Cell Cycle Genes and Related Methods

Description

CROSS REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. provisional application Ser. No. 60/533,036, filed on Dec. 30, 2003, which is specifically incorporated in its entirety herein by reference.

FIELD OF THE INVENTION

The present invention relates generally to the field of plant cell cycle genes and polypeptides encoded by such genes, and the use of such polynucleotide and polypeptide sequences for regulating a plant cell cycle. The invention specifically provides cell cycle polynucleotide and polypeptide sequences isolated from Eucalyptus and Pinus and sequences related thereto.

BACKGROUND OF THE INVENTION

Cell growth and division are controlled by the temporal expression of different sets of genes, allowing the dividing cell to progress through the different phases of the cell cycle. Continued growth and organogesis in plants requires precise function of the cell cycle machinery. Plant development, which is directly affected by cell division rates and patterns, also is influenced by environmental factors, such as temperature, nutrient availability, light, etc. See Gastal and Nelon, Plant Physiol. 105:191-7 (1994), Ben-Haj-Sahal and Tardieu, Plant Physiol. 109:861-7 (1995), and Sacks et al., Plant Physiol. 114:519-27 (1997). Plant development and phenotype are connected with the cell cycle, and altering expression of the genes involved in the cell cycle can be a useful method of modifying plant development and altering plant phenotype.

The ability to alter expression of cell cycle genes is extremely powerful because the cell cycle drives plant development, including growth rates, responses to environmental cues, and resulting plant phenotype. Control of the plant cell cycle and phenotypes associated with alteration of cell cycle gene expression, in the vascular cambium, in particular, has applications for, inter alia, alteration of wood properties and, in particular, lumber and wood pulp properties. For example, improvements to wood pulp that can be effected by altering cell cycle gene expression include increased or decreased lignin and cellulose content, and altered length, diameter, and lumen diameter of cells. Manipulating the plant cell cycle, and in particular the cambium cell cycle (i.e. the rate and angle of cell division), can also engineer better lumber having increased dimensional stability, increased tensile strength, increased shear strength, increased compression strength, increased shock resistance, increased stiffness, increased or decreased hardness, decreased spirality, decreased shrinkage, and desirable characteristics with respect to weight, density, and specific gravity.

A. Cell Cycle Genes and Proteins

1. Cyclin Dependent Protein Kinase

Progression through the cell cycle is regulated primarily by cyclin-dependent kinases (CDKs). CDKs are a conserved family of eukaryotic serine/threonine protein kinases, which require heterodimer formation with a cyclin subunit for activity. For review see, e.g. Joubes et al., Plant Mol. Biol. 43: 607-20 (2000), Stals and Inze, Trends Plant Sci. 6:359-64 (2001), and John et al., Protoplasma 216: 119-42 (2001).

The are five subclasses of CDK's, each having a different cyclin binding consensus sequence. In CDK type A the cyclin binding consensus sequence is PSTAIRE. Id. The cyclin binding consensus sequence in CDK types B-1, B-2, and C are PPTTLRE, PPTALRE, and PITAIRE, respectively. Joubes et al, Plant Physiol, 126: 1403-15 (2001).

Cell cycle progression is directed, in part, by changes in CDK activity. CDK activity is modulated by a number of different cell cycle protein components, such as changes in the abundance of individual cyclins due to changing rates of biosynthesis and proteolysis. Fluctuations in cyclin concentrations result in commensurate fluctuations in CDK activity. Cyclin accumulation is especially important in terminating the G1 phase of the cell cycle because DNA replication is initiated by an increase in CDK activity.

Activation of CDK also requires phosphorylation of a threonine residue within the T-loop of CDK by a CDK-activating kinase (CAK). Umeda et al., Proc. Nat'l Acad. Sci. U.S.A. 97: 13396-400 (2000). It was suggested by Yamaguchi et al., Plant J. 24: 11-20 (2000), that cyclin H is a regulatory subunit of CAK. CDK activity is further regulated by interaction with a CDK regulatory subunit, a small (70-100 AA) protein involved in cell cycle regulation.

A cell must exit the cell cycle in order to commit to differentiation, senescence or apoptosis. This process involves the down-regulation of CDK activities. CDK inhibitors (CKI) are low molecular weight proteins, which are important for cell cycle regulation and development. CKIs bind stoichiometrically to CDK and down-regulate the activity of CDKs.

Many biochemical properties of ICK1, the first plant CKI to be identified from Arabidopsis thaliana, are known. Wang et al., Nature 386:451-2 (1997) Wang et al., Plant J. 24: 613-23 (2000). ICK1 is expressed at low levels in many tissue types, and there can be a threshold level of ICK1 that must be overcome before a cell can enter the cell cycle. Wang et al., Plant J. 24: 613-23 (2000). ICK1 is induced by the plant growth regulator abscisic acid (ABA), which inhibits cell division by blocking DNA replication. When the expression of ICK1 increases, there is a corresponding decrease in Cdc2-like H1 histone activity. ICK1 has been shown to bind in vitro with the cyclins C2c2a and CycD3, and deletion experiments have identified different domain regions for these two interactions.

Altering the expression of CDK regulatory protein or a subunit thereof is known to cause changes in plant phenotype. Overexpression of the Arabidopsis CDK regulatory subunit, CKS1At, resulted in a reduction of leaf size, root growth rates and meristem size. Additionally, overexpression of CKS1At resulted in inhibition of cell-cycle progression, with an extension in the duration of the G1 and G2 phases of the cell cycle.

2. Cyclins

Cyclins are positive regulatory subunits of cyclin-dependent kinase (CDK) enzymes and are required for CDK activity. Fowler et al., Mol. Biotech. 10, 123, 126. Cyclins and CDK complexes provide temporal regulation of transition through the cell cycle. Evidence also suggests that cyclins provide spatial regulation of specific CDK activity, differentially targeting the cytoskeleton, spindle, phragmoplast, nuclear envelope, and chromosomes.

Plant cyclins are classified into five major groups: A, B, C, D, and H. Renaudin et al., Plant Mol. Biol. 32: 1003-18 (1996) and Yamaguchi et al., (supra 2000). Cyclins can be divided into mitotic cyclins (A and B) and G₁ cyclins.

The mitotic cyclins possess a consensus sequence (R-x-x-L-x-x-I-x-N) located at the N-terminal region, termed a destruction box, adjacent to a lysine-rich region. The destruction box and lysine-rich region target the mitotic cyclins for ubiquitin-dependent proteolysis during mitosis. Stals, supra at 361, and Fowler, supra at 126. The destruction box in A versus B cyclins differs slightly and this difference is thought to result in slightly different timing of degradation of A versus B cyclins. Fowler, supra at 126. A-type cyclins accumulate during the S, G2, and early M phase of the cell cycle, whereas B-type cyclins accumulate during the late G2 and early M phase. Mironov et al., Plant Cell 11: 509-22 (1999). Three subgroups of A-type cyclins are known in plants, but only one is known in animals. Cyclin A1 (cycA1;zm;1 from Zea cans) is most concentrated during cytokinesis at the microtubule-containing phragmoplast. Expression of cyclin A2 is upregulated by auxins in roots, and by cytokinins in the shoot apex. Abrahams et al., Biochim. Biophys. Acta 28: 1-2 (2001).

D-type cyclins, of which five subgroups are known, are thought to control the progression through the G1 phase in response to growth factors and nutrients. Riou-Khamlichi et al., Mol. Cell Biol. 20: 4513-21 (2000). For example, the expression of D-type cyclins is upregulated by sucrose as shown by an increase in cycD2 mRNA 30 minutes after sucrose exposure, and an increase in cycD3 four hours after sucrose exposure. This timing corresponds to early G1-phase and late G1-phase, respectively. Cockcroft et al., Nature 405: 575-9 (2000). Furthermore, in Arabidopsis, a D3 cyclin was shown to be upregulated by the brassinosteroid, epi-brassinolide.

Cyclin D2 proteins bind with CDKA to produce an active complex, which binds to and phosphorylates retinoblastoma-related protein (Rb). This process is found in actively proliferating tissue, suggesting it plays an important function during late G1- and early S-phase. Three different D3-type cyclins are active during tomato fruit development. These proteins all contain a retinoblastoma binding motif and a PEST-destruction motif. There are differences in the spatial and temporal expression of these D3 cyclins, inferring different roles during fruit development.

Overexpression of cyclin D was shown to increase overall growth rate. Over-expression of cyclin D2 in tobacco increases causes shortening the G1-phase which producing a faster rate of cell cycling.

C- and H-type cyclins were characterized in poplar (Populus tremula×tremuloides) and rice (Oryza sativa) but their exact function is still unclear. Putative cyclins with a lesser degree of peptide sequence conservation have also been identified. For example, Arabidopsis CycJ18 has only 20% identity with homologues over the cyclin box domain. CycJ18 is expressed predominantly in young seedlings. Arabidopsis F3O9.13 protein also has similarity to the cyclin family.

3. Histone Acetyltransferase/Deacetyltransferase

Histone acetyltransferase (HA) and histone deacetyltransferase (HAD) control the net level of acetylation of histones. Histone acetylation and deacetylation are thought to exert their regulatory effects on gene expression by altering the accessibility of nucleosomal DNA to DNA-binding transcriptional activators, other chromatin-modifying enzymes or multi-subunit chromatin remodeling complexes capable of displacing nucleosomes. Lusser et al., Nucleic Acids Res. 27: 4427-35 (1999). Therefore, in general, the HDAs are involved in the repression of gene expression, while HAs are correlated with gene activation.

HA effects acetylation at the ε-amino group of conserved lysine residues clustered near the amino terminus of core histones which up-regulates gene expression.

HDAs remove acetyl groups from the core histones of the nucleosome. There are numerous family members in the HDA group, many of which are conserved throughout evolution. Lechner et al., Biochim Biophys Acta 5:181-8 (1996). HDAs function as part of multi-protein complexes facilitating chromatin condensation.

HDAs and HAs recognize highly distinct acetylation patterns on the nucleosome. It is thought that different types of HDAs interact with specific regions of the genome, to influence gene silencing.

Schultz et al., Genes Dev. 15: 428-43 (2001), demonstrated that the superfamily of Kruppel-associated-box zinc finger proteins (KRAB-ZFPs) are linked to the nucleosome remodeling and histone deacetylation complex via the PHD (plant homeodomain) and bromodomains of co-repressor KAP-1, to form a cooperative unit that is required for transcriptional repression. A maize HDAC (HD2) has been identified that has no sequence homology to other eukaryotic HDACs, but instead contains sequence similarity to peptidyl-prolyl cis-trans isomerases (PPIases).

The effects of interfering with histone deacetylation are discussed in e.g. Tian and Chen, Proc. Nat'l Acad. Sci. USA 98: 200-5 (2001).

4. Peptidyl Prolyl Cis-Trans Isomerase

Peptidylprolyl isomerases (e.g., peptidylprolyl cis-trans isomerase, peptidyl-prolyl cis-trans isomerase, PPIase, rotamase, cyclophilin) catalyze the interconversion of peptide bonds between the cis and trans conformations at proline residues. Sheldon and Venis, Biochem J. 315: 965-70 (1996). This interconversion is thought to be the rate limiting step of protein folding. PPIases belong to a conserved family of proteins that are present in animals, fungi, bacteria and plants. PPIases are implicated in a number of responses including the response to environmental stress, calcium signals, transcriptional repression, cell cycle control, etc. Viaud, et al., Plant Cell 14: 917-30 (2002).

5. Retinoblastoma-Related Protein

Retinoblastoma (Rb)-related protein putatively regulates progression of the cell cycle through the G1 phase and into S phase. Xie et al., EMBO J. 15: 4900-8 (1996) and Ach et al., Mol. Cell Biol. 17: 5077-86 (1997).

Although Rb is well-characterized in mammalian systems, the role of Rb-related proteins in regulation of G1 phase progression and S phase entry is not well characterized in plants. It is known, however, that RB-related protein functions through its association with various other cellular proteins involved in cell cycle regulation, such as the cyclins, WD40 proteins, Soni et al., Plant. Cell. 7:85-103 (1995); Grafi et al., Proc. Natl. Acad. Sci. U.S.A. 93:8962 (1996); Ach et al., Plant Cell 9:1595-606 (1997); Umen and Goodenough, Genes Dev. 15:1652-61 (2001); Mariconti et al., J. Biol. Chem. 277:9911-9 (2002).

6. WD40 Repeat Protein

WD40 is a common repeating motif involved in many different protein-protein interactions. The WD40 domain is found in proteins having a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly. Goh et al., Eur. J. Biochem. 267: 434-49 (2000).

The WD40 domain, which is 40 residues long, typically contains a GH dipeptide 11-24 residues from the N-terminus and the WD dipeptide at the C-terminus. Id. Between the GH dipeptide and the WD dipeptide lies a conserved core which serves as a stable platform where proteins can bind either stably or reversibly. The core forms a propeller-like structure with several blades. Each blade is composed of a four-stranded anti-parallel β-sheet. Each WD40 sequence repeat forms the first three strands of one blade and the last strand in the next blade. The last C-terminal WD40 repeat completes the blade structure of the first WD40 repeat to create the closed ring propeller-structure. The residues on the top and bottom surface of the propeller are proposed to coordinate interactions with other proteins and/or small ligands.

Studies in yeast demonstrated that Cdc20, which contains the WD40 motif, is required for the proteolysis of mitotic cyclins. This process is mediated by an ubiquitin-protein ligase called anaphase-promoting complex (APC) or cyclosome. Following ubiquitination and proteolysis by the 26S proteasome, the cell can segregate chromosomes, and exit from mitosis. Cdc20 also contains a destruction-box domain.

7. WEE1-Like Protein

WEE1 controls the activity of cyclin-dependent kinases. WEE1 itself is a serine/threonine kinase. Sorrell et al., Planta 215: 518-22 (2002). The enzymatic activity of these protein kinases is controlled by phosphorylation of specific residues in the activation segment of the catalytic domain, sometimes combined with reversible conformational changes in the C-terminal autoregulatory tail. This process is conserved among eukaryotes, from fungi to animals and plants. Similarly, there is a high degree of homology between WEE1 proteins from various organisms. For example, there is 50% identity between the protein kinase domains of the human and maize WEE1 proteins.

Expression of WEE1 is shown to occur only in actively dividing tissues and is believed to inhibit cell division by acting as a negative regulator of mitosis. WEE1 is believed to prevent entry from G2 to M by protecting the nucleus from cytoplasmically-activated cyclin B1-complexed CDC2 before the onset of mitosis. For example, over-expression of AtWEE1 (from Arabidopsis) and ZmWEE1 (from Zea cans) in fission yeast inhibits cell division which results in elongated cells. Sun et al., Proc. Nat'l Acad. Sci. USA 96: 4180-5 (1999).

B. Expression Profiling and Microarray Analysis in Plant Development

The multigenic control of plant phenotype presents difficulties in determining the genes responsible for phenotypic determination. One major obstacle to identifying genes and gene expression differences that contribute to phenotype in plants is the difficulty with which the expression of more than a handful of genes can be studied concurrently. Another difficulty in identifying and understanding gene expression and the interrelationship of the genes that contribute to plant phenotype is the high degree of sensitivity to environmental factors that plants demonstrate.

There have been recent advances using genome-wide expression profiling. In particular, the use of DNA microarrays has been useful to examine the expression of a large number of genes in a single experiment. Several studies of plant gene responses to developmental and environmental stimuli have been conducted using expression profiling. For example, microarray analysis was employed to study gene expression during fruit ripening in strawberry, Aharoni et al., Plant Physiol. 129:1019-1031 (2002), wound response in Arabodopsis, Cheong et al., Plant Physiol. 129:661-7 (2002), pathogen response in Arabodopsis, Schenk et al., Proc. Nat'l Acad. Sci. 97:11655-60 (2000), and auxin response in soybean, Thibaud-Nissen et al., Plant Physiol. 132:118. Whetten et al., Plant Mol. Biol. 47:275-91 (2001) discloses expression profiling of cell wall biosynthetic genes in Pinus taeda L. using cDNA probes. Whetten et al. examined genes which were differentially expressed between differentiating juvenile and mature secondary xylem. Additionally, to determine the effect of certain environmental stimuli on gene expression, gene expression in compression wood was compared to normal wood. 156 of the 2300 elements examined showed differential expression. Whetten, supra at 285. Comparison of juvenile wood to mature wood showed 188 elements as differentially expressed. Id. at 286.

Although expression profiling and, in particular, DNA microarrays provide a convenient tool for genome-wide expression analysis, their use has been limited to organisms for which the complete genome sequence or a large cDNA collection is available. See Hertzberg et al., Proc. Nat'l Acad. Sci. 98:14732-7 (2001a), Hertzberg et al., Plant J., 25:585 (2001b). For example, Whetten, supra, states, “A more complete analysis of this interesting question awaits the completion of a larger set of both pine and poplar ESTs.” Whetten et al. at 286. Furthermore, microarrays comprising cDNA or EST probes may not be able to distinguish genes of the same family because of sequence similarities among the genes. That is, cDNAs or ESTs, when used as microarray probes, may bind to more than one gene of the same family.

Methods of manipulating gene expression to yield a plant with a more desirable phenotype would be facilitated by a better understanding of cell cycle gene expression in various types of plant tissue, at different stages of plant development, and upon stimulation by different environmental cues. The ability to control plant architecture and agronomically important traits would be improved by a better understanding of how cell cycle gene expression effects formation of plant tissues, how cell cycle gene expression causes plant cells to enter or exit cell division, and how plant growth and the cell cycle are connected. Among the large number of genes, the expression of which can change during development of a plant, only a fraction are likely to effect phenotypic changes during any given stage of the plant development.

SUMMARY

Accordingly, there is a need for tools and methods useful in determining the changes in the expression of cell cycle genes that occur during the plant cell cycle. There is also a need for polynucleotides useful in such methods. There is a further need for methods which can correlate changes in cell cycle gene expression to phenotype or stage of plant development. There is a further need for methods of identifying cell cycle genes and gene products that impact plant phenotype, and that can be manipulated to obtain a desired phenotype.

In one aspect, the present invention provides an isolated polynucleotide comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof.

In another aspect, the present invention provides a DNA construct comprising at least one polynucleotide having the sequence of any one of SEQ ID NOs: 1-237 and conservative variants thereof.

Another aspect of the invention is a plant cell transformed with a DNA construct of comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof.

A further aspect of the invention is a transgenic plant comprising a plant cell transformed with a DNA construct comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof.

Another aspect of the invention is an isolated polynucleotide comprising a sequence encoding the catalytic or substrate-binding domain of a polypeptide selected from of any one of SEQ ID NOs: 261-497, wherein the polynucleotide encodes a polypeptide having the activity of said polypeptide selected from any one of SEQ ID NOs: 261-497.

A further aspect of the invention is a method of making a transformed plant comprising transforming a plant cell with a DNA construct comprising at least one polynucleotide having the sequence of any of SEQ ID NOs: 1-237; and culturing the transformed plant cell under conditions that promote growth of a plant.

In another aspect, the invention provides a wood obtained from a transgenic tree.

In a further aspect, the invention provides a wood pulp obtained from a transgenic tree which has been transformed with the DNA construct of the invention.

Another aspect of the invention is a method of making wood, comprising transforming a plant with a DNA construct comprising a polynucleotide having a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof; culturing the transformed plant under conditions that promote growth of a plant; and obtaining wood from the plant.

The invention further provides a method of making wood pulp, comprising transforming a plant with a DNA construct comprising a polynucleotide having a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof; culturing the transformed plant under conditions that promote growth of a plant; and obtaining wood pulp from the plant.

In another aspect, the invention provides an isolated polypeptide comprising an amino acid sequence encoded by the isolated polynucleotide comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof.

The invention also provides, an isolated polypeptide comprising an amino acid sequence selected from the group consisting of 261-497.

The invention further provides a method of altering a plant phenotype of a plant, comprising altering expression in the plant of a polypeptide encoded by any one of SEQ ID NOs: 1-237.

In another aspect, the invention provides a polynucleotide comprising a nucleic acid selected from the group comprising of SEQ ID NOs: 471-697.

An aspect of the invention is a method of correlating gene expression in two different samples, comprising detecting a level of expression of one or more genes encoding a product encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof in a first sample; detecting a level of expression of the one or more genes in a second sample; comparing the level of expression of the one or more genes in the first sample to the level of expression of the one or more genes in the second sample; and correlating a difference in expression level of the one or more genes between the first and second samples.

A further aspect of the invention is a method of correlating the possession of a plant phenotype to the level of gene expression in the plant of one or more genes comprising detecting a level of expression of one or more genes encoding a product encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof in a first plant possessing a phenotype; detecting a level of expression of the one or more genes in a second plant lacking the phenotype; comparing the level of expression of the one or more genes in the first plant to the level of expression of the one or more genes in the second plant; and correlating a difference in expression level of the one or more genes between the first and second plants to possession of the phenotype.

In a further aspect, the invention provides a method of correlating gene expression to a stage of the cell cycle, comprising detecting a level of expression of one or more genes encoding a product encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 and conservative variants thereof in a first plant cell in a first stage of the cell cycle; detecting a level of expression of the one or more genes in a second plant cell in a second, different stage of the cell cycle; comparing the level of the expression of the one or more genes in the first plant cells to the level of expression of the one or more genes in the second plants cells; and correlating a difference in expression level of the one or more genes between the first and second samples to the first or second stage of the cell cycle.

An aspect of the invention is a combination for detecting expression of one or more genes, comprising two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237.

Another aspect of the invention is a combination for detecting expression of one or more genes, comprising two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a nucleic acid sequence encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237.

The invention further provides a microarray comprising a combination for detecting expression of one or more genes, comprising two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 or wherein each oligonucleotide is capable of hybridizing to a nucleic acid sequence encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237, wherein each of said two or more oligonucleotides occupies a unique location on said solid support.

In another aspect, the invention provides a method for detecting one or more genes in a sample, comprising contacting the sample with two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a gene comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 under standard hybridization conditions; and detecting the one or more genes of interest which are hybridized to the one or more oligonucleotides.

The invention also provides a method for detecting one or more nucleic acid sequences encoded by one or more genes in a sample, comprising contacting the sample with two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a nucleic acid sequence encoded by a gene comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-237 under standard hybridization conditions; and detecting the one or more nucleic acid sequences which are hybridized to the one or more oligonucleotides.

The invention further provides a kit for detecting gene expression comprising the microarray of the invention together with one or more buffers or reagents for a nucleotide hybridization reaction.

Other features, objects, and advantages of the present invention are apparent from the detailed description that follows. It should be understood, however, that the detailed description, while indicating preferred embodiments of the invention, are given by way of illustration only, not limitation. Various changes and modifications within the spirit and scope of the invention will be apparent to those skilled in the art from the detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1: Exemplary microarray sampling parameters.

FIG. 2: Plasmid map for pWVK202.

FIG. 3: Plasmid map for pGrowth14.

FIG. 4: Plasmid map for pGrowth15.

FIG. 5: Plasmid map for pGrowth16.

FIG. 6: Plasmid map for pGrowth18.

FIG. 7: Plasmid map for pGrowth19.

FIG. 8: Plasmid map for pGrowth20.

LIST OF TABLES

Table 1: shows genes having greater than doubled signal with any one sample as compared to the mean signal of the other three samples.

Table 2: identifies plasmid(s), genes, and Genesis ID numbers for constructs described in Example 17.

Table 3: Rooting medium for Populus deltoids.

Table 4: pGrowth information.

Table 5: shows genes having greater than doubled signal with any one sample as compared to the mean signal of the other three samples.

Table 6: Differentially expressed cDNAs.

Table 7: Consensus ID information.

Table 8: pGrowth information.

Table 9: Eucalyptus grandis cell cycle genes and proteins.

Table 10: Pinus radiata cell cycle genes and proteins.

Table 11: Annotated peptide sequences of the present invention.

Table 12: Eucalyptus in silico data.

Table 13: Pine in silico data.

Table 14: Oligo table.

Table 15: Peptide table.

Table 16: BLAST sequence alignment table.

DETAILED DESCRIPTION

The inventors have discovered novel isolated cell cycle genes and polynucleotides useful for identifying the multigenic factors that contribute to a phenotype and for manipulating gene expression to affect a plant phenotype. These genes, which are derived from plants of commercially important forestry genera, pine and eucalyptus, are involved in the plant cell cycle and are, at least in part, responsible for expression of phenotypic characteristics important in commercial wood, such as stiffness, strength, density, fiber dimensions, coarseness, cellulose and lignin content, and extractives content. Generally speaking, the genes and polynucleotides encode a protein which can be a cyclin, cyclin dependent kinase, cyclin dependent kinase inhibitor, histone acetyltransferase, histone deacetylase, peptidyl-prolyl cis-trans isomerase, retinoblastoma-related protein, WEE1-like protein, or WD40 repeat protein, or a catalytic domain thereof, or a polypeptide having the same function, and the invention further includes such proteins and polypeptides.

The methods of the present invention for selecting cell cycle gene sequences to target for manipulation will permit better design and control of transgenic plants with more highly engineered phenotypes. The ability to control plant architecture and agronomically important traits in commercially important forestry species will be improved by the information obtained from the methods, such as which genes affect which phenotypes, which genes affect entry into which stage of the cell cycle, which genes are active in which stage of plant development, and which genes are expressed in which tissue at a given point in the cell cycle or plant development.

Unless indicated otherwise, all technical and scientific terms are used herein in a manner that conforms to common technical usage. Generally, the nomenclature of this description and the described laboratory procedures, including cell culture, molecular genetics, and nucleic acid chemistry and hybridization, respectively, are well known and commonly employed in the art. Standard techniques are used for recombinant nucleic acid methods, oligonucleotide synthesis, cell culture, tissue culture, transformation, transfection, transduction, analytical chemistry, organic synthetic chemistry, chemical syntheses, chemical analysis, and pharmaceutical formulation and delivery. Generally, enzymatic reactions and purification and/or isolation steps are performed according to the manufacturers' specifications. Absent an indication to the contrary, the techniques and procedures in question are performed according to conventional methodology disclosed, for example, in Sambrook et al., MOLECULAR CLONING A LABORATORY MANUAL, 2d ed. (Cold Spring Harbor Laboratory Press, 1989), and CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons, 1989). Specific scientific methods relevant to the present invention are discussed in more detail below. However, this discussion is provided as an example only, and does not limit the manner in which the methods of the invention can be carried out.

A. Plant Cell Cycle Genes and Proteins

1. Cell Cycle Genes, Polynucleotide and Polypeptide Sequences

One aspect of the present invention relates to novel plant cell cycle genes and polypeptides encoded by such genes. As used herein, the term “plant cell cycle genes” refers to genes encoding proteins that function during the plant cell cycle, and the term “plant cell cycle proteins” refers to proteins that function during the plant cell cycle. There are several known families of plant cell cycle proteins, including cyclin, cyclin dependent kinase, cyclin dependent kinase inhibitor, histone acetyltransferase, histone deacetylase, peptidyl-prolyl cis-trans isomerase, retinoblastoma-related protein, WEE1-like protein, and WD40 repeat protein. Although there is significant sequence homology within each gene and protein family, each member of each family can display different biochemical properties and altering the expression of at least one of these genes can result in a different plant phenotype.

The present invention provides novel plant cell cycle genes and polynucleotides and novel cell cycle proteins and polypeptides. In accordance with one embodiment of the invention, the novel plant cell cycle genes are the same as those expressed in a wild-type plant of a species of Pinus or Eucalyptus. Exemplary novel plant cell cycle gene sequences of the invention are set forth in Tables 9 and 10, which depict Eucalyptus grandis sequences and Pinus radiata sequences, respectively. Corresponding gene products, i.e., oligonucleotides and polypeptides, are also listed in Tables 14, 15, and 16. The Sequence Listing in APPENDIX 1 provides the sequences of these aspects of the invention.

The sequences of the invention have cell cycle activity and encode proteins that are active in the cell cycle, such as proteins of the cell cycle families discussed above. As discussed in more detail below, manipulation of the expression of the cell cycle genes and polynucleotides, or manipulation of the activity of the encoded proteins and polypeptides, can result in a transgenic plant with a desired phenotype that differs from the phenotype of a wild-type plant of the same species.

Throughout this description, reference is made to cell cycle gene products. As used herein, a “cell cycle gene product” is a product encoded by a cell cycle gene, and includes both nucleotide products, such as RNA, and amino acid products, such as proteins and polypeptides. Examples of specific cell cycle genes of the invention include SEQ ID NOs: 1-237. Examples of specific cell cycle gene products of the invention include products encoded by any one of SEQ ID NOs: 1-237. Reference also is made herein to cell cycle proteins and cell cycle polypeptides. Examples of specific cell cycle proteins and polypeptides of the invention include polypeptides encoded by any of SEQ ID NOs: 1-237 or polypeptides comprising the amino acid sequence of any of SEQ ID NOs: 261-497. One aspect of the invention is directed to a subset of these cell cycle genes and cell cycle gene products, namely SEQ ID NOs: 1-12, 14-58, 60-62, 64-70, 72-75, 77-83, 85-86, 88-91, 93-119, 121-130, 132-148, 150-156, 158-191, 193-207, 209-218, 220-221, 223-231, 233-237, their respective conservative variants (as that term is defined below), and the nucleotide and amino acid products encoded thereby. Another aspect of the invention is directed to a subset of the cell cycle genes and cell cycle gene products, namely SEQ ID NOs: 1-12, 14, 16-26, 30-37, 40-41, 43-76, 78-103, 106, 108-113, 116-121, 124-125, 128-147, 150-152, 154-155, 161-162, 164-172, 174, 177-183, 185-191, 193-197, 200-204, 208-213, and 215-234 their respective conservative variants, and the nucleotide and amino acid products encoded thereby. A further aspect of the invention is directed to a subset of the cell cycle genes and cell cycle gene products, namely SEQ ID NOs: 1-12, 14, 16-26, 30-37, 40-41, 43-58, 60-62, 64-70, 72-75, 78-83, 85-86, 88-91, 93-103, 106, 108-113, 116-119, 121, 124-125, 128-130, 132-147, 150-152, 154-155, 161-162, 164-172, 174, 177-183, 185-191, 193-197, 200-204, 209-213, 215-218, 220-221, 223-231, and 233-234 their respective conservative variants, and the nucleotide and amino acid products encoded thereby.

The present invention also includes sequences that are complements, reverse sequences, or reverse complements to the nucleotide sequences disclosed herein.

The present invention also includes conservative variants of the sequences disclosed herein. The term “variant,” as used herein, refers to a nucleotide or amino acid sequence that differs in one or more nucleotide bases or amino acid residues from the reference sequence of which it is a variant.

Thus, in one aspect, the invention includes conservative variant polynucleotides. As used herein, the term “conservative variant polynucleotide” refers to a polynucleotide that hybridizes under stringent conditions to an oligonucleotide probe that, under comparable conditions, binds to the reference gene the conservative variant is a variant of. Thus, for example, a conservative variant of SEQ ID NO: 1 hybridizes under stringent conditions to an oligonucleotide probe that, under comparable conditions, binds to SEQ ID NO: 1. One aspect of the invention provides conservative variant polynucleotides that exhibit at least about 75% sequence identity to their respective reference sequences.

“Sequence identity” has an art-recognized meaning and can be calculated using published techniques. See COMPUTATIONAL MOLECULAR BIOLOGY, Lesk, ed. (Oxford University Press, 1988), BIOCOMPUTING: INFORMATICS AND GENOME PROJECTS, Smith, ed. (Academic Press, 1993), COMPUTER ANALYSIS OF SEQUENCE DATA, PART I, Griffin & Griffin, eds., (Humana Press, 1994), SEQUENCE ANALYSIS IN MOLECULAR BIOLOGY, Von Heinje ed., Academic Press (1987), SEQUENCE ANALYSIS PRIMER, Gribskov & Devereux, eds. (Macmillan Stockton Press, 1991), and Carillo & Lipton, SIAM J. Applied Math. 48: 1073 (1988). Methods commonly employed to determine identity or similarity between two sequences include but are not limited to those disclosed in GUIDE TO HUGE COMPUTERS, Bishop, ed., (Academic Press, 1994) and Carillo & Lipton, supra. Methods to determine identity and similarity are codified in computer programs. Preferred computer program methods to determine identity and similarity between two sequences include but are not limited to the GCG program package (Devereux et al., Nucleic Acids Research 12: 387 (1984)), BLASTP, BLASTN, FASTA (Atschul et al., J. Mol. Biol. 215: 403 (1990)), and FASTDB (Brutlag et al., Comp. App. Biosci. 6: 237 (1990)).

The invention includes conservative variant polynucleotides having a sequence identity that is greater than or equal to 99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%, 91%, 90%, 89%, 88%, 87%, 86%, 85%, 84%, 83%, 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75%, 74%, 73%, 72%, 71%, 70%, 69%, 68%, 67%, 66%, 65%, 64%, 63%, 62%, 61%, or 60% to any one of SEQ ID NOs: 1 to 237. In such variants, differences between the variant and the reference sequence can occur at the 5′ or 3′ terminal positions of the reference nucleotide sequence or anywhere between those terminal positions, interspersed either individually among nucleotides in the reference sequence or in one or more contiguous groups within the reference sequence.

Additional conservative variant polynucleotides contemplated by and encompassed within the present invention include polynucleotides comprising sequences that differ from the polynucleotide sequences of SEQ ID NO: 1-237, or complements, reverse complements or reverse sequences thereof, as a result of deletions and/or insertions totaling less than 10% of the total sequence length.

The invention also includes conservative variant polynucleotides that, in addition to sharing a high degree of similarity in their primary structure (sequence) to SEQ ID NOs: 1 to 237, have at least one of the following features: (i) they contain an open reading frame or partial open reading frame encoding a polypeptide having substantially the same functional properties in the cell cycle as the polypeptide encoded by the reference polynucleotide, or (ii) they have nucleotide domains or encoded protein domains in common. The invention includes conservative variants of SEQ ID NOs: 1-237 that encode proteins having the enzyme or biological activity or binding properties of the protein encoded by the reference polynucleotide. Such conservative variants are functional variants, in that they have the enzymatic or binding activity of the protein encoded by the reference polynucleotide.

In accordance with the invention, polynucleotide variants can include a “shuffled gene” such as those described in e.g. U.S. Pat. Nos. 6,500,639, 6,500,617 6,436,675, 6,379,964, 6,352,859 6,335,198 6,326,204, and 6,287,862. A variant of a nucleotide sequence of the present invention also can be a polynucleotide modified as disclosed in U.S. Pat. No. 6,132,970, which is incorporated herein by reference.

In accordance with one embodiment, the invention provides a polynucleotide that encodes a cell cycle protein from one of the following families: cyclin, cyclin dependent kinase, cyclin dependent kinase inhibitor, histone acetyltransferase, histone deacetylase, peptidyl-prolyl cis-trans isomerase, retinoblastoma-related protein, WEE1-like protein, or WD40 repeat protein. SEQ ID NOs: 1-237 provide examples of such polynucleotides.

In accordance with another embodiment, a polynucelotide of the invention encodes the catalytic or protein binding domain of a polypeptide encoded by any of SEQ ID NOs: 1-237 or of a polypeptide comprising any of SEQ ID NOs: 261-497. The catalytic and protein binding domains of the cell cycle proteins of the invention are known in the art. The conserved sequences of these proteins are shown in Entries 1-195 as underlined, bold, and/or italicized text.

The invention also encompasses as conservative variants polynucleotides that differ from the sequences discussed above but that, as a consequence of the degeneracy of the genetic code, encode a polypeptide which is the same as that encoded by a polynucleotide of the present invention. The invention also includes as conservative variants polynucleotides comprising sequences that differ from the polynucleotide sequences discussed above as a result of substitutions that do not affect the amino acid sequence of the encoded polypeptide sequence, or that result in conservative substitutions in the encoded polypeptide sequence.

The present invention also includes an isolated polypeptide encoded by a polynucleotide comprising any of SEQ ID NOs: 1-237 or any of the conservative variants thereof discussed above. The invention also includes polypeptides comprising SEQ ID NOs: 261-497 and 495-497 and conservative variants of these polypeptides. Another aspect of the invention include polypeptides comprising SEQ ID NOs: 261-272, 274-318, 320-322, 324-330, 332-335, 337-343, 345-346, 348-351, 353-379, 381-390, 392-408, 410-416, 418-451, 453-467, 469-478, 480-481, 483-491, and 493-494 and conservative variants thereof. A further aspect of the invention includes polypeptides comprising SEQ ID NOs: 261-272, 274, 276-286, 289, 290-297, 300-301, 303-345, 347-363, 366, 368-373, 376-381, 384-385, 388-407, 410-412, 414-415, 420-422, 424-432, 434, 437-443, 445-451, 453-457, 460-464, 468-473, and 475-494 and conservative variants thereof. Another aspect of the invention includes polypeptides comprising SEQ ID NOs: 261-272, 274, 276-286, 290-297, 300-301, 303-318, 320-322, 324-330, 332-335, 337-343, 345, 348-351, 353-363, 366, 368-373, 376-381, 384-385, 388-390, 392-407, 410-412, 414-415, 421-422, 424-432, 434, 437-443, 445-451, 453-457, 460-464, 469-473, 475-478, 480-481, 483-491, and 493-494 and conservative variants thereof.

In accordance with the invention, a variant polypeptide or protein refers to an amino acid sequence that is altered by the addition, deletion or substitution of one or more amino acids.

The invention includes conservative variant polypeptides. As used herein, the term “conservative variant polypeptide” refers to a polypeptide that has similar structural, chemical or biological properties to the protein it is a conservative variant of. Guidance in determining which amino acid residues can be substituted, inserted, or deleted can be found using computer programs well known in the art such as Vector NTI Suite (InforMax, MD) software. In one embodiment of the invention, conservative variant polypeptides that exhibit at least about 75% sequence identity to their respective reference sequences.

Conservative variant protein includes an “isoform” or “analog” of the polypeptide. Polypeptide isoforms and analogs refers to proteins having the same physical and physiological properties and the same biological function, but whose amino acid sequences differs by one or more amino acids or whose sequence includes a non-natural amino acid.

Polypeptides comprising sequences that differ from the polypeptide sequences of SEQ ID NO: 261-497 as a result of amino acid substitutions, insertions, and/or deletions totaling less than 10% of the total sequence length are contemplated by and encompassed within the present invention.

One aspect of the invention provides conservative variant polypeptides that have the same function in the cell cycle as the proteins of which they are variants, as determined by one or more appropriate assays, such as those described below. The invention includes variant polypeptides that function as cell cycle proteins, such as those having the biological activity of cyclin, cyclin dependent kinase, cyclin dependent kinase inhibitor, histone acetyltransferase, histone deacetylase, peptidyl-prolyl cis-trans isomerase, retinoblastoma-related protein, WEE1-like protein, and WD40 repeat protein, and are thus capable of modulating the cell cycle in a plant. As discussed above, the invention includes variant polynucleotides that encode polypeptides that function as cell cycle proteins.

The activities and physical properties of cell cycle proteins can be examined using any method known in the art. The following examples of assay methods are not exhaustive and are included to provide some guidance in examining the activity and distinguishing protein characteristics of cell cycle protein variants.

CDK activity can be assessed using roscovitine as described in Yamaguchi et al., Proc. Natl. Acad. Sci. U.S.A. 100:8019 (2003). CDK histone kinase activity can be assayed using autoradiography to detect histone H1 phosphorylation by CDK as described in Joubés et al., Plant Physiol. 121:857 (1999).

CKI activity can be assayed using a variation of the method described in Zhou et al., Planta. 6:604 (2003). The modified method can employ co-transformation or subsequent transformations to identify the interaction of CKI and cyclins in vivo. For example, in the first transformation pine tissue can be transformed using the method described in U.S. Patent Application Publication No. 2002/0100083 using geneticin selection to obtain transgenic plants possessing cycD3 and cdc2a homologs. The second transformation can be performed using alpha-methyltryptophan as a selectable marker to obtain transformants having an ICK1 homologue as described in U.S. Provisional Application No. 60/476,189. Tissue capable of growing on both on geneticin and on alpha-methyltryptophan contains the ICK1 homologue and the cycD3 and cdc2a homologues. The CKI activity is determined by comparison of the phenotype of transformants having the cycD3 and cdc2a homologues to the transformants having ICK1 homologue and the cycD3 and cdc2a homologs.

Histone deacetylase activity can be assessed by complementation of the Arabidopsis mutants described in Tian et al., Genetics 165:399 (2003). Histone acetyltransferase activity can be assayed using anacardic acid as described in Balasubramanyam et al., J. Biol. Chem. 278:19134 (2003). Histone acetyltransferase also can be assayed using trichostatin A-treated plant lines as is described in Bhat et al., Plant J. 33:455 (2003). The plant lines described in Bhat et al., supra, also can be used to assay retinoblastoma-related proteins using the co-precipitation method described in Rossi et al., Plant Mol. Biol. 51:401 (2003).

Peptidyl-prolyl isomerase can be assayed as described in Edvardsson et al., FEBS Lett. 542:137 (2003). WD40 proteins can be evaluated based on the possession of the WD40 motif as well as their ability to interact with cdc2. WEE-1 can be assayed using any kinase activity assay known in the art.

2. Methods of Using Cell Cycle Genes, Polynucleotide and Polypeptide Sequences

The present invention provides methods of using plant cell cycle genes and conservative variants thereof. The invention includes methods and constructs for altering expression of plant cell cycle genes and/or gene products for purposes including, but not limited to (i) investigating function during the cell cycle and ultimate effect on plant phenotype and (ii) to effect a change in plant phenotype. For example, the invention includes methods and tools for modifying wood quality, fiber development, cell wall polysaccharide content, fruit ripening, and plant growth and yield by altering expression of one or more plant cell cycle genes.

The invention comprises methods of altering the expression of any of the cell cycle genes and variants discussed above. Thus, for example, the invention comprises altering expression of a cell cycle gene present in the genome of a wild-type plant of a species of Eucalyptus or Pinus. In one embodiment, the cell cycle gene comprises a nucleotide sequence selected from SEQ ID NOs: 1-237, from the subset thereof comprising SEQ ID NOs: SEQ ID NOs: 1-12, 14-58, 60-62, 64-70, 72-75, 77-83, 85-86, 88-91, 93-119, 121-130, 132-148, 150-156, 158-191, 193-207, 209-218, 220-221, 223-231, and 233-237, from the subset thereof comprising SEQ ID NOs: 1-12, 14, 16-26, 30-37, 40-41, 43-76, 78-103, 106, 108-113, 116-121, 124-125, 128-147, 150-152, 154-155, 161-162, 164-172, 174, 177-183, 185-191, 193-197, 200-204, 208-213, and 215-234, from the subset thereof comprising SEQ ID NOs: 1-12, 14, 16-26, 30-37, 40-41, 43-58, 60-62, 64-70, 72-75, 78-83, 85-86, 88-91, 93-103, 106, 108-113, 116-119, 121, 124-125, 128-130, 132-147, 150-152, 154-155, 161-162, 164-172, 174, 177-183, 185-191, 193-197, 200-204, 209-213, 215-218, 220-221, 223-231, and 233-234, or the conservative variants thereof, as discussed above.

Techniques which can be employed in accordance with the present invention to alter gene expression, include, but are not limited to: (i) over-expressing a gene product, (ii) disrupting a gene's transcript, such as disrupting a gene's mRNA transcript; (iii) disrupting the function of a polypeptide encoded by a gene, or (iv) disrupting the gene itself Over-expression of a gene product, the use of antisense RNAs, ribozymes, and the use of double-stranded RNA interference (dsRNAi) are valuable techniques for discovering the functional effects of a gene and for generating plants with a phenotype that is different from a wild-type plant of the same species.

Over-expression of a target gene often is accomplished by cloning the gene or cDNA into an expression vector and introducing the vector into recipient cells. Alternatively, over-expression can be accomplished by introducing exogenous promoters into cells to drive expression of genes residing in the genome. The effect of over-expression of a given gene on cell function, biochemical and/or physiological properties can then be evaluated by comparing plants transformed to over-express the gene to plants that have not been transformed to over-express the gene.

Antisense RNA, ribozyme, and dsRNAi technologies typically target RNA transcripts of genes, usually mRNA. Antisense RNA technology involves expressing in, or introducing into, a cell an RNA molecule (or RNA derivative) that is complementary to, or antisense to, sequences found in a particular mRNA in a cell. By associating with the mRNA, the antisense RNA can inhibit translation of the encoded gene product. The use of antisense technology to reduce or inhibit the expression of specific plant genes has been described, for example in European Patent Publication No. 271988, Smith et al., Nature, 334:724-726 (1988); Smith et. al., Plant Mol. Biol., 14:369-379 (1990)).

A ribozyme is an RNA that has both a catalytic domain and a sequence that is complementary to a particular mRNA. The ribozyme functions by associating with the mRNA (through the complementary domain of the ribozyme) and then cleaving (degrading) the message using the catalytic domain.

RNA interference (RNAi) involves a post-transcriptional gene silencing (PTGS) regulatory process, in which the steady-state level of a specific mRNA is reduced by sequence-specific degradation of the transcribed, usually fully processed mRNA without an alteration in the rate of de novo transcription of the target gene itself. The RNAi technique is discussed, for example, in Elibashir, et al., Methods Enzymol. 26: 199 (2002); McManus & Sharp, Nature Rev. Genetics 3: 737 (2002); PCT application WO 01/75164; Martinez et al., Cell 110: 563 (2002); Elbashir et al., supra; Lagos-Quintana et al., Curr. Biol. 12: 735 (2002); Tuschl et al., Nat. Biotechnol. 20:446 (2002); Tuschl, Chembiochem. 2: 239 (2001); Harborth et al., J. Cell Sci. 114: 4557 (2001); et al., EMBO J. 20:6877 (2001); Lagos-Quintana et al., Science. 294: 8538 (2001); Hutvagner et al., loc cit, 834; Elbashir et al., Nature. 411: 494 (2001).

The present invention provides a DNA construct comprising at least one polynucleotide of SEQ ID NOs: 1-235 or conservative variants thereof, such as the conservative variants discussed above. Any method known in the art can be used to generate the DNA constructs of the present invention. See, e.g. Sambrook et al., supra.

The invention includes DNA constructs that optionally comprise a promoter. Any suitable promoter known in the art can be used. A promoter is a nucleic acid, preferably DNA, that binds RNA polymerase and/or other transcription regulatory elements. As with any promoter, the promoters of the invention facilitate or control the transcription of DNA or RNA to generate an mRNA molecule from a nucleic acid molecule that is operably linked to the promoter. The RNA can encode a protein or polypeptide or can encode an antisense RNA molecule or a molecule useful in RNAi. Promoters useful in the invention include constitutive promoters, inducible promoters, temporally regulated promoters and tissue-preferred promoters.

Examples of useful constitutive plant promoters include: the cauliflower mosaic virus (CaMV) 35S promoter, which confers constitutive, high-level expression in most plant tissues (Odel et al. Nature 313:810(1985)); the nopaline synthase promoter (An et al. Plant Physiol. 88:547 (1988)); and the octopine synthase promoter (Fromm et al., Plant Cell 1: 977 (1989)). It should be noted that, although the CaMV 35S promoter is commonly referred to as a constitutive promoter, some tissue preference can be seen. The use of CaMV 35S is envisioned by the present invention, regardless of any tissue preference which may be exhibited during use in the present invention.

Inducible promoters regulate gene expression in response to environmental, hormonal, or chemical signals. Examples of hormone inducible promoters include auxin-inducible promoters (Baumann et al. Plant Cell 11:323-334(1999)), cytokinin-inducible promoters (Guevara-Garcia, Plant Mol. Biol. 38:743-753(1998)), and gibberellin-responsive promoters (Shi et al. Plant Mol. Biol. 38:1053-1060(1998)). Additionally, promoters responsive to heat, light, wounding, pathogen resistance, and chemicals such as methyl jasmonate or salicylic acid, can be used in the DNA constructs and methods of the present invention.

Tissue-preferred promoters allow for preferred expression of polynucleotides of the invention in certain plant tissue. Tissue-preferred promoters are also useful for directing the expression of antisense RNA or siRNA in certain plant tissues, which can be useful for inhibiting or completely blocking the expression of targeted genes as discussed above. As used herein, vascular plant tissue refers to xylem, phloem or vascular cambium tissue. Other preferred tissue includes apical meristem, root, seed, and flower. In one aspect, the tissue-preferred promoters of the invention are either “xylem-preferred,” “cambium-preferred” or “phloem-preferred,” and preferentially direct expression of an operably linked nucleic acid sequence in the xylem, cambium or phloem, respectively. In another aspect, the DNA constructs of the invention comprise promoters that are tissue-specific for xylem, cambium or phloem, wherein the promoters are only active in the xylem, cambium or phloem.

A vascular-preferred promoter is preferentially active in any of the xylem, phloem or cambium tissues, or in at least two of the three tissue types. A vascular-specific promoter is specifically active in any of the xylem, phloem or cambium, or in at least two of the three. In other words, the promoters are only active in the xylem, cambium or phloem tissue of plants. Note, however, that because of solute transport in plants, a product that is specifically or preferentially expressed in a tissue may be found elsewhere in the plant after expression has occurred.

In another embodiment, the promoter is under temporal regulation, wherein the ability of the promoter to initiate expression is linked to factors such as the stage of the cell cycle or the stage of plant development. For example, the promoter of a cyclin D2 gene may be expressed only during the G1 and early S-phase, and the promoters of particular cyclin genes may be expressed only within the primary vascular poles of the developing seedling.

Additionally, the promoters of particular cell cycle genes may be expressed only within the cambium in developing secondary vasculature. Within the cambium, particular cell cycle gene promoters may be expressed exclusively in the stem or in the root. Moreover, the cell cycle promoters may be expressed only in the spring (for early wood formation) or only in the summer.

A promoter may be operably linked to the polynucleotide. As used in this context, operably linked refers to linking a polynucleotide encoding a structural gene to a promoter such that the promoter controls transcription of the structural gene. If the desired polynucleotide comprises a sequence encoding a protein product, the coding region can be operably linked to regulatory elements, such as to a promoter and a terminator, that bring about expression of an associated messenger RNA transcript and/or a protein product encoded by the desired polynucleotide. In this instance, the polynucleotide is operably linked in the 5′- to 3′-orientation to a promoter and, optionally, a terminator sequence.

Alternatively, the invention provides DNA constructs comprising a polynucleotide in an “antisense” orientation, the transcription of which produces nucleic acids that can form secondary structures that affect expression of an endogenous cell cycle gene in the plant cell. In another variation, the DNA construct may comprise a polynucleotide that yields a double-stranded RNA product upon transcription that initiates RNA interference of a cell cycle gene with which the polynucleotide is associated. A polynucleotide of the present invention can be positioned within a t-DNA, such that the left and right t-DNA border sequences flank or are on either side of the polynucleotide.

It should be understood that the invention includes DNA constructs comprising one or more of any of the polynucleotides discussed above. Thus, for example, a construct may comprise a t-DNA comprising one, two, three, four, five, six, seven, eight, nine, ten, or more polynucleotides.

The invention also includes DNA constructs comprising a promoter that includes one or more regulatory elements. Alternatively, the invention includes DNA constructs comprising a regulatory element that is separate from a promoter. Regulatory elements confer a number of important characteristics upon a promoter region. Some elements bind transcription factors that enhance the rate of transcription of the operably linked nucleic acid. Other elements bind repressors that inhibit transcription activity. The effect of transcription factors on promoter activity can determine whether the promoter activity is high or low, i.e. whether the promoter is “strong” or “weak.”

A DNA construct of the invention can include a nucleotide sequence that serves as a selectable marker useful in identifying and selecting transformed plant cells or plants. Examples of such markers include, but are not limited to, a neomycin phosphotransferase (nptII) gene (Potrykus et al., Mol. Gen. Genet. 199:183-188 (1985)), which confers kanamycin resistance. Cells expressing the nptII gene can be selected using an appropriate antibiotic such as kanamycin or G418. Other commonly used selectable markers include a mutant EPSP synthase gene (Hinchee et al., Bio/Technology 6:915-922 (1988)), which confers glyphosate resistance; and a mutant acetolactate synthase gene (ALS), which confers imidazolinone or sulphonylurea resistance (European Patent Application 154,204, 1985).

The present invention also includes vectors comprising the DNA constructs discussed above. The vectors can include an origin of replication (replicons) for a particular host cell. Various prokaryotic replicons are known to those skilled in the art, and function to direct autonomous replication and maintenance of a recombinant molecule in a prokaryotic host cell.

In one embodiment, the present invention utilizes a pWVR8 vector as described in U.S. Application No. 60/476,222, filed Jun. 6, 2003, or pART27 as described in Gleave, Plant Mol. Biol, 20:1203-27 (1992).

The invention also provides host cells which are transformed with the DNA constructs of the invention. As used herein, a host cell refers to the cell in which a polynucleotide of the invention is expressed. Accordingly, a host cell can be an individual cell, a cell culture or cells that are part of an organism. The host cell can also be a portion of an embryo, endosperm, sperm or egg cell, or a fertilized egg. In one embodiment, the host cell is a plant cell.

The present invention further provides transgenic plants comprising the DNA constructs of the invention. The invention includes transgenic plants that are angiosperms or gymnosperms. The DNA constructs of the present invention can be used to transform a variety of plants, both monocotyledonous (e.g. grasses, corn, grains, oat, wheat and barley), dicotyledonous (e.g., Arabidopsis, tobacco, legumes, alfalfa, oaks, eucalyptus, maple), and Gymnosperms (e.g., Scots pine; see Aronen, Finnish Forest Res. Papers, Vol. 595, 1996), white spruce (Ellis et al., Biotechnology 11:84-89, 1993), and larch (Huang et al., In Vitro Cell 27:201-207, 1991).

The plants also include turfgrass, wheat, maize, rice, sugar beet, potato, tomato, lettuce, carrot, strawberry, cassava, sweet potato, geranium, soybean, and various types of woody plants. Woody plants include trees such as palm oak, pine, maple, fir, apple, fig, plum and acacia. Woody plants also include rose and grape vines.

In one embodiment, the DNA constructs of the invention are used to transform woody plants, i.e., trees or shrubs whose stems live for a number of years and increase in diameter each year by the addition of woody tissue. The invention includes methods of transforming plants including eucalyptus and pine species of significance in the commercial forestry industry such as plants selected from the group consisting of Eucalyptus grandis and its hybrids, and Pinus taeda, as well as the transformed plants and wood and wood pulp derived therefrom. Other examples of suitable plants include those selected from the group consisting of Pinus banksiana, Pinus brutia, Pinus caribaea, Pinus clausa, Pinus contorta, Pinus coulteri, Pinus echinata, Pinus eldarica, Pinus ellioti, Pinus jeffreyi, Pinus lambertiana, Pinus massoniana, Pinus monticola, Pinus nigra, Pinus palustris, Pinus pinaster, Pinus ponderosa, Pinus radiata, Pinus resinosa, Pinus rigida, Pinus serotina, Pinus strobus, Pinus sylvestris, Pinus taeda, Pinus virginiana, Abies amabilis, Abies balsamea, Abies concolor, Abies grandis, Abies lasiocarpa, Abies magnifica, Abies procera, Chamaecyparis lawsoniona, Chamaecyparis nootkatensis, Chamaecyparis thyoides, Juniperus virginiana, Larix decidua, Larix laricina, Larix leptolepis, Larix occidentalis, Larix siberica, Libocedrus decurrens, Picea abies, Picea engelmanni, Picea glauca, Picea mariana, Picea pungens, Picea rubens, Picea sitchensis, Pseudotsuga menziesii, Sequoia gigantea, Sequoia sempervirens, Taxodium distichum, Tsuga canadensis, Tsuga heterophylla, Tsuga mertensiana, Thuja occidentalis, Thuja plicata, Eucalyptus alba, Eucalyptus bancroftii, Eucalyptus botryoides, Eucalyptus bridgesiana, Eucalyptus calophylla, Eucalyptus camaldulensis, Eucalyptus citriodora, Eucalyptus cladocalyx, Eucalyptus coccifera, Eucalyptus curtisii, Eucalyptus dalrympleana, Eucalyptus deglupta, Eucalyptus delagatensis, Eucalyptus diversicolor, Eucalyptus dunnii, Eucalyptus ficifolia, Eucalyptus globulus, Eucalyptus gomphocephala, Eucalyptus gunnii, Eucalyptus henryi, Eucalyptus laevopinea, Eucalyptus macarthurii, Eucalyptus macrorhyncha, Eucalyptus maculata, Eucalyptus marginata, Eucalyptus megacarpa, Eucalyptus melliodora, Eucalyptus nicholii, Eucalyptus nitens, Eucalyptus nova-angelica, Eucalyptus obliqua, Eucalyptus occidentalis, Eucalyptus obtusiflora, Eucalyptus oreades, Eucalyptus pauciflora, Eucalyptus polybractea, Eucalyptus regnans, Eucalyptus resinifera, Eucalyptus robusta, Eucalyptus rudis, Eucalyptus saligna, Eucalyptus sideroxylon, Eucalyptus stuartiana, Eucalyptus tereticornis, Eucalyptus torelliana, Eucalyptus urnigera, Eucalyptus urophylla, Eucalyptus viminalis, Eucalyptus viridis, Eucalyptus wandoo, and Eucalyptus youmanni.

As used herein, the term “plant” also is intended to include the fruit, seeds, flower, strobilus, etc. of the plant. A transformed plant of the current invention can be a direct transfectant, meaning that the DNA construct was introduced directly into the plant, such as through Agrobacterium, or the plant can be the progeny of a transfected plant. The second or subsequent generation plant can be produced by sexual reproduction, i.e., fertilization. Furthermore, the plant can be a gametophyte (haploid stage) or a sporophyte (diploid stage).

As used herein, the term “plant tissue” encompasses any portion of a plant, including plant cells. Plant cells include suspension cultures, callus, embryos, meristematic regions, callus tissue, leaves, roots, shoots, gametophytes, sporophytes, pollen, seeds and microspores. Plant tissues can be grown in liquid or solid culture, or in soil or suitable media in pots, greenhouses or fields. As used herein, “plant tissue” also refers to a clone of a plant, seed, progeny, or propagule, whether generated sexually or asexually, and descendents of any of these, such as cuttings or seeds.

In accordance with one aspect of the invention, a transgenic plant that has been transformed with a DNA construct of the invention has a phenotype that is different from a plant that has not been transformed with the DNA construct.

As used herein, “phenotype” refers to a distinguishing feature or characteristic of a plant which can be altered according to the present invention by integrating one or more DNA constructs of the invention into the genome of at least one plant cell of a plant. The DNA construct can confer a change in the phenotype of a transformed plant by modifying any one or more of a number of genetic, molecular, biochemical, physiological, morphological, or agronomic characteristics or properties of the transformed plant cell or plant as a whole.

In one embodiment, transformation of a plant with a DNA construct of the present invention can yield a phenotype including, but not limited to any one or more of increased drought tolerance, herbicide resistance, reduced or increased height, reduced or increased branching, enhanced cold and frost tolerance, improved vigor, enhanced color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced resistance of the wood to decay, enhanced resistance to fungal diseases, altered attractiveness to insect pests, enhanced heavy metal tolerance, increased disease tolerance, increased insect tolerance, increased water-stress tolerance, enhanced sweetness, improved texture, decreased phosphate content, increased germination, increased micronutrient uptake, improved starch composition, improved flower longevity, production of novel resins, and production of novel proteins or peptides.

In another embodiment, the affected phenotype includes one or more of the following traits: propensity to form reaction wood, a reduced period of juvenility, an increased period of juvenility, self-abscising branches, accelerated reproductive development or delayed reproductive development, as compared to a plant of the same species that has not been transformed with the DNA construct.

In a further embodiment, the phenotype that is different in the transgenic plant includes one or more of the following: lignin quality, lignin structure, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization, fiber dimensions, lumen size, other plant components, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape.

Phenotype can be assessed by any suitable means. The plants can be evaluated based on their general morphology. Transgenic plants can be observed with the naked eye, can be weighed and their height measured. The plant can be examined by isolating individual layers of plant tissue, namely phloem and cambium, which is further sectioned into meristematic cells, early expansion, late expansion, secondary wall formation, and late cell maturation. See, e.g., Hertzberg, supra. The plants also can be assessed using microscopic analysis or chemical analysis.

Microscopic analysis includes examining cell types, stage of development, and stain uptake by tissues and cells. Fiber morphology, such as fiber wall thickness and microfibril angle of wood pulp fibers can be observed using, for example, microscopic transmission ellipsometry. See Ye and Sundström, Tappi J., 80:181 (1997). Wood strength, density, and grain slope in wet wood and standing trees can be determined by measuring the visible and near infrared spectral data in conjunction with multivariate analysis. See, U.S. Patent Application Publication Nos. 2002/0107644 and 2002/0113212. Lumen size can be measured using scanning electron microscopy. Lignin structure and chemical properties can be observed using nuclear magnetic resonance spectroscopy as described in Marita et al., J. Chem. Soc., Perkin Trans. I 2939 (2001).

The biochemical characteristic of lignin, cellulose, carbohydrates and other plant extracts can be evaluated by any standard analytical method known including spectrophotometry, fluorescence spectroscopy, HPLC, mass spectroscopy, and tissue staining methods.

As used herein, “transformation” refers to a process by which a nucleic acid is inserted into the genome of a plant cell. Such insertion encompasses stable introduction into the plant cell and transmission to progeny. Transformation also refers to transient insertion of a nucleic acid, wherein the resulting transformant transiently expresses the nucleic acid. Transformation can occur under natural or artificial conditions using various methods well known in the art. Transformation can be achieved by any known method for the insertion of nucleic acid sequences into a prokaryotic or eukaryotic host cell, including Agrobacterium-mediated transformation protocols, viral infection, whiskers, electroporation, microinjection, polyethylene glycol-treatment, heat shock, lipofection, and particle bombardment. Transformation can also be accomplished using chloroplast transformation as described in e.g. Svab et al., Proc. Natl Acad. Sci. 87:8526-30 (1990).

In accordance with one embodiment of the invention, transformation in Eucalyptus is performed as described in U.S. Patent Application No. 60/476,222 (supra) which is incorporated herein by reference in its entirety. In accordance with another embodiment, transformation of Pinus is accomplished using the methods described in U.S. Patent Application Publication No. 2002/0100083.

Another aspect of the invention provides methods of obtaining wood and/or making wood pulp from a plant transformed with a DNA construct of the invention. Methods of producing a transgenic plant are provided above and are known in the art. A transformed plant can be cultured or grown under any suitable conditions. For example, pine can be cultured and grown as described in U.S. Patent Application Publication No. 2002/0100083. Eucalyptus can be cultured and grown as in, for example, Rydelius, et al., GROWING EUCALYPTUS FOR PULP AND ENERGY, presented at the Mechanization in Short Rotation, Intensive Culture Forestry Conference, Mobile, Ala., 1994. Wood and wood pulp can be obtained from the plant by any means known in the art.

As noted above, the wood or wood pulp obtained in accordance with this invention may demonstrate improved characteristics including, but not limited to any one or more of lignin composition, lignin structure, wood composition, cellulose polymerization, fiber dimensions, ratio of fibers to other plant components, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape include increased or decreased lignin content, increased accessibility of lignin to chemical treatments, improved reactivity of lignin, increased or decreased cellulose content increased dimensional stability, increased tensile strength, increased shear strength, increased compression strength, increased shock resistance, increased stiffness, increased or decreased hardness, decreased spirality, decreased shrinkage, and differences in weight, density, and specific gravity.

B. Expression Profiling of Cell Cycle Genes

The present invention also provides methods and tools for performing expression profiling of cell cycle genes. Expression profiling is useful in determining whether genes are transcribed or translated, comparing transcript levels for particular genes in different tissues, genotyping, estimating DNA copy number, determining identity of descent, measuring mRNA decay rates, identifying protein binding sites, determining subcellular localization of gene products, correlating gene expression to a phenotype or other phenomenon, and determining the effect on other genes of the manipulation of a particular gene. Expression profiling is particularly useful for identifying gene expression in complex, multigenic events. For this reason, expression profiling is useful in correlating gene expression to plant phenotype and formation of plant tissues and the interconnection thereof to the cell cycle.

Only a small fraction of the genes of a plant's genome are expressed at a given time in a given tissue sample, and all of the expressed genes may not affect the plant phenotype. To identify genes capable of affecting a phenotype of interest, the present invention provides methods and tools for determining, for example, a gene expression profile at a given point in the cell cycle, a gene expression profile at a given point in plant development, and a gene expression profile a given tissue sample. The invention also provides methods and tools for identifying cell cycle genes whose expression can be manipulated to alter plant phenotype or to alter the biological activity of cell cycle gene products. In support of these methods, the invention also provides methods and tools that distinguish expression of different genes of the same family.

As used herein, “gene expression” refers to the process of transcription of a DNA sequence into an RNA sequence, followed by translation of the RNA into a protein, which may or may not undergo post-translational processing. Thus, the relationship between cell cycle stage and/or developmental stage and gene expression can be observed by detecting, quantitatively or qualitatively, changes in the level of an RNA or a protein. As used herein, the term “biological activity” includes, but is not limited to, the activity of a protein gene product, including enzyme activity.

The present invention provides oligonucleotides that are useful in these expression profiling methods. Each oligonucleotide is capable of hybridizing under a given set of conditions to a cell cycle gene or gene product. In one aspect of the invention, a plurality of oligonucleotides is provided, wherein each oligonucleotide hybridizes under a given set of conditions to a different cell cycle gene product. Examples of oligonucleotides of the present invention include SEQ ID NOs: 471-697. Each of the oligos of SEQ ID NOs 471-697 hybridizes under standard conditions to a different gene product of one of SEQ ID NOs: 1-237. The oligonucleotides of the invention are useful in determining the expression of one or more cell cycle genes in any of the above-described methods.

1. Cell, Tissue, Nucleic Acid, and Protein Samples

Samples for use in methods of the present invention may be derived from plant tissue. Suitable plant tissues include, but are not limited to, somatic embryos, pollen, leaves, stems, calli, stolons, microtubers, shoots, xylem, male strolbili, pollen cones, vascular tissue, apical meristem, vascular cambium, xylem, root, flower, and seed.

According to the present invention “plant tissue” is used as described previously herein. Plant tissue can be obtained from any of the plants types or species described supra.

In accordance with one aspect of the invention, samples are obtained from plant tissue at different stages of the cell cycle, from plant tissue at different developmental stages, from plant tissue at various times of the year (e.g. spring versus summer), from plant tissues subject to different environmental conditions (e.g. variations in light and temperature) and/or from different types of plant tissue and cells. In accordance with one embodiment, plant tissue is obtained during various stages of maturity and during different seasons of the year. For example, plant tissue can be collected from stem dividing cells, differentiating xylem, early developing wood cells, differentiated spring wood cells, and differentiated summer wood cells. As another example, gene expression in a sample obtained from a plant with developing wood can be compared to gene expression in a sample obtained from a plant which does not have developing wood.

Differentiating xylem includes samples obtained from compression wood, side-wood, and normal vertical xylem. Methods of obtaining samples for expression profiling from pine and eucalyptus are known. See, e.g., Allona et al., Proc. Nat'l Acad. Sci. 95:9693-8 (1998) and Whetton et al., Plant Mol. Biol. 47:275-91, and Kirst et al., INT'L UNION OF FORESTRY RESEARCH ORGANIZATIONS BIENNIAL CONFERENCE, S6.8 (June 2003, Umea, Sweden).

In one embodiment of the invention, gene expression in one type of tissue is compared to gene expression in a different type of tissue or to gene expression in the same type of tissue in a difference stage of development. Gene expression can also be compared in one type of tissue which is sampled at various times during the year (different seasons). For example, gene expression in juvenile secondary xylem can be compared to gene expression in mature secondary xylem. Similarly, gene expression in cambium can be compared to gene expression in xylem. Furthermore, gene expression in apical meristems can be compared to gene expression in cambium.

In an alternative embodiment, differences in gene expression are determined as cells from different tissues advance during the cell cycle. In this method, the cells from the different tissues are synchronized and their gene expression is profiled. Methods of synchronizing the stage of cell cycle in a sample are known. These methods include, e.g., cold acclimation, photoperiod, and aphidicoline. See, e.g., Nagata et al., Int. Rev. Cytol. 132:1-30 (1992), Breyne and Zabeau, Curr. Opin. Plant Biol. 4:136-42, 140 (2001). A sample is obtained during a specific stage of the cell cycle and gene expression in that sample is compared to a sample obtained during a different stage of the cell cycle. For example, tissue can be examined in any of the phases of the cell cycle, such as mitosis, G1, G0, S, and G2. In particular, one can examine the changes in gene expression at the G1, G2, and metaphase checkpoints.

In another embodiment of the invention, a sample is obtained from a plant having a specific phenotype and gene expression in that sample is compared to a sample obtained from a plant of the same species that does not have that phenotype. For example, a sample can be obtained from a plant exhibiting a fast rate of growth and gene expression can be compared with that of a sample obtained from a plant exhibiting a normal or slow rate of growth. Differentially expressed genes identified from such a comparison can be correlated with growth rate and, therefore, useful for manipulating growth rate.

In a further embodiment, a sample is obtained from clonally propagated plants. In one embodiment the clonally propagated plants are of the species Pinus or Eucalyptus. Individual ramets from the same genotype can be sacrificed at different times of year. Thus, for any genotype there can be at least two genetically identical trees sacrificed, early in the season and late in the season. Each of these trees can be divided into juvenile (top) to mature (bottom) samples. Further, tissue samples can be divided into, for example, phloem to xylem, in at least 5 layers of peeling. Each of these samples can be evaluated for phenotype and gene expression. See Entry 196.

Where cellular components may interfere with an analytical technique, such as a hybridization assay, enzyme assay, a ligand binding assay, or a biological activity assay, it may be desirable to isolate the gene products from such cellular components. Gene products, including nucleic acid and amino acid gene products, can be isolated from cell fragments or lysates by any method known in the art.

Nucleic acids used in accordance with the invention can be prepared by any available method or process, or by other processes as they become known in the art. Conventional techniques for isolating nucleic acids are detailed, for example, in Tijssen, LABORATORY TECHNIQUES IN BIOCHEMISTRY AND MOLECULAR BIOLOGY: HYBRIDIZATION WITH NUCLEIC ACID PROBES, chapter 3 (Elsevier Press, 1993), Berger and Kimmel, Methods Enzymol. 152:1 (1987), and GIBCO BRL & LIFE TECHNOLOGIES TRIZOL RNA ISOLATION PROTOCOL, Form No. 3786 (2000). Techniques for preparing nucleic acid samples, and sequencing polynucleotides from pine and eucalyptus are known. See, e.g., Allona et al., supra and Whetton et al., supra, and U.S. Application No. 60/476,222.

A suitable nucleic acid sample can contain any type of nucleic acid derived from the transcript of a cell cycle gene, i.e., RNA or a subsequence thereof or a nucleic acid for which an mRNA transcribed from a cell cycle gene served as a template. Suitable nucleic acids include cDNA reverse-transcribed from a transcript, RNA transcribed from that cDNA, DNA amplified from the cDNA, and RNA transcribed from the amplified DNA. Detection of such products or derived products is indicative of the presence and/or abundance of the transcript in the sample. Thus, suitable samples include, but are not limited to, transcripts of the gene or genes, cDNA reverse-transcribed from the transcript, cRNA transcribed from the cDNA, DNA amplified from the genes, and RNA transcribed from amplified DNA. As used herein, the category of “transcripts” includes but is not limited to pre-mRNA nascent transcripts, transcript processing intermediates, and mature mRNAs and degradation products thereof.

It is not necessary to monitor all types of transcripts to practice the invention. For example, the expression profiling methods of the invention can be conducted by detecting only one type of transcript, such as mature mRNA levels only.

In one aspect of the invention, a chromosomal DNA or cDNA library (comprising, for example, fluorescently labeled cDNA synthesized from total cell mRNA) is prepared for use in hybridization methods according to recognized methods in the art. See Sambrook et al., supra.

In another aspect of the invention, mRNA is amplified using, e.g., the MessageAmp kit (Ambion). In a further aspect, the mRNA is labeled with a detectable label. For example, mRNA can be labeled with a fluorescent chromophore, such as CyDye (Amersham Biosciences).

In some applications, it may be desirable to inhibit or destroy RNase that often is present in homogenates or lysates, before use in hybridization techniques. Methods of inhibiting or destroying nucleases are well known. In one embodiment of the invention, cells or tissues are homogenized in the presence of chaotropic agents to inhibit nuclease. In another embodiment, RNase is inhibited or destroyed by heat treatment, followed by proteinase treatment.

Protein samples can be obtained by any means known in the art. Protein samples useful in the methods of the invention include crude cell lysates and crude tissue homogenates. Alternatively, protein samples can be purified. Various methods of protein purification well known in the art can be found in Marshak et al., STRATEGIES FOR PROTEIN PURIFICATION AND CHARACTERIZATION: A LABORATORY COURSE MANUAL (Cold Spring Harbor Laboratory Press 1996).

2. Detecting Level of Gene Expression

For methods of the invention that comprise detecting a level of gene expression, any method for observing gene expression can be used, without limitation. Such methods include traditional nucleic acid hybridization techniques, polymerase chain reaction (PCR) based methods, and protein determination. The invention includes detection methods that use solid support-based assay formats as well as those that use solution-based assay formats.

Absolute measurements of the expression levels need not be made, although they can be made. The invention includes methods comprising comparisons of differences in expression levels between samples. Comparison of expression levels can be done visually or manually, or can be automated and done by a machine, using for example optical detection means. Subrahmanyam et al., Blood. 97: 2457 (2001); Prashar et al., Methods Enzymol. 303: 258 (1999). Hardware and software for analyzing differential expression of genes are available, and can be used in practicing the present invention. See, e.g., GenStat Software and GeneExpress® GX Explorer™ Training Manual, supra; Baxevanis & Francis-Ouellette, supra.

In accordance with one embodiment of the invention, nucleic acid hybridization techniques are used to observe gene expression. Exemplary hybridization techniques include Northern blotting, Southern blotting, solution hybridization, and S1 nuclease protection assays.

Nucleic acid hybridization typically involves contacting an oligonucleotide probe and a sample comprising nucleic acids under conditions where the probe can form stable hybrid duplexes with its complementary nucleic acid through complementary base pairing. For example, see PCT application WO 99/32660; Berger & Kimmel, Methods Enzymol. 152: 1 (1987). The nucleic acids that do not form hybrid duplexes are then washed away leaving the hybridized nucleic acids to be detected, typically through detection of an attached detectable label. The detectable label can be present on the probe, or on the nucleic acid sample. In one embodiment, the nucleic acids of the sample are detectably labeled polynucleotides representing the mRNA transcripts present in a plant tissue (e.g., a cDNA library). Detectable labels are commonly radioactive or fluorescent labels, but any label capable of detection can be used. Labels can be incorporated by several approached described, for instance, in WO 99/32660, supra. In one aspect RNA can be amplified using the MessageAmp kit (Ambion) with the addition of aminoallyl-UTP as well as free UTP. The aminoallyl groups incorporated into the amplified RNA can be reacted with a fluorescent chromophore, such as CyDye (Amersham Biosciences)

Duplexes of nucleic acids are destabilized by increasing the temperature or decreasing the salt concentration of the buffer containing the nucleic acids. Under low stringency conditions (e.g., low temperature and/or high salt) hybrid duplexes (e.g., DNA:DNA, RNA:RNA or RNA:DNA) will form even where the annealed sequences are not perfectly complementary. Thus, specificity of hybridization is reduced at lower stringency. Conversely, at higher stringency (e.g., higher temperature and/or lower salt and/or in the presence of destabilizing reagents) hybridization tolerates fewer mismatches.

Typically, stringent conditions for short probes (e.g., 10 to 50 nucleotide bases) will be those in which the salt concentration is at least about 0.01 to 1.0 M at pH 7.0 to 8.3 and the temperature is at least about 30° C. Stringent conditions can also be achieved with the addition of destabilizing agents such as formamide.

Under some circumstances, it can be desirable to perform hybridization at conditions of low stringency, e.g., 6×SSPE-T (0.9 M NaCl, 60 mM NaH₂PO₄, pH 7.6, 6 mM EDTA, 0.005% Triton) at 37° C., to ensure hybridization. Subsequent washes can then be performed at higher stringency (e.g., 1×SSPE-T at 37° C.) to eliminate mismatched hybrid duplexes. Successive washes can be performed at increasingly higher stringency (e.g., down to as low as 0.25×SSPE-T at 37° C. to 50° C.) until a desired level of hybridization specificity is obtained.

In general, standard conditions for hybridization is a compromise between stringency (hybridization specificity) and signal intensity. Thus, in one embodiment of the invention, the hybridized nucleic acids are washed at successively higher stringency conditions and read between each wash. Analysis of the data sets produced in this manner will reveal a wash stringency above which the hybridization pattern is not appreciably altered and which provides adequate signal for the particular oligonucleotide probes of interest. For example, the final wash may be selected as that of the highest stringency that produces consistent results and that provides a signal intensity greater than approximately 10% of the background intensity.

a. Oligonucleotide Probes

Oligonucleotide probes useful in nucleic acid hybridization techniques employed in the present invention are capable of binding to a nucleic acid of complementary sequence through one or more types of chemical bonds, usually through complementary base pairing via hydrogen bond formation. A probe can include natural bases (i.e., A, G, U, C or T) or modified bases (7-deazaguanosine, inosine, etc.). In addition, the nucleotide bases in the probes can be joined by a linkage other than a phosphodiester bond, so long as it does not interfere with hybridization. Thus, probes can be peptide nucleic acids in which the constituent bases are joined by peptide bonds rather than phosphodiester linkages.

Oligonucleotide probes can be prepared by any means known in the art. Probes useful in the present invention are capable of hybridizing to a nucleotide product of cell cycle genes, such as one of SEQ ID NOs: 1-237. Probes useful in the invention can be generated using the nucleotide sequences disclosed in SEQ ID NOs: 1-237. The invention includes oligonucleotide probes having at least a 2, 10,15, 20, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, or 100 nucleotide fragment of a corresponding contiguous sequence of any one of SEQ ID NOs: 1-237. The invention includes oligonucleotides of less than 2, 1, 0.5, 0.1, or 0.05 kb in length. In one embodiment, the oligonucleotide is 60 nucleotides in length.

Oligonucleotide probes can be designed by any means known in the art. See, e.g., Li and Stormo, Bioinformatics 17: 1067-76 (2001). Oligonucleotide probe design can be effected using software. Exemplary software includes ArrayDesigner, GeneScan, and ProbeSelect. Probes complementary to a defined nucleic acid sequence can be synthesized chemically, generated from longer nucleotides using restriction enzymes, or can be obtained using techniques such as polymerase chain reaction (PCR). PCR methods are well known and are described, for example, in Innis et al. eds., PCR PROTOCOLS: A GUIDE TO METHODS AND APPLICATIONS, Academic Press Inc. San Diego, Calif. (1990). The probes can be labeled, for example, with a radioactive, biotinylated, or fluorescent tag. Optimally, the nucleic acids in the sample are labeled and the probes are not labeled. Oligonucleotide probes generated by the above methods can be used in solution or solid support-based methods.

The invention includes oligonucleotide probes that hybridize to a product of the coding region or a 3′ untranslated region (3′ UTR) of a cell cycle gene. In one embodiment, the oligonucleotide probe hybridizes to the 3′UTR of any one of SEQ ID NOs: 1-237. The 3′ UTR is generally a unique region of the gene, even among members of the same family. Therefore, the probes capable of hybridizing to a product of the 3′ UTR can be useful for differentiating the expression of individual genes within a family where the coding region of the genes likely are highly homologous. This allows for the design of oligonucleotide probes to be used as members of a plurality of oligonucleotides, each capable of uniquely binding to a single gene. In another embodiment, the oligonucleotide probe comprises any one of SEQ ID NOs: 471-697. In another embodiment, the oligonucleotide probe consists of any one of SEQ ID NOs:471-697.

b. Oligonucleotide Array Methods

One embodiment of the invention employs two or more oligonucleotide probes in combination to detect a level of expression of one or more cell cycle genes, such as the genes of SEQ ID NOs: 1-237. In one aspect of this embodiment, the level of expression of two or more different genes is detected. The two or more genes may be from the same or different cell cycle gene families discussed above. Each of the two or more oligonucleotides may hybridize to a different one of the genes.

One embodiment of the invention employs two or more oligonucleotide probes, each of which specifically hybridize to a polynucleotide derived from the transcript of a gene provided by SEQ ID NOs: 1-237. Another embodiment employs two or more oligonucleotide probes, at least one of which comprises a nucleic acid sequence of SEQ ID NOs: 471-697. Another embodiment employs two or more oligonucleotide probes, at least one of which consists of SEQ ID NOs: 471-697.

The oligonucleotide probes may comprise from about 5 to about 60, or from about 5 to about 500, nucleotide bases, such as from about 60 to about 100 nucleotide bases, including from about 15 to about 60 nucleotide bases.

One embodiment of the invention uses solid support-based oligonucleotide hybridization methods to detect gene expression. Solid support-based methods suitable for practicing the present invention are widely known and are described, for example, in PCT application WO 95/11755; Huber et al., Anal. Biochem. 299: 24 (2001); Meiyanto et al., Biotechniques. 31: 406 (2001); Relogio et al., Nucleic Acids Res. 30:e51 (2002). Any solid surface to which oligonucleotides can be bound, covalently or non-covalently, can be used. Such solid supports include filters, polyvinyl chloride dishes, silicon or glass based chips, etc.

One embodiment uses oligonucleotide arrays, i.e. microarrays, which can be used to simultaneously observe the expression of a number of genes or gene products. Oligonucleotide arrays comprise two or more oligonucleotide probes provided on a solid support, wherein each probe occupies a unique location on the support. The location of each probe may be predetermined, such that detection of a detectable signal at a given location is indicative of hybridization to an oligonucleotide probe of a known identity. Each predetermined location can contain more than one molecule of a probe, but each molecule within the predetermined location has an identical sequence. Such predetermined locations are termed features. There can be, for example, from 2, 10, 100, 1,000, 2,000 or 5,000 or more of such features on a single solid support. In one embodiment, each oligonucleotide is located at a unique position on an array at least 2, at least 3, at least 4, at least 5, at least 6, or at least 10 times.

Oligonucleotide probe arrays for detecting gene expression can be made and used according to conventional techniques described, for example, in Lockhart et al., Nat'l Biotech. 14: 1675 (1996), McGall et al., Proc. Nat'l Acad. Sci. USA 93: 13555 (1996), and Hughes et al., Nature Biotechnol. 19:342 (2001). A variety of oligonucleotide array designs is suitable for the practice of this invention.

In one embodiment the one or more oligonucleotides include a plurality of oligonucleotides that each hybridize to a different gene expressed in a particular tissue type. For example, the tissue can be developing wood.

In one embodiment, a nucleic acid sample obtained from a plant can be amplified and, optionally labeled with a detectable label. Any method of nucleic acid amplification and any detectable label suitable for such purpose can be used. For example, amplification reactions can be performed using, e.g. Ambion's MessageAmp, which creates “antisense” RNA or “aRNA” (complementary in nucleic acid sequence to the RNA extracted from the sample tissue). The RNA can optionally be labeled using CyDye fluorescent labels. During the amplification step, aaUTP is incorporated into the resulting aRNA. The CyDye fluorescent labels are coupled to the aaUTPs in a non-enzymatic reaction. Subsequent to the amplification and labeling steps, labeled amplified antisense RNAs are precipitated and washed with appropriate buffer, and then assayed for purity. For example, purity can be assay using a NanoDrop spectrophotometer. The nucleic acid sample is then contacted with an oligonucleotide array having, attached to a solid substrate (a “microarray slide”), oligonucleotide sample probes capable of hybridizing to nucleic acids of interest which may be present in the sample. The step of contacting is performed under conditions where hybridization can occur between the nucleic acids of interest and the oligonucleotide probes present on the array. The array is then washed to remove non-specifically bound nucleic acids and the signals from the labeled molecules that remain hybridized to oligonucleotide probes on the solid substrate are detected. The step of detection can be accomplished using any method appropriate to the type of label used. For example, the step of detecting can accomplished using a laser scanner and detector. For example, on can use and Axon scanner which optionally uses GenePix Pro software to analyze the position of the signal on the microarray slide.

Data from one or more microarray slides can analyzed by any appropriate method known in the art.

Oligonucleotide probes used in the methods of the present invention, including microarray techniques, can be generated using PCR. PCR primers used in generating the probes are chosen, for example, based on the sequences of SEQ ID NOs:1-237, to result in amplification of unique fragments of the cell cycle genes (i.e., fragments that hybridize to only one polynucleotide of any one of SEQ ID NOs: 1-237 under standard hybridization conditions). Computer programs are useful in the design of primers with the required specificity and optimal hybridization properties. For example, Li and Stormo, supra at 1075, discuss a method of probe selection using ProbeSelect which selects an optimum oligonucleotide probe based on the entire gene sequence as well as other gene sequences to be probed at the same time.

In one embodiment, oligonucleotide control probes also are used. Exemplary control probes can fall into at least one of three categories referred to herein as (1) normalization controls, (2) expression level controls and (3) negative controls. In microarray methods, one or more of these control probes may be provided on the array with the inventive cell cycle gene-related oligonucleotides.

Normalization controls correct for dye biases, tissue biases, dust, slide irregularities, malformed slide spots, etc. Normalization controls are oligonucleotide or other nucleic acid probes that are complementary to labeled reference oligonucleotides or other nucleic acid sequences that are added to the nucleic acid sample to be screened. The signals obtained from the normalization controls, after hybridization, provide a control for variations in hybridization conditions, label intensity, reading efficiency and other factors that can cause the signal of a perfect hybridization to vary between arrays. In one embodiment, signals (e.g., fluorescence intensity or radioactivity) read from all other probes used in the method are divided by the signal from the control probes, thereby normalizing the measurements.

Virtually any probe can serve as a normalization control. Hybridization efficiency varies, however, with base composition and probe length. Preferred normalization probes are selected to reflect the average length of the other probes being used, but they also can be selected to cover a range of lengths. Further, the normalization control(s) can be selected to reflect the average base composition of the other probes being used. In one embodiment, only one or a few normalization probes are used, and they are selected such that they hybridize well (i.e., without forming secondary structures) and do not match any test probes. In one embodiment, the normalization controls are mammalian genes.

Expression level controls probes hybridize specifically with constitutively expressed genes present in the biological sample. Virtually any constitutively expressed gene provides a suitable target for expression level control probes. Typically, expression level control probes have sequences complementary to subsequences of constitutively expressed “housekeeping genes” including, but not limited to certain photosynthesis genes.

“Negative control” probes are not complementary to any of the test oligonucleotides (i.e., the inventive cell cycle gene-related oligonucleotides), normalization controls, or expression controls. In one embodiment, the negative control is a mammalian gene which is not complementary to any other sequence in the sample.

The terms “background” and “background signal intensity” refer to hybridization signals resulting from non-specific binding or other interactions between the labeled target nucleic acids (i.e., mRNA present in the biological sample) and components of the oligonucleotide array. Background signals also can be produced by intrinsic fluorescence of the array components themselves.

A single background signal can be calculated for the entire array, or a different background signal can be calculated for each target nucleic acid. In a one embodiment, background is calculated as the average hybridization signal intensity for the lowest 5 to 10 percent of the oligonucleotide probes being used, or, where a different background signal is calculated for each target gene, for the lowest 5 to 10 percent of the probes for each gene. Where the oligonucleotide probes corresponding to a particular cell cycle gene hybridize well and, hence, appear to bind specifically to a target sequence, they should not be used in a background signal calculation. Alternatively, background can be calculated as the average hybridization signal intensity produced by hybridization to probes that are not complementary to any sequence found in the sample (e.g., probes directed to nucleic acids of the opposite sense or to genes not found in the sample). In microarray methods, background can be calculated as the average signal intensity produced by regions of the array that lack any oligonucleotides probes at all.

c. PCR-Based Methods

In another embodiment, PCR-based methods are used to detect gene expression. These methods include reverse-transcriptase-mediated polymerase chain reaction (RT-PCR) including real-time and endpoint quantitative reverse-transcriptase-mediated polymerase chain reaction (Q-RTPCR). These methods are well known in the art. For example, methods of quantitative PCR can be carried out using kits and methods that are commercially available from, for example, Applied BioSystems and Stratagene®. See also Kochanowski, QUANTITATIVE PCR PROTOCOLS (Humana Press, 1999); Innis et al., supra.; Vandesompele et al., Genome Biol. 3: RESEARCH0034 (2002); Stein, Cell Mol. Life Sci. 59: 1235 (2002).

Gene expression can also be observed in solution using Q-RTPCR. Q-RTPCR relies on detection of a fluorescent signal produced proportionally during amplification of a PCR product. See Innis et al., supra. Like the traditional PCR method, this technique employs PCR oligonucleotide primers, typically 15-30 bases long, that hybridize to opposite strands and regions flanking the DNA region of interest. Additionally, a probe (e.g., TaqMan®, Applied Biosystems) is designed to hybridize to the target sequence between the forward and reverse primers traditionally used in the PCR technique. The probe is labeled at the 5′ end with a reporter fluorophore, such as 6-carboxyfluorescein (6-FAM) and a quencher fluorophore like 6-carboxy-tetramethyl-rhodamine (TAMRA). As long as the probe is intact, fluorescent energy transfer occurs which results in the absorbance of the fluorescence emission of the reporter fluorophore by the quenching fluorophore. As Taq polymerase extends the primer, however, the intrinsic 5′ to 3′ nuclease activity of Taq degrades the probe, releasing the reporter fluorophore. The increase in the fluorescence signal detected during the amplification cycle is proportional to the amount of product generated in each cycle.

The forward and reverse amplification primers and internal hybridization probe is designed to hybridize specifically and uniquely with one nucleotide derived from the transcript of a target gene. In one embodiment, the selection criteria for primer and probe sequences incorporates constraints regarding nucleotide content and size to accommodate TaqMan® requirements.

SYBR Green® can be used as a probe-less Q-RTPCR alternative to the Taqman®-type assay, discussed above. ABI PRISM® 7900 SEQUENCE DETECTION SYSTEM USER GUIDE APPLIED BIOSYSTEMS, chap. 1-8, App. A-F. (2002).

A device measures changes in fluorescence emission intensity during PCR amplification. The measurement is done in “real time,” that is, as the amplification product accumulates in the reaction. Other methods can be used to measure changes in fluorescence resulting from probe digestion. For example, fluorescence polarization can distinguish between large and small molecules based on molecular tumbling (see U.S. Pat. No. 5,593,867).

d. Protein Detection Methods

Proteins can be observed by any means known in the art, including immunological methods, enzyme assays and protein array/proteomics techniques.

Measurement of the translational state can be performed according to several protein methods. For example, whole genome monitoring of protein—the “proteome”—can be carried out by constructing a microarray in which binding sites comprise immobilized, preferably monoclonal, antibodies specific to a plurality of proteins having an amino acid sequence of any of SEQ ID NOs: 261-497 or proteins encoded by the genes of SEQ ID NOs:1-237 or conservative variants thereof. See Wildt et al., Nature Biotechnol. 18: 989 (2000). Methods for making polyclonal and monoclonal antibodies are well known, as described, for instance, in Harlow & Lane, ANTIBODIES: A LABORATORY MANUAL (Cold Spring Harbor Laboratory Press, 1988).

Alternatively, proteins can be separated by two-dimensional gel electrophoresis systems. Two-dimensional gel electrophoresis is well-known in the art and typically involves isoelectric focusing along a first dimension followed by SDS-PAGE electrophoresis along a second dimension. See, e.g., Hames et al, GEL ELECTROPHORESIS OF PROTEINS: A PRACTICAL APPROACH (IRL Press, 1990). The resulting electropherograms can be analyzed by numerous techniques, including mass spectrometric techniques, western blotting and immunoblot analysis using polyclonal and monoclonal antibodies, and internal and N-terminal micro-sequencing.

3. Correlating Gene Expression to Phenotype and Tissue Development

As discussed above, the invention provides methods and tools to correlate gene expression to plant phenotype. Gene expression may be examined in a plant having a phenotype of interest and compared to a plant that does not have the phenotype or has a different phenotype. Such a phenotype includes, but is not limited to, increased drought tolerance, herbicide resistance, reduced or increased height, reduced or increased branching, enhanced cold and frost tolerance, improved vigor, enhanced color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced resistance of the wood to decay, enhanced resistance to fungal diseases, altered attractiveness to insect pests, enhanced heavy metal tolerance, increased disease tolerance, increased insect tolerance, increased water-stress tolerance, enhanced sweetness, improved texture, decreased phosphate content, increased germination, increased micronutrient uptake, improved starch composition, improved flower longevity, production of novel resins, and production of novel proteins or peptides.

In another embodiment, the phenotype includes one or more of the following traits: propensity to form reaction wood, a reduced period of juvenility, an increased period of juvenility, self-abscising branches, accelerated reproductive development or delayed reproductive development.

In a further embodiment, the phenotype that is differs in the plants compares includes one or more of the following: lignin quality, lignin structure, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization, fiber dimensions, lumen size, other plant components, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape.

Phenotype can be assessed by any suitable means as discussed above.

In a further embodiment, gene expression can be correlated to a given point in the cell cycle, a given point in plant development, and in a given tissue sample. Plant tissue can be examined at different stages of the cell cycle, from plant tissue at different developmental stages, from plant tissue at various times of the year (e.g. spring versus summer), from plant tissues subject to different environmental conditions (e.g. variations in light and temperature) and/or from different types of plant tissue and cells. In accordance with one embodiment, plant tissue is obtained during various stages of maturity and during different seasons of the year. For example, plant tissue can be collected from stem dividing cells, differentiating xylem, early developing wood cells, differentiated spring wood cells, differentiated summer wood cells.

It will be apparent to those skilled in the art that various modifications and variations can be made in the methods and compositions of the present invention without departing from the spirit or scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.

The following examples are given to illustrate the present invention. It should be understood, however, that the invention is not to be limited to the specific conditions or details described in these examples. Throughout the specification, any and all references to a publicly available document, including a U.S. patent, are specifically incorporated by reference.

Examples

Example 1

Example 1 illustrates a procedure for RNA extraction and purification, which is particularly useful for RNA obtained from conifer needle, xylem, cambium, and phloem.

Tissue is obtained from conifer needle, xylem, cambium or phloem. The tissue is frozen in liquid nitrogen and ground. The total RNA is extracted using Concert Plant RNA reagent (Invitrogen). The resulting RNA sample is extracted into phenol:chloroform and treated with DNase. The RNA is then incubated at 65° C. for 2 minutes followed by centrifugation at 4° C. for 30 minutes. Following centrifugation, the RNA is extracted into phenol at least 10 times to remove contaminants.

The RNA is further cleaned using RNeasy columns (Qiagen). The purified RNA is quantified using RiboGreen reagent (Molecular Probes) and purity assessed by gel electrophoresis.

RNA is then amplified using MessageAmp (Ambion). Aminoallyl-UTP and free UTP are added to the in vitro transcription of the purified RNA at a ratio of 4:1 aminoallyl-UTP-to-UTP. The aminoallyl-UTP is incorporated into the new RNA strand as it is transcribed. The amino-allyl group is then reacted with Cy dyes to attach the colorimetric label to the resulting amplified RNA using the Amersham procedure modified for use with RNA. Unincorporated dye is removed by ethanol precipitation. The labeled RNA is quantified spectrophotometrically (NanoDrop). The labeled RNA is fragmented by heating to 95° C. as described in Hughes et al., Nature Biotechnol. 19:342 (2001).

Example 2

Example 2 illustrates how cell cycle genes important for wood development in Pinus radiata can be determined and how oligonucleotides which uniquely bind to those genes can be designed and synthesized for use on a microarray.

Pine trees of the species Pinus radiata are grown under natural light conditions. Tissue samples are prepared as described in, e.g., Sterky et al., Proc. Nat'l Acad. Sci. 95:13330 (1998). Specifically, tissue samples are collected from woody trees having a height of 5 meters. Tissue samples of the woody trees are prepared by taking tangential sections through the cambial region of the stem. The stems are sectioned horizontally into sections ranging from juvenile (top) to mature (bottom). The stem sections separated by stage of development are further separated into 5 layers by peeling into sections of phloem, differentiating phloem, cambium, differentiating xylem, developing xylem, and mature xylem. Tissue samples, including leaves, buds, shoots, and roots are also prepared from seedlings of the species Pinus radiata.

RNA is isolated and ESTs generated as described in Example 1 or Sterky et al., supra. The nucleic acid sequences of ESTs derived from samples containing developing wood are compared with nucleic acid sequences of genes known to be involved in the plant cell cycle. ESTs from samples that do not contain developing wood are also compared with sequences of genes known to be involved in the plant cell cycle. An in silico hybridization analysis is performed using BLAST (NCBI). Sequences from among the known cell cycle genes that show hybridization in silico to ESTs made from samples containing developing wood, but that do not hybridize to ESTs from samples not containing developing wood are selected for further examination.

cDNA clones containing sequences that hybridize to the genes showing wood-preferred expression are selected from cDNA libraries using techniques well known in the art of molecular biology. Using the sequence information, oligonucleotides are designed such that each oligonucleotide is specific for only one cDNA sequence in the library. The oligonucleotide sequences are provided in Table 14. 60-mer oligonucleotide probes are designed using the method of Li and Stormo, supra or using software such as ArrayDesigner, GeneScan, and ProbeSelect.

The oligonucleotides are then synthesized in situ described in Hughes et al., Nature Biotechnol. 19:324 (2002) or as described in Kane et al., Nucleic Acids Res. 28:4552 (2000) and affixed to an activated glass slide (Sigma-Genosis, The Woodlands, Tex.) using a 5′ amino linker. The position of each oligonucleotide on the slide is known.

Example 3

Example 3 illustrates how cell cycle genes important for wood development in Eucalyptus grandis can be determined and how oligonucleotides which uniquely bind to those genes can be designed and synthesized for use on a microarray.

Eucalyptus trees of the species Eucalyptus grandis are grown under natural light conditions. Tissue samples are prepared as described in, e.g., Sterky et al., Proc. Nat'l Acad. Sci. 95:13330 (1998). Specifically, tissue samples are collected from woody trees having a height of 5 meters. Tissue samples of the woody trees are prepared by taking tangential sections through the cambial region of the stem. The stems are sectioned horizontally into sections ranging from juvenile (top) to mature (bottom). The stem sections separated by stage of development are further separated into 5 layers by peeling into sections of phloem, differentiating phloem, cambium, differentiating xylem, developing xylem, and mature xylem. Tissue samples, including leaves, buds, shoots, and roots are also prepared from seedlings of the species Pinus radiata.

RNA is isolated and ESTs generated as described in Example 1 or Sterky et al., supra. The nucleic acid sequences of ESTs derived from samples containing developing wood are compared with nucleic acid sequences of genes known to be involved in the plant cell cycle. ESTs from samples that do not contain developing wood are also compared with sequences of genes known to be involved in the plant cell cycle. An in silico hybridization analysis is performed as described in, for example, Audic and Claverie, Genome Res. 7:986 (1997). Sequences from among the known cell cycle genes that show hybridization in silico to ESTs made from samples containing developing wood, but do not hybridize to ESTs from samples not containing developing wood are selected for further examination.

cDNA clones containing sequences that hybridize to the genes showing wood-preferred expression are selected from cDNA libraries using techniques well known in the art of molecular biology. Using the sequence information, oligonucleotides are designed such that each oligonucleotide is specific for only one cDNA sequence in the library. The oligonucleotide sequences are provided in Table 14. 60-mer oligonucleotide probes are designed using the method of Li and Stormo, supra or using software such as ArrayDesigner, GeneScan, and ProbeSelect.

The oligonucleotides are then synthesized in situ described in Hughes et al., Nature Biotechnol. 19:324 (2002) or as described in Kane et al., Nucleic Acids Res. 28:4552 (2000) and affixed to an activated glass slide (Sigma-Genosus, The Woodlands, Tex.) using a 5′ amino linker. The position of each oligonucleotide on the slide is known.

Example 4

Example 4 illustrates how to detect expression of Pinus radiata cell cycle genes which are important in wood formation using an oligonucleotide microarray prepared as in Example 2. This is an example of a balanced incomplete block designed experiment carried out using aRNA samples prepared from mature-phase phloem (P), cambium (C), expanding xylem found in a layer below the cambium (X1) and differentiating, lignifying xylem cells found deeper in the same growth ring (X2). In this example, cell cycle gene expression is compared among the four samples, namely P, C, X1, and X2.

In the summer, plants of the species Pinus radiata are felled and the bark of the main stem is immediately pulled gently away to reveal the phloem and xylem. The phloem and xylem are then peeled with a scalpel into separate containers of liquid nitrogen. Needles (leaves) and buds from the trees are also harvested with a scalpel into separate containers of liquid nitrogen. RNA is subsequently isolated from the frozen tissue samples as described in Example 1. Equal microgram quantities of total RNA are purified from each sample using RNeasy Mini columns (Qiagen, Valencia, Calif.) according to the manufacturers instructions.

Amplification reactions are carried out for each of the P, C, X1, and X2 tissue samples. Amplification reactions are performed using Ambion's MessageAmp kit, a T7-based amplification procedure, following the manufacturer's instructions, except that labeled aaUTP is added to the reagent mix during in the amplification step. aaUTP is incorporated into the resulting antisense RNA formed during this step. CyDye fluorescent labels are coupled to the aaUTPs in a non-enzymatic reaction as described in Example 1. Labeled amplified antisense RNAs are precipitated and washed, and then assayed for purity using a NanoDrop spectrophotometer. These labeled antisense RNAs, corresponding to the RNA isolated from the P, C, X1, and X2 tissue samples, constitute the sample nucleic acids, which are referred to as the P, C, X1, and X2 samples.

Normalization control samples of known nucleic acids are added to each sample in a dilution series of 500, 200, 100, 50, 25 and 10 pg/μl for quantitation of the signals. Positive controls corresponding to specific genes showing expression in all tissues of pine, such as housekeeping genes, are also added to the plant sample.

Each of four microarray slides is incubated with 125 μL of a P, C, X1 or X2 sample under a coverslip at 42° C. for 16-18 hours. The arrays are washed in 1×SSC, 0.1% SDS for 10 minutes and then in 0.1×SSC, 0.1% SDS for 10 minutes and the allowed to dry.

The array slides are scanned using an Axon laser scanner and analyzed using GenePix Pro software. Data from the microarray slides are subjected to microarray data analysis using GenStat SAS or Spotfire software. Outliers are removed and ratiometric data for each of the datasets are normalized using a global normalization which employs a cubic spline fit applied to correct for differential dye bias and spatial effects. A second transformation is performed to fit control signal ratios to a mean log²=0 (i.e. 1:1 ratio). Normalized data are then subjected to a variance analysis.

Mean signal intensity for each signal at any given position on the microarray slide is determined for each of three of P, C, X1, and X2 sample microarray slides. This mean signal/probe position is compared to the signal at the same position on sample slide which was not used for calculating the mean. For example, a mean signal at a given position is determined for P, C, and X1 and the signal at that position in the X2 microarray slide is compared to the P, C, and X1 mean signal value.

Table 1 shows genes having greater than doubled signal with any one sample as compared to the mean signal of the other three samples.

	TABLE 1
	Gene	PvCX12	PvX12	CvX12

	WD40 repeat protein A	−1.24	−0.88	−1.07
	CDC2	−1.09	−0.78	−0.92
	CYCLIN	−1.08	−1	−0.26
	WD-40 repeat protein B	−1.01	−0.87	−0.42
	CDC2	−0.83	−0.49	−1.01
	P = Phloem
	C = Cambium
	X1 = xylem layer-1
	X2 = xylem layer-2
	PvCX12 = Ratio of the signal for Phloem target versus mean signal for Cambium, Xylem1, and Xylem2 targets

The data shows that WD40 repeat protein A encodes a WD40 repeat protein is less highly expressed in cambium than in developing xylem, while WD40 repeat protein B encodes a WD40 repeat protein that is more highly expressed in phloem than in the other tissues.

Signal data are then verified with RT-PCR to confirm gene expression in the target tissue of the genes corresponding to the unique oligonucleotides in the probe.

Example 5

Example 5 demonstrates how one can correlate cell cycle gene expression with agronomically important wood phenotypes such as density, stiffness, strength, distance between branches, and spiral grain.

Mature clonally propagated pine trees are selected from among the progeny of known parent trees for superior growth characteristics and resistance to important fungal diseases. The bark is removed from a tangential section and the trees are examined for average wood density in the fifth annual ring at breast height, stiffness and strength of the wood, and spiral grain. The trees are also characterized by their height, mean distance between major branches, crown size, and forking.

To obtain seedling families that are segregating for major genes that affect density, stiffness, strength, distance between branches, spiral grain and other characteristics that may be linked to any of the genes affecting these characteristics, trees lacking common parents are chosen for specific crosses on the criterion that they exhibit the widest variation from each other with respect to the density, stiffness, strength, distance between branches, and spiral grain criteria. Thus, pollen from a plus tree exhibiting high density, low mean distance between major branches, and high spiral grain is used to pollinate cones from the unrelated plus tree among the selections exhibiting the lowest density, highest mean distance between major branches, and lowest spiral grain. It is useful to note that “plus trees” are crossed such that pollen from a plus tree exhibiting high density are used to pollinate developing cones from another plus tree exhibiting high density, for example, and pollen from a tree exhibiting low mean distance between major branches would be used to pollinate developing cones from another plus tree exhibiting low mean distance between major branches.

Seeds are collected from these controlled pollinations and grown such that the parental identity is maintained for each seed and used for vegetative propagation such that each genotype is represented by multiple ramets. Vegetative propagation is accomplished using micropropagation, hedging, or fascicle cuttings. Some ramets of each genotype are stored while vegetative propagules of each genotype are grown to sufficient size for establishment of a field planting. The genotypes are arrayed in a replicated design and grown under field conditions where the daily temperature and rainfall are measured and recorded.

The trees are measured at various ages to determine the expression and segregation of density, stiffness, strength, distance between branches, spiral grain, and any other observable characteristics that may be linked to any of the genes affecting these characteristics. Samples are harvested for characterization of cellulose content, lignin content, cellulose microfibril angle, density, strength, stiffness, tracheid morphology, ring width, and the like. Samples are also examined for gene expression as described in Example 4. Ramets of each genotype are compared to ramets of the same genotype at different ages to establish age:age correlations for these characteristics.

Example 6

Example 6 demonstrates how the stage of plant development and responses to environmental conditions such as light and season can be correlated to cell cycle gene expression using microarrays prepared as in Example 4. In particular, the changes in gene expression associated with wood density are examined.

Trees of three different clonally propagated Eucalyptus grandis hybrid genotypes are grown on a site with a weather station that measures daily temperatures and rainfall. During the spring and subsequent summer, genetically identical ramets of the three different genotypes are first photographed with north-south orientation marks, using photography at sufficient resolution to show bark characteristics of juvenile and mature portions of the plant, and then felled as in Example 4. The age of the trees is determined by planting records and confirmed by a count of the annual rings. In each of these trees, mature wood is defined as the outermost rings of the tree below breast height, and juvenile wood as the innermost rings of the tree above breast height. Each tree is accordingly sectored as follows:

NM—NORTHSIDE MATURE

SM—SOUTHSIDE MATURE

NT—NORTHSIDE TRANSITION

ST—SOUTHSIDE TRANSITION

NJ—NORTHSIDE JUVENILE

SJ—SOUTHSIDE JUVENILE

Tissue is harvested from the plant trunk as well as from juvenile and mature form leaves. Samples are prepared simultaneously for phenotype analysis, including plant morphology and biochemical characteristics, and gene expression analysis. The height and diameter of the tree at the point from which each sector was taken is recorded, and a soil sample from the base of the tree is taken for chemical assay. Samples prepared for gene expression analysis are weighed and placed into liquid nitrogen for subsequent preparation of RNA samples for use in the microarray experiment. The tissues are denoted as follows:

P—phloem

C—cambium

X1—expanding xylem

X2—differentiating and lignifying xylem

Thin slices in tangential and radial sections from each of the sectors of the trunk are fixed as described in Ruzin, Plant Microtechnique and Microscopy, Oxford University Press, Inc., New York, N.Y. (1999) for anatomical examination and confirmation of wood developmental stage. Microfibril angle is examined at the different developmental stages of the wood, for example juvenile, transition and mature phases of Eucalyptus grandis wood. Other characteristics examined are the ratio of fibers to vessel elements and ray tissue in each sector. Additionally, the samples are examined for characteristics that change between juvenile and mature wood and between spring wood and summer wood, such as fiber morphology, lumen size, and width of the S2 (thickest) cell wall layer. Samples are further examined for measurements of density in the fifth ring and determination of modulus of elasticity using techniques well known to those skilled in the art of wood assays. See, e.g., Wang, et al., Non-destructive Evaluations of Trees, EXPERIMENTAL TECHNIQUES, pp. 28-30 (2000).

For biochemical analysis, 50 grams from each of the harvest samples are freeze-dried and analyzed, using biochemical assays well known to those skilled in the art of plant biochemistry for quantities of simple sugars, amino acids, lipids, other extractives, lignin, and cellulose. See, e.g., Pettersen & Schwandt, J. Wood Chem. & Technol. 11:495 (1991).

In the present example, the phenotypes chosen for comparison are high density wood, average density wood, and low density wood. Nucleic acid samples are prepared as described in Example 3, from trees harvested in the spring and summer. Gene expression profiling by hybridization and data analysis is performed as described in Examples 3 and 4.

Using similar techniques and clonally propagated individuals one can examine cell cycle gene expression as it is related to other complex wood characteristics such as strength, stiffness and spirality.

Example 7

Example 7 demonstrates the ability of the oligonucleotide probes of the invention to distinguish between highly homologous members of a family of cell cycle genes. Hybridization to a particular oligonucleotide on the array identifies a unique WD40 gene that is expressed more strongly in a genotype having a higher density wood than in observed in other genotypes examined. The WD40 gene is also expressed more strongly in mature wood than in juvenile wood and more strongly in summer wood than in spring wood. This gene is not found to be expressed at high levels either in leaves or buds.

The gene expression pattern is confirmed by RT-PCR. This gene, the putative “density-related” gene, is used for in situ hybridization of fixed radial sections. The density-related WD40 gene hybridizes most strongly to the vascular cambium in regions of the stem where the xylem is comprised primarily of fibers with few vessel elements and few xylem ray cells.

These results suggest that the WD40 gene product functions in radial cell division, which occurs in the cambium and results in diameter growth, rather than in axial cell division such as may be important in the apex or leaves. Such a gene would be difficult to identify by cDNA microarrays or other traditional hybridization means because the highly conserved regions present in the gene would result in confusing it with genes encoding enzymes having similar catalytic functions, but acting in axial or radial divisions. Furthermore, from the sequence similarity-based annotation suggesting a function of this gene product in cell division and the observation of this microarray hybridization pattern, confirmed by RT-PCR and in silico hybridization, this gene product functions specifically in developing secondary xylem to guide the cell division patterns of fibers, such that higher expression of this gene results in greater fiber production relative to vessel element or ray production. The fiber content is correlated with a principal components analysis (PCA) variable that accounts for at least 10% of the variation in basic density.

Example 8

Example 8 demonstrates how the use of oligonucleotide probes of the invention can be used to identify one wood “density related” WD40 repeat protein gene and its promoter from among the family of homologous genes. Further, this example demonstrates how a promoter sequence identified using this method is used to transform other hardwood species to result in increased diameter growth rates as compared to wild-type plants of the same species.

The sequence of the WD40 gene is used to probe a Genome Walker library in order to isolate 5′ flanking sequences comprising a promoter region. The promoter region is then operably linked to a beta-glucuronidase reporter gene and cloned into a binary vector for transformation into Eucalyptus using the method described in U.S. Application Ser. No. 60/476,222. Regenerated transgenic tobacco and Eucalyptus plants are then sectioned and stained using X-gluc, demonstrating that the microarray data results in isolation of a promoter capable of highly cambial-specific expression solely in those portions of the stem that develop more fibers than vessel elements or xylem rays.

Using techniques well known to those skilled in the art of molecular biology, the promoter is then operably linked to a cell division promoting gene and this construct placed in a binary vector for transformation into hardwood plants such as Sweetgum and Populus, such that the cell division promoting gene is expressed more strongly than normally in the vascular cambium. This results in increased diameter growth rate in the transgenic hardwood plants relative to control hardwood plants.

Example 9

Example 9 demonstrates how a density related polypeptide can be linked to a tissue-preferred promoter and expressed in pine resulting in a plant with increased wood density.

A density-related polypeptide, which is more highly expressed during the early spring, is identified by the method described in Example 7. A DNA construct having the density-related polypeptide operably linked to a promoter is placed into an appropriate binary vector and transformed into pine using the method of Connett et al. (U.S. patent application Ser. Nos. 09/973,088 and 09/973,089). Pine plants are transformed as described in Connett et al., supra, and the transgenic pine plants are used to establish a forest planting. Increased density even in the spring wood (early wood) is observed in the transgenic pine plants relative to control pine plants which are not transformed with the density related DNA construct.

Example 10

Using techniques well known to those skilled in the art of molecular biology, the sequence of the putative density-related gene isolated in Example 7 is analyzed in genomic DNA isolated from alfalfa. This enables the identification of an orthologue in alfalfa whose sequence is then used to create an RNAi knockout construct. This construct is then transformed into alfalfa. See, e.g., Austin et al., Euphytica 85, 381 1995. The regenerated transgenic plants show lower fiber content and increased ray cells content in the xylem. Such properties improved digestability which results in higher growth rates in cattle fed on this alfalfa as compared to wild-type alfalfa of the same species.

Example 11

Example 11 demonstrates how gene expression analysis can be used to find gene variants which are present in mature plants having a desirable phenotype. The presence or absence of such a variant can be used to predict the phenotype of a mature plant, allowing screening of the plants at the seedling stage. Although this example employs eucalyptus, the method used herein is also useful in breeding programs for pine and other tree species.

The sequence of a putative density-related gene is used to probe genomic DNA isolated from Eucalyptus that vary in density as described in previous examples. Non-transgenically produced Eucalyptus hybrids of different wood phenotypes are examined. One hybrid exhibits high wood density and another hybrid exhibits lower wood density. A molecular marker in the 3′ portion of the coding region is found which distinguishes a high-density gene variant from a lower density gene variant.

This molecular marker enables tree breeders to assay non-transgenic Eucalyptus hybrids for likely density profiles while the trees are still at seedling stage, whereas in the absence of the marker, tree breeders must wait until the trees have grown for multiple years before density at harvest age can be reliably predicted. This enables selective outplanting of the best trees at seedling stage rather than an expensive culling operation and resultant erosion at thinning age. This molecular marker is further useful in the breeding program to determine which parents will give rise to high density outcross progeny.

Molecular markers found in the 3′ portion of the coding region of the gene that do not correspond to variants seen more frequently in higher or lower wood density non-transgenic Eucalyptus hybrid trees are also useful. These markers are found to be useful for fingerprinting different genotypes of Eucalyptus, for use in identity-tracking in the breeding program and in plantations.

Example 12

This Example describes microarrays for identifying gene expression differences that contribute to the phenotypic characteristics that are important in commercial wood, namely wood appearance, stiffness, strength, density, fiber dimensions, coarseness, cellulose and lignin content, extractives content and the like.

As in Examples 2-4, woody trees of genera that produce commercially important wood products, in this case Pinus and Eucalyptus, are felled from various sites and at various times of year for the collection and isolation of RNA from developing xylem, cambium, phloem, leaves, buds, roots, and other tissues. RNA is also isolated from seedlings of the same genera.

All contigs are compared to both the ESTs made from RNA isolated from samples containing developing wood and the sequences of the ESTs made from RNA of various tissues that do not contain developing wood. Contigs containing primarily ESTs that show more hybridization in silico to ESTs made from RNA isolated from samples containing developing wood than to ESTs made from RNA isolated from samples not containing developing wood are determined to correspond to possible novel genes particularly expressed in developing wood. These contigs are then used for BLAST searches against public domain sequences. Those contigs that hybridize with high stringency to no known genes or genes annotated as having only a “hypothetical protein” are selected for the next step. These contigs are considered putative novel genes showing wood-preferred expression.

The longest cDNA clones containing sequences hybridizing to the putative novel genes showing wood-preferred expression are selected from cDNA libraries using techniques well known to those skilled in the art of molecular biology. The cDNAs are sequenced and full-length gene-coding sequences together with untranslated flanking sequences are obtained where possible. Stretches of 45-80 nucleotides (or oligonucleotides) are selected from each of the sequences of putative novel genes showing wood-preferred expression such that each oligonucleotide probe hybridizes at high stringency to only one sequence represented in the ESTs made from RNA isolated from trees or seedlings of the same genus.

Oligomers are then chemically synthesized and placed onto a microarray slide as described in Example 3. Each oligomer corresponds to a particular sequence of a putative novel gene showing wood-preferred expression and to no other gene whose sequence is represented among the ESTs made from RNA isolated from trees or seedlings of the same genus.

Sample preparation and hybridization are carried out as in Example 4. The technique used in this example is more effective than use of a microarray using cDNA probes because the presence of a signal represents significant evidence of the expression of a particular gene, rather than of any of a number of genes that may contain similarities to the cDNA due to conserved functional domains or common evolutionary history. Thus, it is possible to differentiate homologous genes, such as those in the same family, but which may have different functions in phenotype determination.

Thus hybridization data, gained using the method of Example 4, enable the user to identify which of the putative novel genes actually has a pattern of coordinate expression with known genes, a pattern of expression consistent with a particular developmental role, and/or a pattern of expression that suggests that the gene has a promoter that drives expression in a valuable way.

The hybridization data thus using this method can be used, for example, to identify a putative novel gene that shows an expression pattern particular to the tracheids with the lowest cellulose microfibril angle in developing spring wood (early wood). The promoter of this gene can also be isolated as in Example 8, and operably linked to a gene that has been shown as in Example 9 to be associated with late wood (summer wood). Transgenic pine plants containing this construct are generated using the methods of Example 9, and the early wood of these plants is then shown to display several characteristics of late wood, such as higher microfibril angle, higher density, smaller average lumen size, etc.

Example 13

Example 13 demonstrates the use of a cambium-specific promoter functionally linked to a cell cycle gene for increased plant biomass.

Cambium-specific cell cycle transcripts are identified via array analyses of different secondary vasculature layers as described in Example 4. Candidate promoters linked to the genes corresponding to these transcripts are cloned from pine genomic DNA using, e.g., the BD Clontech GenomeWalker kit and tested in transgenic tobacco via a reporter assay(s) for cambium specificity/preference. The cambium-specific promoter overexpressing a cell cycle gene involved in secondary xylem cell division is used to increased wood biomass. A tandem cambium-specific promoter is constructed driving the cell cycle ORF. Boosted transcript levels of the candidate cell cycle gene result in an increased xylem biomass phenotype.

Example 14

Isolation and Characterization of cDNA Clones from Eucalyptus Grandis

Eucalyptus grandis cDNA expression libraries were prepared from mature shoot buds, early wood phloem, floral tissue, leaf tissue (two independent libraries), feeder roots, structural roots, xylem or early wood xylem and were constructed and screened as follows.

Total RNA was extracted from the plant tissue using the protocol of Chang et al. (Plant Molecular Biology Reporter 11:113-116 (1993). mRNA was isolated from the total RNA preparation using either a Poly(A) Quik mRNA Isolation Kit (Stratagene, La Jolla, Calif.) or Dynal Beads Oligo (dT)₂₅ (Dynal, Skogen, Norway). A cDNA expression library was constructed from the purified mRNA by reverse transcriptase synthesis followed by insertion of the resulting cDNA clones in Lambda ZAP using a ZAP Express cDNA Synthesis Kit (Stratagene), according to the manufacturer's protocol. The resulting cDNAs were packaged using a Gigapack II Packaging Extract (Stratagene) using an aliquot (1-5 αl) from the 5 μl ligation reaction dependent upon the library. Mass excision of the library was done using XL1-Blue MRF′ cells and XLOLR cells (Stratagene) with ExAssist helper phage (Stratagene). The excised phagemids were diluted with NZY broth (Gibco BRL, Gaithersburg, Md.) and plated out onto LB-kanamycin agar plates containing X-gal and isopropylthio-beta-galactoside (IPTG).

Of the colonies plated and selected for DNA miniprep, 99% contained an insert suitable for sequencing. Positive colonies were cultured in NZY broth with kanamycin and cDNA was purified by means of alkaline lysis and polyethylene glycol (PEG) precipitation. Agarose gel at 1% was used to screen sequencing templates for chromosomal contamination. Dye primer sequences were prepared using a Turbo Catalyst 800 machine (Perkin Elmer/Applied Biosystems Division, Foster City, Calif.) according to the manufacturer's protocol.

DNA sequence for positive clones was obtained using a Perkin Elmer/Applied Biosystems Division Prism 377 sequencer. cDNA clones were sequenced first from the 5′ end and, in some cases, also from the 3′ end. For some clones, internal sequence was obtained using either Exonuclease III deletion analysis, yielding a library of differentially sized subclones in pBK-CMV, or by direct sequencing using gene-specific primers designed to identified regions of the gene of interest.

The determined cDNA sequences were compared with known sequences in the EMBL database using the computer algorithms FASTA and/or BLASTN. Multiple alignments of redundant sequences were used to build reliable consensus sequences. Based on similarity to known sequences from other plant species, the isolated polynucleotide sequences were identified as encoding transcription factors, as detailed herein. The predicted polypeptide sequences corresponding to the polynucleotide sequences are also depicted therein.

Example 15

Isolation and Characterization of cDNA Clones from Pinus Radiata

Pinus radiata cDNA expression libraries (prepared from either shoot bud tissue, suspension cultured cells, early wood phloem (two independent libraries), fascicle meristem tissue, male strobilus, root (unknown lineage), feeder roots, structural roots, female strobilus, cone primordia, female receptive cones and xylem (two independent libraries) were constructed and screened as described above in Example 14.

DNA sequence for positive clones was obtained using forward and reverse primers on a Perkin Elmer/Applied Biosystems Division Prism 377 sequencer and the determined sequences were compared to known sequences in the database as described above.

Based on similarity to known sequences from other plant species, the isolated polynucleotide sequences were identified as encoding transcription factors, as detailed herein. The predicted polypeptide sequences corresponding to the polynucleotide sequences are also depicted therein.

Example 16

5′ RACE Isolation

To identify additional sequence 5′ or 3′ of a partial cDNA sequence in a cDNA library, 5′ and 3′ rapid amplification of cDNA ends (RACE) was performed using the SMART RACE cDNA amplification kit (Clontech Laboratories, Palo Alto, Calif.). Generally, the method entailed first isolating poly(A) mRNA, performing first and second strand cDNA synthesis to generate double stranded cDNA, blunting cDNA ends, and then ligating of the SMART RACE. Adaptor to the cDNA to form a library of adaptor-ligated ds cDNA. Gene-specific primers were designed to be used along with adaptor specific primers for both 5′ and 3′ RACE reactions. Using 5′ and 3′ RACE reactions, 5′ and 3′ RACE fragments were obtained, sequenced, and cloned. The process may be repeated until 5′ and 3′ ends of the full-length gene were identified. A full-length cDNA may generated by PCR using primers specific to 5′ and 3′ ends of the gene by end-to-end PCR.

For example, to amplify the missing 5′ region of a gene from first-strand cDNA, a primer was designed 5′→3′ from the opposite strand of the template sequence, and from the region between ˜100-200 bp of the template sequence. A successful amplification should give an overlap of ˜100 bp of DNA sequence between the 5′ end of the template and PCR product.

RNA was extracted from four pine tissues, namely seedling, xylem, phloem and structural root using the Concert Reagent Protocol (Invitrogen, Carlsbad, Calif.) and standard isolation and extraction procedures. The resulting RNA was then treated with DNase, using 10 U/ul DNase I (Roche Diagnostics, Basel, Switzerland). For 100 μg of RNA, 9 μl 10× DNase buffer (Invitrogen, Carlsbad, Calif.), 10 μl of Roche DNase I and 90 μl of Rnase-free water was used. The RNA was then incubated at room temperature for 15 minutes and 1/10 volume 25 mM EDTA is added. A RNeasy mini kit (Qiagen, Venlo, The Netherlands) was used for RNA clean up according to manufacturer's protocol.

To synthesize cDNA, the extracted RNA from xylem, phloem, seedling and root was used and the SMART RACE cDNA amplification kit (Clontech Laboratories Inc, Palo Alto, Calif.) was followed according to manufacturer's protocol. For the RACE PCR, the cDNA from the four tissue types was combined. The master mix for PCR was created by combining equal volumes of cDNA from xylem, phloem, root and seedling tissues. PCR reactions were performed in 96 well PCR plates, with 1 μl of primer from primer dilution plate (10 mM) to corresponding well positions. 49 μl of master mix is aliquoted into the PCR plate with primers. Thermal cycling commenced on a GeneAmp 9700 (Applied Biosystems, Foster City, Calif.) at the following parameters:

94° C. (5 sec),

72° C. (3 min), 5 cycles;

94° C. (5 sec),

70° C. (10 sec),

72° C. (3 min), 5 cycles;

94° C. (5 sec),

68° C. (10 sec),

72° C. (3 min), 25 cycles.

cDNA was separated on an agarose gel following standard procedures. Gel fragments were excised and eluted from the gel by using the Qiagen 96-well Gel Elution kit, following the manufacturer's instructions.

PCR products were ligated into pGEMTeasy (Promega, Madison, Wis.) in a 96 well plate overnight according to the following specifications: 60-80 ng of DNA, 5 μl 2× rapid ligation buffer, 0.5 μl pGEMT easy vector, 0.1 μl DNA ligase, filled to 10 μl with water, and incubated overnight.

Each clone was transformed into E. coli following standard procedures and DNA was extracted from 12 clones picked by following standard protocols. DNA extraction and the DNA quality was verified on an 1% agarose gel. The presence of the correct size insert in each of the clones was determined by restriction digests, using the restriction endonuclease EcoRI, and gel electrophoresis, following standard laboratory procedures.

Example 17

Curation of an EST Sequence.

During the production of cDNA libraries, the original transcripts or their DNA counterparts may have features that prevent them from coding for functional proteins. There may be insertions, deletions, base substitutions, or unspliced or improperly spliced introns. If such features exist, it is often possible to identify them so that they can be changed. Similar curation can be performed on any other sequences that have homology to sequences in the public databases.

After determination of the DNA sequence, BLAST analysis shows that it is related to an Arabidopsis gene on the publicly available Arabidopsis genome sequence). However, instead of coding for an approximately 240 amino acid polypeptide, the consensus being curated is predicted to code for a product of only 157 amino acid residues, suggesting an error in the DNA sequence. To identify where the genuine coding region might be, the DNA sequence to the end of each EST is translated in each of the three reading frames and the predicted sequences are aligned with the Arabidopsis gene's amino acid sequence. It is found that the DNA segment in one portion of the EST codes for a sequence with similarity to the carboxyl terminus of the Arabidopsis gene. Therefore, it appears that an unspliced intron is present in the EST.

Unspliced introns are a relatively minor issue with regard to use of a cloned sequence for overexpression of the gene of interest. The RNA resulting from transcription of the cDNA can be expected to undergo normal processing to remove the intron. Antisense and RNAi constructs are also expected to function to suppress the gene of interest. On other occasions, it may be desirable to identify the precise limits of the intron so that it can be removed. When the sequence in question has a published sequence that is highly similar, it may be possible to find the intron by aligning the two sequences and identifying the locations where the sequence identity falls off, aided by the knowledge that introns start with the sequence GT and end with the sequence AG.

When there is some doubt about the site of the intron because highly similar sequences are not available, the intron location can be verified experimentally. For example, DNA oligomers can be synthesized flanking the region where the suspected intron is located. RNA from the source species, either Pinus or Eucalyptus, is isolated and used as a template to make cDNA using reverse transcriptase. The selected primers are then used in a PCR reaction to amplify the correctly spliced DNA segment (predicted size of approximately 350 by smaller than the corresponding segment of the original consensus) from the population of cDNAs. The amplified segment is then subjected to sequence analysis and compared to the consensus sequence to identify the differences.

The same procedure can be used when an alternate splicing event (partial intron remaining, or partial loss of an exon) is suspected. When an EST has a small change, such as insertion or deletion of a small number of bases, computer analysis of the EST sequence can still indicate its location when a translation product of the wrong size is predicted or if there is an obvious frameshift. Verification of the true sequence is done by synthesis of primers, production of new cDNA, and PCR amplification as described above.

Example 18

Transformation of Populus deltoides with constructs containing cell cycle genes.

Constructs made as described in the preceding example and shown in Table 2 below were each inoculated into Agrobacterium cultures by standard techniques.

Table 2 identifies plasmid(s), genes, and Genesis ID numbers for constructions described in Example 17.

	TABLE 2
	Plasmid(s)	Gene	Genesis ID
	pGrw14	Cyclin A	prga001823
	pGrw15	Cyclin A	prpe001264
	pGrw16	Cyclin D	prxa004540
	pGrw18	Cyclin D	prxl006271
	PGrw19	Cyclin D	prpb019661
	PGrw20	WEE1-like protein	prrd041233

Populus deltoides stock plant cultures were maintained on DKW medium (Driver and Kuniyuki, 1984, McGranahan et al. 1987, available commercially from Sigma/Aldrich) with 2.5 uM zeatin in a growth room with a 16 h photoperiod. For transformation, petioles were excised aseptically using a sharp scalpel blade from the stock plants, cut into 4-6 mm lengths, placed on DKW medium with 1 ug/ml BAP and 1 ug/ml NAA immediately after harvest, and incubated in a dark growth chamber (28 degrees) for 24 hours.

Agrobacterium cultures containing the desired constructs were grown to log phase, indicated by an OD600 between 0.8-1.0 A, then pelleted and resuspended in an equal volume of Agrobacterium Induction Medium (AIM), which contains Woody Plant Medium salts (Lloyd, G., and McCown, B., 1981. Woody plant medium. Proc. Intern. Plant Prop. Soc. 30:421, available commercially from Sigma/Aldrich), 5 g/L glucose and 0.6 g/L MES at pH 5.8, with the addition of 1 ul of a 100 mM stock solution of acetosyringone per ml of AIM. The pellet was resuspended by vortexing. The bacterial cells were incubated for an hour in this medium at 28 degrees C. in an environmental chamber, shaking at 100 rpm.

After the induction period, Populus deltoides explants were exposed to the Agrobacterium mixture for 15 minutes. The explants were then lightly blotted on sterile paper towels, replaced onto the same plant medium and cultured in the dark at 18-20 degrees C. After a three-day co-cultivation period, the explants were transferred to DKW medium in which the NAA concentration was reduced to 0.1 ug/ml and to which was added 400 mg/L timentin to eradicate the Agrobacterium.

After 4 days on eradication medium, explants were transferred to small magenta boxes containing the same medium supplemented with timentin (400 mg/L) as well as the selection agent geneticin (50 mg/L). Explants were transferred every two weeks to fresh selection medium. Calli that grow in the presence of selection were isolated and sub-cultured to fresh selection medium every three weeks. Calli were observed for the production of adventitious shoots.

Adventitious shoots were normally observed within two months from the initiation of transformation. These shoot clusters were transferred to DKW medium to which no NAA was added, and in which the BAP concentration was reduced to 0.5 ug.ml, for shoot elongation, typically for about 14 weeks. Elongated shoots were excised and transferred to BTM medium (Chalupa, Communicationes Instituti Forestalis Checosloveniae 13:7-39, 1983, available commercially from Sigma/Aldrich) at pH5.8, containing 20 g/l sucrose and 5 g/l activated charcoal. See Table 3 below.

TABLE 3
Rooting medium for Populus deltoids.

	BTM-1 Media Components	mg/L
	NH4NO3	412
	KNO3	475
	Ca(NO3)2•4H2O	640
	CaCl2•2H2O	440*
	MgSO4•7H2O	370
	KH2PO4	170
	MnSO4•H2O	2.3
	ZnSO4•7H2O	8.6
	CuSO4•5H2O	0.25
	CoCl2•6H2O	0.02
	KI	0.15
	H3BO3	6.2
	Na2MoO4•2H2O	0.25
	FeSO4•7H2O	27.8
	Na2EDTA•2H2O	37.3
	Myo-inositol	100
	Nicotinic acid	0.5
	Pyridoxine HCl	0.5
	Thiamine HCl	1
	Glycine	2
	Sucrose	20000
	Activated Carbon	5000

After development of roots, typically four weeks, transgenic plants were propagated in the greenhouse by rooted cutting methods, or in vitro through axillary shoot induction for four weeks on DKW medium containing 11.4 uM zeatin, after which the multiplied shoots were separated and transferred to root induction medium. Rooted plants were transferred to soil for evaluation of growth in glasshouse and field conditions.

Example 19

Production of disproportionately large leaves mediated by ectopic expression of certain cyclin D genes

Approximately 100 explants of Populus deltoides per construct were transformed with pGRW16 and pGRW19, which contain genes that are normally show preferred expression in the vasculature, driven by a constitutive promoter (the Pinus radiata superubiquitin promoter). Upon regeneration, many of the ramets of many of the translines were observed to have disproportionately large leaves relative to control plants. The leaves were both longer and broader than those of control plants.

Disproportionately large leaves could be a very useful early indicator of growth potential large leaf size and thus high growth potential. Lage leaf size can be a function of either increased numbers of leaf cells or increased leaf cell size or both.

Example 20

Production of unusual vascular development mediated by ectopic expression of a cyclin D gene.

Approximately 100 explants of Populus deltoides per construct were transformed with pGRW18. Multiple transgenic lines regenerated from this experiment showed a very unique pleiotropic phenotype. Leaves of these transgenic lines symmetrically folded on both sides of the midrib down the entire length of the leaf. Many petioles of these lines spiraled, and in many cases turned 360 degrees, in a right-handed fashion towards the leaf. The stem showed some thickening and slight bending near the middle.

One ramet of the transgenic line TDL002534 showing these phenotypes was sacrificed to investigate these aberrancies at the tissue level. Transverse sections of a curling petiole stained with toluidine blue revealed retardation of vascular development, but the presence of additional vascular cylinders developing as indicated by the black arrows. The xylem and phloem within the vascular cylinders of the curling petiole appeared to be developmentally similar and spatially oriented correctly. Longitudinal sections of straight and curled petioles may offer an explanation for the spiraling phenomenon. Curled petioles showed more elongated cells on the outside turn of the curl and more compressed cells on the opposite side of the petiole.

Perhaps the most striking phenotype was identified in the leaves. As with the petioles, aberrant vascular development was noted, comprising additional forming vascular cylinders lateral to the larger midrib. In some sections almost fully-formed veins could be seen immediately adjacent to the midrib. In all instances where the folding phenotype was noted, this type of leaf configuration was associated with the phenotype.

The development of additional vascular cylinders in the space where normally a small number of vascular bundles or a single midrib are seen is indicative of unusual cell division activity at the level of early vascular development. Thus, this gene expressed under the control of a vascular-preferred promoter rather than a constitutive promoter could have utility in increasing cell division in later vascular development, creating additional wood.

Example 21

This example illustrates how polynucleotides important for wood development in P. radiata can be determined and how oligonucleotides which uniquely bind to those genes can be designed and synthesized for use on a microarray.

Open pollinated trees of approximately 16 years of age are selected from plantation-grown sites, in the United States for loblolly pine, and in New Zealand for radiata pine. Trees are felled during the spring and summer seasons to compare the expression of genes associated with these different developmental stages of wood formation. Trees are felled individually and trunk sections are removed from the bottom area approximately one to two meters from the base and within one to two meters below the live crown. The section removed from the basal end of the trunk contains mature wood. The section removed from below the live crown contains juvenile wood. Samples collected during the spring season are termed earlywood or springwood, while samples collected during the summer season are considered latewood or summerwood (Larson et al., Gen. Tech. Rep. FPL-GTR-129. Madison, Wis.: U.S. Department of Agriculture, Forest Service, Forest Products Laboratory. p. 42).

Tissues are isolated from the trunk sections such that phloem, cambium, developing xylem, and maturing xylem are removed. These tissues are collected only from the current year's growth ring. Upon tissue removal in each case, the material is immediately plunged into liquid nitrogen to preserve the nucleic acids and other components. The bark is peeled from the section and phloem tissue removed from the inner face of the bark by scraping with a razor blade. Cambium tissue is isolated from the outer face of the peeled section by gentle scraping of the surface. Developing xylem and lignifying xylem are isolated by sequentially performing more vigorous scraping of the remaining tissue. Tissues are transferred from liquid nitrogen into containers for long term storage at −70 until RNA extraction and subsequent analysis is performed.

Example 22

This example illustrates a procedure for RNA extraction and purification, which is particularly useful for RNA obtained from conifer needle, xylem, cambium, and phloem.

Tissue is obtained from conifer needle, xylem, cambium or phloem. The tissue is frozen in liquid nitrogen and ground. The total RNA is extracted using Concert Plant RNA reagent (Invitrogen). The resulting RNA sample is extracted into phenol:chloroform and treated with DNase. The RNA is then incubated at 65° C. for 2 minutes followed by centrifugation at 4° C. for 30 minutes. Following centrifugation, the RNA is extracted into phenol at least 10 times to remove contaminants.

The RNA is further cleaned using RNeasy columns (Qiagen). The purified RNA is quantified using RiboGreen reagent (Molecular Probes) and purity assessed by gel electrophoresis.

RNA is then amplified using MessageAmp (Ambion). Aminoallyl-UTP and free UTP are added to the in vitro transcription of the purified RNA at a ratio of 4:1 aminoallyl-UTP-to-UTP. The aminoallyl-UTP is incorporated into the new RNA strand as it is transcribed. The amino-allyl group is then reacted with Cy dyes to attach the colorimetric label to the resulting amplified RNA using the Amersham procedure modified for use with RNA. Unincorporated dye is removed by ethanol precipitation. The labeled RNA is quantified spectrophotometrically (NanoDrop). The labeled RNA is fragmented by heating to 95° C. as described in Hughes et al., Nature Biotechnol. 19:342 (2001).

Example 23

This Example illustrates how genes important for wood development in P. radiata can be determined and how oligonucleotides which uniquely bind to those genes can be designed and synthesized for use on a microarray.

Pine trees of the species P. radiata are grown under natural light conditions. Tissue samples are prepared as described in, e.g., Sterky et al., Proc. Nat'l Acad. Sci. 95:13330 (1998). Specifically, tissue samples are collected from woody trees having a height of 5 meters. Tissue samples of the woody trees are prepared by taking tangential sections through the cambial region of the stem. The stems are sectioned horizontally into sections ranging from juvenile (top) to mature (bottom). The stem sections separated by stage of development are further separated into 5 layers by peeling into sections of phloem, differentiating phloem, cambium, differentiating xylem, developing xylem, and mature xylem. Tissue samples, including leaves, buds, shoots, and roots are also prepared from seedlings of the species P. radiata.

RNA is isolated and ESTs generated as described in the Example above or Sterky et al., supra. The nucleic acid sequences of ESTs derived from samples containing developing wood are compared with nucleic acid sequences of genes known to be involved in polysaccharide synthesis. ESTs from samples that do not contain developing wood are also compared with sequences of genes known to be involved in the plant cell cycle. An in silico hybridization analysis is performed using BLAST (NCBI) as follows.

Example 24

Eucalyptus in Silico Data

In silico gene expression can be used to determine the membership of the consensi EST libraries. For each library, a consensus is determined from the number of ESTs in any tissue class divided by the total number of ESTs in a class multiplied by 1000. These values provide a normalized value that is not biased by the extent of sequencing from a library. Several libraries were sampled for a consensus value, including reproductive, bud reproductive, bud vegetative, fruit, leaf, phloem, cambium, xylem, root, stem, sap vegetative, whole plant libraries.

As shown below, a number of the inventive sequences exhibit vascular-preferred expression (more than 50% of the hits by these sequences if the databases were searched at random would be in libraries made from developing vascular tissue) and thus are likely to be involved in wood-related developmental processes. The data are shown in Table 12.

Example 25

Pinus in Silico Data

In silico gene expression can be used to determine the membership of the consensi EST libraries. For each library, a consensus is determined from the number of ESTs in any tissue class divided by the total number of ESTs in a class multiplied by 1000. These values provide a normalized value that is not biased by the extent of sequencing from a library. Several libraries were sampled for a consensus value, including needles, phloem, cambium, xylem, root, stem and, whole plant libraries.

As shown below, a number of the inventive sequences exhibit vascular-preferred expression (more than 50% of the hits by these sequences if the databases were searched at random would be in libraries made from developing vascular tissue) and thus are likely to be involved in wood-related developmental processes. The data are shown in Table 13.

Example 26

Sequences that show hybridization in silico to ESTs made from samples containing developing wood, but that do not hybridize to ESTs from samples not containing developing wood are selected for further examination.

cDNA clones containing sequences that hybridize to the genes showing wood-preferred expression are selected from cDNA libraries using techniques well known in the art of molecular biology. Using the sequence information, oligonucleotides are designed such that each oligonucleotide is specific for only one cDNA sequence in the library. The oligonucleotide sequences are provided in Table 14. 60-mer oligonucleotide probes are designed using the method of Li and Stormo, supra or using software such as ArrayDesigner, GeneScan, and ProbeSelect.

The oligonucleotides are then synthesized in situ described in Hughes et al., Nature Biotechnol. 19:324 (2002) or as described in Kane et al., Nucleic Acids Res. 28:4552 (2000) and affixed to an activated glass slide (Sigma-Genosis, The Woodlands, Tex.) using a 5′ amino linker. The position of each oligonucleotide on the slide is known.

Example 27

This example illustrates how to detect expression of Pinus radiata genes of the instant application which are important in wood formation using an oligonucleotide microarray prepared as described above. This is an example of a balanced incomplete block designed experiment carried out using aRNA samples prepared from mature-phase phloem (P), cambium (C), expanding xylem found in a layer below the cambium (X1) and differentiating, lignifying xylem cells found deeper in the same growth ring (X2). In this example, cell cycle gene expression is compared among the four samples, namely P, C, X1, and X2.

In the summer, plants of the species Pinus radiata are felled and the bark of the main stem is immediately pulled gently away to reveal the phloem and xylem. The phloem and xylem are then peeled with a scalpel into separate containers of liquid nitrogen. Needles (leaves) and buds from the trees are also harvested with a scalpel into separate containers of liquid nitrogen. RNA is subsequently isolated from the frozen tissue samples as described in Example 1. Equal microgram quantities of total RNA are purified from each sample using RNeasy Mini columns (Qiagen, Valencia, Calif.) according to the manufacturers instructions.

Amplification reactions are carried out for each of the P, C, X1, and X2 tissue samples. Amplification reactions are performed using Ambion's MessageAmp kit, a T7-based amplification procedure, following the manufacturer's instructions, except that labeled aaUTP is added to the reagent mix during in the amplification step. aaUTP is incorporated into the resulting antisense RNA formed during this step. CyDye fluorescent labels are coupled to the aaUTPs in a non-enzymatic reaction as described in Example 1. Labeled amplified antisense RNAs are precipitated and washed, and then assayed for purity using a NanoDrop spectrophotometer. These labeled antisense RNAs, corresponding to the RNA isolated from the P, C, X1, and X2 tissue samples, constitute the sample nucleic acids, which are referred to as the P, C, X1, and X2 samples.

Normalization control samples of known nucleic acids are added to each sample in a dilution series of 500, 200, 100, 50, 25 and 10 pg/μl for quantitation of the signals. Positive controls corresponding to specific genes showing expression in all tissues of pine, such as housekeeping genes, are also added to the plant sample.

Each of four microarray slides is incubated with 125 μL of a P, C, X1 or X2 sample under a coverslip at 42° C. for 16-18 hours. The arrays are washed in 1×SSC, 0.1% SDS for 10 minutes and then in 0.1×SSC, 0.1% SDS for 10 minutes and the allowed to dry.

The array slides are scanned using an Axon laser scanner and analyzed using GenePix Pro software. Data from the microarray slides are subjected to microarray data analysis using GenStat SAS or Spotfire software. Outliers are removed and ratiometric data for each of the datasets are normalized using a global normalization which employs a cubic spline fit applied to correct for differential dye bias and spatial effects. A second transformation is performed to fit control signal ratios to a mean log²=0 (i.e. 1:1 ratio). Normalized data are then subjected to a variance analysis.

Mean signal intensity for each signal at any given position on the microarray slide is determined for each of three of P, C, X1, and X2 sample microarray slides. This mean signal/probe position is compared to the signal at the same position on sample slide which was not used for calculating the mean. For example, a mean signal at a given position is determined for P, C, and X1 and the signal at that position in the X2 microarray slide is compared to the P, C, and X1 mean signal value.

Table 5 shows genes having greater than doubled signal with any one sample as compared to the mean signal of the other three samples.

	TABLE 5
	Gene	PvCX12	PvX12	CvX12

	WD40 repeat protein A	−1.24	−0.88	−1.07
	CDC2	−1.09	−0.78	−0.92
	CYCLIN	−1.08	−1	−0.26
	WD-40 repeat protein B	−1.01	−0.87	−0.42
	CDC2	−0.83	−0.49	−1.01
	P = Phloem
	C = Cambium
	X1 = xylem layer-1
	X2 = xylem layer-2
	PvCX12 = Ratio of the signal for Phloem target versus mean signal for Cambium, Xylem1, and Xylem2 targets

The data shows that WD40 repeat protein A encodes a WD40 repeat protein is less highly expressed in cambium than in developing xylem, while WD40 repeat protein B encodes a WD40 repeat protein that is more highly expressed in phloem than in the other tissues.

Signal data are then verified with RT-PCR to confirm gene expression in the target tissue of the genes corresponding to the unique oligonucleotides in the probe.

Example 28

This example illustrates how RNAs of tissues from multiple pine species, in this case both P. radiata and loblolly pine P. taeda trees, are selected for analysis of the pattern of gene expression associated with wood development in the juvenile wood and mature wood forming sections of the trees using the microarrays derived from P. radiata cDNA sequences described in Example 4.

Open pollinated trees of approximately 16 years of age are selected from plantation-grown sites, in the United States for loblolly pine, and in New Zealand for radiata pine. Trees are felled during the spring and summer seasons to compare the expression of genes associated with these different developmental stages of wood formation. Trees are felled individually and trunk sections are removed from the bottom area approximately one to two meters from the base and within one to two meters below the live crown. The section removed from the basal end of the trunk contains mature wood. The section removed from below the live crown contains juvenile wood. Samples collected during the spring season are termed earlywood or springwood, while samples collected during the summer season are considered latewood or summerwood. Larson et al., Gen. Tech. Rep. FPL-GTR-129. Madison, Wis.: U.S. Department of Agriculture, Forest Service, Forest Products Laboratory. p. 42.

Tissues are isolated from the trunk sections such that phloem, cambium, developing xylem, and maturing xylem are removed. These tissues are collected only from the current year's growth ring. Upon tissue removal in each case, the material is immediately plunged into liquid nitrogen to preserve the nucleic acids and other components. The bark is peeled from the section and phloem tissue removed from the inner face of the bark by scraping with a razor blade. Cambium tissue is isolated from the outer face of the peeled section by gentle scraping of the surface. Developing xylem and lignifying xylem are isolated by sequentially performing more vigorous scraping of the remaining tissue. Tissues are transferred from liquid nitrogen into containers for long term storage at −70° C. until RNA extraction and subsequent analysis is performed.

Example 29

This example illustrates procedures alternative to those used in the example above for RNA extraction and purification, particularly useful for RNA obtained from a variety of tissues of woody plants, and a procedure for hybridization and data analysis using the arrays described in Example 4.

RNA is isolated according to the protocol of Chang et al., Plant Mol. Biol. Rep. 11:113. DNA is removed using DNase I (Invitrogen, Carlsbad, Calif.) according to the manufacturer's recommendations. The integrity of the RNA samples is determined using the Agilent 2100 Bioanalyzer (Agilent Technologies, USA).

10 μg of total RNA from each tissue is reverse transcribed into cDNA using known methods.

In the case of Pinus radiata phloem tissue, it can be difficult to extract sufficient amounts of total RNA for normal labelling procedures. Total RNA is extracted and treated as previously described and 100 ng of total RNA is amplified using the Ovation™ Nanosample RNA Amplification system from NuGEN™ (NuGEN, CA, USA). Similar amplification kits such as those manufactured by Ambion may alternatively be used. The amplified RNA is reverse transcribed into cDNA and labelled as described above.

Hybridization and stringency washes are performed using the protocol as described in the US Patent Application for “Methods and Kits for Labeling and Hybridizing cDNA for Microarray Analysis” (supra) at 42 C. The arrays (slides) are scanned using a ScanArray 4000 Microarray Analysis System (GSI Lumonics, Ottawa, ON, Canada). Raw, non-normalized intensity values are generated using QUANTARRAY software (GSI Lumonics, Ottawa, ON, Canada).

A fully balanced, incomplete block experimental design (Kerr and Churchill, Gen. Res. 123:123, 2001) is used in order to design an array experiment that would allow maximum statistical inferences from analyzed data.

Gene expression data is analyzed using the SAS® Microarray Solution software package (The SAS Institute, Cary, N.C., USA). Resulting data was then visualized using JMP® (The SAS Institute, Cary, N.C., USA).

Analysis done for this experiment is an ANOVA approach with mixed model specification (Wolfinger et al., J. Comp. Biol. 8:625-637). Two steps of linear mixed models are applied. The first one, normalization model, is applied for global normalization at slide-level. The second one, gene model, is applied for doing rigorous statistical inference on each gene. Both models are stated in Models (1) and (2).

log₂(Y_ijkls)=θ_ij+D_k+S_l+DS_kl+ω_ijkls   (1)

R_ijkls^(g)=μ_ij^(g)+D_k^(g)+S_l^(g)+DS_kl^(g)+SS_ls^(g)+ε_ijkls^(g)   (2)

Y_ijkls represents the intensity of the s^th spot in the 1^th slide with the k^th dye applying the j^th treatment for the i^th cell line. θ_ij, D_k, S_l, and D_Skl represent the mean effect of the jth treatment in the ith cell line, the kth dye effect, the l^th slide random effect, and the random interaction effect of the k^th dye in the l^th slide. ω_ijkls is the stochastic error term. represent the similar roles as θ_ij, D_k, S_l, and D_Skl except they are specific for the g^th gene. R_ijkls^(g) represents the residual of the g^th gene from model (1). μ_ij^(g), D_k^(g), S_l^(g), and DS_kl^(g) represent the similar roles as θ_ij, D_k, S_l, and DS_kl except they are specific for the g^th gene. SS_ls^(g) represent the spot by slide random effect for the g^th gene. ε_ijkls^(g) represent the stochastic error term. All random terms are assumed to be normal distributed and mutually independent within each model.

According to the analysis described above, certain cDNAs, some of which are shown in Table 6 below, are found to be differentially expressed.

TABLE 6
Gene corresponding
to SEQ ID	Oligo ID	Gene_Family	Expression
162	Pra_000171_O_4	Peptidylprolyl isomerase	steady state RNA higher
			in xylem than cambium
164	Pra_001480_O_3	Peptidylprolyl isomerase	steady state RNA lower
			in xylem than cambium
control	Pra_000218_O_2	RIBONUCLEOSIDE-DIPHOSPHATE	steady state RNA lower
		REDUCTASE LARGE CHAIN (EC1.17.4.1).	in xylem than cambium
control	Pra_000193_O_2	PUTATIVE SURFACE PROTEIN.	steady state RNA lower
			in xylem than cambium

The involvement of these specific genes in wood development is inferred through the association of the up-regulation or down-regulation of genes to the particular stages of wood development. Both the spatial continuum of wood development across a section (phloem, cambium, developing xylem, maturing xylem) at a particular season and tree trunk position and the relationships of season and tree trunk position are considered when making associations of gene expression to the relevance in wood development.

Example 30

This example demonstrates how one can correlate polysaccharide gene expression with agronomically important wood phenotypes such as density, stiffness, strength, distance between branches, and spiral grain.

Mature clonally propagated pine trees are selected from among the progeny of known parent trees for superior growth characteristics and resistance to important fungal diseases. The bark is removed from a tangential section and the trees are examined for average wood density in the fifth annual ring at breast height, stiffness and strength of the wood, and spiral grain. The trees are also characterized by their height, mean distance between major branches, crown size, and forking.

To obtain seedling families that are segregating for major genes that affect density, stiffness, strength, distance between branches, spiral grain and other characteristics that may be linked to any of the genes affecting these characteristics, trees lacking common parents are chosen for specific crosses on the criterion that they exhibit the widest variation from each other with respect to the density, stiffness, strength, distance between branches, and spiral grain criteria. Thus, pollen from a tree exhibiting high density, low mean distance between major branches, and high spiral grain is used to pollinate cones from the unrelated plus tree among the selections exhibiting the lowest density, highest mean distance between major branches, and lowest spiral grain. It is useful to note that “plus trees” are crossed such that pollen from a plus tree exhibiting high density are used to pollinate developing cones from another plus tree exhibiting high density, for example, and pollen from a tree exhibiting low mean distance between major branches would be used to pollinate developing cones from another plus tree exhibiting low mean distance between major branches.

Seeds are collected from these controlled pollinations and grown such that the parental identity is maintained for each seed and used for vegetative propagation such that each genotype is represented by multiple ramets. Vegetative propagation is accomplished using micropropagation, hedging, or fascicle cuttings. Some ramets of each genotype are stored while vegetative propagules of each genotype are grown to sufficient size for establishment of a field planting. The genotypes are arrayed in a replicated design and grown under field conditions where the daily temperature and rainfall are measured and recorded.

The trees are measured at various ages to determine the expression and segregation of density, stiffness, strength, distance between branches, spiral grain, and any other observable characteristics that may be linked to any of the genes affecting these characteristics. Samples are harvested for characterization of cellulose content, lignin content, cellulose microfibril angle, density, strength, stiffness, tracheid morphology, ring width, and the like. RNA is then collected from replicated samples of trees showing divergent stiffness and density, or other characteristics, from genotypes that are otherwise as similar as possible in growth habit, in spring and fall so that early and late wood development is assayed. These samples are examined for gene expression similarly as described in above examples.

TABLE 7
Concensus ID Information.

Patent app	SEQ ID	Gene Family	Consensus_ID	Expression
—	control	Ribonucleoside-	pinusRadiata_000218	up in early spring xylem
		diphosphate reductase		vs late summer xylem
Cell Cycle	168	Peptidylprolyl	pinusRadiata_001692	up in juvenile
		isomerase		developing wood vs
				mature developing xylem
—	control	Nitrite transporter	pinusRadiata_016801	up mature developing xylem
				vs juvenile cambium

Ramets of each genotype are compared to ramets of the same genotype at different ages to establish age:age correlations for these characteristics.

Example 31

Example 8 demonstrates how responses to environmental conditions such as light and season alter plant phenotype and can be correlated to polysaccharide synthesis gene expression using microarrays. In particular, the changes in gene expression associated with wood density are examined.

Trees of three different clonally propagated E. grandis hybrid genotypes are grown on a site with a weather station that measures daily temperatures and rainfall. During the spring and subsequent summer, genetically identical ramets of the three different genotypes are first photographed with north-south orientation marks, using photography at sufficient resolution to show bark characteristics of juvenile and mature portions of the plant, and then felled. The age of the trees is determined by planting records and confirmed by a count of the annual rings. In each of these trees, mature wood is defined as the outermost rings of the tree below breast height, and juvenile wood as the innermost rings of the tree above breast height. Each tree is accordingly sectored as follows:

NM—NORTHSIDE MATURE

SM—SOUTHSIDE MATURE

NT—NORTHSIDE TRANSITION

ST—SOUTHSIDE TRANSITION

NJ—NORTHSIDE JUVENILE

SJ—SOUTHSIDE JUVENILE

Tissue is harvested from the plant trunk as well as from juvenile and mature form leaves. Samples are prepared simultaneously for phenotype analysis, including plant morphology and biochemical characteristics, and gene expression analysis. The height and diameter of the tree at the point from which each sector was taken is recorded, and a soil sample from the base of the tree is taken for chemical assay. Samples prepared for gene expression analysis are weighed and placed into liquid nitrogen for subsequent preparation of RNA samples for use in the microarray experiment. The tissues are denoted as follows:

P—phloem

C—cambium

X1—expanding xylem

X2—differentiating and lignifying xylem

Thin slices in tangential and radial sections from each of the sectors of the trunk are fixed as described in Ruzin, PLANT MICROTECHNIQUE AND MICROSCOPY, Oxford University Press, Inc., New York, N.Y. (1999) for anatomical examination and confirmation of wood developmental stage. Microfibril angle is examined at the different developmental stages of the wood, for example juvenile, transition and mature phases of Eucalyptus grandis wood. Other characteristics examined are the ratio of fibers to vessel elements and ray tissue in each sector. Additionally, the samples are examined for characteristics that change between juvenile and mature wood and between spring wood and summer wood, such as fiber morphology, lumen size, and width of the S2 (thickest) cell wall layer. Samples are further examined for measurements of density in the fifth ring and determination of modulus of elasticity using techniques well known to those skilled in the art of wood assays. See, e.g., Wang, et al., Non-destructive Evaluations of Trees, EXPERIMENTAL TECHNIQUES, pp. 28-30 (2000).

For biochemical analysis, 50 grams from each of the harvest samples are freeze-dried and analyzed, using biochemical assays well known to those skilled in the art of plant biochemistry for quantities of simple sugars, amino acids, lipids, other extractives, lignin, and cellulose. See, e.g., Pettersen & Schwandt, J. Wood Chem. & Technol. 11:495 (1991).

In the present example, the phenotypes chosen for comparison are high density wood, average density wood, and low density wood. Nucleic acid samples are prepared as described in Example 3, from trees harvested in the spring and summer. Gene expression profiling by hybridization and data analysis is performed as described above.

Using similar techniques and clonally propagated individuals one can examine polysaccharide gene expression as it is related to other complex wood characteristics such as strength, stiffness and spirality.

Example 32

Example 32 demonstrates the use of a vascular-preferred promoter functionally linked to one of the genes of the instant application.

A vascular-preferred promoter is then linked to one of the genes in the instant application and used to transform tree species. Boosted transcript levels of the candidate gene in the xylem of the transformants results in an increased xylem biomass phenotype.

In another example, a vascular-preferred promoter such as any of those in ArborGen's November 2003 patent applications is then linked to an RNAi construct containing sequences from one of the genes in the instant application and used to transform a tree of the genus from which the gene was isolated. Reduced transcript levels of the candidate gene in the xylem of the transformants results in an increased xylem biomass phenotype.

Example 33

The vector pARB476 was developed using the following steps. The Bluescript vector (Stratagene, La Jolla, Calif.) was modified by adding the Superubiquitin 3′UTR and nos 3′terminator sequence at the KpnI and ClaI sites to produce the vector pARB005 (SEQ ID NO. 773). To this vector the P. radiata superubiquitin promoter with intron was added. The promoter/intron sequence was first amplified from the P. radiata superubiquitin sequence identified in U.S. Pat. No. 6,380,459 using standard PCR techniques and the primers of SEQ ID NOS 774 and 775. The amplified fragment was then ligated into pARB005 using XbaI and PstI restriction digestion to produce the vector pARB119 (SEQ ID NO. 776).

The poplus tremuloises UDB Glucose binding domain gene (patent WO 0071670, ptCelA Genbank number AF072131) was amplified using standard PCR techniques and primers including and ATG and a ClaI site as part of the 5′ primer and a TGA and a ClaI site as part of the 3′ primer. The amplified fragment was then cloned into the ClaI site of pARB119 to produce the vector pARB476 (SEQ ID NO. 777).

The NotI cassette containing the P. radiata superubiquitin promoter with intron::UDP Glucose Binding domain::3′UTR: nos terminator from pARB476 was removed and cloned into the NotI site of pART29 to produce the vector pARB483. The binary vector pART29 is a modified pART27 vector (Gleave, Plant Mol. Biol. 20:1203-1207, 1992) that contains the Arabidopsis thaliana ubiquitin 3 (UBQ3) promoter instead of the nos5′ promoter and no lacZ sequences.

SEQ ID 773

CGATGGGTGTTATTTGTGGATAATAAATTCGGGTGATGTTCAGTGTTTGTCGTATTTCTCACGAATAAA
TTGTGTTTATGTATGTGTTAGTGTTGTTTGTCTGTTTCAGACCCTCTTATGTTATATTTTTCTTTTCGT
CGGTCAGTTGAAGCCAATACTGGTGTCCTGGCCGGCACTGCAATACCATTTCGTTTAATATAAAGACTC
TGTTATCCGTGAGCTCGAATTTCCCCGATCGTTCAAACATTTGGCAATAAAGTTTCTTAAGATTGAATC
CTGTTGCCGGTCTTGCGATGATTATCATATAATTTCTGTTGAATTACGTTAAGCATGTAATAATTAACA
TGTAATGCATGACGTTATTTATGAGATGGGTTTTTATGATTAGAGTCCCGCAATTATACATTTAATACG
CGATAGAAAACAAAATATAGCGCGCAAACTAGGATAAATTATCGCGCGCGGTGTCATCTATGTTACTAG
ATCGCGGCCGCATTTAAATGGTACCCAATTCGCCCTATAGTGAGTCGTATTACGCGCGCTCACTGGCCG
TCGTTTTACAACGTCGTGACTGGGAAAACCCTGGCGTTACCCAACTTAATCGCCTTGCAGCACATCCCC
CTTTCGCCAGCTGGCGTAATAGCGAAGAGGCCCGCACCGATCGCCCTTCCCAACAGTTGCGCAGCCTGA
ATGGCGAATGGGACGCGCCCTGTAGCGGCGCATTAAGCGCGGCGGGTGTGGTGGTTACGCGCAGCGTGA
CCGCTACACTTGCCAGCGCCCTAGCGCCCGCTCCTTTCGCTTTCTTCCCTTCCTTTCTCGCCACGTTCG
CCGGCTTTCCCCGTCAAGCTCTAAATCGGGGGCTCCCTTTAGGGTTCCGATTTAGTGCTTTACGGCACC
TCGACCCCAAAAAACTTGATTAGGGTGATGGTTCACGTAGTGGGCCATCGCCCTGATAGACGGTTTTTC
GCCCTTTGACGTTGGAGTCCACGTTCTTTAATAGTGGACTCTTGTTCCAAACTGGAACAACACTCAACC
CTATCTCGGTCTATTCTTTTGATTTATAAGGGATTTTGCCGATTTCGGCCTATTGGTTAAAAAATGAGC
TGATTTAACAAAAATTTAACGCGAATTTTAACAAAATATTAACGCTTACAATTTAGGTGGCACTTTTCG
GGGAAATGTGCGCGGAACCCCTATTTGTTTATTTTTCTAAATACATTCAAATATGTATCCGCTCATGAG
ACAATAACCCTGATAAATGCTTCAATAATATTGAAAAAGGAAGAGTATGAGTATTCAACATTTCCGTGT
CGCCCTTATTCCCTTTTTTGCGGCATTTTGCCTTCCTGTTTTTGCTCACCCAGAAACGCTGGTGAAAGT
AAAAGATGCTGAAGATCAGTTGGGTGCACGAGTGGGTTACATCGAACTGGATCTCAACAGCGGTAAGAT
CCTTGAGAGTTTTCGCCCCGAAGAACGTTTTCCAATGATGAGCACTTTTAAAGTTCTGCTATGTGGCGC
GGTATTATCCCGTATTGACGCCGGGCAAGAGCAACTCGGTCGCCGCATACACTATTCTCAGAATGACTT
GGTTGAGTACTCACCAGTCACAGAAAAGCATCTTACGGATGGCATGACAGTAAGAGAATTATGCAGTGC
TGCCATAACCATGAGTGATAACACTGCGGCCAACTTACTTCTGACAACGATCGGAGGACCGAAGGAGCT
AACCGCTTTTTTGCACAACATGGGGGATCATGTAACTCGCCTTGATCGTTGGGAACCGGAGCTGAATGA
AGCCATACCAAACGACGAGCGTGACACCACGATGCCTGTAGCAATGGCAACAACGTTGCGCAAACTATT
AACTGGCGAACTACTTACTCTAGCTTCCCGGCAACAATTAATAGACTGGATGGAGGCGGATAAAGTTGC
AGGACCACTTCTGCGCTCGGCCCTTCCGGCTGGCTGGTTTATTGCTGATAAATCTGGAGCCGGTGAGCG
TGGGTCTCGCGGTATCATTGCAGCACTGGGGCCAGATGGTAAGCCCTCCCGTATCGTAGTTATCTACAC
GACGGGGAGTCAGGCAACTATGGATGAACGAAATAGACAGATCGCTGAGATAGGTGCCTCACTGATTAA
GCATTGGTAACTGTCAGACCAAGTTTACTCATATATACTTTAGATTGATTTAAAACTTCATTTTTAATT
TAAAAGGATCTAGGTGAAGATCCTTTTTGATAATCTCATGACCAAAATCCCTTAACGTGAGTTTTCGTT
CCACTGAGCGTCAGACCCCGTAGAAAAGATCAAAGGATCTTCTTGAGATCCTTTTTTTCTGCGCGTAAT
CTGCTGCTTGCAAACAAAAAAACCACCGCTACCAGCGGTGGTTTGTTTGCCGGATCAAGAGCTACCAAC
TCTTTTTCCGAAGGTAACTGGCTTCAGCAGAGCGCAGATACCAAATACTGTCCTTCTAGTGTAGCCGTA
GTTAGGCCACCACTTCAAGAACTCTGTAGCACCGCCTACATACCTCGCTCTGCTAATCCTGTTACCAGT
GGCTGCTGCCAGTGGCGATAAGTCGTGTCTTACCGGGTTGGACTCAAGACGATAGTTACCGGATAAGGC
GCAGCGGTCGGGCTGAACGGGGGGTTCGTGCACACAGCCCAGCTTGGAGCGAACGACCTACACCGAACT
GAGATACCTACAGCGTGAGCTATGAGAAAGCGCCACGCTTCCCGAAGGGAGAAAGGCGGACAGGTATCC
GGTAAGCGGCAGGGTCGGAACAGGAGAGCGCACGAGGGAGCTTCCAGGGGGAAACGCCTGGTATCTTTA
TAGTCCTGTCGGGTTTCGCCACCTCTGACTTGAGCGTCGATTTTTGTGATGCTCGTCAGGGGGGCGGAG
CCTATGGAAAAACGCCAGCAACGCGGCCTTTTTACGGTTCCTGGCCTTTTGCTGGCCTTTTGCTCACAT
GTTCTTTCCTGCGTTATCCCCTGATTCTGTGGATAACCGTATTACCGCCTTTGAGTGAGCTGATACCGC
TCGCCGCAGCCGAACGACCGAGCGCAGCGAGTCAGTGAGCGAGGAAGCGGAAGAGCGCCCAATACGCAA
ACCGCCTCTCCCCGCGCGTTGGCCGATTCATTAATGCAGCTGGCACGACAGGTTTCCCGACTGGAAAGC
GGGCAGTGAGCGCAACGCAATTAATGTGAGTTAGCTCACTCATTAGGCACCCCAGGCTTTACACTTTAT
GCTTCCGGCTCGTATGTTGTGTGGAATTGTGAGCGGATAACAATTTCACACAGGAAACAGCTATGACCA
TGATTACGCCAAGCGCGCAATTAACCCTCACTAAAGGGAACAAAAGCTGGGGCCGCTCTAGAACTAGTG
GATCCCCCGGGCTGCAGGAATTCGTCCAGCAGTTGTCTGGAGCTCCACCAGAAATCTGGAAGCTTAT

SEQ ID 774

AAATCTAGAGGTACCATTTAAATGCGGCCGCAAAACCCCTCACAAATACATAA

SEQ ID 775

TTTCTGCAGCTTGAAATTGAAATATGACTAACGAAT

SEQ ID 776

tctagaggtaccatttaaatgcggccgcaaaacccctcacaaatacataaaaaaaattctttatttaat
tatcaaactctccactacctttcccaccaaccgttacaatcctgaatgttggaaaaaactaactacatt
gatataaaaaaactacattacttcctaaatcatatcaaaattgtataaatatatccactcaaaggagtc
tagaagatccacttggacaaattgcccatagttggaaagatgttcaccaagtcaacaagatttatcaat
ggaaaaatccatctaccaaacttactttcaagaaaatccaaggattatagagtaaaaaatctatgtatt
attaagtcaaaaagaaaaccaaagtgaacaaatattgatgtacaagtttgagaggataagacattggaa
tcgtctaaccaggaggcggaggaattccctagacagttaaaagtggccggaatcccggtaaaaaagatt
aaaatttttttgtagagggagtgcttgaatcatgttttttatgatggaaatagattcagcaccatcaaa
aacattcaggacacctaaaattttgaagtttaacaaaaataacttggatctacaaaaatccgtatcgga
ttttctctaaatataactagaattttcataactttcaaagcaactcctcccctaaccgtaaaacttttc
ctacttcaccgttaattacattccttaagagtagataaagaaataaagtaaataaaagtattcacaaac
caacaatttatttcttttatttacttaaaaaaacaaaaagtttatttattttacttaaatggcataatg
acatatcggagatccctcgaacgagaatcttttatctccctggttttgtattaaaaagtaatttattgt
ggggtccacgcggagttggaatcctacagacgcgctttacatacgtctcgagaagcgtgacggatgtgc
gaccggatgaccctgtataacccaccgacacagccagcgcacagtatacacgtgtcatttctctattgg
aaaatgtcgttgttatccccgctggtacgcaaccaccgatggtgacaggtcgtctgttgtcgtgtcgcg
tagcgggagaagggtctcatccaacgctattaaatactcgccttcaccgcgttacttctcatcttttct
cttgcgttgtataatcagtgcgatattctcagagagcttttcattcaaaggtatggagttttgaagggc
tttactcttaacatttgtttttctttgtaaattgttaatggtggtttctgtgggggaagaatcttttgc
caggtccttttgggtttcgcatgtttatttgggttatttttctcgactatggctgacattactagggct
ttcgtgctttcatctgtgttttcttcccttaataggtctgtctctctggaatatttaattttcgtatgt
aagttatgagtagtcgctgtttgtaataggctcttgtctgtaaaggtttcagcaggtgtttgcgtttta
ttgcgtcatgtgtttcagaaggcctttgcagattattgcgttgtactttaatattttgtctccaacctt
gttatagtttccctcctttgatctcacaggaaccctttcttctttgagcattttcttgtggcgttctgt
agtaatattttaattttgggcccgggttctgagggtaggtgattattcacagtgatgtgctttccctat
aaggtcctctatgtgtaagctgttagggtttgtgcgttactattgacatgtcacatgtcacatattttc
ttcctcttatccttcgaactgatggttctttttctaattcgtggattgctggtgccatattttatttct
attgcaactgtattttagggtgtctctttctttttgatttcttgttaatatttgtgttcaggttgtaac
tatgggttgctagggtgtctgccctcttcttttgtgcttctttcgcagaatctgtccgttggtctgtat
ttgggtgatgaattatttattccttgaagtatctgtctaattagcttgtgatgatgtgcaggtatattc
gttagtcatatttcaatttcaagcgatcccccgggctgcaggaattcgtccagcagttgtctggagctc
caccagaaatctggaagcttatcgatgggtgttatttgtggataataaattcgggtgatgttcagtgtt
tgtcgtatttctcacgaataaattgtgtttatgtatgtgttagtgttgtttgtctgtttcagaccctct
tatgttatatttttcttttcgtcggtcagttgaagccaatactggtgtcctggccggcactgcaatacc
atttcgtttaatataaagactctgttatccgtgagctcgaatttccccgatcgttcaaacatttggcaa
taaagtttcttaagattgaatcctgttgccggtcttgcgatgattatcatataatttctgttgaattac
gttaagcatgtaataattaacatgtaatgcatgacgttatttatgagatgggtttttatgattagagtc
ccgcaattatacatttaatacgcgatagaaaacaaaatatagcgcgcaaactaggataaattatcgcgc
gcggtgtcatctatgttactagatcgcggccgcatttaaatggtacccaattcgccctatagtgagtcg
tattacgcgcgctcactggccgtcgttttacaacgtcgtgactgggaaaaccctggcgttacccaactt
aatcgccttgcagcacatccccctttcgccagctggcgtaatagcgaagaggcccgcaccgatcgccct
tcccaacagttgcgcagcctgaatggcgaatgggacgcgccctgtagcggcgcattaagcgcggcgggt
gtggtggttacgcgcagcgtgaccgctacacttgccagcgccctagcgcccgctcctttcgctttcttc
ccttcctttctcgccacgttcgccggctttccccgtcaagctctaaatcgggggctccctttagggttc
cgatttagtgctttacggcacctcgaccccaaaaaacttgattagggtgatggttcacgtagtgggcca
tcgccctgatagacggtttttcgccctttgacgttggagtccacgttctttaatagtggactcttgttc
caaactggaacaacactcaaccctatctcggtctattcttttgatttataagggattttgccgatttcg
gcctattggttaaaaaatgagctgatttaacaaaaatttaacgcgaattttaacaaaatattaacgctt
acaatttaggtggcacttttcggggaaatgtgcgcggaacccctatttgtttatttttctaaatacatt
caaatatgtatccgctcatgagacaataaccctgataaatgcttcaataatattgaaaaaggaagagta
tgagtattcaacatttccgtgtcgcccttattcccttttttgcggcattttgccttcctgtttttgctc
acccagaaacgctggtgaaagtaaaagatgctgaagatcagttgggtgcacgagtgggttacatcgaac
tggatctcaacagcggtaagatccttgagagttttcgccccgaagaacgttttccaatgatgagcactt
ttaaagttctgctatgtggcgcggtattatcccgtattgacgccgggcaagagcaactcggtcgccgca
tacactattctcagaatgacttggttgagtactcaccagtcacagaaaagcatcttacggatggcatga
cagtaagagaattatgcagtgctgccataaccatgagtgataacactgcggccaacttacttctgacaa
cgatcggaggaccgaaggagctaaccgcttttttgcacaacatgggggatcatgtaactcgccttgatc
gttgggaaccggagctgaatgaagccataccaaacgacgagcgtgacaccacgatgcctgtagcaatgg
caacaacgttgcgcaaactattaactggcgaactacttactctagcttcccggcaacaattaatagact
ggatggaggcggataaagttgcaggaccacttctgcgctcggcccttccggctggctggtttattgctg
ataaatctggagccggtgagcgtgggtctcgcggtatcattgcagcactggggccagatggtaagccct
cccgtatcgtagttatctacacgacggggagtcaggcaactatggatgaacgaaatagacagatcgctg
agataggtgcctcactgattaagcattggtaactgtcagaccaagtttactcatatatactttagattg
atttaaaacttcatttttaatttaaaaggatctaggtgaagatcctttttgataatctcatgaccaaaa
tcccttaacgtgagttttcgttccactgagcgtcagaccccgtagaaaagatcaaaggatcttcttgag
atcctttttttctgcgcgtaatctgctgcttgcaaacaaaaaaaccaccgctaccagcggtggtttgtt
tgccggatcaagagctaccaactctttttccgaaggtaactggcttcagcagagcgcagataccaaata
ctgtccttctagtgtagccgtagttaggccaccacttcaagaactctgtagcaccgcctacatacctcg
ctctgctaatcctgttaccagtggctgctgccagtggcgataagtcgtgtcttaccgggttggactcaa
gacgatagttaccggataaggcgcagcggtcgggctgaacggggggttcgtgcacacagcccagcttgg
agcgaacgacctacaccgaactgagatacctacagcgtgagctatgagaaagcgccacgcttcccgaag
ggagaaaggcggacaggtatccggtaagcggcagggtcggaacaggagagcgcacgagggagcttccag
ggggaaacgcctggtatctttatagtcctgtcgggtttcgccacctctgacttgagcgtcgatttttgt
gatgctcgtcaggggggcggagcctatggaaaaacgccagcaacgcggcctttttacggttcctggcct
tttgctggccttttgctcacatgttctttcctgcgttatcccctgattctgtggataaccgtattaccg
cctttgagtgagctgataccgctcgccgcagccgaacgaccgagcgcagcgagtcagtgagcgaggaag
cggaagagcgcccaatacgcaaaccgcctctccccgcgcgttggccgattcattaatgcagctggcacg
acaggtttcccgactggaaagcgggcagtgagcgcaacgcaattaatgtgagttagctcactcattagg
caccccaggctttacactttatgcttccggctcgtatgttgtgtggaattgtgagcggataacaatttc
acacaggaaacagctatgaccatgattacgccaagcgcgcaattaaccctcactaaagggaacaaaagc
tggggccgctctag

SEQ ID 777

TCTAGAGGTACCATTTAAATGCGGCCGCAAAACCCCTCACAAATACATAAAAAAAATTCTTTATTTAAT
TATCAAACTCTCCACTACCTTTCCCACCAACCGTTACAATCCTGAATGTTGGAAAAAACTAACTACATT
GATATAAAAAAACTACATTACTTCCTAAATCATATCAAAATTGTATAAATATATCCACTCAAAGGAGTC
TAGAAGATCCACTTGGACAAATTGCCCATAGTTGGAAAGATGTTCACCAAGTCAACAAGATTTATCAAT
GGAAAAATCCATCTACCAAACTTACTTTCAAGAAAATCCAAGGATTATAGAGTAAAAAATCTATGTATT
ATTAAGTCAAAAAGAAAACCAAAGTGAACAAATATTGATGTACAAGTTTGAGAGGATAAGACATTGGAA
TCGTCTAACCAGGAGGCGGAGGAATTCCCTAGACAGTTAAAAGTGGCCGGAATCCCGGTAAAAAAGATT
AAAATTTTTTTGTAGAGGGAGTGCTTGAATCATGTTTTTTATGATGGAAATAGATTCAGCACCATCAAA
AACATTCAGGACACCTAAAATTTTGAAGTTTAACAAAAATAACTTGGATCTACAAAAATCCGTATCGGA
TTTTCTCTAAATATAACTAGAATTTTCATAACTTTCAAAGCAACTCCTCCCCTAACCGTAAAACTTTTC
CTACTTCACCGTTAATTACATTCCTTAAGAGTAGATAAAGAAATAAAGTAAATAAAAGTATTCACAAAC
CAACAATTTATTTCTTTTATTTACTTAAAAAAACAAAAAGTTTATTTATTTTACTTAAATGGCATAATG
ACATATCGGAGATCCCTCGAACGAGAATCTTTTATCTCCCTGGTTTTGTATTAAAAAGTAATTTATTGT
GGGGTCCACGCGGAGTTGGAATCCTACAGACGCGCTTTACATACGTCTCGAGAAGCGTGACGGATGTGC
GACCGGATGACCCTGTATAACCCACCGACACAGCCAGCGCACAGTATACACGTGTCATTTCTCTATTGG
AAAATGTCGTTGTTATCCCCGCTGGTACGCAACCACCGATGGTGACAGGTCGTCTGTTGTCGTGTCGCG
TAGCGGGAGAAGGGTCTCATCCAACGCTATTAAATACTCGCCTTCACCGCGTTACTTCTCATCTTTTCT
CTTGCGTTGTATAATCAGTGCGATATTCTCAGAGAGCTTTTCATTCAAAGGTATGGAGTTTTGAAGGGC
TTTACTCTTAACATTTGTTTTTCTTTGTAAATTGTTAATGGTGGTTTCTGTGGGGGAAGAATCTTTTGC
CAGGTCCTTTTGGGTTTCGCATGTTTATTTGGGTTATTTTTCTCGACTATGGCTGACATTACTAGGGCT
TTCGTGCTTTCATCTGTGTTTTCTTCCCTTAATAGGTCTGTCTCTCTGGAATATTTAATTTTCGTATGT
AAGTTATGAGTAGTCGCTGTTTGTAATAGGCTCTTGTCTGTAAAGGTTTCAGCAGGTGTTTGCGTTTTA
TTGCGTCATGTGTTTCAGAAGGCCTTTGCAGATTATTGCGTTGTACTTTAATATTTTGTCTCCAACCTT
GTTATAGTTTCCCTCCTTTGATCTCACAGGAACCCTTTCTTCTTTGAGCATTTTCTTGTGGCGTTCTGT
AGTAATATTTTAATTTTGGGCCCGGGTTCTGAGGGTAGGTGATTATTCACAGTGATGTGCTTTCCCTAT
AAGGTCCTCTATGTGTAAGCTGTTAGGGTTTGTGCGTTACTATTGACATGTCACATGTCACATATTTTC
TTCCTCTTATCCTTCGAACTGATGGTTCTTTTTCTAATTCGTGGATTGCTGGTGCCATATTTTATTTCT
ATTGCAACTGTATTTTAGGGTGTCTCTTTCTTTTTGATTTCTTGTTAATATTTGTGTTCAGGTTGTAAC
TATGGGTTGCTAGGGTGTCTGCCCTCTTCTTTTGTGCTTCTTTCGCAGAATCTGTCCGTTGGTCTGTAT
TTGGGTGATGAATTATTTATTCCTTGAAGTATCTGTCTAATTAGCTTGTGATGATGTGCAGGTATATTC
GTTAGTCATATTTCAATTTCAAGCGATCCCCCGGGCTGCAGGAATTCGTCCAGCAGTTGTCTGGAGCTC
CACCAGAAATCTGGAAGCTTATCGATATGGATCAGTTCCCCAAGTGGAATCCTGTCAATAGAGAAACGT
ATATCGAAAGGCTGTCGGCAAGGTATGAAAGAGAGGGTGAGCCTTCTCAGCTTGCTGGTGTGGATTTTT
TCGTGAGTACTGTTGATCCGCTGAAGGAACCGCCATTGATCACTGCCAATACAGTCCTTTCCATCCTTG
CTGTGGACTATCCCGTCGATAAAGTCTCCTGCTACGTGTCTGATGATGGTGCAGCTATGCTTTCATTTG
AATCTCTTGTAGAAACAGCTGAGTTTGCAAGGAAGTGGGTTCCGTTCTGCAAAAAATTCTCAATTGAAC
CAAGAGCACCGGAGTTTTACTTCTCACAGAAAATTGATTACTTGAAAGACAAGGTTCAACCTTCTTTCG
TGAAAGAACGTAGAGCAATGAAAAGGGATTATGAAGAGTACAAAGTCCGAGTTAATGCCCTGGTAGCAA
AGGCTCAGAAAACACCTGAAGAAGGATGGACTATGCAAGATGGAACACCTTGGCCTGGGAATAACACAC
GTGATCACCCTGGCATGATTCAGGTCTTCCTTGGAAATACTGGAGCTCGTGACATTGAAGGAAATGAAC
TACCTCGTCTAGTATATGTCTCCAGGGAGAAGAGACCTGGCTACCAGCACCACAAAAAGGCTGGTGCAG
AAAATGCTCTGGTGAGAGTGTCTGCAGTACTCACAAATGCTCCCTACATCCTCAATGTTGATTGTGATC
ACTATGTAAACAATAGCAAGGCTGTTCGAGAGGCAATGTGCATCCTGATGGACCCACAAGTAGGTCGAG
ATGTATGCTATGTGCAGTTCCCTCAGAGGTTTGATGGCATAGATAAGAGTGATCGCTACGCCAATCGTA
ACGTAGTTTTCTTTGATGTTAACATGAAAGGGTTGGATGGCATTCAAGGACCAGTATACGTAGGAACTG
GTTGTGTTTTCAACAGGCAAGCACTTTACGGCTACGGGCCTCCTTCTATGCCCAGCTTACGCAAGAGAA
AGGATTCTTCATCCTGCTTCTCATGTTGCTGCCCCTCAAAGAAGAAGCCTGCTCAAGATCCAGCTGAGG
TATACAGAGATGCAAAAAGAGAGGATCTCAATGCTGCCATATTTAATCTTACAGAGATTGATAATTATG
ACGAGCATGAAAGGTCAATGCTGATCTCCCAGTTGAGCTTTGAGAAAACTTTTGGCTTATCTTCTGTCT
TCATTGAGTCTACACTAATGGAGAATGGAGGAGTACCCGAGTCTGCCAACTCACCAACACTCATCAAGG
AAGCAATTCATGTCATCGGCTGTGGCTATGAAGAGAAGACTGAATGGGGAAAAGAGATTGGTTGGATAT
ATGGGTCAGTCACTGAGGATATCTTAAGTGGCTTCAAGATGCACTGCCGAGGATGGAGATCAATTTACT
GCATGCCCGTAAGGCCTGCATTCAAAGGATCTGCACCCATCAACCTGTCTGATAGATTGCACCAGGTCC
TCCGATGGGCTCTTGGTTCTGTGGAAATTTTCTTTAGCAGACACTGTCCCCTCTGGTACGGGTTTGGAG
GAGGCCGTCTTAAATGGCTCCAAAGGCTTGCGTATATAAACACCATTGTGTACCCATGAATCGATGGGT
GTTATTTGTGGATAATAAATTCGGGTGATGTTCAGTGTTTGTCGTATTTCTCACGAATAAATTGTGTTT
ATGTATGTGTTAGTGTTGTTTGTCTGTTTCAGACCCTCTTATGTTATATTTTTCTTTTCGTCGGTCAGT
TGAAGCCAATACTGGTGTCCTGGCCGGCACTGCAATACCATTTCGTTTAATATAAAGACTCTGTTATCC
GTGAGCTCGAATTTCCCCGATCGTTCAAACATTTGGCAATAAAGTTTCTTAAGATTGAATCCTGTTGCC
GGTCTTGCGATGATTATCATATAATTTCTGTTGAATTACGTTAAGCATGTAATAATTAACATGTAATGC
ATGACGTTATTTATGAGATGGGTTTTTATGATTAGAGTCCCGCAATTATACATTTAATACGCGATAGAA
AACAAAATATAGCGCGCAAACTAGGATAAATTATCGCGCGCGGTGTCATCTATGTTACTAGATCGCGGC
CGCATTTAAATGGTACCCAATTCGCCCTATAGTGAGTCGTATTACGCGCGCTCACTGGCCGTCGTTTTA
CAACGTCGTGACTGGGAAAACCCTGGCGTTACCCAACTTAATCGCCTTGCAGCACATCCCCCTTTCGCC
AGCTGGCGTAATAGCGAAGAGGCCCGCACCGATCGCCCTTCCCAACAGTTGCGCAGCCTGAATGGCGAA
TGGGACGCGCCCTGTAGCGGCGCATTAAGCGCGGCGGGTGTGGTGGTTACGCGCAGCGTGACCGCTACA
CTTGCCAGCGCCCTAGCGCCCGCTCCTTTCGCTTTCTTCCCTTCCTTTCTCGCCACGTTCGCCGGCTTT
CCCCGTCAAGCTCTAAATCGGGGGCTCCCTTTAGGGTTCCGATTTAGTGCTTTACGGCACCTCGACCCC
AAAAAACTTGATTAGGGTGATGGTTCACGTAGTGGGCCATCGCCCTGATAGACGGTTTTTCGCCCTTTG
ACGTTGGAGTCCACGTTCTTTAATAGTGGACTCTTGTTCCAAACTGGAACAACACTCAACCCTATCTCG
GTCTATTCTTTTGATTTATAAGGGATTTTGCCGATTTCGGCCTATTGGTTAAAAAATGAGCTGATTTAA
CAAAAATTTAACGCGAATTTTAACAAAATATTAACGCTTACAATTTAGGTGGCACTTTTCGGGGAAATG
TGCGCGGAACCCCTATTTGTTTATTTTTCTAAATACATTCAAATATGTATCCGCTCATGAGACAATAAC
CCTGATAAATGCTTCAATAATATTGAAAAAGGAAGAGTATGAGTATTCAACATTTCCGTGTCGCCCTTA
TTCCCTTTTTTGCGGCATTTTGCCTTCCTGTTTTTGCTCACCCAGAAACGCTGGTGAAAGTAAAAGATG
CTGAAGATCAGTTGGGTGCACGAGTGGGTTACATCGAACTGGATCTCAACAGCGGTAAGATCCTTGAGA
GTTTTCGCCCCGAAGAACGTTTTCCAATGATGAGCACTTTTAAAGTTCTGCTATGTGGCGCGGTATTAT
CCCGTATTGACGCCGGGCAAGAGCAACTCGGTCGCCGCATACACTATTCTCAGAATGACTTGGTTGAGT
ACTCACCAGTCACAGAAAAGCATCTTACGGATGGCATGACAGTAAGAGAATTATGCAGTGCTGCCATAA
CCATGAGTGATAACACTGCGGCCAACTTACTTCTGACAACGATCGGAGGACCGAAGGAGCTAACCGCTT
TTTTGCACAACATGGGGGATCATGTAACTCGCCTTGATCGTTGGGAACCGGAGCTGAATGAAGCCATAC
CAAACGACGAGCGTGACACCACGATGCCTGTAGCAATGGCAACAACGTTGCGCAAACTATTAACTGGCG
AACTACTTACTCTAGCTTCCCGGCAACAATTAATAGACTGGATGGAGGCGGATAAAGTTGCAGGACCAC
TTCTGCGCTCGGCCCTTCCGGCTGGCTGGTTTATTGCTGATAAATCTGGAGCCGGTGAGCGTGGGTCTC
GCGGTATCATTGCAGCACTGGGGCCAGATGGTAAGCCCTCCCGTATCGTAGTTATCTACACGACGGGGA
GTCAGGCAACTATGGATGAACGAAATAGACAGATCGCTGAGATAGGTGCCTCACTGATTAAGCATTGGT
AACTGTCAGACCAAGTTTACTCATATATACTTTAGATTGATTTAAAACTTCATTTTTAATTTAAAAGGA
TCTAGGTGAAGATCCTTTTTGATAATCTCATGACCAAAATCCCTTAACGTGAGTTTTCGTTCCACTGAG
CGTCAGACCCCGTAGAAAAGATCAAAGGATCTTCTTGAGATCCTTTTTTTCTGCGCGTAATCTGCTGCT
TGCAAACAAAAAAACCACCGCTACCAGCGGTGGTTTGTTTGCCGGATCAAGAGCTACCAACTCTTTTTC
CGAAGGTAACTGGCTTCAGCAGAGCGCAGATACCAAATACTGTCCTTCTAGTGTAGCCGTAGTTAGGCC
ACCACTTCAAGAACTCTGTAGCACCGCCTACATACCTCGCTCTGCTAATCCTGTTACCAGTGGCTGCTG
CCAGTGGCGATAAGTCGTGTCTTACCGGGTTGGACTCAAGACGATAGTTACCGGATAAGGCGCAGCGGT
CGGGCTGAACGGGGGGTTCGTGCACACAGCCCAGCTTGGAGCGAACGACCTACACCGAACTGAGATACC
TACAGCGTGAGCTATGAGAAAGCGCCACGCTTCCCGAAGGGAGAAAGGCGGACAGGTATCCGGTAAGCG
GCAGGGTCGGAACAGGAGAGCGCACGAGGGAGCTTCCAGGGGGAAACGCCTGGTATCTTTATAGTCCTG
TCGGGTTTCGCCACCTCTGACTTGAGCGTCGATTTTTGTGATGCTCGTCAGGGGGGCGGAGCCTATGGA
AAAACGCCAGCAACGCGGCCTTTTTACGGTTCCTGGCCTTTTGCTGGCCTTTTGCTCACATGTTCTTTC
CTGCGTTATCCCCTGATTCTGTGGATAACCGTATTACCGCCTTTGAGTGAGCTGATACCGCTCGCCGCA
GCCGAACGACCGAGCGCAGCGAGTCAGTGAGCGAGGAAGCGGAAGAGCGCCCAATACGCAAACCGCCTC
TCCCCGCGCGTTGGCCGATTCATTAATGCAGCTGGCACGACAGGTTTCCCGACTGGAAAGCGGGCAGTG
AGCGCAACGCAATTAATGTGAGTTAGCTCACTCATTAGGCACCCCAGGCTTTACACTTTATGCTTCCGG
CTCGTATGTTGTGTGGAATTGTGAGCGGATAACAATTTCACACAGGAAACAGCTATGACCATGATTACG
CCAAGCGCGCAATTAACCCTCACTAAAGGGAACAAAAGCTGGGGCCGCTCTAG

TABLE 8
pGrowth Information.

CW AR	Plasmid(s)	Promoter	Gene	Genesis ID
88	pGrowth14	SUBIN	Cyclin A	prga001823
88	pGrowth15	SUBIN	Cyclin A	prpe001264
88	pGrowth16	SUBIN	Cyclin D	prxa004540
88	pGrowth18	SUBIN	Cyclin D	prxl006271
88	pGrowth19	SUBIN	Cyclin D	prpb019661
88	pGrowth20	SUBIN	WEE1-like protein	prrd041233

To make the growth100 plasmids, an acceptor vector (pWVK202) was built by first inserting the NotI-SUBIN::UDPGBD::nos term-NotI cassette from pARB483a into plasmid pWVK147 at NotI. Next, the UDPGBD gene was removed using restriction sites PstI and ClaI. A polylinker containing the restriction sites PstI, NheI, AvrII, ScaI, and ClaI was inserted in place of the UDPGBD gene. Sites AvrII and NheI are both compatible with SpeI, a site found often in the plasmids provided by Genesis. ScaI is blunt, so any fragment can be blunted and then inserted at that position into the acceptor vector. Plasmids were received from Genesis and analyzed to determine which restriction sites would be most suitable for subcloning into the acceptor vector pWVK202. After the ligations were performed, the resulting products were checked by extensive restriction digest analysis to make sure that the desired plasmid had been created.

TABLE 9
Eucalyptus grandis Cell Cycle Genes and Proteins.

			Patent	Patent
DNA SEQ	Protein SEQ		ORF	ORF
ID NO	ID NO	Sequence Identifier	start	stop

1	236	eucalyptusSpp_003910	387	1820
2	237	eucalyptusSpp_019213	99	1007
3	238	eucalyptusSpp_036800	120	1004
4	239	eucalyptusSpp_040260	23	937
5	240	eucalyptusSpp_041965	149	1033
6	241	eucalyptusSpp_002906	199	1116
7	242	eucalyptusSpp_001518	41	982
8	243	eucalyptusSpp_008078	291	2042
9	244	eucalyptusSpp_009826	107	2236
10	245	eucalyptusSpp_010364	82	1749
11	246	eucalyptusSpp_011523	151	1560
12	247	eucalyptusSpp_024358	82	1644
13	248	eucalyptusSpp_039125	626	2782
14	249	eucalyptusSpp_005362	13	1467
15	250	eucalyptusSpp_044857	113	1558
16	251	eucalyptusSpp_001743	187	1686
17	252	eucalyptusSpp_012405	238	1653
18	253	eucalyptusSpp_003739	235	1539
19	254	eucalyptusSpp_022338	158	1618
20	255	eucalyptusSpp_028605	205	1530
21	256	eucalyptusSpp_041006	174	1499
22	257	eucalyptusSpp_006643	94	1332
23	258	eucalyptusSpp_045338	176	1342
24	259	eucalyptusSpp_046486	150	1283
25	260	eucalyptusSpp_012070	101	367
26	261	eucalyptusSpp_006617	9	1352
27	262	eucalyptusSpp_007827	89	1486
28	263	eucalyptusSpp_008036	80	1477
29	264	010212EGLA007017HT	160	1062
30	265	eucalyptusSpp_001596	172	1077
31	266	eucalyptusSpp_005870	66	989
32	267	eucalyptusSpp_006901	111	1541
33	268	eucalyptusSpp_006902	116	1615
34	269	eucalyptusSpp_007440	155	1453
35	270	eucalyptusSpp_008994	228	2033
36	271	eucalyptusSpp_024580	110	1258
37	272	eucalyptusSpp_037831	50	1462
38	273	eucalyptusSpp_034958	176	739
39	274	001209EGXC004488HT	150	1529
40	275	010310EGXD012820HT	247	1971
41	276	010310EGXD013036HT	136	1644
42	277	010316EGXF999037HT	48	836
43	278	010324EGXF002118HT	49	822
44	279	011019EGKA001923HT	185	751
45	280	eucalyptusSpp_000966	103	621
46	281	eucalyptusSpp_001037	41	559
47	282	eucalyptusSpp_004603	127	693
48	283	eucalyptusSpp_005465	28	639
49	284	eucalyptusSpp_006571	135	812
50	285	eucalyptusSpp_006786	119	613
51	286	eucalyptusSpp_007057	38	562
52	287	eucalyptusSpp_008670	109	1872
53	288	eucalyptusSpp_009137	74	1159
54	289	eucalyptusSpp_010285	54	2045
55	290	eucalyptusSpp_010600	53	1879
56	291	eucalyptusSpp_011551	7	690
57	292	eucalyptusSpp_020743	83	601
58	293	eucalyptusSpp_023739	125	535
59	294	eucalyptusSpp_024103	55	573
60	295	eucalyptusSpp_031985	147	842
61	296	eucalyptusSpp_032025	167	487
62	297	eucalyptusSpp_032173	195	890
63	298	eucalyptusSpp_033340	68	586
64	299	eucalyptusSpp_009143	182	3265
65	300	eucalyptusSpp_000349	165	1145
66	301	eucalyptusSpp_000575	529	1569
67	302	eucalyptusSpp_000804	156	1136
68	303	eucalyptusSpp_000805	90	1073
69	304	eucalyptusSpp_000806	66	1049
70	305	eucalyptusSpp_002248	277	1512
71	306	eucalyptusSpp_003203	33	1076
72	307	eucalyptusSpp_003209	65	973
73	308	eucalyptusSpp_004429	82	1047
74	309	eucalyptusSpp_004607	43	1101
75	310	eucalyptusSpp_004682	142	1095
76	311	eucalyptusSpp_005786	61	1257
77	312	eucalyptusSpp_005887	193	1527
78	313	eucalyptusSpp_005981	109	1155
79	314	eucalyptusSpp_006766	71	1213
80	315	eucalyptusSpp_006769	109	1785
81	316	eucalyptusSpp_006907	364	2685
82	317	eucalyptusSpp_007518	96	1412
83	318	eucalyptusSpp_007717	116	1702
84	319	eucalyptusSpp_007718	46	1101
85	320	eucalyptusSpp_007741	23	1258
86	321	eucalyptusSpp_007884	404	2644
87	322	eucalyptusSpp_008258	107	2383
88	323	eucalyptusSpp_008465	243	1625
89	324	eucalyptusSpp_008616	126	1127
90	325	eucalyptusSpp_008690	257	1390
91	326	eucalyptusSpp_008708	178	1632
92	327	eucalyptusSpp_008850	290	2917
93	328	eucalyptusSpp_009072	148	1197
94	329	eucalyptusSpp_009465	140	1567
95	330	eucalyptusSpp_009472	376	1737
96	331	eucalyptusSpp_009550	69	1010
97	332	eucalyptusSpp_010284	149	1423
98	333	eucalyptusSpp_010595	365	2677
99	334	eucalyptusSpp_010657	24	923
100	335	eucalyptusSpp_012636	221	3598
101	336	eucalyptusSpp_012748	44	1447
102	337	eucalyptusSpp_012879	196	1314
103	338	eucalyptusSpp_015515	193	1668
104	339	eucalyptusSpp_015724	78	1634
105	340	eucalyptusSpp_016167	85	2826
106	341	eucalyptusSpp_016633	74	1246
107	342	eucalyptusSpp_017485	100	4377
108	343	eucalyptusSpp_018007	58	2439
109	344	eucalyptusSpp_020775	159	1064
110	345	eucalyptusSpp_023132	118	1665
111	346	eucalyptusSpp_023569	57	1628
112	347	eucalyptusSpp_023611	250	1566
113	348	eucalyptusSpp_024934	106	1434
114	349	eucalyptusSpp_025546	190	1917
115	350	eucalyptusSpp_030134	102	2942
116	351	eucalyptusSpp_031787	75	1079
117	352	eucalyptusSpp_034435	99	1148
118	353	eucalyptusSpp_034452	232	1806
119	354	eucalyptusSpp_035789	72	1124
120	355	eucalyptusSpp_035804	315	2069
121	356	eucalyptusSpp_043057	145	1968
122	357	eucalyptusSpp_046741	130	1488
123	358	eucalyptusSpp_047161	269	1693
698	718	eucalyptusSpp_008994
699	719	eucalyptusSpp_009143
700	720	eucalyptusSpp_006366
701	721	eucalyptusSpp_006907
702	722	eucalyptusSpp_012636
703	723	eucalyptusSpp_015724
704	724	eucalyptusSpp_016167
705	725	eucalyptusSpp_017485
706	726	eucalyptusSpp_030134
707	727	eucalyptusSpp_046741
708	728	eucalyptusSpp_047161
709	729	eucalyptusSpp_017378

TABLE 10
Pinus radiata cell cycle genes and proteins.

			Patent	Patent
DNA SEQ	Protein SEQ		ORF	ORF
ID NO	ID NO	Sequence Identifier	start	stop

124	359	pinusRadiata_001766	1163	2545
125	360	pinusRadiata_002927	152	1582
126	361	990309PRCA009171HT	389	1297
127	362	pinusRadiata_013714	38	946
128	363	pinusRadiata_016332	180	1088
129	364	pinusRadiata_021677	40	948
130	365	pinusRadiata_027562	229	1134
131	366	pinusRadiata_001504	105	2642
132	367	pinusRadiata_015211	187	2580
133	368	pinusRadiata_020421	220	1749
134	369	pinusRadiata_003187	438	1748
135	370	pinusRadiata_015661	240	1631
136	371	pinusRadiata_013874	252	1604
137	372	pinusRadiata_014615	261	1817
138	373	pinusRadiata_004578	167	1576
139	374	pinusRadiata_023387	183	1598
140	375	pinusRadiata_006970	98	1126
141	376	pinusRadiata_010322	148	894
142	377	pinusRadiata_022721	287	1363
143	378	pinusRadiata_023407	251	1348
144	379	pinusRadiata_001945	229	510
145	380	pinusRadiata_008233	92	409
146	381	pinusRadiata_008234	64	381
147	382	pinusRadiata_022054	68	349
148	383	pinusRadiata_012137	125	1849
149	384	pinusRadiata_012582	70	1602
150	385	pinusRadiata_015285	140	1465
151	386	pinusRadiata_017229	628	2565
152	387	pinusRadiata_020724	55	1818
153	388	pinusRadiata_004555	259	1710
154	389	pinusRadiata_004556	356	1807
155	390	pinusRadiata_005729	261	1298
156	391	pinusRadiata_007395	365	2251
157	392	pinusRadiata_009503	156	1454
158	393	pinusRadiata_011283	203	1348
159	394	pinusRadiata_012322	229	1644
160	395	pinusRadiata_018671	156	1454
161	396	pinusRadiata_023236	27	2222
162	397	pinusRadiata_000171	71	1759
163	398	pinusRadiata_000172	358	2040
164	399	pinusRadiata_001480	238	756
165	400	pinusRadiata_001481	285	803
166	401	pinusRadiata_001483	190	708
167	402	pinusRadiata_001484	156	674
168	403	pinusRadiata_001692	176	1912
169	404	pinusRadiata_005313	64	765
170	405	pinusRadiata_006362	93	881
171	406	pinusRadiata_006493	372	1070
172	407	pinusRadiata_006983	28	594
173	408	pinusRadiata_006984	34	648
174	409	pinusRadiata_007665	481	1611
175	410	pinusRadiata_012196	93	584
176	411	pinusRadiata_013382	250	1869
177	412	pinusRadiata_016461	84	422
178	413	pinusRadiata_017611	128	1213
179	414	pinusRadiata_019776	265	837
180	415	pinusRadiata_020659	38	781
181	416	pinusRadiata_022559	38	526
182	417	pinusRadiata_024188	37	1158
183	418	pinusRadiata_027973	61	768
184	419	pinusRadiata_001353	421	2172
185	420	pinusRadiata_001978	163	1647
186	421	pinusRadiata_002810	192	1172
187	422	pinusRadiata_002811	131	1111
188	423	pinusRadiata_002812	149	1726
189	424	pinusRadiata_003514	948	2228
190	425	pinusRadiata_004104	332	1465
191	426	pinusRadiata_005595	232	1590
192	427	pinusRadiata_005754	207	1550
193	428	pinusRadiata_006463	221	1171
194	429	pinusRadiata_006665	221	3679
195	430	pinusRadiata_006750	269	1252
196	431	pinusRadiata_007030	214	1242
197	432	pinusRadiata_007854	119	2065
198	433	pinusRadiata_007917	186	1550
199	434	pinusRadiata_007989	244	3671
200	435	pinusRadiata_008506	163	1431
201	436	pinusRadiata_008692	155	1081
202	437	pinusRadiata_008693	537	1463
203	438	pinusRadiata_009170	284	1909
204	439	pinusRadiata_009408	610	1659
205	440	pinusRadiata_009522	241	1452
206	441	pinusRadiata_009734	223	1173
207	442	pinusRadiata_009815	251	1777
208	443	pinusRadiata_010670	367	1419
209	444	pinusRadiata_011297	284	1303
210	445	pinusRadiata_013098	684	1784
211	446	pinusRadiata_013172	336	2738
212	447	pinusRadiata_013589	81	1622
213	448	pinusRadiata_013608	399	1460
214	449	pinusRadiata_014299	207	1673
215	450	pinusRadiata_014498	263	1309
216	451	pinusRadiata_014548	232	2529
217	452	pinusRadiata_014610	56	2950
218	453	pinusRadiata_015460	56	1234
219	454	pinusRadiata_016090	193	2577
220	455	pinusRadiata_016722	187	1233
221	456	pinusRadiata_016785	51	1436
222	457	pinusRadiata_017094	525	2351
223	458	pinusRadiata_017527	152	1099
224	459	pinusRadiata_017591	470	4114
225	460	pinusRadiata_017769	196	2007
226	461	pinusRadiata_018047	214	1323
227	462	pinusRadiata_018414	68	2146
228	463	pinusRadiata_018986	874	3705
229	464	pinusRadiata_019479	360	1754
230	465	pinusRadiata_020144	185	1384
231	466	pinusRadiata_022480	241	1533
232	467	pinusRadiata_023079	230	1435
233	468	pinusRadiata_026739	101	2857
234	469	pinusRadiata_026951	43	1548
235	470	pinusRadiata_026529	206	1657
710	730	pinusRadiata_000888
711	731	pinusRadiata_004578
712	732	pinusRadiata_007989
713	733	pinusRadiata_009522
714	734	pinusRadiata_014610
715	735	pinusRadiata_017591
716	736	pinusRadiata_017769
717	737	pinusRadiata_026951

TABLE 11
Annotated Peptide Sequences of the Present Invention.

Entry	Sequence Description	Annotated Peptide Sequence

1	The amino acid sequence of SEQ ID	MGDGSLGSGGRGNSGGGGGGGSRPEWLQQYDLIGKIGEG
	261. The conserved eukaryotic	TYGLVFLARIKHPSTNRGKYIAIKKFKQSKDGDGVSPTA
	protein kinase domain is	IREIMLLREISHENVVKLVNVHINPVDMSLYLAFDYADH
	underlined and the	DLYEIIRHHRDKVNQAINPYTVKSLLWQLLNGLNYLHSN
	serine/threonine protein kinases	WIIHRDLKPSNILVMGEGEEQGVVKIADFGLARVYQAPL
	active-site signature is in bold.	KPLSDNGVVVTIWYRAPELLLGAKHYTSAVDMWAVGCIF
		AELLTLKPLFQGQEVKANPNPFQLDQLDKIFKVLGHPTQ
		EKWPMLVNLPHWQSDVQHIQRHKYDDNALGNVVRLSSKN
		ATFDLLSKMLEYDPQKRITAAQALEHEYFRMEPLPGRNA
		LVPSSPGDKVNYPTRPVDTTTDIEGTTSLQPSQSASSGN
		AVPGNMPGPHVVTNRPMPRPMHMVGMQRVPASGMAGYNL
		NPSGMGGGMNPSGIPMQRGVANQAQQSRRKDPGMGMGGY
		PPQQKQRRF
2	The amino acid sequence of SEQ ID	MEKYQQLAKIGEGTYGIVYKAKDKKSGELLALKKIRLEA
	262. The conserved eukaryotic	EDEGIPSTAIREISLLKQLQHPNIVRLYDVVHTEKKLTL
	protein kinase domain is	VFEFLDQDLKKYLDACGDNGLEPYTVKSFLYQLLQGIAF
	underlined and the protein kinases	CHEHRVLHRDLKPQNLLINMEGELKLADFGLARAFGIPV
	ATP-binding region and	RNYTHEVVTLWYRAPDVLMGSRKYSTQVDIWSVGCIFAE
	serine/threonine protein kinases	MVNGRPLFPGSSEQDQLLRIFKTLGTPSLKTWPGMAELP
	active-site signatures are in	DFKDNFPKYVVQSFKKICPKKLDKTGLDLLSRMLQYDPA
	bold.	KRISAEQAMGHPYFKDLKLRKPKAAGPGP
3	The amino acid sequence of SEQ ID	MDQYEKIEKIGEGTYGVVYKAIDRSTNKTIALKKIRLEQ
	263. The conserved eukaryotic	EDEGVPSTAIREISLLKEMQHGNIVKLQDVVHSERRLYL
	protein kinase domain is	VFEYLDLDLKKHMDSCPEFSKDTHTIKMFLYQILRGISY
	underlined and the protein kinases	CHSHRVLHRDLKPQNLLLDRRTNSLKLADFGLARAFGIP
	ATP-binding region and	VRTFTHEVVTLWYRAPEILLGSRHYSTPVDVWSVGCIFA
	serine/threonine protein kinases	EMVNRRPLFPGDSEIDELFKIFRIMGTPNEDSWPGVTSL
	active-site signatures are in	PDFKSTFPKWASQDLKTVTPTVDPAGIDLLSKMLCMDPR
	bold.	RRITAKVALEHEYFKDVGVIP
4	The amino acid sequence of SEQ ID	MVMKSKLDKYEKLEKLGEGTYGVVYKAQDKTTKEIYALK
	264. The conserved eukaryotic	KIRLESEDEGIPSTAIREIALLKELQHPNVVRIHDVIHT
	protein kinase domain is	NKKLILVFEFVDYDLKKFLHNFDKGIDPKIVKSLLYQLV
	underlined and the protein kinases	RGVAHCHQQKVLHRDLKPQNLLVSQEGILKLGDFGLARA
	ATP-binding region and	FGIPVKNYTNEVVTLWYRAPDILLGSKNYSTSVDIWSIG
	serine/threonine protein kinases	CIFVEMLNQKPLFPGSSEQDQLKKIFKIMGTPDATKWPG
	active-site signatures are in	IAELPDWKPENFEKYPGEPLNKVCPKMDPDGLDLLDKML
	bold.	KCNPSERIAAKNAMSHPYFKDIPDNLKKLYN
5	The amino acid sequence of SEQ ID	MDQYEKVEKIGEGTYGVVYKAIDRLTNETIALKKIRLEQ
	265. The conserved eukaryotic	EDEGVPSTAIREISLLKEMQHGNIVRLQDVVHSENRLYL
	protein kinase domain is	VFEYLDLDLKKHMDSSPDFAKDPRLVKIFLYQILRGIAY
	underlined and the protein kinases	CHSHRVLHRDLKPQNLLIDRRTNALKLADFGLARAFGIP
	ATP-binding region and	VRTFTHEVVTLWYRAPEILLGSRHYSTPVDVWSVGCIFA
	serine/threonine protein kinases	EMVNQRPLFPGDSEIDELFKIFRILGTPNEDTWPGVTAL
	active-site signatures are in	PDFKSAFPKWPAKNLQDMVPGLNSAGIDLLSKMLCLDPS
	bold.	KRITARSALEHEYFKDIGFVP
6	The amino acid sequence of SEQ ID	MEKYEKLEKVGEGTYGKVYKAKDKATGQLVALKKTRLEM
	266. The conserved eukaryotic	DEEGVPPTALREVSLLQLLSQSLYVVRLLSVEHVDGGSK
	protein kinase domain is	RKAAAAAAAEGGGGEAHGGGAVGGGKPMLYLVFEYLDTD
	underlined and the protein kinases	LKKFIDSHRKGPNPRPVPAATVQNFLYQLLKGVAHCHSH
	ATP-binding region and	GVLHRDLKPQNLLVDKEKGILKIADLGLGRAFTVPLKSY
	serine/threonine protein kinases	THEVFAFLAILLWRSEGESAADFDSXFRVSPVQVVTLWY
	active-site signatures are in	RAPEVLLGSAHYSIGVDMWSVGCIFAEMVRRQALFPGDS
	bold.	EFQQLLHIFRLLGTPTEKQWPGVTTLRDWHVYPQWEPQN
		LARAVPSLGPDGVDLLSKMLKYDPAERISAKAALDHPFF
		DSLDKSQF
7	The amino acid sequence of SEQ ID	MERPATAAVSAMEAFEKLEKVGEGTYGKVYRAREKATGK
	267. The conserved eukaryotic	IVALKKTRLHEDEEGVPPTTLREISILRMLSRDPHIVRL
	protein kinase domain is	MDVKQGQNKEGKTVLYLVFEYMETDLKKYIRGFRSSGES
	underlined and the protein kinases	IPVNIVKSLMYQLCKGVAFCHGHGVLHRDLKPHNLLMDK
	ATP-binding region and	KTLTLKIADLGLARAFTVPIKKYTHEILTLWYRAPEVLL
	serine/threonine protein kinases	GATHYSTAVDMWSVGCIFAELVTKQALFPGDSELQQLLH
	active-site signatures are in	IFRLLGTPNEKMWPGVSSLMNWHEYPQWKPQSLSTAVPN
	bold.	LDKDGLDLLSQMLHYEPSRRISAKAAMEHPYFDDVNKTCL
8	The amino acid sequence of SEQ ID	MGCVLGREVSSGIVTESKGRDSSEVETSKRDDSVAAKVE
	268. The conserved eukaryotic	GEGKAEEVRTEETQKKEKVEDDQQSREQRRRSKPSTKLG
	protein kinase domain is	NLPKHIRGEQVAAGWPSWLSDICGEALNGWIPRRANTFE
	underlined and the	KIDKIGQGTYSNVYKAKDLLTGKIVALKKVRFDNLEPES
	serine/threonine protein kinases	VRFMAREILILRHLDHPNVVKLEGLVTSRMSCSLYLVFE
	active-site signature is in bold.	YMEHDLAGLAASPAIKFTEPQVKCYMHQLLSGLEHCHNR
		RVLHRDIKGSNLLIDNGGVLKIGDFGLASFYDPDHKHRM
		TSRVVTLWYRPPELLLGANDYGVGIDLWSAGCILAELLA
		GKPIMPGRTEVEQLHKIYKLCGSPSEEYWKKYKLPNATL
		FKPREPYRRCIRETFKDFPPSSLPLIETLLAIDPAERGT
		ATDALQSEFFRTEPYACEPSSLPQYPPSKEMDAKKRDDE
		ARRLRAASKGQADGSKKERTRDRRVRAVPAPEANAELQH
		NIDRRRLISHANAKSKSEKFPPPHQDGALGFPLGASHRF
		DPAVVPPDVPFTSTSFTSSKEHDQTWSGPLVDPPGAPRR
		KKHSAGGQRESSKLSMGTNKGRRADSHLKAYESKSIA
9	The amino acid sequence of SEQ ID	MYSKSSAVDDSRESPKDRVSSSRRLSEVKTSRLDSSRRE
	269. The conserved eukaryotic	NGFRARDKVGDVSVMLIDKKVNGSARFCDDQIEKKSDRL
	protein kinase domain is	QKQRRERAEAAAAADHPGAGRVPKAVEGEQVAAGWPVWL
	underlined and the	SAVAGEAIKGWLPRRADTFEKLDKIGQGTYSSVYKARDV
	serine/threonine protein kinase	TNNKIVALKRVRFDNLDTESVKFMAREIHILRMLDHPNV
	active-site signature is in bold.	IKLEGLITSRMSCSLYLVFEYMEHDLTGLASRPDVKFSE
		PQIKCYMKQLLSGLDHCHKHGVLHRDIKGSNLLIDNNGI
		LKIADFGLASVFDPHQTAPLTSRVVTLWYRPPELLLGAS
		RYGVEVDLWSTGCILGELYTGKPILPGKTEVEQLHKIFK
		LCGSPSDDYWRRLHLPHAAVFKPPQPYRRCVAEIFKELP
		PVALGLLETLISVDPSQRGTAAFALRSEFFTASPLPCDP
		SSLPKYPPSKEIDMKLREEEARRRGAAGGKNELEKRGTK
		DSRTNSAYYPNAGQLQVKQCHSNANGRSEIFGPYQEKTV
		SGFLVAPPKQARVSKETRKDYAEQPDRASFSGPLVPGPG
		FSKAGKELGHSITVSRNTNLSTLSSLVTSRTGDNKQKSG
		PLVSESANQASRYSGPIREMEPARKQDRRSHVRTNIDYR
		SREDGNSSTKEPALYGRGSAGNKIYVSGPLLVSSNNVDQ
		MLKEHDRRIQEHARRARFDKARVGNNHPQAAVDSKLVSV
		HDAG
10	The amino acid sequence of SEQ ID	MGCIPTIISDGRRRSAAPDKRRPRPRRSSSEGEAPPHAT
	270. The conserved eukaryotic	AAGSEGGESARGAPGKERPEPAPRFVVRSPQGWPPWLVA
	protein kinase domain is	AVGHAIGEFVPRCADSFRKLAKIGEGTYSNVYKARDLVT
	underlined and the	GKTVALKKVRFDNLEAESIKFMAREILVLTRLNHPNVIK
	serine/threonine protein kinase	LEGPVTSRMSSGLYLAFEYMEHDLSGIAARQNGKFTEPQ
	active-site is in bold	VKCFMRQLLSGLEHCHNHDVLHRDIKCSNLLIDNEGNLK
		IADFGLATFYDPERKQVMTNRVVTLWYRAPELLLGATSY
		GIGIDLWSAGCILAELLYGKPIMPGRTEVEQLHKIFKLC
		GSPSEAYWNKFKLPNANIFKPPQPYARCIAETFKDFPPS
		ALPLLETLLSIDPDERGTATTALNSEFFAAEPHACEPSS
		LPKYPPSKEMDLKLIKEKTRRDSSKRPSAIHGSRRDGIH
		DRAGRVIPAPEATAENQATLHRPRAMKKANPMSRSEKFP
		PAHMDGVVGSSANAWLSGPASNAAPDSRRHRSLNQNPSS
		SVGKASTGSSTTQETLKVAPELLQVGSSSLHPCHRMLVY
		GSNLTIRSK
11	The amino acid sequence of SEQ ID	MGCICAKQADRGPASPGSGILTGAGTGTGTRSSKIPSGL
	271. The conserved protein kinase	FEFEKSGVKEHGGRSGELRKLEEKGSLSKRLRLELGFSH
	family domain is underlined, and	RYVEAEQAAAGWPSWLTAVAGDAIQGLVPLKADSFEKLE
	the serine/threonine protein	KIGQGTYSSVFRARELANGRMVALKKVRFDNFQPESIQF
	kinases active-site signature is	MAREISILRRLDHPNIMKLEGIITSRMSNSIYLVFEYME
	in bold	HDLYGLISSPQVKFSDAQVKCYMKQLLSGIEHCHQHGVI
		HRDVKSSNILVNNEGILRIGDFGLANILNPKDRQQLTSH
		VVTLWYRPPELLMGSTSYGVTVDLWSVGCVFAELMFRKP
		ILRGRTEVEQLHKIFKLCGSPPDGYWKMCKVPQATMFRP
		RHAYECTLRERCKGIATSAMKLMETFLSIEPHKRGTASS
		ALISEYFRTVPYACDPSSLPKYPPNKEIDAKHREEARRK
		KARSRVREAEVGKRPTRIHRASQEQGFSSNIAPKEKRSYA
12	The amino acid sequence of SEQ ID	MAVAAPGHLNVNESPSWGSRSVDCFEKLEQIGEGTYGQV
	272. The conserved eukaryotic	YMAKEKKTGEIVALKKIRMDNEREGFPITAIREIKILKK
	protein kinase domain is	LHHENVIKLKEIVTSPGPEKDEQGRPEGNKYKGGIYMVF
	underlined and the protein kinases	EYMDHDLTGLADRPGMRFSVPQIKCYMRQLLTGLHYCHI
	ATP-binding region and	NQVLHRDIKGSNLLIDNEGNLKLADFGLARSFSNDHNAN
	serine/threonine protein kinases	LTNRVITLWYRPPELLLGATKYGPAVDMWSVGCIFAELL
	active-site signatures are in	HGKPIFPGKDEPEQLNKIFELCGAPDEINWPGVSKIPWY
	bold.	NNFKPTRPMKRRLREVFRHFDRHALELLERMLTLDPSQR
		ISAKDALDAEYFWADPLPCDPKSLPKYESSHEFQTKKKR
		QQQRQHEETAKRQKLQHPPQHPRLPPVQQSGQAHAQMRP
		GPNQLMHGSQPPVATGPPGHHYGKPRGPSGGAGRYPSSG
		NPGGGYNHPSRGGQGGSGGYNSGPYPPQGRAPPYGSSGM
		PGAGPRGGGGNNYGVGPSNYPQGGGGPYGGSGAGRGSNM
		MGGNRNQQYGWQQ
13	The amino acid sequence of SEQ ID	MGCICTKGILPAHYRIKDGGLKLSKSSKRSVGSLRRDEL
	273. The conserved	AVSANGGGNDAADRLISSPHEVENEVEDRKNVDFNEKLS
	serine/threonine protein kinase	KSLQRRATMDVASGGHTQAQLKVGKVGGFPLGERGAQVV
	domain is underlined, and the	AGWPSWLTAVAGEAINGWVPRRADSFEKLEKIGQGTYSS
	serine/threonine protein kinase	VYRARDLETNTIVALKKVRFANMDPESVRFMAREIIIMR
	active-site signature is in bold.	KLDHPNVMKLEGLITSRVSGSLYLVFEYMDHDLAGLAAT
		PSIKLTESQIKCYMQQLLRGLEYCHSHGVLHRDIKGSNL
		LVDNNGNLKIGDFGLATFFRTNQKQPLTSRVVTLWYRPP
		ELLLGSSDYGASVDLWSSGCILAELFAGKPIMPGRTEVE
		QLHKIFKLCGSPSEEYWKKSKLPHATIFKPQQPYKRCLL
		ETFKDFPSSALGLLDVLLAVEPECRGTASSALQNEFFTS
		NPLPSDPSSLPKYPSSKEFDARLRDEEARKHKATAGKAR
		GLESIRKGSKESKVVPTSNANADLKASIQKRQEQSNPRS
		TGEKPGGTTQNNFILSGQSAKPSLNGSTQIGNANEVEAL
		IVPDRELDSPRGGAELRRQRSFMQRRASQLSRFSNSVAV
		GGDSHLDCSREKGANTQWRDEGFVARCSHPDGGELAGKH
		DWSHHLLHRPISLFKKGGEHSRRDSIASYSPKKGRIHYS
		GPLLPSGDNLDEMLKEHERQIQNAVRKARLDKVKTKREY
		ADHGQTESLLCWANGR
14	The amino acid sequence of SEQ ID	MDPDPSPDPDPPKSWSIHTRREIIARYEILERVGSGAYS
	274. The conserved protein kinase	DVYRGRRLSDGLAVALKEVHDYQSAFREIEALQILRGSP
	family domain is underlined and	HVVLLHEYFWREDEDAVLVLEFLRSDLAAVIADASRRPR
	the serine/threonine protein	DGGGGGAAALRAGEVKRWMLQVLEGVDACHRNSIVHRDL
	kinases active-site signature is	KPGNLLISEEGVLKIADFGQARILLDDGNVAPDYEPESF
	in bold.	EERSSEQADILQQPETMEADTTCPEGQEQGAITREAYLR
		EVDEFKAKNPRHEIDKETSIFDGDTSCLATCTTSDIGED
		PFKGSYVYGAEEAGEDAQGCLTSCVGTRWFRAPELLYGS
		TDYGLEVDLWSLGCIFAELLTLEPLFPGISDIDQLSRIF
		NVLGNLSEEVWPGCTKLPDYRTISFCKIENPIGLESCLP
		NCSSDEVSLVRRLLCYDPAARATPMELLQDKYFTEEPLP
		VPISALQVPQSKNSHDEDSAGGWYDYNDMDSDSDFEDFG
		PLKFTPTSTGFSIQFP
15	The amino acid sequence of SEQ ID	MDPDPSPSPDPPKSWSIHTRREIIARYEILERVGSGAYS
	275. The conserved	DVYRGRRLSDGLAVALKEVHDYQSAFREIEALQILRGSP
	serine/threonine protein kinase	HVVLLHEYFWREDEDAVLVLEFLRSDLAAVIADASRRPR
	domain is underlined, and the	GGGVAPLRAGEGKRWMLQVLEGVDACHRNSIVHRDLKPG
	serine/threonine protein kinase	NLLISEEGVLKIADFGQARILLDDGNVAPDYEPESFEER
	active-site signature is in bold.	SSEQADILQQPETMEADTTCPEGQEQGAITREAYLREVD
		EFKAKNPRHEIDKETSIYDGDTSCLATCTTSDIGEDPFK
		GSYVYGAEEAGEDAQGSLTSCVGTRWFRAPELLYGSTDY
		GLEVDLWSLGCIFAELLTLEPLFPGISDIDQLSRIFNVL
		GNLSEEVWPGCTKLPDYRTISFCKIENPIGLESCLPNCS
		SDEVSLVRRLLCYDPAARATPMELLQDKYFTEEPLPVPI
		SALQVPQSKNSHDEDSAGGWYDYNDMDSDSDFEDFGPLK
		FTPTSTGFSIQFP
16	The amino acid sequence of SEQ ID	MSNQHRRSSFSSSTTSSLAKRHASSSSSSLENAGKAFAA
	276. The conserved cyclin and	AAVPSHLAKKRAPLGNLTNLKAGDGNSRSSSAPSTLVAN
	cyclin C-terminal domains are	ATKLAKTRKGSSTSSSIMGLSGSALPRYASTKPSGVLPS
	underlined and the cyclins	VNPSIPRIEIAVDPMSCSMVVSPSRSDMQSVSLDESMST
	signature is in bold.	CESFKSPDVEYIDNEDVSAVDSIDRKTFSNLYISDAAAK
		TAVNICERDVLMEMETDEKIVNVDDNYSDPQLCATIACD
		IYQHLRASEAKKRPSTDFMDRVQKDITASMRAILIDWLV
		EVAEEYRLVPDTLYLTVNYIDRYLSGNVMNRQRLQLLGV
		ACMMIAAKYEEICAPQVEEFCYITDNTYFKEEVLQMESS
		VLNYLKFEMTAPTVKCFLRRFVRAAQGVNEVPSLQLECM
		ANYIAELSLLEYDMLCYAPSLVAASAIFLAKFVITPSKR
		PWDPTLQHYTLYQPSDLGNCVKDLHRLCFNNHGSTLPAI
		REKYSQHKYKYVAKKYCPPSIPPEFFHNLVY
17	The amino acid sequence of SEQ ID	MNKENAVGTKSEAPTIRITRSRSKALGTSTGMLPSSRPS
	277. The conserved cyclin and	FKQEQKRTVRANAKRSASDENKGTMVGNASKQHKKRTVL
	cyclin C-terminal domains are	NDVTNIFCENSYSNCLNAAKAQTSRQGRKWSMKKDRDVH
	underlined.	QSGAVQIMQEDVQAQFVEESSKIKVAESMEITIPDKWAK
		RENSEHSISMKDTVAESSRKPQEFICGEKSAALVQPSIV
		DIDSKLEDPQACTPYALDIYNYKRSTELERRPSTIYMET
		LQKDVTPNMRGILVDWLVEVSEEYKLVPDTLYLTVNLID
		RSLSQKFIEKQRLQLLGVTCMLIASKYEEICPPRVEEFC
		FITDNTYTSLEVLKMESRVLNLLHFQLSVPTVKTFLRRF
		VQAAQVSSEVPSVELEYLANYLAELTLVEYSFLKFLPSL
		MAASAVLLARWTLNQSDNPWNLTLEHYTKYKASELKAAV
		LALEDLQLNTSGSTLNAIREKYRQQKVNYSLLIHSKANH
		EIL
18	The amino acid sequence of SEQ ID	MAGSDENNPGVVGGAHVQEGLRVGAGKMGAGNVQQRRAL
	278. The conserved cyclin N- and	SNINSNIIGAPPYPCAVNKRVLSEKNVNSENDLLNAAHR
	C-terminal family domains are	PITRQFAAQMAYKQQLRPEENKRTTQSVSNPSKSEDCAI
	underlined and the cyclins	LDVDDDKMADDFPVPMFVQHTEAMLEEIDRMEEVEMEDV
	signature is in bold.	AEEPVTDIDSGDKENQLAVVEYIDDLYMFYQKAEASSCV
		PPNYMDRQQDINERMRGILIDWLIEVHYKFELMDETLYL
		TVNLIDRFLAVQPVVKKKLQLVGVTAMLLACKYEEVSVP
		VVEDLILISDRAYSRKEVLEMERLMVNTLHFNMSVPTPY
		VFMRRFLKAAQSDKKLELLSFFIIELSLVEYDMLKFPPS
		LLAASAIYTALSTITRTKQWSTTCEWHTSYSEEQLLECA
		RLMVTFHQRAGSGKLTGVHRKYSTSKFGHAARTEPANFL
		LDFRL
19	The amino acid sequence of SEQ ID	MASRPIVPVQARGEAAIGGGAGKAAIGGGAGKQQKKNGA
	279. The conserved cyclin and	AEGRNRKALGDIGNLVTVRGIEGKVQPHRPITRSFCAQL
	cyclin C-terminal domains are	LANAQAAAAAENNKKQAVVNVNGAPSILDVPGAGKRAEP
	underlined.	AAAAAAAVAKAAQKKVVKPKQKAEVIDLTSDSEERSRPR
		RSNNIMSLRRRKERNHREGICPLSLRSSLLEARLVDWLI
		EIHNKFDLMPETLYLTINIIDRFLSVKAVPRRELQLLGM
		GALFTASKYEEIWAPEVNDLVCIADRAYSHEQVLAMEKT
		ILGKLEWTLTVPTHYVFLVRFIKASLGDRKLENMVYFLA
		ELGVMNYATLTYCPSMVAASAVYAARCTLGLTPLWNDTL
		KLHTGFSESQLMDCARLLVGYHAKAKENKLQVVYKKYSS
		SQREGVALIPPAKALLCEGGGLSSSSSLASSS
20	The amino acid sequence of SEQ ID	MGLPDENNAALSKPTNLQVGGLEIGGRKFGQEIRQTRRA
	280. The conserved cyclin and	LSVINQNLVGDRAYPCHVVNKRGHSKRDAVCGKDQVDPV
	cyclin C-terminal domains are	HRPLTRKFAAQTASTQQHCIEEAKKPRTAVQERNEFGDC
	underlined and the cyclins	IFVDVEDCQPSSENQPVPMFLEIPESRLDDDMEEVEMED
	signature is in bold.	IVEEEEEEPIMDIDGRDKKNPLAVVDYIEDIYANYRRTE
		NCSCVSANYMAQQADINEKMRSILIDWLIEVHDKFDLMH
		ETLFLTVNLIDRFLARQSVVRKKLQLVGLVAMLLACKYE
		EVSVPVVGDLILISDKAYTRKEVLEMESLMLNSLQFNMS
		VPTPYVFMRRFLKAAESDKKLEVLSFFLIELSLVEYEMV
		KFPPSLLAAAAIFTAQCTLYGFKQWTKTCEWHSNYTEDQ
		LLECARMMVGFHQKAATGKLTGVHRKYGTSKFGYTSKCE
		PANFLLGEMKNP
21	The amino acid sequence of SEQ ID	MGLPDENNAALSKPTNLQVGGLEIGGRKFGQEIRQTRRA
	281. The conserved cyclin and	LSVINQNLVGDRAYPCHVVNKRGHSKRDAVCGKDQVDPV
	cyclin C-terminal domains are	HRPLTRKFAAQTASTQQHCIEEAKKPRTAVQERNEFGDC
	underlined and the cyclins	IFVDVEDCQPSSENQPVPMFLEIPESRLDDDMEEVEMED
	signature is in bold.	IVEEEEEEPIMDIDGRDKKNPLAVVDYIEDIYANYRRTE
		NCSCVSANYMAQQADINEKMRSILIDWLIEVHDKFDLMH
		ETLFLTVNLIDRFLARQSVVRKKLQLVGLVAMLLACKYE
		EVSVPVVGDLILISDKAYTRKEVLEMEKLMLNSLQFNMS
		VPTPYVFMRRFLKAAESDKKLEVLSFFLIELSLVEYEMV
		KFPPSLLAAAAIFTAQCTLYGFKQWTKTCEWHSNYTEDQ
		LLECARMMVGFHQKAATGKLTGVHRKYGTSKFGYTSKCE
		AANFLLGEMKNP
22	The amino acid sequence of SEQ ID	MAMVQRQGHDPSSPQEQEDGPSSFLSDDALYCEEGRFEE
	282. The conserved cyclin N- and	DDGGGGGQVDGIPLFPSQPADRQQDSPWADEDGEEKEEE
	C-terminal family domains are	EAELQSLFSKERGARPELAKDDGGAVAARREAVEWMLMV
	underlined.	RGVYGFSALTAVLAVDYLDRFLAGFRLQRDNRPWMTQLV
		AVACLALAAKVEETDVPLLVELQEVGDARYVFEAKTVQR
		MELLVLSTLGWEMHPVTPLSFVHHVARRLGASPHHGEFT
		HWAFLRRCERLLVAAVSDARSLKHLPSVLAAAAMLRVIE
		EVEPFRSSEYKAQLLSALHMSQEMVEDCCRFILGIAETA
		GDAVTSSLDSFLKRKRRCGHLSPRSPSGVIDASFSCDDE
		SNDSWATDPPSDPDDNDDLNPLPKKSRSSSPSSSPSSVP
		DKVLDLPFMNRIFEGIVNGSPI
23	The amino acid sequence of SEQ ID	MEASYQPHHHGHLRQHDPSSSQQEEQVPFDALYCSEEHW
	283. The conserved cyclin and	GEEDEEEGLASDGLLSEERDHRLLSPRALLDQDLLWEDE
	cyclin C-terminal domains are	ELASLFSKEEPGGMRLNLENDPSLADARREAVEWIMRVH
	underlined.	AHYAFSALTALLAVNYWDRFTCSFALQEDKPWMTQLSAV
		ACLSLAAKVEETQVPLLIDFQVEDSSPVFEAKNIQRMEL
		LVLSSLEWKMNPVTPLSFLDYMTRRLGLTGHLCWEFLRR
		CENVLLSVISDCRFTCYLPSVIAASTMLHVINGLKPRLD
		VEDQTQLLGILAMGMDKIDACYKLIDDDHALRSQRYSHN
		KRKFGSVPGSPRGVMELCFSSDGSNDSWSVAASVSSSPE
		PHSKKSRAGEEAEDRLLRGLEGEEDDPASADIFSFPH
24	The amino acid sequence of SEQ ID	MALQEEDTRRHYPTAPPFSPDGLYCEDETFGEDLADNAC
	284. The conserved cyclin and	EYAGGGARDGLCEIKDPTLPPSLLGQDLFWEDGELASLV
	cyclin C-terminal domains are	SRETGTHPCWDELISDGSVALARKDAVGWILRVHGHYGF
	underlined.	RPLTAMLAVNYLDRFFLSRSYQRDRPWISQLVAVACLSV
		AAKVEETQVPILLDLQVANAKFVFESRTIQRMELLLMST
		LDWRMNSVTPISFFDHILRRFGLTTNLHRQFFWMCERLL
		LSVVADVRLASFLPSVVATAAMLYVNKEIEPCICSEFLD
		QLLSLLKINEDRVNECYELILELSIDHPEILNYKHKRKR
		GSVPSSPSGVIDTSFSCDSSNDSWGVASSVSSSLEPRFK
		RSRFQDQQMGLPSVNVSSMGVLNSSY
25	The amino acid sequence of SEQ ID	MGQIQYSEKYFDDTYEYRHVVLPPDVAKLLPKNRLLSEN
	285. The conserved cyclin-	EWRAIGVQQSRGWVHYAIHRPEPHIMLFRRPLNYQQQQE
	dependent kinases regulatory	NQAQQNMLAK
	subunit domain is underlined and
	the cyclin-dependent kinases
	regulatory subunits signature 1 is
	in bold.
26	The amino acid sequence of SEQ ID	MGSIDPPKAEQNGTAAAAVADPGQKPGAGDAMPPPPPVK
	286. The conserved chromo domain	HSNGTAAEPDVATKRRRMSVLPLEVGTRVMCRWRDGKYH
	is underlined and the MOZ/SAS-like	PVKVIERRKLNPGDPNDYEYYVHYTEFNRRLDEWVKLEQ
	protein domain is in bold/italics.	LDLNSVETVVDEKVEDKVTGLKMTRHQKRKIDETHVEGH
		EELDAASLREHEEFTKVKNIATIELGRYEIETWYFSPFP
		PEYNDCSKLYFCEFCLNFMKRKEQLQRHMKKCD
		PKVLDRHLKAAGRG
		GLEVDVSKLIWTPYREQG
27	The amino acid sequence of SEQ ID	MDTGGNSLPSGPDGVKRKVCYFYDPEVGNYYLLQHMQVL
	292. The conserved histone	KPVPARDRDLCRFHADDYVAFLRSITPETQQDQLRQLKR
	deacetylase family domain is	FNVGEDCPVFDGLHSFCQTYAGGSVGGAVKLNHGLCDIA
	underlined.	INWAGGLHHAKKCEASGFCYVNDIVLGILELLKQHERVL
		YVDIDIHHGDGVEEAFYTTDRVMTVSFHKFGDYFPGTGD
		IRDIGYGKGKYYSLNVPLDDGIDDESYHSLFKPIIGKVM
		EVFKPGAVVLQCGADSLSGDRLGCFNLSIKGHAECVRYM
		RSFNVPVLLLGGGGYTIRNVARCWCYETGVALGLEVDDK
		MPQHEYYEYFGPDYTLHVAPSNMENKNSRQLLEEIRSKL
		LENLSKLQHAPSVPFQERPPDTELPEADEDQEDPDERWD
		PDSDMDVDEDRKPLPSRVKRELIVEPEVKDQDSQKASID
		HGRGLDTTQEDNASIKVSDMNSMITDEQSVKMEQDNVNK
		PSEQIFPK
28	The amino acid sequence of SEQ ID	MDTGGNSLPSGPDGVKRKVCYFYDPEVGNYYYGQGHPMK
	293. The conserved histone	PHRIRMTHALLAHYGLLQHMQVLKPVPARDRDLCRFHAD
	deacetylase family domain is	DYVAFLRSITPETQQDQLRQLKRFNVGEDCPVFDGLHSF
	underlined.	CQTYAGGSVGGAVKLNHGLCDIAINWAGGLHHAKKCEAS
		GFCYVNDIVLGILELLKQHERVLYVDIDIHHGDGVEEAF
		YTTDRVMTVSFHKFGDYFPGTGDIRDIGYGKGKYYSLNV
		PLDDGIDDESYHSLFKPIIGKVMEVFKPGAVVLQCGADS
		LSGDRLGCFNLSIKGHAECVRYMRSFNVPVLLLGGGGYT
		IRNVARCWCYETGVALGLEVDDKMPQHEYYEYFGPDYTL
		HVAPSNMENKNSRQLLEDIRSKLLENLSKLQHAPSVPFQ
		ERPPDTELPEADEDQEDPDERWDPDSDMDVDEDRKPLPS
		RVKRELIVEPEVKDQDSQKASIDHGRGLDTTQEDNASIK
		VSDMNSMITDEQSVKMEQDNVNKPSEQIFPK
29	The amino acid sequence of SEQ ID	MRPKDRISYFYDGDVGSVYFGPNHPMKPHRLCMTHHLVL
	294. The conserved histone	SYELHTKMEIYRPHKAYPAELAQFHSPDYVEFLHRITPD
	deacetylase domain is underlined.	TQHLFPNDLAKYNLGEDCPVFENLFEFCQIYAGGTIDAA
		RRLNNQLCDIAINWAGGLHHAKKCEASGFCYINDLVLGI
		LELLKYHARVLYIDIDVHHGDGVEEAFYFTDRVMTVSFH
		KFGDMFFPGTGDVKEIGGKEGKFYAINVPLKDGIDDTSF
		TRLFKAIISKVVETYQPGAIVLQCGADSLAGDRLGCFNL
		SIDGHSECVRFVKKFNLPLLVTGGGGYTKENVARCWVVE
		TGVLLDTELPNEIPENEYFKYFAPDYSLKIPRGNIVLEN
		LNSKSYLSAIKVQVLENLRNIQHAPSVQMQEVPPDFYIP
		DFDEDEQNPDERMDQHTQDKQIQRDDEYYDGDNDNDHNM
		DD
30	The amino acid sequence of SEQ ID	MTVAEDFHVNNRSKMVSQATPESRLTGGEDDNSLHNQVD
	295. The conserved histone	ELLCQELPERQVILEFEGTRPKPYFSDHNGGENSALGVR
	deacetylase family domain is	ATEDDLNSDVEAEEKQKEMTLEDMYKNDGTLYDDDEDDS
	underlined and the Zinc finger	DWEPVKRQVELMRWFCTNCTMVNVEDVFLCDICGEHRDS
	RanBP2-type profile is in bold.	GILRHGFYASPFMQDVGAPSVEAEVQESREDHARSSPPS
		SSTVVGFDEKMLLHSEVEMKSHPHPERADRLQAIAASLA
		TAGIFPGRCRSLPVREITKEELQMVHSSEHVDAVEMTSH
		MFSSYFTPDTYANEHSARAARIAAGLCADLASTIISGRS
		KNGFALVRPPGHHAGIKHAMGFCLHNNAAVAALAAQGAG
		AKKVLIVDWDVHHGNGTQEIFDGNKSVLYISLHRHEGGN
		FYPGTGAAHEVGTMGAEGYCVNIPWSRRGVGDNDYVFAF
		HHIVLPIASAFAPDFTIISAGFDAARGDPLGCCDVTPAG
		YAQMTHMLSALSGGKLLVILEGGYNLRSISSSAVAVIKV
		LLGDSPISEIADAVPSKAGLRTVLEVLKIQRSYWPSLES
		IFWELQSQWGMFLVDNRRKQIRKRRRVLVPIWWKWGRKS
		VLYHLLNGHLHVKTKR
31	The amino acid sequence of SEQ ID	MAAAPSSPPTNRVDVFWHDGMLSHDTGRGVFDTGSDPGF
	296. The conserved histone	LDVLEKHPENPDRVRNMVSILKRGPISPFISWHTATPAL
	deacetylase family domain is	ISQLLSFHSPEYINELVEADKNGGKVLCAGTFLNPGSWD
	underlined.	AALLAAGNTLSAMKYVLDGKGKIAYALVRPPGHHAQPSQ
		ADGYCFLNNAGLAVRLALDSGCKRVVVVDIDVHYGNGTA
		EGFYQSSDVLTISLHMNHGSWGPSHPQSGSVDELGEDEG
		YGYNMNIPLPNGTGDRGYEYAVTELVVPAVESFKPEMVV
		LVVGQDSSAFDPNGRQCLTMDGYRAIGRTIRGLADRHSG
		GRILIVQEGGYHVTYSAYCLHATVEGILDLPDPLLADPI
		AYYPEDEAFPVKVVDSIKRYLVDKVPFLKEH
32	The amino acid sequence of SEQ ID	MVESSGGASLPSVGQDARKRRVSYFYEPTIGDYYYGQGH
	297. The conserved histone	PMKPHRIRMAHNLIVHYYLHRRMEISRPFPAATTDIRRF
	deacetylase family domain is	HSEDYVTFISSVTPETVSDPAFSRQLKRFNVGEDCPVFD
	underlined.	GIFGFCQASAGGSMGAAVKLNRGDSDIALNWAGGLHHAK
		KSEASGFCYVNDIVLGILELLKVHKRVLYVDIDVHHGDG
		VEEAFYTTDRVMTVSFHKFGDFFPGSGHIKDTGAGPGKN
		YALNVPLNDGIDDESFRGMFRPIIQKVMEVYQPDAVVLQ
		CGADSLSGDRLGCFNLSVKGHADCLRFLRSFNVPLMVLG
		GGGYTMRNVARCWCYETAVAVGVEPENDLPYNEYYEYFG
		PDYTLHVEPCSMENLNAPKDLERIRNMLLEQLSRIPHAP
		SVPFQMTPPITQEPEEAEEDMDERPKPRIWNGEDYESDA
		EEDKSQHRSSNADALHDENVEMRDSVGENSGDKTREDRS
		PS
33	The amino acid sequence of SEQ ID	MAAIISCHHYHSCCSSLIASKWVGARIPTSCFGRSSTQS
	299. The conserved cyclophilin-	NNAASVRQFVTRCSSSPSSRGQWQPHQNGEKGRSFSLRE
	type peptidyl-prolyl cis-trans	CAISIALAVGLVTGVPSLDMSTGNAYAASPALPDLSVLI
	isomerase family domain is	SGPPIKDPEALLRYALPINNKAIREVQKPLEDITDSLKV
	underlined.	AGLRALDSVERNVRQASRVLKQGKNLIVSGLAESKKDHG
		VELLDKLEAGMDELQQIVEDGNRDAVAGKQRELLNYVGG
		VEEDMVDGFPYEVPEEYKNMPLLKGRAAVDMKVKVKDNP
		NLEECVFRIVLDGYNAPVTAGNFVDLVERHFYDGMEIQR
		ADGFVVQTGDPEGPAESFIDPSTEKPRTIPLEIMVDGEK
		APVYGATLEELGLYKAQTKLPFNAFGTMAMARDEFEDNS
		ASSQIFWLLKESELTPSNANILDGRYAVFGYVTENQDFL
		ADLKVGDVIESVQVVSGLDNLANPSYKIAG
34	The amino acid sequence of SEQ ID	MAGEDFDIPPADEMNEDFDLPDDDDDAPVMKAGDEKEIG
	300. The conserved FKBP-type	KQGLKKKLVKEGDAWETPDNGDEVEVHYTGTLLDGTQFD
	peptidylprolyl isomerase domains	SSRDRGTPFKFTLGQGQ
	are underlined. The FKBP-type	EAGSPPTIPPNATLQFDVELLSWTSVKDICKD
	peptidyl-prolyl cis-trans	GGIFKKILVEGEKWENPKDLDEVLVKYEFQLEDGTTIAR
	isomerase signature 1 is in bold	SDGVEFTVKEGHFCPAVAKAVKTMKKGEKVLLTVKPQYG
	and the FKBP-type peptidyl-prolyl	FGEKGKPASGDEGAVPPNATLQITLELVSWKTVSEVTDD
	cis-trans isomerase signature 2 is	KKVIKKILKEGEGYERPNEGAVVEVKLIGKLQDGTVFVK
	in bold/italics.	KGHDDCEELFKFKIDEEQ
		SSESKQDLAVVPPSSTVYYEVELVSFVKDKE
		SWDMNTEEKIEAAGKKKEEGNVIFKAGKYAKASKRYEKA
		VKYIEYDTSFSEDEKKQAKALKVACNLNDAACKLKLKDY
		NQAEKLCTKVLELDSRNVKALYRRAQAYIELSDLDLAEF
		DIKKALEIDPHNRDVKLEYKVLKEKVKEFNKKDAKFYGN
		MFAKMSKLEPVEKTAAKEPEPMSIDSKA
35	The amino acid sequence of SEQ ID	MSTVYVLEPPTKGKVVLNTTHGPLDVELWPKEAPKAVRN
	301. The conserved cyclophilin-	FVQLCLEGYYDNTIFHRIIKDFLVQGGDPTGSGTGGESI
	type peptidyl-prolyl cis-trans	YGDAFSDEFHSRLRFKHRGLVACANAGSPHSNGSQFFIT
	isomerase family domain is	LDRCDWLDRKNTIFGKITGDSIYNLSGLAEVETDKSDRP
	underlined and the cyclophilin-	LDPPPKIISVEVLWNPFEDIVPRAPVRSLVPTVPDVQNK
	type peptidyl-prolyl cis-trans	EPKKKAVKKLNLLSFGEEAEEEEKALVVVKQKIKSSHDV
	isomerase signature is in bold.	LDDPRLLKEHIPSKQVDSYDSKTARDVQSVREALSSKKQ
		ELQKESGAEFSNSFREIADDEDDDDDDASFDARMRRQIL
		QKRKELGDLPPKPKPKSRDGISARKERETSISRDKDDDD
		DDDQPRVEKLSLKKKGIGSEARGERMANADADLQLLNDA
		ERGRQLQKQKKHRLRGREDEVLTKLETFKASVFGKPLAS
		SAKVGDGDGDLSDWRSVKLKFAPEPGKDRMTRNEDPNDY
		VVVDPLLEKGKEKFNRMQAKEKRRGREWAGKSLT
36	The amino acid sequence of SEQ ID	MASAISMHSSGLLLLQGTNGKDVTEMGKAPASSRVANMQ
	302. The conserved cyclophilin-	QRKYGATCCVARGLTSRSHYASSLAFKQFSKTPSIKYDR
	type peptidyl-prolyl cis-trans	MVEIKAMATDLGLQAKVTNKCFFDVEIGGEPAGRIVIGL
	isomerase family domain is	FGDDVPKTVENFRALCTGEKGFGYKGCSFHRIIKDFMIQ
	underlined and the cyclophilin-	GGDFTRGNGTGGKSIYGSTFEDENFALKHVGPGVLSMAN
	type peptidyl-prolyl cis-trans	AGPSTNGSQFFICTVKTPWLDNRHVVFGQVVDGMDVVQK
	isomerase signature is in bold.	LESQETSRSDVPRQPCRIVNCGELPLDG
37	The amino acid sequence of SEQ ID	MAASFTALSNVGSLSSPRNGSEIRRFRPSCNVAASVRPP
	303. The conserved cyclophilin-	PLKAGLSASSSSSFSGSLRLIPLSSSPQRKSRPCSVRAS
	type peptidyl-prolyl cis-trans	AEAAAAQSKVTNKVYLDISIGNPVGKLVGRIVIGLYGDD
	isomerase signature is underlined.	VPQTAENFRALCTGEKGFGYKGSTVHRVIKDFMIQGGDF
		DKGNGTGGKSIYGRTFKDENFKLSHVGPGVVSMANAGPN
		TNGSQFFICTVKTPWLDQRHVVFGQVLEGMDIVRLIESQ
		ETDRGDRPRKRVVVSDCGELPVV
38	The amino acid sequence of SEQ ID	MAEAIDLTGDGGVMKTIVRRAKPDAVSPSETLPLVDVRY
	304. The conserved FKBP-type	EGVLAETGEVFDSTHEDNTLFSFEIGKGSVISAWDTALR
	peptidyl-prolyl cis-trans	TMKVGEVAKITCKPEYAYGSTGSPPDIPPDATLIFEVEL
	isomerase signature is underlined	VACKPCKGFSVTSVTEDKARLEELKKQREIAAATKEEEK
	and the FKBP-type peptidyl-prolyl	KRREEAKAAAAARVQAKLDAKKGHGKGKGKAK
	cis-trans isomerase signature 2 is
	in bold.
39	The amino acid sequence of SEQ ID	MGNPKVFFDMSIGGQPAGRIVMELYADVVPRTAENFRAL
	305. The conserved cyclophilin-	CTGEKGAGRSGKPLHYKGSSFHRVIPGFMCQGGDFTAGN
	type peptidyl-prolyl cis-trans	GTGGESIYGSKFADENFVKKHTGPGVLSMANAGPGTNGS
	isomerase family domain is	1QFFVCTAKTEWLDGKHVVFGQIVDGMDVVKAIEKVGSSS
	underlined and the cyclophilin-	GRTSKPVVVADCGQLS
	type peptidyl-prolyl cis-trans
	isomerase signature is in bold.
40	The amino acid sequence of SEQ ID	MPNPKVFFDMTIGGAAAGRVVMELYADTTPRTAENFRAL
	306. The conserved cyclophilin-	CTGEKGVGRSKKPLHYKGSKFHRVIPSFMCQGGDFTAGN
	type peptidyl-prolyl cis-trans	GTGGESIYGVKFADENFIKKHTGPGILSMANAGPGTNGS
	isomerase signature is underlined	QFFICTTKTEWLDGKHVVFGKVVEGMEVVKAIEKVGSSS
	and the cyclophilin-type peptidyl-	GRTSKPVVVADCGQLP
	prolyl cis-trans isomerase
	signature is in bold.
41	The amino acid sequence of SEQ ID	MAEAIDLTGDGGVMKTIVRRAKPDAVSPSETLPLVDVRY
	307. The conserved FKBP-type	EGVLAETGEVFDSTHEDNTLFSFEIGKGSVISAWDTALR
	peptidyl-prolyl cis-trans	TMKVGEVAKITCKPEYAYGSTGSPPDIPPDATLIFEVEL
	isomerase signature is underlined	VACKPCKGFSVTSVTEDKARLEELKKQREIAAATKEEEK
	and the FKBP-type peptidyl-prolyl	KRREEAKAAAAARVQAKLDAKKGHGKGKGKAK
	cis-trans isomerase signature 2 is
	in bold.
42	The amino acid sequence of SEQ ID	MATARSFFLCALLLLATLYLAQAKKSEDLKEVTHKVYFD
	308. The conserved cyclophilin-	VEIAGKPAGRIVMGLYGKAVPKTAENFRALCTGEKGTGK
	type peptidyl-prolyl cis-trans	SGKPLHYKGSSFHRIIPSFMLQGGDFTLGDGRGGESIYG
	isomerase signature is underlined	EKFADENFKLKHTGPGLLSMANAGPDTNGSQFFITTVTT
	and the cyclophilin-type peptidyl-	SWLDGRHVVFGKVLSGMDVVYKVEAEGRQSGTPKSKVVI
	prolyl cis-trans isomerase	ADSGELPL
	signature is in bold.
43	The amino acid sequence of SEQ ID	MMRREISVLLQPRFVLAFLALAVLLLVFAFPFSRQRGDQ
	309. The conserved cyclophilin-	VEEEPEITHRVYLDVDIDGQHLGRIVIGLYGEVVPRTVE
	type peptidyl-prolyl cis-trans	NFRALCTGEKGKSANGKKLHYKGTPFHRIISGFMIQGGD
	isomerase family domain is	VIYGDGKGYESIYGGTFADENFRIKHSHAGIISMVNSGP
	underlined and the cyclophilin-	DSNGSQFFITTVKASWLDGEHVVFGRVIQGMDTVYAIEG
	type peptidyl-prolyl cis-trans	GAGTYNGKPRKKVIIADSGEIPKSKWDEER
	isomerase signature is in bold.
44	The amino acid sequence of SEQ ID	MWATAEGGPPEVTLETSMGSFTVELYFKHAPRTSRNFIE
	310. The conserved cyclophilin-	LSRRGYYDNVKFHRIIKDFIVQGGDPTGTGRGGESIYGK
	type peptidyl-prolyl cis-trans	KFEDEIKPELKHTGAGILSMANAGPNTNGSQFFITLAPC
	isomerase family domain is	PSLDGKHTIFGRVCRGMEIIKRLGSVQTDNNDRPIHDVK
	underlined and the cyclophilin-	ILRTSVKD
	type peptidyl-prolyl cis-trans
	isomerase signature is in bold.
45	The amino acid sequence of SEQ ID	MSNPKVFFDILIGKMKAGRVVMELFADVTPKTAENFRAL
	311. The conserved cyclophilin-	CTGEKGIGRSGKPLHYKGSTFHRIIPNFMCQGGDFTRGN
	type peptidyl-prolyl cis-trans	GTGGESIYGMKFADENFKIKHTGLGVLSMANAGPDTNGS
	isomerase family domain is	QFFICTEKTPWLDGKHVVFGKVIDGYNVVKEMESVGSDS
	underlined and the cyclophilin-	GSTRETVAIEDCGQLSEN
	type peptidyl-prolyl cis-trans
	isomerase signature is in bold.
46	The amino acid sequence of SEQ ID	MDDDFEFPASSNVENDDDDGMDMDDMGGDVPEEEDPVAS
	312. The conserved FKBP-type	PAVLKVGEEREIGKAGFKKKLVKEGEGWETPSSGDEVEV
	peptidylprolyl isomerase domains	HYTGTLLDGTKFDSSRDRGTPFKFKLGRGQ
	are underlined. The FKBP-type	ESGSPPTIPPNATLQFDVE
	peptidyl-prolyl cis-trans	LLSWSSVKDICKDGGILKKVLVEGEKWDNPKDLDEVFVK
	isomerase signature 1 is in bold	YEASLEDGTLISKSDGVEFTVGDGYFCAALAKAVKTMKK
	and the FKBP-type peptidyl-prolyl	GEKVLLTVMPQYAFGETGRPASGDEAAVPPDASLQIMLE
	cis-trans isomerase signature 2 is	LVSWKTVSDVTKDKKVLKKTLKEGEGYERPNDGAAVQVR
	in bold/italics. The TPR repeat	LCGKLQDGTVFVKKDDEEPFEFKIDEEQ
	is in italics.	PTESQQDLAVVPANSTVYYEV
		ELLSFVKEKESWEMNNQEKIEAAARKKEEGNAAFKAGKY
		VRASKRYEKAVRFIEYDSSFSDEEKQQAKTLKNTCNLND
		AACKLKLKDFKEAEKLCTKVLEGDGKNVKALYRRAQAYI
		QLVDLDLAEQDIKKALEIDPNNRDVKLEYKILKEKVREY
		NKRDAQFYGNMFAKMNKLEHSRTAGMGAKHEAAPMTIDS
		KA
47	The amino acid sequence of SEQ ID	MAKPRCFMDISIGGELEGRIVGELYTDVAPKTAENFRAL
	313. The conserved cyclophilin-	CTGEKGIGPHTGAPLHYKGVRFHRVIKGFMVQGGDISAG
	type peptidyl-prolyl cis-trans	DGTGGESIYGLKFEDENFDLKHERKGMLSMANSGPNTNG
	isomerase family domain is	SQFFITTTRTSHLDGKHVVFGRVVKGMGVVRSVEHVTTA
	underlined and the cyclophilin-	AGDCPTVDVVIADCGEIPAGADDGIRNFFKDGDTYPDWP
	type peptidyl-prolyl cis-trans	ADLDESPAELSWWMDAVDSIKAFGNGSYKKQDYKMALRK
	isomerase signature is in bold.	YRKALRYLDICWEKEGIDEVESSSLRKTKSQIFTNSSAC
	The TPR repeat is in bold/italics.	KLKLCDLKGALLDAEFAVRDGENN
		GIKKELNAAKKKIFERREQ
		EKRAYRKMFL
48	The amino acid sequence of SEQ ID	MTKRKNPLVFLDVSIDGDPVERIVIELFADTVPRTAENF
	314. The conserved cyclophilin-	RSLCTGEKGVGKTTGKPLHYKGSYFHRIIKGFMAQGGDF
	type peptidyl-prolyl cis-trans	SNGNGTGGESIYGGKFADENFKLAHDGPGLLSMANGGPN
	isomerase signature is underlined	TNGSQFFIIFKRQPHLDGKHVVFGKVMRGMEVVKKIEQV
	and the cyclophilin-type peptidyl-	GSANGKPLQPVKIVDCGETSETGTQDAVVEEKSKSATLK
	prolyl cis-trans isomerase	AKKKRSARDSSSESRGKRRQRKSRKERTRKRRRYSSSDS
	signature is in bold.	YSSESSDSDSESYSSDTESESKSHSESSVSDSSSSDGRR
		RKRKSTKREKLRRQRGKDSRGEQKSARYDKKSRHKSADS
		SSDSESESSSRSRSRDDKKKSSRRESARSVSKLKDAEAN
		SPENLESPRDREIKKVEDNSSHEEGEFSPKNDVQHNGHG
		TDAKFGKYDDQRPRSDGSKKSSGSMRDSPKRLANSVPQG
		SPSSSPAHKASEPSSSIRARNPSRSPAPDGNSKRIRKGR
		GFTERFSYARRYRTPSPEDVTYRPYHYGRRNFHDRRNDR
		YSNYRSYSERSPHRRYRSPPRGRSPPRYQRRRSRSRSVS
		RSPGGNKGRYRGRDQSRSRSRSRSRSPRRGSSPANKQLP
		LSERLKSRLGTRVDEHSPRRRRSSSRSHDSSRSRSPDEV
		PDKHEGKAAPVSPARSRSSSPSGRGLVSYGDASPDSGIN
49	The amino acid sequence of SEQ ID	MSVLLVTSLGDIVVDLHADRCPLTCKNFLKLCRIKYYNG
	315. The conserved cyclophilin-	CVFHTVQKDFTAQTGDPTGTGTGGDSVYKFLYGDQARFF
	type peptidyl-prolyl cis-trans	MDEIHLDLKHSKTGTVAMASGGENLNASQFYFTLRDDLD
	isomerase signature is underlined.	YLDGKHTVFGEVAEGLETLTRINEAYVDEKGRPYKNIRI
	The CCHC type zinc finger is in	RHTYILDDPFDDPPQLAELIPDASPEGKPKDEVVDDVRL
	bold and the RNA-binding region	EDDWVPLDEQLGPAQLEEAIRAKEAHSRAVVLESIGDIP
	RNP-1 (RNA recognition motif) is	DAEIKPPDNV
	in bold/italics.
		DFSQSVAKLWSQFKRKDSQAAKGKGCFKCGAPDHM
		ARECPGSSTRQPLSKYILKEDNAQRGGDDSRYEMVFDED
		APESPSHGKKRRGRDDRDDRHKMSRQSVEETKFNDREGG
		HSVDKHRQSERSKHREDEMSRDSKASEAGRRRIDRDFPE
		EERDGEKYTESHRDRDGKRGDYRDYRKGRADVQTHGDRR
		GDENYRRKSAAYDDGHEGAGAARRKDSNDDHHAYRRGYG
		DSRKGTRDEDDDGRGRRDDPSYRRSSGHKDSSNGGREEQ
		KYRSGETDGKSHPERSHRGDRRR
50	The amino acid sequence of SEQ ID	MRPFNGGSSIACLVLVIAAGALAESQGPHLGSARVVFQT
	316. The conserved cyclophilin-	NYGDIEFGFFPGVAPRTVDHIFKLVRLGCYNTNHFFRVD
	type peptidyl-prolyl cis-trans	KGFVAQVADVANGRTAPMNDEQRTEAEKTIVGEFSNVKH
	isomerase signature is underlined.	VRGILSMGRYDDPDSAQSSFSILLGDAPHLDGKYAIFGR
		VTKGDETLKKLEQLPTRREGMFVMPTERITILSSYYYDT
		GAESCEEENSTLRRRLAASAVEVERQRMKCFP
51	The amino acid sequence of SEQ ID	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRAL
	317. The conserved cyclophilin-	CTGEKGTGRSGKPLHFKGSSFHRVIPGFMCQGGDFTRGN
	type peptidyl-prolyl cis-trans	GTGGESIYGEKFADENFVKKHTGPGILSMANAGPNTNGS
	isomerase signature is underlined	QFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGS
	and the cyclophilin-type peptidyl-	GRTSKPVVIADSGQLA
	prolyl cis-trans isomerase
	signature is in bold.
52	The amino acid sequence of SEQ ID	MRFTSITSAIALFAAAASALDKPLDIKVDKAVECSRKTK
	318. The conserved FKBP-type	AGDKIQVHYRGTLEADGSEFDASYKRGQPLSFHVGKGQV
	peptidyl-prolyl cis-trans	IKGWDQGLLDMCPGEKRTLTIQPDWGYGSRGMGPIPANS
	isomerase signature is underlined	VLIFETELVEIAGVAREEL
	and the FKBP-type peptidyl-prolyl
	cis-trans isomerase signature 2 is
	in bold.
53	The amino acid sequence of SEQ ID	MGNPKVFFDMSIGGQPAGRIVMELYADVVPRTAENFRAL
	319. The conserved cyclophilin-	CTGEKGAGRSGKPLHYKGSSFHRVIPGFMCQGGDFTAGN
	type peptidyl-prolyl cis-trans	GTGGESIYGSKFADENFVKKHTGPGVLSMANAGPGTNGS
	isomerase signature is underlined	QFFVCTAKTEWLDGKHVVFGQIVDGMDVVKAIEKVGSSS
	andThe cyclophilin-type peptidyl-	GRTSKPVVVADCGQLS
	prolyl cis-trans isomerase
	signature 2 is in bold.
54	The amino acid sequence of SEQ ID	MAVATRSRWVAMSVAWILVLFGTLALIQNRLSDTGASSD
	320. The conserved FKBP-type	PKLVHRKVGEEKKKPDDLEEVTHKVFFDVEIGGKPAGRI
	peptidyl-prolyl cis-trans	VMGLFGKTVPKTVENFRALCTGEKGIGKSGKPLNYKGSQ
	isomerase signature is underlined	FHRIIPKFMIQGGDFTLGDGRGGESIYGNKFSDENFKLK
	and the Cyclophilin-type peptidyl-	HTDAGRLSMTNAGPDTNGSQFFITTVTTSWLDGRHVVFG
	prolyl cis-trans isomerase	KVLSGMDVVHKIEAEGGQSGQPKSIVVISDSGELDL
	signature is in bold.
55	The amino acid sequence of SEQ ID	MAVTLHTNLGDIKCEIFCDEVPKAAEHNARGILSMANSG
	321. The conserved cyclophilin-	PNTNGSQFFIAYAKQPHLNGLYTIFGRVIHGFEVLDIME
	type peptidyl-prolyl cis-trans	KTQTGPGDRPLAEIRLNRVTIHANPLAG
	isomerase signature is underlined
56	The amino acid sequence of SEQ ID	MAVATRSRWVAMSVAWILVLFGTLALIQNRLSDTGASSD
	322. The conserved FKBP-type	PKLVHRKVGEEKKKPDDLEEVTHKVFFDVEIGGKPAGRI
	peptidyl-prolyl cis-trans	VMGLFGKTVPKTVENFRALCTGEKGIGKSGKPLNYKGSQ
	isomerase signature is underlined	FHRIIPKFMIQGGDFTLGDGRGGESIYGNKFSDENFKLK
	and the Cyclophilin-type peptidyl-	HTDAGRLSMANAGPDTNGSQFFITTVTTSWLDGRHVVFG
	prolyl cis-trans isomerase	KVLSGMDVVHKIEAEGGQSGQPKSIVVISDSGELDL
	signature is in bold.
57	The amino acid sequence of SEQ ID	MGNPKVFFDMSIGGQPAGRIVMELYADVVPRTAENFRAL
	323. The conserved cyclophilin-	CTGEKGAGRSGKPLHYKGSSFHRVIPGFMCQGGDFTAGN
	type peptidyl-prolyl cis-trans	GTGGESIYGSKFADENFVKKHTGPGVLSMANAGPGTNGS
	isomerase signature is underlined	QFFVCTAKTEWLDGKHVVFGQIVDGMDVVKAIEKVGSSS
	andThe cyclophilin-type peptidyl-	GRTSKPVVVADCGQLS
	prolyl cis-trans isomerase
	signature 2 is in bold.
58	The amino acid sequence of SEQ ID	MSPVAANAMEEAAEPEVPAPVTPSKDDADTDAAVSRFLG
	324. The conserved A-box of the	FCKSKLGLAEGNCVQSSTLLRKTAHVLRSSGTVIGTGTA
	Retinoblastoma-associated protein	EEAERYWFAFVLYTVRRVGERKAEDEQNGSDETEVPLSR
	is underlined and the B-box of the	ILKASVLNLIDFFKEIPQFVIKAGAIVSGIYGANWDSRL
	Retinoblastoma-associated protein	EAREMQTNYVHLCILCKFYKRICGEFFILNDAKDDMKSA
	is in bold.	DSSTSDPVIMYQPFGWLLFLALRIHALSRFKDLVSSTNA
		LVSVLAILIIHLPTRFRKFSISDSSQLVKRSEKGVDLVG
		SLAYRYDTSEDEIKRTLEKANNVIAEILGITPPPASECK
		AENLENVDTDGLIYFGNLMEETSLSSILSTLEKIYEDAT
		RNDSEFDERVFINDDDSLLVSGSLSGAAINLTGAKRKYD
		SFASPAKTITRPLSPSRSPASHINGIIGGTNLRITATPV
		ATAMTTAKWLRTFVSPLPSKPSTDLQGFLASCDRDVTSD
		VIRRANIILEAIFPNSPIGERTVTGGLQNANLMDNMWAE
		QRRLEALKLYYRVLEAMCRAEAQILHSNNLTSLLTNERF
		HRCMLACSAELVLATHKTVTMLFPAVLERTGITAFDLSK
		VIESFVRHEETLPRELRRHLNTLEERLLENMVWERGSSM
		YNSLVVARPALAPEINRLGLLPEPMPSLDAIALLINFSS
		SGLPQSPVQKHEASPGQNGDIRSPKRISTEYRSVLVERN
		FTSPVKDRLLALSNIKSKLPPPPLQSAFASPTRPHPGGG
		GETCAETAIHIFFSKITKLAAVRINAMLERLQLSQQIKE
		GVYCLFQQILSQRTNLFFNRHIDQVILCCFYGVAKINQI
		NLTFREIIYNYRKQPQCKPQVFRNVFVDWSTRRNGKAGN
		EHVDIISFYNEIFIPSVKPLLVELGPTGATTRTNRTSEV
		GNKNDAQCPGSPKISSFPTLPDMSPKKVSASHNVYVSPL
		RSSKMDASISHSSKSYYACVGESTHAYQSPSKDLVAINS
		RLNGNRKVRGTLNFDDVDAGLVSDSMVANSLYLQNGSSM
		SSSTAKSSEK
59	The amino acid sequence of SEQ ID	MRPILMKGHERPLTFLKYNREGDLLFSCAKDHTPTVWFA
	325. The conserved G-protein beta	DNGERLGTYRGHNGAVWCCDVSRDSMRLITGSADTTAKL
	WD-40 repeat domains are	WSVQNGTQLFTFNFDSPARSVDFSIGDKLAVITTDPFME
	underlined.	LPSAIHVKRIARDPADQASESVLVLRGHQGRIARAVWGP
		LNKTIISAGEDAVIRIWDSETGKLLRESDKETGHKKAVT
		SLMKSVDGSHFVTGSQDKSAKLWDIRTLTLIKTYVTERP
		VNAVTMSPLLDHVVLGGGQDASAVTMTDHRAGKFEAKFF
		DKILQEEIGGVKGHFGPINALAFNPDGKSFSSGGEDGYV
		RLHHFDPDYFNIKI
60	The amino acid sequence of SEQ ID	MDKKRTVVPLVCHGHSRPVVDLFYSPITPDGFFLISASK
	326. The conserved G-protein beta	DSSPMLRNGETGDWIGTFEGHKGAVWSCCLDTNALRAAS
	domain is underlined and the WD-40	GSADFSAKLWDALSGDELHSFEHKHIVRSCAFSEDTHLL
	repeat domains are in bold	LTGGVEKILRIFDLNRPDAPPREVDNSPGSIRTVAWLHS
		DQTILSSCTDIGGVRLWDVRSGKIVQTLETKSPVTSSEV
		SQDGRYITTADGSTVKFWDANHFGLVKSYNMPCNIESAS
		LEPKLGNKFIAGGEDMWVHIFDFHTGEEIGCNKGHHGPV
		HCVRFSPGGESYASGSEDGTIRIWQTGPANNVEGDANPS
		NGPVTGKAKVGADEVTRKVEDLQIGKEGKDWREG
61	The amino acid sequence of SEQ ID	MAEGLILKGTMRAHTDMVTAIAIPIDNSDMVVTSSRDKS
	327. The conserved G-protein beta	IILWHLTKEEKVYGVPRRRLTGHSHFVQDVVLSSDGQFA1
	WD-40 repeat domains are	LSGSWDGELRLWDLATGVSARRFVGHTKDVLSVAFSIDN
	underlined.	RQIVSASRDRTIKLWNTLGECKYTIQEGEAHTDWVSCVR
		FSPNTLQPTIVSASWDRTIKVWNLTNCKRNTLAGHNGY
		VNTVAVSPDGSLCASGGKDGVILLWDLAEGKRLYNLEAG
		AIIHSLCFSPNRYWLCAATENSIKIWDLESKSIVEDLRV
		DLKNEADKTDGTTTAASNKKVIYCTSLNWSADGSTLFSG
		YNDGVIRVWGTGRY
62	The amino acid sequence of SEQ ID	MAEGLHLKGTMKAHTDMVTAIAVPIDNADMIVTSSRDKS
	328. The conserved G-protein beta	IILWHLTKEDKVYGVPRRRLTGHSHFVQDVVLSSDGQFA
	WD-40 repeat domains are	LSGSWDGELRLWDLATGVSARRFVGHTKDVLSVAFSIDN
	underlined.	RQIVSASRDRTIKLWNTLGECKYTIQEGEAHNDWVSCVR
		FSPNTLQPTIVSASWDRTVKVWNLTNCKLRNTLQGHSGY
		VNTVAVSPDGSLCASGGKDGVILLWDLAEGKKLYSLEAG
		AIIHSLCFSPNRYWLCAATENSIKIWDLESKSIVEDLRV
		DLKNEADMSDGTTGAMSSNKKVIYCTSLNWSADGSTLFS
		GYNDGVIRVWGIGRY
63	The amino acid sequence of SEQ ID	MAEGLHLKGTMKAHTDMVTAIAVPIDNADMIVTSSRDKS
	329. The conserved G-protein beta	IILWHLTKEDKVYGVPRRRLTGHSHFVQDVVLSSDGQFA
	WD-40 repeat domains are	LSGSWDGELRLWDLATGVSARRFVGHTKDVLSVAFSIDN
	underlined and the Trp-Asp (WD)	RQIVSASRDRTIKLWNTLGECKYTIQEGEAHNDWVSCVR
	repeats signature is in bold.	FSPNTLQPTIVSASWDRTVKVWNLTNCKLRNTLQGHSGY
		VNTVAVSPDGSLCASGGKDGVILLWDLAEGKKLYSLEAG
		AIIHSLCFSPNRYWLCAATENSIKIWDLESKSIVEDLRV
		DLKNEADMSDGTTGAMSSNKKVIYCTSLNWSADGSTLFS
		GYNDGVIRVWGIGRY
64	The amino acid sequence of SEQ ID	MSGVPAPPFATTTPENGTMSSNSPAFHRDSDDDDDQGEV
	330. The conserved G-protein beta	FLDDSDIIHEVAVDDEDLPDADDEADEAEEADDSLHIFT
	WD-40 repeat domains are	GHNGEVYSLACSPTDATLVATGAGDDKGFLWRIGHGDWA
	underlined.	VELQGHKDSISSLAFSLDGQLLASGSLDGVIQIWDVPSG
		NLKGTLDGPGGGIEWIRWHPKGHIILAGSEDSTVWMWNA
		DKMAYLNMFSGHGNSVTCGDFTPDGKTICTGSDDATLRI
		WNPKSGENIHVVKGHPYHAEGLTSMAISSDSGLAITGAK
		DGSVRIVNISSGRVVSSLDAHADSVEFVGLALSSPWAAT
		GSLDQKLIIWDLQHSSPRATCDHEDGVTCLSWVGASRFL
		ASGCVDGKVRVWDSLSGDCVRTFHGHSDAIQSLSVSANE
		EFLVSVSIDGTARVFEIAEFH
65	The amino acid sequence of SEQ ID	MGTSQHQLSSCLQLLPRRRGNKNLIFRRTMASGGAAAVA
	331. The conserved G-protein beta	PPPGYKPYRHLKTLTGHVAAVSCVKFSNDGTLLASASLD
	WD-40 repeat domains are	KTLIIWSSAALSLLHRLVGHSEGVSDLAWSSDSHYICSA
	underlined.	SDDRTLRIWSSRSPFDCLKTLRGHTDFVFCVNFNPQSSL
		IVSGSFDETIRIWEVKTGRCLNVIRAHSMPVTSVHFNRD
		GSLIVSGSHDGSCKIWDTKNGACLKTLIDDTVPAVSFAK
		FSPNGKFILVATLNDTLKLWNYATGKFLKIYTGHKNSVY
		CLTSTFSVTNGKYIVSGSEDRCICIWDLQGKNLIQKLEG
		HSDTVISVTCHPSENKIASAGLDSDRTVRIWLQDA
66	The amino acid sequence of SEQ ID	MPSQKIETGHQDIVHDVAMDYYGKRVATASSDTTIKIIG
	332. The conserved G-protein beta	VSNSSGSQHLASLSGHKGPVWQVAWAHPKFGSILASCSY
	WD-40 repeat domains are	DGQVILWKEGNQNDWAQAHVFNDHKSSVNSIAWAPHELG
	underlined.	LCLACGSSDGNISVFTARPDGGWDTTRIEQAHPVGVTSV
		SWAPSMAPGALVGSGLLDPVQKLASGGCDNTVKVWKLYN
		GTWKMDCFPALQMHSDWVRDVAWAPNLGLPKSTIASASQ
		DGTVVIWTVAKEGEQWQGKVLKDFKTPVWRVSWSLTGNL
		LAVADGNNNVTLWNEAVDGEWQQVTTVEP
67	The amino acid sequence of SEQ ID	MKIAGLKSVENAHDESVWAAAWVPATESRPALLLTGSLD
	333. The conserved G-protein beta	ETVKLWRPDELALERTNAGHFLGVVSVAAHPSGVIAASA
	WD-40 repeat domains are	SIDSFVRVFDVDTNATIATLEAPPSEVWQMQFDPKGTTL
	underlined and the Trp-Asp (WD)	AVAGGGSASIKLWDTATWELNATLSIPRPEQPKPSEKGN
	repeats signature is in bold.	KKFVLSVAWSPDGRRLACGSMDGTISIFDVARAKFLHHL
		EGHFMPVRSLVFSPVEPRLLFSASDDAHVHMYDSEGKSL
		VGSMSGHASWVLSVDVSPDGAALATGSSDRTVRLWDLSM
		RAAVQTMSNHSDQVWGVAFRPMAGAGVRAGGRLASVSDD
		KSISLYDYS
68	The amino acid sequence of SEQ ID	MEIDLGNLAFDVDFHPSEQLVASGLITGDLLLYRYGDGS
	334. The conserved G-protein beta	SPEKLLEVRAHGESCRAVRFINDGKAILTGSPDCSILAT
	WD-40 repeat domains are	DVETGSVVARVENAHEAAVNRLVNLTESTIATGDDNGCI
	underlined and the Trp-Asp (WD)	KVWDTRQRSCCNTFSAHEDFISDMTFASDSMKLVVTSGD
	repeats signature is in bold.	GTLSVCNLRSNKVQTRSEFSEDELLSVVIMKNGRKVVCG
		TQSGTLLLYSWGFFKDCSDRFVDLSPSSVDALLKLDEDR
		IIAGTENGLISLIGILPNRIIQPIAEHSDHPIERLAFSH
		DKKFLGSISHDQTLKLWDLNDILGSEDSPSSQAAIDDSD
		SDEMDVDANPPDSSKGNKKKHSGKGNDVGNANNFFADLGD
69	The amino acid sequence of SEQ ID	MSQQPSVILATASYDHTIRFWEAKSGRCYRTIQYPDSQV
	335. The conserved G-protein beta	NRLEITPHKRYLAVAGNPSIRLFDVNSNTPQPVMSFDSH
	WD-40 repeat domains are	TNNVMAVGFQYDGNWMYSGSEDGTVRIWDLRARGCQREY
	underlined and the Trp-Asp (WD)	ESRGAVNTVVLHPNQTELISGDQNGNIRVWDLTANSCSC
	repeats signature is in bold.	ELVPEVDTAVRSLTVMWDGSLVVAANNNGTCYVWRLLRG
		SQTMTNFEPLHKLQAHNGYILKCLLSPEFCEPHRYLATA
		SSDHTVKIWNVEGFTLEKTLIGHQRWVWDCVFSVDGAYL
		ITASSDTTARLWSMSTSQDIRVYQGHHKATTCCALHDGA
		EGSPG
70	The amino acid sequence of SEQ ID	MEDAMDMEVEVEVEAEEHSPSSSNPSGSSFRRFGLKNSI
	336. The conserved G-protein beta	QTNFGSDYVFEITPKFDWSLMGVSLSSNAVKLYSPTTGQ
	WD-40 repeat domains are	YCGECRGHSDTVNGISFSGPSSPHVLHSCSSDGTIRAWD
	underlined.	TRSFKEVSCISAGPSQEIFSFSFGGSSDSLLSAGCKSQI
		LFWDWRNKKQVACLEDSHVDDVTQVCFVPHHQNKLISAS
		VDGLICIFDTAGDINDDEHMESVINVGTSIGKVGIFGQT
		FEKLWCLTHIETLSVWDWKEGTNEANFEDARKLASDSWS
		LDHIDYFVDCHSAEEGEGLWVIGGTNAGTLGYFPVKYKG
		GAAIGSPEAVLGGGHSDVVRSVLPMSGMAGTTSKTRGIF
		GWTGGEDGRLCCWLSDDSSATSRSWMSSNLVLKSSRSHH
		KKNRHQPY
71	The amino acid sequence of SEQ ID	MSQHQEYPMEYAADDYDVGEVEDDMYFHERVMGDSDTDE
	337. The conserved G-protein beta	DEEYDHLDNKITDTSAADARRGKDIQGIPWERLSVTREK
	domain is underlined and the WD-40	YRRTRIEQYKNYENVPQSGESSEKDCKPTRKGGNYYEFW
	repeat domains are in bold	RNTRSVKSTILHFQLRNLVWSTTKHDVYLMSHFSIIHWS
		SLTCKKTEVLDVYGHVAPREKHPGSLLEGFTQTQVSTLA
		VRDKLLIAGGFQGELICKNLDRPGVSYCCRTTYDDNAIT
		NAVEIYDYPSGAVHFMASNNDCGVRDFDMEKFELSRHFT
		FPWPVNHTSLSPDGKLLVIVGDNPEGIVVDSQRGKTIRP
		LQGHLDFSFASAWHPDGHIFATGNQDKTCRIWDIRNLSK
		SVAVLKGNLGAIRSIRFTSDGRFMAMAEPADFVHVYDVK
		SGYEKEQEIDFFGEISGVSFSPDTESLFVGVWDRTYGSL
		LQYNRCRNYSYLDSM
72	The amino acid sequence of SEQ ID	MGASSDPNPDVSDEHQKRSEIYTYEAPWHIYAMNWSVRR
	338. The conserved G-protein beta	DKKYRLAIASLLDHPAAAAAVPNRVEIVQLDDSTGEIRA
	WD-40 repeat domains are	DPNLSFDHPYPATKAAFVPDKDCQRADLLATSSDFLRIW
	underlined.	RIADDSSRVDLRSFLNGNKNSEFCRPLTSFDWNEAEPKR
		IGTSSIDTTCTIWDIERETVDTQLIAHDKEVYDIAWGGV
		SVFASVSADGSVRVFDLRDKEHSTIIYESSEPDTPLVRL
		GWNKQDPRYMATIIMDSAKVVVLDIRYPTMPVVELQRHQ
		ASVNAIAWAPHSSCHICTAGDDSQALIWDLSSMAQPVEG
		GLDPILAYTAGAEIEQLQWSSSQPDWVAIAFSLKLQ
73	The amino acid sequence of SEQ ID	MRGGGGGGDATGWDEDAYRESVLKEREVQTRTVFRAAFA
	339. The conserved G-protein beta	PSPSPSPSPDAVVVASSDGSVASYSISACLSDHRLQSLR
	WD-40 repeat domains are	FADAKSQNVLEAEPACFLQGHDGPAYDVKFYGEGEDSLL
	underlined.	LSCGDDGRIRGWMWRDITSSEAHDHSQGNSAKPVLDLVN
		PQSRGPWGALSPIPENNALAVDVKRGSIYAAAGDSCAYC
		WDVECGKIKTVFKGHSDYLHCIAARNSSSQIITGSEDGT
		ARIWDCRSGKCVQVIDPDKDHKKGFFASVSCLALDASES
		WLVCGRGRDLSVWSISASDCIAKISTNAPAQDVLFDDNQ
		ILLVGAEPLISRLDMNGAVLSQIHCAPQSVFSVSLHQSG
		VTAVGGYGGLVDVISQFGSHLCTFRCKCI
74	The amino acid sequence of SEQ ID	MEAPIIDPLQGDFPEVIEEYLEHGIMKCIAFNRRGTLLA
	340. The conserved G-protein beta	AGCTDGSCIIWDFETRGVAKELRDKECTAAITSVCWSKY
	WD-40 repeat domains are	GHRILVSASDKSLILWDVLSGEKIAHTTLQHTVLQACLH
	underlined.	PGSSTPSICLACPFSSAPMIVDLNTGSTTALPVLTADVS
		NGATPLSRNKTSDTSVTYSPCNACFNKHGDLVYAGTSKG
		EILIIDHKNVRVCAIVLVSGGAVIKNVVFSRNGQYMLTN
		SNDRLIRIYKNLLPPKDGLKMLDELNESFNESDDVEKLK
		AIGSKCLELLHEFQDSITRVQWKAPCFSGDGEWVIGGAA
		SRGEHKIYIWDRAGHLVKILEGPKEALMDLAWHPVHPII
		ISVSLTGLVYIWAKDYTENWSAFAPDFKELEENEEYVER
		EDEFDLVPETEKVKGLDVHEDDEVDVLTVERDSVFSDSD
		MSQEELCFLPAVPCLDIPEQQDKCVGSCSKLPDGNHSGS
		PLSVEAGQNGNASNHNSSPLEPMENSTADDTDGVRLKRK
		RKPSEKGLELQAEKVKKPVKPLKSSGRLSKTNKPVIDPD
		SSNGVYGDDGSD
75	The amino acid sequence of SEQ ID	MRGVSWPEDGNNPSTSSSSQRNQQQAHAPRAVSGHAASH
	341. The conserved G-protein beta	PSASNIFKLLVQREVSPRSKHSSKKLWREASKCQPYPFQ
	WD-40 repeat domains are	QSCEAVRDVRQGLISWVESASLRHLSAKYCPLVPPPRST
	underlined.	IAAAFSPDGKILASTHGDHTVKLIDSQTGSCLKVLRGHR
		RTPWVVRFHPLYPEILASGSLDHEVRLWDANTAECIGSR
		NFYRPIASIAFHARGELLAVASGHKLYIWHYNRRGETSS
		PTIVLRTQRSLRAVHFHPHAAPFLLTAEVNDLDSADSAM
		TLATSPGYLHYPPPTVYFADAHSHERSRLADELPLMPLP
		LLMWPSFTRDDGRVPLQRIDGDVGLNGQQRVDSSSSVRL
		WTYSTPSGQYELLLSPVESGNSPSMPEETGNNAFSSAVE
		AEVSQSAMDTVEDMEVQPEERNTQFFSFSDPRFWELPLL
		HGWLVGQTQAGPRSVRQSSPGDIETQSAFGEVASVSPIT
		SGVMPVSMDPSRFGGRSGSRYRSPGSRGVHVTGPNNDGP
		RDENDPQSVVSKLRSELAASLAAAASTELPCTVKLRIWP
		HDVKDPCAQLDLESCRLTIPHAVLCSEMGAHFSPCGRFL
		AACVACVLPHLESDPGLHGQVNQDVTGVATSPTRHPISA
		HQIMYELRIYSLEEATFGIVLASRPVRAAHCLTSIQFSP
		TSEHLLLAYGRRHSSLLKSIVIDGENTVPIYTILEVYRV
		SDMELVRVLPSAEDEVNVACFHPSVGGGLIYGTKEGKLR
		ILHYDSSHGLNLKSSGFLDENVPEVQTYALEC
76	The amino acid sequence of SEQ ID	MDSAVAIAALSLVVGAAIALLFFGNYFRKRRSEVVAMAE
	342. The conserved G-protein beta	ADLQPHPKNPSRPPPQPAAKKVHAKSHAHGADKDKNKRH
	WD-40 repeat domains are	HPLDLNTLKGHGDSVTGLCFASDGRSLATACADGVVRVF
	underlined and the Trp-Asp (WD)	KLDDASNKSFKFLRINLPAGGHPTAVAFGDGVSSVIVAS
	repeats signature is in bold.	QHLSGCSLYMYGEEKPTNLDSNKQQTKLPMPEIKWEHHK
		VHEQKAILTLSGAAANYDSGDGSTIIASCSEGTDIIIWH
		AKTGKILGNVDTNQLKNTMSAISPNGRFIAAAAFTADVK
		VWEIVYSKDGSVKGVTKVMQLKGHKSAVTWLCFTPNSEQ
		IVTASKDGSIRIWNINVRYHLDEDTKTLKVFPIPLQDSS
		GTTLHYERLSLSPDGKILAATHGSMLQWLCIETGKVLDT
		AEKAHDGDITCMSWAPQSIPTGDKKVNVLATASGDKKVK
		LWAAPPLPS
77	The amino acid sequence of SEQ ID	MEVEPKKASKTFPVKPKLKPKPRTPSGKTPESKYWSSFK
	343. The conserved G-protein beta	TTHPLDNLSFSVPSLAFSPSPPHLLAAAHSATVSLFSPH
	WD-40 repeat domains are	RTTISSFSDVVSSLSFRSDGQLLAASDLSGLIQVFDVRS
	underlined.	RTPLRRLRSHARPVRFVRYPVLDKLHLVSGGDDALVKYW
		DVAGESVVSELRGHKDYVRCGDCSPADANCFVTGSYDHV
		VKLWDVRVRDGNRAATEVNHGSPVQDVIFLPSGSLVATA
		GGNSVKIWDLIGGGRMVYSMESHNKTVTSICVGTMGAQQ
		SGEEGVQLRILSVGLDGYMKVFDYSRMKVTHSMRFPAPL
		LSIGFSPDSNVRAIGTSNGILYVGKRKAKENAEGGANGI
		LGLGSVEEPRRRVLKPSFYRYFHRGQSEKPSEGDYLVMR
		PKKVKLAEHDKLLKKFQHKNALISVLGGNDPEKVVAVME
		ELVARRALLKCVLNLDADELGLILTFLHKNSTVPRYSSL
		LLGLAKKVIDLRLEDIRASDALKGHIRNLKRSVDEEIRI
		QEGLQEIQGMVSPLLRIAGRR
78	The amino acid sequence of SEQ ID	MQGGSSGVGYGLKYQARCISDVKADTDHTSFLTGTLSLK
	344. The conserved G-protein beta	EENEVHLLRLSSGGTELICEGLFSHPSEIWDLSSCPFDQ
	WD-40 repeat domains are	RIFSTVFSTGESYGAAVWQIPELYGQLNSPQLEKIASLD
	underlined.	AHSRKISCVLWWPSGRHDKLVSIDEENIFLWGLDCSKKS
		AQVQSQESAGMLHNLSGGAWDPHDVNTVAATCESSIQFW
		DLRTMKKANSLESVHARDLDYDMRKKHLLVTSEDESGVR
		VWDLRMPKAPIQEFPGHTHWTWAVRCNPDYEGLILSAGT
		DSAVNLWWSSTASSDELISERLIDSPTRKLDPLLHSYND
		YEDSVYGLAWSSREPWIFASLSYDGRVVVESVKPFLSRK
79	The amino acid sequence of SEQ ID	MAEEEGSAELEQQLEEEFAVWKKNTPILYDLLISHALEW
	345. The conserved G-protein beta	PSLTVHWAPLLPQPSSSAAAAAGDPSLAAHRLVLGTHTS
	WD-40 repeat domains are	DGAPNFLILADALLPSSESDHCGDDAVLPKVEISQKIRV
	underlined.	DGEVNRARFMPQNHNIVGAKTNGCEVYVFDCSKQAAKQH
		DGGFDPDLRLTGHDGEGYGLSWSPLKENYLLSASHDKKI
		CLWDISAAAQDKVLGAMHVFEAHEGAVGDASWHSKNDNL
		FGSAGDDCQLMIWDLRTNKAQQCVKAHEKEVNSVSFNSY
		NDWILATASSDTTVGLFDMRKLTTPLHVFSSHEGEVLQV
		EWDPNHEAVLASSSEDRRVMVWDLNRIGDEQQEGDASDG
		PAELLFSHGGHKAKISDFSWNKNEPWVISSVAEDNSVQV
		WQMAESICGDDDDMQAMEGYI
80	The amino acid sequence of SEQ ID	MGNYGEEDEDQYFDALEETASVSDRGSNSSDCCSSGSGL
	346. The conserved G-protein beta	DENVLDSLGFEFWTKFPESVRARRNRFLMLTGLGIEANS
	WD-40 repeat domains are	VDKEDAFPPSCNEIEVYTCKVTRDDGAVQRSLDSYNCIS
	underlined.	LLQSSTSIRSNQEVESLRGDSLLSSFRGRSKESDDLTEL
		CGMGCPESKRNAVSEFGSVSQGSIEELRRIVASSPLVHP
		LLHRKLEYERELIETKQKMGAGWLRKFGSATCISGRQGD
		TWSDPDDLEITAGMKMRRVRAHSSKKKYKELSSLYAAQE
		FLAHEGSISTMKFSMDGQYLASAGEDTVVRVWKVTEEDR
		SERVNVTVDPSCLYFALNESTQLASLNTNKEHIGKAKTF
		QRSSDSSCVILPLKVFQITEKPWHEFKGHNGEVLDLSWS
		SKGYLLSSSTDKTVRLWRVGCDRCQRVYSHNDYVTCISF
		NPVNENFFISGSIDGKVRIWNVFGGQVVAYIDCREIVSA
		VCYRSDGKGAIVGTMTGNCLFYSIKDNHLQMDAQVYLHG
		KKKSPGKRITGFQFPPNDPGKLMITSADSVIRVLSGLDV
		VCKLKGPRNSGGPMIATFTSDGKHVISASEDSNVYIWNY
		AGQDKTSSRVKKIWSCESFWSSNASVALPWCGIRTVPEA
		LAPPSRSEERRASCAENGENHHMLEEYFQKMPPYSPDCF
		SLSRGFFLELLPKGSATWPEEKLSDTSPPTVSSQAISKL
		EYKFLKSACHSVLSSAHMWGLVIVTAGWDGRIRTYHNYG
		LPVRS
81	The amino acid sequence of SEQ ID	MDIDFKEYRLRCELRGHEDDVRGVCVCGDGSIGTSSRDR
	347. The conserved G-protein beta	TVRLWAPSAGERRKYEVARVLLGHKSFVGPLAWVPPSEE
	WD-40 repeat domains are	LPEGGIVSGGMDTLVMAWDLRNGEAQTLKGHQLQVTGIV
	underlined.	LDGGDIVSASVDCTLIRWKNGQLTEHWEAHKAPIQAVIR
		LPSGELVTGSSDTTLKLWRGKTCTQTFVGHTDTVRGLAV
		MPDLGILSASHDGSIRLWAVSGECLMEMVDHTSIVYSVD
		SHASGLIVSGSEDRFAKIWKDGVCFQSIEHPGCVWDVKF
		LEDGDIVTACSDGTIRIWTNQEDRMANSTELELFDLELS
		SYKRSRKRVGGLKLEELPGLEALQVPGTSDGQTKVIREG
		DNGVAYAWNSTELKWDKIGEVVDGPEDSMNRPALDGVQY
		DYVFDVDIGDGEPTRKLPYNRSDNPYDTADKWLLKENLP
		LSYRQQIVEFILANSGQRDFNLDPSFRDPYTGSSAYVPG
		APSQLAAKQARPTFKHIPKKGMLVFDAAQFDGILKKINE
		FNNTLLSNQEKKNLSLTDIEISRLGAVVKILKDTSHYHS
		SKFADADFDLMLKLLESWPYEMMFPVIDIFRMVILHPDG
		ADGLLRHQEDKKDVLMESIKRATGNPSVPANFLTSIRAV
		TNLFKNSAYYSWLQKHRSEMLDAFSSCSSSSNKNLQLSY
		ATLLLNYAVLLIEKKDEEGQSQVLSAALELAENESLEVD
		ARYRALVAIGSLMLDGLVKRIALDFDVEHIAKAARTSKE
		AKIAEVGADIELLIKQS
82	The amino acid sequence of SEQ ID	MEFTEAYKQSGPCCFSPNARFIAVAVDYRLVIRDTLSLK
	348. The conserved G-protein beta	VVQLFSCLDKISYIEWALDSEYILCGLYKRPMIQAWSLI
	domain is underlined and the WD-40	QPEWTCKIDEGPAGIAYARWSPDSRHILTTSDFQLRLTV
	repeat domains are in bold	WSLVNTACVHVQWPKHASKGVSFTRDGKFAAICTRHDCK
		DYINLLSCHNWEIMGVFAVDTLDLADIQWSPDDSAIVIW
		DSPLEYKVLVYSPDGRCLFKYQAYESGLGVKSVSWSPCG
		QFLAVGSYDQMLRVLSHLTWKTFAEFTHLSNVRAPCCAA
		IFKEVDEPLQIDMSELSLSDDYMQGNSGDAPEGHYRVRY
		DVTEVPITLPCQKPPADRPNPKQGIGLMSWSNDSQYICT
		RNDSMPTILWIWDMRHLELAAILVQKDPIRAAVWDPTGT
		RLVLCTGSSHLYMWTPSGAYCVSVPLSQFNITDLKWNSD
		GSCLLLKDKESFCCAAAPLPPDESSDYSSDD
83	The amino acid sequence of SEQ ID	MATIAALDDDMVRSMSIGAVFSDFVGKLNSLDFHRKDDI
	349. The conserved G-protein beta	LVTAGEDDSVRLYDIANARLLKTTFHKKHGTDRVCFTHH
	WD-40 repeat domains are	PNSLICSSTKNLDTGESLRYISMYDNRSLRYFKGHKQRV
	underlined.	VSLCMSPINDSFMSGSLDHSVRMWDLRVNACQGILRLRG
		RPTVAYDQQGLVFAVAMEGGAIKLFDSRSYDKGPFDAFL
		VGGDTSEVCDIKFSNDGKSVLLSTTNNNIYVLDAYAGDK
		QCGFNLEPSPSTPIEASFSPDGQYVVSGSGDGTLHAWNI
		SRRNEVACWNSHIGVASCLKWAPRRAMFVAASTVLTFWI
		PNSEPELASAKGEAGVPPEQV
84	The amino acid sequence of SEQ ID	MSVAELKERHRAATETVNSLRERLKQKRVQLLDTDVAGY
	350. The conserved G-protein beta	ARTQGKTPVTFGATDLVCCRTLQGHTGKVYSLDWTPERN
	WD-40 repeat domains are	RIVSVSQDGRFIVWNALTSQKTHAIRLPCAWVMTCAFAP
	underlined and the beta G-protein	NGQSVACGGLDSVCSIFNLNSPVDRDGNLPVSRMLSGHK
	(transducin) is in bold.	GYVSSCQYVPDGDAHLITGSGDQTCVLWDITTGLRTSVF
		GGEFQSGHTADVLSVSINGSSPRIFVSGSCDSTARMWDT
		RVASRAVHTYHGHEGDVNAVKFFPDGNRFGTGSDDGTCR
		LFDIRTGHELQVYYQQRGIDEIPHVTSIAFSISGRLLIA
		GYSNGDCFVWDTLLAQVVLNLGSLQNSHEGRISCLGVSA
		DGSALCTGSWDTNLKIWAFGGIRRVT
85	The amino acid sequence of SEQ ID	MKKRPRGASLDQAVVDIRRREVGGLSGLSFARRLAASEG
	351. The conserved G-protein beta	LVLRLDIYNKLKGHRGCVNTVGFNLDGDIVISGSDDRHV
	domain is underlined and the WD-40	KLWDWQTGKVKLSFDSGHLSNVFQAKIMPYTDDRSIVTC
	repeat domains are in bold	AADGQARHAQILEGGQVQTMLLAKHRGRAHKLAIDPGSP
		HIVYTCGEDGLVQRLDLRSNTARELFTCREVYGTHVEVV
		HLNAIAIDPRNPNLFVIGGSDEYARVYDIRNYKWNGSHN
		FGRSANYFCPSHLIGEAHVGITGLAFSGQSELLVSYNDE
		SIYLFTQEMGLGPDPLSASTKSVDSNSSEVTSPTAVNVD
		DNVTPQVYKGHRNCETVKGVGFFGPKCEYVVSGSDCGRI
		FIWKKKGGQLIRVMAADKHVVNCIEPHPHIPALASSGIE
		NDIKIWTPKAIERATLPMNVEQLKPKARGWMNRISSPRQ
		LLLQLYSLERWPEHGGETSSGLAASQEELTELFFALSAN
		GNGSPDGGGDPSGPLL
86	The amino acid sequence of SEQ ID	MSKRGYKLQEFVAHSSNVNCLSIGKKACRLFLTGGDDCK
	352. The conserved G-protein beta	VNLWAIGKPNSLMSLCGHTNAVESVAFDSAEVLVLAGAS
	WD-40 repeat domains are	SGVIKLWDVEEAKLVRGLTGHRSNCTAMEFHPFGEFFAS
	underlined and the Trp-Asp (WD)	GSTDTNLKIWDIRKKGCIHTYKGHTRGISTIRFSPDGRW
	repeats signature is in bold.	VVSGGNDNVVKVWDLTAGKLLHDFKFHENHIRSIDFHPL
		EFLLATGSADRTVKFWDLETFELIGSSRPEAAGVRAIAF
		HPDGRTLFCGLEDSLKVYSWEPVICHDGVDMGWSTLADL
		CIHDGKLLGCSYYQSSVGVWVADASLIEPYGTNVKPQQK
		DSGDDEIEHQESRPSAKVGTTIRSTSIMRCASPDYETKD
		IKNIYVDTASGNPVSSQRVGTTNFAKVTQPLDFNDTPNL
		TLRRQGLVTETPDGLSGHVPSKSITQPKVVSRDSPDGKD
		SSRRESITFSRTKPGMLLRPAHSRRPSSTKYDVDRLSAC
		AEIGVLSSAKSGSESLVDSFLNIKVAPEDGARNGCEDNH
		SSVKNVSVESEKVLPLQTPKTEKCDQTVGFKEEINSVKF
		VNGVAVVPGRTRTLVEKFEKREKLNSTEDQTINTPENPT
		LDKTPPPSLAENEEKSDRLNIVERKATRMSSHMVTAEDR
		TPVTLVGSPEDQSTVMAPQRELPADESSKTPPLPVEDLE
		IHHGSNVSEDKATILSSQTVSEEDSKRSTLIRNFRRRDR
		FKSTEGRSPVMATQRKLPTDESGKTSSLPMEDLEIKGGL
		NVSEDKATSFSSRAPPREDRAHSALVRNVRKRDKFKSTN
		DTITVMVHQRGLSTDEASTVSVERVERRQLSNNVENPLN
		NLPPHSVPPTTTRGEPQYVGSESDSVNHEDVTELLLGNH
		EVFLSTLRSRLTKLQVV
87	The amino acid sequence of SEQ ID	MSTFLTGTALSNPNPNKSYEVVQPPNDSVSSLSFNPKAN
	353. The conserved G-protein beta	FLVATSWDNQVRCWEIVRSGTSLGTTPKASISHDQPVLC
	WD-40 repeat domains are	STWKDDGTTVFSGGCDKQVKMWPLSGGQPMTVAMHDAPI
	underlined.	KEISWIPEMNLLVTGSWDKTLRYWDTRQANPVHIQQLPE
		RCYALTVRHPLMVVGTADRNLIIYNLQSPQTEFKRISSP
		LKYQTRCLAAFPDQQGFLVGSIEGRVGVHHLDDSQQSKN
		FTFKCHREGSEIYSVNSLNFHPVHHTFATAGSDGAFNFW
		DKDSKQRLKAMSRCSQPIPCSTFNNDGSIFAYSACYDWS
		KGAENHNPATAKTYIFLHLPQESEVKGKPRLGTTGRK
88	The amino acid sequence of SEQ ID	MEVEAQQRDVNNVMCQLVDPEGTTLGPPMYLPQDVGPQQ
	354. The conserved G-protein beta	LQQMVNKLLSNEDKLPYTFYISDQELVVPLESYLQKNKV
	WD-40 repeat domains are	SVEKVLSIVYQPQAIFRIRPVNRCSATIAGHSEAVLSVA
	underlined and the Trp-Asp (WD)	FSPDGKQLASGSGDTTVRLWDLSTQTPMFTCKGHKNWVL
	repeats signatures are in bold.	SIAWSPDGKHLVSGSKAGEIQCWDPLTGQPSGNPLVGHK
		KWITGISWEPVHLSSPCRRFVSSSKDGDARIWDVTLRRC
		VICLSGHTLAVTCVKWGGDGVIYTGSQDCTIKVWETSQG
		KLIRELKGHGHWVNSLALSTEYVLRTGAFDHTGKQYSSA
		EEMKQVALERYKKMKGNAPERLVSGSDDFTMFLWEPSVS
		KHPKTRMTGHQQLVNHVYFSPDGQWVASASFDKSVKLWN
		GITGKFVAAFRGHVGPVYQISWSADSRLLLSGSKDSTLK
		IWDIRTKKLKRDLPGHADEVFAVDWSPDGEKVVSGGKDK
		VLKLWMG
89	The amino acid sequence of SEQ ID	MDAGSAHSSSNMKTQSRSPLQEQFLQRRNSRENLDRFIP
	355. The conserved G-protein beta	NRSAMDFDYAHYMLTEGRKGKENPAVSSPSREAYRKQLA
	WD-40 repeat domains are	ETLNMNRTRILAFKNKPPTPVELIPHELTSAQPAKPTKT
	underlined.	RRYIPQTSERTLDAPDLLDDYYLNLLDWGSSNVLSIALG
		NTVYLWNASDGSTSELVTIDDETGPVTSVSWAPDGRHIA
		VGLNNSDVQLWDSADNRLLRTLRGGHRSRVGSLAWNNHI
		LTTGGMDGLIVNNDVRVRSHIVDTYRGHTQEVCGLKWSA
		SGQQLASGGNDNILHIWDRSTASSNSPTQWLHRLEEHTA
		AVKALAWCPFQGNLLASGGGGGDRTIKFWNTHTGACLNS
		VDTGSQVCALLWNKNERELLSSHGFTQNQLTLWKYPSMV
		KIAELTGHTSRVLFMAQSPDGCTVASAAGDETLRFWNVF
		GVPEVAKPAPKANPEPFAHLNRIR
90	The amino acid sequence of SEQ ID	MEEAIPFKNLPSREYQGHKKKVHSVAWNCTGTKLASGSV
	356. The conserved G-protein beta	DQTARVWHIEPHGHGKVKDIELKGHTDSVDQLCWDPKHA
	WD-40 repeat domains are	DLIATASGDKTVRLWDARSGKCSQQAELSGENINITYKP
	underlined and the Trp-Asp (WD)	DGTHVAVGNRDDELTILDVRKFKPIHKRKFNYEVNEIAW
	repeats signature is in bold.	NMSGEMFFLTTGNGTVEVLAYPSLRPVDTLMAHTAGCYC
		IAIDPVGRYFAVGSADSLVSLWDISEMLCVRTFTKLEWP
		VRTISFNHTGDYVASASEDLFIDISNVQTGRTVHQIPCR
		AAMNSVEWNPKYNLLAYAGDDKNKYQADEGVFRIFGFESA
91	The amino acid sequence of SEQ ID	MGKDEEEMRGEIEERLINEEYKVWKKNTPFLYDLVITHA
	357. The conserved G-protein beta	LEWPSLTVEWLPDREEPPGKDYSVQKLVLGTHTSENEPN
	WD-40 repeat domains are	YLMLAQVQLPLEDAENDARHYDDDRADVGGFGCANGKVQ
	underlined.	IIQQINHDGEVNRARYMPQNSFIIATKTVSAEVYVFDYS
		KHPSKPPLDGACSPDLRLRGHSTEGYGLSWSKFKQGHLL
		SGSDDAQICLWDINATPKNKSLDAMQIFKVHEGVVEDVA
		WHLRHEYLFGSVGDDQYLLIWDLRTPSVTKPVQSVVAHQ
		SEVNCLAFNPFNEWVVATGSTDKTVKLFDLRKISTALHT
		FDAHKEEVFQVGWNPKNETILASCCLGRRLMVWDLSRID
		EEQTPEDAEDGPPELLFIHGGHTSKISDFSWNTCEDWVV
		ASVAEDNILQIWQMAENIYHDEDDVPGEESNKGS
92	The amino acid sequence of SEQ ID	MMRGFSCTEDGDAPSTSSTSPPPPPPPPHRQQMQAPRAS
	358. The conserved G-protein beta	SSSSGQPTSRRSTGNVFKLLARREVSPRSKHSLKKFWGE
	WD-40 repeat domains are	ASECQLCPFQQSYEAVRDVRRSLISWVEAFSLQHLSAKY
	underlined.	CPLMPPPRSTIAAAFSPDGKILASTHGDHTVKLIDSQTG
		SCLKVLRGHRRTPWVVRFHPLYPEILASGSLDHEVHLWD
		ANTAECIGSRNFYRPIASIAFHAQGDLLAVASGHKLYIW
		HYNRSGETSSPTIVLRTPRSLRAVHFHPHAAPFLLTAEV
		NDLDLTDSAMTLATSPGYLHYPPPTIYLADAHSNERSRL
		EDELPLMPSPLLMWPSFTRDDGRATLPHIGGDVGLSGQQ
		RVDSLSSGQYEFHPSPIEPSSSTSMHEEMGTDPFSSVRE
		SEVTQSAMNIVDNTEVQPEERSTYSFSFSDPRFWELPSV
		YGWLVGQTQAAPRTAPSPGALETASALGEVASVSPVRSE
		FMPGGMDQPRLGGRSGSGCRSSGSRMMRTAGLNDHPHDE
		NYPQSVVSKLRSELEASLAAAASTELPCTVKLRVWPYDM
		KDPCALFRSESCRLTIPHAVLCSEMGAHFSPCGRFFAAC
		VACVLPQLEADPVLHGQVDPDVTGVATSPTRHPVSAYQI
		MYELRIYSLEEATFGMVLASRSIRAAHCLTSIQFSPTSE
		HLLLAYGRRHNSLLKSIVIDGENTVPIYSILEVYRVSDM
		ELVRVLPSAEDEVNVACFHPSVGGGLVYGTKEGKLRILQ
		IDSSGGLNPKSTGFLDENMAEVPTYALEC
93	The amino acid sequence of SEQ ID	MGEGDLPRTEAGVLRGHEGAVLAARFNGDGNYCLSCGKD
	359. The conserved G-protein beta	RTIRLWNPHRGIHIKTYKSHGREVRDVHCTSDNSKLISC
	WD-40 repeat domains are	GGDRQIFYWDVSTGRVIRRFRGHDSEVNAVKFNDYASVV
	underlined.	VSAGYDRSVRAWDCRSHSTEPIQIINTFQDSVMSVCLTK
		TEIIGGSVDGTVRTFDIRIGREISDDLGQPVNCISMSND
		GNCILASCLDSTLRLVDRSAGELLQEYKGHTCKSYKLDC
		CLTNTDAHVAGGSEDGYVFFWDLVDASVISKFRAHSSVV
		TSVSYHPKEDCMITASVDGTIKVWKT
94	The amino acid sequence of SEQ ID	MACIKGVGRSASVAMAPDGGYLATGTMAGTVDLSFSSSA
	360. The conserved G-protein beta	SLEIFGLDFQSDDRDLPLIAESPSSERFNRLSWGKNGSG
	WD-40 repeat domains are	SDEFSLGLIAGGLVDGTIGLWNPLSLIRSEAGDKAIVGH
	underlined	LSRHKGPVRGLEFNVIAPNLLASGADDGEICIWDLAAPR
		EPSHFPPLRGSGSAAQGEISFLSWNSKVQHILASTSYNG
		TTVVWDLKKQKPVISFSDSVRRRCSVLQWNPDLATQLVV
		ASDEDSSPTLRLWDMRNIMSPVKEFAGHTRGVIAMSWCP
		NDSSYLVTCAKDNRTICWDTVTGEIVCELPAGSNWNFDV
		HWYPKIPGVISASSFDGKIGIYNVEGCSRYGVRENEFGA
		ATLRAPKWFKRPVGASFGFGGKVVSFHTRSTGGPSVNSS
		EVFVHDIITEQTLVSRSSEFEAAIQSGDRPSLRALCEKK
		SQHCESTDDQETWGFLKVLLEDDGTARSKLLAHLGFDIP
		TETNDGSQEDLSQQVNALGLEDVTADKVVQEDNNESMVF
		PTDNGEDFFNNLPSPRADTPVSTSADGFPTVNAAVEPSQ
		DEVDGLEESSDPSFDDSVQRALVVGDYKAAVALCMSANK
		LADALVIAHVGGASLWESTRDKYLKMSRLPYLKVVFAMV
		NNDLQSLVDTRPLKFWKETLAILCSFAQGEEWAMLCNSL
		ASKLMAAGNMLAATLCFICAGNIDKTVEIWSRSLATEHD
		GMSYMDLLQDLMEKTIVLALASGQKQFSASVCKLVEKYA
		EILASQGLLTTAMDYLKLLGTDDLSPELAVLRDRIAFSV
		EAEKGANISAFNGSQDPRGAVYGVDQSNYGMVDTSQHYY
		PEAAQPQVPHTVPGSPYGENYQQPFGSSFGKGYNTPMQY
		QAPSQASMFVPSEPPQNAQPSFVPTPVTSQPTTRSQFIP
		APPLALRNPEQYQQPTLGSHLYPGSVNPTFQPLPHAPGP
		VAPVPPQVSSVPGQNMPQAVAPTQMRGFMPVTNPGVVQN
		PGPISMQPATPIESAAAQPVVSPAAPPPTVQTADTSNVP
		APQKPVIATL
95	The amino acid sequence of SEQ ID	MKERGKGAGRSVDERYTQWKSLVPVLYDWLANHNLVWPS
	361. The conserved G-protein beta	LSCRWGPQLEQATYKNRQRLYLSEQTDGSVPNTLVIANV
	WD-40 repeat domains are	EVVKPRVAAAEHISQFNEEARSPFVKKFKTIIHPGEVNR
	underlined.	IRELPQNSKIVATHTDSPDVLIWDVETQPNRHAVLGAST
		SRPDLILTGHKDNAEFALAMSPTEPFVLSGGKDRYVVLW
		SIQDHISTLAADPGSAKSPGSAGTNNKQSSKAAGGNDKT
		GDSPSIEPRGVYLGHGDTVEDVTFCPSSAQEFCSVGDDS
		CLILWDARTGSSPAIKVEKAHHADLHCVDWNPHDVNLIL
		TGSADNTVRMFDRRNLTSGGVGSPVHTFEGHNAAVLCVQ
		WSPDKSSVFGSSAEDGILNIWDHEKIGRKIETVGSKVPN
		SPPGLFFRHAGHRDKVVDFHWNSSDPWTIVSVSDDGEST
		GGGGTLQIWRMIDLIYRPEEEVLAELDKFKSHILSCTS
96	The amino acid sequence of SEQ ID	MAKIAPGCEPVAGTLTPSKKREYRVTNRLQEGKRPLYAV
	362. The conserved G-protein beta	VFNFIDSRYFNVFATVGGNRVTVYQCLEGGVIAVLQSYI
	WD-40 repeat domains are	DEDKDESFYTVSWACNIDRTPFVVAGGINGIIRVIDAGN
	underlined and the Trp-Asp (WD)	EKIHRSFVGHGDSINEIRTQPLNPSLIVSASKDESVRLW
	repeats signature is in bold.	NVHTGICILIFAGAGGHRNEVLSVDFHPSDKYRIASCGM
		DNTVKIWSMKEFWTYVEKSFTWTDLPSKFPTKYVQFPVF
		IAPVHSNYVDCNRWLGDFVLSKSVDNEIVLWEPKMKEQS
		PGEGSVDILQKYPVPECDIWFIKFSCDFHYHSIAIGNRE
		GKIYVWELQSSPPVLIAKLSHPQSKSPIRQTAMSFDGST
		ILSCCEDGTIWRWDAITASTS
97	The amino acid sequence of SEQ ID	MNTAMHFGAGWRSIAEMGYTMSRLEIEPESCEDEKSLDG
	363. The conserved G-protein beta	VGNSQGPNELPRCLDHELAHLTNLKSRPHEHLIRDFPGR
	WD-40 repeat domains are	RALPVSTVKMLAGRECNYSRRGRFSSADCCHMLSRYVPV
	underlined.	NGPSPLDQMNSRAYVSQFSADGSLFVAGFQGSHIRIYNV
		DKGWKCQKNILTKSLRWTITDTSLSPDQRYLVYASMSPI
		VHIVDIGSAAMDSLANITEIHEGLDFSADSGPYSFGIFS
		VKFSTDGREVVAGSSDDSIYVYDLVANKLSLRIPAHESD
		VNTVCFADESGHIIYSGSDDTYCKVWDRRCLSARNKPAG
		VLMGHLEGITFIDSRGDGRYFISNGKDQTIKLWDIRKMG
		SDICRRGFRNFEWDYRWMDYPPRARDSKHPFDLSVATYK
		GHSVLRTLIRCYFSPVHSTGQKYIYTGSHDSCVYIYDVV
		TGAQVAALKHHKSPVRDCSWHPEYPMIVSSSWDGDIVKW
		EFFGNGETEIPAMKKRIRRRHLY
98	The amino acid sequence of SEQ ID	MEPQPQAPKKRGRKPKPKEDKKEEQLHQPPPPPPPQQQA
	364. The conserved G-protein beta	APAPAPAATRSSTSGSAGGRDRRPQQQHAVDEKYARWKS
	WD-40 repeat domains are	LVPVLYDWLANHNLLWPSLSCRWGPQLEQATYKNRQRLY
	underlined.	ISEQTDGSVPNTLVIANCEVVKPRVAAAEHVSQFNEEAR
		SPFIRKYKTIIHPGEVNRVRELPQNPNIVATHTDSPDVL
		IWDVESQPNRHAVYGATASRPNLILTGHQENAEFALAMC
		PAEPFVLSGGKDKTVVLWSIQDHITASATDQTTNKSPGS
		GGSIIKKTGEGNEETGNGPSVGPRGIYCGHEDTVEDVAF
		CPSTAQEFCSVGDDSCLILWDARVGTNPVAKVEKAHNGD
		LHCVDWNPHDNNLILTGSADNSVNMFDRRNLTSNGVGSP
		VYKFEGHKAAVLCVQWSPDKPSVFGSSAEDGLLNIWDYE
		RVDKKVDRAPNAPAGLFFQHAGHRDKIVDFHWNAADPWT
		MVSVSDDCDTAGGGGTLQIWRMSDLIYRPEEEVLAELEN
		FKAHVLECSKA
99	The amino acid sequence of SEQ ID	MGIFEPYRAVGYITTGVPFSVQRLGTETFVTVSVGKAFQ
	365. The conserved G-protein beta	VYNCAKLSLVLVGPQLPKKIRALASYREYTFAAYGSDIG
	WD-40 repeat domains are	IFKRAHQLATWSGHTAKVCLLLLFGEHILSVDVDGNAYI
	underlined and the Trp-Asp (WD)	WAFKGMNYNLSPVGHILLDSNFTPSCIMHPDTYLNKVIL
	repeats signature is in bold. The	GSQEGPLQLWNISTKTKLYEFKGWNSSVSSCVSSPALDV
	Utp21 specific WD40 associated	VAVGCADGKIHVHNIRYDEELVTFSHSMRGSVTALSFST
	putative domain is in italics.	DGQPLLASGSSSGVVSIWNLDKRRLQSVIRDAHDGSIIS
		LHFFANEPVLMSSSADNSIKMWIFDTSDGDPRLLRFRSG
		HSAPPLCIRFYANGRHILSAGQDRAFRLFSVVQDQQSRE
		LSQRHVSKRAKKLKLKEEEIKLKPVIAFDVAEIRERDWC
		NVVTSHMDTPQAYVWRLQNFVIGEHILRPCPNKPTPVKA
		CMISACGNFAILGTAGGWIERFNLQSGISRGSYIDQLEG
		TNSAHDGEVVGVACDATNTLMISAGYAGDIKVWDFKGRE
		LKSRWEIGSSLVKISYHRLNGLLATVADDFIIRLFDAVA
		LRMVRKFEGHTDRITDLCFSEDGKWLLSSSMDGSLRIWD
		IILARQVDAVFVDVSITALSLSPNMDILATTHVDQNGVF
		LWVNQSMFSGDSDINLYASGKEVVTVKLPSVSSVEGSQV
		EESNEPTIRHSESKDVPSFRPSLEQIPDLVTLSLLPKSQ
		WQSLINLDIIKVRNKPVEPPKKPEKAPFFLPSIPSLSGE
		ILFKPSEMSDKGDMKADEDKSKITPEVPSSRFLQLLHSC
		SEAKNFSPFTTYIKGLSPSTLDLELRMLQIIDDDAVDAD
		ADDPQDVDKRQELLSIELLMDYFIHEISCRSNFEFVQAL
		VRLFLKIHGETIRRQSVLQNKAKVLLETQCSVWQRVDKL
		FQGARCMVAFLSNSQF
100	The amino acid sequence of SEQ ID	MEETKVTCGSWIRRPENVNLAVLGRSPRRRGSAALEIFA
	366. The conserved G-protein beta	FDPKSTSLSSSPLVAHVIEEIEGDPLAIAVHPNGEDIVC
	WD-40 repeat domains are	FASSGSCLSFELSGQESNLKLLTKELPPLRGIGPQKCMA
	underlined.	FSVDGSRFATGGVDGRLRILEWPSLRIILDEPKAHKSIR
		DLDFSLDSEFLATTSTDGSARIWKAEDGLPCTTLTRRSD
		EKIELCRFSKDGTKPFLFCTVQRGDKAVTGVWDISTWNK
		IGHKRLLRKPAVVMSISLDGKYLAQGSKDGDMCVVEVKK
		MEVSHWSKRLHLGTSLTSLEFCPIERVVITTSDEWGVLV
		TKLNVPADWKAWQVYLLLLGLFLASLVAFYIFYENSDSF
		WGFPLGKDQPARPKIGSVLGDPKSADDQNMWGEFGPLDM
101	The amino acid sequence of SEQ ID	MADPVEHQHQQHQQHQLQQQRRRGWRIQGGQYLGEISAL
	367. The conserved G-protein beta	CFLHLPPPPLSLSSSPVLSLSSGLDSESRDRPACSFRFP
	WD-40 repeat domains are	SAGSGSQVSLFDLASGAMVRTFYVFRGIRVHGIVLGCAD
	underlined.	FPGGSSSSSSTLDYVIAVYGERRVKLFRLSVRLGRGAGE
		GSGTVLSADLELVSAAPRLSHWVMDVRFLKENGTSEDEL
		QRCLTVAIGCSDNSIRLWDVDKCSFVLAVSSPERCLLYS
		MRLWGDNLEDLQVASGTIYNEILIWKVVPNHDAPSSNEL
		TEEGLTNSCAGNSVHECLRYEAYHICRLVGHEGSIFRIA
		WSSDGSKLVSVSDDRSARIWEVHCKVQYSEDAGEVGLLF
		GHSARVWDCYISDNLIVTAGEDCSCRVWGLDGQQHDVIK
		EHIGRGIWRCLYDPWSSLLVTGGFDSAIKVHKLDASLAE
		ASAKQSNIKDLSDGTELFTTHLPNSSGHSGHMDSKSEYV
		RCLSFSCEDVMYIATNHGYLYHAKLCNDGDLRWTELAQV
		SNEVQIICMELLPSNPYDPRIDADDWVAVGDGKGWTTVV
		RVVKNSDSPKVSTSFSWAAEMDRQLLGIHWCKSLGHRFI
		FTADPRGALKLWRFFEVSQSSSLYPENSPRISLIAEFKS
		DLGARIMCLDVAFESELLICGDLRGNLVLFPLLKDLLLD
		TFVVSAAKISPVNHFKGAHGISAVSSISVAHMSFNHIEL
		RSTGADGCICYMEYDKGLQSLNFVGMKQVKELSMIESVS
		TENESTGYRTSGSYASGFASTDFIIWNLVTEAKVLQVSC
		GGWRRPHSYYLGDVPEMKNCFAYVKDDIIYIRRHWIKDS
		KDKILPQNLRLQFHGREVHSLCFVTGDFQLRKNKQSSWI
		VTGCEDGTVRLTRYTQCTDNWSSSKLLGEHVGGSAVRSI
		CCVSNIHTTSSGTSVSDVKGIENLPKDIKGTLMEDECNP
		SLLISVGAKRVLTSWLLRRRKQDGKEDDVTDLQEAENSS
		LPSSAGSSTFSFQWLSTDMPVKYSVPSKKSGSIKKLIGV
		SDTNVRCKSL
102	The amino acid sequence of SEQ ID	MPYKLSATLSNHSSDVRAVASPSDDLILSASRDSTAISW
	368. The conserved G-protein beta	FRQSPSSFTPASVIRAGSRFVNAIAYLPPTPRAPQGYAV
	WD-40 repeat domains are	VGGQDTVVNVFALGPGDKEEPEYTLVGHTDNVCALSVNS
	underlined.	DDTIISGSWDKTAKVWKDFALVYDLKGHQQSVWAVLAMN
		EKEFLTASADRTIKYWVQHKTMQTYEGHRDAVRGLALIP
		DIGFASCSNDSEIRVWTMGGDVVYTLSGHTSFVYSLSVL
		PNGDLVSAGEDRSVRVWRDGECSQVIVHPAISVWAVSTM
		PNGDIISGSSDGVVRVFSESEKRWATASELKALEDQIAS
		QSLPSQQVGDVKKTDLPGPEALSVPGKKAGEVKMIRSGD
		VVEAHQWDSLASSWQKIGEVVDAIGSGRKQLHDGKEYDY
		VFDVDIQEGAPPLKLPYNVSENPYTAAQRFLEQNDLPTG
		YLDQVVKFIEQNTAGVKLGNDGYVDPFTGASRYQPATQS
		TSNTASSSYMDPFTGGSRHIAESAPSNVPQGSHATGIIP
		FSKPIFFKLANVSAMQAKMFQFDEVLRNEISTATLAMRP
		DEVIMVNETFTYLSKVVTSTSSARTSLGWIHIETIMQIL
		DRWPVPQRFPVIDLGRLVTAYCMNAFSGPGDLEKFFSCL
		FRTSEWTSITSGSKALTKAQETNVLLLFRTIANSLDGAP
		LNDMEWIKQIFRELAQTPQLVLNKSHRLALASVLFNFSC
		IGLKGPVPADVRTLHLTIILQVLRSPNDDPEVAYRTCVA
		LGNMLYSDKTRGTPRDAQSPSPTELKSAVAAIKGGFSDP
		RINDVHREIMSLI
103	The amino acid sequence of SEQ ID	MPPQKIESGHKDTVHDLAMDYYGKRLATASSDHTINVVG
	369. The conserved G-protein beta	VSSSGSQHLATLIGHQGPVWQISWAHPKFGSLLASCSYD
	domain is underlined and the WD-40	GRVIIWREGNPNEWTQAQVFEEHKSSVNSVAWAPHELGL
	repeat domains are in bold	CLACGSSDGNISVFTARQDGGWDTSRIDQAHPVGVTSVS
		WAPSTAPGALVGSGMMEPVQKLCSGGCDNTVKVWKLYNR
		VWKLDCFPVLQMHTDWVRDVAWAPNLGLPKSTIASASQD
		GRVIIWTLAKEGDQWQGKVLYDFRTPVWRVSWSLTGNIL
		AVADGNNNVSLWNEAVDGEWIQVSTVEP
104	The amino acid sequence of SEQ ID	MSAPMLEIEARDVVKIVLQFCKENSLHQTFQTLQSECQV
	370. The conserved G-protein beta	SLNTVDSIETFVADINSGRWDAILPQVAQLKLPRNTLED
	WD-40 repeat domains are	LYEQIVLEMIELRELDTARAILRQTQAMGVMKQEQPERY
	underlined and the Trp-Asp (WD)	LRLEHLLVRTYFDPNEAYQDSTKEKRRAQIAQALAAEVT
	repeats signature is in bold.	VVPPSRLMALVGQALKWQQHQGLLPPGTQFDLFRGTAAM
		KQDVDDMYPTTLSHTIKFGTKSHAECARFSPDGQFLVSC
		SVDGFIEVWDYMSGKLKKDLQYQADETFMMHDDPVLCVD
		FSRDSEMLASGSQDGKIKVWRIRTGQCLRRLERAHSQGV
		TSVLFSRDGSQLLSTSFDGSARIHGLKSGKQLKEFRGHS
		SYVNDAIFSNDGSRVITASSDCTVKVWDVKTSDCLQTFK
		PPPPLRGGDASVNSVHLFPKNADHIVVCNKTSSIYIMTL
		QGQVVKSLSSGKREGGDFVAACVSPKGEWIYCVGEDRNL
		YCFSCQSGKLEHLMKVHEKDVIGVTHHPHRNLVATYSED
		STMKLWKP
105	The amino acid sequence of SEQ ID	MDLLQSYAEDNDGDLGRHSSPEPSPPRLLPSKSAAPKVD
	371. The conserved G-protein beta	DTTLALTVAQTNQTLARPIDPSQHAVAFNPTYDQLWAPI
	WD-40 repeat domains are	CGPAHPYAKDGIAQGMRNHKLGFVEDAAIGSFLFDEQYN
	underlined.	TFQRYGYAADPCASTGNEYVGDLDALKQNDGISVYNIRQ
		QEQKKYAEEYAKKKGEERGEGGREKAEVVSDKSTFHGKE
		ERDYQGRSWIAPPKDAKATNDHCYIPKRLVHTWSGHTKG
		VSAIRFFPKHGHLILSAGMDTKVKIWDVFNSGKCMRTYM
		GHSKAVRDISFCNDGTKFLTAGYDKNIKYWDTETGKVIS
		TFSTGKIPYVVKLHPDDEKQNILLAGMSDKKIVQWDMNT
		GQITQEYDQHLGAVNTITFVDDNRRFVTSSDDKSLRVWE
		FGIPVVIKYISEPHMHSMPSISLHPNTNWLAAQSLDNQI
		LIYSTRERFQLNKKKRFAGHIVAGYACQVNFSPDGRFVM
		SGDGEGRCWFWDWKSCKVFRTLKCHEGVCIGCEWHPLEQ
		SKVATCGWDGLIKYWD
106	The amino acid sequence of SEQ ID	MESNGNLEQTLQDGRIYRQLNSLIVAHLRDHNFPQAASA
	372. The conserved G-protein beta	VALATMTPLNVEAPRNRLLELVAKGLAVEKGELLRGVSH
	WD-40 repeat domains are	AGTNDLGGSIPASYGLVPAPWTAIDFSSLRDTKGMSKSF
	underlined.	TKHETRHLSDHKNVARCARFSTDGRFFATGSADTSIKLF
		EVSKIKQMMLPDSTDGAIRAVIRTFYDHTHPVNDLDFHP
		QNTVLISAAKDHTVKFFDYSKATAKRAFRVIQDTHNVRS
		VAFHPSGDFLLAGTDHPIPHLYDVNTFQCYLSANVPEFA
		VNAAINQVRYSSSGGMYVTASKDGTIRFWDGASANCVRS
		IAGAHGAAEVTSANFTKDQRYVLSCGKDSTVKLWEVGTG
		RLVKQYLGATHMQLRCQAVFNNTEEFVLSIDEPSNEIVV
		WDAMTAEKVARWPSNHNGPPRWIEHSPTEAAFVSCSTDR
		SIRFWKETH
107	The amino acid sequence of SEQ ID	MSNFQGEDGEYVADDFEAEDGDEELHGRESADPESDVDE
	373. The conserved G-protein beta	IDTPSNRFTDTTADQARRGRDIQGIPWERLSITREKYRR
	WD-40 repeat domains are	TRLEQYKNYENVPQSGEKSGKDCTVTEKGNSFYEFRRNS
	underlined.	RSVKSTILHFQLRNLVWATSKHDVYLMSNYSVVHWSSLT
		GKKSEVLNLAGHVAPNEKHPGSLLEGFTQTQVSTLAVKD
		RFLVAGGFQGELICKFLDRPGISFCSRTTYDDNAITNAV
		EIYVSPSGGIHFIASNNDCGVRDFDMENFELSKHFRFPW
		PVNHTSLSPDGKLLVIVGDDPEGILVDAKTGKTIMPLRG
		HLDFSFASEWHPDGVTFATGNQDKTCRIWDIRNLSKSIA
		VLKGNLGAIRSIRYTSDGRYMAIAEPADFVHVYDTKTGY
		KKEQEIDFFGEISGMSFSPDTESLFIGVWDRTYGSLLEY
		GRRRNFSYLDCLV
108	The amino acid sequence of SEQ ID	MGVEEDLEDLNALAESTDAAVDGQAALASAVDSVTLQPA
	374. The conserved G-protein beta	PPILPPVIPPPAVPVVAPVPTIPPVLRPLAPLPIRPPVL
	WD-40 repeat domains are	RPPAPKRDEAGSSDSDSDHDGTAAGSTAEYEITEESRLV
	underlined and the splicing factor	RERHEKAMQDLMMKRRGAALAVPTNDKAVRARLRRLGEP
	motif is in bold.	MTLFGEREMERRDRLRMLMAKLDAEGQLEKLMKAHEDEE
		AAASAAPEDVEEEMLQYPFYTEGSKALFNARIDIAKFSI
		TRAALRLERARRRRDDPDEDVDAEIDWALKKAESLSLHC
		SEIGDDRPLSGCSFSHDGKLLATCSMSGVAKLWDTCRMP
		QVNRVLTLKGHTERATDVAFSPVQNHIATASADRTAKLW
		NTEGTILKTFEGHLDRLGRIAFHPSGKYLGTTSFDKTWR
		LWDIESGEELLLQEGHSRSIYGIDFHRDGSLVASCGLDA
		LARVWDLRTGRSILALEGHVKPVLGVSFSPNGYHLATGG
		EDNTCRIWDLRKKKSLYTIPAHANLISEVKFEPQEGYFL
		VTASYDTTAKVWSARDFKPVKTLSVHEAKITSVDITADA
		SHIVTVSHDRTIKLWTSNDDVKEQAMDVD
109	The amino acid sequence of SEQ ID	MVKAYLRYEPAAAFGVIASVESNIAYDASGKHLLAPALE
	375. The conserved G-protein beta	KVGVWHVRQGVCTKALAPSASSAAGPSLAVTAIASSPSS
	WD-40 repeat domains are	LIASGYADGSIRIWDFEKGSCETTLNGHKGAVSVLRYGK
	underlined, and the conserved	LGSLLASGSKDNDIILWDVVGETGLYRLRGHRDQVTDLV
	Dip2/Utp12 domain is in bold.	FLDSDKKLVSSSKDKYLRVWDLETQHCMQIVGGHHSEIW
		SLDTDPEERYLVTGSADPELRFYTVKNDSSDERSEADAS
		GGVGNGDLASHNKWDVLKQFGEIQRQSKDRVATVRFNKN
		GNLLACQAAGKLVEVFRVLDEAEAKRKAKRRLHRKREKK
		GADVNENSDSSRGIGEGHDTMVTVADVFKLLQTIRASKK
		ICSISFCPVAPKSSLATLALSLNNNLLEFHSIEADKTSK
		MLTIELQGHRSDVRSVTLSSDNTLLMSTSHNSVKIWNPS
		TGSCLRTIDSGYGLCGLIVPQNKHALIGTKDGAIEIFDV
		GSGTCIEVVEAHGGSIRSIVAIPNQNGFVTGSADHDIKF
		WEYGMKQKPGDNSKHLTVSNVRTLKMNDDVLVVAVSPDA
		QKIAVALLDCTVKVFFMDSLKLMHSLYGHRLPVLCLDIS
		SDGDLIVTGSADKNLMIWGLDFGDRHKSIFAHGDSIMAV
		QFVGNTHYMFSVGKDRLVKYWDADKFELLLTLEGHHADI
		WCLAISNRGDFLVTGSHDRSIRRWDRTEEPFFIEEEKEK
		RLEEMFESDLDNAFGNKYVPKEEIPEEGAVALAGKKTQE
		TLSATDSIIEALDIAEVELKRIAEHEEEKNNGKTAEFHP
		NYVMLGLSPSDFILRALSNVQTNDLEQTLLALPFSDALK
		LLSYLKDWTTYPDKVELVSRIATVLLQTHYNQLVSTPAA
		RPLLTTLKDILHKKVKECKDTIGFNLAAMDHLKQLMALR
		SDALFQDAKVKLLEIRSQLSKRLEERTDPREAKRRKKKQ
		KKSTNMHAWP
110	The amino acid sequence of SEQ ID	MGGVQAEREDKDKVSLELTEEILQSMEVGMTFRDYSGRI
	376. The conserved G-protein beta	SSMDFHRASSYLVTASDDESIRLYDVASATCLKTINSKK
	WD-40 repeat domains are	YSVDLVSFTSHPMTVIYSSKNGWDESLRLLSLHDNKYLR
	underlined.	YFKGHHDRVVSLSLCPRNECFISGSLDRTVLLWDQRAEK
		CQGLLRVQGRPATAYDDPGLVFAIAFGGCVRMFDARKYE
		KGPFEIFSVGGDVSDANVVKFSNDGRLMLLTTTDGHIHV
		LDSFRGTLLYTFNVKPTSSKSTLEASFSPEGMFVISGSG
		DGSVYAWSVRGGKEVASWLSTDTEPPVIKWAPGNLMFAT
		GSSELSFWIPDLSKLGAYVGRK
111	The amino acid sequence of SEQ ID	MAAFGAAPAGNHNPNKSSEVIQPPSDSVSSLCFSPRANH
	377. The conserved G-protein beta	LVATSWDNQVRCWELTKNGASVTSVPKASMSHDQPVLCS
	WD-40 repeat domains are	AWKDDGTTVFSGGCDKQAKMWSLMSGGQPVTVAMHDAPI
	underlined.	KEIAWIPEMNVLVTGSWDKTLKYWDTRQSNPVHTQQLPE
		RCYAMTVRYPLMVVGTADRNLIVFNLQNPQAEFKRFSSP
		LKYQTRCVAAFPDQQGFLVGSIEGRVGVHHLDDSQISKN
		FTFKCHRDNNDIYSVNSLNFHPVHHTFATAGSDGTFNFW
		DKDSKQRLKAMSRCSQPIPCSTFNNDGTIYAYSVCYDWS
		KGAENHNPATAKTYIFLHLPQESEVKAKPRVGTTNRK
112	The amino acid sequence of SEQ ID	MNCSISGEVPEEPVVSTKSGHVFERRLIERYVSDYGKCP
	378. The conserved G-protein beta	VSGEPLTMDDVLPVKMGKIVKPRPLQAASIPGLLSIFQN
	WD-40 repeat domains are	EWDSLMLSNFALEQQLHTARQELSHALYQHDAACRVIAR
	underlined.	LKKERDEARSLLALAERQIPMTASSDIAVNAPAMSNGRK
		ASLDEEPGYAGKKMRPGISASIIAEITDCNLALSQQRKK
		RQIPSTLAPVEDLERYTQLSSYPLHKTGKPGITSLDICH
		SKDIIATGGIDTSAVLFDRSSGQIMSTLSGHSKKVTSVN
		FDAQGDMVLTGSADKTVRIWQGSEDGSYNCRHILKDHTA
		EVQAITVHATNNYFATASLDNTWCFYEFSTGLCLTQVEG
		ASGSEGYTSAAFHPDGLILGTGTSNADVKIWDVKTQANV
		TTFSGHTGAITAISFSENGYFLATAAQDGVKLWDLRKLK
		NFRTFSAYDKDTGTNSVEFDHSGCYLGLAGSDIRVYQVA
		SVKSEWNCVKTFPDLSGTGKVTCVKFGPDSKYIAVGSMD
		HNLRIFGLPSEDGAMES
113	The amino acid sequence of SEQ ID	MAAPGVETLKKEIKELKEKIAQHRLDTDGEQPLPAAAKS
	379. The conserved G-protein beta	KSVPEVSAALKQRRILKGHFGKIYALHWSADSRHLVSAS
	domain is underlined and the WD-40	QDGKLIIWNGFTTNKVHAIPLRSSWVMTCAYSPSGNLVA
	repeat domains are in bold	CGGLDNLCSVYKVPHGGNKESSSAQKTYGELAQHEGYLS
		CCRFIKDNEIVTSSGDSTCILWDVETKTPKAIFNDHTGD
		VMSLAVFDDKGVFVSGSCDATAKLWDHRVHKQCVMTFQG
		HESDINSVQFFPDGDAFGTGSDDSSCRLFDIRAYQQINK
		YSSDKILCGITSVAFSKTGKSLFAGYDDYNTYVWDTLSG
		NQVEVLTGHENRVSCLGVSEDGKALATGSWDTLLKIWA
114	The amino acid sequence of SEQ ID	MGGVEDESEPASKRMKLSSRVLRGLANGSSRTEPAAGSS
	380. The conserved G-protein beta	LDLMARPLPIEGDEEVIGSKGVIKRVEFVRLIAKALYSL
	WD-40 repeat domains are	GYEKSGARLEEESGIPLQSSVVNLFMQQISDGLWDESVV
	underlined.	TLHKIGLSDENLVKSASFLILEQKFLELLDQEKAMDALK
		TLRTEITPLCIKNSRVRELSSCIISPSSCGLLNQNKRNS
		TRARSRSELLEELQKLLPPAVIIPERRLEHLVEQALVLQ
		TDACMLHNSIDMEMSLYTDHQCGKEHIPCRTLQILQSHN
		DEVWLVQFSHNGKYLASASNDRSAIIWEVDENGSVSLKH
		KLTGHQKPISSVCWSPDDRQLLTCGVGETVRRWDVSSGE
		CLRVYEKAGHGLISCAWFPDGKWICYGVSDRSICMCDLE
		GKEIECWKGQRTLSISDLEITSDGKQIISICRETAILLL
		DREAKYERMIEENQTITSFSLSKDNRYLLVNLLNQEIHL
		WDIKGDFRLVAKYKGLKRSRFVIRSCFGGLKQAFVASGS
		EDSQVYIWHKGSGELIEPLPGHSGAVNCVSWNPANHHML
		ASASDDRTIRIWGLNELNTRHKGARPNGVHYCNGNGTS
115	The amino acid sequence of SEQ ID	MTQLAETYACMPSTERGRGILIAGNPKPGSNSVLYTNGR
	381. The conserved G-protein beta	SVVILNLDNPLDISVYAEHAYPATVARFSPNGEWVASAD
	WD-40 repeat domains are	SSGAVRIWGAYNDHVLKKEFKVLSGRIDDLQWSPDGLRI
	underlined.	VASGDGKGKSLVRAFMWDSGTNVGEFDGHSRRVLSCAFK
		PTRPFRIVTCGEDFLVNFYEGPPFKFKLSRRDHSNFVNC
		LRFSPDGNRFISVSSDKKGIIYDGKTGEKIGELSSDGGH
		TGSIYAVSWSPDSKQVITVSADKSAKIWDISEDGSGNLR
		KTLTSSGSGGVDDMLVGCLWQNNHLVTVSLGGTISIYTA
		GDLDKAPVSFSGHMKNVSSLSVLKGDPKVILSSSYDGLI
		IKWIQGIGFSGRVQRKESTQIKCLAAVDEEIVTSGYDNK
		VCRVSGSGDAEFIDIGCQPKDLSLALQCPEFALVSTDTG
		VVLLRGAKIVSTINLGFAVTASTVAPDGTEAIIGAQDGK
		LRIYSISGDTLTEEAVLEKHRGAISVIHYSPDLSMFASG
		DLNREAVVWDRASREVRLKNILYHTARINCLAWSPDSST
		VATGSLDTCVIIYEVDKPASNRLTIKGAHLGGVYGLAFT
		DDFSVVSSGEDACIRVWKINRQ
116	The amino acid sequence of SEQ ID	MKVKVISRSTDEFTRERSQDLQRVFRNFDPNLRTQEKAV
	382. The conserved G-protein beta	EYVRALNAAKLDKVFARPFVGAMDGHVDSVSCMAKNPNY
	WD-40 repeat domains are	LKGIFSGSMDGDIRLWDIASRRTVCQFPGHQGPVRGLAA
	underlined and the SOF1 protein	STDGQILVSCGIDSTVRLWNVPVATLGESDGTHENLAKP
	domain is in bold.	LAVYVWKNAFWAVDHQWDGELFATAGAQVDIWNQNRSQP
		ISSFEWGTDTVISVRFNPGEPNVLATSGSDRSITLYDLR
		MSSPTRKVIMRTKTNAISWNPMEPMNFTAANEDCNCYSY
		DARKLEEAKCVHKDHVSAVMDIDYSPTGREFVTGSYDRT
		VRIFQYNGGHSREVYHTKRMQRVFCVKFSCDASYVISGS
		DDTNLRLWKAKASEQLGVVLPRERRKHEYHEAVKSRYKH
		LPEVKRIVRHRHLPKPIYKAGILRRTVNEADRRKEERRK
		AHSAPGSSSAEPLRKRRIIKEIE
117	The amino acid sequence of SEQ ID	MVRSIKNPKKAKRKNKGSKNGDGSSSSSSIPSMPTKVWQ
	383. The conserved G-protein beta	PGVDKLEEGEELQCDPSAYNSLHAFHIGWPCLSFDIVRD
	WD-40 repeat domains are	TLGLVRTEFPHQVYFVAGTQAEKPTWNSIGIFKVSNITG
	underlined.	KRRELVPSKPTDDADEESDSSDSDEDSDDEVGGSGTPIL
		QLRKVGHEGCVNRIRAMNQNPHICASWGDSGHVQIWDFS
		SHLNALAESEADVSQGASSVFNQAPLVKFGGHKDEGYAL
		DWSPLVPGRLVSGDCKNSIHLWEPTSGSTWNVDSTPFIG
		HAASVEDLQWSPTEENVFASCSVDGTIAIWDTRLGKTPA
		ASFKAHDADVNVISWNRLATCMLASGCDDGTFSIHDLRL
		LKEGDSVVAHFEYHKHPVTSIEWSPHEASTLAVSSADCQ
		LTIWDLSLEKDEEEEAEFKAKTKEQVNAPEDLPPQLLFV
		HQGQKDLKELHWHAQIPGMIVSTAADGFNILMPSNIQST
		LPSDGA
118	The amino acid sequence of SEQ ID	MERYKVIKELGDGTYGSVWKALNQQTHEIVAIKKMKRKY
	384. The conserved eukaryotic	YIWEECINLREVKSLRKLNHPNIIKLKEVIRENNELFFI
	protein kinase domain is	FEYMECNLYQIMKERSTPFSETAIIKFCYQILQGLSYMH
	underlined and the protein kinases	RNGYFHRDLKPENLLVTSDLIKIADFGLAREVLTSPPYT
	ATP-binding region and	DYVSTRWYRAPEVLLQSPTYTTAIDMWAVGAILAELFTL
	serine/threonine protein kinases	HPLFPGESELDEIYKICGVLGTPDYETWPDGMQLAAFRN
	active-site signatures are in	FIFPQFLPVNLSVLIPHASPEAIDLITRLCSWDPQKRPT
	bold.	AEQALHHPFFRIGMSIPLSLGGHFQDNTCAAEVDTKFHS
		KKACKAWNGEKESSLECFLGLSLGLKPSLGHLGAMGSQG
		VGAVKQEVGSSPGCQSNPKQSLFQVLNSRAILPLFSSSP
		NLNVVPVKSSLPSAYTVNSQVMWPTIAGPPAAAVTVSTL
		QPSILGDFKIFGKSMGLASQYAGKEASPFS
119	The amino acid sequence of SEQ ID	MGEMGRGINNSSNNNNSNRPAWLQHYDLVGKIGEGTYGL
	385. The conserved eukaryotic	VFLARSKLPNNRGLRIAIKKFKQSKDGDGVSPTAIREIM
	protein kinase domain is	LLREFSHENVVKLVNVHINHVDMSLYLAFDYAEHDLYEI
	underlined and the protein kinases	IRHHREKLNHHNINQYTVKSLLWQLLNGLNYLHSNWIVH
	ATP-binding region and	RDLKPSNILVMGEGEEHGVVKIADFGLARIYQAPLKPLS
	serine/threonine protein kinases	DNGVVVTIWYRAPELLLGAKHYTSAVDMWAVGCIFAELI
	active-site signatures are boxed	TLKPLFQGVEVKASPNPFQLDQLDKIFKVLGHPTIEKWP
	in bold.	TLMNLPHWSKNLQQIQQHKYDNAGLHIGPIPAKSPAYDL
		LSKMLEYDPRKRITAAQALEHEYFRIDPQPGRNALVPSQ
		PGEKAINYPPRLVDANTDFDGTIAPQPSQVSSGNAPSGS
		IASAAVPAVRPLPQQMQLMGMQRMQNPGMAAFNLGAQAS
		MSGLNHNNIALQRGSSQQQAHQQVRRKEPNSGFPNTGYP
		PPPKSRRL
120	The amino acid sequence of SEQ ID	MDKYEKLEKVGEGTYGKVYKARDKMTGQLVALKKTRLEM
	386. The conserved protein kinase	DEEGVPPSSLREISLLQMLSQSIYVVRLLCVEHVTKKGK
	family domain is underlined. The	PLLYLVFEYLDTDLKKFIDYRRSVNAGPLPQNVIQSFMY
	protein kinases ATP-binding region	QLLKGVAHCHSHGVLHRDLKPQNLLVDKSKGLLKVGDLG
	is in bold and the	LGRAFTVPLKCYTHEVVTLWYRAPEVLLGSTHYSTPVDI
	serine/threonine protein kinases	WSVGCIFAEMVRRQPLFPGDCEIQQLLHIFTLLGTPTEE
	active-site signature is in	MWPGVKRLRDWHEYPQWKPENLARAVPNLSPTGLDLISK
	bold/italics.	MLQCDPAKRISAKAAMNHPYFDDLDKSQF
121	The amino acid sequence of SEQ ID	MDGYEKMDKVGEGTYGKVYMARDKKTGQLVALKKTRLEN
	387. The conserved protein kinase	DGEGIPPTALREISLLQMLSQDIYIVRLLDVKHTENKLG
	family domain is underlined. The	KPLLYLVFEYMESDLKKYIDSYRRSHTKMPPSMIKSFMY
	protein kinases ATP-binding region	QLCRGVAYCHSRG DKEKGVLKIADLG
	is in bold and the	LSRAFTVPVKKYTHEIVTLWYRAPEVLLGATHYSLPVDI
	serine/threonine protein kinases	WSVGCIFAEMSRMQALFTGDSEVQQLMNIFRFLGTPNEE
	active-site signature is in	VWPGVTKLKDWHIYPEWKPQDISHAVPDLEPSGLDLLSQ
	bold/italics.	MLVYEPSKRISAKKALEHPYFDDLDKSQF
122	The amino acid sequence of SEQ ID	MDAYEKLEKVGEGTYGKVYKAKDKNTGQLVALKKTRLES
	388. The conserved eukaryotic	DDEGIPPTALREISLLQMLSQDIHIVRLLDVEHTENKNG
	protein kinase domain is	KPLLYLVFEYMDSDLKKYIDGYRRSHTKVPPNIIKSFMY
	underlined and the protein kinases	QLCQGVAYCHSRGVMHRDLKPHNLLVDKQRGVVKIADLG
	ATP-binding region and	LGRAFTIPIKKYTHEIVTLWYRAPEVLLGATHYSTPVDI
	serine/threonine protein kinases	WSVGCIFAEMVRLQALFIGDSEVQQLFKIFSFLGTPNEE
	active-site signatures are in	IWPGVTKFRDWHIYPQWKPQDISSAVPDLEPSGVDLLSK
	bold.	MLVYEPSKRISAKKALEHPYFDDLDKSQF
123	The amino acid sequence of SEQ ID	MDSYEKLEKVGEGTYGKVYKAKDKKTGKLVALKKTRLEN
	389. The conserved protein kinase	DGEGIPPTALREISLLQMLSQDMNIVRLLDVEHTENKNG
	family domain is underlined. The	KPLLYLVFEYMDSDLKKYVDGYRRSHTKMPPKIIKSFMY
	protein kinases ATP-binding region	QLCQGVAYCHSRG DKQRGVLKIADLG
	is in bold and the	LGRAFTVPIKKYTHEIVTLWYRAPEVLLGATHYSTPVDI
	serine/threonine protein kinases	WSVGCIFAEMSRMHALFCGDSEVQQLMSIFKFLGTPNEG
	active-site signature is in	VWPGVTKLKDWHIYPEWRPQDLSRAVPDLEPSGVDLLTK
	bold/italics.	MLVYEPSKRISAKKALQHPYFDDLDKSQF
124	The amino acid sequence of SEQ ID	MEKYEKLEKVGEGTYGKVYKGRDKRTGRLVALKKTPFHQ
	390. The conserved eukaryotic	EEGIPPTAIREISLLKSLSQCIYIVKLLDVKASFNGKGK
	protein kinase domain is	HVLFMVFEYADSDLKKHIDAHRQCNTKLSPRSIQSYMFQ
	underlined and the protein kinases	LCKGIAYCHSHGVLHRDLKPQNILVDQKIGLLKIADLGL
	ATP-binding region and	GRACTVPIKSYTFEVVTLWYRAPEVLLGAKRYSMALDIW
	serine/threonine protein kinases	SLGCIFAELCNLQALFAGDSQIQQLINIFRLLGTPNEQL
	active-site signatures are in	WPGVTQLSDWHEFPQWRPQDLSKVVFNLDPNGVDLLSKM
	bold.	LQYDPAKRISAKEALDHPYFDSLDKSQF
125	The amino acid sequence of SEQ ID	MGCVCGKPSARAADYVESPAEKGASSNSRSSSMASRRLV
	391. The conserved eukaryotic	APAVMDQGIDAENGHEGDYRTKLRGKQSNGADPVSLLSD
	protein kinase domain is	DAEKQRHSRHHQHQQHHPIRPHHLRPQGEFVPNANSNPR
	underlined and the	FGNPPRHIEGEQVAAGWPAWLTAVAGEAIKGWIPRRADS
	serine/threonine protein kinases	FEKLDKIGQGTYSNVYKARDLDTGKIVALKKVRFDNLEP
	active-site signatures are in	ESVRFMAREIQVLRRLDHPNVVKLEGLVTSRMSCSLYLV
	bold.	FEYMDHDLAGLAACPGIKFTEPQVKCYMQQLLRGLDHCH
		SRGVLHRDIKGSNLLIDNGGILKIADFGLATFFHPDQRQ
		PLTSRVVTLWYRPPELLLGATEYGVAVDLWSTGCILAEL
		LAGKPIMPGRTEVEQLHKIFKLCGSPSEDYWKKSKLPHA
		TIFKPQQPYKRCVAETFKDFPPSALALMEVLLAIEPADR
		GTATSALKSDFFTTKPLACDPSSLPKYPPSKEFDAKIRD
		EEARRQRAAGGRGRDAARRPSRESRAIPAPEANAELAIS
		IQKRRLSSQGPSKSKSEKFNPQQEDGAVGFPIEPPRPMH
		IGIDAGATSRMYSQQFGPSHSGPLSNQISSSIWGKNQKE
		DEIQMAPGRPSRSSKATISDFRKPGACAPQPGADLSHLS
		SLVATARSNAGIDTHKDRSGMWQHNRIDAIDGVHNNGKH
		EFLEVPEHPNRQDWTRFQQPESFKGLDNYHLQDLPATHH
		RKDERVASKEATMNWQGYGGQGGDKIHYSGPLLPPSGNI
		DEILKEHERHIQHAVRRARQDKGRPQRSNLSQNERKAFE
		HRSFVSGVNGNAGYSDLVNELPISVGSNRLKVSKTRGTE
		EIVELRELEREPLSSVMEKYEREHEM
126	The amino acid sequence of SEQ ID	MGCVCAKQSDILGEPESPKVKGSNLASSRWSVSSETKQL
	392. The conserved eukaryotic	PQHSDSGILHHQHYYHPRDESDEAKLKESNYGGSKRRTR
	protein kinase domain is	QGRDPADLDMGIFVRTPSSQSEAELVAAGWPAWMAAFAG
	underlined and serine/threonine	EAIHGWIPRRAESFEKLYKIGQGTYSNVYKARDLDNGKI
	protein kinases active-site	VALKKVRFDSLDAESVRFMAREILVLRKLDHPNIVKLEG
	signatures is in bold.	LVTSEVSSSLYLVFEYMEHDLAGLAACPGIKFTEPQVKC
		YMQQLLQGLDHCHRHGVLHRDIKGSNLLIDNGGILKIAD
		FGLATFFYPDQKQLLTSRVVTLWYRPPELLLGATDYGVA
		VDIWSAGCILAELLAGKPILPGRTEVEQLHKIFKLCGSP
		SEDYWKESKLPHATIFKPQHPYKSCIAEAFKDFSPSALA
		LLETLLAIEPGHRGEASGALKSEFFTTEPLSCDPSSLPK
		YPPSKEFDAKLRAQETRRQRDVGVRGHGSEAARRTSRLS
		RAGPTPNEGAELTALTQKQHSTSHATSNIGSEKPSTKKE
		DYTAGLHIDPPRPVNHSYETTGVSRAYDAIRGVAYSGPL
		SQTHVSGSTSGKKPKRDHVKGLSGQSSLQPSKPFIVSDS
		RSERIYEKSHVTDLSNHSRLAVGRNRDTTDPHKSLSTLM
		QQIQDGTLDGIDIGTHEYARAPVSSTKQKSAQLQRPSAL
		KYVDNVQLQNTRVGSRQSDERPANKESDMVSHRQGQRIH
		CSGPLLHPSANIEDLLQKHEQQIQQAVRRAHHGKREALS
		NKSSLPGKKPVDHRAWVSSGKGNKESPYFKGKGNKELSD
		LKGGPTAKVTNFRQKVM
127	The amino acid sequence of SEQ ID	MAVANPGQLNLQEAPSWGSRSVNCFEKLEQIGEGTYGQV
	393. The conserved protein kinase	YMAKEIETGEIVALKKIRMDNEREGFPITAIREIKLLKK
	family domain is underlined. The	LQHENVIKLKEIVTSPGPEKDEQGKSDGNKYNGSIYMVF
	protein kinases ATP-binding region	EYMDHDLTGLAERPGMRFSVPQIKCYMKQLLIGLHYCHI
	is in bold and the	NQ DNNGILKLADFGLARSFCSDQNGN
	serine/threonine protein kinases	LTNRVITLWYRPPELLLGSTKYGPAVDMWSVGCIFAELL
	active-site signature is in	YGKPILPGKNEPEQLTKIFELCGSPDESNWPGVSKLPWY
	bold/italics.	SNFKPQRQMKRRVRESFKNFDRHALDLVEKMLTLDPSQR
		ISAKDALDAEYFWTDPVPCAPSSLPRYEPSHDFQTKRKR
		QQQRQHDEMTKRQKISQHPPQQHVRLPPIQNAGQGHLPL
		RPGPNPTMHNPPPQFPVGPSHYTGGPRGAGGQNRHPQNI
		RPLHAAQGGGYNANRGYGGPPQQQGGGYPPHGMGNQGPR
		GGQFGGRGAGYSQGGPYGGPVGGRGPNVGGGNRGPQFWS
		EQ
128	The amino acid sequence of SEQ ID	MQNMEDNVQSSWSLHGNKEICARYEILERVGSGTYSDVY
	394. The conserved eukaryotic	RGRRKADGLIVALKEVHDYQSSWREIEALQRLCGCPNVV
	protein kinase domain is	RLYEWFWRENEDAVLVLEFLPSDLYSVIKSGKNKGENGI
	underlined and the	PEAEVKAWMIQILQGLADCHANWVIHRDLKPSNLLISAD
	serine/threonine protein kinases	GILKLADFGQARILEEPEAIYEVEYELPQEDIVADAPGE
	active-site signature is in bold.	RLMEEDDSVKGVRNEGEEDSSTAVETNFGDMAETANLDL
		SWKNEGDMVMQGFTSGVGTRWYRAPELLYGATIYGKEID
		LWSLGCILGELLILEPLFSGTSDIDQLSRLVKVLGTPTE
		ENWPGCSNLPDYRKLCFPGDGSPVGLKNHVPSCSDSVFS
		ILERLVCYDPAARLNAKEVLENKYFVEDPYPVLTHELRV
		PSPLREENNFSEDWAKWKDMEADSDLENIDEFNVVHSSD
		GFCIKFS
129	The amino acid sequence of SEQ ID	MDLNQYPEDLNPELPEGTDNVDNPDNNKGSPVPSPHPPL
	395. The conserved eukaryotic	KPLDPSERYRKGITLGQGTYGIVYKAFDTVTNKTVAVKK
	protein kinase domain is	IHLGKAKEGVNVTALREIKLLKELSHPNIIQLIDAYPHK
	underlined and the protein kinases	QNLHIVFEFMETDLEAVIKDRNLVFSPADIKSYLQMTLK
	ATP-binding region and	GLAVCHKKWVLHRDMKPNNLLIAADGQLKLGDFGLARLF
	serine/threonine protein kinases	GSPDRKFTHQVFAVWYRAPELLFGAKQYGPAVDIWATGC
	active-site signatures are in	IFAELLLRKPFLQGVSDLDQIGKIFAAFGTPRQSQWPDV
	bold.	ASLPDFVEFQFVPAPSLRSLFPMASEDALDLLSKMFTLD
		PKNRITAQQALEHRYFSSVPAPTRPDLLPKPSKVDSSRP
		PKHASPDGPVVLSPSKARRVMLFPNNLAGILPKQVSQST
		TGGTPIEFDMPTQKLREVCPRSRITESGKKHLKRKTMDM
		SAALDECAREQEGQEGKTILDPDHQRSAKKEKHM
130	The amino acid sequence of SEQ ID	MAGGQENCVRITRARAACVSKASAPVIQSQVDEKKSRKR
	396. The conserved cyclin N- and	APKRAAVDDLAANASGSQPKRRAVLGDVTNLHAAATDCL
	C-terminal family domains are	STAEDQVDAPNPSIKGRARNKKKEARTSTKVVKDEIHPE
	underlined.	SNPLADHSSNLSECQKPPAAKLAEQRSLRGVPSKAKQGG
		SSNSQSCSKHTDIDKDHTDPQMCTTYVEDIYEYLRNAEL
		KNRPSANFMETAQNDITPNMRAILVDWLVEVSEEYKLVP
		DTLYLTVSYIDRYLSANPTSRHKLQLLGVSCMLIASKYE
		EVCPPHVEEFCYITDNTYTRDEMLSMERKILIFLNFEMT
		KPTTKSFLRRFVRASQAGNKAPSLHMEFLANYLAELTLM
		ECSFLQYLPSLIAASTVFLSRLTLDFLTNPWNPTLAHYT
		GYKASQLKDCVMAIYNVQMNRKGSTLVAIREKYQQHKFK
		CVASLPPPPFIAERFFDTPN
131	The amino acid sequence of SEQ ID	MTGTQASNVRITRARAAKSTLNNALPPLPPAQGKPRGKR
	397. The conserved cyclin and	AATESNISGFSVAAEPLKRRAVLSDVSNICKEAAAVDCL
	cyclin C-terminal domains are	KKPKAVKVVSQNANAKGRGRGIPRNNKKITQEAEIKKET
	underlined and the cyclins	SPAICNVDDASAGNAIGDDKQNNNVNPLKEVQDNPKELN
	signature is in bold.	PIAEQISVHPHCKQSVEKPNEKEIVVSDNKAAIASLKQQ
		STLQSLRIPKQPKYSLKQGNPVPLANLHEDVGRSSCSDF
		IDIDSEYKDPQMCTAYVTDIYANMRVVELKRRPLPNFME
		TTQRDINANMRSVLIDWLVEVSEEYKLVPDTLYLTVSYI
		DRFLSANVVNRQRLQLLGVSCMLVASKYEEICAPPVEEF
		CYITDNTYKKEEVLEMEISVLNRLQYDLTTPTTKTFLRR
		FIRAAQASCKVSSLHLEFMGNYLAELTLVEYDFLKYLPS
		LIAAAAVFVARMTLDPMVHPWNSTLQHYTGYKVSDMRDC
		ICAIHDLQLNRKGCTLAAIREKYNQPKFKCVANLFPPPI
		ISPQFLIDNEV
132	The amino acid sequence of SEQ ID	MAAPNQNALLINNNNRRPLVDIGNLVGALNAQCNISKNG
	398. The conserved cyclin and	ARKRAFGDIGNLVEDLDAKCTISKYWVRKRPRTNFGVNA
	cyclin C-terminal domains are	NKGASSSTQGQGIVVRGEQKAWDRIVWGNKQSCAIKMNA
	underlined and the cyclins	QHVTATQRGTAISISDIIDSSVQDGGIKAPSQLKARKQT
	signature is in bold.	VRTVTATLTARSEDSLRDVLEVPPGIDDGDRDNPLAVVE
		YVEDIYHFYRKIEVRSCVPPDYMTRQLEIKDSMRGVIID
		WLIEVHRTFLLMPETLYLTVNIIDRYLSIQSVTRNELQL
		MGITAMFIASKYEEISPPKINDLVYITKDAYTSKQIVNM
		EHTILNRLKFKLTVPTPYVFLVRFLKAAGPDKVMKNLAF
		FLVDLCLLHYKMIKYSPSMLAAAAVYTAQCTLKKHPYWN
		KTLILHIGYSEAHLRECAHLMADLHLKAEGSNLKSVYKK
		YSYPIFGSVAFLSPAKIPAGTVAAPAIDKCAHQIYLRNLR
133	The amino acid sequence of SEQ ID	MFPNKQTQGLVQNKKMASKAAQPKAMVPPQRVPPAANNR
	399. The conserved cyclin N- and	RALGDIGNIVADVGGKCNVTKDGVNGKPLAQVSRPITRS
	C-terminal family domains are	FGAQLLAQAAANKGISAANNQTQVPVVIPKADVRGNKQR
	underlined.	RTSKSKDIPPTTVVTNESDDCVIIEQAQRIKPTCNHNVG
		AVGNKEKPQLLTAKPKSLTASLTSRSAVALRGFRFDDEM
		TEAEEDPLPNIDVGDRDNQLAVVEYVEDIYKFYRRTEQM
		SCVPDYMPRQQEINPKMRAVLINWLIEVHYRFGLMPETL
		YLTTNLIDRYLATQLVSRSNYQLVGATAMLLASKYEEIW
		APEMNDFLDILENKFERKHVLVMEKAMLNKLKFHLTVPT
		PYVFLVRFLKAAASDEEMENLVFFLMELSLMQYVMIKFP
		PSMLAAAAVYTAQITLKKTTVWNDVLKRHTGYSEIDLKE
		CTRLMVAFHQSSEESKLNVVFKKYSMPEYDSVALIKPAK
		LPA
134	The amino acid sequence of SEQ ID	MAPSFDCVANAYIESCEDQEKLRQNAQILAQSGENDVDE
	400. The conserved cyclin and	PVSMLVQRETHYMLPEDYLQRLRNRTLDVNVRREAVGWI
	cyclin C-terminal domains are	LKVHSFYNFSAPTAYLAVNYLDRFLSRHRMPQGVKAWMI
	underlined	QLMAVACLSLAAKMEETQVPLPSDLQREDARFIFDARTI
		QRMELLILSTLQWGMRSITPFSFIDYFAYRAVQGHGHGH
		DATPKAVMSRAIELILSTTEEIDFMEYRPSAIAAAALLC
		AAEEVVPLQAVHYKRALSSSITDVDKDKMFGCYNLIQET
		IIEGGCYWTPMSLQSTEKTPVGVLDAAACLSNTPTSSYS
		VKPYASVTAAKRRKLNEICSALLVSQAHPC
135	The amino acid sequence of SEQ ID	MAANFWTSSHCKELLDAEKVGIVHPLDKDQGLTQEDVKI
	401. The conserved cyclin and	IKINMSNCIRTLAQYVKLRQRVVATAITYCRRVYTRKSF
	cyclin C-terminal domains are	TEYDPQLVAPTCLYLASKAEESTVQAKLVIFYMKKYSKH
	underlined.	RYEIKDMLEMEMKLLEALDYYLVIYHPYRPLIQFLQDAG
		LNDLKVTAWALVNDTYRTDLILTYPPYMIALACIYFACI
		MEEKDAQAWFEELRVDMNEIKNISMEIVDYYDNYRVIPD
		EKMNSALNKLPHRF
136	The amino acid sequence of SEQ ID	MAPALSSSYECLSHLLCAEDASNVVGCWDEDESKIFCEE
	402. The conserved cyclin domain	EEGFGIQHFPDFPVPDDDEIRVLVRKESQYMPGKSYVQS
	is underlined.	YQNLGLDFTARQNAIGWILKVHGSYNFGPLTAYLSINYL
		DRFLSRNPLPKAKVWMLQLLSVACLSLAAKMEETQVPLL
		LDLQAEEPDFLFEPRTIQRMELLVLSTLEWRMLSVTPFS
		FVDYFLQGGGGRKPPPRAMVARANELIFNTHTVLDFLEH
		RPSAIAAAAVICAAEEVLPLEAAQYKETILSCSLVDKEW
		VFGSYNLIQEVLIEKFSTPKKAKSASSSIPQSPVGVLDA
		FCLSNNSNNTSLEASLSVNLYASVAAKRRKLNDYCNTWR
		MFQHSTC
137	The amino acid sequence of SEQ ID	MAPNCIDCAPSDLFCAEDAFGVVEWGDAETGSLYGDEDQ
	403. The conserved cyclin domain	LHYNLDICDQHDEHLWDDGELVAFAEKETLYVPNPVEKN
	is underlined.	SAEAKARQDAVDWILKVHAHYGFGPVTAVLSINYLDRFL
		SANQLQQDKPWMTQLAAVACLSLAAKMDETEVPLLLDFQ
		VEEAKYIFESRTIQRMELLVLSTLEWRMSPVTPLSYIDH
		ASRMIGLENHHCWIFTMRCKEILLNTLRDAKFLGLLPSV
		VAAAIMLHVIKETELVNPCEYENRLLSAMKVNKDMCERC
		IGLLIAPESSSLGSFSLGLKRKSSTINIPVPGSPDGVLD
		ATFSCSSSSCGSGQSTPGSYDSNNSSILCISPAVIKKRK
		LNYEFCSDLHCLED
138	The amino acid sequence of SEQ ID	MPQIQYSEKYTDDTYEYRHVVLPPETAKLLPKNRLLNEN
	404. The conserved cyclin-	EWRAIGVQQSRGWVHYAIHRPEPHIMLFRRPLNYQQNQQ
	dependent kinases regulatory	QQAGAQSQPMGLKAQ
	subunit domain is underlined and
	the cyclin-dependent kinases
	regulatory subunits signature 1 is
	in bold.
139	The amino acid sequence of SEQ ID	MDQIEYSEKYYDDTYEYRHVELPPDVARLLPKNRLLTEN
	405. The conserved cyclin-	EWRGIGVQQSRGWVHYAIHCSEPHIMLFRRPLNYEQNHQ
	dependent kinases regulatory	HPEPHIMLFRRPLNCQPNHQPQAHHPT
	subunit domain is underlined and
	the cyclin-dependent kinases
	regulatory subunits signature 1 is
	in bold.
140	The amino acid sequence of SEQ ID	MDQIEYSEKYYDDTYEYRHVELPPDVARLLPKNRLLTEN
	406. The conserved cyclin-	EWRGIGVQQSRGWVHYAIHCSEPHIMLFRRPLNYEQNHQ
	dependent kinases regulatory	HPEPHIMLFRRPLNCQPNHQPQAHHPT
	subunit domain is underlined and
	the cyclin-dependent kinases
	regulatory subunits signature 1 is
	in bold.
141	The amino acid sequence of SEQ ID	MPQIQYSEKYYDDTYEYRHVVLPPDVARLLPKNRLLNEN
	407. The conserved cyclin-	EWRGIGVQQSRGWVHYAIHRPEPHIMLFRRHLNYQQNQQ
	dependent kinases regulatory	QQAQQQPAQAMGLQA
	subunit domain is underlined and
	the cyclin-dependent kinases
	regulatory subunits signature 1 is
	in bold.
142	The amino acid sequence of SEQ ID	MALVETEPVTLIHPEEPKKFKKKPTPGRGGVISHGLTEE
	408. The conserved GCN5-related N-	EARVKAIAEIVGAMVEGCRKGEDVDLNALKAAACRRYGL
	acetyltransferase family domain is	SRAPKLVEMIAALPDGERAAVLPKLKAKPVRTASGIAVV
	underlined and the radical SAM	AVMSKPHRCPHIATTGNICVYCPGGPDSDFEYSTQSYTG
	family domain is in bold.	YEPTSMRAIRARYNPYVQTRSRIDQLKRLGHTVDKVEFI
		LMGGTFMSLPADYRDYFIRNLHDALSGHTSSNVEEAVCY
		SEHSATKCIGLTIETRPDYCLGPHLRQMLSYGCTRLEIG
		VQSTYEDVARDTNRGHTVAAVADCFCLAKDAGFKVVAHM
		MPDLPNVGVERDMESFREFFENPAFRADGLKIYPTLVIR
		GTGLYELWKTGRYRNYPPEQLVDIIARVLALVPPWTRVY
		RVQRDIPMPLVTSGVEKGNLRELALARMDDLGLKCRDVR
		TREAGIQDIHHKIRPEVVELVRRDYCANEGWETFLSYED
		TRQDILVGLLRLRKCGHNTTCPELKGRCSIVRELHVYGT
		AVPVHGRDADKLQHQGYGTLLMEQAERIAWKEHRSIKIA
		VISGVGTRHYYRKLGYELEGPYMMKYLN
143	The amino acid sequence of SEQ ID	MLGFRDLYTSICEHLQRASGRLPIIAAATSLISTPEIAA
	409. The conserved chromo domain	VEKENKAPNSVDKMGMGSADESGRFSTSNGQFMNMNNGV
	is underlined and the MOZ/SAS-like	VKEEWKGGVPVVPSAPTTVPVITNVKLETPSSPDHDMAR
	protein domain is in bold.	KRKLGFLPLEVGTRVLCKWRDGKFHPVKIIERRKLPNGA
		TNDYEYYVHYTEFNRRLDEWVKLEQLELDSVETDADEKV
		DDKAGSLKMTRHQKRKIDETHVEGNEELDAASLREHEEF
		TKVKNITKIELGRYEIETWYFSPFPSEYNNCEKLYFCEF
		CLNFMKRKEQLQRHMRKCDLKHPPGDEIYRSGTLSMFEV
		DGKKNKVYAQNLCYLAKLFLDHKTLYYDVDLFLFYILCE
		CDERGCHMVGYFSKEKHSEESYNLACILTLPPYQRKGYG
		KFLISFSYELSKKEGKVGTPERPLSDLGLLSYRGYWTRV
		LLDILKKHKSNISIKELSDMTAIKADDVLSTLQGLDLIQ
		YRKGQHAICADPKVLDRHLKAVGRGGLEVDVCKLIWTPY
		KEQ
144	The amino acid sequence of SEQ ID	MGSLDESTCSEEIRDEGKDSIRTKFKVESTVNNAQNGGN
	410. The conserved MOZ/SAS-like	DNSKKKRAAGLPLEVGIRLLCKWRDSKLHPVKIIERRKL
	protein domain is underlined.	PNGFPQDYEYYVHYTEFNRRLDEWVKLEQFELDSVETDA
		DEKIEDKGGSLKMTRHQKRKIDEIHVEEGQGHEDFDPAS
		LREHEEFTKVKNIAKVELGRYEIETWYFSPFPPEYSHCE
		KLFFCEFCLNFMKRKEQLQRHMRKCDLKHPPGDEIYRNG
		TLSMFEVDGKKNKIYGQNLCYLAKLFLDHKTLYYDVDLF
		LFYVLCECDDRGCHVVGYFSKEKHSDEAYNLACILTLPP
		YQRKGYGKFLIAFSYELSKKEGKVGTPERPLSDLGLLSY
		RGYWTRILLDILKKQRGNISIKELSDMTAIKVEDVISTL
		QVLDLIQYRKGQHVICADPKVLDRHLKAAGIAGLEVDVS
		KLIWTPYKEQCG
145	The amino acid sequence of SEQ ID	MASAPMVGCDDSRDKHRWVESKVYMRKGHGKGSKGNAGF
	411. The conserved bromo family	NAQNSTAQVRRENDNMGNSIADNGKSEAASEGLSSLSRK
	domain is underlined.	QITVNQDHPPNETSSMPAVGGLQNIDTHVTFKLEGCSKQ
		EIWELRKKLTNELEQVRGTFKKLEARELQLRGYSVSAGV
		NTSYSASQFSGNDMRNNGGKEVTSEVASGGAITPKQAQR
		ESNPPRQLSISLMENNQAASDMGEKGKRTPKANQYYRNS
		EFVLGKDKFPPAESKKSKSTGNKKISQSKVFSKETMQVG
		KEFMPQKSVNEVFKQCSLLLTKLMKHKYGWVFNLPVDAQ
		ALGLHDYHTIIKRPMDLGTVKSKLEKNLYNSPASFAEDV
		KLTFSNAMTYNPKGHEVHTMAEQLLQLFEERWKTIYEEH
		LDGKMRFGSGQGLGASSSTKKLPFQDSKKNIKKSEPAGG
		PSPPKPKSTNHHASRTPSAKKPKAKDPHKRDMTYEEKQK
		LSTNLQNLPQERLELIVQIIKKRNPSLCQHDEEIEVDID
		SFDTETLWELDRFVTNYKKSLSKNKKKALLADQAKRASE
		HGSARNKHPMIGRELPMNNKKGEQGEKVVEIDHMPPVNP
		PVVEVEKDGVYAKRSSSSSSSSSDSGSSSSDSDSGSSSG
		SESDAYAATSPPAGSNTSARG
146	The amino acid sequence of SEQ ID	MEGHSGALGFGQGFSRSSQSPNLSPSPSHSASASVTSSG
	412. The conserved GCN5-related N-	QKRKRNEVEHAGVASNSTGMFAVPPSHIYSHLHPMSMSM
	acetyltransferase family domain is	PMPMHNSHPSSLSESRDGALTSNDDDDNLTGGNQSQLDS
	underlined and the bromodomain is	MSAGNTDGREDFDDEDDDDDDEEDDDEVEGDEEDQDHDP
	in bold.	DADDDSDDGHDSMRTFTAARLDNGAPNSRNLKPKADAAG
		VAIAPTVKTEPILDTVKEEKVSGNNNNNSVSANNAQVAP
		SGSAVLLSAVKEEANKPTSTDHIQTSGAYCAREESLKRE
		EDADRLKFVCFGNDGIDQHMIWLIGLKNIFARQLPNMPK
		EYIVRLVMDRSHKSVMIIKQNQVVGGITYRPYLSQKFGE
		IAFCAITADEQVKGYGTRLMNHLKQHARDVDGLTHFLTY
		ADNNAVGYFIKQDFTKEIKLEKERWHGYIKDYDGGILME
		CKIDPKLPYTDLPAMIRWQRQTIDEKIRELSNCHIVYSG
		IDIQKKEAGIPRKPIKVEDIPGLKEAGWTTDQWGHSRFR
		LLNSPSEGLPNRQVLHAFMRSLHKAMVEHADAWPFKEPV
		DPRDVPDYYDIIKDPMDVKRMFTNARTYNTHETIYYKCA
		NR
147	The amino acid sequence of SEQ ID	MEESGNSLTSGPDGSKRRVSYFYDSDIGNYYYSQGHPMK
	413. The conserved histone	PHRIRMAHSLIVHYALDEKMEVCRPNLLQSRELRVFHAD
	deacetylase family domain is	DYISFLQSVTPETQHEQLRQLKRFNVGEDCPVFDGLYNF
	underlined.	CQTYAGGSVGAAIKLNNKEADIAINWSGGLHHAKKCEAS
		GFCYVNDIVLAILELLKVHQRVLYIDIDIHHGDGVEEAF
		YSTDRVMSVSFHKFGDYFPGTGHLKDVGYGKGKYYSLNV
		PLNDGIDDESYKNLFRPIIQKVMEIYQPEAVVLQCGADS
		LSGDRLGCFNLSVKGHADCVRFLRSFNVPLVLVGGGGYT
		IRNVARCWCYETAVAVGVEPQDKLPYNEYYEYFGPDYTL
		HVAPSNMENQNSAKELAKIRNTLLEQLKRIQHVPSVPFQ
		ERPPDTKFPEEDEEDYEKRPKGHKWGGEYFGSESDEEQK
		PQNRDIDISDKPGIRRQSPPNVEAAKKIKVEEEDGDIGI
		VNENDGAKWPLGEAG
148	The amino acid sequence of SEQ ID	MEESGNSLTSGPDGSKRRVSYFYDSDIGNYYYSQGHPMK
	414. The conserve histone	PHRIRMAHSLIVHYALDEKMEVCRPNLLQSRELRVFHAD
	deacetylase domain is underlined.	DYISFLQSVTPETQHEQLRQLKRFNVGEDCPVFDGLYNF
		CQTYAGGSVGAAIKLNNKEADIAINWSGGLHHAKKCEAS
		GFCYVNDIVLAILELLKVHQRVYIDIDIHHGDGVEEAF
		YSTDRVMSVSFHKFGDYFPGTGHLKDVGYGKGKYYSLNV
		PLNDGIDDESYKNLFRPIIQKVMEIYQPEAVVLQCGADS
		LSGDRLGCFNLSVKGHADCVRFLRSFNVPLVLVGGGGYT
		IRNVARCWCYETAVGVEVEPQDKLPYNEYYEYFGPDYTL
		HVAPSNMENQNSAKELAKIRNTLLEQLKRIQHVPSVPFQ
		ERPPDTKFPEEDEEDYEKRPKGHKWGGEYFGSESDEEQK
		PQNRDIDISDKPGIRRQSPPNVEAAKKIKVEEEDGDIGI
		VNENDGAKWPLGEAG
149	The amino acid sequence of SEQ ID	MMETGGNSLPSGPDGVKRKVAYFYDPEVGNYYYGQGHPM
	416. The conserved histone	KPHRIRMTHALLVQYGLHKEMQILKPYPARDRDLCRFHA
	deacetylase family domain is	DDYVAFLRGITPETIQDQVKALKRFNVGDDCPVFDGLYQ
	underlined.	YCQTYAGGSVGGAVKLNHKLCDIAINWAGGLHHAKKCEA
		SGFCYVNDIVLAILELLKYHKRVLYVDIDIHHGDGVEEA
		FYTTDRVMTVSFHKFGDYFPGTGDIRDIGCGKGKYYAVN
		VPLDDGIDDESFQSLFKPIIQQVMLVYNPEAIVLQCGAD
		SLSGDRLGCFNLSVKGHAECVRYMRSFNVPLLMVGGGGY
		TVRNVARCWCYETGVAVGVEIDDKMPQHEYYEYFGPDYT
		VHVAPSNMENKNTKQYLDKIRSKILENINSLPCAPSAQF
		QVQPPDTDFPELEEEDYDERTRSHKWDGASCDSDSENGD
		LKHRNHDVEESAFPRHNLANISYNTKIKLEGVGTGGLDM
		AAGTDTKKNDESFEAMDYESGEELRQDHFASTINASQPC
		DPALLTGVQNQLQSTDTVKPIEQSGNAPGIPPPSVATVS
		TGTRPSSISRTSSLNSMSSVKQGSILGPNPPQGLNASGL
		QFPVPTSNSPIRQGGSYSITVQAPDKQGLQNHMKGPQNM
		PGNS
150	The amino acid sequence of SEQ ID	MPPKDRVAYFYDGDVGSVYFGPNHPMKPHRLCMTHHLVL
	417. The conserved histone	SYELHKKMEIYRPHKAYPVELAQFHSADYVEFLHRITPD
	deacetylase family domain is	TQHLFTKELVKYNMGEDCPVFENLFEFCQIYAGGTIDAA
	underlined.	HRLNNQICDIAINWSGGLHHAKKCEASGFCYINDLVLGI
		LELLKHHARVLYVDIDVHHGDGVEEAFYFTDRVMTVSFH
		KYGDMFFPGTGDVKEVGEREGKYYAINVPLKDGIDDASF
		TRLFKTIITKVVDIYQPGAIVLQCGADSLAGDRLGCFNL
		SIDGHAQCVRIVKKFNLPLLVTGGGGYTKENVARCWSVE
		TGVLLDTELPNEIPDNDYIKYFAPDYSLKINTAGNMENL
		NSKTYLSAIKVQVMENLRAIQHAPSVQMHEVPPDFYIPD
		IDEDELNPDERMDQHTQDRQIQRDDEYYDGDNDIDHDME
		EAS
151	The amino acid sequence of SEQ ID	MDSSKSEEANILHVFWHEGMLNHDLGTGVFDTLEDPGFL
	418. The conserved histone	EVLEKHPENADRVRNMLSILRKGPIAPYTEWHTGRAAYL
	deacetylase family domain is	SELYSFHRPDYVDMLAKTSTAGGKTLCHGTRLNPGSWEA
	underlined.	ALLAAGTTLEAMRYILDGHGKLSYALVRPPGHHAQPTQA
		DGYCFLNNAGLAVELAVASGCKRVAVVDIDVHYGNGTAE
		GFYERDDVLTISLHMNHGSWGPSHPQTGFHDEVGRGKGL
		GFNLNVPLPNGTGDKGYEHAMHELVVPAISKFMPEMIVL
		VIGQDSSAFDPNGRECLTMEGYRKIGQIMRQQADQFSGG
		RLVVVQEGGYHITYAAYCLHATLEGVLCLPHPLLSDPIA
		YYPEHDIYSERVTFIKNYWQGGIISTTDKRN
152	The amino acid sequence of SEQ ID	MEESGNALVSGPDGSKRRVTYFYDADIGNYYYGQGHPMK
	419. The conserved histone	PHRMRMAHNLIVHYGLHQRMEVCRPHLAQSKDIRAFHTD
	deacetylase family domain is	DYIHFLSSVAPDTQQEQLRQLKRFNVGEDCPVFDGLFNF
	underlined.	CQSSAGGSIGAALKLNRKDADIAINWAGGLHHAKKCEAS
		GFCYVNDIVLGILELLKVHQRVLYIDIDIHHGDGVEEAF
		YTTDRVMTVSFHKFGDYFPGTGHIKDVGYGKGKYYALNV
		PLNDGIDDESYKHLFRPIIQKVMEVYQPEAVVLQCGADS
		LSGDRLGCFNLSVKGHADCVRFVRSFNIPLMLVGGGGYT
		IRNVARCWCYETAVAVGVEPQDKLPYNEYYEYFGPDYTL
		YVAPSNMENLNTEKDLEKMRNVLLEQLSKIQHTPSVPFQ
		ERPPDTEFNDEEEEDMEKRSKCRIWDGEYVGSEPEEDGK
		LPRFDADTYERSVLKHENKRLVPVSNVEPLKRIKQEEDG
		AAV
153	The amino acid sequence of SEQ ID	MDLNLVSHGEEEEGVRRRKVGIVYDERMCKHATPEDQPH
	421. The conserved histone	PEQPDRIRVIWDKLNSAGVLHKCVMVEAKEASEEQLAGV
	deacetylase family domain is	HSRKHIEVMKSIGTARYNKKKRDKLAASYSSIYFSQGSS
	underlined.	EAALLAAGSVVEISEKVASGELDAGVAIVRPPGHHAEAD
		KAMGFCLFNNIAIAAKHLVHERPELGVQKVLIVDWDVHH
		GNGTQHMFWTDPHVLYFSVHRFDAGTFYPGGDDGFYDKI
		GEGKGAGYNINVPWEQGKCGDADYLAVWDHVLVPVAKSY
		DPDMVLISGGFDAALGDPLGGCRLTPYGYSLMTKKLMEF
		AGGKIVLALEGGYNLKSLADSFLACVEALLKDGPGRSSV
		LTHPFGSTWRVIQAVRKELSSFWPALNEELQLPRLLKDA
		SESFDKLSSSSSDESSASEDEKKFAEVTSIMEVSPDPSS
		ILALTAEDIAQPLAGLKIEEAGTDSQRSSDHTLLDLTND
		DTQKLKQFEGEIFVMIGDEESVPSASSSKDQNESTVVLS
		KSNIKAHSWRLTFSSIYVWYASYGSNMWNPRFLCYIEGG
		QVEGMAKRCCGSEDKLLLKGYSGKLFLIECFLGDHTQIH
		GVQEECPFLIQIVVIRVKRMSACIK
154	The amino acid sequence of SEQ ID	MADEDLDLSDVGEVEDEPGEEIESTPPLAVGQEKEINSL
	422. The conserved FKBP-type	ALKKKLLKVGTRWETPENGDEVTVHYTGTLPDGTKFDSS
	peptidyl-prolyl cis-trans	RDRGEPFTFKLGQGQVIKGWDQGIVTMKKGERALFTIPP
	isomerase signature is underlined	ELAYGSSGVRPTIPPNATLQFDVELLSWTNIVDVCNDGG
	and the FKBP-type peptidyl-prolyl	ILKRIISEGEKYERPKDPDEVTVKYEAKLEDGTLVAKSP
	cis-trans isomerase signatures 1	EEGVEFYVNDGHFCPAIAKAVKTMKRGESVILTIKPTYA
	and 2 are in bold.	FGERGKDAEEGFAAIPPNATLTTSLELVSFKAVIAVTED
		KKVIKKILKEADGYDKPSDGTVVQIRYTAKLQDGTIFEK
		KGYEGEEPFQFVVDEEQVIAGLDKAVETMKTGEIALITI
		GAEYGFGNFETQRDLAVIPPNSTLIYEVEMISFTKEKES
		WDMDTTEKIEASKQKKEQGNSLFKVGKYQRAAKKYEKAA
		KYIEHDSSFSAEEKKQSKVLKVSCNLNHAACRLKLKDFK
		EAVKLCSKVLELESQNVKALYRRAQAYIETADLDLAEFD
		IKKALEIEPQNREVQLEYKILKQKQIEYNKKDAKLYGNM
		FAKLNKLEAFEGKVLS
155	The amino acid sequence of SEQ ID	MADEGLELSDVAEVEDEPGEEFESAPPLVVGQEKELNSS
	423. The conserved FKBP-type	GLKKKLLKAGTRCETPENGDEVTVHYTGTLLDGTKFDSS
	peptidyl-prolyl cis-trans	RDRGEPFTFNIGQGQVIKGWDQGIVTMKKREHALFTIPP
	isomerase family domains are	ELAYGASGMPPTIPPNATLQFDVELLSWTNIVDVCKDGG
	underlined. The FKBP-type	ILKRIISDGEKYERPKDPDEVTVKYEAKLEDGMLVAKSP
	peptidyl-prolyl cis-trans	EEGVEFYVNDGNFCPAIVKAVKTMKKGENVTLTIKPAYA
	isomerase signatures 1 and 2 are	FGEQGKDAEEGFAAIPPNATITINLQLVSFKAVKEVTED
	in bold. The TPR repeat is in	KKVIKKILKEADGYDKPSDGTVVQIRYTAKLQDGTIFEK
	bold/italics.	KGYAGEEPFQFVVDEEQVIAGLDKAVETMKTGEVALITI
		GPEYGFGNIETQRDLAVIPPYSTLIYEVEMVSFTKEKES
		WDMNTTENIEASKQKKEQGNSLFKVGKYLRAAKKYDKAA
		KYIEHDNSFSAEEKKQSKVLKVSCNLNHAACCLKLKDFK
		KAVKLCSKVLELESQN
		REVRLEYLILKQKQIEYNKKDAKLYGNM
		FARQNKLEAIEGKD
156	The amino acid sequence of SEQ ID	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRAL
	424. The conserved cyclophilin-	CTGEKGTGRSGKPLHFKGSSFHRVIPGFMCQGGDFTRGN
	type peptidyl-prolyl cis-trans	GTGGESIYGEKFADENFVKKHTGPGILSMANAGPNTNGS
	isomerase signature is underlined	QFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGS
	and the cyclophilin-type peptidyl-	GRTSKPVVIADSGQLA
	prolyl cis-trans isomerase
	signature 2 is in bold.
157	The amino acid sequence of SEQ ID	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRAL
	425. The conserved cyclophilin-	CTGEKGNGRSGKPLHFKGSSFHRVIPGFMCQGGDFTRGN
	type peptidyl-prolyl cis-trans	GTGGESIYGEKFADENFVKKHTGPGILSMANAGPNTNGS
	isomerase signature is underlined	QFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGS
	and The cyclophilin-type peptidyl-	GRTSKPVVIADSGQLA
	prolyl cis-trans isomerase
	signature 2 is in bold.
158	The amino acid sequence of SEQ ID	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRAL
	426. The conserved cyclophilin-	CTGEKGTGRSGKPLHFKGSSFHRVIPGFMCQGGDFTRGN
	type peptidyl-prolyl cis-trans	GTGGESIYGEKFADENFVKKHTGPGILSMANAGPNTNGS
	isomerase signature is underlined	QFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGS
	and The cyclophilin-type peptidyl-	GRTSKPVVIADSGQLA
	prolyl cis-trans isomerase
	signature 2 is in bold.
159	The amino acid sequence of SEQ ID	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRAL
	427. The conserved cyclophilin-	CTGEKGTGRSGKPLHFKGSSFHRVIPGFMCQGGDFTRGN
	type peptidyl-prolyl cis-trans	GTGGESIYGEKFADENFVKKHTGPGILSMANAGPNTNGS
	isomerase signature is underlined	QFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGS
	and The cyclophilin-type peptidyl-	GRTSKPVVIADSGQLA
	prolyl cis-trans isomerase
	signature 2 is in bold.
160	The amino acid sequence of SEQ ID	MADDFELPESAGMMENEDFGDTVFKVGEEKEIGKQGLKK
	428. The conserved FKBP-type	LLVKEGGSWETPETGDEVEVHYTGTLLDGTKFDSSRDRG
	peptidyl-prolyl cis-trans	TPFKFKLGQGQVIKGWDQGIATMKKGENAVFTIPPDLAY
	isomerase signature is underlined	GESGSQPTIPPNATLKFDVELLSWASVKDICKDGGIFKK
	and the FKBP-type peptidyl-prolyl	IIKEGEKWEHPKEADEVLVKYEARLEDGTVVSKSEEGVE
	cis-trans isomerase signature 1 is	FYVKDGYFCPAFAIAVKTMKKGEKVLLTVKPQYGFGHQG
	in bold and underlined. The TPR	REAIGNDVARSTNATLLVDLELVSWKVVDEVTDDKKVLK
	repeat is in bold/italics.	KILKQGEGYERPNDGAVVKVKYTGKLEDGTIFEEKGSDE
		EPFEFMAGEEQVVDGLDRAVMTMKKGEVALVSVAAEYGY
		QTEIKTDLAVVPPKSTLIYEVELVSFVKEKESWDMNTAE
		KIEAAGKKKEEGNALFKVGKYFRASKKYEKATKYIEYDT
		SFSEEEKKQSKPLK
		RDVKLEYRALKEKQKEYNKKEAKFYGNMFARMSKL
		EELESRKSGSQKVETANKEEGSDAMAVDGESA
161	The amino acid sequence of SEQ ID	MAASLTPLGAGLAYATIYDQAKVRKLEPTKRSLIALCQH
	429. The conserved FKBP-type	SDSQHRRFITRKYHVNVQILNRRDAIRLIGLAAGLCIDL
	peptidylprolyl isomerase domain is	SLMYDARGAGLPPQENAKLCDTTCEKELENAPMITTESG
	underlined.	LQYKDIKIGNGPSPPIGFQVAANYVAMVPSGQVFDSSLD
		KGQPYIFRVGSGQVIKGLDEGLLSMKVGGKRRLYIPGPL
		AFPKGLNSAPGRPRVAPSSPVIFDVSLEFIPGLESEEE
162	The amino acid sequence of SEQ ID	MSAASLSADMAIRGTILGKTALHVLGPQVVSQCRQPVMF
	430. The conserved FKBP-type	KCPPHTLRKMRFSAQDLQSKNFYSGFTPFKSVFISTSKR
	peptidylprolyl isomerase domain is	SWQAGSARAMSQDAAFQSKVTTKCFLDIEIGGDPAGRIV
	underlined and the Cyclophilin-	LGLFGEDVPKTAENFRALCTGEKGFGYKGSSFHRIIKDF
	type peptidyl-prolyl cis-trans	MLQGGDFDRGDGTGGKSIYGRTFEDENFKLAHVGPGVLS
	isomerase signature is in bold.	MANAGPNTNGSQFFICTVKTPWLDKRHVVFGQVIEGMEI
		VKKLESEETNRTDRPKRPCRIVDCGELP
163	The amino acid sequence of SEQ ID	MGRIKPQTLLQQSKKKKVPGRISVSTIIVCNLIIIFLMF
	431. The conserved FKBP-type	SLVGIYRQRAKRNRATSRSDGDEEMENFGRSKINSVPHQ
	peptidylprolyl isomerase domain is	AIVNTTKGLITLELFGKSSAHTVEKFVEWSERGYFNGLP
	underlined.	FYRVIKHFVIQVGDPKFAGNREDWTVGGQLNVQLEFSPK
		HEAFMLGTSKLEDQGDGFELFITTAPIPDLNDKLNVFGR
		VIKGQDVVQEIEEVDTDEHFQPKSPIIINDVRLKDEL
164	The amino acid sequence of SEQ ID	MARQSTLLLFWSLVFLGAIVFTQAKHEELEEVTHKVYFD
	432. The conserved cyclophilin-	VDIAGKPAGRVVIGLFGKAVPKTVENFRALCTGEKGVGK
	type peptidyl-prolyl cis-trans	SGKPLHYKGSFFHRIIPSFMIQGGDFTLGDGRGGESIYG
	isomerase signature is underlined	TKFADENFKLKHTGPVFITTVTTDWLDGRHVVFGKIISG
	and the cyclophilin-type peptidyl-	MDVVYKVEAEGRQSGQPKRKVKIADSGELSMD
	prolyl cis-trans isomerase
	signature is in bold.
165	The amino acid sequence of SEQ ID	MEMDEIQEQSQPQSSEKQDISQESDTGNDKTINAEKITS
	434. The conserved FKBP-type	ENAEVEEDDMLPPKVNTEVEVLHDKVTKQIIKEGSGNKP
	peptidyl-prolyl cis-trans	SRNSTCFLHYRAWAESTMHKFQDTWQEQQPLELVLGREK
	isomerase signature is underlined	KELSGFAIGVAGMKAGERALLHVDWQLGYGEEGNFSFPN
	and the TPR repeat is in bold.	VPPRANLIYEAELIGFEEAKEGKARSDMTVEERIEAADR
		RRQQGNELFKEDKLAEAMQQYEMALAYMGDDFMFQLFGK
		YKDMANAVKNPCHLNMAQCLLKLNRYEEAIGQCNMVLAE
		DEKNIKALFRRGKARATLGQTDDAREDFQKVRKFSPEDK
		AVIRELRLLAEHDKQVYQKQKEMFKGLFGQKPEQKPKKL
		HWFVVFWQWLLSMIRTIFRMRSKTD
166	The amino acid sequence of SEQ ID	MAGAGEGTPEVTLETSMGPITVELYHKHAPKTCRNFLEL
	435. The conserved cyclophilin-	SRRGYYNNVKFHRVIKDFMVQGGDPTGTGRGGESIYGPR
	type peptidyl-prolyl cis-trans	FEDEITRDLKHTGAGILSMANAGPNTNGSQFFISLAPTP
	isomerase signature is underlined	WLDEKHTIFGRVCKGMDVVKRLGNVQTDKNDRPIHDVKI
	and the cyclophilin-type peptidyl-	LRTTVKD
	prolyl cis-trans isomerase
	signature is in bold.
167	The amino acid sequence of SEQ ID	MMDPELMRLAQEQMSKISPDELMKMQRQIMANPDLMRMA
	436. The conserved TPR repeat	SENMKNLKPEDIRFAAEQMKNVRKEEMAEISERISRASP
	domain is underlined.	EEIEAMKARANLQSAYQLQVAQNLKDQGNQLHARMKYSE
		AAEKYLQARNNLTGIPFSEAKSLLLASSSNLMSCYLKTG
		QYEECVQTGSEVLAYDAMNVKALYRRGQAYKQIGKLELA
		VADLRKAVEVSPEDETIAQALREASTELMEKGGTQDQNG
		PRIEEIIEEEAVQPTAEKYPQSAPMVTSVTEDVSDDEQG
		SEDQNGFSRDSFQATNAPDGQMYAESLRNLTENPDMLRT
		MQSLMKNVDPDSLVALSGGKLSPDMVKTVSGMFGRMSPE
		EIQNMMKMSSTLSRQNPSTSSRFDDITRGHSNMDSSPQS
		VSVDNDLFEENQNRVGESSTNLSSSAAFSGMPNFSAEMQ
		EQVRNQMNDPATRQMFTSMIQNMSPEMMASMSEQFGVKL
		SPEDAVKAQNAMASLSPNDLDRLMNWATRLQTAIDYARK
		IKNWILGRPGLIFAISMLLLAIILHRFGYIGD
168	The amino acid sequence of SEQ ID	MGVEKEILRPGNGPKPRPGQSVTVHCTGYGKNEDLSQKF
	437. The conserved FKBP-type	WSTKDPGQKPFTFTIGQGRVIKGWDEGVLDMQLGEIFKL
	peptidylprolyl isomerase domain is	RCSPDYGYGSNGFPAWGIRPNSVLVFEIEVLSVN
	underlined and the Cyclophilin-
	type peptidyl-prolyl cis-trans
	isomerase signature is in bold.
169	The amino acid sequence of SEQ ID	MPNPRCYLDITIGEELEGRILVELYSDVVPKTAENFRAL
	438. The conserved cyclophilin-	CTGEKGIGPHTGVPLHYKGLPFHRVIKGFMIQGGDISAQ
	type peptidyl-prolyl cis-trans	NGTGGESIYGLKFDDENFQLKHERRGMLSMANSGPNTNG
	isomerase family domain is	SQFFITTTRTSHLDGKHVVFGKVIKGMGVVRGIEHTPTE
	underlined and the cyclophilin-	SNDRPSLDVVISDCGEIPEGSDDGIANFFKDGDLYPDWP
	type peptidyl-prolyl cis-trans	ADLDEKSAEISWWMNAVDSAKCFGNENYKKGDYKMALRK
	isomerase signature is in bold.	YRKALRYLDICWEKEEIDEEKSNHLRKTKSQIFTNSSAC
		KLKLGDLKGALLDTEFAMRDGEDNVKALFRQGQAYMALK
		DVDSAVASFKKALQLEPNDAGIRKELAVATKMINDRRDQ
		ERRAYARMFQ
170	The amino acid sequence of SEQ ID	MGDVIDLNGDGGVLKTIIRSAKPGAMQPTEDLPNVDVHY
	439. The conserved FKBP-type	EGTLADTGEVFDTTREDNTLFSFELGKGTVIKAWDIAVK
	peptidylprolyl isomerase domain is	TMKVGEVARITCKPEYAYGSAGSPPDIPENATLIFEVEL
	underlined and the Cyclophilin-	VACKPRKGSTFGSVSDEKARLEELKKQREIAAASKEEEK
	type peptidyl-prolyl cis-trans	KRREEAKATAAARVQAKLEAKKGQGRGKGKSKGK
	isomerase signature is in bold.
171	The amino acid sequence of SEQ ID	MGLGLKIASASFLPIFNIMATRSLCILLVCFIPVLAHVL
	440. The conserved cyclophilin-	SLQDPELGTVRVYFQTTYGDIEFGFFPHVAPKTVEHIYK
	type peptidyl-prolyl cis-trans	LVRLGCYNSNHFFRVDKGFVAQVADVVGGREVPLNSEQR
	isomerase signature is underlined.	KEGEKTIVGEFSEVKHVRGILSMGRYSDPDSASSSFSIL
		LGNAPHLDGQYAVFGKVTKGDDTLKRLEEVPTRQEGIFV
		MPLERIRILSTYYYDTNERESNLTCDHEVSILKRRLVES
		AYEIEYQRRKCLP
172	The amino acid sequence of SEQ ID	MASKRSLRTMNVWPTLPPLVLLLLLCFSSMSSSVVAKKS
	441. The conserved FKBP-type	DVSELQIGVKHKPKSCDIQAHKGDRIKVHYRGSLTDGTV
	peptidylprolyl isomerase domain is	FDSSFERGDPIEFELGSGQVIKGWDQGLLGMCVGEKRKL
	underlined and the Cyclophilin-	RIPSKLGYGAQGSPPKIPGGATLIFDTELVAVNGKGISN
	type peptidyl-prolyl cis-trans	DGDSDL
	isomerase signatures are in bold.
173	The amino acid sequence of SEQ ID	MSGAPAERPISYFDITIGGKPIGRIVFSLYADLVPKTAE
	442. The conserved FKBP-type	NFRALCTGEKGIGKSGKPLCYAGSGFHRVIKGFMCQGGD
	peptidylprolyl isomerase domain is	FTAGNGTGGESIYGEKFEDEAFPVKHTKPFLLSMANAGK
	underlined and the Cyclophilin-	DTNGSQFFITVSQTPHLDDKHVVFGEVIKGKSIVRAIEN
	type peptidyl-prolyl cis-trans	YPTASGDVPTSPIIISACGVLSPDDPSLAASEETIGDSY
	isomerase signatures are in bold.	EDYPEDDDSDVQNPEVALDIARKIRELGNKLFKEGQIEL
		ALKKYLKSIRYLDVHPVLPDDSPPELKDSYDALLAPLLL
		NSALAALRTQPADAQTAVKNATRALERLELSDADKAKAL
		YRRASAHVILKQEDEAEEDLVAASQLSPEDMAISSKLKE
		VKDEKKKKREKEKKAFKKMFSS
174	The amino acid sequence of SEQ ID	MASSLRSSLFSSWALDSKSVCSLFNLNPGKMGLPSISTP
	443. The conserved FKBP-type	LNWRTCCCSHSSELLELNEGLQSSRRKTVMGLSTVIALS
	peptidylprolyl isomerase domain is	LVYCDEVGAVSTSKRALRSQKVPEDEYTTLPNGLKYYDL
	underlined.	KVGSGTEAVKGSRVAVHYVAKWKGITFMTSRQGMGITGG
		TPYGFDVGASERGAVLKGLDLGVQGMRVGGQRILIVPPE
		LAYGNTGIQEIPPNATLEFDVELISIKQSPFGSSVKIVEG
175	The amino acid sequence of SEQ ID	MGAIEDEEPPLKRLKVSSPGLRRGLEEEAPSLSVGSVSI
	444. The conserved G-protein beta	LMAKSLSLEEGETVGSKGLIRRVEFVRIITQALYSLGYQ
	WD-40 repeat domains are	KAGALLEEESGILLQSSNVALFRKQILDGKWDESVVTLR
	underlined.	GIDQVEVEGNTLKAASFLILQQKFFELLDKGNIPEAMKT
		LRLEISPMQLNTKRVHELASCIVFPSRCEELGYSKQGNP
		KSSQRMKVLQEIQQLLPPSIMIPEKRLERLVEQALNVQR
		EACIFHNSLDPALSLYTDHQCGRDQIPTTTLQVLESHKN
		EVWFLQFSNNGKYLASASKDCSAIIWEITEGDSFSMKHR
		LSAHQKPVSFVAWSPDDKLLLTCGIEEVVKLWNVETGEC
		KLTYDKANSGFTSCGWFPDGERFISGGVDKCIYIWDLEG
		KELDSWKGQGMPKISDLAVTSDGKEIISICGDNAIVMYN
		LDTKTERLIEEESGITSLCVSKDSRFLLLNLANQEIHLW
		DIGARSKLLLKYKSHRQSRYVIRSCFSSSDLAFVVSGSE
		DSQVYIWHRGNGELLAVLPGHSGTVNCVSWNPVNPHVFA
		SASDDYTIRIWGVNRNTFRSKNASSSNGVVHLANGGP
176	The amino acid sequence of SEQ ID	MPGTTAGAGIEPTEPQSLKKLSLKSLKRSFDLFASLHGE
	445. The conserved G-protein beta	PQPPDQRSQRIRIACKVRAEYEVVKNLPTLPQREVGSSV
	WD-40 repeat domains are	SNSNVGETHSSLTTNQAQGFPTDTSGDLSKDEGKEITSI
	underlined and the Trp-Asp (WD)	AVHLQPQTGLIDGKAGAIAGTSTAISSVGSSDRYQPSAA
	repeats signature is in bold.	IMKRLPSKWPRPIWHPPWKNYRVISGHLGWVRSVAFDPG
		NEWFCTGSADRTIKIWEVATGKLKLTLTGHIEQIRGLAV
		SSRHPYLFSAGDDKQVKCWDLEYNKAIRSYHGHLSGVYC
		LALHPTLDILCTGGRDSVCRVWDIRTKAQIFALSGHENT
		VCSVFTQAIDPQVVTGSHDTTIKLWDLAAGKTMSTLTYH
		KKSVRAIAKHPFEHTFASASADNIKKFKLPKGEFLHNML
		SQQKTIVNAMAINEDNVLVSAGDNGSLWFWDWKSGHNFQ
		QAQTIVQPGSLDSEAGIYALQYDITGSRLVSCEADKTIK
		MWKEDETATPESHPINFKAPKDIRRF
177	The amino acid sequence of SEQ ID	MRPILMKGHERPLTFLKYNRDGDLLFSCAKDHTPTVWYG
	446. The conserved G-protein beta	HNGERLGTYRGHNGAVWCCDVSRDSTRLITSSADQTAKL
	WD-40 repeat domains are	WNVETGAQLFSFNFESPARAVDLAIGDKLVVITTDPFME
	underlined.	LPSAIHIKRIEKDLSKQTADSVLTITGIKGRINRAVWGP
		LNSTIISGGEDSVVRIWDSETGKLLRESDKETGHQKPIT
		SLCKSADGSHFLTGSLDKSARLWDIRTLTLIKTYVTERP
		VNAVAISPLLDHVVIGGGQEASHVTTTDREAGKFEAKFF
		HKILEEEIGGVKGHFGPINSLAFNPDGRSFASGGEDGYV
		RLHHFDPDYFHIKM
178	The amino acid sequence of SEQ ID	MRPILMKGHERPLTFLKYNRDGDLLFSCAKDHTPTVWYG
	447. The conserved G-protein beta	HNGERLGTYRGHNGAVWCCDVSRDSTRLITSSADQTAKL
	WD-40 repeat domains are	WNVETGNQLFSFNFESPARAVDLAIGDKLVVITTDPFME
	underlined.	LPSAIHIKRIEKDLSKQTADSVLTITGIKGRINRAVWGP
		LNSTIISGGEDSVVRIWDSETGKLLRESDKETGHQKAIT
		SLCKSADGSHFLTGSLDKSARLWDIRTLTLIKTYVTERP
		VNAVAISPLLDHVVIGGGQEASHVTTTDRRAGKFEAKFF
		HKILEEEIGGVKGHFGPINSLAFNPDGRSFASGGEDGYV
		RLHHFDPDYFHIKM
179	The amino acid sequence of SEQ ID	MAENNVGDFIPLDRQEYPSKPAPGAVDSSFWKSFKKKEV
	448. The conserved G-protein beta	SRQIAGVTCINFCPEPPHDFAVTSSTRVHIYDGKSCELK
	WD-40 repeat domains are	KTITKFKDVAYSGVFRSDGQIIAAGGETGVIQVFNAKSQ
	underlined.	MVLRQLKGHGRPVRVVRYSPQDKLHLLSGGDDSMVKWWD
		ITTQEELLNLEGHKDYVRCGAASPSSVNLWATGSYDHTV
		RLWDLRNSKTVLQLKHGKPLEDVLFFPSGGLLATAGGNV
		VKVWDILGGGRPIHTMETHQKTVMAMCISKVPRSGQALG
		DAPSRLVTASLDGYMKVFDLDHFKVTHSARYPAPILSMG
		ISSLCRTMAVGTSSGLLFIRQRKGQIEDKIHSDSSGLQV
		NPVNDEKDSAVLKPNQYRYYLRGRSEKPSEGDYVVKRMA
		KVYFQEYDKDLRHFNHSKALVSALKAADSKGTVAVIEEL
		VARKRLIQTLSILNLDELELLINFLSRFILVPKYSRFLI
		SLTDRVLDARAVDLGKSENLKKQIADLKGIVVQELRVQQ
		SMQELQGIIEPLIRASAR
180	The amino acid sequence of SEQ ID	MDVETSSKPTGNKRTYTRLPRQVCVFWQEGRCTRESCNF
	449. The conserved C-x8-C-x5-C-x3-	LHVDEPGSVKRGGATNGFAPKRSYNGSDERDTLAAGPPG
	H type zinc finger is underlined	GSRRNISARWGRGRGGIFISDERQKIRNKV NYWLAGN
	and in italics and the conserved	QRGEE KYL SFVMGSDVKFLTQLSGHVKAIRGIAFPSD
	Cys and His residues in bold, The	SGKLYSGGQDKKVIVWDCQTGQGTDIPLNDEVGCLMSEG
	conserved G-protein beta WD-40	PWIFVGLPNAVKAWNILTSTELSLVGPRGQVHALAVGNG
	repeat domains are underlined and	MLFAGTHDGSILAWKFSPASNTFEPAASLVGHTQAVVSL
	the Trp-Asp (WD) repeats signature	VSGADRLYSGSMDKTIRVWDLGTFQCLQTLRDHTSVVMS
	is in bold (non-italics).	LLCWDQFLLSCSLDNTVKVWVATSSGALEVTYTHNEEHG
		VLALCGMNDEQAKPVLLCSCNDNTVRLYDLPSFSERGRI
		FSRNEVRTFQIAPGGLFFTGDATGELKVWNWATQKS
181	The amino acid sequence of SEQ ID	MSVQELRERHAAATAKVNALRERIKAKRLQLLDTDVATY
	450. The conserved G-protein beta	ASSNGRTPISFSFTDLVCCRTLQGHTGKVYSLDWTSEKN
	WD-40 repeat domains are	RIVSASQDGRLIVWNALTSQKTHAIKLPCAWVMTCAFSP
	underlined.	SGQAVACGGLDSVCSIFQLNNQLDRDGHLPVSRILSGHR
		SYVSSCQYVPDGDTHVITGSGDRTCIQWDVTTGQRIAIF
		GGEFPLGHTADVMSVSISAANPKEFVSGSCDTTTRLWDT
		RIASRAIRTFHGHEADVNTVKFFPDGLRFGSGSDDGTCR
		LFDIRTGHQLQVYRQPPRENQSPTVTAIAFSFSGRLLFA
		GYSNGDCFVWDTILEKVVLNLGELQNTHNGRISCLGLSA
		DGSALCTGSWDKNLKIWAFGGHRKIV
182	The amino acid sequence of SEQ ID	MKVKIISRSTDEFTRERSNDLQRVFRNFDPNLHTQARAQ
	451. The conserved G-protein beta	EYVRALNAAKLDKIFAKPFLAAMSGHIDGISAMAKSPRH
	WD-40 repeat domains are	LKSIFSGSVDGDIRLWDIAARRTVQQFPGHRGAVRGLTV
	underlined.	STEGGRLISCGDDCTVRLWDIPVAGIGESSYGSENVQKP
		LATYVGKNSFRAVDYQWDSNVFATGGAQVDIWDHDRSEP
		TNSFAWGSDTVISVRFNPAEKDIFATTASDRSIVLYDLR
		MASPLNKLIMQTRNNAIAWNPREPMNFTAANEDCNCYSY
		DMRRMNISTCVHQDHVSAVMDIDYSPSGREFVTGSYDRT
		VRIFPYNAGHSREIYHTKRMQRVFCVKFSGDATYVVSGS
		DDANIRLWKAKASEQLGVLLPRERKRHEYLDAVKERFKH
		LPEIKRIERHRHLPKPIYKAALLRHTVNAAAKRKEERKR
		AHSAPGSVVTNPLRKKRIVAQLE
183	The amino acid sequence of SEQ ID	MDHYYQDDFDYLVDDEMVDFADDVEDDVRTRRRSDIDSD
	452. The conserved G-protein beta	SENDFDLNNKSPDTTALQAKRGKDIQGIPWNRLNFTREK
	WD-40 repeat domains are	YRETRLQQYKNYENLPRPRRSRNLDKECTNFERGSSFYD
	underlined.	FRHNTRSVKATIVHFQLRNLVWATSKHNVYLMQNYSIMH
		WSSLKQKGEEVLNVAGPIVPSVKHPGSSPQGLTRVQVSA
		MSVKDNLVVAGGFQGELICKYLDKPGVSFCTKISHDENG
		ITNAVEIYNDASGATRLMTANNDLAVRVFDTEKFTVLER
		FSFPWSVNHTSVSPDGKLVAVLGDNADCLLADCKTGKTV
		GTLRGHLDYSFAAAWHPDGYILATGNQDTTCRLWDVRKL
		SSSLAVLKGRMGAIRSIRFSSDGRFMAMAEPADFVHLYD
		TRQNYTKSQEIDLFGEIAGISFSPDTEAFFVGVADRTYG
		SLLEFNRRRMNYYLDSIL
184	The amino acid sequence of SEQ ID	MAEALVLRGTMEGHTDAVTAIATPIDNSDMIVSSSRDKS
	453. The conserved G-protein beta	ILLWNLTKEPEKYGVPRRRLTGHSHFVQDVVISSDGQFA
	WD-40 repeat domains are	LSGSWDSELRLWDLNTGLTTRRFVGHTKDVLSVAFSIDN
	underlined and the Trp-Asp (WD)	RQIVSASRDRTIKLWNTLGECKYTIQPDAEGHSNWISCV
	repeats signatures are in bold.	RFSPSATNPTIVSCSWDRTVKVWNLTNCKLRNTLVGHGG
		YVNTAAVSPDGSLCASGGKDGVTMLWDLAEGKRLYSLDA
		GDIIYALCFSPNRYWLCAATQQCVKIWDLESKSIVADLR
		PDFIPNKKAQIPYCTSLSWSADGSTLFSGYTDGKIRVWG
		IGHV
185	The amino acid sequence of SEQ ID	MAAIKSTSRSASVAFAPDAPLLAAGTMAGAIDLSFSSLA
	454. The conserved G-protein beta	NLEIFKLDFQSDDPELPVVGECPSNERLNRLSWGSAGGS
	WD-40 repeat domains are	FGIIAGGLVDGTINIWNPATLINSEDNGDALIARLEQHT
	underlined.	GPVRGLEFNTISTNLLASGAEDGELCIWDLANPTAPTHF
		PPLKGVGSGAQGEISFLAWNRKVQHILASTSYSGTTVVW
		DLRRQKPIISFPDATRRRCSVLQWNPDASTQLIVASDDD
		NSPTLEAWDLRNTISPYKEFVGHSRGVIAMSWCPSDSLF
		LLTCAKDNRTLCWDTGSGEIVCELPAGANWNFDVQWSPK
		IPGILSTSSFDGKIGIHNIEACSRNVSGEVEFGGAIVRG
		GPSALLKAPKWLERPAGVSFGFGGKLASFRPSTVAQAAD
		HRHSEVFIHNLVTEDNLVIRSTEFEAAIADGEKVSLRAL
		CDRKAEESQSDEEKETWNFLRVMFEDEGTARTKLLEHLG
		FKVQSEENGDLQETHSSKIDDIGSEIGKTLTLDDKTEED
		VLPQLKGGQDAAIPQDNGEDFFDNLHSPKEEVSLSHVGN
		DFVGEKDKDMVVNGAEIEHETEDLTEYSDWNEAIQHSLV
		VGDYKGAVLQCLSANRMADALIIAHLGGNSLWEKTRDEY
		LKKAKSSYLKVVSAMVNNDLTGLVNSRPLKSWKETLAML
		CTYSQREEWTVLCDMLASRLIAAGNVMAATLCYICAGNI
		EKTVEIWSRSLKYDYDGRSFVDHLQDVMEKTVVLALATG
		QKRVSPSLSKLVENYAELLASQGLLTTAMEYLKLLGTEE
		SSHELSILRDRLYLSGTDNKVEASSFPFETRQDLTESQY
		NMHQTGFGAPETQKNYQENVHQVLPSGSYTDNYQPTANT
		HYIAGYQPAPQQQPSFQNYFTPASYQPAPSPNVFYPSQV
		SQAEQSNFAPPVNQPPMKTFVPSTPPILRNVDQYQTPSL
		NPQLYQGVSSATVETHPYQTGAPASVSVGTTPGQPSVVP
		NFMVPGPVTAPTVTPRGFMPVTTPTQHPLGSANPPVQPQ
		SPQSSQVQSV
186	The amino acid sequence of SEQ ID	MAGAADSQLQTLSERDSTPNFKNLHTREYAAHKKKVHSV
	455. The conserved G-protein beta	AWNCTGTKLASGSVDQTARVWNIEPHGHSKTKDLELKGH
	WD-40 repeat domains are	ADSVDQLCWDPKHSELLATASGDRTVRLWDARSGKCSQQ
	underlined and the Trp-Asp (WD)	VELSGENINITFKPDGTHIAVGNRDDELTIIDVRKFKPL
	repeats signature is in bold.	HKRKFSYEVNEIAWNTTGELFFLTTGNGTVEVLSYPSLQ
		VLHTLVAHTAGCYCIAIDPIGRYFAVGSADALVSLWDLS
		EMLCVRTFTKLEWPVRTISFNHDGQYIASASEDLFIDIA
		DVQTGRTVHQISCRAAMNSVEWNPKYNLLAFAGDDKNKY
		MQDEGVFRVFGFETP
187	The amino acid sequence of SEQ ID	MAATSPVGAGSGRELANPPTDGISNLRFSNHSDHLLVSS
	456. The conserved G-protein beta	WDRKVRLYDASANSLKGQFVHGGPVLDCCFHDDASGFSG
	WD-40 repeat domains are	SADNTVRRYDFSTRKEDILGRHEAPVRCVEYSYAAGQVI
	underlined.	TGSWDKTLKCWDPRGASGQEKTLVGTYSQLERVYSMSLV
		GHRLVVATAGRHINVYDLRNMSQPEQRRESSLKYQTRCV
		RCYPNGTGFALSSVEGRVAMEFFDLSEAGQAKKYAFKCH
		RKSEAGRDTVYPVNAIAFHPIYGTFATGGCDGYVNVWDG
		NNKKRLYQYSKYPTSIAALSFSRDGRLLAVASSYTFEEG
		EKPHEPDAVFVRSVNEAEVKPKPKVYAAPP
188	The amino acid sequence of SEQ ID	MASDDEEGFKNEEAPGVVDEAEVQEGLRACFPLSFGKQE
	457. The conserved G-protein beta	KKQAPLESIHSATKRPEDPRPRRQLGPPRPPPSILAEQE
	WD-40 repeat domains are	DSDRFVGPPRPPQFVRDDNDDGEAEIMIGPPRPPAQYSD
	underlined and the Trp-Asp (WD)	DHDNEETIGPPKPSYLEKGEETDQMVGPSKRGSDDETSG
	repeats signature is in bold.	DSDDGDDAVDFRVPLSNEIVLRGHTKVVSALAIDQTGSR
		VLTGSYDYSVRMYDFQGMTSQLKSFRQLEPAEGHQVRSL
		SWSPTSDRFLCVTGSAQAKIFDRDGLTLGEFVKGDMYLR
		DLKNTKGHISGLTCGEWHPKEKQTILTCSEDGSLRIWDV
		NDFNTQKQVIKPKLAKPGRVPVTACAWGRDGKCIAGGVG
		DGSIQVWNLKPGWGSRPDLYVAKGHDDDITGLQFSADGN
		ILLTRSTDETLKVWDLRKAITPLQVFRDLPNNYAQTNVA
		FSPDERLIFTGTSVERDGNSGGLLCFYDRQTLELVLRIG
		VSPVHSVVRCTWHPRHNQVFATVGDKKEGGAHILYDPAL
		SERGALVCVARAPRKKSLDDFEAKPVIHNPHALPLFRDE
		PSRKRQREKARMDPMKSQRPDLPVTGPGFGGRVGSTKGS
		LLTQYLLKEGGLIKETWMEEDPREAILKYADVAAKDPKF
		IAPAYAQTQPETVFAETDSEEEQK
189	The amino acid sequence of SEQ ID	MKERGQSHAGQPSVDERYTQWKSLVPVLYDWLANHNLVW
	458. The conserved G-protein beta	PSLSCRWGPQMHQATYKNSQRLYLSEQTDGTVPNTLVIA
	WD-40 repeat domains are	TCEVVKPRVAAAEHISQFNEEARSPFVKKFKTIIHPGEV
	underlined.	NRIRELPQNSKIVATHTDGPDVLIWDVDTQPNRQATLGA
		ADSRPDLVLTGHKDNAEFALAMSPSAPFVLSGGKDKCVL
		LWSIQDHISAATEPSSAKASKTPSSAHGEKVPKIPSIGP
		RGVYKGHKDTVEDVQFCPSNAQEFCSVGDDSALILWDAR
		NGNEPVIKVEKAHNADLHCVDWNPHDENLILTGSADNSV
		RMFDRRNLTSSGVGSPVHKFEGHSAPVLCVQWCPDKASV
		FGSAAEDSYLNVWDYEKVGKNVGKKTPPGLFFQHAGHRD
		KVVDFHWNSFDPWTIVSVSDDGESTGGGGTLQIWRMSDL
		IYRPEDEVLAELERFEAHILSCQNK
190	The amino acid sequence of SEQ ID	MSSLSRELVFLILQFLDEEKFKESVHKLEQESG NMK
	459. The conserved G-protein beta	YFDEKAQAGEWDEVERYLSGFTKVDDNRYSMKIFFEIRK
	WD-40 repeat domains are	QKYLEALDRQDRAKAVDILVKDLKVFSTFNEELYKEITQ
	underlined. The Lissencephaly	LLTLDNFRENEQLSKYGDTKSARTIMMSELKKLIEANPL
	type-1-like homology motif is in	FREKLIYPNLKASRLRTLINQSLNWQHQLCKNPRPNPDI
	bold and the CTLH, C-terminal to	KTLFTDHACGPPNGARTPTQPTASLGVLPKATTFTPIGP
	LisH motif is in italics.	HGPFPSSSTATSGLASWMSNPNMVTSPQAPVAVGPSVPV
		PPNQATLLKRPRTPPGSSSVVDYQTADSEQLIKRLRPVS
		QSIDEATYPGPTLRVPWSTDDLPKTLARALNEPYPVTSI
		DFHPSQQTFLLVGTKNGEITLWEVGSREKLATRSFKIWD
		NANCSNHLEAAFVKDSSVSINRVLWSPDGTLIGIAFTKH
		LVHTYTFQGLDLRQHLEIDAHVGGVNDLAFSHPNKQLCV
		VTCGDDKMIKVWDAVTGRKLYNFEGHDAPVYSVCPHHKE
		NIQFIFSTAVDGKIKAWLYDHLGSRVDYDAPGHSCTTMM
		YSADGTRLFSCGTSKEGESFLVEWNESEGAIKRTYSGLR
		KKGSGVVQFDTTQNHFLAVGDEHLIKFWDMDSTNMLTSC
		DAEGGLLNLPRLRFNKEGSLLAVTTVNGIKILANADGQK
		LLKTMENRTFDLPSRAHIDAASATSSPATGRMERIERTS
		SANTVSGINGVDPAQSSEKLRLSDDLSEKTKIWKLTEIT
		DSIQCRCITLPENAAEPASKVSRLLYTNSGVGLLALGSN
		AVHKLWKWNRSEQNPSGKATASVHPQRWQPTSGLLMTND
		ITDINPEEAVPCIALSKNDSYVMSASGGKVSLFNMMTFK
		VMTTFMPPPPASTFLAFHPQDNNIIAIGMEDSTIHIYNV
		RVDEVKTKLKGHQKRITGLAFSSTQNILVSSGADAQLCV
		WNTETWEKRKSKTIQMPVGKTVSGDTRVQFHSDQLHILV
		VHETQLAIYDAYKLERQYQWVPQDALSAPILYATYSCNR
		QLIYATFSDG
191	The amino acid sequence of SEQ ID	MAKDEEEFRGEMEERLVNEEYKIWKKNTPFLYDLVITHA
	460. The conserved G-protein beta	LEWPSLTVQWLPDREEPPGKDYSVQKMILGTHTSDNEPN
	WD-40 repeat domains are	YLMLAQVQLPLEDAENDARQYDDERGEIGGFGCANGKVQ
	underlined.	VIQQINHDGEVNRARYMPQNPFIIATKTVSAEVYVFDYS
		KHPSKPPQDGGCHPDLRLRGHNTEGYGLSWSPFKHGHLL
		SGSDDAQICLWDINVPAKNKVLEAQQIFKVHEGVVEDVA
		WHLRHEYLFGSVGDDRHLLIWDLRTSATNKPLHSVVAHQ
		GEVNCLAFNPFNEWVLATGSADRTVKLFDLRKISSALHT
		FSCHKEEVFQIGWSPKNETILASCSADRRLMVWDLSRID
		EFQTPEDALDGPPELLFIHGGHTSKISDFSWNPCEDWVI
		ASVAEDNILQIWQMAENIYHDEEDDMPPEEVV
192	The amino acid sequence of SEQ ID	MSPGVKQTGSQKFESGHQDVVHDVTMDYYGKRIATCSAD
	461. The conserved G-protein beta	RTIKLFGLNASDTPSLLASLTGHEGPVWQVAWAHPKFGS
	WD-40 repeat domains are	MLASCSYDGRVIIWREGQQENEWSQVQVFKEHEASVNSI
	underlined.	SWAPHELGLCLACGSSDGSITVFTCREDGSWDKTKIDQA
		HQVGVTAVSWAPASAPGSLVGQPSDPIQKLVSGGCDNTA
		KVWKFYNGSWKLDCFPPLQMHTDWVRDVAWAPNLGLPKS
		TIASCSQDGKVVIWTQGKEGDKWEGRILNDFKIPVWRVN
		WSLTGNILAVADGNNSVTLWKEAVDGDWNQVTTVQ
193	The amino acid sequence of SEQ ID	MSSGVKQTGSQKFESGHQDVVHDVTMDYYGKRIATCSAD
	462. The conserved G-protein beta	RTIKLFGMNTSDTPTLLASLTGHEGPVWQVAWAHPKFGS
	WD-40 repeat domains are	MLASCSYDRRVIIWREGQQENEWSQVQVFKEHEASVNSI
	underlined.	SWAPHELGLCLACGSSDGSITVFTGREDGSWDKTKIDQA
		HQVGVTAVSWAPASAPGSLVGQPSDPVQKLVSGGCDNTA
		KVWKFYNGSWKLDCFPPLQMHTDWVRDVAWAPNLGLPKS
		TIASCSQDGRVVIWTQGKEGDKWEGKILNDFKTPVWRIS
		WSLTGNILAVADGNNNVTLWKEAVDGEWNQVTTVQ
194	The amino acid sequence of SEQ ID	MKKRSRPSNGHLSTAAKNKSRKTAPITKDPFFDSAHNRN
	463. The conserved G-protein beta	KSKGKGKSRGKGEEIFSSDEDDDAIGRDAPAEEEEEIAE
	WD-40 repeat domains are	EERETADEKRLRVAKAYLDKIRAITKANEEDNEEEAGED
	underlined.	EETEAERRGKRDSLVAEILQQEQLEESGRVQRQLASRVV
		TPSKLVECRVVKRHKQSVTAVALTEDDLRGFSASKDGTI
		IHWDVETGASEKYEWPSQAVSVSSSNEVSKTQKSKGSKK
		QGSKHVLSMAVSSDGRYLATGGLDRYIHLWDTRTQKHIQ
		AFRGHRGAVSCLAFRQGTQQLISGSFDRTIKLWSAEDRA
		YMDTLYGHQSEILAVDCLRKERVLSVGRDHTLRLWKVPE
		ETQLVFRGHAASLECCCFINNEDFLSGSDDGSIELWSML
		RKKPVFMAKNAHGHAIVENLSEDTSTREEPDEEVTTRQL
		PNGNSIGNGMTNQMGITPSVESWVGAVTVCRGTDLAASG
		AGNGVVRLWAIENSSKSLRALHDIPLTGFVNSLTFARSG
		RFLIAGVGQEPRLGRWGRIQAARNGVTLCPIELS
195	The amino acid sequence of SEQ ID	MAATFGTINTATSPHNPNKSFEIVQPPNDSISSLSFSPK
	464. The conserved G-protein beta	ANYLVATSWDNQVRCWEVLQTGASMPKAAMSHDQPVLCS
	WD-40 repeat domains are	TWKDDGTAVFSAGCDKQAKMWPLLTGGQPVTVAMHDAPI
	underlined.	KDIAWIPEMNLLATGSWDKTLKYWDTRQSNPVHTQQLPE
		RCFALSVRHPLMVVGTADRNLIIFNLQNPQTEFKRISSP
		LKYQTRCVAAFPDKQGFLVGSIEGRVGVHHVEEAQQSKN
		FTFKCHRDSNDIYAVNSLNFHPVHQTFATAGSDGAFNFW
		DKDSKQRLKAMARSNQPIPCSTFNSDGSLYAYAVSYDWS
		KGAENHNPATAKHHILLHVPQESEIKGKPRVTTSGRK
196	The amino acid sequence of SEQ ID	MVVMDKGTHQTNEDESESEFIDEDDVIDEISIDEEDLPD
	465. The conserved G-protein beta	ADVEGEDVQEDNKRSEPDENSSSLDDAIHTFEGHEDTLF
	WD-40 repeat domains are	AVACSPVDATWVASGGGDDKAFMWRIGHATPFFELKGHT
	underlined.	DSVVALSFSNDGLLLASGGLDGVVRIWDASTGNLIHVLD
		GPGGGIEWVRWHPKGHLVLAGSEDYSTWMWNADLGKCLS
		VYTGHCESVTCGDFTPDGKAICTGSADGSLRVWNPQTQE
		SKLTVKGYPYHTEGLTCLSISSDSTLVVSGSTDGSVHVV
		NIKNGKVVASLVGHSGSIECVRFSPSLTWVATGGMDKKL
		MIWELQSSSLRCTCQHEEGVMRLSWSLSSQHIITSSLDG
		IVRLWDSRSGVCERVFEGHNDSIQDMVVTVDQRFILTGS
		DDTTAKVFEIGAF
197	The amino acid sequence of SEQ ID	MPVFRTAFNGYAVKFSPFVETRLAVATAQNFGIIGNGRQ
	466. The conserved G-protein beta	HVLELTPNGIVEVCAFDSSDGLYDCTWSEANENLVVSAS
	WD-40 repeat domains are	GDGSVKIWDIALPPVANPIRSLEEHAREVYSVDWNLVRK
	underlined and the Trp-Asp (WD)	DCFLSASWDDTIRLWTIDRPQSMRLFKEHTYCIYAAVWN
	repeats signature is in bold.	PRHADVFASASGDCTVRIWDVREPNATIIIPAHEHEILS
		CDWNKYNDCMLVTGSVDKLIKVWDIRTYRTPMTVLEGHT
		YAIRRVKFSPHQESLIASCSYDMTTCMWDYRAPEDALLA
		RYDHHTEFAVGIDISVLVEGLLASTGWDETVYVWQHGMD
		PRAC
198	The amino acid sequence of SEQ ID	MDSRNRRSRLNLPPGMSPSSLHLETTAGSPGLSRVNSSP
	467. The conserved G-protein beta	STPSPSRTTTYSDRFIPSRTGSRLNGFALIDKQPQPLPS
	WD-40 repeat domains are	PTRSAAEGRDDASSSSASAYSTLLRNELFGEDVVGPATP
	underlined.	ATPEKSTGLYGGSRDSIKSPMSPSRNLFRFKNDHGGNSP
		GSPYSASTVGSEGLFSSNVGTPPKPARKITRSPYKVLDA
		PALQDDFYLNLVDWSSNNVLAVGLGTCVYLWSACTSKVT
		KLCDLGVNDSVCSVGWTPQGTHLAVGTNIGEVQIWDTSR
		CKKVRTMGGHCTRAGALAWSSYILSSGSRDRNILHRDIR
		VQDDFIRKLVGHKSEVCGLKWSYDDRELASGGNDNQLLV
		WNQQSAQPLLRFNEHTAAVKAIAWSPHQHGILASGGGTA
		DRCLRFWNTATDTRLNCVDTGSQVCNLVWCKNVNELVST
		HGYSQNQIMVWRYPSMSKLATLTGHTLRVLYLAISPDGQ
		TIVTGAGDETLRFWSIFPSPKSQSAVHDSGLWSLGRTHIR
199	The amino acid Sequence of SEQ ID	MEKKKVVVPIVCHGHSRPIVDLFYSPVTPDGLFLISASK
	468. The Conserved G-protein beta	DSSTMLRNGETGDWIGTFEGHKGAVWSCCLDNRALRAAS
	WD-40 repeat domains are	GSADFSAKIWDALTGDELHCFVHKHIVRACAFSESTSLL
	underlined.	LTGGHEKILRIFDLNRPDAPPKEVDNSPGSIRTVAWLHS
		DQTILSSNSDAGGVRLWDLRTEKIVRVLETKSPVTSAEV
		SQDGRYITTADGNSVKFWDANHFGMVKSYTMPCMVESAS
		LEPTMGNMFVAGGEDMWVRLFDFHTGEEIACNKGHHGPV
		HCVRFAPGGESYSSGSEDGTIRIWQTLNMNSEENESYGV
		NGLSGKVRVGVDDVVQKVEGFQITADGHLNDKPEKPNP
200	The amino acid Sequence of SEQ ID	MERYSQGTQKKSEIYTYEAPWQIYGMNWSVRKDKKFRLG
	469. The Conserved G-protein beta	IGSFLEEYNNRVEIIELDEESGEFKSDPRLAFDHPYPTT
	WD-40 repeat domains are	KIMFVPDKECQRPDLLATTGDYLRIWQVCEDRVEPKSLL
	underlined.	NNNKNSEFCAPLTSFDWNDADPKRIGTSSIDTTCTIWDI
		EKEVVDTQLIAHDKEVYDIAWGEVGVFASVSADGSVRVF
		DLRDKEHSTIIYESSQPETPLLRLGWNKQDPRFIATILM
		DSCKVVILDIRFPTLPVAELQRHQASVNTIAWAPHSPCH
		ICTAGDDSQALIWELSSVSQPLVEGGGLDPILAYTAAAE
		INQLQWSSMQPDWVAIAFSNEVQILRV
201	The amino acid sequence of SEQ ID	MQSENNLDESLHLREVQELQGHTDTVWAVAWNPVTGIDG
	470. The conserved G-protein beta	APSMLASCSGDKTVRIWENTHTLNSTSPSWACKAVLEET
	WD-40 repeat domains are	HTRTVRSCAWSPNGKLLATASFDATTAIWENVGGEFECI
	underlined.	ASLEGHENEVKSVSWSASGMLLATCGRDKSVWIWDVQPG
		NEFECVSVLQGHTQDVKMVQWHPNRDILVSASYDNSIKV
		WAEDGDGDDWACMQTLGNSVSGHTSTVWAVSFNSSGDRM
		VSCSDDLTLMVWDTSINPAERSGNAGPWKHLCTISGYHD
		RTIFSVHWSRSGLIASGASDDCIRLFS
202	The amino acid sequence of SEQ ID	MKRAYKLQEFVAHASNVNCLKIGKKSSRVLVTGGEDHKV
	471. The conserved G-protein beta	NMWAIGKPNAILSLSGHSSAVESVTFDSAEALVVAGAAS
	WD-40 repeat domains are	GTIKLWDLEEAKIVRTLTGHRSNCISVDFHPFGEFFASG
	underlined and the Trp-Asp (WD)	SLDTNLKIWDIRRKGCIHTYKGHTRGVNSIRFSPDGRWV
	repeats signature is in bold.	VSGGEDNIVKLWDLTAGKLMHDFKCHEGQIQCMDFHPQE
		FLLATGSADRTVKFWDLETFELIGSAGPETTGVRAMIFN
		PDGRTLLTGLHESLKVFSWEPLRCYDAVDVGWSKLADLN
		IHEGKLLGCSYNQSCVGVWVVDISRVGPYAAGNVSRTNG
		HNEAKLASSGHPSVQQLDNNLKTNMARLSLSHSTESGIK
		EPKTTTSLTTTEGLSSTPQRAGIAFSSKNLPASSGPPSY
		VSTPKKNSTSRVQPTTNFQTLSRPDIVPVIVPRSNSLRP
		ETTSDVKKEMNNFGRVVPSTVSTKSTDVIKSGSNRDESD
		KIDSINQKRMTGNDKTDLNIARAEQHVSSRLDNTNTSSV
		VCDGNQPAARWIGAAKFRRNSPVDPVVSPHDRSPTFPWS
		ATDDGVTCQPDRQVTAPELSKRVVEPGRARALVASWETR
		EKALTADTPVLVSGRPPTSPGVDMNSFIPRGSHGTSESD
		LTVSDDNSAIEELMQQHNAFTSILQARLTKLQVIRRFWQ
		RNDLKGAIDATGKMGDHSVSADVISVLIERSEIFTLDIC
		TVILPLLTRLLQSETDRHLTVAMETLLVLVKTFGDVIRA
		TISATPTIGVDLQAEQRLERCNLCYVELENIKQILVPLI
		RRGGAVAKSAQELSLALQEV
203	The amino acid sequence of SEQ ID	MSTLEIEARDVIKIVLQFCKENSLHQTFQTLQNECQVSL
	472. The conserved G-protein beta	NTVDSLETFVADINSGRWDVILPQVAQLKLPRKKLEDLY
	WD-40 repeat domains are	EQIVLEMIELRELDTARAILRQTQAMGFMKQEQPERYLR
	underlined and the Trp-Asp (WD)	LEHLLVRTYFDPREAYHESSKEKRRSQIAQALASEVTVV
	repeats signature is in bold.	PPSRLMALIGQSLKWQQHQGLLPPGTQFDLFRGTAAVKA
		DEEEMYPTTLAHTIKFGKQSHPECARFSPDGQYLVSCSV
		DGFIEVWDYISGKLKKDLQYQADDSFMMHDDAVLCVDFS
		RDSEMLASGSQDGKIKVWRIRTGQCLRRLERAHSQGVTS
		LSFSRDGSQLLSTSFDSTARIHGLKSGKALKEFRGHTSY
		VNDAIFTSDGGRVITASSDCTVKVWDVKTTDCIQTFKPP
		PPLKGGDVSVNSVHLFPKNSEHIVVCNKASSIYIMTLQG
		QVVKSFSSGKREGGDFVAACISPKGEWIYCVGEDRNIYC
		FSQQSGKLEHLMKAHDKDIIGVTPHPHRNLLVTYSEDST
		MKIWKP
204	The amino acid sequence of SEQ ID	MDIELEDQPFDLDFHPSAPIVAVALITGRLQLFRYVDIS
	473. The conserved G-protein beta	SEPERLWTVTAHTESCRAARFINAGSSVLTASPDCSILA
	WD-40 repeat domains are	TNVETGQPVARLDNAHGAAINCLTNLTESTIASGDENGI
	underlined.	IKVWDTRQNSCCNKFKAHEDYISDMEFVPDTMQLLGTSG
		DGTLSVCNLRKNKVHARSEFSEDELLSVALMKNGKKVVC
		GSQEGVLLLYSWGYFKDCSDRFVGHPHSVDALLKLDEDT
		VLTGSSDGIIRVVSILPNKMIGVIGEHSSYPIERLAFSH
		DRNVLGSASHDQILKLWDIHYLHEDDEPETNKQEAVNDE
		NVDMDLDVDTEKRPRGSKRKKRAEKGQTSSQKQSSDFFA
		DI
205	The amino acid sequence of SEQ ID	MDRIQQIPHTCVARKINLPLGMSKESLALNLPANLAPTM
	474. The conserved G-protein beta	SPPSITYSDRFIPSRKASNFEEFALPDKTSPSPNSAGGQ
	WD-40 repeat domains are	SSSTNGEGRDDACAAYSALLRTELFPATPDKTEGCRRPV
	underlined.	IGSPSGNVFRFKSQQCKSQSPFSLCPVGEDGDLSETGAV
		ARKTTRKIPRSPFKVLDAPALQDDFYLNLVDWSSHNILA
		VGLSACVYLWSASSSKVTKLCDLGLDDNVCSVAWTQRGT
		YLAVGTNNGGVQIWDAAHCKQVRTMEGHCTRVGTLAWNS
		HILSSGGRDRNILQRDIRAQDDFVSKFSGHKSEVCGLKW
		SYDNRELASGGNDNQLFVWNQQSQQPVLKYNEHTAAVKA
		IAWSPHQHGLLASGGGTADRCIRFWNTATNTSLNCVDTG
		SQVCNLVWSKNVNELVSTHGYSQNQIIVWRYPTMSKLAT
		LTGHTLRVLYLAISPDGQTIVTGAGDETLRFWNVFPSSK
		TQQNTIRDMGVWSSGRTHIR
206	The amino acid sequence of SEQ ID	MAGGQGEGEEKVDKLSMELTEDVMKSMEIGAVFKDYNGK
	475. The conserved G-protein beta	INSLDFHRTNNYLVTASDDEAIRLFDTASATWQKTSYSK
	WD-40 repeat domains are	KYGVDLICFTNHQTSVLYSSKNGWDESLRHLSLMDNKYL
	underlined.	RYFKGHHDRVVSLCMSPKGECFMSGSLDRTVLLWDLRID
		KCQGLIRVRGRPAVAYDEQGLVFAISNEGGLIKMFDARL
		YDKGPFDTFVVEGDKSEASGIKFSNDGKLILLSTMDSNI
		HVLDAYQGTTVHSFSVEAVPNGGEAVPNGGTLEASFSPD
		GKFVISGSGNGNIHAWSVNSGKEVACWTTEGVIPAVVKW
		APRRLMFASGSSVLSLWVPDLSKLASLTGSNSNSAY
207	The amino acid sequence of SEQ ID	MHRVGSTGNTSNSSRPRREKRLTYVLNDANDSRHCSGIN
	476. The conserved G-protein beta	CLVISKLSLLGGNDYLFSGSRDGTLKRWELADDSAVCSA
	WD-40 repeat domains are	TFESHVDWVNDAVLTGETLVSCSSDTTLKTWRPFSDGVC
	underlined.	TRTLRQHSDYVTCLAAASKNSNIVASGGLGREVFIWDIE
		AAMAPVSRTSEAMDDDTSNGVLSSGNSVLSTTVRSTNAT
		NSASLHTSQLQGYTPIAAKGHKESVYALAMNDVGTLLVS
		GGTEKVVRVWDPRSGAKQMKLRGHTDNVRALILDSTGRF
		CLSGSSDSIIRLWDLGQQRCVHSYAVHTDSVWALASTPN
		FSHVYSGGRDLSLYLTDLTTRESLLLCMEKHPLLRLTLQ
		DDSIWVATTDSSLHRWPAEGQNPPKMFQRGGSFLAGNLS
		FTRARACLEGSAPVPVNTQPSFVIPGSPGIVQHEILNNR
		RHVLTKDAEGTVKLWEITRGAVLDDYGKVSFEEKKEELF
		EMVSIPAWFTMDTRLGSMSVHLDTPQCFTAEMYAVDLNV
		PDAPEEQKINLAQETLRGLLAHWLSRRRQRLATQASANG
		DFPAGQENALRNHISSRIDVHDDAETHIAGILPAFDFST
		TSPPSIITEGSQGGPWRKKITDLDGTEDEKDFPWWCLEC
		VLHGRLSPRESLKCSFYLHPYEGTTVQVLTQGKLSAPRI
		LRIQKVINYVLEKMVLDRPLDSSNSETTFTPGLSGNQSH
		AAVVGDGSLRSGARVWQQKAKPLVEILCNNQVLSPDMSL
		ATVRTYIWKKPDDLYLYYRLVQNR
208	The amino acid sequence of SEQ ID	MMKGKTIQMQAAHQNHDGETSVACVLWDWHAKHLITAGA
	477. The conserved G-protein beta	DNTILIHSYPSSSSSKPITLRHHKNAVTALAINSNVRSL
	WD-40 repeat domains are	ASGSVDHSVKLYSYPGGEFQSNVTRFTLPIRSLAFNKSG
	underlined.	ELLAAAGDDEGIKLISTIDNSIARVLKGHNGPVTSISFD
		PKNEFLASSDSDGTVIYWELSTGKPVHTLKKIAPNTTSN
		PTSLNQISWRPDGEMLAVPGRKSEVSMYDRDTAEKLFSL
		KGGHSDTICSLAWSPNGKYIATAGTDRQVMVWDADRRQD
		IDKQRFDNPICSVAWKPSDNALAVIDVLGRFGVWESPIA
		SHMKSPADGAERYDNMEDEEPLMARYEEELEDSVSGSLN
		EIINDDDDDDEMGKIPRKILQKKPSVKVEKGKEESNAKA
		FKSGQDSFKLKSAMQEAFQPGATQRQSGKRNFLAYNMLG
		SVITFDNDGFSHIEVDFHDIGKGCRVPSMTDYFGFTMAS
		LSESGSVFGSPQKGEKNPSTLMYRPFSSWANNSEWSMRF
		PMGEEVKAVALGSGWVAAVTSLNFLRVFSEGGLQKFVLS
		MDGPVVTAAGYENLLVVVSHASNPLLSGDQVLSFTVYDI
		SQKTCPLSGRLPLSPGSHLTWLGFSEEGLLSSYDSEGNL
		RVFTNDYNGCWVPIFSAARERKSETESIWMVGLNSTQVF
		CVVCKLPDTYPQVAPKPVLSVLNLSLPLACSDLGADDLE
		NEYLRGSLLLSQMQKKAEDAVACGRESNMEEDSIFKMEA
		ALDRCLLRLIANCCKGDKLVRATELARLLSLEKSLQGAI
		KLVSAMKLPMLAERFNTILEEKILQENMETISCRRLTSE
		AQDMDTPISISVKQVSYGANLGDSPFLPNRQVEPKHSTP
		VFSKPDTKIEVDTSEAIAKGCDAQNGNIKSGDAEVQPAS
		HNDSIQKPSNPFAKASNTSANQAVQRNASLLSSIKQMKT
		ATENEGKRKERARSGSLPQKPAKQSKIS
209	The amino acid Sequence of SEQ ID	MKQKRKGHQVDDPKYSVQTPQEDDTPNESGPASEEVESS
	478. The conserved G-protein beta	DEEGGNSSNIEDDIIYSSSEEDPVVSSDYEEDEDAESDA
	WD-40 repeat domains are	EGVTAEQELEGDIDNALQNYMGTLTVLSNFHGENLKNAE
	underlined.	GEDTSGDDDDEEEMPKRAEESDSPEDENDERPKRAEESD
		FSEDEDEERPKRAEESDSSEDEVPSRNTVGDVPLRWYKD
		EQHIGYDIKGKKIKKQPKKDQLDSFLASTDDSSDWRKVY
		DEYNDEEVELTKDEIKFISRLRKGTIPHADVNPYEPYVD
		WFDWKDKGHPLSNAPEPKRRFIPSKWEAKKVVKLVRAIR
		KGWITFQKAEEKPRFYLMWGDDLKPSEKMANGLSYIPAP
		KPKLPGHEESYNPPPEYIPTQEEINSYQLMYEEDRPKFI
		PKRFDSLRNVPAYDRFLSEIFERCLDLYLCPRTRKKRIN
		IDPESLIPKLPKPKDLQPFPSICFLEYKGHTGAVSCISP
		ESSGQWLASGSKDGTVRIWEVETARCLKVWDIGRPIQHI
		AWNPVSQLSILAVAVDEEVLVLNTGLGSEDSQEKVAELL
		HVKSKPVSADDLGDNTSLTKWIKHEKFDGIKLTHLKPVH
		LISWHHKGDYFATVAPDGNTRAVLVHQLSKQQTQNPFKK
		MQGRVVHVLFHPSRAIFFVATKTHVRVYDLVKQQLVKRL
		VTGLHEVSSMAVHHKGDNLLVGSKEGKVCWFDMDLSTQP
		YKTLKNHSKDIHSVAFHDSYPLFASCSDDCKAYVFYGLV
		YSDLLQNPLIVPLKVLQGHQSVNGMGVLDCQFHPKQPWL
		FTAGADSVVKLYCN
210	The amino acid sequence of SEQ ID	MMSLKRGFEESLVPAKRQKTELSTVTYGDGPRRTSSLES
	479. The conserved G-protein beta	PIMLLTGHHAAIYTMKFNPTGTVIASGSHEREIFLWNVH
	WD-40 repeat domains are	GDCKNFMVLKGHKNAVLDLHWTTDGCQIISASPDKTLRA
	underlined.	WDVETGKQIKKMAEHSSFVNSCCPSRRGPPLVVSGSDDG
		TAKLWDLRHRGAIQTFPDKYQITAVGFSDAADKIYSGGI
		DNEIKVWDLRRGEVTMRLQGHTDTITGMQLSSDGSYLLT
		NSMDCSLRIWDMRPYAPQNRCVKILTGHQHNFEKNLLKC
		SWSSDGSKVTAGSADRMVYIWDTTTRRILYKLPGHTGSV
		NETGFHPTQPIIGSCSSDKQIYLGEIEPNVGYQAVI
211	The amino acid sequence of SEQ ID	MEFSDTYKHTGPCCFSPDARYLAIAVDYRLVIRDVVTLK
	480. The conserved G-protein beta	VVQLYSCMDKISNIEWALDSEYILCGLYKRAMVQAWSLS
	WD-40 repeat domains are	QPEWTCKIDEGPAGIAHARWSPDSRHIITTSDFQLRLTV
	underlined.	WSLVNTACIHIQWPKHASKGVSETQDSKfAAIATRRDCK
		DYVNLLSCHTWEVMGTFTVDTIDLADLEWSPNDSAIVVW
		DSPLEYKVLIYSPDGRCLFKYQAYDSWLGVKTVAWSPCS
		QFLAVGSYDQTLRTLNHLTWKPFAEFVHVSTVRGPASAV
		VFKEVEEPWNLDVSGLHLNDDNAHDIQDGKPAEGHSRVR
		YKVVEFPVNVSSQKHPVDKPNPKQGIGLLAWSRDSQYLF
		TRNDNMPTALWIWDICRLELAALLIQKEPIRAAAWDPVY
		PRVALCTGSSHLYMWTPSGACCVNIPLPQFVVSDLKWNP
		DGTSMLLKDRESFCCTFVPMLPEFNDDETNEE
212	The amino acid sequence of SEQ ID	MAKLIETHSCVPSTERGRGILIAGDAKTNSIIYCNGRSV
	481. The conserved G-protein beta	IMRNLDNPLEASVYGEHSYPATVARFSPNGEWVASGDTS
	WD-40 repeat domains are	GTVRIWGRGSDHTLKYEYKALAGRIDDLEWSADGQRIVV
	underlined.	CGDSKGKSMVRAFMWDSGTNVGEFDGHSRRVLSCSFKPT
		RPFRVATCGEDFLVNFYEGPPFRFKTSHRDHSNYVNCVR
		FAPDGSKFITVGSDRKGVIFDGKMGEKIGELSKEGGHTG
		SIYAASWSPDSKQVLTVSADKSAKIWEISETGNGTVKKT
		LTFGSQGGADDMLVGCLWLNDYLITVSLGGIVSLLSAVD
		PDKPPKTISGHMKSINAIALSLQSGQSEVCSSSYDGVIV
		RWILGVGYAGRVERKDSTQIKCLATIEGELVTCGFDNKV
		RRVPLLSEQHKESEPIDIGAQPKDLDVAVGCPELTFVST
		DAGIIIIRASKIVSTTNVGYAVTAAAISPDGTEAVVGGQ
		DGKLRVYSIKGDTLLEESVLERHRGPINAIRFSPDGSMF
		ASGDLNREAVVWDRITREVKLKNMVYHTARINCIAWSPD
		SSKVATGSLDTCILIYEVGKPASSRITIKGAHLGGVYGL
		AFSDQSTVISAGEDACVRVWSLP
213	The amino acid sequence of SEQ ID	MPQPSVILATAGYDHTVRFWEATSGRCYRTLQYPDSQVN
	482. The conserved G-protein beta	HLEITPDKQYLAAAGNPHIRLFEVNSNNPQPVISYDSHT
	WD-40 repeat domains are	NNVTAVGFQCDGKWMYSGSEDGTVKIWDLRAPGFQREYE
	underlined and the Trp-Asp (WD)	SRAAVNTVVLHPNQTELISGDQNGNIRVWDLNANSCSCE
	repeats signature is in bold.	LVPEDTAVRSLTVMWDGSLVVAANNHGTCYVWRLMRGTQ
		TMTNFEPLHKLQAHNSYILKCLLSPEFCEHHRYLATTSS
		DQTVKIWNVDGFTLERTLTGHQRWVWDCVFSVDGAFLVT
		ASSDSTARLWDLSTGEAIRTYQGHHKATVCCALHDGTDG
		ASC
214	The amino acid sequence of SEQ ID	MLTKFETKSNRVKGLSFHPKRPWILASLHSGVIQLWDYR
	483. The conserved G-protein beta	MGTLIDKFDEHDGPVRGVHFHKTQPLFVSGGDDYKIKVW
	WD-40 repeat domains are	NYKMRQCLFTFVGHLDYIRTVHFHNEYPWIVSASDDQTI
	underlined and the Trp-Asp (WD)	RLWNWQSRVCISVLTGHNHYVMSASFHPKEDLVVSASLD
	repeats signature is in bold. The	QTVRVWDISGLRKKTVSPADDLSRLAQMNTDLFGGGDVV
	coatomer WD associated region is	VKYVLEGHDRGVNWAAFHTSLPLIVSGADDRQVKLWRMN
	in bold/italics.	DTKAWEVDTLRGHTNNVSCVIFHARQDIIVSNSEDKSIR
		VWDMSKRTSVQTFRREHDRFWILAAHPEMNLLAAGHDSG
		MIVFKLERERPAYVVYGGSLLYVK
		IPVLPPGKKSSLLMPPAPILHGGDWPLLRVTKGIFE
		GGLENSTSAAYEEEDEEAAADWGEDIDIENIEGENGEAT
		VLDDQEVKGGEDDEGGWDMEDLELPPDVAAANVGTNQKT
		LFVAPTLGMPVSQIWMQKSSLAGEHAAAGNFETALRLLT
		RQLGIKNFSPLKPLFLELYMGSHTFLPSFASVPAFSLAL
		QRGWSESASPNIRGPPALVYRLSVLEEKLTVAYRATTEG
		RFSEALRLFL
215	The amino acid sequence of SEQ ID	MDLLQNYQDDSEDSNPELRNHPPLEDATATSAPAGVENE
	484. The conserved G-protein beta	TSSSPDSSPLRLALPAKSCAPDVDETLMALGVPGSEKKN
	WD-40 repeat domains are	NHNKPIDPTQHSVTFNPSYDQLWAPLYGPAHPYAKDGIA
	underlined.	QGMRNHKLGFVEDSAIEPFMFDEQYNTFHRYGYAADPSA
		SLGSHIVGDLESLKKNDGASVYNLPKREHKRQKLEKKMI
		QKDENEEEEKEVGEEVDNPSTEEWLKKNRKSPWAGKKEG
		LQTELTEEQKKYAQEHAEKKGDREKGEKVEIVDKTTFHG
		KEERDYQGRSWIDPPKDAKATNDHCYIPKRWVHTWSGHT
		KGVSAIRFFPKYGHLLLSAGMDTKVKIWDVFNSGKCMRT
		YMGHSKAVRDISFSNDGSRFLSAGYDRNIKLWDTETGKV
		ISTFSTGKIPYVVKLHPDEDKQNVLLAGMSDKKIVQWDM
		NSGEITQEYDQHLGAVNTITFVDNNRRFVTSSDDKSLRV
		WEFGIPVVIKYISEPHMHSMPSISLHPNTNWLAAQSLDN
		QILIYSTRERFQLNKKKRFAGHIAAGYACQVNFSPDGRF
		VMSGDGEGRCWFWDWKTCKVFRTLKCHDNVCIGCEWHPL
		EQSKVATCGWDGMIKYWD
216	The amino acid sequence of SEQ ID	MARKGLGTDPAIGSLMSSKKRKEYKVTNRFQEGKRPLYA
	485. The conserved G-protein beta	IAFNFIDARYHNIFATAGGTRVTIYQCLEGGAISVLQAY
	WD-40 repeat domains are	VDDDKDESFYTLSWACDVNGSPLLVAGGHNGIIRVLDVA
	underlined and the Trp-Asp (WD)	NEKVHKSFVGHGDSVNEIRTQALKPSLILSASKDESVRL
	repeats signature is in bold.	WNVQTGICILIFAGAGGHRNEVLSVDFHPSDVYRIASCG
		MDNTVKIWSMKEFWTYVEKSFTWTDLPSKFPTKYVQFPV
		FIAAVHSNYVDCTRWLGNFILSKSVDNEVVLWEPYSKEQ
		STSDGVVDILQKYPVPECDIWFIKFSCDFHYNSMAVGNR
		EGKVYVWELQSSPPNLIARLSHAHCKNPIRQTAISHDGS
		TILCCCDDGSMWRWDVVQ
217	The amino acid sequence of SEQ ID	MESGAGGSVGARVPSAKPEMLQQPPYSNGDDDNDMERGT
	486. The conserved G-protein beta	APVPSSNPNTVSKWELDKDFLCPICMQTMKDAFLTACGH
	WD-40 repeat domains are	SFCYMCIMTHLNNKSNCPCCSLYLTNNQLFPNFLLNKLL
	underlined and the Trp-Asp (WD)	KKTSACQMASTASPVENLCLSLQQGAEVSVKELDFLLTL
	repeats signature is in bold.	LAEKKRKMEQEEAETNMEILLDFLQRLRQQKQAELNEVQ
		ADLHYIKDDILALEKRRLELSRARERYSRKLHMLLDDPM
		DTTLGHAAIDDGNNVRTAFVRGGQGDAISGKFQQKKAEI
		KAQASSQGMQKRANFCHSDSQVLPTLSGLTIARKRRVLA
		QFDDLQECYLQKRRRWATQLRKQCDGGLRKERDGNSISR
		EGYHAGLEEFQSILTTFTRYSRLRVISELRHGDLFHSAN
		IVSSIEFDRDDELFATAGVSRRIKVFDFATVVNEPADVH
		CPVVEMSTRSKLSCLSWNKCIKSQIASSDYEGIVTVWDV
		NTRQSVMMYEEHEKRAWSVDFSRTEPTRLISGSDDGKVK
		VWCTRQETSVLNIDMKANICCVKYNPGSSYYVAVGSADH
		HIHYYDLRNPSVPLYEFNGHRKTVSYVKFISTNELASAS
		TDSTLRLWDVRDNCLVRTFKGHTNEKNFVGLTVNSEYIA
		CGSETNGVFVYHKAISKPAAWHQFGSPDLDDSDDDTSHF
		ISAVCWKSESPTMLAANSQGTIKVLVLAP
218	The amino acid sequence of SEQ ID	MANYVDSKKNFKCVPALQQFYTGGPFRLSSDGSFLVCAC
	487. The conserved G-protein beta	NDEVKVVDLATGSVKNTLEGDSELIVALALTPDNKYLFS
	WD-40 repeat domains are	ASRSTQIKFWDLSSATCKRTWKAHNGPVADMACDASGGL
	underlined.	LATAGADRSILVWDVDGGYCTHSFRGHQGVVTTVIFHPD
		PHCLLLFSGSDDATVRIWDLVAKKCISVLEKHFSTVTSL
		AISENGWNLLSAGRDKVVNIWDLRDYHCRATIPTYEPLE
		AVCVLPTGSRLVSVMNQSRALPENRKKSGAAPVYFLTVG
		ERGIVRIWYSEGALCLYEQKSSDAIISSDKDELKGGFVS
		AVLLPLTQGVMCVTADQRFLFYNLDESDEGKCDLKVSKR
		LIGYNEEIVDLKFLGDEEKFLAVATNLEQVRMYDLSSMT
		CVYELSGHTDIVLCLDTVVFSGHSLLASGSKDHTVRIWD
		TESKSCICVAAGHMGAVGAVAFSKKAKNFFVSGSSDRTI
		KVWSFASVLDFGGISKSIKLSSQAAVAAHDKDINSVAVA
		PNDSLICTGSQDRTARIWRLPDLVPVLVLRGHKRGVWCV
		EFSPVDQCVMTASGDKTIKIWALSDGSCLKTFEGHTASV
		LRASFLTRGTQFVSSGADGLLKLWTIKSNECIATFDQHE
		DKIWAMAVGKKTEMLATGGSDSLVNLWHDCTTTDEEEAL
		LKEEEAALKDQELLNALADTDYVKAIQLAFELRRPYKLL
		NVFTELYSKGHAQDQIQKVIRELGNEELRLLLEYVREWN
		TKPKFAHVAQFVLFQLFNVLPPKEIIEVQGISELLEGLI
		PYAQRHYSRIDRLMRSTFLLDYTLSSMSVLSPTETDLSS
		SNLLARTADPLHAQIDQFHPTHFPEPNLTPIQSLLDSGN
		TDSVEVTARRAKKKRVSGNDSEKTTVAEVKIGDMENAFD
		EPDVADQGSSRKHKPASSKKRKSIAVGNASIKRIASGNA
		VTIALQV
219	The amino acid sequence of SEQ ID	MESSCSSMNSNRHSTEKRCLRPLQKQGASMNKHSSDRFI
	488. The conserved G-protein beta	PARGSIDLDVARFMVTQKQKDNNDIHALSPSPSPSKKAY
	WD-40 repeat domains are	QKEMADTLLKNAGAADNNCRILSFNGKSSTVSQGSQENV
	underlined.	LANLSISRRARRYIPQSADRTLDAPDLLDDYYLNLLDWS
		STNVLSTALGNTVYLWDASNSSISELLIADEEEGPVTSV
		SWAPDGSQIAVGLNNSVVQLWDSQSNKKLRALKGHHDRV
		GALSWNGPILTTGGLDGIIINHDVRTRDHIVQTYKGHTQ
		EVCGLKWSPSGQQLASGGNDNLLYIWDKSMASHNPSSQY
		FHQLDEHCAAVKALAWCPFQTNLLASGGGTSDGSIKFWN
		TQTGACLNTVDTHSQVCSLLWNRHERELLSSHGLNQNQL
		TLWKYPSMVKITELTGHTARVLHMAQSPDGYTVASAAAD
		ETLKFWQVFGAPDASKKTKDTKGAFNMFHMHIR
220	The amino acid sequence of SEQ ID	MLDEIVADEEEEFNIWKKNTPLLYDVVITHALEWPSLTV
	489. The conserved G-protein beta	QWLPDRHQSPTKDYSLQKMIVGTHTSGDEPNYLMIAEVQ
	WD-40 repeat domains are	MPLQYSEDGNVGGFESTEAKVHIIQQINHEGEVNRAQYM
	underlined.	PQNSFIIATKTVSSDVYVFDYTKHSSNAPQERVCNPELI
		LKGHTNEGYSLSWSPLKEGQLLSGSNDAQICFWDINAAS
		GRKVVEAKQIFKVHEGAVEDVSWHLKHEYLFGSVGDDCH
		LLIWDTRTAAPNKPQHSVVAHESEVNSLAFNPFNEWLLA
		TGSADKTVKLFDLRKLSCSLHTFSNHTEEVFQIEWSPMN
		ETILASSGGDRRLMVWDLRRIGDEQTSEDAEDGPPRLIF
		IHGGHTSKISDFSWNLHDDWLIASVAEDNILQIWQMAEN
		IYHDDADIL
221	The amino acid sequence of SEQ ID	MTKEDHGESRDEMGERMVNEEYKLWKKNTPFLYDLVITH
	490. The conserved G-protein beta	ALEWPSLTVQWLPPSCKQQQDIIKDDDIDHPNTQMVILG
	WD-40 repeat domains are	THTSDNEPNYLILAEVQLHDGTEDEDGDGDVKRPQDKMK
	underlined.	PGTSGGAMGKVRILQQINHQKEVNRARYMPQKPTIIATK
		TVNADVYVFDYSKHPSKPPQEGRCNPELRLQGHESEGYG
		LSWSPLKEGHLLSASDDAQICLWDITAATKAPKVVEANQ
		IFRYHDGPVEDVAWHAIHDHLFGSVGDDHHLLLWDIRND
		SEKPLHIVEAHQAEVNCLAFNPFNEWIVATGSADRTVAL
		HDIRKLDKVLHTCAHHMEEVFQIGWSPQNGAILASCGSD
		RRLMVWDLSRIGDEQNPEDAEEAPPELLFIHGGHTSKIS
		DFSWNPAEEWVIASVAEDNILQVWQMSEHIYNDDNDSPTA
222	The amino acid sequence of SEQ ID	MAMAMGDENAADPVEEFNIWKKNTPFLYDLVITHALEWP
	491. The conserved G-protein beta	SLTVQWLPDRHQSSTADYSLQKMIVGTHTSEDEPNYLMI
	WD-40 repeat domains are	AEVQIPLQNSEDNIIGGFESTEAKVQIIQKINHEGEVNK
	underlined.	ARYMPQNSFVIATKTVSSDVYVFDYSKHPSKAPQERVCN
		PELILKGHSNEGYGLSWSPLKEGYLLSGSNDAQICLWDI
		NAAFGKKVLEANQIFKVHEGAVGDVSWHLKHEYLFGSVG
		DDCHLLIWDMRTAAPNKPQQSVIAHQSEVNSLAFNPFNE
		WLLATGSMDKTVKLFDLRKLSCSLHTFSNHTDQVFQIEW
		SPMNETILASSGADRRLMVWDLARIGETPEDEEDGPPEL
		LFVHGGHTSKISDFSWNLNDDRVIASVAEDNILQIWQMA
		ENIYHDDEDML
223	The amino acid sequence of SEQ ID	MGLFEPFRALGYITDGVPFAVQRRGIETFVTLSVGKAWQ
	492. The conserved G-protein beta	IYNCAKLIPVLVGPQMDKKIRALACWRDFTFAATGHDIA
	WD-40 repeat domains are	VFRRAHQVATWSGHKAKVTLLLSFGQHVLSVDLEGCLFI
	underlined and the Trp-Asp (WD)	WAVAEVNQNKPPIGQIQLGEKFSPSCIMHPDTYLNKVLI
	repeats signature is in bold.	GSEEGTLQLWNVNTRKKLYEFKGWGSSIRCCVSSPALDV
		VGIGCSDGKIHVHNLRYDEEIVTFMHSTRGAVTALSFRT
		DGQPLLAAGGSSGVISIWNLEKKKLQSVIKDAHDSSVCS
		LHFFANEPVLMSSATDNSIKMWIFDTTDGEARLLKYRSG
		HSAPPMCIRYYGKGRHILSAGQDRAFRIFSVIQDQQSRE
		LSQGHVGKRAKKLKVKDEEIKLPPVIAFDAAEIRERDWC
		NVVTCHLDDPCAYTWRLQNFVIGEHILKPCLEDPTPVKS
		CSISACGNFAVLGTEGGWLERFNLQSGISRGTYIDIGEK
		RQCAHNGAVVGLACDATNTLLISGGYNGDIKVWDFKGRE
		LKFRWEIEVPLIKIVYHPGNGILATAADDMILRLFDVTA
		MRLVRIFVGHMDRVTDLCFSGDGKWLLSSSMDGTIRVWD
		IISSRQLNAMHMDSAVTALSLSPGMDMLATTHVGHNGIY
		LWANRMIYSKATDIEPFISGKQVVKVSMPTVSSKRESEE
		GDEKRTIVAESNVNKSDVSGSLIGDSYSAQLTPELVTLA
		LLPKAQWQSLVNLDIIKMRNKPIEPPKKPEKAPFFLPSL
		PTLSGERIFIPSSMNGDGDQDETRNDKTVFEARGKKLGG
		ESLSFMQLLQSCAKIKDFTTFTNYLKGLSPSAVDMELRL
		LQIVDNENISETEHSVELQGIGMLLDYFVNEVSCNNNFE
		FVQALIRLFLKIHGETIRCQVSLQEKARKLLEIQSSTWE
		RLDTSFQNARCMITFLSSSQF
224	The amino acid sequence of SEQ ID	MIAAVCWVPKGVAKVLPDSAEPPTQEEIQELLKCNVVAE
	493. The conserved G-protein beta	SDDNEDSDEESEEMDTETDKNTDAVAKALAAANALGSQS
	WD-40 repeat domains are	SDFQRQHKVDDIANGLKELDMDHYDDEDEGIDIFGSGSL
	underlined and the Trp-Asp (WD)	GNCYYPANDMDPYLVEQDDDDEDEIEDMTIKPSDLIILS
	repeats signature is in bold.	ARNEDDVSHLEVWIYEEETEEGGSNMYVHHDIILPAFPL
		SLAWLDCNLKGGEKGNFVAVGTMQPEIELWDLDVLDEVE
		PAVVLGGAVKDEASGKTTKLKKKKKNKQAVNFKEGSHTD
		AVLGLAWNMEYRNVLASASADKSVKIWDIVAEKCEHTMQ
		PHTDKVQAVAWNPNQATVLLSGSFDRSVIMMDMRAPTHS
		GIRWPVPADVESLAWDPHTDHSFMVSAEDGTVRGFDIRA
		AASTADFDGKPMFILHAHDKAVCAISYNPAAPSLLTTGS
		TDKMVKLWDITNNQPSCIASTNPNVGAVFSAAFSKNSPF
		LLATGGSKGILHVWDTLDNSEVARRFGKFRPQN
225	The amino acid sequence of SEQ ID	MIMDENEFCDIFSLRKRLCLLSSQEGEEEEELEAMSQLD
	494. The conserved eukaryotic	AGEFTVTGNEEVVAIAEDDVNTGILSQDLFSSQDYCTPS
	protein kinase domain is	QPQDSTDLDSKDKAPCPLSPVKSTIQRKRCRPELLSNPP
	underlined.	DSIQFSFQRLERVRSEESIQSSSQQLARVRSEVSSSDDF
		KTPKITASGQKNYVSQSALALRARVMSPPCIKNPYLDEN
		EELNEKIQRSTRRSPACVTPIQSGACLSRYRADFHELEE
		IGRGNFSRVYKALNRLDGCCYAVKCSQSELRLDTERKVA
		LMEVQSLAALGPHKNIVGYHTAWFENDHLYIQMELCDHN
		LTTANDRGILRTDTDFLEAVYQIAQALEFIHGRGVAHLD
		VKPENIYVRDGTYKLGDFGRATLINGTLHVEEGDARYMS
		REILNDNYEHLDKVDMFSLGATFFELLMRKQYPGSGKRI
		DRDTEIKIPILPGFSIYFQKLLQDLVSNDPGKRPSAKDV
		LKNPIFNKVRGAKEV
226	The amino acid sequence of SEQ ID	MLAPALEMEPVEPQSLKKLSFKSLKRALDLFSPVHGQIA
	495. The conserved G-protein beta	PPDPESKKMRISYKLNFEYGGGSGSEDQVPKRKESGAAQ
	WD-40 repeat domains are	NQGQQAAGASNALALPGPEGSKIPPMEKSQNALTVGPSL
	underlined and the Trp-Asp (WD)	RPQGLNDVGLHGKGTAIISASGSSDRNLSTSAIMERLPS
	repeats signature is in bold.	RWPRPVWHPPWKNYRVISGHLGWVRSIAFDPSNQWFCTG
		SADRTIKIWDLASGRLKLTLTGHIEQIRGLAVSSKHTYM
		FSAGDDKQVKCWDLEQNKVIRSYHGHLSGVYCLALHPTI
		DILLTGGRDSVCRVWDIRSKMQIFALSGHDNTVCSVFAR
		PTDPQVVTGSHDTTIKFWDLRHGKTMTTLTNHKKSVRAM
		AQHPKENCFASASADNIKKFQLPRGEFLHNMLSQQKTII
		NTMAVNEEGVMATGGDNGSLWFWDWKSGHNFQQAHTIVQ
		PGSLESEAGIYALSYDLTGSRLVSCEADKTIKMWKEDEL
		ATPETHPLNFKPPKDIRRF
227	The amino acid sequence of SEQ ID	MEEAAKEQSAGSGKPKLLRYGLRSAAKPKEDKKEEQLHQ
	496. The conserved G-protein beta	PPPPPPPQQQAAPAPAPAATRSSTSGSAGGRDRRPQQQH
	WD-40 repeat domains are	AVDEKYARWKSLVPVLYDWLANHNLLWPSLSCRWGPQLE
	underlined.	QATYKNRQRLYISEQTDGSVPNTLVIANCEVVKPRVAAA
		EHVSQFNEEARSPFIRKYKTIIHPGEVNRIRELPQNPNI
		VATHTDSPDVLIWDVESQPNRHAVYGATASRPNLILTGH
		QENAEFALAMCPAEPFVLSGGKDKTVVLWSIQDHITASA
		TDQTTNKSPGSGGSIIKKTGEGNEETGNGPSVGPRGIYC
		GHEDTVEDVAFCPSTAQEFCSVGDDSCLILWDARIGTNP
		VAKVEKAHNGDLHCVDWNPHDNNLILTGSADNSVNMFDR
		RNLTSNGVGSPVYKFEGHKAAVLCVQWSPDKPSVFGSSA
		EDGLLNIWDYERVDKKVDRAPNAPAGLFFQHAGHRDKIV
		DFHWNTADPWTMVSVSDDCDTAGGGGTLQIWRMSDLIYR
		PEEEVLAELENFKAHVLECSKA
228	The amino acid sequence of SEQ ID	MAKDEEEFRGEMEERLVNEEYKIWKKNTPFLYDLVITHA
	497. The conserved G-protein beta	LEWPSLTVQWLPDREEPPGKDYSVQKMILGTHTSDNEPN
	WD-40 repeat domains are	YLMLAQVQLPLEDAENDARQYDDERGEIGGFGCANGKVQ
	underlined.	VIQQINHDGEVNRARYMPQNPFIIATKTVSAEVYVFDYS
		KHPSKPPQDGGCHPDLRLRGHNTEGYGLSWSPFKHGHLL
		SGSDDAQICLWDINVPAKNKVLEAQQIFKVHEGVVEDVA
		WHLRHEYLFGSVGDDRHLLIWDLRTSATNKPLHSVVAHQ
		GEVNCLAFNPFNEWVLATGSADRTVKLFDLRKISSALHT
		FSCHKEEVFQIGWSPKNETILASCSADRRLMVWDLSRID
		EFQTPEDALDGPPELLFIHGGHTSKISDFSWNPCEDWVI
		ASVAEDNILQIWQMAENIYHDEEDDMPPEEVV
229	The amino acid sequence of SEQ ID	MGKYMRKGKGVGEVAVMEVSQGSLGVRTRARTLAAASSQ
	498. The conserved cyclin-	KDHRRLGASKSVTTKHQSSAPPASPCVESSMHTCYLELR
	dependent kinase inhibitor domain	SRKLEKFSRCYHSAHGATSHGESKRSLSLSEPSRLAVSE
	is underined.	EARVASDKSSHRVLQQQSSVAHSRNNSATFSHNAKPAKA
		AQRKERRDDDHTSARPSEAPHEDEDGMEVEASFGENVMD
		LDSRERRTRETTPSSYTRDVETMETPGSTTRPPSNAGRR
		RFQTEGGHGTRNQFHVPTTNEIEEFFAGAEQQEQRRFTD
		RYNYDPVSDSPLPGRFEWVRLRP
230	The amino acid sequence of SEQ ID	MQNMEENVQSSWSLHGNKEICARYEILKRVSSGTYLDVY
	499. The conserved	RGRRKEDGLIVALKEVHDYQSSWREIEALQRLCGCPNVV
	serine/threonine protein kinase	RLYEVILEFLTSDLYSVIKSAKNKGENGIPEAEVKAWMI
	domain is underlined, and the	QILQGLANCHANWVIHRDLKPSNMLISAYGILKLADFGS
	serine/threonine protein kinase	MSFLKRAIYEVEYELPQEDILADAPGERLMDEDDSVKGV
	active-site signature is in bold.	WNEGEEDSSTAVETNFDDMAETANLDLSWKNEGDMVMQG
		FTSGVGTRWYRAPDFLYGATIYGKEIDLWSLGCILGELL
		ILEPLFSGTSNIDQLSRLVKVLGLQQKKNWPGCSNLPDY
		RKLCFPGDGSPVGLKNHVPNCSDNMFSILERLVCYDPAA
		RLNAKEIVENKYFVEDPYPVLTHELRVPSPLREENNFSE
		DWAKWKDMEVDSDLENIDEFNVVHSSDGFCIKFS
231	The amino acid sequence of SEQ ID	MADVPESLQQEKDEQGTDKNCCDGKFQKEIDIDDMEEEY
	502. The conserved histone	NESSIDDEEENLSDNVATNNMGTTPQGQACMAVTVEGIE
	deacetylase family domain is	HANSVGCGRNGREGSEEVTAAEDMGHVSIENIREQGRNR
	underlined	KSSEQLLALYEQEGLLEDDEDDDDVDWEPFEGVTVQMKW
		YCTNCTMANSDDSVHCDSCGEHRNSDILRQGFLASPYLP
		AESPSSSDVPDERLEESKCVMTTLTPSISPMIGVCCSSL
		QSERRTVVGFDERMLLHSEIQMETYPHPERPDRLRAIAA
		SLRAAGLFPGKCFSIPAREATCEELQTIHSLEHVNAVES
		TSCGMLSHLSPDTYANEHSSLAARLAAGLCADLAKAIMT
		GQAQNGFALVRPPGHHAGVKDSMGFCLHNNAAIAVSASR
		VVGAKKVLIVDWDVHHGNGTQEIFEADQSVLYISLHRHG
		EGFYPGSGAVTEVGSSKGEGYSVNIPWKCGGVGDNDYIF
		AFQHAVLPIAEQFEPDLTIISAGFDAAKGDPLGRCEVTP
		DGFAHMAQMLSCLSKGKMLVILEGGYNLRSISASATAVI
		KVLLGDNPKALPIDIQPSKGGLQTLLEVFEIQSKYWSSL
		KGHDQKLRSQWEAQYGSKKRKVIRKRHMHIVGGPVWWKW
		GRKRVVYYHWFARVSSRKHL
232	The amino acid sequence of SEQ ID	MASGAGAAGVVEWHQKPPNPKNPVVFFDVTIGTIPAGRI
	503. The conserved cyclophilin-	KMELFADIVPRTAENFRQFCTGEYRKAGIPIGYKGCHFH
	type peptidyl-prolyl cis-trans	RVIKDFMIQAGDFVKGDGSGCISIYGSKFEDENFIAKHT
	isomerase family domain is	GPGLLSMANSGPNTNGCQFFLTCAKCDWLDNKHVVFGRV
	underlined and the cyclophilin-	LGEGLLVLRKIENVQTGQHNRPKLPCVIAECGEM
	type peptidyl-prolyl cis-trans
	isomerase signature is in bold.
233	The amino acid sequence of SEQ ID	MDHYYQDDFDYLVDDEMVDFADDVEDDVRTRRRSDIDSD
	505. The conserved G-protein beta	SENDFDSNNKSPDTTALQAKRGKDIQGIPWNRLNFTREK
	WD-40 repeat domain is underlined.	YRETRLQQYKNYENLPRPRRSRNLDKECTNFERGSSFYD
		FRHNTRSVKATIVHFQLRNLVWATSKHNVYLMQNYSIMH
		WSSLKQKGEEVLNVAGPIIPSVKHPGSSPQGLTRVQVSA
		MSVKDNLVVAGGFQGELICKYLDKPGVSFCTKISHDENG
		ITNAVEIYNDASGATRLMTANNDLAVRVFDTEKFTVLER
		FSFPWSVNHTSVSPDGKLVAVLGDNADCLLADCKTGKTV
		GTLRGHLDYSFAAAWHPDGYILATGNQDTTCRLWDVRKL
		SSSLAVLKGRMGAIRSIRFSSDGRFMAMAEPADFVHLYD
		TRQNYTKSQEIDLFGEIAGISFSPDTEAFFVGVADRTYG
		SLLEFNRRRMNYYLDSIL
234	The amino acid sequence of SEQ ID	MDCSGDEEEEQFFESLEEMLSPSDSGSEAADNETGCRNA
	506. The conserved G-protein beta	DARSKYEIWKRAPSSIQERRQRFLVRMGLANPSELGNQV
	WD-40 repeat domains are	NSTSAESTCSTETANIPNGIERLRENSGAVLRTAGSSGR
	underlined.	KTHCKNVINIGLREGSVRSSSSSNGTPDVGEDNGEFGGT
		IFSRSGGTWECMCKIKNLDSGKEFVVDELGQDGLWNKLR
		EVGTDRQLTMDEFERSLGLSPLVQELMRRESGVAQADCN
		GVHHHDAEISSSKRRSWLKALKSAAYSMRRPKEDQSNYD
		SERSGRRSGSFDVPWGKPQWTKVRHYRKRYKEFTALYMG
		QEIEAHEGSIWTMKFSLDGRYLASAGQDCVIHVREVIES
		MRTFGADTPDLYASSAYFSMNGLQELVPLSIEDHANKMK
		RGKIIGSKKSSNSDCIVLPNKVFQLSEEPVCSFHGHLLD
		VFDLSWSPSQYLLSSSMDKTVRLWKLGHESCLKVFSHND
		IVTCIQFNPVDERYFISGSLDGKARIWSIPDRQVVDWSD
		LREMVTAVCYTPDGQGGLVGSIKGSCRFYNTSGNKLQLE
		NQLNVRSKKKKSSGKKITGFQFAPGGDSQKVLITSADSR
		VRVYNGSELVCKYKGFRNTCSQISASFAPNGQHFVCASE
		DSRVYIWNHESPRGSGARHEKSSWSHEHFLSQGVSVAIP
		WSGMKLQPPVWNSPEFMLGQRHNLLSLQGGKDVGCQNGL
		LSREAGEGQESETPLHYISQVSHSCGSQNMVDRDGQDDL
		SRYSACISDSRLSSFMAFPESPGNPDDLNSKVFFSDSSS
		KGSATWPEEKLPPTRKQSRSNSTSSHYDTLKTHLGNTIQ
		GQSGASAAVAWGLVIVTAGHGGEIRSFQNYGLPVRL
235	The amino acid sequence of SEQ ID	MPSIPAIGEFTVCEINRELLTTKDESDTQAKDAYAKILG
	507. The conserved G-protein beta	LVFPPISFQIEEGFGSASRQQFDQDLDREDTIVTPSTSE
	WD-40 repeat domain is underlined.	GTNALQEGGLLLKGVSVLKNILASSFGPIFSPNDTKVLK
		KVELLQGISWHRHKHILAFISGSNQVTVHDFQDPEWRES
		SLLVSESQRGIEALEWRPNGGTTLSVACRGGICIWSASY
		PGSVAPVRSGVASFLGTSTRGSSVRWTLVDFLQIPGGKA
		VTALSWSPTGRLLASASREDSSFTIWDVAQGVGTPLRRG
		LGGISLLKWSPTGDYLFSAKPNGTFYLWETNTWTLEQWS
		SSGGCVISATWGPDGRMLFMAFSESTTLGSLHFAGRPPS
		LDAHLLPMELPEIGSITGGFGNIEKMAWDGCGERLAVSY
		TGGDLMYVGLIAIYDTRRTPFISASLVGFIRGPGEQVKP
		LAFAFHDKFKQGPLLSVCWSSGLCCTYPLIFRAH
236	The amino acid sequence of SEQ ID	MEEENAKHTEETRQVQVRFTTKLQPALRVPTTSIAIPAH
	508. The conserved G-protein beta	LTRYGLSDIVNTLLGNDKPQPFDFLVESELVRTSLEKLL
	WD-40 repeat domains are	LIKGISAEKILNIEYILAVVPPKQEEPSLHDDWVSVVDG
	underlined.	SYPNFIFSGSFDSIGRIWKGEGLCTHVLEGHRDAITSAA
		FIMPSDSSDSFINLATASKDRTLRLWQFKPNEHMTNGKM
		VRPYKLLKGHTSSVQTVSACPRRNLICSGSWDCSIKIWQ
		TAGEMDIESNAGSVKKRKLEDSTEQIISQIEASRTLEGH
		SQCVSSVVWLEKDTIYSASWDHSVRSWDVETGVNSLTVG
		CRKALHCLSIGGEGSALIAAGGADSVLRIWDPRMPGTFT
		PILQLSSHKSWITACKWHPKSRHHLISASHDGTLKLWDV
		RSKVPLTTLEAHKDKVLCADWWKEDCVISGGADSTLQIF
		SNLNLT
237	The amino acid sequence of SEQ ID	MNRLRSKRNHILELRLGQSEPEKEATLASNRSRGTNAPI
	509. The conserved RING-type zinc	VVEDDDDVVVSSPRSFALARSSVSQRSSRIPIVNEEDLE
	finger is underlined.	LRLGLAVTGRTSAEHNPRRRHGRVPPNKPIVLCDDAGEA
		DQSSSKKRRTGQQLSSDVQSDESKEVKLTCAICISTMEE
		ETSTICGHIFCKKCITNAIHRWKRCPTCRKKLAINNIIHR
		IYISSSTG
238	The amino acid sequence of SEQ TD	MEEPPPPAVLPSSEDTSIVSSHSFVNAPPTVPVGLDASI
	510. The conserved G-protein beta	PQISTPGINQPGLTIPVPPEAAPLTASLVAASAGMPPAV
	WD-40 repeat domains are	VPSFVRPAIVAHPSVMPPPSMPLAALPMPVASAVPVAAP
	underlined and the splicing factor	HFPPSTPNDNSITPSMPVPTPIVASSSVPPSVTIPGIAP
	motif is in bold.	LPFIAPIPVPSSRPVAPSPFMPPARPLGASVSVAMDVDN
		TDEQDQDADNKGESPSSSPDHPEDPSAAEYEITEESRKV
		RERQEQAIQELLLRRRAYALAVPTNDSSVRARLRRLNEP
		ITLFGEREMERRDRLRALMAKLDAEGQLEKLMKVQEEEE
		AAANVDAEEVQEMEGPQVYPFYTEGSQELLKARTEITKF
		SLPRAVSRLQRARRKREDPDEDEDEELKCVLQQSAQINM
		DCSEIGDDRPLSGCAFSSDGTLLATSAWSGVTKLWSVPN
		INKVATLKGHTERVTDVAFSPTNCHLATACADRTAMLWN
		SEGVLMKTYEGHLDRLARLAFHPSGLYLGTASFDKTWRL
		WDVNTGIELLLQEGHSRSVYGIAFQCDGSLAATCGLDGL
		ARIWDLRTGRSILALEGHVKPVLGIDFSPNGYHLATGSE
		DHTCRIWDLRKRQSVYIIPAHSHLVSQVKFEPQEGYFLV
		TASYDSTAKVWSARDFKSIKVLAGHEAKVTSVDITADGQ
		YIATVSHDRTIKLWSSKNSTNDMNIG
239	The amino acid sequence of SEQ ID	MKRAYKLQEFVAHASNVNCLKIGKKSSRVLVTGGEDHKV
	511. The conserved G-protein beta	NMWAIGKPNAILSLSGHSSAVESVTFDSAEALVVAGAAS
	WD-40 repeat domains are	GTIKLWDLEEAKIVRTLTGHRSNCISVDFHPFGEFFASG
	underlined and the Trp-Asp (WD)	SLDTNLKIWDIRRKGCIHTYKGHTRGVNSIRFSPDGRWV
	repeats signature is in bold.	VSGGEDNIVKLWDLTAGKLMHDFKCHEGQIQCMDFHPQE
		FLLATGSADRTVKFWDLETFELIGSAGPETTGVRAMIFN
		PDGRTLLTGLHESLKVFSWEPLRCYDAVDVGWSKLADLN
		IHEGKLLGCSYNQSCVGVWVVDISRVGPYAAGNVSRTNG
		HNEAKLASSGHPSVQQLDNNLKTNMARLSLSHSTESGIK
		EPKTTTSLTTTEGLSSTPQRAGIAFSSKNLPASSGPPSY
		VSTPKKNSTSRVQPTTNFQTLSRPDIVPVIVPRSNSLRP
		ETTSDAKKEMNNFGRVVPSTVSTKSTDVIKSGSNRDESD
		KIDSINQKRMTGNDKTDLNIARAEQHVSSRLDNTNTSSV
		VCDGNQPAARWIGAAKFRRNSPVDPVVSPHDRSPTFPWS
		ATDDGVTCQPDRQVTAPELSKRVVEPGRARALVASWETR
		EKALTADTPVLVSGRPPTSPGVDMNSFIPRGSHGTSESD
		LTVSDDNSAIEELMQQHNAFTSILQARLTKLQVIRRFWQ
		RNDLKGAIDATGKMGDHSVSADVISVLIERSEIFTLDIC
		TVILPLLTRLLQSETDRHLTVAMETLLVLVKTFGDVIRA
		TISATPTIGVDLQAEQRLERCNLCYVELENIKQILVPLI
		RRGGAVAKSAQELSLALQEV
240	The amino acid sequence of SEQ ID	MAGSDENNPGVVGGAHVQEGLRVGAGKMGAGNVQQRRAL
	512. The conserved cyclin N- and	SNINSNIIGAPPYPCAVNKRVLSEKNVNSENDLLNAAHR
	C-terminal family domains are	PITRQFAAQMAYKQQLRPEENKRTTQSVSNPSKSEDCAI
	underlined.	LDVDDDKMADDFPVPMFVQHTEAMLEEIDRMEEVEMEDV
		AEEPVTDIDSGDKENQLAVVEYIDDLYMFYQKAEASSCV
		PPNYMDRQQDINERMRGILIDWLIEVHYKFELMDETLYL
		TVNLIDRFLAVQPVVKKKLQLVGVTAMLLACKYEEVSVP
		VVEDLILISDRAYSRKEVLEMERLMVNTLHFNMSVPTPY
		VFMRRFLKAAQSDKKLELLSFFIIELSLVEYDMLKFPPS
		LLAASAIYTALSTITRTKQWSTTCEWHTSYSEEQLLECA
		RLMVTFHQRAGSGKLTGVHRKYSTSKFGHAARTEPANFL
		LDFRL
241	The amino acid sequence of SEQ ID	MQAPREGKSAAAIVGMGKYMKKSKAIPRDVSLLEASPRS
	513. The conserved cyclin-	PSATGVRTRAKTLASRRLRRASQRRPPPPAAAAAAAAPS
	dependent kinase inhibitor domain	LDASPCPFSYLQLRSRRLRRPRLAPSPEARIDEGPAGSG
	is underlined.	SRGSRDASCSARTASSSGGVEGEGACVGRGDRGNGGECV
		RDAAVDASYGENDLEIEDRDRSTRESTPCSLIRDSNANT
		PPGSTTRQQSSCTAHRTQMSILRSIPTSDEMEEFFAYAE
		QRQQRSFIEKYNFDIVKDRPLPGRFEWVQVIP
242	The amino acid sequence of SEQ ID	MDGHSSHLAAQNRSRGSQTPSPSHSAASASATSSIHLKR
	514. The conserved GCN5-related N-	KLSAANASAASAAAAAAAAAAAADDHAPPFPPSSISADT
	acetyltransferase family domain is	RDGALTSNDDLESISARGGGAGDDSDDDSDDEEEDDGDN
	underlined and the bromodomain is	DGGSSLRTFTAARLENVGPAAARNRKIKAESNATVKVEK
	in bold.	EDSAKDGGNGAGVGALGPAATSGAGSGSGTVPKEDAVKI
		FTENLQASGAYSAREENLKREEEAGRLKFECLSNDGVDD
		HMVWLIGLKNIFARQLPNMPKEYIVRLVMDRNHKSVMVI
		RRNLVVGGITYRPYASQKFGEIAFCAIKADEQVKGYGTR
		LMNHLKQHARDVDGLTHFLTYADNNAVGYFIKQGFTKEI
		YLDKDRWHGYIKDYDGGILMECKIDPKLPYTDLSTMVRR
		QRQAIDEKIRELSNCHIVYQGIDFQKRDAGVPQNTIKME
		DIPGLREAGWTPDQWGYSRFRGLSDQKRLTFFIRQLLKV
		LNDHSDAWPFKEPVDAREVPDYYDIIKDPMDLKTMTKRV
		ESEQYYVTLEMFIADVKRMFANARTYNSPDTIYFKIATR
		LEAHFQSKVQSNLQSGAGKIQQ
243	The amino acid sequence of SEQ ID	MFNGMMDPELFKLAQEQMNRMSPAELAKIQQQMMSNPEL
	515. The conserved TPR repeat	MRMASESMKNMRPEDLRQAAEQLKHVRPEEMAEIGEKMA
	domain is underlined	NASPEEIAAVRARADAQMTYEINAAKILKKEGNELHSQG
		RFKDASQKYLRAKNNLKGIPSSEGKNLLLACSLNLMSCY
		LKTRQYEECIKEGSEALACEEKNLKAFYRRGQAYRELGQ
		LKDAVSDLRKAHEISPDDETIAQVLRDTEESLTKEGGSA
		PRGVVIEEITEEDETLASVNHESPSEYSEKRHQESEDAH
		KGPINGDIMGQMTNSESLKALKGDPDAIRSFQNFISNAD
		PTTLAAMGAGNAGEVSPDLIKTASSMIGKMSAEELQKMI
		QLASSFPGENPYVTRNSDSNSNSFGNGSIPNVSPDMLKT
		ASDMMSKMSPDDLQRMFEMASSSRGKDPSLDANHASSSS
		GANLAANLNHILGESEPSSSYHIPSSSRNISSSPLSNFP
		SSPGDMQEQIRNQMKDPAMRQMFTSMMKNMSPEMMANMG
		KQFGLELSPEDAAKAQEAMSSLSPEMLDKMMRWADRAQR
		GVETAKKTKNWLLGRPGMILAICMLLLAVILHRLGFIGS
244	The amino acid sequence of SEQ ID	MIAAISWVPRGASKAVPEVAEPPSKEEIEEILKSGVVER
	516. The conserved G-protein beta	SGDSDGEEDDENMDAVASEKADEVSTALSAADALGRISK
	WD-40 repeat domains are	VTKAGSGFEDIADGLRELDMDNYDEEDEDVKLFSTGLGD
	underlined.	LYYPSNDMDPYLKDKDDDDDTEEIEDLSIKPMDSLIVCA
		RTDDEVNLLEVYLLEPSLSDESNMYVHHEVVISEFPLCT
		AWLDCPIKGGDKGNFIAVGSMEPAIEIWDLDIIDAVEPC
		LVLGGQEELKKKKKKGKKASIKYKEGSHTDSVLGLAWNK
		EFRNILASASADRQVKIWDVAAGKCNITMEHHTDKVQAV
		AWNHHAPQVLLSGSFDHSVVMKDGRIPSHSGYRWSVTAD
		VESLAWDPHSEHFFVVSLEDGTVRGFDVRAAISNSASQS
		LPSFTLHAHEKAVSTISYNPAAPNLLATGSTDKMVKLWD
		LSNNQPSCIASRNPKAGAVFSVSFSEDSPLLLAIGGSKG
		RLEVWDTSSDAAVSRRFGKHGKPKTAEPGS
245	The amino acid sequence of SEQ ID	MKFCKKYQEYMQGQEGKKLPGLGFKKLKKILKRCRRRDS
	517. The conserved Zn-finger, RING	LHSQKALQAVQNPRTCPAHCSVCDGSFFPSLLEEMSAVL
	domain is underlined, and the SPX,	GCFNKQAQKLLELHLASGFQKYLMWFKGKLRGNHVALIQ
	N-terminal is in bold	EGKDLVTYALINAIAIRKILKKYDKIHLSTQGQAFKSQV
		QRMHMEILQSPWLCELIAFHINVRETKANSGKGHALFEG
		CSLVVDDGKPSLSCELFDSIKLDIDLTCSICLDTVFDSV
		SLTCGHIYCYMCACSAASVTIVDGLKAAEPKEKCPLCRE
		ARVFEGAVHLDELNILLSRSCPEYWAERLQTERVERVRQ
		AKEHWESQCRAFMGVE
246	The amino acid sequence of SEQ ID	MVSTQSTRENPSIFFPPPLKPWLLPVVLSLSLSRQLGMA
	518. The conserved G-protein beta	AAAAASLPFKKNYRSSQALQQFYAGGPFAVSSDGSFIAC
	WD-40 repeat domains are	NCGDSIKIVDSSNASLRPSIDCGSDTITALSLSPDGKLL
	underlined.	FSAGHSRQIRVWDLSTSTCLRSWKGHDGPVMSMACPVSG
		GLLATGGADRKVMVWDVDGGFCTHFFKGHDGVVSTVLFH
		PDSNRSLLFSGSDDGTIRVWDLLAKKCASTLRGHDSTVT
		SLAFSEDGLTLLAAGRDKVVSLWDLHNYACKKTIPMYEV
		LESVCVIHSGTVLASQLGLDDQLKVTKESAQNIHFITVG
		ERGILRIWKSEGSVCLFKQEHSDVTVISDEDDSRSGFTA
		AVMLPLDQGLLCVTADQQFLFYYPEKHPEGIFSLTLCRR
		LVGYNEEIVDMKFLGEEENFLAVATNLEQVRVYELASMS
		CSYVLAGHTETVLCLDTCISSSGRTLIVTGSKDNSVRLW
		DSESRHCIGVGVGHMGAVGAVAFSRKRQDFFVSGSSDRT
		LKVWSLDGISEDGVDSTNLKAKAVVAAHDKDINSVAVAP
		NDSLVCSGSQDRTACVWRLPDLVSVVVLKGHKRGIWSVE
		FSPVDQCVLTASGDKTVKIWAISDGSCLKTFEGHVSSVL
		RASFLTRGTQFVSCGADGLVKLWTVRTNECIATYDQHSD
		KVWALAVGKKTEMLATGGSDAVVNLWYDSTASDKEDAFR
		KEEEGVLKGQELENAVSDADYTKAIELALELRRPHKLFE
		LFSELCRTREVGDRVERILSALSGEEVCLLLEYIREWNA
		KPKLCHVAQSVLSQVFRILSPTEIVEIKGIGELLEGLIP
		YSQRHFSRIDRLVRSTYLLDYTLTGMSVIEPEADRSAVN
		DGSPDKSGLEKLEDGLLGENVGEEKIQNKEELESSAYKK
		RKLPRSKDRSKKKSKNVVYADAAAISFRA
247	The amino acid sequence of SEQ ID	MDSAPRRKSGGINLPSGMSETSLRLDGFSGSSSSFRAIS
	519. The conserved G-protein beta	NLTSPSKSSSISDRFIPCRSSSRLHTFGLVERGSPVKEG
	WD-40 repeat domains are	GNEAYSRLLKAELFGSDFGSLSPAGQGSPMSPSKNMLRF
	underlined.	KTESSGPNSPFSPSILRQDSGFSSEASTPPKPPRKVPKT
		PHKVLDAPSLQDDFYLNLVDWSSQNTLAVGLGTCVYLWS
		ASNSKVTKLCDLGPNDGVCAVQWTREGSYISIGTSLGQV
		QIWDGTQCKRVRTMGGHQTRTGVLAWNSRILASGSRDRV
		ILQHDLRVPNEFIGKLVGHKSEVCGLKWSHDDRELASGG
		NDNQLLVWNQHSQQPVLKLTEHTAAVKAIAWSPHQNGLL
		ASGGGTADRCIRFWNTTNGHQTSSVDTGSQVCNLAWSKN
		VNELVSTHGYSQNQIMVWKYPSMAKVATLTGHSLRVLYL
		AMSPDGQTIVTGAGDETLRFWNVFPSAKAPAPVKDTGLW
		SLGRTHIR
248	The amino acid sequence of SEQ ID	MEDEAEIYDGVRAQFPLTFGKQSKPQTSLESVHSATRRG
	520. The conserved G-protein beta	GPAPAPAPASSSSLPSTTSPSAAGGAGKSSGLPSLSSSS
	WD-40 repeat domains are	TAWLEGLRAGNPRAGREAGIGSRGGDGEDGGRAMIGPPR
	underlined.	PPPGFSANDDGGGEDDDDDGDGVMVGPPPPPPGNLGDGD
		DDEEEEEAMIGPPRPPVVDSDEEEEEEEEENRYRLPLSN
		EIVLKGHNKIVSALAVDPTGSRVLSGSYDYTVRMFDFQG
		MNSRLSSFRDFEPVEGHQVRNLSWSPTADRFLCVTGSAQ
		AKIYDRDGLTLGEFVKGDMYIRDLKNTKGHITGLTWGEW
		HPKTKETILTSSEDGSLRIWDVNDFKSQKQVIKPKLARP
		GRVPVTTCTWDREGKCIAGGIGDGSIQIWNLKPGWGSRP
		DIHVEQAHADDITGLKFSSDGKILLTRSFDDSLKVWDLR
		LMKNPLKVFEDLPNHYAQTNIACSPDEQLFLTGTSVERE
		STIGGLLCFFDRSKLELVSRIGISPTCSVVQCAWHPRLN
		QIFATSGDKSQGGTHVLYDPTLSERGALVCVARAPRKKS
		VDDFELKPVIHNPHALPLFRDQPSRKRQREKILKDPLKS
		HKPELPMNGPGHGGRVGASKGSLLTQYLLKQGGMIKETW
		MDEDPREAILKHADAAEKNPKFTRAYAETQPDPVFAKSD
		SEDEDK

TABLE 12
Eucalyptus in silico Data.

SEQ	ConsID
ID	eucSpp	Family	1	2	3	4	5	6	7	8	9	10	11	12

1	3910	Cyclin-		0.25				0.11		0.20				0.73
		dependant
		protein
		kinase
2	19213	Cyclin-								0.59				0.64
		dependant
		protein
		kinase
3	36800	Cyclin-							0.11	0.36
		dependant
		protein
		kinase
4	40260	Cyclin-				0.85
		dependant
		protein
		kinase
5	41965	Cyclin-					0.35							0.86
		dependant
		protein
		kinase
6	2906	Cyclin-		0.93										0.81
		dependant
		protein
		kinase
7	1518	Cyclin-		0.08	0.28	0.08		0.06	0.11
		dependant
		protein
		kinase
8	8078	Cyclin-					0.17							3.20
		dependant
		protein
		kinase
9	9826	Cyclin-			0.36	0.23			0.15	0.04		0.24		0.43
		dependant
		protein
		kinase
10	10364	Cyclin-						0.11	1.52					0.13
		dependant
		protein
		kinase
11	11523	Cyclin-				0.15		0.06	0.15					2.40
		dependant
		protein
		kinase
12	24358	Cyclin-		0.76					0.07	0.04		0.24
		dependant
		protein
		kinase
13	39125	Cyclin-				0.23
		dependant
		protein
		kinase
14	5362	Cyclin-		0.68				0.06		0.08				1.17
		dependant
		protein
		kinase
15	44857	Cyclin-		0.68				0.06		0.08				1.17
		dependant
		protein
		kinase
16	1743	Cyclin A			0.19		2.10	0.06	0.15
17	12405	Cyclin A						0.06	0.59			2.84
18	3739	Cyclin B		0.42	1.99	0.08								2.33
19	22338	Cyclin B												0.86
20	28605	Cyclin B						0.39		0.04		0.47
21	41006	Cyclin B										0.71
22	6643	Cyclin D		0.85			0.83	0.06	1.06	0.08				0.26
23	45338	Cyclin D												2.03
24	46486	Cyclin D							0.30
25	12070	Cyclin-	0.24		0.82			0.06	0.26					0.92
		dependent
		kinase
		regulatory
		subunit
26	6617	Histone		0.08				0.06	0.04	0.55			0.51	0.26
		acetyltransferase
27	7827	Histone			2.27			0.11		0.04
		acetyltransferase
28	8036	Histone					1.16
		acetyltransferase
30	1596	Histone		0.17	0.16	0.08	2.98	0.88	0.26	0.98				0.71
		deacetylase
31	5870	Histone			0.19		0.17			0.12				5.43
		deacetylase
32	6901	Histone	1.21	0.08				2.01	1.16	0.08
		deacetylase
33	6902	Histone		0.08				0.11	1.21					0.47
		deacetylase
34	7440	Histone	0.48		1.23	0.15		0.22	0.48	0.20				2.02
		deacetylase
35	8994	Histone			0.09				0.15
		deacetylase
36	24580	Histone		0.42					1.22
		deacetylase
37	37831	Histone		0.08				0.22		0.40		1.19		0.12
		deacetylase
38	34958	MAT1 CDK-							0.15	0.23
		activating
		kinase
		assembly
		factor
39	22967	Peptidyl-			0.72									0.69
		prolyl cis-
		trans
		isomerase
40	8599	Peptidyl-			0.46	0.08	0.50	0.17	0.51	0.28				3.01
		prolyl cis-
		trans
		isomerase
41	9919	Peptidyl-			0.51		0.35	0.06	0.15	0.43				4.24
		prolyl cis-
		trans
		isomerase
42	15820	Peptidyl-							0.04					6.78
		prolyl cis-
		trans
		isomerase
43	8327	Peptidyl-						0.06		0.04				6.86
		prolyl cis-
		trans
		isomerase
44	4604	Peptidyl-												0.68
		prolyl cis-
		trans
		isomerase
45	966	Peptidyl-		0.59	1.02	0.54	0.69	0.50	0.93	0.59		0.95		18.65
		prolyl cis-
		trans
		isomerase
46	1037	Peptidyl-		0.59
		prolyl cis-
		trans
		isomerase
47	4603	Peptidyl-		0.17				0.17	1.24	0.04				0.34
		prolyl cis-
		trans
		isomerase
48	5465	Peptidyl-			1.21	0.08	0.66	0.11	0.29	0.16				6.99
		prolyl cis-
		trans
		isomerase
49	6571	Peptidyl-		0.51		0.08			0.41	0.08				1.14
		prolyl cis-
		trans
		isomerase
50	6786	Peptidyl-		0.42				0.33	0.06	0.41	0.04
		prolyl cis-
		trans
		isomerase
51	7057	Peptidyl-		0.42				0.11	0.04
		prolyl cis-
		trans
		isomerase
52	8670	Peptidyl-			1.56			0.39		0.20				0.12
		prolyl cis-
		trans
		isomerase
53	9137	Peptidyl-							0.04	0.59
		prolyl cis-
		trans
		isomerase
54	10285	Peptidyl-					0.60	1.16	0.04	0.04				0.45
		prolyl cis-
		trans
		isomerase
55	10600	Peptidyl-			0.16		0.17	0.06						0.46
		prolyl cis-
		trans
		isomerase
56	11551	Peptidyl-				0.08		0.06	0.04	0.08				1.89
		prolyl cis-
		trans
		isomerase
57	20743	Peptidyl-								0.76
		prolyl cis-
		trans
		isomerase
58	23739	Peptidyl-		0.59
		prolyl cis-
		trans
		isomerase
60	31985	Peptidyl-					1.99
		prolyl cis-
		trans
		isomerase
61	32025	Peptidyl-					0.99
		prolyl cis-
		trans
		isomerase
62	32173	Peptidyl-					1.99
		prolyl cis-
		trans
		isomerase
64	9143	Retinoblastoma			0.90				0.15
		related
		protein
65	349	WD40 repeat	0.24		0.34	0.08	0.17	0.22	0.33	0.08			0.25	2.24
		protein
66	575	WD40 repeat		0.25	0.94	0.31	0.34	0.11		0.16		0.47		1.87
		protein
67	804	WD40 repeat				0.15	0.34	0.39	0.33	0.39				1.82
		protein
68	805	WD40 repeat	0.97	0.51	4.66	0.23	0.17	0.77	0.33	1.07		0.24		4.43
		protein
69	806	WD40 repeat					0.83			0.04
		protein
70	2248	WD40 repeat		0.08		0.08	1.92	0.06		0.08				0.91
		protein
71	3203	WD40 repeat		0.34	0.18	0.15	0.17	0.11	0.30	0.04				0.72
		protein
72	3209	WD40 repeat		0.08		0.15	0.17			0.12				0.61
		protein
73	4429	WD40 repeat		0.08	1.16	0.08								0.13
		protein
74	4607	WD40 repeat		0.76		0.54		0.06	0.07
		protein
75	4682	WD40 repeat		0.08	0.28	0.23			1.13	0.08				0.12
		protein
76	5786	WD40 repeat		0.08				0.06	0.46	0.08				0.13
		protein
77	5887	WD40 repeat		1.61	1.23	0.08		0.06	0.15	0.28				1.41
		protein
78	5981	WD40 repeat		0.08										0.37
		protein
79	6766	WD40 repeat	0.24	0.08	1.31		0.51	0.06	0.74	0.51				0.28
		protein
80	6769	WD40 repeat		0.93			0.17			0.12				2.28
		protein
81	6907	WD40 repeat		0.25			0.17	0.06	0.45	0.32		0.47		1.67
		protein
82	7518	WD40 repeat			0.91			0.28	0.15	0.55				0.59
		protein
83	7717	WD40 repeat			0.47									0.38
		protein
84	7718	WD40 repeat	0.24		1.88	0.08		0.22		0.04				0.92
		protein
85	7741	WD40 repeat			1.42			0.11				0.47
		protein
86	7884	WD40 repeat			1.33	0.15						0.24
		protein
87	8258	WD40 repeat	0.72		0.19	0.23	0.87		0.15	0.08				0.08
		protein
88	8465	WD40 repeat			0.47	0.08	1.75
		protein
89	8616	WD40 repeat			0.57	0.08	0.69			0.16				0.13
		protein
90	8690	WD40 repeat			0.26	0.08	0.35	1.39	0.34	0.32		2.13		0.80
		protein
91	8708	WD40 repeat			0.57					0.04
		protein
92	8850	WD40 repeat			0.09			0.06		0.27				2.03
		protein
93	9072	WD40 repeat			1.21		0.17							0.48
		protein
94	9465	WD40 repeat	0.24		0.72		0.33		0.15
		protein
95	9472	WD40 repeat			0.36		1.99	0.11	0.61					6.90
		protein
96	9550	WD40 repeat			0.90			0.11	1.78
		protein
97	10284	WD40 repeat	0.24	0.08			1.82		1.22	0.16		0.47		0.28
		protein
98	10595	WD40 repeat			0.16		0.17	0.11	6.52					0.85
		protein
99	10657	WD40 repeat						0.06		0.12
		protein
100	12636	WD40 repeat						0.06						0.65
		protein
101	12748	WD40 repeat			1.50	0.08		0.06	1.67	0.04				0.38
		protein
102	12879	WD40 repeat				0.08	0.33	0.06	0.04	0.08				2.00
		protein
103	15515	WD40 repeat					0.35		0.30
		protein
104	15724	WD40 repeat		0.25	0.33	0.15			0.47	0.04				0.39
		protein
105	16167	WD40 repeat	0.24				0.52
		protein
106	16633	WD40 repeat			1.96					0.12				0.42
		protein
107	17485	WD40 repeat			0.65
		protein
108	18007	WD40 repeat								0.12
		protein
109	20775	WD40 repeat					0.17			0.08
		protein
110	23132	WD40 repeat												2.42
		protein
111	23569	WD40 repeat							0.91					0.91
		protein
112	23611	WD40 repeat							4.15
		protein
113	24934	WD40 repeat		0.34						0.04
		protein
114	25546	WD40 repeat			0.09
		protein
115	30134	WD40 repeat							0.07
		protein
116	31787	WD40 repeat			0.19									1.19
		protein
117	34435	WD40 repeat					0.35			0.08
		protein
118	34452	WD40 repeat			1.44					0.20				0.25
		protein
119	35789	WD40 repeat								0.20
		protein
120	35804	WD40 repeat							0.19	0.27				0.08
		protein
121	43057	WD40 repeat							0.30					0.57
		protein
122	46741	WD40 repeat							0.46
		protein
123	47161	WD40 repeat							1.78
		protein
235	6366	WD40 repeat		0.08	0.68	0.23	0.93	0.11	0.36	0.83		0.24		0.94
		protein
236	17378	WD40 repeat			0.65					0.12				0.08
		protein
252	45414	Cyclin B												3.13
253	44328	Cyclin-												0.38
		dependant
		kinase
		inhibitor
254	15615	Histone							0.22	0.04
		acetyltransferase
255	17239	Peptidyl-				0.08	0.50			0.08
		prolyl cis-
		trans
		isomerase
256	18643	WD40 repeat								0.04				0.90
		protein
257	19127	WD40 repeat								0.04				0.89
		protein
258	22624	WD40 repeat												1.16
		protein
259	32424	WD40 repeat					0.50
		protein
260	37472	WD40 repeat								0.08				0.17
		protein
In Table 12, the following numbers 1-12 represent the following tissues:
1 is bud reproductive;
2 is bud vegetative;
3 is cambium;
4 is fruit;
5 is leaf 6 is phloem;
7 is reproductive;
8 is root;
9 is sap vegetative;
10 is stem;
11 is whole; and
12 is xylem.

TABLE 13
Pine in silico data.

	ConsID
SEQ	pinus
ID	Radiata	Family	1	2	3	4	5	6	7	8	9	10	11	12

124	1766	Cyclin-				1.02	0.05	1.58	0.15	0.22	0.22	0.18	2.16	4.91
		dependant
		protein
		kinase
125	2927	Cyclin-	0.16					0.19	0.11	0.14	0.04	0.36	0.38	0.17
		dependant
		protein
		kinase
126	7642	Cyclin-			0.22	0.21	0.05				0.07
		dependant
		protein
		kinase
127	13714	Cyclin-						0.11	0.11
		dependant
		protein
		kinase
128	16332	Cyclin-						0.54	0.26		0.14		0.04	0.91
		dependant
		protein
		kinase
129	21677	Cyclin-					0.05	0.14						0.17
		dependant
		protein
		kinase
130	27562	Cyclin-												0.41
		dependant
		protein
		kinase
131	1504	Cyclin-	0.16					0.36		0.35	0.21	0.54	0.09	0.65
		dependant
		protein
		kinase
132	15211	Cyclin-						0.13	0.15				0.19	0.19
		dependant
		protein
		kinase
133	20421	Cyclin-									0.04		0.05	0.95
		dependant
		protein
		kinase
134	3187	Cyclin-						0.34	0.15		0.04	0.18	0.38
		dependant
		protein
		kinase
135	15661	Cyclin-									0.04		0.13
		dependant
		protein
		kinase
136	13874	Cyclin A	0.31					0.27	0.15				0.05
137	14615	Cyclin A	0.16					0.15
138	4578	Cyclin B	0.47	0.14				0.13	0.22				0.74	0.38
139	23387	Cyclin B						0.29	0.26					0.17
140	6970	Cyclin D		0.14						0.27	0.04
141	10322	Cyclin D	0.16			0.19		0.06			0.14		1.12	1.36
142	22721	Cyclin D						0.27		0.36
143	23407	Cyclin D						0.15	0.26					0.31
144	1945	Cyclin-		0.28	0.55	0.41	0.16	1.62	5.02	0.22	0.72		0.39	3.06
		dependent
		kinase
		regulatory
		subunit
145	8233	Cyclin-				0.21
		dependent
		kinase
		regulatory
		subunit
146	8234	Cyclin-	0.16		0.11
		dependent
		kinase
		regulatory
		subunit
147	22054	Cyclin-					0.05		0.22				0.18
		dependent
		kinase
		regulatory
		subunit
148	12137	Histone						0.06					1.51	0.19
		acetyltransferase
149	12582	Histone						0.64	0.15	1.09			0.33	0.63
		acetyltransferase
150	15285	Histone				0.21					0.12		0.70	0.14
		acetyltransferase
151	17229	Histone											0.94	0.16
		acetyltransferase
152	20724	Histone									0.04		0.19	0.19
		acetyltransferase
153	4555	Histone	0.16	0.14				0.97		0.14			0.89	0.89
		deacetylase
154	4556	Histone												0.14
		deacetylase
155	5729	Histone	0.31	0.28	0.22	0.58	0.22	2.00	0.48	0.07	0.04		2.73	1.46
		deacetylase
156	7395	Histone		0.14		0.14			0.19	0.93	0.04		0.14	1.33
		deacetylase
157	9503	Histone			0.11					0.14
		deacetylase
158	11283	Histone				0.19			0.15				0.96	1.35
		deacetylase
159	12322	Histone	0.16					0.06	0.11		0.04		0.05	0.29
		deacetylase
161	23236	Histone						0.13			0.11
		deacetylase
162	171	Peptidyl-									0.07			0.46
		prolyl
		cis-trans
		isomerase
163	172	Peptidyl-						0.19			0.11	0.18	0.11	0.46
		prolyl
		cis-trans
		isomerase
164	1480	Peptidyl-	2.51	4.20	0.88	2.97	1.58	3.53	7.36	1.33	2.74	0.72	6.62	10.14
		prolyl
		cis-trans
		isomerase
168	1692	Peptidyl-	0.16		0.22		0.65	0.61	0.26		0.29	0.18	1.28	0.34
		prolyl
		cis-trans
		isomerase
169	5313	Peptidyl-		0.14						0.07			0.37	0.17
		prolyl
		cis-trans
		isomerase
170	6362	Peptidyl-		0.14	0.33	0.05		0.06	0.60		0.04		2.92	0.68
		prolyl
		cis-trans
		isomerase
171	6493	Peptidyl-		0.42	0.11	0.21			0.11		0.04		0.25	0.32
		prolyl
		cis-trans
		isomerase
172	6983	Peptidyl-				0.61		0.13					0.04
		prolyl
		cis-trans
		isomerase
174	7665	Peptidyl-			0.11	0.39	0.05	0.62					0.25
		prolyl
		cis-trans
		isomerase
175	12196	Peptidyl-						0.19	0.15	0.14	0.16
		prolyl
		cis-trans
		isomerase
176	13382	Peptidyl-				0.25		0.06		0.07	0.04		0.87	0.15
		prolyl
		cis-trans
		isomerase
177	16461	Peptidyl-				0.19		0.15	0.15		0.04		0.04	0.74
		prolyl
		cis-trans
		isomerase
178	17611	Peptidyl-				0.24	0.11	0.27	0.41				0.99
		prolyl
		cis-trans
		isomerase
179	19776	Peptidyl-						0.13		0.07	0.16		0.05	0.61
		prolyl
		cis-trans
		isomerase
180	20659	Peptidyl-								0.15			0.19
		prolyl
		cis-trans
		isomerase
181	22559	Peptidyl-							0.11	0.14				0.20
		prolyl
		cis-trans
		isomerase
182	24188	Peptidyl-									0.23
		prolyl
		cis-trans
		isomerase
183	27973	Peptidyl-											1.01
		prolyl
		cis-trans
		isomerase
184	1353	WD40			0.44		0.05	0.73			0.11	1.07	0.70	1.32
		repeat
		protein
185	1978	WD40		0.14		0.05		0.44	0.11	0.21	0.27	0.36	1.46	0.82
		repeat
		protein
186	2810	WD40		0.42		0.79	0.11	0.39		0.27		0.36	1.69	1.03
		repeat
		protein
187	2811	WD40									0.14		0.09	0.14
		repeat
		protein
188	2812	WD40							0.15			0.18	0.04	0.16
		repeat
		protein
189	3514	WD40				0.63		0.06		0.14		0.18	0.48	0.56
		repeat
		protein
190	4104	WD40		0.14		0.25		0.27	0.37	0.36	0.19	0.18	0.39	0.53
		repeat
		protein
191	5595	WD40		0.14		0.25			0.15	0.14	0.07		0.23
		repeat
		protein
192	5754	WD40	0.31	0.14				0.06		0.07	0.16		0.10	0.16
		repeat
		protein
193	6463	WD40	0.16	0.56	0.22	0.43		0.81	0.53	0.21	0.08		1.00	0.70
		repeat
		protein
194	6665	WD40	0.31	0.28		0.45	0.44	0.96			0.07		3.37	2.68
		repeat
		protein
195	6750	WD40		0.14		0.59	0.05		0.37	0.42	0.04		0.18	0.52
		repeat
		protein
196	7030	WD40	0.31			0.40	0.54	0.45	0.37		0.07		1.58	3.41
		repeat
		protein
197	7854	WD40			0.11					0.14			0.05
		repeat
		protein
198	7917	WD40			0.22	0.39		0.13	0.15				0.18	0.56
		repeat
		protein
199	7989	WD40			0.11						0.04		0.11
		repeat
		protein
200	8506	WD40	0.47		0.33		0.11	0.86	0.19	1.28	0.04		1.23	3.12
		repeat
		protein
201	8692	WD40				0.21		0.06	0.11		0.15		0.10	0.87
		repeat
		protein
202	8693	WD40			0.11	0.80		0.25		0.14	0.18		0.53	0.31
		repeat
		protein
203	9170	WD40	0.16		0.11	0.05							0.05
		repeat
		protein
204	9408	WD40			0.33		0.05	0.41	0.15	0.14			0.41	0.33
		repeat
		protein
205	9522	WD40			0.11								0.18
		repeat
		protein
206	9734	WD40			0.11	0.05	0.11	0.15		0.07	0.25		0.11
		repeat
		protein
207	9815	WD40			0.11								0.18	0.14
		repeat
		protein
208	10670	WD40				0.40	0.16	0.11			0.16		0.34	0.31
		repeat
		protein
209	11297	WD40				0.53			0.15		0.16		0.05
		repeat
		protein
210	13098	WD40				0.19	0.11	0.54	0.31	0.14	0.26		1.85	0.14
		repeat
		protein
211	13172	WD40									0.04
		repeat
		protein
212	13589	WD40					0.11	0.06		0.21			0.05	0.37
		repeat
		protein
213	13608	WD40						0.11			0.04		0.59	0.33
		repeat
		protein
214	14299	WD40	0.16			0.05				1.09			0.38
		repeat
		protein
215	14498	WD40				0.21							0.44	0.30
		repeat
		protein
216	14548	WD40	0.16								0.11		0.11	0.82
		repeat
		protein
217	14610	WD40	0.16					0.27
		repeat
		protein
218	16090	WD40						0.43			0.04		0.37	0.85
		repeat
		protein
219	16722	WD40											0.10
		repeat
		protein
220	16785	WD40				0.05		0.13					0.38	0.50
		repeat
		protein
221	17094	WD40						0.29	0.15				0.24	0.81
		repeat
		protein
222	17527	WD40									0.04		0.10
		repeat
		protein
223	17591	WD40						0.14					0.10
		repeat
		protein
224	17769	WD40											0.39
		repeat
		protein
225	18047	WD40				0.05	0.22	0.98	0.15	2.68	0.07		0.19	0.80
		repeat
		protein
226	18414	WD40					0.16	0.15			0.34		0.23	0.19
		repeat
		protein
227	18986	WD40						0.41					0.15
		repeat
		protein
228	19479	WD40					0.05						0.28	0.32
		repeat
		protein
229	20144	WD40				0.43			0.29				0.05
		repeat
		protein
230	22480	WD40							0.15	0.27
		repeat
		protein
231	23079	WD40						0.13			0.04
		repeat
		protein
232	26739	WD40							0.15				0.18
		repeat
		protein
233	26951	WD40				0.21								0.20
		repeat
		protein
234	26529	WEE1-like									0.04		0.18
		protein
237	888	WD40							0.11				0.18
		repeat
		protein
238	14166	Cyclin-	0.16			0.05							0.05
		dependant
		kinase
		inhibitor
239	3189	Cyclin-						0.06
		dependant
		protein
		kinase
240	9356	Histone			0.11				0.22					0.46
		acetyltransferase
241	65	Histone	0.16				0.22	0.27	0.22				0.24	0.34
		deacetylase
242	14197	Histone	0.16				0.33						0.05
		deacetylase
243	9081	Peptidyl-			0.11		0.05		0.29		0.26		0.69
		prolyl
		cis-trans
		isomerase
244	13417	Peptidyl-						0.06					0.59
		prolyl
		cis-trans
		isomerase
245	5755	WD40	0.16
		repeat
		protein
246	6670	WD40		0.14		0.05
		repeat
		protein
247	7027	WD40		0.14				0.15					1.30	0.15
		repeat
		protein
248	7276	WD40		0.14					0.11				0.05
		repeat
		protein
249	7390	WD40	0.31	0.14			0.11		0.44				1.29	0.38
		repeat
		protein
250	12648	WD40				0.05		0.06					0.05	0.94
		repeat
		protein
251	13171	WD40				0.19		0.63					0.19	0.34
		repeat
		protein
Table 13, the following numbers 1-12 represent the following tissues:
1 is bud reproductive;
2 is bud vegetative;
3 is callus;
4 is cambium;
5 is meristem vegetative;
6 is phloem;
7 is reproductive female;
8 is reproductive male;
9 is root;
10 is vascular;
11 is whole; and
12 is xylem.

TABLE 14
Oligo Table.

Oligo
SEQ
ID	Oligo ID	Microarray Oligo Seq
521	Euc_003910_O_4	GATTTTAAGTAACTCAATTAGCAGTTCCAACATTAAACCATTATTATTACCCCTTTTATC
522	Euc_019213_O_1	CTCAAAAAGTACTTGGATGCGTGCGGTGACAACGGACTCGAACCGTACACTGTCAAATCT
523	Euc_036800_O_4	TTGTCAAGTTGCAGGACGTAGTGCACAGTGAGAGGCGTCTATATCTAGTTTTTGAGTACT
524	Euc_040260_O_1	GAAGAAATTATATAACTAGATACAAGGTTAGCTAGGTATATAATAGCGGTACAAGTCTTT
525	Euc_041965_O_1	GGACAAATCAAGTAGAACTTCTCTCGGCAGCATCAGTTTTTCTAATCCATGCCTTGTTGC
526	Euc_002906_O_1	CTCAGTTCTGATAATGCCTCGGATATATGGCCGAGTGTTCGCTGGACGGCCTCTTATGTT
527	Euc_001518_O_3	GGAGATTCTGAACTGCAACAGCTCCTACACATTTTCAGACTGTTGGGTACTCCAAATGAA
528	Euc_008078_O_2	GACTGGTAAAATCGTTGCACTAAAAAAGGTCCGGTTTGACAACTTGGAACCTGAAAGCGT
529	Euc_009826_O_4	AAACACCAATCTATCAACACTGTCGAGTTTAGTCACTAGTAGAACCGGAGATAACAAACA
530	Euc_010364_O_1	CTATGATCCTGAGCGCAAGCAAGTTATGACCAATAGAGTCGTTACACTATGGTACCGAGC
531	Euc_011523_O_1	TGTTGTGAAGGTAGTTATAGCCATCGATTAGACAGTGATTAAAGTAGTACCCGTGCCAAT
532	Euc_024358_O_2	CCACATACAAGAGTTGTTACGCTACACATCCTATACCATCAAAGGAACGTTGGAATGCCA
533	Euc_039125_O_3	TATGATCGACACAAGCATTTTGTGTTGGAGCCTCAGCTAATTGTATGTCATCGAGTACTT
534	Euc_005362_O_3	AAAATTTTTGCTACGGATAATGTTGTGAGGCGAGGCAGTCGAAATTACGGAGGTTGACTT
535	Euc_044857_O_1	ATGCAGGGATCAAATTTGTGAGTACTACGTAAAATTTTGCTACGGAGGCGAGGCAGTCGA
536	Euc_001743_O_1	GAAGAATACAGGCTCGTACCTGATACACTGTACCTGACTGTTAACTACATAGATCGGTAT
537	Euc_012405_O_1	TCCACCCTAAATGCGATACGTGAAAAGTATAGACAACAGAAGGTAAACTATTCATTACTG
538	Euc_003739_O_2	AGGCTTCTAGTTGCGTTCCCCCAAACTACATGGATCGGCAGCAGGATATTAATGAGCGGA
539	Euc_022338_O_2	GAGAAAAATGACAGATTGATATCGATGATGATGACTGTCGTGTCATCAGTAGTGTGCTTT
540	Euc_028605_O_5	TTTCCAATTGTAGTTCGTCTTTTATTGTAACAATAAATTGATAGATACTGATTCGAAATA
541	Euc_041006_O_1	ACATTTATGCTAACTATAGGAGAACGGAGAATTGTAGCTGCGTCTCTGCTAACTACATGG
542	Euc_006643_O_1	TTCTGGCTTAAAGGCTATTCTTTGTGCACAATGACCTGAGGGAGGTCTCGACAGACCACT
543	Euc_045338_O_1	TTCATCCGGGTCCTGGTTATCATACTCTTATATATGTTGGGGAATAACGGTTCATATGTT
544	Euc_046486_O_3	GGGTGTGCTTAATAGTTCTTATTAGTCTTAGCTTATTATCTTTGATTGGACATGCTATAA
545	Euc_012070_O_2	CTTGCTAAGTAGACATGTTATATTTCTAATGCTTTGAGAACAATATTACAGTATAATTAG
546	Euc_006617_O_2	AATCATCGACTAGACCGATGGTCAAAGTGGTAATCATGTAATTAAACGCGTTTGTCATTG
547	Euc_007827_O_2	ATGGAAAAATCTATGGATATGAAGGATTGAAGATATCCGTCTGGGTAAGCTGTGTATCAT
548	Euc_008036_O_3	TTATGATTTGAGAAAACCCTTGCAGGCTGCGATTTGCGGATCATGACAGCATAGTTTTGC
549	Euc_001596_O_2	GTTTTGTTGTGAGGGCTTGGTAGGTTTTCATTATATTGTAATGTCGACGACAGAGATTTT
550	Euc_005870_O_3	CCAATTAATGTTACTGCTCAAGCTGACGTACCTGCGAAAAAAGCACCAGTGACTGCTAAT
551	Euc_006901_O_3	TGATGTCAAAACGTAGCTCTTTTTTGTGTGAGCTATCCTGCTAAATTAAACCTCAGCAAA
552	Euc_006902_O_1	ACATGAGTATTATGAATACTTCGGTCCTGACTATACACTTCATGTTGCTCCGAGTAACAT
553	Euc_007440_O_2	GAATTGGCGATCACAATCTACTGTAGTCAATACTCAAGTGGGAGGTGTAAATAGATTCCA
554	Euc_008994_O_1	GATCATGTGTAATCAGTATATCAGGTTAGAAACAGTACTCTTGAGCTTAGCGGGCACTGT
555	Euc_024580_O_2	TCCTGTGAAGGTGGTCGACTCAATCAAAAGGTACCTTGTAGATAAGGTACCTTTTCTCAA
556	Euc_037831_O_5	GCATTTTATACGACGGATAGAGTCATGACCGTATCTTTCCATAAGTTTGGGGACTTCTTC
557	Euc_034958_O_3	CCTCGTTTCTTTGCGGTTCGGACGCATCATGGATGTATCTCCAAAGAGTAATCTGTCGAT
558	Euc_022967_O_2	AATTCAGATCTATTAGTGAAAGTTGGCATGAGTCTCAATCTTAGGGGAATACAGTACGGA
559	Euc_008599_O_3	TGATATGAGTATCATAACTCGGATGGTGACAACTTTGTACTACGGTCGGCACCGGTAGAT
560	Euc_009919_O_1	CATATACAATCTTAGTGGATTAGCTGAGGTCGAAACTGACAAGAGTGATCGCCCGTTGGA
561	Euc_015820_O_2	CATGGCTAACGCTGGCCCTAGCACTAATGGGAGCCAATTTTTCATATGCACTGTAAAGAC
562	Euc_008327_O_2	AACAAAGTCTACCTTGACATTAGCATCGGTAACCCTGTCGGGAAACTAGTCGGAAGAATT
563	Euc_004604_O_2	TGTGCTTGGATATACTGTATAAGCATTCTATATTATGCTTGTTGGCTTCGTTTTGAGGGA
564	Euc_000966_O_1	TTAACGTCGACCGCTTCTCTGCCCCTTGAATTTTCCCGAGAAAACCAGGAACCTGCCAAA
565	Euc_001037_O_1	TGTTGAATACGATGTATTATAATGTTGGTGTCTTGGTGAAATACAGAATTATGCTTGCGT
566	Euc_004603_O_2	ATCGCTGTGGCTGATCTCGTCGCTCCGGCTTTTCATAAAAATCATGGCTGAGGCAATCGA
567	Euc_005465_O_2	CTCGCAACCCTATATCTCGCTCAGGCGAAGAAGTCTGAGGATTTGAAAGAGGTGACTCAC
568	Euc_006571_O_1	TGTTTTTGGGTACACGCAGTTAGGATAACTAGCATGAAAGCCCGATCCCGCATATACAGG
569	Euc_006786_O_2	GAGGACTAGCCGGAACTTCATCGAACTCTCTCGGAGGGGTTACTACGATAACGTCAAGTT
570	Euc_007057_O_1	GATGGCTAGCACTGTGTAGAAAGGTGAATTTAAAGTACTTGTCTACACTGCTTATTAAAT
571	Euc_008670_O_2	TGAGACTGTCTTGGCGTGTATTTTGGAATAAACTATTATCACGTTTTGTTAAATATAATA
572	Euc_009137_O_3	TTACAAAATGGCTCTCAGAAAGTATCGAAAGGCCCTGCGCTATCTGGATATCTGCTGGGA
573	Euc_010285_O_2	AATTTTATGTTTGCTACTGCTTAGTGCTTAATGGACTTGCGTAGGTATTCAAATTACAGA
574	Euc_010600_O_1	TGGAACCGTGGTATCGGCTGACGTTATCCGTGATTTTAAGACTGGAGATAGTTTATGCTA
575	Euc_011551_O_2	CTTTGATGTATCCTCAGTGTACTGCTTTTAGCTATGTATAGATCGAGTCAACTCATTGAA
576	Euc_020743_O_3	TTTTTATTATTTACCTTCGCCTTTACGCTGCATACGTTAATAGGTTATTATTTCCTTCAA
577	Euc_023739_O_1	ATTTGTCCATGACAATCGTAGTCGAAGACACGATACGCTCTTAGATGGTACGGAAATCTG
578	Euc_031985_O_2	TGAATAGAGATAACTTTTCTGAGTGTGAATTGGATATTACGTTGCAAATAGCCGAATGAA
579	Euc_032025_O_2	GCTTTAGGTTAGGGATCCCTGTAAGCTGATGATAGATATTGGAGATGGTACTTGTAAGAT
580	Euc_032173_O_1	TGTTGTGTTTGGAAAGGTGCTGTCTGGGATGGATGTTGTCCACAAGATTGAGGCTGAAGG
581	Euc_009143_O_1	GGAAAGCGGGGAATGAGCATGTGGATATTATCTCTTTCTACAATGAAATATTCATTCCTT
582	Euc_000349_O_1	CATCAGGACGTTGACTCTAATTAAGACATATGTGACAGAGCGCCCTGTTAATGCGGTTAC
583	Euc_000575_O_2	CTTTAGGTTTGATCTGTCTGTTTTGTCTATCCTGCGAGTTTCGAGCATGTGCGTGTGTGA
584	Euc_000804_O_1	CAGCCCCAATAGATACTGGCTCTGTGCCGCTACTGAGAACAGTATTAAAATCTGGGACCT
585	Euc_000805_O_2	AAGAATGAAGCTGATATGAGTGATGGAACTACGGGGGCCATGAGCTCAAATAAGAAGGTC
586	Euc_000806_O_1	TGACTACAATTAGCACCTCACCATTATCGAACTGTATAATTGTGCTTGCCTGCTATTATT
587	Euc_002248_O_4	TTGAAGCGGAAATATATATTTATGCTACTACATAAGTAATGTACTACTTGACAAGATGAG
588	Euc_003203_O_1	TACTCGATGTGGTATAGAATTTATCCAATGTACTCCTAAATGTAGATACATCGTGTATTG
589	Euc_003209_O_2	GCTTCGTCTGATACCACTATCAAGATAATAGGCGTGAGCAATAGCTCTGGATCACAGCAC
590	Euc_004429_O_4	GGTCGGCTTGCTAGTGTATCTGATGACAAGAGCATATCACTCTATGATTACTCATGAAGG
591	Euc_004607_O_3	GAAAGGAGAAAAGCATGGAGATCGATCTCGGAAACCTCGCATTCGACGTCGATTTTCATC
592	Euc_004682_O_1	GATTCAGTACCCGGATTCGCAAGTCAACCGGTTGGAGATAACTCCACATAAGCGGTACCT
593	Euc_005786_O_1	TTCCATGTATCAAGCCGCATCAATGTTTGTCGCTGCAATTAACATGTGTGCAGTCGATCC
594	Euc_005887_O_2	TTCAGCGCATTGTGTAAATGTAGATAGGTGATATATTTCTCGTTGCAATGTAGGGTAAGA
595	Euc_005981_O_2	TCCAATAATCACATTTACCATCAACAGGCATCAGCAACATACTGTTGTAGTGTAATTAAT
596	Euc_006766_O_1	GGGCATTCTGACTACCTGCACTGTATAGCTGCACGGAACTCTTCTAGTCAGATTATAACA
597	Euc_006769_O_1	AATCGTCTGGTAGATTGTCAAAAACTAATAAACCTGTGATTGATCCGGATTCTAGTAATG
598	Euc_006907_O_2	AGTTGAGGATTCTCCACTATGACAGCTCTCATGGCTTGAATCTAAAGTCATCTGGTTTTC
599	Euc_007518_O_1	GAACAATCATTCTGTAGAACACTAGAGTCTATATGCTTGACTGTATCGGTTAATTAATTC
600	Euc_007717_O_1	AGATAGCGATAGAGTTATACTGCATGTACTGAGGTAAATGTTTTGATTACTCCACCCAAT
601	Euc_007718_O_1	AAGAATTGTTAGGAGGTGTATACTTTCTGTAACTGTATTCAATGAGCATACACCTGACGG
602	Euc_007741_O_2	CAACTCATATAATGACTGGATTCTGGCAACCGCGTCTTCAGACACAACAGTTGGACTATT
603	Euc_007884_O_1	AGTGTAAAAGGATGCCCCTAATAGATTATATGCCAAGTGTAGTATATATAATAGTGCTTT
604	Euc_008258_O_2	AAGAATCTACAGTTGTCTTATGCTACTCTATTACTCAATTATGCTGTGCTATTGATTGAG
605	Euc_008465_O_4	TCTGAATACATACTTTGTGGTCTCTATAAAAGACCAATGATACAGGCATGGTCATTAATT
606	Euc_008616_O_5	TAAATCTTCTCATGTGCCTGGCGTAAATTTTGCAGTTATTACTAGACCAAGATAGTTTCA
607	Euc_008690_O_4	ACATGGATTCGATCAATCGCCACATGACAACTAAAACAAGCGGTTCACGTGATTGTAATT
608	Euc_008708_O_4	AGATGAGTATGCTCGGGTGTATGATATTCGCAATTACAAGTGGAATGGATCGCATAATTT
609	Euc_008850_O_5	TCTTTGATTCTGTTGTATGGTGTATCTTATTGTATCTTCTATCTGCCCCCCATGTAATTC
610	Euc_009072_O_1	TTCGTTGTGTAGTACTGGGAGTTACTACTTGTATGTATGTAAATCATGTGGCGTCTGTCC
611	Euc_009465_O_1	GGAGATGTGTAATATGTCTGAGCGGTCACACTCTAGCTGTTACATGCGTAAAGTGGGGAG
612	Euc_009472_O_3	CCACCGTTGCGTAACTCGAATAGCCGGATTTTCGTTTTCGTTTTTATTTCCCCGTTAATT
613	Euc_009550_O_1	TGAGATGCTCTGTGTGAGGACTTTTACGAAACTTGAATGGCCCGTAAGGACAATAAGCTT
614	Euc_010284_O_3	TGGGTTGTTGCGACGGGTTCTACAGATAAGACTGTTAAGTTATTTGATCTACGCAAGATC
615	Euc_010595_O_1	GCAGAGGTGCCTACATATGCTTTAGAATGCTAGTAGCTTGGAAGTGCAACACGCTCGTGA
616	Euc_010657_O_1	AGTAAAGTTTAACGACTATGCATCTGTCGTAGTATCAGCCGGCTATGATCGTTCAGTGCG
617	Euc_012636_O_2	CGTTAGGATAGTCTTTAAAGGAGTTGGTGATTATTGATTTCCACCCAATATATGTAGCGT
618	Euc_012748_O_2	GAGCAAGCTACTTACAAAAATCGACAGCGTCTTTACCTATCTGAACAGACAGATGGCAGT
619	Euc_012879_O_2	TCCTTCCGACAAGTACCGTATTGCAAGTTGTGGTATGGACAATACGGTTAAAATCTGGTC
620	Euc_015515_O_1	TTTCACTCGATGACGGTTGGCCGGATAAATAATCGCTTATATAGTCCTAATAAGTTCCAT
621	Euc_015724_O_3	ATATGTAGGTGGTAGAGGTGTGGATATTGCATAGACCGAACCTCCGCAGGTCCGCATTCT
622	Euc_016167_O_1	CCATTGAACTACTTATGGATTACTTTATACATGAAATATCATGCCGGAGTAATTTTGAGT
623	Euc_016633_O_3	AGCATTAGAGACCTGGATTTTAGTCTAGATTCAGAGTTTTTGGCTACGACATCTACTGAT
624	Euc_017485_O_3	AAAGGTTTATCCCTCATTGGATTTGATATATAAACTGAGAGTGTTTTGCCCCCCATTAAA
625	Euc_018007_O_1	GTACAGCGTGTATTTCTTGTTACGATACTTGAGGGGTTAGAGGCACCTACGAATTAGGAA
626	Euc_020775_O_3	ATATCCTTATGAATGAAGTTTGGATGATAAGTGGCGCCAGACTTTCTACTCACCCTTTTT
627	Euc_023132_O_3	TGATCACATCGTTGTTTGCAATAAGACGTCATCAATTTATATCATGACTCTACAGGGACA
628	Euc_023569_O_2	TTTTCCCAGTGTACTGCGAGAGTGATGCTACATAAGTTTACTCTTGTGTCTAACTTTTCC
629	Euc_023611_O_1	AGATTCTACAGATGGCGCTATACGAGCTGTTATACGGACATTTTATGACCATACACATCC
630	Euc_024934_O_3	TGCTACGGGAAACCAGGACAAAACTTGTAGGATTTGGGACATACGAAACTTATCTAAGTC
631	Euc_025546_O_1	CAAGTCATATAGTTACAGTGTCGCATGACAGAACAATTAAGCTCTGGACTAGTAACGACG
632	Euc_030134_O_2	TGCCACATCGTAACCATCATAGCACTTATCATCTAATTATGGTGAAAGGGAGTTATATAT
633	Euc_031787_O_5	GTTTATACTTATAAACAACAGAGAGACAACTGTACAGGTGTTGTAAACACTCCCAGTGTG
634	Euc_034435_O_1	CTGTGTTTTAGCCCGAGGGCCAATCACTTAGTTGCTACTTCGTGGGATAATCAGGTACGG
635	Euc_034452_O_3	GCAAAGTAGAGTTTAAGTTTCGTTGTGCTTGGACCGGAAAACTCACATGCTTAGAGTTTA
636	Euc_035789_O_5	AAGATTTGGGCATAACTTGTATGAACTTTTTCTGTTGTCGACACTGTAATTACACGAGCT
637	Euc_035804_O_4	AAACAGATGCATGTATGCTTCATAACTCTATAGATATGGAAATGTCACTGTACACTGATC
638	Euc_043057_O_2	TTATTGGTGCACAGGACGGAAAATTGCGCATATATTCTATTTCAGGTGATACATTAACAG
639	Euc_046741_O_1	AGGCACAGACACTTGCCTAAACCAATATACAAGGCAGGTATTCTAAGGCGCACCGTGAAT
640	Euc_047161_O_4	CATGCGAAGGTTTCTGGGAATTTTCAGTAGAAAATTCGGTCGTGGCGGCCATCCTCGATA
641	Pra_001766_O_1	TTAAGCTGATAGCTTTAGTTCCTACGTGGAATGTATAAATGCACCATTGTCCATAAGGCA
642	Pra_002927_O_2	GGATGCTCTGGTTACATGACTACTCCTTAGGGAATCAGTCAGACATTTTAAATAACTTCC
643	Pra_007642_O_2	TCATTAAGCGGTACTGGCAGAGGACATGTCTATTTATACAAGCAAATGGTCCTATTGGCT
644	Pra_013714_O_1	ATGTTGGTCAGACCTCAAATATTGTACTCCCCACACTAGGGAGCATTTACGGTGAATATA
645	Pra_016332_O_1	TCCTCTCGACCCTTAGAGTCCTCTGCGAATCTTGTTGTTAGTTACTGTGTACGCTGTAAC
646	Pra_021677_O_3	AAGCATGTTTTGAATTTATGGTGGTGGCATGTGGATATTTGAACTTGGTTGAGAAAAATT
647	Pra_027562_O_2	CATTCCTATTGAAGGGTCAACCTTTAATTTTGGCTAGCAGGACTGTATAGGATTATATGC
648	Pra_001504_O_2	TTATTGTATTTTAGATTCTTGATGGCCATCTAAACTTCTGGCTGCTTGGTGCAACATTGA
649	Pra_015211_O_2	ATAGCTAATGATTCCATGCTATCCATGGTATCTACTTCACGATAATAAAGGTCTTAGTCC
650	Pra_020421_O_2	CACCTAATAGGCCTGAGTATTGCTCACCACTATGCTGATATGGGGAGCAATAACGTTAGT
651	Pra_003187_O_2	TTTCTTTTCACTTTGTACTAATGATCATTGTGACCACAAAATCTTTATACACAATACAGA
652	Pra_015661_O_1	CTTGTCACTATCCTCATATTGATATCACCTCGTGTATGTTGTGGGGTGGCAAAATTACTT
653	Pra_013874_O_1	TATTTTAACTCAGCGACTTACCAGCCTAGTAAGCAATGGGGAGCTTGCATGTATTAGTTT
654	Pra_014615_O_1	ATTCGTCCTGGTCCTTTAGGACATGTACTTATGTCCATGCAAGTGCTTCTTGCCTAAGCT
655	Pra_004578_O_2	TTCTAGGCGATATATATCGCCGTAACTTTGGATGTGTTAAGAATATAGGGGATCATTAGC
656	Pra_023387_O_3	AGTTGCAGAGTGTGTAGCAACTGATGAGCATAGTTGTTATGTTTCTCAACTCAGTTGCAC
657	Pra_006970_O_1	AAGAAACTCATACACTGGACAGGCCAACCTTCCAAATATGTGTTTAGAAAACCTTTGTCT
658	Pra_010322_O_1	AAGGGGTGCTATCCATATCTAGAATCTACCATGCTCAATGAGGTATCTTCATTAGTATAC
659	Pra_022721_O_1	ATCTAATGCTAGTTTATTGATTTCTATGATCCAAGACCTCGTCATAGATCAAGTGCCTAG
660	Pra_023407_O_1	TTGTTATTAAATACCATTCAATATGCTTATGATTCATGAATGCTTAAGAGATTCTGCTGC
661	Pra_001945_O_2	GCTTCTAAACTGTAGAAGCCTGTTATCTTTAGACTCGTGGTTATGTGAACTACTTTTACA
662	Pra_008233_O_1	GGCTGTGGGGATTCGAGCCTGATGGTTATGCACTGTGGCCAGCAAGATGTTGAAGTTTTA
663	Pra_008234_O_4	GCCTGATGGTTATGCACTGTAAGTGATCTGATTTGATTAACTATTTTATCAATTAATTTT
664	Pra_022054_O_2	ATGGTCATTATCCGAGATAGTGCGCTTTGTCATGGGAAAATGACTATTGAATGTGAGTTT
665	Pra_012137_O_2	TTTTCTGGTGCATCCTTAACACAGCTTGGTTACATGGTGAATTACAGTATTTGAAGGAGT
666	Pra_012582_O_2	AGATTTAATGCCACTTAGGTGATCGGTGACCCACTTGTACATATAGATGTTGGCGATGTT
667	Pra_015285_O_2	AAGAAATTCATCAATTCTTTGAAATTATTGTTCCCTTTTGATGCGGCCCCTTTCTGGAGG
668	Pra_017229_O_1	TAAAGTATATTTTAGCCGCTGTTGTTGTAAATTTATGTTTTTCATTGCTATCAACATTTA
669	Pra_020724_O_2	GGTTTTCCTATAAGATGTATGAATTCGCACTGTGGTGCAATTTTATGAATTAAACTCAAA
670	Pra_004555_O_1	TTTACTATTCCGTCTGGGCTTAGAGATGTACGTTAATTGGTCATTTAAGACGACTCAGTT
671	Pra_004556_O_5	TCAAATCTAGTCAATATCCGTGTTGAGCTAAACAAGCGCTGAAAGTTTGCTCGAATCAGC
672	Pra_005729_O_2	AGAAAGTTGTGTACTAATTTGTATTGTAACGTCCATTTATCCAACGAGTCCTCCATTCAT
673	Pra_007395_O_3	CAGTACTGTATTCGAAGATCCTGAAAATTTACTAAAACAAATGGAATATCAACAACCTAG
674	Pra_009503_O_1	TTGCTCTATATAATTTGTGCTCGTGTGTGTACTTGAAGATCCATCCTCACATAGTCCAAT
675	Pra_011283_O_1	GTGTGTATAGTTTTATAACACTCTATGGTATCACTACCACTATGGGCCTGTTTAGTCCAA
676	Pra_012322_O_3	GAAGCAGAATCAGCTTTGACCAGTATTTAGTGTCTTGTATACAATTCTTGTTTCAGTGAA
677	Pra_023236_O_3	AAATCAAGATTAAAATCCGAAACCAAGGCTAACCAGCAAACTGTGAGGTGTACATTGTTG
678	Pra_000171_O_2	TTCCAAGCAGAAGGGCACATGTTGTGACATCAAGTAGTAGATTGTTCTGCAGATTCTGGT
679	Pra_000172_O_1	GTTAATGTAATACATTTAGTTTTTAGATAACTGTTAATGTGTAGTAAAGCACTAGGAAGA
680	Pra_001480_O_3	GAGGCTTCAAAGGTTTTTGTGTCTTTTCTAGTTATTATAAACGCTTCATAGGTTCCTAGG
681	Pra_001692_O_2	GAAGATTGTAAGTTGGGTGAACTTTTTTACCACGCTAGGTTGATCTATTTTAAGACTCTT
682	Pra_005313_ORF_O1	AAAATAGCTGCGCGTACCACAAAGGTGACAAACGCCGGATTTCTCTTATCAGACTTGTCA
683	Pra_006362_O_1	TTTAATTATCATAGTTTTATTCCGGCTATCTTGATCATTCACGGAAGTCCCGAGAGTCAA
684	Pra_006493_O_3	GTGGAGTGAACGTGGTTACTTCAATGGATTACCCTTCTATCGTGTCATTAAACACTTTGT
685	Pra_006983_O_1	GCTAACTCTTCTAGTTGAGATCTCCATCAATTAATGGATACAAACATTGAGTTTCACTTT
686	Pra_007665_O_1	GGATCACTACTGGATTCCGTTACATTAGTTATTGCAAGTTGGTTATTATGTACGTTTATA
687	Pra_012196_O_1	ATGAACAAATGCAATTACCCTGTTTTATTCTATCCCGCTTTAATTAATATTGGTCATGTT
688	Pra_013382_O_1	TTTGCTTGTGGATTGTACTGTGGTACATGGTATAAATCTATAGGCTATGTCGATTATTTT
689	Pra_016461_O_1	ATATAAGATATAAGATATTGCCAGCAAACTATTTGACAGGTTATTTAATAAAGTGTGCTA
690	Pra_017611_O_1	TTTTAAATGTGGACAGAGGCACTATAAGAATGCGAAATATCGTCGGAGCACGACTAATTG
691	Pra_019776_O_1	ATAGACTAGTTCTACAAAGCCCTAGGATGATGGACTTCATTTCTTTTGCATTAAGATGAA
692	Pra_020659_O_1	GATTTCTTATGGGGTTGGAACATTCCTCGCTGCCTTCTGGTAATATTAGGTTATGCGTTT
693	Pra_022559_O_3	AATTGAGGTTGACTGTGTACTTCTCCAGTGGACAGGAGAAAGCGATAAAATTCAAACGTT
694	Pra_024188_O_5	AAGGAAGGGCAAATAGAGCTCGCGCTCAAGAAATACCTTAAATCGATACGGTATTTGGAT
695	Pra_027973_O_2	TAATTTAAGAGCTATGAAACAACTACCTTTTGGAATGGTTTTGTTTTTAGCATCCCAATT
696	Pra_001353_O_1	TTGTAAATTATGCTGGTTCCATATGGGGGTTAATCAGTATCCTGGTTATTTGTGACACCA
697	Pra_001978_O_3	GTTGTGAACTATCAATAGACGGGGATGGTCCTTTTTAGCTGCTCCTTAAGCAGCTCAAAT
698	Pra_002810_O_2	TCAATTCCGGTCATATGTAGACGACTATAATGTTGTTTGTGTCCTATAACTATAGTGTTG
699	Pra_002811_O_1	CATTTTACACCCTATAACAAAATATAGTGTCATAAGTTTACACCAGGTAACAACTCTATA
700	Pra_002812_O_3	ATGGAGAGTTTTATTCATTACATGAAAGAGTATGTCACCTTTCGTGCTCCATCTATTGAT
701	Pra_003514_O_1	TTTCACGTCCTGTATACTCACTCAAGCAACTTTAGGATGAAGAGCTAAAGTATATCAAAG
702	Pra_004104_O_2	AATGCACTCTTTATAAAGTGGGATGAGGTATGTGTTTCCTTCCTATTGGCTAACCTGAAT
703	Pra_005595_O_1	ATTGGGCAATCGTTATTGATTTTACCTATCGCTATCTCACTGTCCGCCAATTTAGTGTAA
704	Pra_005754_O_1	TTTCAGCGGATATAAAGTCTTCCAACTTGTAAACCGGTGCTGTGAAGATTAAAAGTCCTT
705	Pra_006463_O_1	GCTTTAGAGGCAATGGTAGATTATGAAGTCAACACCAGGGAGTTTGACCGTTTGGGACAT
706	Pra_006665_O_1	CATTCAATTTGACATTGGAGTTTCAAGGCATTCCAAGGATAGCATGTACACAAGTTGAAT
707	Pra_006750_O_1	CATAAAATTACTATGGAAGTTGGATCATTATCTATGCCATAGTGGAGTAGAACTAGATTT
708	Pra_007030_O_1	CTCTTGATTCTAGAATCTAAACTACTACCTTGCGGACATGACTGAGCATCTCTCTAACAG
709	Pra_007854_O_1	CAGGGTTGTGCTAGTTTAACATTTTAACTTAATGTAATCATGTAAGCTTTAGAGAGGTGG
710	Pra_007917_O_1	GTAAATGTTTACATTGAGGTCATGCATGAGTGTTAATTACGCTTTCACTACTGTTCACTT
711	Pra_007989_ORF_O2	AATTAAAGCTTGGTTGTATGATCATTTGGGATCGAGAGTAGATTATGATGCTCCTGGGCA
712	Pra_008506_O_1	TTATCTAGCTAGAAGTTGTGAAATTAAGAGGGATGTGAGGATTGGGTTATAACTAGTGTA
713	Pra_008692_ORF_O2	AATGAATCAGGCATTAAAGCGGGAATCATTTATGACTTGGCAACCTGAAAATTCTATTAA
714	Pra_008693_O_2	TTCTTGACGTTTTAATATGGTATGGTATTAAATTTGGAAGGCCTATTCGATTGTTTGCAA
715	Pra_009170_O_1	TTCTTATAACCTGTACGATTGCCGATATATCACCAATTTTGCTGATTTTAATCTGAGTTT
716	Pra_009408_O_1	CAATTTCATATTCGGGTTCAATGTAGTGCCTCTCATTTTAGGGTGATAGCATGAGTTTTT
717	Pra_009522_O_1	TCCACAAGTTAACATAGGTAACTATCGACTGAAGTGAACTGGGGGGCAGAAGCTAACTAT
718	Pra_009734_O_2	TTTAGATAGCCATTTACATTTTACTTATTATTGGACTTGTAAAGATTTTTGTACCCTTGT
719	Pra_009815_O_4	TTGCTGAAATATTTCAAGCTGAAAGTTATGATTCTGGCCAAGAAGTCTACTGAAAATTTG
720	Pra_010670_O_2	AAACATAAGTTTGGCCCAGATTCGGTTTATCATAAAATCTGGCTGCATATAAGGTGTCAG
721	Pra_011297_O_1	ATGTTCTAGAATTTGTCTAAGCTAGCTACTGGTGTTTAACTGATATGGAAAACTTTTGCC
722	Pra_013098_O_2	TTTGGGGAGTACTTTAGTCAATAAAAGTGAAGTGAATCATGATATAAAGGGTTTAAGTAA
723	Pra_013172_O_2	AGAAGTTACTAATTTGTAGATAAATTCTAACGAAGGTGATGATAGCATACACGTAATGAA
724	Pra_013589_O_2	GAATTTTGATGGTAGCGTATGGTTGAAGGAAAACTTGGATATATCATGTAAACATTTTTC
725	Pra_013608_O_1	TTAATGAACCGCTTTTTCCTTGAGAGGCTATGAATGCCTGTAGAACTAATCCTTTAAGTA
726	Pra_014299_O_2	TTTCTCTAACACTATATTTTCTGGTATGACCGCTCTACATTGTATATTAACCCTTGCAAA
727	Pra_014498_O_1	TATATTCACTGTGCTGGGATTATCCTCTCCCCTTTTTGACCCACTGTTGTGTGTATTTGA
728	Pra_014548_O_1	GAGCATACAGCGTTATCTTTGAGACGAGTCATCAATGATAATATCCTCGTAAAAGGTTAC
729	Pra_014610_O_2	TTTATTCAATTACGACGGATTCAGTTGGCCTTTTGTAACATTCAAGTATCCATCTATCAC
730	Pra_016090_O_2	ATGTTCAGGGGTATTAAAAATTCAGAGGATAAATTTCCTCACTCTCAAGTGTTAGATGGT
731	Pra_016722_O_2	CAAAGTCTAGACGTTAATGTTTTGGAACTCTTTTTTCGAATTTGTGCCTATTGAATCACT
732	Pra_016785_O_3	TATAAATATATTGTACTGGGGATCCAAGACATGGCAATATATGTCGAGATTTTCATTTTC
733	Pra_017094_O_3	CTTTTGCATGAGTTCAAATGTCTTTGTGACATATTGTCTTGAACCACCGAGGATATATCA
734	Pra_017527_O_2	GTTTGTATGTCCAATAGATTATAACCTATTTACTGTGACACTATTCTTCACACCCATGTC
735	Pra_017591_ORF_O2	AGATCTAGTTGTTTCAGCATCGTTGGACCAAACTGTTCGTGTATGGGATATAAGTGGCCT
736	Pra_017769_O_2	TGCCGTATCAAAAGATTGGTACTTCCTTATGGACACACAAGATCGTAAGCATGGCTGAAT
737	Pra_018047_O_2	TTGATGGCCACATGAGTTGTTTATACAAGTCGTTGTTTTATGAGAGAACCTTCTTCAGAT
738	Pra_018414_O_1	ATTTCTATAGTGCCATATGCTTGTCGGTTGTCATTGACCTCTAATAGAATAGCCAGAGTA
739	Pra_018986_O_1	TTCACGGCAGTTGAACTAGTCATAGTGGAATATTATTTAAATGGTGTATTCTAGTCACAT
740	Pra_019479_ORF_O1	TGCAGGCGCTCTATAGTTCTGTTCTCTAGCATGAAGTGTGTATTTTATCTATTGTGGACC
741	Pra_020144_O_1	TGTCTTTAATCTTCAGGGTTCGTTACTAACAATTGAGCTCAAATCTCTATTCTGACCAGC
742	Pra_022480_O_1	CATTTATAGAGTTGTGCAAAATCACCCATAATGCTATGAATTGACAGGTGACTGTAATCT
743	Pra_023079_O_2	GGAGAAAATTTCCTATCCCTTTGTGGGTGTGTGAAAAACGAAATATAGAGGAACAATGTG
744	Pra_026739_O_2	ACCAATCATTTATTTGCAGTGTAGTTGATATGAAGGGAGAAATATGACAGTTGGTTTCAA
745	Pra_026951_O_2	AAGTTAATGTTCTCATAGGTTATTCATTGGAGTTGTCTCGTATGTACGCTGTGCCGTAGT
746	Pra_026529_O_2	CTCATAAATTGAGGCTTGCCTACGTTAATTGTTATATATGGAGAGCCATGCTAATTGTTA
747	Euc_006366_O_2	GCAGATCATGTAATTGTATCTCAAATTATAGTATCCGTATTCTGTACAAATGCTCCGGAA
748	Euc_017378_O_1	TCTTTACGCAGATGGTGACTGAAGCTGGTTCCGAGATCGGCATATGTAGCTGGTAGAGGT
749	Pra_000888_O_1	TTCACATTGAGGGTTGCCGTCGGTATTCGCCGATGATATCCTGTTTTACGCGCAACAGTT
750	Pra_014166_O_1	TCATTATTTAGGGTGCAGGCTGTATAAAATGTTGTAAATTGTAGTATCAATGTGTACAAT
751	Pra_003189_O_1	GCATTCACCACGACAGTAAAGTAATCATTATGATTACTAATGTATTGCTTTCATGGGGTG
752	Pra_009356_O_4	AAAGGGTATATTTTGTCTCATGTTGGGGTGATAATTCTCCCTGAAAGTCTCCAAAATATA
753	Pra_000065_ORF_O_2	AAATTTCCGGTTGCCATAGTCTAGTGGGGTGAGGGTTCATTCTAGGGGATTTATTGTGTT
754	Pra_014197_ORF_O1	GCAGTGATAAAGGTACTTCTTGGTGATAATCCTAAAGCCTTACCCATGGATATCCAGCCT
755	Pra_009081_O_2	TTCTTTAACAAGGTAAAAATCCCCCCCTTGGCATGTAGCTCAATTAGTTGTAATGGAACT
756	Pra_013417_O_1	AGTTGTAAACAGTGTAATAAGGAGCAGAAGTTGTGATAGCTTTTAGGAACGATAGACTTT
757	Pra_005755_O_1	TGAACCAATTCTTGTATATTAGATATGTAACATGTATGAATGTCCATAGAGCAGAGCTTT
758	Pra_006670_O_2	AGCCAGGCACGCTTAACTAAATTTCGTTTAGTTCACCATGACTATTCGTTGAACTTAATG
759	Pra_007027_O_1	CAAAACCCCTTGTAGGGTGGACTTCTGTTGTATCCAATTTTTATGGCATAATTAGCTAGT
760	Pra_007276_O_1	AATTTGGTGATTATTCCTTACCATATCGTACTGTACAGATACGGTAAGGTCGAAATATAT
761	Pra_007390_ORF_O1	CATGCCGTGATCGGTCGATTGCATTAAGTGCTGCAAGGATCAAATAGTGGCACTGTCATG
762	Pra_012648_ORF_O1	CAAACATAAATAAGGTTGCTACTTTAAAGGGACATACGGAACGAGTTACTGATGTGGCAT
763	Pra_013171_O_2	ATTTATGGATGAGGTACTCCTTATGAATATCTTCAAACTAAGAAATAACTATATATGCAA
764	Euc_045414_O_2	CTTGGTTTTTGTTGAGCTTTCTATTTCAAGCAATTTGTGATTGGGGGGTTCTGCATTCTT
765	Euc_044328_O_2	ATGTCTAAAGAGCCGTGATCTATGAGTAGATTAGAAACCGCCTTTTTAGTTGCAAACGCC
766	Euc_015615_O_2	TTGCAACAAGGTATACTTAGTCAGTCCTTGTTATGTATGTCTTTTGTCAACCCTTCAGGG
767	Euc_017239_O_3	GGCGGAATCCCTTTGTTCTTTCGAGCTTTACGTGACAAGTCGGCCAGAAAGCAGTAGCAT
768	Euc_018643_O_3	TTGATGTACGAGCCGCTATATCTAATTCTGCCTCCCAGTCACTGCCAAGTTTTACTCTTC
769	Euc_019127_O_5	GTCTTGCATGTCAGCTATTATACAGTCCTGTTTATAGTCCTGTGATGTAATAAAAAGCTG
770	Euc_022624_O_3	AAGTAGGAGATCGTGTAGAGAGAATACTTTCTGCTCTCAGCGGCGAAGAGGTTTGTCTGC
771	Euc_032424_O_1	AATTGTGAGTAGAATAGGAGAAACTTTTGTACAAGATTAATACGTGTGGCATAATAAGAT
772	Euc_037472_O_1	TGATGTGCAGTTTACATTATTATGGTTCGAGTATTATTTAGCTGCCCTATCTTAAGTCAT

TABLE 15
Peptide Table.

			Patent	Patent
Protein			ORF	ORF
SEQ ID	Target	Patent PEPTIDE Sequence	start	stop

261	CDK type A	MGDGSLGSGGRGNSGGGGGGGSRPEWLQQYDLIGKIGEGTYGLVFLARIKHPST	387	1820
		NRGKYIAIKKFKQSKDGDGVSPTAIREIMLLREISHENVVKLVNVHINPVDMSL
		YLAFDYADHDLYEIIRHHRDKVNQAINPYTVKSLLWQLLNGLNYLHSNWIIHRD
		LKPSNILVMGEGEEQGVVKIADFGLARVYQAPLKPLSDNGVVVTIWYRAPELLL
		GAKHYTSAVDMWAVGCIFAELLTLKPLFQGQEVKANPNPFQLDQLDKIFKVLGH
		PTQEKWPMLVNLPHWQSDVQHIQRHKYDDNALGNVVRLSSKNATFDLLSKMLEY
		DPQKRITAAQALEHEYFRMEPLPGRNALVPSSPGDKVNYPTRPVDTTTDIEGTT
		SLQPSQSASSGNAVPGNMPGPHVVTNRPMPRPMHMVGMQRVPASGMAGYNLNPS
		GMGGGMNPSGIPMQRGVANQAQQSRRKDPGMGMGGYPPQQKQRRF
262	CDK type A	MEKYQQLAKIGEGTYGIVYKAKDKKSGELLALKKIRLEAEDEGIPSTAIREISL	99	1007
		LKQLQHPNIVRLYDVVHTEKKLTLVFEFLDQDLKKYLDACGDNGLEPYTVKSFL
		YQLLQGIAFCHEHRVLHRDLKPQNLLINMEGELKLADFGLARAFGIPVRNYTHE
		VVTLWYRAPDVLMGSRKYSTQVDIWSVGCIFAEMVNGRPLFPGSSEQDQLLRIF
		KTLGTPSLKTWPGMAELPDFKDNFPKYVVQSFKKICPKKLDKTGLDLLSRMLQY
		DPAKRISAEQAMGHPYFKDLKLRKPKAAGPGP
263	CDK type A	MDQYEKIEKIGEGTYGVVYKAIDRSTNKTIALKKIRLEQEDEGVPSTAIREISL	120	1004
		LKEMQHGNIVKLQDVVHSERRLYLVFEYLDLDLKKHMDSCPEFSKDTHTIKMFL
		YQILRGISYCHSHRVLHRDLKPQNLLLDRRTNSLKLADFGLARAFGIPVRTFTH
		EVVTLWYRAPEILLGSRHYSTPVDVWSVGCIFAEMVNRRPLFPGDSEIDELFKI
		FRIMGTPNEDSWPGVTSLPDFKSTFPKWASQDLKTVTPTVDPAGIDLLSKMLCM
		DPRRRITAKVALEHEYFKDVGVIP
264	CDK type A	MVMKSKLDKYEKLEKLGEGTYGVVYKAQDKTTKEIYALKKIRLESEDEGIPSTA	23	937
		IREIALLKELQHPNVVRIHDVIHTNKKLILVFEFVDYDLKKFLHNFDKGIDPKI
		VKSLLYQLVRGVAHCHQQKVLHRDLKPQNLLVSQEGILKLGDFGLARAFGIPVK
		NYTNEVVTLWYRAPDILLGSKNYSTSVDIWSIGCIFVEMLNQKPLFPGSSEQDQ
		LKKIFKIMGTPDATKWPGIAELPDWKPENFEKYPGEPLNKVCPKMDPDGLDLLD
		KMLKCNPSERIAAKNAMSHPYFKDIPDNLKKLYN
265	CDK type A	MDQYEKVEKIGEGTYGVVYKAIDRLTNETIALKKIRLEQEDEGVPSTAIREISL	149	1033
		LKEMQHGNIVRLQDVVHSENRLYLVFEYLDLDLKKHMDSSPDFAKDPRLVKIFL
		YQILRGIAYCHSHRVLHRDLKPQNLLIDRRTNALKLADFGLARAFGIPVRTFTH
		EVVTLWYRAPEILLGSRHYSTPVDVWSVGCIFAEMVNQRPLFPGDSEIDELFKI
		FRILGTPNEDTWPGVTALPDFKSAFPKWPAKNLQDMVPGLNSAGIDLLSKMLCL
		DPSKRITARSALEHEYFKDIGFVP
266	CDK type B-1	MEKYEKLEKVGEGTYGKVYKAKDKATGQLVALKKTRLEMDEEGVPPTALREVSL	199	1116
		LQLLSQSLYVVRLLSVEHVDGGSKRKPMLYLVFEYLDTDLKKFIDSHRKGPNPR
		PVPAATVQNFLYQLLKGVAHCHSHGVLHRDLKPQNLLVDKEKGILKIADLGLGR
		AFTVPLKSYTHEVVTLWYRAPEVLLGSAHYSIGVDMWSVGCIFAEMVRRQALFP
		GDSEFQQLLHIFRLLGTPTEKQWPGVTTLRDWHVYPQWEPQNLARAVPSLGPDG
		VDLLSKMLKYDPAERISAKAALDHPFFDSLDKSQF
267	CDK type B-2	MERPATAAVSAMEAFEKLEKVGEGTYGKVYRAREKATGKIVALKKTRLHEDEEG	41	982
		VPPTTLREISILRMLSRDPHIVRLMDVKQGQNKEGKTVLYLVFEYMETDLKKYI
		RGFRSSGESIPVNIVKSLMYQLCKGVAFCHGHGVLHRDLKPHNLLMDKKTLTLK
		IADLGLARAFTVPIKKYTHEILTLWYRAPEVLLGATHYSTAVDMWSVGCIFAEL
		VTKQALFPGDSELQQLLHIFRLLGTPNEKMWPGVSSLMNWHEYPQWKPQSLSTA
		VPNLDKDGLDLLSQMLHYEPSRRISAKAAMEHPYFDDVNKTCL
268	CDK type C	MGCVLGREVSSGIVTESKGRDSSEVETSKRDDSVAAKVEGEGKAEEVRTEETQK	291	2042
		KEKVEDDQQSREQRRRSKPSTKLGNLPKHIRGEQVAAGWPSWLSDICGEALNGW
		IPRRANTFEKIDKIGQGTYSNVYKAKDLLTGKIVALKKVRFDNLEPESVRFMAR
		EILILRHLDHPNVVKLEGLVTSRMSCSLYLVFEYMEHDLAGLAASPAIKFTEPQ
		VKCYMHQLLSGLEHCHNRRVLHRDIKGSNLLIDNGGVLKIGDFGLASFYDPDHK
		HRMTSRVVTLWYRPPELLLGANDYGVGIDLWSAGCILAELLAGKPIMPGRTEVE
		QLHKIYKLCGSPSEEYWKKYKLPNATLFKPREPYRRCIRETFKDFPPSSLPLIE
		TLLAIDPAERGTATDALQSEFFRTEPYACEPSSLPQYPPSKEMDAKKRDDEARR
		LRAASKGQADGSKKERTRDRRVRAVPAPEANAELQHNIDRRRLISHANAKSKSE
		KFPPPHQDGALGFPLGASHRFDPAVVPPDVPFTSTSFTSSKEHDQTWSGPLVDP
		PGAPRRKKHSAGGQRESSKLSMGTNKGRRADSHLKAYESKSIA
269	CDK type C	MYSKSSAVDDSRESPKDRVSSSRRLSEVKTSRLDSSRRENGFRARDKVGDVSVM	107	2236
		LIDKKVNGSARFCDDQIEKKSDRLQKQRRERAEAAAAADHPGAGRVPKAVEGEQ
		VAAGWPVWLSAVAGEAIKGWLPRRADTFEKLDKIGQGTYSSVYKARDVTNNKIV
		ALKRVRFDNLDTESVKFMAREIHILRMLDHPNVIKLEGLITSRMSCSLYLVFEY
		MEHDLTGLASRPDVKFSEPQIKCYMKQLLSGLDHCHKHGVLHRDIKGSNLLIDN
		NGILKIADFGLASVFDPHQTAPLTSRVVTLWYRPPELLLGASRYGVEVDLWSTG
		CILGELYTGKPILPGKTEVEQLHKIFKLCGSPSDDYWRRLHLPHAAVFKPPQPY
		RRCVAEIFKELPPVALGLLETLISVDPSQRGTAAFALRSEFFTASPLPCDPSSL
		PKYPPSKEIDMKLREEEARRRGAAGGKNELEKRGTKDSRTNSAYYPNAGQLQVK
		QCHSNANGRSEIFGPYQEKTVSGFLVAPPKQARVSKETRKDYAEQPDRASFSGP
		LVPGPGFSKAGKELGHSITVSRNTNLSTLSSLVTSRTGDNKQKSGPLVSESANQ
		ASRYSGPIREMEPARKQDRRSHVRTNIDYRSREDGNSSTKEPALYGRGSAGNKI
		YVSGPLLVSSNNVDQMLKEHDRRIQEHARRARFDKARVGNNHPQAAVDSKLVSV
		HDAG
270	CDK type C	MGCIPTIISDGRRRSAAPDKRRPRPRRSSSEGEAPPHATAAGSEGGESARGAPG	82	1749
		KERPEPAPRFVVRSPQGWPPWLVAAVGHAIGEFVPRCADSFRKLAKIGEGTYSN
		VYKARDLVTGKTVALKKVRFDNLEAESIKFMAREILVLTRLNHPNVIKLEGPVT
		SRMSSGLYLAFEYMEHDLSGIAARQNGKFTEPQVKCFMRQLLSGLEHCHNHDVL
		HRDIKCSNLLIDNEGNLKIADFGLATFYDPERKQVMTNRVVTLWYRAPELLLGA
		TSYGIGIDLWSAGCILAELLYGKPIMPGRTEVEQLHKIFKLCGSPSEAYWNKFK
		LPNANIFKPPQPYARCIAETFKDFPPSALPLLETLLSIDPDERGTATTALNSEF
		FAAEPHACEPSSLPKYPPSKEMDLKLIKEKTRRDSSKRPSAIHGSRRDGIHDRA
		GRVIPAPEATAENQATLHRPRAMKKANPMSRSEKFPPAHMDGVVGSSANAWLSG
		PASNAAPDSRRHRSLNQNPSSSVGKASTGSSTTQETLKVAPELLQVGSSSLHPC
		HRMLVYGSNLTIRSK
271	CDK type C	MGCICAKQADRGPASPGSGILTGAGTGTGTRSSKIPSGLFEFEKSGVKEHGGRS	151	1560
		GELRKLEEKGSLSKRLRLELGFSHRYVEAEQAAAGWPSWLTAVAGDAIQGLVPL
		KADSFEKLEKIGQGTYSSVFRARELANGRMVALKKVRFDNFQPESIQFMAREIS
		ILRRLDHPNIMKLEGIITSRMSNSIYLVFEYMEHDLYGLISSPQVKFSDAQVKC
		YMKQLLSGIEHCHQHGVIHRDVKSSNILVNNEGILRIGDFGLANILNPKDRQQL
		TSHVVTLWYRPPELLMGSTSYGVTVDLWSVGCVFAELMFRKPILRGRTEVEQLH
		KIFKLCGSPPDGYWKMCKVPQATMFRPRHAYECTLRERCKGIATSAMKLMETFL
		SIEPHKRGTASSALISEYFRTVPYACDPSSLPKYPPNKEIDAKHREEARRKKAR
		SRVREAEVGKRPTRIHRASQEQGFSSNIAPKEKRSYA
272	CDK type C	MAVAAPGHLNVNESPSWGSRSVDCFEKLEQIGEGTYGQVYMAKEKKTGEIVALK	82	1644
		KIRMDNEREGFPITAIREIKILKKLHHENVIKLKEIVTSPGPEKDEQGRPEGNK
		YKGGIYMVFEYMDHDLTGLADRPGMRFSVPQIKCYMRQLLTGLHYCHINQVLHR
		DIKGSNLLIDNEGNLKLADFGLARSFSNDHNANLTNRVITLWYRPPELLLGATK
		YGPAVDMWSVGCIFAELLHGKPIFPGKDEPEQLNKIFELCGAPDEINWPGVSKI
		PWYNNFKPTRPMKRRLREVFRHFDRHALELLERMLTLDPSQRISAKDALDAEYF
		WADPLPCDPKSLPKYESSHEFQTKKKRQQQRQHEETAKRQKLQHPPQHPRLPPV
		QQSGQAHAQMRPGPNQLMHGSQPPVATGPPGHHYGKPRGPSGGAGRYPSSGNPG
		GGYNHPSRGGQGGSGGYNSGPYPPQGRAPPYGSSGMPGAGPRGGGGNNYGVGPS
		NYPQGGGGPYGGSGAGRGSNMMGGNRNQQYGWQQ
273	CDK type C	MGCICTKGILPAHYRIKDGGLKLSKSSKRSVGSLRRDELAVSANGGGNDAADRL	626	2782
		ISSPHEVENEVEDRKNVDFNEKLSKSLQRRATMDVASGGHTQAQLKVGKVGGFP
		LGERGAQVVAGWPSWLTAVAGEAINGWVPRRADSFEKLEKIGQGTYSSVYRARD
		LETNTIVALKKVRFANMDPESVRFMAREIIIMRKLDHPNVMKLEGLITSRVSGS
		LYLVFEYMDHDLAGLAATPSIKLTESQIKCYMQQLLRGLEYCHSHGVLHRDIKG
		SNLLVDNNGNLKIGDFGLATFFRTNQKQPLTSRVVTLWYRPPELLLGSSDYGAS
		VDLWSSGCILAELFAGKPIMPGRTEVEQLHKIFKLCGSPSEEYWKKSKLPHATI
		FKPQQPYKRCLLETFKDFPSSALGLLDVLLAVEPECRGTASSALQNEFFTSNPL
		PSDPSSLPKYPSSKEFDARLRDEEARKHKATAGKARGLESIRKGSKESKVVPTS
		NANADLKASIQKRQEQSNPRSTGEKPGGTTQNNFILSGQSAKPSLNGSTQIGNA
		NEVEALIVPDRELDSPRGGAELRRQRSFMQRRASQLSRFSNSVAVGGDSHLDCS
		REKGANTQWRDEGFVARCSHPDGGELAGKHDWSHHLLHRPISLFKKGGEHSRRD
		SIASYSPKKGRIHYSGPLLPSGDNLDEMLKEHERQIQNAVRKARLDKVKTKREY
		ADHGQTESLLCWANGR
274	CDK type D	MDPDPSPDPDPPKSWSIHTRREIIARYEILERVGSGAYSDVYRGRRLSDGLAVA	13	1467
		LKEVHDYQSAFREIEALQILRGSPHVVLLHEYFWREDEDAVLVLEFLRSDLAAV
		IADASRRPRDGGGGGAAALRAGEVKRWMLQVLEGVDACHRNSIVHRDLKPGNLL
		ISEEGVLKIADFGQARILLDDGNVAPDYEPESFEERSSEQADILQQPETMEADT
		TCPEGQEQGAITREAYLREVDEFKAKNPRHEIDKETSIFDGDTSCLATCTTSDI
		GEDPFKGSYVYGAEEAGEDAQGCLTSCVGTRWFRAPELLYGSTDYGLEVDLWSL
		GCIFAELLTLEPLFPGISDIDQLSRIFNVLGNLSEEVWPGCTKLPDYRTISFCK
		IENPIGLESCLPNCSSDEVSLVRRLLCYDPAARATPMELLQDKYFTEEPLPVPI
		SALQVPQSKNSHDEDSAGGWYDYNDMDSDSDFEDFGPLKFTPTSTGFSIQFP
275	CDK type D	MDPDPSPSPDPPKSWSIHTRREIIARYEILERVGSGAYSDVYRGRRLSDGLAVA	113	1558
		LKEVHDYQSAFREIEALQILRGSPHVVLLHEYFWREDEDAVLVLEFLRSDLAAV
		IADASRRPRGGGVAPLRAGEGKRWMLQVLEGVDACHRNSIVHRDLKPGNLLISE
		EGVLKIADFGQARILLDDGNVAPDYEPESFEERSSEQADILQQPETMEADTTCP
		EGQEQGAITREAYLREVDEFKAKNPRHEIDKETSIYDGDTSCLATCTTSDIGED
		PFKGSYVYGAEEAGEDAQGSLTSCVGTRWFRAPELLYGSTDYGLEVDLWSLGCI
		FAELLTLEPLFPGISDIDQLSRIFNVLGNLSEEVWPGCTKLPDYRTISFCKIEN
		PIGLESCLPNCSSDEVSLVRRLLCYDPAARATPMELLQDKYFTEEPLPVPISAL
		QVPQSKNSHDEDSAGGWYDYNDMDSDSDFEDFGPLKFTPTSTGFSIQFP
276	Cyclin A	MSNQHRRSSFSSSTTSSLAKRHASSSSSSLENAGKAFAAAAVPSHLAKKRAPLG	187	1686
		NLTNLKAGDGNSRSSSAPSTLVANATKLAKTRKGSSTSSSIMGLSGSALPRYAS
		TKPSGVLPSVNPSIPRIEIAVDPMSCSMVVSPSRSDMQSVSLDESMSTCESFKS
		PDVEYIDNEDVSAVDSIDRKTFSNLYISDAAAKTAVNICERDVLMEMETDEKIV
		NVDDNYSDPQLCATIACDIYQHLRASEAKKRPSTDFMDRVQKDITASMRAILID
		WLVEVAEEYRLVPDTLYLTVNYIDRYLSGNVMNRQRLQLLGVACMMIAAKYEEI
		CAPQVEEFCYITDNTYFKEEVLQMESSVLNYLKFEMTAPTVKCFLRRFVRAAQG
		VNEVPSLQLECMANYIAELSLLEYDMLCYAPSLVAASAIFLAKFVITPSKRPWD
		PTLQHYTLYQPSDLGNCVKDLHRLCFNNHGSTLPAIREKYSQHKYKYVAKKYCP
		PSIPPEFFHNLVY
277	Cyclin A	MNKENAVGTKSEAPTIRITRSRSKALGTSTGMLPSSRPSFKQEQKRTVRANAKR	238	1653
		SASDENKGTMVGNASKQHKKRTVLNDVTNIFCENSYSNCLNAAKAQTSRQGRKW
		SMKKDRDVHQSGAVQIMQEDVQAQFVEESSKIKVAESMEITIPDKWAKRENSEH
		SISMKDTVAESSRKPQEFICGEKSAALVQPSIVDIDSKLEDPQACTPYALDIYN
		YKRSTELERRPSTIYMETLQKDVTPNMRGILVDWLVEVSEEYKLVPDTLYLTVN
		LIDRSLSQKFIEKQRLQLLGVTCMLIASKYEEICPPRVEEFCFITDNTYTSLEV
		LKMESRVLNLLHFQLSVPTVKTFLRRFVQAAQVSSEVPSVELEYLANYLAELTL
		VEYSFLKELPSLMAASAVLLARWTLNQSDNPWNLTLEHYTKYKASELKAAVLAL
		EDLQLNTSGSTLNAIREKYRQQKVNYSLLIHSKANHEIL
278	Cyclin B	MAGSDENNPGVVGGAHVQEGLRVGAGKMGAGNVQQRRALSNINSNIIGAPPYPC	235	1539
		AVNKRVLSEKNVNSENDLLNAAHRPITRQFAAQMAYKQQLRPEENKRTTQSVSN
		PSKSEDCAILDVDDDKMADDFPVPMFVQHTEAMLEEIDRMEEVEMEDVAEEPVT
		DIDSGDKENQLAVVEYIDDLYMFYQKAEASSCVPPNYMDRQQDINERMRGILID
		WLIEVHYKFELMDETLYLTVNLIDRFLAVQPVVKKKLQLVGVTAMLLACKYEEV
		SVPVVEDLILISDRAYSRKEVLEMERLMVNTLHFNMSVPTPYVFMRRFLKAAQS
		DKKLELLSFFIIELSLVEYDMLKFPPSLLAASAIYTALSTITRTKQWSTTCEWH
		TSYSEEQLLECARLMVTFHQRAGSGKLTGVHRKYSTSKFGHAARTEPANFLLDF
		RL
279	Cyclin B	MASRPIVPVQARGEAAIGGGAGKAAIGGGAGKQQKKNGAAEGRNRKALGDIGNL	158	1618
		VTVRGIEGKVQPHRPITRSFCAQLLANAQAAAAAENNKKQAVVNVNGAPSILDV
		PGAGKRAEPAAAAAAAVAKAAQKKVVKPKQKAEVIDLTSDSERAIEAKKKQQHH
		EPTKKEGEKSSRRNMPTLTSVLTARSKAACGMTKKPKEKVVDIDAGDAHNELAA
		FEYIEDIYTYYKEAENESLPRNYMSSQPEINEKMRAILVDWLIEIHNKFDLMPE
		TLYLTINIIDRFLSVKAVPRRELQLLGMGALFTASKYEEIWAPEVNDLVCIADR
		AYSHEQVLAMEKTILGKLEWTLTVPTHYVFLVRFIKASLGDRKLENMVYFLAEL
		GVMNYATLTYCPSMVAASAVYAARCTLGLTPLWNDTLKLHTGFSESQLMDCARL
		LVGYHAKAKENKLQVVYKKYSSSQREGVALIPPAKALLCEGGGLSSSSSLASSS
280	Cyclin B	MGLPDENNAALSKPTNLQVGGLEIGGRKFGQEIRQTRRALSVINQNLVGDRAYP	205	1530
		CHVVNKRGHSKRDAVCGKDQVDPVHRPLTRKFAAQTASTQQHCIEEAKKPRTAV
		QERNEFGDCIFVDVEDCQPSSENQPVPMFLEIPESRLDDDMEEVEMEDIVEEEE
		EEPIMDIDGRDKKNPLAVVDYIEDIYANYRRTENCSCVSANYMAQQADINEKMR
		SILIDWLIEVHDKFDLMHETLFLTVNLIDRFLARQSVVRKKLQLVGLVAMLLAC
		KYEEVSVPVVGDLILISDKAYTRKEVLEMESLMLNSLQFNMSVPTPYVFMRRFL
		KAAESDKKLEVLSFFLIELSLVEYEMVKFPPSLLAAAAIFTAQCTLYGFKQWTK
		TCEWHSNYTEDQLLECARMMVGFHQKAATGKLTGVHRKYGTSKFGYTSKCEPAN
		FLLGEMKNP
281	Cyclin B	MGLPDENNAALSKPTNLQVGGLEIGGRKFGQEIRQTRRALSVINQNLVGDRAYP	174	1499
		CHVVNKRGHSKRDAVCGKDQVDPVHRPLTRKFAAQTASTQQHCIEEAKKPRTAV
		QERNEFGDCIFVDVEDCQPSSENQPVPMFLEIPESRLDDDMEEVEMEDIVEEEE
		EEPIMDIDGRDKKNPLAVVDYIEDIYANYRRTENCSCVSANYMAQQADINEKMR
		SILIDWLIEVHDKFDLMHETLFLTVNLIDRFLARQSVVRKKLQLVGLVAMLLAC
		KYEEVSVPVVGDLILISDKAYTRKEVLEMEKLMLNSLQFNMSVPTPYVFMRRFL
		KAAESDKKLEVLSFFLIELSLVEYEMVKFPPSLLAAAAIFTAQCTLYGFKQWTK
		TCEWHSNYTEDQLLECARMMVGFHQKAATGKLTGVHRKYGTSKFGYTSKCEAAN
		FLLGEMKNP
282	Cyclin D	MAMVQRQGHDPSSPQEQEDGPSSFLSDDALYCEEGRFEEDDGGGGGQVDGIPLF	94	1332
		PSQPADRQQDSPWADEDGEEKEEEEAELQSLFSKERGARPELAKDDGGAVAARR
		EAVEWMLMVRGVYGFSALTAVLAVDYLDRFLAGFRLQRDNRPWMTQLVAVACLA
		LAAKVEETDVPLLVELQEVGDARYVFEAKTVQRMELLVLSTLGWEMHPVTPLSF
		VHHVARRLGASPHHGEFTHWAFLRRCERLLVAAVSDARSLKHLPSVLAAAAMLR
		VIEEVEPFRSSEYKAQLLSALHMSQEMVEDCCRFILGIAETAGDAVTSSLDSFL
		KRKRRCGHLSPRSPSGVIDASFSCDDESNDSWATDPPSDPDDNDDLNPLPKKSR
		SSSPSSSPSSVPDKVLDLPFMNRIFEGIVNGSPI
283	Cyclin D	MEASYQPHHHGHLRQHDPSSSQQEEQVPFDALYCSEEHWGEEDEEEGLASDGLL	176	1342
		SEERDHRLLSPRALLDQDLLWEDEELASLFSKEEPGGMRLNLENDPSLADARRE
		AVEWIMRVHAHYAFSALTALLAVNYWDRFTCSFALQEDKPWMTQLSAVACLSLA
		AKVEETQVPLLIDFQVEDSSPVFEAKNIQRMELLVLSSLEWKMNPVTPLSFLDY
		MTRRLGLTGHLCWEFLRRCENVLLSVISDCRFTCYLPSVIAASTMLHVINGLKP
		RLDVEDQTQLLGILAMGMDKIDACYKLIDDDHALRSQRYSHNKRKFGSVPGSPR
		GVMELCFSSDGSNDSWSVAASVSSSPEPHSKKSRAGEEAEDRLLRGLEGEEDDP
		ASADIFSFPH
284	Cyclin D	MALQEEDTRRHYPTAPPFSPDGLYCEDETFGEDLADNACEYAGGGARDGLCEIK	150	1283
		DPTLPPSLLGQDLFWEDGELASLVSRETGTHPCWDELISDGSVALARKDAVGWI
		LRVHGHYGFRPLTAMLAVNYLDRFFLSRSYQRDRPWISQLVAVACLSVAAKVEE
		TQVPILLDLQVANAKFVFESRTIQRMELLLMSTLDWRMNSVTPISFFDHILRRF
		GLTTNLHRQFFWMCERLLLSVVADVRLASFLPSVVATAAMLYVNKEIEPCICSE
		FLDQLLSLLKINEDRVNECYELILELSIDHPEILNYKHKRKRGSVPSSPSGVID
		TSFSCDSSNDSWGVASSVSSSLEPRFKRSRFQDQQMGLPSVNVSSMGVLNSSY
285	Cyclin-	MGQIQYSEKYFDDTYEYRHVVLPPDVAKLLPKNRLLSENEWRAIGVQQSRGWVH	101	367
	dependent	YAIHRPEPHIMLFRRPLNYQQQQENQAQQNMLAK
	kinase
	regulatory
	subunit
286	Histone	MGSIDPPKAEQNGTAAAAVADPGQKPGAGDAMPPPPPVKHSNGTAAEPDVATKR	9	1352
	acetyltransferase	RRMSVLPLEVGTRVMCRWRDGKYHPVKVIERRKLNPGDPNDYEYYVHYTEFNRR
		LDEWVKLEQLDLNSVETVVDEKVEDKVTGLKMTRHQKRKIDETHVEGHEELDAA
		SLREHEEFTKVKNIATIELGRYEIETWYFSPFPPEYNDCSKLYFCEFCLNFMKR
		KEQLQRHMKKCDLKHPPGDEIYRSGTLSMFEVDGKKNKVYGQNLCYLAKLFLDH
		KTLYYDVDLFLFYVLCECDDRGCHMVGYFSKEKHSEESYNLACILTLPPYQRKG
		YGKFLIAFSYELSKKEGKVGTPERPLSDLGLLSYKGYWTRVLLDILKKHKANIS
		IKELSDMTAIKADDILNTLQSLDLIQYRKGQHVICADPKVLDRHLKAAGRGGLE
		VDVSKLIWTPYREQG
287	Histone	MAQKHSTAPDPAAEPKKRRRVGFSGIDAGVDPNGCFKVYLVSREEEVGAPDSFC	89	1486
	acetyltransferase	LDPVDLSHFFEEEDGKIYGYEGLKISVWVSCVSFHSYAEIAFESKSDGGKGITD
		LNTALKNMFGETLVDNKDDFLQTFSKETQFIRSTVSAGEILKHKHSDDHVNDSV
		SNLKVGSDVEAVRMLMGDMTAGHLYSRLVPLVLLLVDGSSPIDVTDSSWELYLL
		IQKTSDQQGNFHDRLLGFAAVYRFYHYPDSSRLRLGQILVLPLYQRKGYGRYLL
		EVLNNVAIADDVYDFTIEEPVDNLQHLRTCIDVQRLLSFDKVQQAVNSTVSQLK
		QGKLSKKTYIPRLLPPPSVVEDARKRFKINKKQFLQCWEILVYLGLDPADKSIQ
		DYFSVISNRVRADILGKDSETAGKKVIEVPSDFDPEMSFVMHRAKAGGEANGIQ
		VEDNQNKQEEQLQQLIDERLKDIKLIAEKVTQK
288	Histone	MAQKHSTAPDPAAEPKKRRRVGFSGIDAGVDPNGCFKVYLVSREEEVGAPDSFC	89	1477
	acetyltransferase	LDPVDLSHFFEEEDGKIYGYEGLKISVWVSCVSFHSYAEIAFESKSDGGKGITD
		LNTALKNMFGETLVDNKDDFLQTFSKETQFIRSTVSAGEILKHKHSDGHVNDSV
		SNLKVGSDVEAVRMLMGDMTAGHLYSRLVPLVLLLVDGSNPIDVTDSSWELYLL
		IQKTSDQQGNFHDRLLGFAAVYRFYHYPDSLRLRLGQILVLPLYQRKGYGHYLL
		EVLNNVAIADDVYDFTIEEPVDNLQHLRTCIDVQRLLSFDKVQQAVNSTVSQLK
		QGKLSKKTYIPRLLPPPSVVEDARKRFKINKKQFLQCWEILVYLGLDPADKSIQ
		DYFSVISNRVRADILGKDSETAGKKVIEVPSDFDPEMSFVLHRAKAGGETNGIQ
		VEDNQNKQEEQLQQLIDERLKDIKLIAQKVSRK
289	Histone	MALPMEFWGVEVKAGQPLKVNPGNAKILHLSQASLGECKSSKGNESVPLHVKFG	160	1062
	deacetylase	DQKLVLGTLSTENFPQLAFDLVFEKEFELSHNWKSGSVYFCGYKSVVHDDDDEF
		SDLESDSEEEDLPMIGVENGKVAAQASAKTATASANASKVESSGKQKARIPQPM
		KVDEDDSDEDDDDEDEDESDEEGVDGEADSDEEEDESDEEETPKKAEIGKKRAA
		DSATKTPVPAKKSKLPTPQKTDGKKGGHTATPHPAKQAGKNPANSANKSQSPKS
		AGQVSCKSCSKTFNSDGALQSHSKAKHGGK;
290	Histone	MEFWGVEVKAGQPLKVNPGNAKILHLSQASLGECKSSKGNESVPLHVKFGDQKL	172	1077
	deacetylase	VLGTLSTENFPQLAFDLVFEKEFELSHNWKSGSVYFCGYKSVVHDDDDEFSDLE
		SDSEEEDLPMIGVENGKVAAQASAKTATASANASKVESSGKQKASIPQPMKVDE
		DDSDEDDDEDDDDEDESDEGVDGEADSDEEEDESDEEETPKKAEIGKKRAADSA
		TKTPVPAKKSKLPTPQKTDGKKGGHTATPHPAKQAGKNPANSANKSQSPKSAGQ
		VSCKSCSKTFNSDGALQSHSKAKHGGK
291	Histone	MEFWGVEVKSGEPLNVEPGAETVVHLSQACLGETKEKTKESVLLYVHIGVQKLV	66	989
	deacetylase	LGTLSADKFPQIPFDLVFEKSFKLSHNWKNGSVFFSGYKTLLPCGSDADSPYSD
		SDTDEGLPINVTAQADVPAKKAPVTANANAAKPNLASAKQKVKIVESNEDGKNE
		GDDDEDADVSSDDDAEDDSGDEDMVDGGDESSDEDDDDSEEGESSEEEEPKAQP
		SKKRPADSVLKTPASDKKSKLETPQKTDGKKASEHVATPYPSKQAGKAIASKGQ
		AKQQTPNSNEFSCKPCNRSFKSDQALQSHNKAKHGGS
292	Histone	MDTGGNSLPSGPDGVKRKVCYFYDPEVGNYYLLQHMQVLKPVPARDRDLCRFHA	111	1541
	deacetylase	DDYVAFLRSITPETQQDQLRQLKRFNVGEDCPVFDGLHSFCQTYAGGSVGGAVK
		LNHGLCDIAINWAGGLHHAKKCEASGFCYVNDIVLGILELLKQHERVLYVDIDI
		HHGDGVEEAFYTTDRVMTVSFHKFGDYFPGTGDIRDIGYGKGKYYSLNVPLDDG
		IDDESYHSLFKPIIGKVMEVFKPGAVVLQCGADSLSGDRLGCFNLSIKGHAECV
		RYMRSFNVPVLLLGGGGYTIRNVARCWCYETGVALGLEVDDKMPQHEYYEYFGP
		DYTLHVAPSNMENKNSRQLLEEIRSKLLENLSKLQHAPSVPFQERPPDTELPEA
		DEDQEDPDERWDPDSDMDVDEDRKPLPSRVKRELIVEPEVKDQDSQKASIDHGR
		GLDTTQEDNASIKVSDMNSMITDEQSVKMEQDNVNKPSEQIFPK
293	Histone	MDTGGNSLPSGPDGVKRKVCYFYDPEVGNYYYGQGHPMKPHRIRMTHALLAHYG	116	1615
	deacetylase	LLQHMQVLKPVPARDRDLCRFHADDYVAFLRSITPETQQDQLRQLKRFNVGEDC
		PVFDGLHSFCQTYAGGSVGGAVKLNHGLCDIAINWAGGLHHAKKCEASGFCYVN
		DIVLGILELLKQHERVLYVDIDIHHGDGVEEAFYTTDRVMTVSFHKFGDYFPGT
		GDIRDIGYGKGKYYSLNVPLDDGIDDESYHSLFKPIIGKVMEVFKPGAVVLQCG
		ADSLSGDRLGCFNLSIKGHAECVRYMRSFNVPVLLLGGGGYTIRNVARCWCYET
		GVALGLEVDDKMPQHEYYEYFGPDYTLHVAPSNMENKNSRQLLEDIRSKLLENL
		SKLQHAPSVPFQERPPDTELPEADEDQEDPDERWDPDSDMDVDEDRKPLPSRVK
		RELIVEPEVKDQDSQKASIDHGRGLDTTQEDNASIKVSDMNSMITDEQSVKMEQ
		DNVNKPSEQIFPK
294	Histone	MRPKDRISYFYDGDVGSVYFGPNHPMKPHRLCMTHHLVLSYELHTKMEIYRPHK	155	1453
	deacetylase	AYPAELAQFHSPDYVEFLHRITPDTQHLFPNDLAKYNLGEDCPVFENLFEFCQI
		YAGGTIDAARRLNNQLCDIAINWAGGLHHAKKCEASGFCYINDLVLGILELLKY
		HARVLYIDIDVHHGDGVEEAFYFTDRVMTVSFHKFGDMFFPGTGDVKEIGGKEG
		KFYAINVPLKDGIDDTSFTRLFKAIISKVVETYQPGAIVLQCGADSLAGDRLGC
		FNLSIDGHSECVRFVKKFNLPLLVTGGGGYTKENVARCWVVETGVLLDTELPNE
		IPENEYFKYFAPDYSLKIPRGNIVLENLNSKSYLSAIKVQVLENLENIQHAPSV
		QMQEVPPDFYIPDFDEDEQNPDERMDQHTQDKQIQRDDEYYDGDNDNDHNMDDS
295	Histone	MTVAEDFHVNNRSKMVSQATPESRLTGGEDDNSLHNQVDELLCQELPERQVILE	228	2033
	deacetylase	FEGTRPKPYFSDHNGGENSALGVRATEDDLNSDVEAEEKQKEMITLEDMYKNDGT
		LYDDDEDDSDWEPVKRQVELMRWFCTNCTMVNVEDVFLCDICGEHRDSGILRHG
		FYASPFMQDVGAPSVEAEVQESREDHARSSPPSSSTVVGFDEKMLLHSEVEMKS
		HPHPERADRLQAIAASLATAGIFPGRCRSLPVREITKEELQMVHSSEHVDAVEM
		TSHMFSSYFTPDTYANEHSARAARIAAGLCADLASTIISGRSKNGFALVRPPGH
		HAGIKHAMGFCLHNNAAVAALAAQGAGAKKVLIVDWDVHHGNGTQEIFDGNKSV
		LYISLHRHEGGNFYPGTGAAHEVGTMGAEGYCVNIPWSRRGVGDNDYVFAFHHI
		VLPIASAFAPDFTIISAGFDAARGDPLGCCDVTPAGYAQMTHMLSALSGGKLLV
		ILEGGYNLRSISSSAVAVIKVLLGDSPISEIADAVPSKAGLRTVLEVLKIQRSY
		WPSLESIFWELQSQWGIFLVDNRRKQIRKRRRVLVPIWWKWGRKSVLYHLLNGH
		LHVKTKR
296	Histone	MAAAPSSPPTNRVDVFWHDGMLSHDTGRGVFDTGSDPGFLDVLEKHPENPDRVR	110	1258
	deacetylase	NMVSILKRGPISPFISWHTATPALISQLLSFHSPEYINELVEADKNGGKVLCAG
		TFLNPGSWDAALLAAGNTLSAMKYVLDGKGKIAYALVRPPGHHAQPSQADGYCF
		LNNAGLAVRLALDSGCKRVVVVDIDVHYGNGTAEGFYQSSDVLTISLHMNHGSW
		GPSHPQSGSVDELGEDEGYGYNMNIPLPNGTGDRGYEYAVTELVVPAVESFKPE
		MVVLVVGQDSSAFDPNGRQCLTMDGYRAIGRTIRGLADRHSGGRILIVQEGGYH
		VTYSAYCLHATVEGILDLPDPLLADPIAYYPEDEAFPVKVVDSIKRYLVDKVPF
		LKEH
297	Histone	MVESSGGASLPSVGQDARKRRVSYFYEPTIGDYYYGQGHPMKPHRIRMAHNLIV	50	1462
	deacetylase	HYYLHRRMEISRPFPAATTDIRRFHSEDYVTFISSVTPETVSDPAFSRQLKRFN
		VGEDCPVFDGIFGFCQASAGGSMGAAVKLNRGDSDIALNWAGGLHHAKKSEASG
		FCYVNDIVLGILELLKVHKRVLYVDIDVHHGDGVEEAFYTTDRVMTVSFHKFGD
		FFPGSGHIKDTGAGPGKNYALNVPLNDGIDDESFRGMFRPIIQKVMEVYQPDAV
		VLQCGADSLSGDRLGCFNLSVKGHADCLRFLRSFNVPLMVLGGGGYTMRNVARC
		WCYETAVAVGVEPENDLPYNEYYEYFGPDYTLHVEPCSMENLNAPKDLERIRNM
		LLEQLSRIPHAPSVPFQMTPPITQEPEEAEEDMDERPKPRIWNGEDYESDAEED
		KSQHRSSNADALHDENVEMRDSVGENSGDKTREDRSPS
298	MAT1 CDK-	MVVPSSNPHNREMAIRRRMASTFNKREDDFPSLREYNDYLEEVEEMTFNLIEGV	176	739
	activating	DVPTIEAKIAKYQEENAEQIMINRAKKAEEFAAALAASKGLPPQTDPDGALNSQ
	kinase assembly	AGLSVGTQGQYAPAIAGGQPRPTGMAPQPVPLGTGLDTHGYDDEEMIKLRAERG
	factor	GRAGGWSIELSKKRALEEAFGSLWL
299	Peptidylprolyl	MAAIISCHHYHSCCSSLIASKWVGARIPTSCFGRSSTQSNNAASVRQFVTRCSS	150	1529
	isomerase	SPSSRGQWQPHQNGEKGRSFSLRECAISIALAVGLVTGVPSLDMSTGNAYAASP
		ALPDLSVLISGPPIKDPEALLRYALPINNKAIREVQKPLEDITDSLKVAGLRAL
		DSVERNVRQASRVLKQGKNLIVSGLAESKKDHGVELLDKLEAGMDELQQIVEDG
		NRDAVAGKQRELLNYVGGVEEDMVDGFPYEVPEEYKNMPLLKGRAAVDMKVKVK
		DNPNLEECVFRIVLDGYNAPVTAGNFVDLVERHFYDGMEIQRADGFVVQTGDPE
		GPAESFIDPSTEKPRTIPLEIMVDGEKAPVYGATLEELGLYKAQTKLPFNAFGT
		MAMARDEFEDNSASSQIFWLLKESELTPSNANILDGRYAVFGYVTENQDFLADL
		KVGDVIESVQVVSGLDNLANPSYKIAG;
300	Peptidylprolyl	MAGEDFDIPPADEMNEDFDLPDDDDDAPVMKAGDEKEIGKQGLKKKLVKEGDAW	247	1971
	isomerase	ETPDNGDEVEVHYTGTLLDGTQFDSSRDRGTPFKFTLGQGQVIKGWDQGIKTMK
		KGENAIFTIPPELAYGEAGSPPTIPPNATLQFDVELLSWTSVKDICKDGGIFKK
		ILVEGEKWENPKDLDEVLVKYEFQLEDGTTIARSDGVEFTVKEGHFCPAVAKAV
		KTMKKGEKVLLTVKPQYGFGEKGKPASGDEGAVPPNATLQITLELVSWKTVSEV
		TDDKKVIKKILKEGEGYERPNEGAVVEVKLIGKLQDGTVFVKKGHDDCEELFKF
		KIDEEQVVDGLDKAVMNMKKGEVALLTVAPEYAFGSSESKQDLAVVPPSSTVYY
		EVELVSFVKDKESWDMNTEEKIEAAGKKKEEGNVIFKAGKYAKASKRYEKAVKY
		IEYDTSFSEDEKKQAKALKVACNLNDAACKLKLKDYNQAEKLCTKVLELDSRNV
		KALYRRAQAYIELSDLDLAEFDIKKALEIDPHNRDVKLEYKVLKEKVKEFNKKD
		AKFYGNMFAKMSKLEPVEKTAAKEPEPMSIDSKA;
301	Peptidylprolyl	MSTVYVLEPPTKGKVVLNTTHGPLDVELWPKEAPKAVRNFVQLCLEGYYDNTIF	136	1644
	isomerase	HRIIKDFLVQGGDPTGSGTGGESIYGDAFSDEFHSRLRFKHRGLVACANAGSPH
		SNGSQFFITLDRCDWLDRKNTIFGKITGDSIYNLSGLAEVETDKSDRPLDPPPK
		IISVEVLWNPFEDIVPRAPVRSLVPTVPDVQNKEPKKKAVKKLNLLSFGEEAEE
		EEKALVVVKQKIKSSHDVLDDPRLLKEHIPSKQVDSYDSKTARDVQSVREALSS
		KKQELQKESGAEFSNSFREIADDEDDDDDDASFDARMRRQILQKRKELGDLPPK
		PKPKSRDGISARKERETSISRDKDDDDDDDQPRVEKLSLKKKGIGSEARGERMA
		NADADLQLLNDAERGRQLQKQKKHRLRGREDEVLTKLETFKASVFGKPLASSAK
		VGDGDGDLSDWRSVKLKFAPEPGKDRMTRNEDPNDYVVVDPLLEKGKEKFNRMQ
		AKEKRRGREWAGKSLT;
302	Peptidylprolyl	MASAISMHSSGLLLLQGTNGKDVTEMGKAPASSRVANMQQRKYGATCCVARGLT	48	836
	isomerase	SRSHYASSLAFKQFSKTPSIKYDRMVEIKAMATDLGLQAKVTNKCFFDVEIGGE
		PAGRIVIGLFGDDVPKTVENFRALCTGEKGFGYKGCSFHRIIKDFMIQGGDFTR
		GNGTGGKSIYGSTFEDENFALKHVGPGVLSMANAGPSTNGSQFFICTVKTPWLD
		NRHVVFGQVVDGMDVVQKLESQETSRSDVPRQPCRIVNCGELPLDG;
303	Peptidylprolyl	MAASFTALSNVGSLSSPRNGSEIRRFRPSCNVAASVRPPPLKAGLSASSSSSFS	49	822
	isomerase	GSLRLIPLSSSPQRKSRPCSVRASAEAAAAQSKVTNKVYLDISIGNPVGKLVGR
		IVIGLYGDDVPQTAENFRALCTGEKGFGYKGSTVHRVIKDFMIQGGDFDKGNGT
		GGKSIYGRTFKDENFKLSHVGPGVVSMANAGPNTNGSQFFICTVKTPWLDQRHV
		VFGQVLEGMDIVRLIESQETDRGDRPRKRVVVSDCGELPVV;
304	Peptidylprolyl	MAEAIDLTGDGGVMKTIVRRAKPDAVSPSETLPLVDVRYEGVLAETGEVFDSTH	185	751
	isomerase	EDNTLFSFEIGKGSVISAWDTALRTMKVGEVAKITCKPEYAYGSTGSPPDIPPD
		ATLIFEVELVACKPCKGFSVTSVTEDKARLEELKKQREIAAATKEEEKKRREEA
		KAAAAARVQAKLDAKKGHGKGKGKAK;
305	Peptidylprolyl	MGNPKVFFDMSIGGQPAGRIVMELYADVVPRTAENFRALCTGEKGAGRSGKPLH	103	621
	isomerase	YKGSSFHRVIPGFMCQGGDFTAGNGTGGESIYGSKFADENFVKKHTGPGVLSMA
		NAGPGTNGSQFFVCTAKTEWLDGKHVVFGQIVDGMDVVKAIEKVGSSSGRTSKP
		VVVADCGQLS
306	Peptidylprolyl	MPNPKVFFDMTIGGAAAGRVVMELYADTTPRTAENFRALCTGEKGVGRSKKPLH	41	559
	isomerase	YKGSKFHRVIPSFMCQGGDFTAGNGTGGESIYGVKFADENFIKKHTGPGILSMA
		NAGPGTNGSQFFICTTKTEWLDGKHVVFGKVVEGMEVVKAIEKVGSSSGRTSKP
		VVVADCGQLP
307	Peptidylprolyl	MAEAIDLTGDGGVMKTIVRRAKPDAVSPSETLPLVDVRYEGVLAETGEVFDSTH	127	693
	isomerase	EDNTLFSFEIGKGSVISAWDTALRTMKVGEVAKITCKPEYAYGSTGSPPDIPPD
		ATLIFEVELVACKPCKGFSVTSVTEDKARLEELKKQREIAAATKEEEKKRREEA
		KAAAAARVQAKLDAKKGHGKGKGKAK
308	Peptidylprolyl	MATARSFFLCALLLLATLYLAQAKKSEDLKEVTHKVYFDVEIAGKPAGRIVMGL	28	639
	isomerase	YGKAVPKTAENFRALCTGEKGTGKSGKPLHYKGSSFHRIIPSFMLQGGDFTLGD
		GRGGESIYGEKFADENFKLKHTGPGLLSMANAGPDTNGSQFFITTVTTSWLDGR
		HVVFGKVLSGMDVVYKVEAEGRQSGTPKSKVVIADSGELPL
309	Peptidylprolyl	MMRREISVLLQPRFVLAFLALAVLLLVFAFPFSRQRGDQVEEEPEITHRVYLDV	135	812
	isomerase	DIDGQHLGRIVIGLYGEVVPRTVENFRALCTGEKGKSANGKKLHYKGTPFHRII
		SGFMIQGGDVIYGDGKGYESIYGGTFADENFRIKHSHAGIISMVNSGPDSNGSQ
		FFITTVKASWLDGEHVVFGRVIQGMDTVYAIEGGAGTYNGKPRKKVIIADSGEI
		PKSKWDEER
310	Peptidylprolyl	MWATAEGGPPEVTLETSMGSFTVELYFKHAPRTSRNFIELSRRGYYDNVKFHRI	119	613
	isomerase	IKDFIVQGGDPTGTGRGGESIYGKKFEDEIKPELKHTGAGILSMANAGPNTNGS
		QFFITLAPCPSLDGKHTIFGRVCRGMEIIKRLGSVQTDNNDRPIHDVKILRTSV
		KD
311	Peptidylprolyl	MSNPKVFFDILIGKMKAGRVVMELFADVTPKTAENFRALCTGEKGIGRSGKPLH	38	562
	isomerase	YKGSTFHRIIPNFMCQGGDFTRGNGTGGESIYGMKFADENFKIKHTGLGVLSMA
		NAGPDTNGSQFFICTEKTPWLDGKHVVFGKVIDGYNVVKEMESVGSDSGSTRET
		VAIEDCGQLSEN
312	Peptidylprolyl	MDDDFEFPASSNVENDDDDGMDMDDMGGDVPEEEDPVASPAVLKVGEEREIGKA	109	1872
	isomerase	GFKKKLVKEGEGWETPSSGDEVEVHYTGTLLDGTKFDSSRDRGTPFKFKLGRGQ
		VIKGWDEGIKTMKKGENAIFTIPPELAYGESGSPPTIPPNATLQFDVELLSWSS
		VKDICKDGGILKKVLVEGEKWDNPKDLDEVFVKYEASLEDGTLISKSDGVEFTV
		GDGYFCAALAKAVKTMKKGEKVLLTVMPQYAFGETGRPASGDEAAVPPDASLQI
		MLELVSWKTVSDVTKDKKVLKKTLKEGEGYERPNDGAAVQVRLCGKLQDGTVFV
		KKDDEEPFEFKIDEEQVIDGLDRAVKNMKKGEVALVTIQPEYAFGPTESQQDLA
		VVPANSTVYYEVELLSFVKEKESWEMNNQEKIEAAARKKEEGNAAFKAGKYVRA
		SKRYEKAVRFIEYDSSFSDEEKQQAKTLKNTCNLNDAACKLKLKDFKEAEKLCT
		KVLEGDGKNVKALYRRAQAYIQLVDLDLAEQDIKKALEIDPNNRDVKLEYKILK
		EKVREYNKRDAQFYGNMFAKMNKLEHSRTAGMGAKHEAAPMTIDSKA
313	Peptidylprolyl	MAKPRCFMDISIGGELEGRIVGELYTDVAPKTAENFRALCTGEKGIGPHTGAPL	74	1159
	isomerase	HYKGVRFHRVIKGFMVQGGDISAGDGTGGESIYGLKFEDENFDLKHERKGMLSM
		ANSGPNTNGSQFFITTTRTSHLDGKHVVFGRVVKGMGVVRSVEHVTTAAGDCPT
		VDVVIADCGEIPAGADDGIRNFFKDGDTYPDWPADLDESPAELSWWMDAVDSIK
		AFGNGSYKKQDYKMALRKYRKALRYLDICWEKEGIDEVESSSLRKTKSQIFTNS
		SACKLKLCDLKGALLDAEFAVRDGENNAKAYFRQGQAHMELNDIDAAAESFSKA
		LELEPNDVGIKKELNAAKKKIFERREQEKRAYRKMFL
314	Peptidylprolyl	MTKRKNPLVFLDVSIDGDPVERIVIELFADTVPRTAENFRSLCTGEKGVGKTTG	54	2045
	isomerase	KPLHYKGSYFHRIIKGFMAQGGDFSNGNGTGGESIYGGKFADENFKLAHDGPGL
		LSMANGGPNTNGSQFFIIFKRQPHLDGKHVVFGKVMRGMEVVKKIEQVGSANGK
		PLQPVKIVDCGETSETGTQDAVVEEKSKSATLKAKKKRSARDSSSESRGKRRQR
		KSRKERTRKRRRYSSSDSYSSESSDSDSESYSSDTESESKSHSESSVSDSSSSD
		GRRRKRKSTKREKLRRQRGKDSRGEQKSARYDKKSRHKSADSSSDSESESSSRS
		RSRDDKKKSSRRESARSVSKLKDAEANSPENLESPRDREIKKVEDNSSHEEGEF
		SPKNDVQHNGHGTDAKFGKYDDQRPRSDGSKKSSGSMRDSPKRLANSVPQGSPS
		SSPAHKASEPSSSIRARNPSRSPAPDGNSKRIRKGRGFTERFSYARRYRTPSPE
		DVTYRPYHYGRRNFHDRRNDRYSNYRSYSERSPHRRYRSPPRGRSPPRYQRRRS
		RSRSVSRSPGGNKGRYRGRDQSRSRSRSRSRSPRRGSSPANKQLPLSERLKSRL
		GTRVDEHSPRRRRSSSRSHDSSRSRSPDEVPDKHEGKAAPVSPARSRSSSPSGR
		GLVSYGDASPDSGIN
315	Peptidylprolyl	MSVLLVTSLGDIVVDLHADRCPLTCKNFLKLCRIKYYNGCVFHTVQKDFTAQTG	53	1879
	isomerase	DPTGTGTGGDSVYKFLYGDQARFFMDEIHLDLKHSKTGTVAMASGGENLNASQF
		YFTLRDDLDYLDGKHTVFGEVAEGLETLTRINEAYVDEKGRPYKNIRIRHTYIL
		DDPFDDPPQLAELIPDASPEGKPKDEVVDDVRLEDDWVPLDEQLGPAQLEEAIR
		AKEAHSRAVVLESIGDIPDAEIKPPDNVLFVCKLNPVTEDEDLHTIFSRFGTVV
		SADVIRDFKTGDSLCYAFIEFENKDSCEQAYFKMDNALIDDRRIKVDFSQSVAK
		LWSQFKRKDSQAAKGKGCFKCGAPDHMARECPGSSTRQPLSKYILKEDNAQRGG
		DDSRYEMVFDEDAPESPSHGKKRRGRDDRDDRHKMSRQSVEETKFNDREGGHSV
		DKHRQSERSKHREDEMSRDSKASEAGRRRIDRDFPEEERDGEKYTESHRDRDGK
		RGDYRDYRKGEADVQTHGDRRGDENYRRKSAAYDDGHEGAGAARRKDSNDDHHA
		YRRGYGDSRKGTRDEDDDGRGRRDDPSYRRSSGHKDSSNGGREEQKYRSGETDG
		KSHPERSHRGDRRR
316	Peptidylprolyl	MRPFNGGSSIACLVLVIAAGALAESQGPHLGSARVVFQTNYGDIEFGFFPGVAP	7	690
	isomerase	RTVDHIFKLVRLGCYNTNHFFRVDKGFVAQVADVANGRTAPMNDEQRTEAEKTI
		VGEFSNVKHVRGILSMGRYDDPDSAQSSFSILLGDAPHLDGKYAIFGRVTKGDE
		TLKKLEQLPTRREGMFVMPTERITILSSYYYDTGAESCEEENSTLRRRLAASAV
		EVERQRMKCFP
317	Peptidylprolyl	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRALCTGEKGTGRSGKPLH	83	601
	isomerase	FKGSSFHRVIPGFMCQGGDFTRGNGTGGESIYGEKFADENFVKKHTGPGILSMA
		NAGPNTNGSQFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGSGRTSKP
		VVIADSGQLA
318	Peptidylprolyl	MRFTSITSAIALFAAAASALDKPLDIKVDKAVECSRKTKAGDKIQVHYRGTLEA	125	535
	isomerase	DGSEFDASYKRGQPLSFHVGKGQVIKGWDQGLLDMCPGEKRTLTIQPDWGYGSR
		GMGPIPANSVLIFETELVEIAGVAREEL
319	Peptidylprolyl	MGNPKVFFDMSIGGQPAGRIVMELYADVVPRTAENFRALCTGEKGAGRSGKPLH	55	573
	isomerase	YKGSSFHRVIPGFMCQGGDFTAGNGTGGESIYGSKFADENFVKKHTGPGVLSMA
		NAGPGTNGSQFFVCTAKTEWLDGKHVVFGQIVDGMDVVKAIEKVGSSSGRTSKP
		VVVADCGQLS
320	Peptidylprolyl	MAVATRSRWVAMSVAWILVLFGTLALIQNRLSDTGASSDPKLVHRKVGEEKKKP	147	842
	isomerase	DDLEEVTHKVFFDVEIGGKPAGRIVMGLFGKTVPKTVENFRALCTGEKGIGKSG
		KPLNYKGSQFHRIIPKFMIQGGDFTLGDGRGGESIYGNKFSDENFKLKHTDAGR
		LSMTNAGPDTNGSQFFITTVTTSWLDGRHVVFGKVLSGMDVVHKIEAEGGQSGQ
		PKSIVVISDSGELDL
321	Peptidylprolyl	MAVTLHTNLGDIKCEIFCDEVPKAAEHNARGILSMANSGPNTNGSQFFIAYAKQ	167	487
	isomerase	PHLNGLYTIFGRVIHGFEVLDIMEKTQTGPGDRPLAEIRLNRVTIHANPLAG
322	Peptidylprolyl	MAVATRSRWVAMSVAWILVLFGTLALIQNRLSDTGASSDPKLVHRKVGEEKKKP	195	890
	isomerase	DDLEEVTHKVFFDVEIGGKPAGRIVMGLFGKTVPKTVENFRALCTGEKGIGKSG
		KPLNYKGSQFHRIIPKFMIQGGDFTLGDGRGGESIYGNKFSDENFKLKHTDAGR
		LSMANAGPDTNGSQFFITTVTTSWLDGRHVVFGKVLSGMDVVHKIEAEGGQSGQ
		PKSIVVISDSGELDL
323	Peptidylprolyl	MGNPKVFFDMSIGGQPAGRIVMELYADVVPRTAENFRALCTGEKGAGRSGKPLH	68	586
	isomerase	YKGSSFHRVIPGFMCQGGDFTAGNGTGGESIYGSKFADENFVKKHTGPGVLSMA
		NAGPGTNGSQFFVCTAKTEWLDGKHVVFGQIVDGMDVVKAIEKVGSSSGRTSKP
		VVVADCGQLS
324	Retinoblastoma	MSPVAANAMEEAAEPEVPAPVTPSKDDADTDAAVSRFLGFCKSKLGLAEGNCVQ	182	3265
	related protein	SSTLLRKTAHVLRSSGTVIGTGTAEEAERYWFAFVLYTVRRVGERKAEDEQNGS
		DETEVPLSRILKASVLNLIDFFKEIPQFVIKAGAIVSGIYGANWDSRLEAREMQ
		TNYVHLCILCKFYKRICGEFFILNDAKDDMKSADSSTSDPVIMYQPFGWLLFLA
		LRIHALSRFKDLVSSTNALVSVLAILIIHLPTRFRKFSISDSSQLVKRSEKGVD
		LVGSLAYRYDTSEDEIKRTLEKANNVIAEILGITPPPASECKAENLENVDTDGL
		IYFGNLMEETSLSSILSTLEKIYEDATRNDSEFDERVFINDDDSLLVSGSLSGA
		AINLTGAKRKYDSFASPAKTITRPLSPSRSPASHINGIIGGTNLRITATPVATA
		MTTAKWLRTFVSPLPSKPSTDLQGFLASCDRDVTSDVIRRANIILEAIFPNSPI
		GERTVTGGLQNANLMDNMWAEQRRLEALKLYYRVLEAMCRAEAQILHSNNLTSL
		LTNERFHRCMLACSAELVLATHKTVTMLFPAVLERTGITAFDLSKVIESFVRHE
		ETLPRELRRHLNTLEERLLENMVWERGSSMYNSLVVARPALAPEINRLGLLPEP
		MPSLDAIALLINFSSSGLPQSPVQKHEASPGQNGDIRSPKRISTEYRSVLVERN
		FTSPVKDRLLALSNIKSKLPPPPLQSAFASPTRPHPGGGGETCAETAIHIFFSK
		ITKLAAVRINAMLERLQLSQQIKEGVYCLFQQILSQRTNLFFNRHIDQVILCCF
		YGVAKINQINLTFREIIYNYRKQPQCKPQVFRNVFVDWSTRRNGKAGNEHVDII
		SFYNEIFIPSVKPLLVELGPTGATTRTNRTSEVGNKNDAQCPGSPKISSFPTLP
		DMSPKKVSASHNVYVSPLRSSKMDASISHSSKSYYACVGESTHAYQSPSKDLVA
		INSRLNGNRKVRGTLNFDDVDAGLVSDSMVANSLYLQNGSSMSSSTAKSSEKPES
325	WD40 repeat	MRPILMKGHERPLTFLKYNREGDLLFSCAKDHTPTVWFADNGERLGTYRGHNGA	165	1145
	protein	VWCCDVSRDSMRLITGSADTTAKLWSVQNGTQLFTFNFDSPARSVDFSIGDKLA
		VITTDPFMELPSAIHVKRIARDPADQASESVLVLRGHQGRIARAVWGPLNKTII
		SAGEDAVIRIWDSETGKLLRESDKETGHKKAVTSLMKSVDGSHFVTGSQDKSAK
		LWDIRTLTLIKTYVTERPVNAVTMSPLLDHVVLGGGQDASAVTMTDHRAGKFEA
		KFFDKILQEEIGGVKGHFGPINALAFNPDGKSFSSGGEDGYVRLHHFDPDYFNI
		KI
326	WD40 repeat	MDKKRTVVPLVCHGHSRPVVDLFYSPITPDGFFLISASKDSSPMLRNGETGDWI	529	1569
	protein	GTFEGHKGAVWSCCLDTNALRAASGSADFSAKLWDALSGDELHSFEHKHIVRSC
		AFSEDTHLLLTGGVEKILRIFDLNRPDAPPREVDNSPGSIRTVAWLHSDQTILS
		SCTDIGGVRLWDVRSGKIVQTLETKSPVTSSEVSQDGRYITTADGSTVKFWDAN
		HFGLVKSYNMPCNIESASLEPKLGNKFIAGGEDMWVHIFDFHTGEEIGCNKGHH
		GPVHCVRFSPGGESYASGSEDGTIRIWQTGPANNVEGDANPSNGPVTGKAKVGA
		DEVTRKVEDLQIGKEGKDWREG
327	WD40 repeat	MAEGLILKGTMRAHTDMVTAIAIPIDNSDMVVTSSRDKSIILWHLTKEEKVYGV	156	1136
	protein	PRRRLTGHSHFVQDVVLSSDGQFALSGSWDGELRLWDLATGVSARRFVGHTKDV
		LSVAFSIDNRQIVSASRDRTIKLWNTLGECKYTIQEGEAHTDWVSCVRFSPNTL
		QPTIVSASWDRTIKVWNLTNCKLRNTLAGHNGYVNTVAVSPDGSLCASGGKDGV
		ILLWDLAEGKRLYNLEAGAIIHSLCFSPNRYWLCAATENSIKIWDLESKSIVED
		LRVDLKNEADKTDGTTTAASNKKVIYCTSLNWSADGSTLFSGYNDGVIRVWGTG
		RY
328	WD40 repeat	MAEGLHLKGTMKAHTDMVTAIAVPIDNADMIVTSSRDKSIILWHLTKEDKVYGV	90	1073
	protein	PRRRLTGHSHFVQDVVLSSDGQFALSGSWDGELRLWDLATGVSARRFVGHTKDV
		LSVAFSIDNRQIVSASRDRTIKLWNTLGECKYTIQEGEAHNDWVSCVRFSPNTL
		QPTIVSASWDRTVKVWNLTNCKLRNTLQGHSGYVNTVAVSPDGSLCASGGKDGV
		ILLWDLAEGKKLYSLEAGAIIHSLCFSPNRYWLCAATENSIKIWDLESKSIVED
		LRVDLKNEADMSDGTTGAMSSNKKVIYCTSLNWSADGSTLFSGYNDGVIRVWGI
		GRY
329	WD40 repeat	MAEGLHLKGTMKAHTDMVTAIAVPIDNADMIVTSSRDKSIILWHLTKEDKVYGV	66	1049
	protein	PRRRLTGHSHFVQDVVLSSDGQFALSGSWDGELRLWDLATGVSARRFVGHTKDV
		LSVAFSIDNRQIVSASRDRTIKLWNTLGECKYTIQEGEAHNDWVSCVRFSPNTL
		QPTIVSASWDRTVKVWNLTNCKLRNTLQGHSGYVNTVAVSPDGSLCASGGKDGV
		ILLWDLAEGKKLYSLEAGAIIHSLCFSPNRYWLCAATENSIKIWDLESKSIVED
		LRVDLKNEADMSDGTTGAMSSNKKVIYCTSLNWSADGSTLFSGYNDGVIRVWGI
		GRY
330	WD40 repeat	MSGVPAPPFATTTPENGTMSSNSPAFHRDSDDDDDQGEVFLDDSDIIHEVAVDD	227	1512
	protein	EDLPDADDEADEAEEADDSLHIFTGHNGEVYSLACSPTDATLVATGAGDDKGFL
		WRIGHGDWAVELQGHKDSISSLAFSLDGQLLASGSLDGVIQIWDVPSGNLKGTL
		DGPGGGIEWIRWHPKGHIILAGSEDSTVWMWNADKMAYLNMFSGHGNSVTCGDF
		TPDGKTICTGSDDATLRIWNPKSGENIHVVKGHPYHAEGLTSMAISSDSGLAIT
		GAKDGSVRIVNISSGRVVSSLDAHADSVEFVGLALSSPWAATGSLDQKLIIWDL
		QHSSPRATCDHEDGVTCLSWVGASRFLASGCVDGKVRVWDSLSGDCVRTFHGHS
		DAIQSLSVSANEEFLVSVSIDGTARVFEIAEFH
331	WD40 repeat	MGTSQHQLSSCLQLLPRRRGNKNLIFRRTMASGGAAAVAPPPGYKPYRHLKTLT	33	1076
	protein	GHVAAVSCVKFSNDGTLLASASLDKTLIIWSSAALSLLHRLVGHSEGVSDLAWS
		SDSHYICSASDDRTLRIWSSRSPFDCLKTLRGHTDFVFCVNFNPQSSLIVSGSF
		DETIRIWEVKTGRCLNVIRAHSMPVTSVHFNRDGSLIVSGSHDGSCKIWDTKNG
		ACLKTLIDDTVPAVSFAKFSPNGKFILVATLNDTLKLWNYATGKFLKIYTGHKN
		SVYCLTSTFSVTNGKYIVSGSEDRCICIWDLQGKNLIQKLEGHSDTVISVTCHP
		SENKIASAGLDSDRTVRIWLQDA
332	WD40 repeat	MPSQKIETGHQDIVHDVAMDYYGKRVATASSDTTIKIIGVSNSSGSQHLASLSG	65	973
	protein	HKGPVWQVAWAHPKFGSILASCSYDGQVILWKEGNQNDWAQAHVFNDHKSSVNS
		IAWAPHELGLCLACGSSDGNISVFTARPDGGWDTTRIEQAHPVGVTSVSWAPSM
		APGALVGSGLLDPVQKLASGGCDNTVKVWKLYNGTWKMDCFPALQMHSDWVRDV
		AWAPNLGLPKSTIASASQDGTVVIWTVAKEGEQWQGKVLKDFKTPVWRVSWSLT
		GNLLAVADGNNNVTLWNEAVDGEWQQVTTVEP
333	WD40 repeat	MKIAGLKSVENAHDESVWAAAWVPATESRPALLLTGSLDETVKLWRPDELALER	82	1047
	protein	TNAGHFLGVVSVAAHPSGVIAASASIDSFVRVFDVDTNATIATLEAPPSEVWQM
		QFDPKGTTLAVAGGGSASIKLWDTATWELNATLSIPRPEQPKPSEKGNKKFVLS
		VAWSPDGRRLACGSMDGTISIFDVARAKFLHHLEGHFMPVRSLVFSPVEPRLLF
		SASDDAHVHMYDSEGKSLVGSMSGHASWVLSVDVSPDGAALATGSSDRTVRLWD
		LSMRAAVQTMSNHSDQVWGVAFRPMAGAGVRAGGRLASVSDDKSISLYDYS
334	WD40 repeat	MEIDLGNLAFDVDFHPSEQLVASGLITGDLLLYRYGDGSSPEKLLEVRAHGESC	43	1101
	protein	RAVRFINDGKAILTGSPDCSILATDVETGSVVARVENAHEAAVNRLVNLTESTI
		ATGDDNGCIKVWDTRQRSCCNTFSAHEDFISDMTFASDSMKLVVTSGDGTLSVC
		NLRSNKVQTRSEFSEDELLSVVIMKNGRKVVCGTQSGTLLLYSWGFFKDCSDRF
		VDLSPSSVDALLKLDEDRIIAGTENGLISLIGILPNRIIQPIAEHSDHPIERLA
		FSHDKKFLGSISHDQTLKLWDLNDILGSEDSPSSQAAIDDSDSDEMDVDANPPD
		SSKGNKKKHSGKGNDVGNANNFFADLGD
335	WD40 repeat	MSQQPSVILATASYDHTIRFWEAKSGRCYRTIQYPDSQVNRLEITPHKRYLAVA	142	1095
	protein	GNPSIRLFDVNSNTPQPVMSFDSHTNNVMAVGFQYDGNWMYSGSEDGTVRTWDL
		RARGCQREYESRGAVNTVVLHPNQTELISGDQNGNIRVWDLTANSCSCELVPEV
		DTAVRSLTVMWDGSLVVAANNNGTCYVWRLLRGSQTMTNFEPLHKLQAHNGYIL
		KCLLSPEFCEPHRYLATASSDHTVKIWNVEGFTLEKTLIGHQRWVWDCVFSVDG
		AYLITASSDTTARLWSMSTGQDIRVYQGHHKATTCCALHDGAEGSPG
336	WD40 repeat	MEDAMDMEVEVEVEAEEHSPSSSNPSGSSFRRFGLKNSIQTNFGSDYVFEITPK	61	1257
	protein	FDWSLMGVSLSSNAVKLYSPTTGQYCGECRGHSDTVNGISFSGPSSPHVLHSCS
		SDGTIRAWDTRSFKEVSCISAGPSQEIFSFSFGGSSDSLLSAGCKSQILFWDWR
		NKKQVACLEDSHVDDVTQVCFVPHHQNKLISASVDGLICIFDTAGDINDDEHME
		SVINVGTSIGKVGIFGQTFEKLWCLTHIETLSVWDWKEGTNEANFEDARKLASD
		SWSLDHIDYFVDCHSAEEGEGLWVIGGTNAGTLGYFPVKYKGGAAIGSPEAVLG
		GGHSDVVRSVLPMSGMAGTTSKTRGIFGWTGGEDGRLCCWLSDDSSATSRSWMS
		SNLVLKSSRSHHKKNRHQPY
337	WD40 repeat	MSQHQEYPMEYAADDYDVGEVEDDMYFHERVMGDSDTDEDEEYDHLDNKITDTS	193	1527
	protein	AADARRGKDIQGIPWERLSVTREKYRRTRIEQYKNYENVPQSGESSEKDCKPTR
		KGGNYYEFWRNTRSVKSTILHFQLRNLVWSTTKHDVYLMSHFSIIHWSSLTCKK
		TEVLDVYGHVAPREKHPGSLLEGFTQTQVSTLAVRDKLLIAGGFQGELICKNLD
		RPGVSYCCRTTYDDNAITNAVEIYDYPSGAVHFMASNNDCGVRDFDMEKFELSR
		HFTFPWPVNHTSLSPDGKLLVIVGDNPEGIVVDSQRGKTIRPLQGHLDFSFASA
		WHPDGHIFATGNQDKTCRIWDIRNLSKSVAVLKGNLGAIRSIRFTSDGRFMAMA
		EPADFVHVYDVKSGYEKEQEIDFFGEISGVSFSPDTESLFVGVWDRTYGSLLQY
		NRCRNYSYLDSM
338	WD40 repeat	MGASSDPNPDVSDEHQKRSEIYTYEAPWHIYAMNWSVRRDKKYRLAIASLLDHP	109	1155
	protein	AAAAAVPNRVEIVQLDDSTGEIRADPNLSFDHPYPATKAAFVPDKDCQRADLLA
		TSSDFLRIWRIADDSSRVDLRSFLNGNKNSEFCRPLTSFDWNEAEPKRIGTSSI
		DTTCTIWDIERETVDTQLIAHDKEVYDIAWGGVSVFASVSADGSVRVFDLRDKE
		HSTIIYESSEPDTPLVRLGWNKQDPRYMATIIMDSAKVVVLDIRYPTMPVVELQ
		RHQASVNAIAWAPHSSCHICTAGDDSQALIWDLSSMAQPVEGGLDPILAYTAGA
		EIEQLQWSSSQPDWVAIAFSLKLQ
339	WD40 repeat	MRGGGGGGDATGWDEDAYRESVLKEREVQTRTVFRAAFAPSPSPSPSPDAVVVA	71	1213
	protein	SSDGSVASYSISACLSDHRLQSLRFADAKSQNVLEAEPACFLQGHDGPAYDVKF
		YGEGEDSLLLSCGDDGRIRGWMWRDITSSEAHDHSQGNSAKPVLDLVNPQSRGP
		WGALSPIPENNALAVDVKRGSIYAAAGDSCAYCWDVECGKIKTVFKGHSDYLHC
		IAARNSSSQIITGSEDGTARIWDCRSGKCVQVIDPDKDHKKGFFASVSCLALDA
		SESWLVCGRGRDLSVWSISASDCIAKISTNAPAQDVLFDDNQILLVGAEPLISR
		LDMNGAVLSQIHCAPQSVFSVSLHQSGVTAVGGYGGLVDVISQFGSHLCTFRCK
		CI
340	WD40 repeat	MEAPIIDPLQGDFPEVIEEYLEHGIMKCIAFNRRGTLLAAGCTDGSCIIWDFET	109	1785
	protein	RGVAKELRDKECTAAITSVCWSKYGHRILVSASDKSLILWDVLSGEKIAHTTLQ
		HTVLQACLHPGSSTPSICLACPFSSAPMIVDLNTGSTTALPVLTADVSNGATPL
		SRNKTSDTSVTYSPCNACFNKHGDLVYAGTSKGEILIIDHKNVRVCAIVLVSGG
		AVIKNVVFSRNGQYMLTNSNDRLIRIYKNLLPPKDGLKMLDELNESFNESDDVE
		KLKAIGSKCLELLHEFQDSITRVQWKAPCFSGDGEWVIGGAASRGEHKIYIWDR
		AGHLVKILEGPKEALMDLAWHPVHPIIISVSLTGLVYIWAKDYTENWSAFAPDF
		KELEENEEYVEREDEFDLVPETEKVKGLDVHEDDEVDVLTVERDSVFSDSDMSQ
		EELCFLPAVPCLDIPEQQDKCVGSCSKLPDGNHSGSPLSVEAGQNGNASNHNSS
		PLEPMENSTADDTDGVRLKRKRKPSEKGLELQAEKVKKPVKPLKSSGRLSKTNK
		PVIDPDSSNGVYGDDGSD
341	WD40 repeat	MRGVSWPEDGNNPSTSSSSQRNQQQAHAPRAVSGHAASHPSASNIFKLLVQREV	364	2685
	protein	SPRSKHSSKKLWREASKCQPYPFQQSCEAVRDVRQGLISWVESASLRHLSAKYC
		PLVPPPRSTIAAAFSPDGKILASTHGDHTVKLIDSQTGSCLKVLRGHRRTPWVV
		RFHPLYPEILASGSLDHEVRLWDANTAECIGSRNFYRPIASIAFHARGELLAVA
		SGHKLYIWHYNRRGETSSPTIVLRTQRSLRAVHFHPHAAPFLLTAEVNDLDSAD
		SAMTLATSPGYLHYPPPTVYFADAHSHERSRLADELPLMPLPLLMWPSFTRDDG
		RVPLQRIDGDVGLNGQQRVDSSSSVRLWTYSTPSGQYELLLSPVESGNSPSMPE
		ETGNNAFSSAVEAEVSQSAMDTVEDMEVQPEERNTQFFSFSDPRFWELPLLHGW
		LVGQTQAGPRSVRQSSPGDIETQSAFGEVASVSPITSGVMPVSMDPSRFGGRSG
		SRYRSPGSRGVHVTGPNNDGPRDENDPQSVVSKLRSELAASLAAAASTELPCTV
		KLRIWPHDVKDPCAQLDLESCRLTIPHAVLCSEMGAHFSPCGRFLAACVACVLP
		HLESDPGLHGQVNQDVTGVATSPTRHPISAHQIMYELRIYSLEEATFGIVLASR
		PVRAAHCLTSIQFSPTSEHLLLAYGRRHSSLLKSIVIDGENTVPIYTILEVYRV
		SDMELVRVLPSAEDEVNVACFHPSVGGGLIYGTKEGKLRILHYDSSHGLNLKSS
		GFLDENVPEVQTYALEC
342	WD40 repeat	MDSAVAIAALSLVVGAAIALLFFGNYFRKRRSEVVAMAEADLQPHPKNPSRPPP	96	1412
	protein	QPAAKKVHAKSHAHGADKDKNKRHHPLDLNTLKGHGDSVTGLCFASDGRSLATA
		CADGVVRVFKLDDASNKSFKFLRINLPAGGHPTAVAFGDGVSSVIVASQHLSGC
		SLYMYGEEKPTNLDSNKQQTKLPMPEIKWEHHKVHEQKAILTLSGAAANYDSGD
		GSTIIASCSEGTDIIIWHAKTGKILGNVDTNQLKNTMSAISPNGRFIAAAAFTA
		DVKVWEIVYSKDGSVKGVTKVMQLKGHKSAVTWLCFTPNSEQIVTASKDGSIRI
		WNINVRYHLDEDTKTLKVFPIPLQDSSGTTLHYERLSLSPDGKILAATHGSMLQ
		WLCIETGKVLDTAEKAHDGDITCMSWAPQSIPTGDKKVNVLATASGDKKVKLWA
		APPLPS
343	WD40 repeat	MEVEPKKASKTFPVKPKLKPKPRTPSGKTPESKYWSSFKTTHPLDNLSFSVPSL	116	1702
	protein	AFSPSPPHLLAAAHSATVSLFSPHRTTISSFSDVVSSLSFRSDGQLLAASDLSG
		LIQVFDVRSRTPLRRLRSHARPVRFVRYPVLDKLHLVSGGDDALVKYWDVAGES
		VVSELRGHKDYVRCGDCSPADANCFVTGSYDHVVKLWDVRVRDGNRAATEVNHG
		SPVQDVIFLPSGSLVATAGGNSVKIWDLIGGGRMVYSMESHNKTVTSICVGTMG
		AQQSGEEGVQLRILSVGLDGYMKVFDYSRMKVTHSMRFPAPLLSIGFSPDSNVR
		AIGTSNGILYVGKRKAKENAEGGANGILGLGSVEEPRRRVLKPSFYRYFHRGQS
		EKPSEGDYLVMRPKKVKLAEHDKLLKKFQHKNALISVLGGNDPEKVVAVMEELV
		ARRALLKCVLNLDADELGLILTFLHKNSTVPRYSSLLLGLAKKVIDLRLEDIRA
		SDALKGHIRNLKRSVDEEIRIQEGLQEIQGMVSPLLRIAGRR
344	WD40 repeat	MQGGSSGVGYGLKYQARCISDVKADTDHTSFLTGTLSLKEENEVHLLRLSSGGT	46	1101
	protein	ELICEGLFSHPSEIWDLSSCPFDQRIFSTVFSTGESYGAAVWQIPELYGQLNSP
		QLEKIASLDAHSRKISCVLWWPSGRHDKLVSIDEENIFLWGLDCSKKSAQVQSQ
		ESAGMLHNLSGGAWDPHDVNTVAATCESSIQFWDLRTMKKANSLESVHARDLDY
		DMRKKHLLVTSEDESGVRVWDLRMPKAPIQEFPGHTHWTWAVRCNPDYEGLILS
		AGTDSAVNLWWSSTASSDELISERLIDSPTRKLDPLLHSYNDYEDSVYGLAWSS
		REPWIFASLSYDGRVVVESVKPFLSRK
345	WD40 repeat	MAEEEGSAELEQQLEEEFAVWKKNTPILYDLLISHALEWPSLTVHWAPLLPQPS	23	1258
	protein	SSAAAAAGDPSLAAHRLVLGTHTSDGAPNFLILADALLPSSESDHCGDDAVLPK
		VEISQKIRVDGEVNRARFMPQNHNIVGAKTNGCEVYVFDCSKQAAKQHDGGFDP
		DLRLTGHDGEGYGLSWSPLKENYLLSASHDKKICLWDISAAAQDKVLGAMHVFE
		AHEGAVGDASWHSKNDNLFGSAGDDCQLMIWDLRTNKAQQCVKAHEKEVNSVSF
		NSYNDWILATASSDTTVGLFDMRKLTTPLHVFSSHEGEVLQVEWDPNHEAVLAS
		SSEDRRVMVWDLNRIGDEQQEGDASDGPAELLFSHGGHKAKISDFSWNKNEPWV
		ISSVAEDNSVQVWQMAESICGDDDDMQAMEGYI
346	WD40 repeat	MGNYGEEDEDQYFDALEETASVSDRGSNSSDCCSSGSGLDENVLDSLGFEFWTK	404	2644
	protein	FPESVRARRNRFLMLTGLGIEANSVDKEDAFPPSCNEIEVYTCKVTRDDGAVQR
		SLDSYNCISLLQSSTSIRSNQEVESLRGDSLLSSFRGRSKESDDLTELCGMGCP
		ESKRNAVSEFGSVSQGSIEELRRIVASSPLVHPLLHRKLEYERELIETKQKMGA
		GWLRKFGSATCISGRQGDTWSDPDDLEITAGMKMRRVRAHSSKKKYKELSSLYA
		AQEFLAHEGSISTMKFSMDGQYLASAGEDTVVRVWKVTEEDRSERVNVTVDPSC
		LYFALNESTQLASLNTNKEHIGKAKTFQRSSDSSCVILPLKVFQITEKPWHEFK
		GHNGEVLDLSWSSKGYLLSSSTDKTVRLWRVGCDRCQRVYSHNDYVTCISFNPV
		NENFFISGSIDGKVRIWNVFGGQVVAYIDCREIVSAVCYRSDGKGAIVGTMTGN
		CLFYSIKDNHLQMDAQVYLHGKKKSPGKRITGFQFPPNDPGKLMITSADSVIRV
		LSGLDVVCKLKGPRNSGGPMIATFTSDGKHVISASEDSNVYIWNYAGQDKTSSR
		VKKIWSCESFWSSNASVALPWCGIRTVPEALAPPSRSEERRASCAENGENHHML
		EEYFQKMPPYSPDCFSLSRGFFLELLPKGSATWPEEKLSDTSPPTVSSQAISKL
		EYKFLKSACHSVLSSAHMWGLVIVTAGWDGRIRTYHNYGLPVRS
347	WD40 repeat	MDIDFKEYRLRCELRGHEDDVRGVCVCGDGSIGTSSRDRTVRLWAPSAGERRKY	107	2383
	protein	EVARVLLGHKSFVGPLAWVPPSEELPEGGIVSGGMDTLVMAWDLRNGEAQTLKG
		HQLQVTGIVLDGGDIVSASVDCTLIRWKNGQLTEHWEAHKAPIQAVIRLPSGEL
		VTGSSDTTLKLWRGKTCTQTFVGHTDTVRGLAVMPDLGILSASHDGSIRLWAVS
		GECLMEMVDHTSIVYSVDSHASGLIVSGSEDRFAKIWKDGVCFQSIEHPGCVWD
		VKFLEDGDIVTACSDGTIRIWTNQEDRMANSTELELFDLELSSYKRSRKRVGGL
		KLEELPGLEALQVPGTSDGQTKVIREGDNGVAYAWNSTELKWDKIGEVVDGPED
		SMNRPALDGVQYDYVFDVDIGDGEPTRKLPYNRSDNPYDTADKWLLKENLPLSY
		RQQIVEFILANSGQRDFNLDPSFRDPYTGSSAYVPGAPSQLAAKQARPTFKHIP
		KKGMLVFDAAQFDGILKKINEFNNTLLSNQEKKNLSLTDIEISRLGAVVKILKD
		TSHYHSSKFADADFDLMLKLLESWPYEMMFPVIDIFRMVILHPDGADGLLRHQE
		DKKDVLMESIKRATGNPSVPANFLTSIRAVTNLFKNSAYYSWLQKHRSEMLDAF
		SSCSSSSNKNLQLSYATLLLNYAVLLIEKKDEEGQSQVLSAALELAENESLEVD
		ARYRALVAIGSLMLDGLVKRIALDFDVEHIAKAARTSKEAKIAEVGADIELLIK
		QS
348	WD40 repeat	MEFTEAYKQSGPCCFSPNARFIAVAVDYRLVIRDTLSLKVVQLFSCLDKISYIE	243	1625
	protein	WALDSEYILCGLYKRPMIQAWSLIQPEWTCKIDEGPAGIAYARWSPDSRHILTT
		SDFQLRLTVWSLVNTACVHVQWPKHASKGVSFTRDGKFAAICTRHDCKDYINLL
		SCHNWEIMGVFAVDTLDLADIQWSPDDSAIVIWDSPLEYKVLVYSPDGRCLFKY
		QAYESGLGVKSVSWSPCGQFLAVGSYDQMLRVLSHLTWKTFAEFTHLSNVRAPC
		CAAIFKEVDEPLQIDMSELSLSDDYMQGNSGDAPEGHYRVRYDVTEVPITLPCQ
		KPPADRPNPKQGIGLMSWSNDSQYICTRNDSMPTILWIWDMRHLELAAILVQKD
		PIRAAVWDPTGTRLVLCTGSSHLYMWTPSGAYCVSVPLSQFNITDLKWNSDGSC
		LLLKDKESFCCAAAPLPPDESSDYSSDD
349	WD40 repeat	MATIAALDDDMVRSMSIGAVFSDFVGKLNSLDFHRKDDILVTAGEDDSVRLYDI	126	1127
	protein	ANARLLKTTFHKKHGTDRVCFTHHPNSLICSSTKNLDTGESLRYISMYDNRSLR
		YFKGHKQRVVSLCMSPINDSFMSGSLDHSVRMWDLRVNACQGILRLRGRPTVAY
		DQQGLVFAVAMEGGAIKLFDSRSYDKGPFDAFLVGGDTSEVCDIKFSNDGKSVL
		LSTTNNNIYVLDAYAGDKQCGFNLEPSPSTPIEASFSPDGQYVVSGSGDGTLHA
		WNISRRNEVACWNSHIGVASCLKWAPRRAMFVAASTVLTFWIPNSEPELASAKG
		EAGVPPEQV
350	WD40 repeat	MSVAELKERHRAATETVNSLRERLKQKRVQLLDTDVAGYARTQGKTPVTFGATD	257	1390
	protein	LVCCRTLQGHTGKVYSLDWTPERNRIVSVSQDGRFIVWNALTSQKTHAIRLPCA
		WVMTCAFAPNGQSVACGGLDSVCSIFNLNSPVDRDSNLPVSRMLSGHKGYVSSC
		QYVPDGDAHLITGSGDQTCVLWDITTGLRTSVFGGEFQSGHTADVLSVSTNGSS
		PRIFVSGSCDSTARMWDTRVASRAVHTYHGHESGVNAVKFFPDGNRFGTGSDDG
		TCRLFDIRTGHELQVYYQQRGIDEIPHVTSIAFSISGRLLIAGYSNGDCFVWDT
		LLAQVVLNLGSLQNSHEGRISCLGVSADGSALCTGSWDTNLKIWAFGGIRRVT
351	WD40 repeat	MKKRPRGASLDQAVVDIRRREVGGLSGLSFARRLAASEGLVLRLDIYNKLKGHR	178	1632
	protein	GCVNTVGFNLDGDIVISGSDDRHVKLWDWQTGKVKLSFDSGHLSNVFQAKIMPY
		TDDRSIVTCAADGQARHAQILEGGQVQTMLLAKHRGRAHKLAIDPGSPHIVYTC
		GEDGLVQRLDLRSNTARELFTCREVYGTHVEVVHLNAIAIDPRNPNLFVIGGSD
		EYARVYDIRNYKWNGSHNFGRSANYFCPSHLIGEAHVGITGLAFSGQSELLVSY
		NDESIYLFTQEMGLGPDPLSASTKSVDSNSSEVTSPTAVNVDDNVTPQVYKGHR
		NCETVKGVGFFGPKCEYVVSGSDCGRIFIWKKKGGQLIRVMAADKHVVNCIEPH
		PHIPALASSGIENDIKIWTPKAIERATLPMNVEQLKPKARGWMNRISSPRQLLL
		QLYSLERWPEHGGETSSGLAAGQEELTELFFALSANGNGSPDGGGDPSGPLL
352	WD40 repeat	MSKRGYKLQEFVAHSSNVNCLSIGKKACRLFLTGGDDCKVNLWAIGKPNSLMSL	290	2917
	protein	CGHTNAVESVAFDSAEVLVLAGASSGVIKLWDVEEAKMVRGLTGHRSNCTAMEF
		HPFGEFFASGSTDTNLKIWDIRKKGCIHTYKGHTRGISTIRFSPDGRWVVSGGN
		DNVVKVWDLTAGKLLHDFKFHENHIRSIDFHPLEFLLATGSADRTVKFWDLETF
		ELIGSSRPEAAGVRAIAFHPDGRTLFCGLEDSLKVYSWEPVICHDGVDMGWSTL
		ADLCIHDGKLLGCSYYQSSVGVWVADASLIEPYGTNVKPQQKDSGDDEIEHQES
		RPSAKVGTTIRSTSIMRCASPDYETKDIKNIYVDTASGNPVSSQRVGTTNFAKV
		TQPLDFNDTPNLTLRRQGLVTETPDGLSGHVPSKSITQPKVVSRDSPDGKDSSR
		RESITFSRTKPGMLLRPAHSRRPSSTKYDVDRLSACAEIGVLSSAKSGSESLVD
		SFLNIKVAPEDGARNGCEDNHSSVKNVSVESEKVLPLQTPKTEKCDQTVGFKEE
		INSVKFVNGVAVVPGRTRTLVEKFEKREKLNSTEDQTINTPENPTLDKTPPPSL
		AENEEKSDRLNIVERKATRMSSHMVTAEDRTPVTLVGSPEDQSTVMAPQRELPA
		DESSKTPPLPVEDLEIHHGSNVSEDKATILSSQTVSEEDSKRSTLIRNFRRRDR
		FKSTEGRSPVMATQRKLPTDESGKTSSLPMEDLEIKGGLNVSEDKATSFSSRAP
		PREDRAHSALVRNVRKRDKFKSTNDTITVMVHQRGLSTDEASTVSVERVERRQL
		SNNVENPLNNLPPHSVPPTTTRGEPQYVGSESDSVNHEDVTELLLGNHEVFLST
		LRSRLTKLQVV
353	WD40 repeat	MSTFLTGTALSNPNPNKSYEVVQPPNDSVSSLSFNPKANFLVATSWDNQVRCWE	148	1197
	protein	IVRSGTSLGTTPKASISHDQPVLCSTWKDDGTTVFSGGCDKQVKMWPLSGGQPM
		TVAMHDAPIKEISWIPEMNLLVTGSWDKTLRYWDTRQANPVHIQQLPERCYALT
		VRHPLMVVGTADRNLIIYNLQSPQTEFKRISSPLKYQTRCLAAFPDQQGFLVGS
		IEGRVGVHHLDDSQQSKNFTFKCHREGSEIYSVNSLNFHPVHHTFATAGSDGAF
		NFWDKDSKQRLKAMSRCSQPIPCSTFNNDGSIFAYSACYDWSKGAENHNPATAK
		TYIFLHLPQESEVKGKPRLGTTGRK
354	WD40 repeat	MEVEAQQRDVNNVMCQLVDPEGTTLGPPMYLPQDVGPQQLQQMVNKLLSNEDKL	140	1567
	protein	PYTFYISDQELVVPLESYLQKNKVSVEKVLSIVYQPQAIFRIRPVNRCSATIAG
		HSEAVLSVAFSPDGKQLASGSGDTTVRLWDLSTQTPMFTCKGHKNWVLSIAWSP
		DGKHLVSGSKAGEIQCWDPLTGQPSGNPLVGHKKWITGISWEPVHLSSPCRRFV
		SSSKDGDARIWDVTLRRCVICLSGHTLAVTCVKWGGDGVIYTGSQDCTIKVWET
		SQGKLIRELKGHGHWVNSLALSTEYVLRTGAFDHTGKQYSSAEEMKQVALERYK
		KMKGNAPERLVSGSDDFTMFLWEPSVSKHPKTRMTGHQQLVNHVYFSPDGQWVA
		SASFDKSVKLWNGITGKFVAAFRGHVGPVYQISWSADSRLLLSGSKDSTLKIWD
		IRTKKLKRDLPGHADEVFAVDWSPDGEKVVSGGKDKVLKLWMG
355	WD40 repeat	MDAGSAHSSSNMKTQSRSPLQEQFLQRRNSRENLDRFIPNRSAMDFDYAHYMLT	376	1737
	protein	EGRKGKENPAVSSPSREAYRKQLAETLNMNRTRILAFKNKPPTPVELIPHELTS
		AQPAKPTKTRRYIPQTSERTLDAPDLLDDYYLNLLDWGSSNVLSIALGNTVYLW
		NASDGSTSELVTIDDETGPVTSVSWAPDGRHIAVGLNNSDVQLWDSADNRLLRT
		LRGGHRSRVGSLAWNNHILTTGGMDGLIVNNDVRVRSHIVDTYRGHTQEVCGLK
		WSASGQQLASGGNDNILHIWDRSTASSNSPTQWLHRLEEHTAAVKALAWCPFQG
		NLLASGGGGGDRTIKFWNTHTGACLNSVDTGSQVCALLWNKNERELLSSHGFTQ
		NQLTLWKYPSMVKIAELTGHTSRVLFMAQSPDGCTVASAAGDETLRFWNVFGVP
		EVAKPAPKANPEPFAHLNRIR
356	WD40 repeat	MEEAIPFKNLPSREYQGHKKKVHSVAWNCTGTKLASGSVDQTARVWHIEPHGHG	69	1010
	protein	KVKDIELKGHTDSVDQLCWDPKHADLIATASGDKTVRLWDARSGKCSQQAELSG
		ENINITYKPDGTHVAVGNRDDELTILDVRKFKPIHKRKFNYEVNEIAWNMSGEM
		FFLTTGNGTVEVLAYPSLRPVDTLMAHTAGCYCIAIDPVGRYFAVGSADSLVSL
		WDISEMLCVRTFTKLEWPVRTISFNHTGDYVASASEDLFIDISNVQTGRTVHQI
		PCRAAMNSVEWNPKYNLLAYAGDDKNKYQADEGVFRIFGFESA
357	WD40 repeat	MGKDEEEMRGEIEERLINEEYKVWKKNTPFLYDLVITHALEWPSLTVEWLPDRE	149	1423
	protein	EPPGKDYSVQKLVLGTHTSENEPNYLMLAQVQLPLEDAENDARHYDDDRADVGG
		FGCANGKVQIIQQINHDGEVNRARYMPQNSFIIATKTVSAEVYVFDYSKHPSKP
		PLDGACSPDLRLRGHSTEGYGLSWSKFKQGHLLSGSDDAQICLWDINATPKNKS
		LDAMQIFKVHEGVVEDVAWHLRHEYLFGSVGDDQYLLIWDLRTPSVTKPVQSVV
		AHQSEVNCLAFNPFNEWVVATGSTDKTVKLFDLRKISTALHTFDAHKEEVFQVG
		WNPKNETILASCCLGRRLMVWDLSRIDEEQTPEDAEDGPPELLFIHGGHTSKIS
		DFSWNTCEDWVVASVAEDNILQIWQMAENIYHDEDDVPGEESNKGS
358	WD40 repeat	MMRGFSCTEDGDAPSTSSTSPPPPPPPPHRQQMQAPRASSSSSGQPTSRRSTGN	365	2677
	protein	VFKLLARREVSPRSKHSLKKFWGEASECQLCPFQQSYEAVRDVRRSLISWVEAF
		SLQHLSAKYCPLMPPPRSTIAAAFSPDGKILASTHGDHTVKLIDSQTGSCLKVL
		RGHRRTPWVVRFHPLYPEILASGSLDHEVHLWDANTAECIGSRNFYRPIASIAF
		HAQGDLLAVASGHKLYIWHYNRSGETSSPTIVLRTPRSLRAVHFHPHAAPFLLT
		AEVNDLDLTDSAMTLATSPGYLHYPPPTIYLADAHSNERSRLEDELPLMPSPLL
		MWPSFTRDDGRATLPHIGGDVGLSGQQRVDSLSSSQYEFHPSPIEPSSSTSMHE
		EMGTDPFSSVRESEVTQSAMNIVDNTEVQPEERSTYSFSFSDPRFWELPSVYGW
		LVGQTQAAPRTAPSPGALETASALGEVASVSPVRSEFMPGGMDQPRLGGRSGSG
		CRSSGSRMMRTAGLNDHPHDENYPQSVVSKLRSELEASLAAAASTELPCTVKLR
		VWPYDMKDPCALFRSESCRLTIPHAVLCSEMGAHFSPCGRFFAACVACVLPQLE
		ADPVLHGQVDPDVTGVATSPTRHPVSAYQIMYELRIYSLEEATFGMVLASRSIR
		AAHCLTSIQFSPTSEHLLLAYGRRHNSLLKSIVIDGENTVPIYSILEVYRVSDM
		ELVRVLPSAEDEVNVACFHPSVGGGLVYGTKEGKLRILQIDSSGGLNPKSTGFL
		DENMAEVPTYALEC
359	WD40 repeat	MGEGDLPRTEAGVLRGHEGAVLAARFNGDGNYCLSCGKDRTIRLWNPHRGIHIK	24	923
	protein	TYKSHGREVRDVHCTSDNSKLISCGGDRQIFYWDVSTGRVIRRFRGHDSEVNAV
		KFNDYASVVVSAGYDRSVRAWDCRSHSTEPIQIINTFQDSVMSVCLTKTEIIGG
		SVDGTVRTFDIRIGREISDDLGQPVNCISMSNDGNCILASCLDSTLRLVDRSAG
		ELLQEYKGHTCKSYKLDCCLTNTDAHVAGGSEDGYVFFWDLVDASVISKFRAHS
		SVVTSVSYHPKEDCMITASVDGTIKVWKT
360	WD40 repeat	MACIKGVGRSASVAMAPDGGYLATGTMAGTVDLSFSSSASLEIFGLDFQSDDRD	221	3598
	protein	LPLIAESPSSERFNRLSWGKNGSGSDEFSLGLIAGGLVDGTIGLWNPLSLIRSE
		AGDKAIVGHLSRHKGPVRGLEFNVIAPNLLASGADDGEICIWDLAAPREPSHFP
		PLRGSGSAAQGEISFLSWNSKVQHILASTSYNGTTVVWDLKKQKPVISFSDSVR
		RRCSVLQWNPDLATQLVVASDEDSSPTLRLWDMRNIMSPVKEFAGHTRGVIAMS
		WCPNDSSYLVTCAKDNRTICWDTVTGEIVCELPAGSNWNFDVHWYPKIPGVISA
		SSFDGKIGIYNVEGCSRYGVRENEFGAATLRAPKWFKRPVGASFGFGGKVVSFH
		TRSTGGPSVNSSEVFVHDIITEQTLVSRSSEFEAAIQSGDRPSLRALCEKKSQH
		CESTDDQETWGFLKVLLEDDGTARSKLLAHLGFDIPTETNDGSQEDLSQQVNAL
		GLEDVTADKVVQEDNNESMVFPTDNGEDFFNNLPSPRADTPVSTSADGFPTVNA
		AVEPSQDEVDGLEESSDPSFDDSVQRALVVGDYKAAVALCMSANKLADALVIAH
		VGGASLWESTRDKYLKMSRLPYLKVVFAMVNNDLQSLVDTRPLKFWKETLAILC
		SFAQGEEWAMLCNSLASKLMAAGNMLAATLCFICAGNIDKTVEIWSRSLATEHD
		GMSYMDLLQDLMEKTIVLALASGQKQFSASVCKLVEKYAEILASQGLLTTAMDY
		LKLLGTDDLSPELAVLRDRIAFSVEAEKGANISAFNGSQDPRGAVYGVDQSNYG
		MVDTSQHYYPEAAQPQVPHTVPGSPYGENYQQPFGSSFGKGYNTPMQYQAPSQA
		SMFVPSEPPQNAQPSFVPTPVTSQPTTRSQFIPAPPLALRNPEQYQQPTLGSHL
		YPGSVNPTFQPLPHAPGPVAPVPPQVSSVPGQNMPQAVAPTQMRGFMPVTNPGV
		VQNPGPISMQPATPIESAAAQPVVSPAAPPPTVQTADTSNVPAPQKPVIATLTR
		LYNETSEALGGSRANPAKKREIEDNSRKIGALFAKLNSGDISKNAADKLVQLCQ
		ALDNGDYSTALQIQVLLTTSEWDECNFWLATLKRMIKTRQNVRLS
361	WD40 repeat	MKERGKGAGRSVDERYTQWKSLVPVLYDWLANHNLVWPSLSCRWGPQLEQATYK	44	1447
	protein	NRQRLYLSEQTDGSVPNTLVIANVEVVKPRVAAAEHISQFNEEARSPFVKKFKT
		IIHPGEVNRIRELPQNSKIVATHTDSPDVLIWDVETQPNRHAVLGASTSRPDLI
		LTGHKDNAEFALAMSPTEPFVLSGGKDRYVVLWSIQDHISTLAADPGSAKSPGS
		AGTNNKQSSKAAGGNDKTGDSPSIEPRGVYLGHGDTVEDVTFCPSSAQEFCSVG
		DDSCLILWDARTGSSPAIKVEKAHHADLHCVDWNPHDVNLILTGSADNTVRMFD
		RRNLTSGGVGSPVHTFEGHNAAVLCVQWSPDKSSVFGSSAEDGILNIWDHEKIG
		RKIETVGSKVPNSPPGLFFRHAGHRDKVVDFHWNSSDPWTIVSVSDDGESTGGG
		GTLQIWRMIDLIYRPEEEVLAELDKFKSHILSCTS
362	WD40 repeat	MAKIAPGCEPVAGTLTPSKKREYRVTNRLQEGKRPLYAVVFNFIDSRYFNVFAT	196	1314
	protein	VGGNRVTVYQCLEGGVIAVLQSYIDEDKDESFYTVSWACNIDRTPFVVAGGING
		IIRVIDAGNEKIHRSFVGHGDSINEIRTQPLNPSLIVSASKDESVRLWNVHTGI
		CILIFAGAGGHRNEVLSVDFHPSDKYRIASCGMDNTVKIWSMKEFWTYVEKSFT
		WTDLPSKFPTKYVQFPVFIAPVHSNYVDCNRWLGDFVLSKSVDNEIVLWEPKMK
		EQSPGEGSVDILQKYPVPECDIWFIKFSCDFHYHSIAIGNREGKIYVWELQSSP
		PVLIAKLSHPQSKSPIRQTAMSFDGSTILSCCEDGTIWRWDAITASTS
363	WD40 repeat	MNTAMHFGAGWRSIAEMGYTMSRLEIEPESCEDEKSLDGVGNSQGPNELPRCLD	193	1668
	protein	HELAHLTNLKSRPHEHLIRDFPGRRALPVSTVKMLAGRECNYSRRGRFSSADCC
		HMLSRYVPVNGPSPLDQMNSRAYVSQFSADGSLFVAGFQGSHIRIYNVDKGWKC
		QKNILTKSLRWTITDTSLSPDQRYLVYASMSPIVHIVDIGSAAMDSLANITEIH
		EGLDFSADSGPYSFGIFSVKFSTDGREVVAGSSDDSIYVYDLVANKLSLRIPAH
		ESDVNTVCFADESGHIIYSGSDDTYCKVWDRRCLSARNKPAGVLMGHLEGITFI
		DSRGDGRYFISNGKDQTIKLWDIRKMGSDICRRGFRNFEWDYRWMDYPPRARDS
		KHPFDLSVATYKGHSVLRTLIRCYFSPVHSTGQKYIYTGSHDSCVYIYDVVTGA
		QVAALKHHKSPVRDCSWHPEYPMIVSSSWDGDIVKWEFFGNGETEIPAMIKKRIR
		RRHLY
364	WD40 repeat	MEPQPQAPKKRGRKPKPKEDKKEEQLHQPPPPPPPQQQAAPAPAPAATRSSTSG	78	1634
	protein	SAGGRDRRPQQQHAVDEKYARWKSLVPVLYDWLANHNLLWPSLSCRWGPQLEQA
		TYKNRQRLYISEQTDGSVPNTLVIANCEVVKPRVAAAEHVSQFNEEARSPFIRK
		YKTIIHPGEVNRVRELPQNPNIVATHTDSPDVLIWDVESQPNRHAVYGATASRP
		NLILTGHQENAEFALAMCPAEPFVLSGGKDKTVVLWSIQDHITASATDQTTNKS
		PGSGGSIIKKTGEGNEETGNGPSVGPRGIYCGHEDTVEDVAFCPSTAQEFCSVG
		DDSCLILWDARVGTNPVAKVEKAHNGDLHCVDWNPHDNNLILTGSADNSVNMFD
		RRNLTSNGVGSPVYKFEGHKAAVLCVQWSPDKPSVFGSSAEDGLLNIWDYERVD
		KKVDRAPNAPAGLFFQHAGHRDKIVDFHWNAADPWTMVSVSDDCDTAGGGGTLQ
		IWRMSDLIYRPEEEVLAELENFKAHVLECSKA
365	WD40 repeat	MGIFEPYRAVGYITTGVPFSVQRLGTETFVTVSVGKAFQVYNCAKLSLVLVGPQ	85	2826
	protein	LPKKIRALASYREYTFAAYGSDIGIFKRAHQLATWSGHTAKVCLLLLFGEHILS
		VDVDGNAYIWAFKGMNYNLSPVGHILLDSNFTPSCIMHPDTYLNKVILGSQEGP
		LQLWNISTKTKLYEFKGWNSSVSSCVSSPALDVVAVGCADGKIHVHNIRYDEEL
		VTFSHSMRGSVTALSFSTDGQPLLASGSSSGVVSIWNLDKRRLQSVIRDAHDGS
		IISLHFFANEPVLMSSSADNSIKMWIFDTSDGDPRLLRFRSGHSAPPLCIRFYA
		NGRHILSAGQDRAFRLFSVVQDQQSRELSQRHVSKRAKKLKLKEEEIKLKPVIA
		FDVAEIRERDWCNVVTSHMDTPQAYVWRLQNFVIGEHILRPCPNKPTPVKACMI
		SACGNFAILGTAGGWIERFNLQSGISRGSYIDQLEGTNSAHDGEVVGVACDATN
		TLMISAGYAGDIKVWDFKGRELKSRWEIGSSLVKISYHRLNGLLATVADDFIIR
		LFDAVALRMVRKFEGHTDRITDLCFSEDGKWLLSSSMDGSLRIWDIILARQVDA
		VFVDVSITALSLSPNMDILATTHVDQNGVFLWVNQSMFSGDSDINLYASGKEVV
		TVKLPSVSSVEGSQVEESNEPTIRHSESKDVPSFRPSLEQIPDLVTLSLLPKSQ
		WQSLINLDIIKVRNKPVEPPKKPEKAPFFLPSIPSLSGEILFKPSEMSDKGDMK
		ADEDKSKITPEVPSSRFLQLLHSCSEAKNFSPFTTYIKGLSPSTLDLELRMLQI
		IDDDAVDADADDPQDVDKRQELLSIELLMDYFIHEISCRSNFEFVQALVRLFLK
		IHGETIRRQSVLQNKAKVLLETQCSVWQRVDKLFQGARCMVAFLSNSQF
366	WD40 repeat	MEETKVTCGSWIRRPENVNLAVLGRSPRRRGSAALEIFAFDPKSTSLSSSPLVA	74	1246
	protein	HVIEEIEGDPLAIAVHPNGEDIVCFASSGSCLSFELSGQESNLKLLTKELPPLR
		GIGPQKCMAFSVDGSRFATGGVDGRLRILEWPSLRIILDEPKAHKSIRDLDFSL
		DSEFLATTSTDGSARIWKAEDGLPCTTLTRRSDEKIELCRFSKDGTKPFLFCTV
		QRGDKAVTGVWDISTWNKIGHKRLLRKPAVVMSISLDGKYLAQGSKDGDMCVVE
		VKKMEVSHWSKRLHLGTSLTSLEFCPIERVVITTSDEWGVLVTKLNVPADWKAW
		QVYLLLLGLFLASLVAFYIFYENSDSFWGFPLGKDQPARPKIGSVLGDPKSADD
		QNMWGEFGPLDM
367	WD40 repeat	MADPVEHQHQQHQQHQLQQQRRRGWRIQGGQYLGEISALCFLHLPPPPLSLSSS	100	4377
	protein	PVLSLSSGLDSESRDRPACSFRFPSAGSGSQVSLFDLASGAMVRTFYVFRGIRV
		HGIVLGCADFPGGSSSSSSTLDYVIAVYGERRVKLFRLSVRLGRGAGEGSGTVL
		SADLELVSAAPRLSHWVMDVRFLKENGTSEDELQRCLTVAIGCSDNSIRLWDVD
		KCSFVLAVSSPERCLLYSMRLWGDNLEDLQVASGTIYNEILIWKVVPNHDAPSS
		NELTEEGLTNSCAGNSVHECLRYEAYHICRLVGHEGSIFRIAWSSDGSKLVSVS
		DDRSARIWEVHCKVQYSEDAGEVGLLFGHSARVWDCYISDNLIVTAGEDCSCRV
		WGLDGQQHDVIKEHIGRGIWRCLYDPWSSLLVTGGFDSAIKVHKLDASLAEASA
		KQSNIKDLSDGTELFTTHLPNSSGHSGHMDSKSEYVRCLSFSCEDVMYIATNHG
		YLYHAKLCNDGDLRWTELAQVSNEVQIICMELLPSNPYDPRIDADDWVAVGDGK
		GWTTVVRVVKNSDSPKVSTSFSWAAEMDRQLLGIHWCKSLGHRFIFTADPRGAL
		KLWRFFEVSQSSSLYPENSPRISLIAEFKSDLGARIMCLDVAFESELLICGDLR
		GNLVLFPLLKDLLLDTFVVSAAKISPVNHFKGAHGISAVSSISVAHMSFNHIEL
		RSTGADGCICYMEYDKGLQSLNFVGMKQVKELSMIESVSTENESTGYRTSGSYA
		SGFASTDFIIWNLVTEAKVLQVSCGGWRRPHSYYLGDVPEMKNCFAYVKDDIIY
		IRRHWIKDSKDKILPQNLRLQFHGREVHSLCFVTGDFQLRKNKQSSWIVTGCED
		GTVRLTRYTQCTDNWSSSKLLGEHVGGSAVRSICCVSNIHTTSSGTSVSDVKGI
		ENLPKDIKGTLMEDECNPSLLISVGAKRVLTSWLLRRRKQDGKEDDVTDLQEAE
		NSSLPSSAGSSTFSFQWLSTDMPVKYSVPSKKSGSIKKLIGVSDTNVRCKSLLP
		DSEALQSKVSAVDKNEDDWRYLAVTAFLVRHSGSRLIVCFIIVACSDATLAIRA
		LVLPYRLWFDVALMVPLSSPVLSLQHVIIGRCQLPDENVQIGNVYVVISGATDG
		SIAFWDLTESVEAFMRRLSNIHLEKFMDCQKRPRTGRGSQGGRWWRSLSKIACK
		EQPINDPVTAKAIKELNRKLTGGVACGSSSSMLDASPELDSNAANSSFEIIEVN
		PFHVLNGVHQSGVNCLHVCETKHGQSSDGRFLYQLVSGGDDQALHLLKFEVLVQ
		PPVQVPDVPNSDIRNSILVEEFLLDEQNQKTKCTIEFISQEKIASAHNSAVKGV
		WTDGTWVFSTGLDQRVRCWISKDRGTPTELAHFIISVPEPEALDARSICWDQYQ
		IAVAGRGMQMIEFHVPSSEIR
368	WD40 repeat	MPYKLSATLSNHSSDVRAVASPSDDLILSASRDSTAISWFRQSPSSFTPASVIR	58	2439
	protein	AGSRFVNAIAYLPPTPRAPQGYAVVGGQDTVVNVFALGPGDKEEPEYTLVGHTD
		NVCALSVNSDDTIISGSWDKTAKVWKDFALVYDLKGHQQSVWAVLAMNEKEFLT
		ASADRTIKYWVQHKTMQTYEGHRDAVRGLALIPDIGFASCSNDSEIRVWTMGGD
		VVYTLSGHTSFVYSLSVLPNGDLVSAGEDRSVRVWRDGECSQVIVHPAISVWAV
		STMPNGDIISGSSDGVVRVFSESEKRWATASELKALEDQIASQSLPSQQVGDVK
		KTDLPGPEALSVPGKKAGEVKMIRSGDVVEAHQWDSLASSWQKIGEVVDAIGSG
		RKQLHDGKEYDYVFDVDIQEGAPPLKLPYNVSENPYTAAQRFLEQNDLPTGYLD
		QVVKFIEQNTAGVKLGNDGYVDPFTGASRYQPATQSTSNTASSSYMDPFTGGSR
		HIAESAPSNVPQGSHATGIIPFSKPIFFKLANVSAMQAKMFQFDEVLRNEISTA
		TLAMRPDEVIMVNETFTYLSKVVTSTSSARTSLGWIHIETIMQILDRWPVPQRF
		PVIDLGRLVTAYCMNAFSGPGDLEKFFSCLFRTSEWTSITSGSKALTKAQETNV
		LLLFRTIANSLDGAPLNDMEWIKQIFRELAQTPQLVLNKSHRLALASVLFNFSC
		IGLKGPVPADVRTLHLTIILQVLRSPNDDPEVAYRTCVALGNMLYSDKTRGTPR
		DAQSPSPTELKSAVAAIKGGFSDPRINDVHREIMSLI
369	WD40 repeat	MPPQKIESGHKDTVHDLAMDYYGKRLATASSDHTINVVGVSSSGSQHLATLIGH	159	1064
	protein	QGPVWQISWAHPKFGSLLASCSYDGRVIIWREGNPNEWTQAQVFEEHKSSVNSV
		AWAPHELGLCLACGSSDGNISVFTARQDGGWDTSRIDQAHPVGVTSVSWAPSTA
		PGALVGSGMMEPVQKLCSGGCDNTVKVWKLYNRVWKLDCFPVLQMHTDWVRDVA
		WAPNLGLPKSTIASASQDGRVIIWTLAKEGDQWQGKVLYDFRTPVWRVSWSLTG
		NILAVADGNNNVSLWNEAVDGEWIQVSTVEP
370	WD40 repeat	MSAPMLEIEARDVVKIVLQFCKENSLHQTFQTLQSECQVSLNTVDSIETFVADI	118	1665
	protein	NSGRWDAILPQVAQLKLPRNTLEDLYEQIVLEMIELRELDTARAILRQTQAMGV
		MKQEQPERYLRLEHLLVRTYFDPNEAYQDSTKEKRRAQIAQALAAEVTVVPPSR
		LMALVGQALKWQQHQGLLPPGTQFDLFRGTAAMKQDVDDMYPTTLSHTIKFGTK
		SHAECARFSPDGQFLVSCSVDGFIEVWDYMSGKLKKDLQYQADETFMMHDDPVL
		CVDFSRDSEMLASGSQDGKIKVWRIRTGQCLRRLERAHSQGVTSVLFSRDGSQL
		LSTSFDGSARIHGLKSGKQLKEFRGHSSYVNDAIFSNDGSRVITASSDCTVKVW
		DVKTSDCLQTFKPPPPLRGGDASVNSVHLFPKNADHIVVCNKTSSIYIMTLQGQ
		VVKSLSSGKREGGDFVAACVSPKGEWIYCVGEDRNLYCFSCQSGKLEHLMKVHE
		KDVIGVTHHPHRNLVATYSEDSTMKLWKP
371	WD40 repeat	MDLLQSYAEDNDGDLGRHSSPEPSPPRLLPSKSAAPKVDDTTLALTVAQTNQTL	57	16828
	protein	ARPIDPSQHAVAFNPTYDQLWAPICGPAHPYAKDGIAQGMRNHKLGFVEDAAIG
		SFLFDEQYNTFQRYGYAADPCASTGNEYVGDLDALKQNDGISVYNIRQQEQKKY
		AEEYAKKKGEERGEGGREKAEVVSDKSTFHGKEERDYQGRSWIAPPKDAKATND
		HCYIPKRLVHTWSGHTKGVSAIRFFPKHGHLILSAGMDTKVKIWDVFNSGKCMR
		TYMGHSKAVRDISFCNDGTKFLTAGYDKNIKYWDTETGKVISTFSTGKIPYVVK
		LHPDDEKQNILLAGMSDKKIVQWDMNTGQITQEYDQHLGAVNTITFVDDNRRFV
		TSSDDKSLRVWEFGIPVVIKYISEPHMHSMPSISLHPNTNWLAAQSLDNQILIY
		STRERFQLNKKKRFAGHIVAGYACQVNFSPDGRFVMSGDGEGRCWFWDWKSCKV
		FRTLKCHEGVCIGCEWHPLEQSKVATCGWDGLIKYWD
372	WD40 repeat	MESNGNLEQTLQDGRIYRQLNSLIVAHLRDHNFPQAASAVALATMTPLNVEAPR	250	1566
	protein	NRLLELVAKGLAVEKGELLRGVSHAGTNDLGGSIPASYGLVPAPWTAIDFSSLR
		DTKGMSKSFTKHETRHLSDHKNVARCARFSTDGRFFATGSADTSIKLFEVSKIK
		QMMLPDSTDGAIRAVIRTFYDHTHPVNDLDFHPQNTVLISAAKDHTVKFFDYSK
		ATAKRAFRVIQDTHNVRSVAFHPSGDFLLAGTDHPIPHLYDVNTFQCYLSANVP
		EFAVNAAINQVRYSSSGGMYVTASKDGTIRFWDGASANCVRSIAGAHGAAEVTS
		ANFTKDQRYVLSCGKDSTVKLWEVGTGRLVKQYLGATHMQLRCQAVFNNTEEFV
		LSIDEPSNEIVVWDAMTAEKVARWPSNHNGPPRWIEHSPTEAAFVSCGTDRSIR
		FWKETH
373	WD40 repeat	MSNFQGEDGEYVADDFEAEDGDEELHGRESADPESDVDEIDTPSNRFTDTTADQ	106	1434
	protein	ARRGRDIQGIPWERLSITREKYRRTRLEQYKNYENVPQSGEKSGKDCTVTEKGN
		SFYEFRRNSRSVKSTILHFQLRNLVWATSKHDVYLMSNYSVVHWSSLTGKKSEV
		LNLAGHVAPNEKHPGSLLEGFTQTQVSTLAVKDRFLVAGGFQGELICKFLDRPG
		ISFCSRTTYDDNAITNAVEIYVSPSGGIHFIASNNDCGVRDFDMENFELSKHFR
		FPWPVNHTSLSPDGKLLVIVGDDPEGILVDAKTGKTIMPLRGHLDFSFASEWHP
		DGVTFATGNQDKTCRIWDIRNLSKSIAVLKGNLGAIRSIRYTSDGRYMAIAEPA
		DFVHVYDTKTGYKKEQEIDFFGEISGMSFSPDTESLFIGVWDRTYGSLLEYGRR
		RNFSYLDCLV
374	WD40 repeat	MGVEEDLEDLNALAESTDAAVDGQAALASAVDSVTLQPAPPILPPVIPPPAVPV	190	1917
	protein	VAPVPTIPPVLRPLAPLPIRPPVLRPPAPKRDEAGSSDSDSDHDGTAAGSTAEY
		EITEESRLVRERHEKAMQDLMMKRRGAALAVPTNDKAVRARLRRLGEPMTLFGE
		REMERRDRLRMLMAKLDAEGQLEKLMKAHEDEEAAASAAPEDVEEEMLQYPFYT
		EGSKALFNARIDIAKFSITRAALRLERARRRRDDPDEDVDAEIDWALKKAESLS
		LHCSEIGDDRPLSGCSFSHDGKLLATCSMSGVAKLWDTCRMPQVNRVLTLKGHT
		ERATDVAFSPVQNHIATASADRTAKLWNTEGTILKTFEGHLDRLGRIAFHPSGK
		YLGTTSFDKTWRLWDIESGEELLLQEGHSRSIYGIDFHRDGSLVASCGLDALAR
		VWDLRTGRSILALEGHVKPVLGVSFSPNGYHLATGGEDNTCRIWDLRKKKSLYT
		IPAHANLISEVKFEPQEGYFLVTASYDTTAKVWSARDFKPVKTLSVHEAKITSV
		DITADASHIVTVSHDRTIKLWTSNDDVKEQAMDVD
375	WD40 repeat	MVKAYLRYEPAAAFGVIASVESNIAYDASGKHLLAPALEKVGVWHVRQGVCTKA	102	2942
	protein	LAPSASSAAGPSLAVTAIASSPSSLIASGYADGSIRIWDFEKGSCETTLNGHKG
		AVSVLRYGKLGSLLASGSKDNDIILWDVVGETGLYRLRGHRDQVTDLVFLDSDK
		KLVSSSKDKYLRVWDLETQHCMQIVGGHHSEIWSLDTDPEERYLVTGSADPELR
		FYTVKNDSSDERSEADASGGVGNGDLASHNKWDVLKQFGEIQRQSKDRVATVRF
		NKNGNLLACQAAGKLVEVFRVLDEAEAKRKAKRRLHRKREKKGADVNENGDSSR
		GIGEGHDTMVTVADVFKLLQTIRASKKICSISFCPVAPKSSLATLALSLNNNLL
		EFHSIEADKTSKMLTIELQGHRSDVRSVTLSSDNTLLMSTSHNSVKIWNPSTGS
		CLRTIDSGYGLCGLIVPQNKHALIGTKDGAIEIFDVGSGTCIEVVEAHGGSIRS
		IVAIPNQNGFVTGSADHDIKFWEYGMKQKPGDNSKHLTVSNVRTLKMNDDVLVV
		AVSPDAQKIAVALLDCTVKVFFMDSLKLMHSLYGHRLPVLCLDISSDGDLIVTG
		SADKNLMIWGLDFGDRHKSIFAHGDSIMAVQFVGNTHYMFSVGKDRLVKYWDAD
		KFELLLTLEGHHADIWCLAISNRGDFLVTGSHDRSIRRWDRTEEPFFIEEEKEK
		RLEEMFESDLDNAFGNKYVPKEEIPEEGAVALAGKKTQETLSATDSIIEALDIA
		EVELKRIAEHEEEKNNGKTAEFHPNYVMLGLSPSDFILRALSNVQTNDLEQTLL
		ALPFSDALKLLSYLKDWTTYPDKVELVSRIATVLLQTHYNQLVSTPAARPLLTT
		LKDILHKKVKECKDTIGFNLAAMDHLKQLMALRSDALFQDAKVKLLEIRSQLSK
		RLEERTDPREAKRRKKKQKKSTNMHAWP
376	WD40 repeat	MGGVQAEREDKDKVSLELTEEILQSMEVGMTFRDYSGRISSMDFHRASSYLVTA	75	1079
	protein	SDDESIRLYDVASATCLKTINSKKYGVDLVSFTSHPMTVIYSSKNGWDESLRLL
		SLHDNKYLRYFKGHHDRVVSLSLCPRNECFISGSLDRTVLLWDQRAEKCQGLLR
		VQGRPATAYDDPGLVFAIAFGGCVRMFDARKYEKGPFEIFSVGGDVSDANVVKF
		SNDGRLMLLTTTDGHIHVLDSFRGTLLYTFNVKPTSSKSTLEASFSPEGMFVIS
		GSGDGSVYAWSVRGGKEVASWLSTDTEPPVIKWAPGNLMFATGSSELSFWIPDL
		SKLGAYVGRK
377	WD40 repeat	MAAFGAAPAGNHNPNKSSEVIQPPSDSVSSLCFSPRANHLVATSWDNQVRCWEL	99	1148
	protein	TKNGASVTSVPKASMSHDQPVLCSAWKDDGTTVFSGGCDKQAKMWSLMSGGQPV
		TVAMHDAPIKEIAWIPEMNVLVTGSWDKTLKYWDTRQSNPVHTQQLPERCYAMT
		VRYPLMVVGTADRNLIVFNLQNPQAEFKRFSSPLKYQTRCVAAFPDQQGFLVGS
		IEGRVGVHHLDDSQISKNFTFKCHRDNNDIYSVNSLNFHPVHHTFATAGSDGTF
		NFWDKDSKQRLKAMSRCSQPIPCSTFNNDGTIYAYSVCYDWSKGAENHNPATAK
		TYIFLHLPQESEVKAKPRVGTTNRK
378	WD40 repeat	MNCSISGEVPEEPVVSTKSGHVFERRLIERYVSDYGKCPVSGEPLTMDDVLPVK	232	1806
	protein	MGKIVKPRPLQAASIPGLLSIFQNEWDSLMLSNFALEQQLHTARQELSHALYQH
		DAACRVIARLKKERDEARSLLALAERQIPMTASSDIAVNAPAMSNGRKASLDEE
		PGYAGKKMRPGISASIIAEITDCNLALSQQRKKRQIPSTLAPVEDLERYTQLSS
		YPLHKTGKPGITSLDICHSKDIIATGGIDTSAVLFDRSSGQIMSTLSGHSKKVT
		SVNFDAQGDMVLTGSADKTVRIWQGSEDGSYNCRHILKDHTAEVQAITVHATNN
		YFATASLDNTWCFYEFSTGLCLTQVEGASGSEGYTSAAFHPDGLILGTGTSNAD
		VKIWDVKTQANVTTFSGHTGAITAISFSENGYFLATAAQDGVKLWDLRKLKNFR
		TFSAYDKDTGTNSVEFDHSGCYLGLAGSDIRVYQVASVKSEWNCVKTFPDLSGT
		GKVTCVKFGPDSKYIAVGSMDHNLRIFGLPSEDGAMES
379	WD40 repeat	MAAPGVETLKKEIKELKEKIAQHRLDTDGEQPLPAAAKSKSVPEVSAALKQRRI	72	1124
	protein	LKGHFGKIYALHWSADSRHLVSASQDGKLIIWNGFTTNKVHAIPLRSSWVMTCA
		YSPSGNLVACGGLDNLCSVYKVPHGGNKESSSAQKTYGELAQHEGYLSCCRFIK
		DNEIVTSSGDSTCILWDVETKTPKAIFNDHTGDVMSLAVFDDKGVFVSGSCDAT
		AKLWDHRVHKQCVMTFQGHESDINSVQFFPDGDAFGTGSDDSSCRLFDIRAYQQ
		INKYSSDKILCGITSVAFSKTGKSLFAGYDDYNTYVWDTLSGNQVEVLTGHENR
		VSCLGVSEDGKALATGSWDTLLKIWA
380	WD40 repeat	MGGVEDESEPASKRMKLSSRVLRGLANGSSRTEPAAGSSLDLMARPLPIEGDEE	315	2069
	protein	VIGSKGVIKRVEFVRLIAKALYSLGYEKSGARLEEESGIPLQSSVVNLFMQQIS
		DGLWDESVVTLHKIGLSDENLVKSASFLILEQKFLELLDQEKAMDALKTLRTEI
		TPLCIKNSRVRELSSCIISPSSCGLLNQNKRNSTRARSRSELLEELQKLLPPAV
		IIPERRLEHLVEQALVLQTDACMLHNSIDMEMSLYTDHQCGKEHIPCRTLQILQ
		SHNDEVWLVQFSHNGKYLASASNDRSAIIWEVDENGSVSLKHKLTGHQKPISSV
		CWSPDDRQLLTCGVGETVRRWDVSSGECLRVYEKAGHGLISCAWFPDGKWICYG
		VSDRSICMCDLEGKEIECWKGQRTLSISDLEITSDGKQIISICRETAILLLDRE
		AKYERMIEENQTITSFSLSKDNRYLLVNLLNQEIHLWDIKGDFRLVAKYKGLKR
		SRFVIRSCFGGLKQAFVASGSEDSQVYIWHKGSGELIEPLPGHSGAVNCVSWNP
		ANHHMLASASDDRTIRIWGLNELNTRHKGARPNGVHYCNGNGTS
381	WD40 repeat	MTQLAETYACMPSTERGRGILIAGNPKPGSNSVLYTNGRSVVILNLDNPLDISV	145	1968
	protein	YAEHAYPATVARFSPNGEWVASADSSGAVRIWGAYNDHVLKKEFKVLSGRIDDL
		QWSPDGLRIVASGDGKGKSLVRAFMWDSGTNVGEFDGHSRRVLSCAFKPTRPFR
		IVTCGEDFLVNFYEGPPFKFKLSRRDHSNFVNCLRFSPDGNRFISVSSDKKGII
		YDGKTGEKIGELSSDGGHTGSIYAVSWSPDSKQVITVSADKSAKIWDISEDGSG
		NLRKTLTSSGSGGVDDMLVGCLWQNNHLVTVSLGGTISIYTAGDLDKAPVSFSG
		HMKNVSSLSVLKGDPKVILSSSYDGLIIKWIQGIGFSGRVQRKESTQIKCLAAV
		DEEIVTSGYDNKVCRVSGSGDAEFIDIGCQPKDLSLALQCPEFALVSTDTGVVL
		LRGAKIVSTINLGFAVTASTVAPDGTEAIIGAQDGKLRIYSISGDTLTEEAVLE
		KHRGAISVIHYSPDLSMFASGDLNREAVVWDRASREVRLKNILYHTARINCLAW
		SPDSSTVATGSLDTCVIIYEVDKPASNRLTIKGAHLGGVYGLAFTDDFSVVSSG
		EDACIRVWKINRQ
382	WD40 repeat	MKVKVISRSTDEFTRERSQDLQRVFRNFDPNLRTQEKAVEYVRALNAAKLDKVF	130	1488
	protein	ARPFVGAMDGHVDSVSCMAKNPNYLKGIFSGSMDGDIRLWDIASRRTVCQFPGH
		QGPVRGLAASTDGQILVSCGIDSTVRLWNVPVATLGESDGTHENLAKPLAVYVW
		KNAFWAVDHQWDGELFATAGAQVDIWNQNRSQPISSFEWGTDTVISVRFNPGEP
		NVLATSGSDRSITLYDLRMSSPTRKVIMRTKTNAISWNPMEPMNFTAANEDCNC
		YSYDARKLEEAKCVHKDHVSAVMDIDYSPTGREFVTGSYDRTVRIFQYNGGHSR
		EVYHTKRMQRVFCVKFSCDASYVISGSDDTNLRLWKAKASEQLGVVLPRERRKH
		EYHEAVKSRYKHLPEVKRIVRHRHLPKPIYKAGILRRTVNEADRRKEERRKAHS
		APGSSSAEPLRKRRIIKEIE
383	WD40 repeat	MVRSIKNPKKAKRKNKGSKNGDGSSSSSSIPSMPTKVWQPGVDKLEEGEELQCD	269	1693
	protein	PSAYNSLHAFHIGWPCLSFDIVRDTLGLVRTEFPHQVYFVAGTQAEKPTWNSIG
		IFKVSNITGKRRELVPSKPTDDADEESDSSDSDEDSDDEVGGSGTPILQLRKVG
		HEGCVNRIRAMNQNPHICASWGDSGHVQIWDFSSHLNALAESEADVSQGASSVF
		NQAPLVKFGGHKDEGYALDWSPLVPGRLVSGDCKNSIHLWEPTSGSTWNVDSTP
		FIGHAASVEDLQWSPTEENVFASCSVDGTIAIWDTRLGKTPAASFKAHDADVNV
		ISWNRLATCMLASGCDDGTFSIHDLRLLKEGDSVVAHFEYHKHPVTSIEWSPHE
		ASTLAVSSADCQLTIWDLSLEKDEEEEAEFKAKTKEQVNAPEDLPPQLLFVHQG
		QKDLKELHWHAQIPGMIVSTAADGFNILMPSNIQSTLPSDGA
384	CDK type A	MERYKVIKELGDGTYGSVWKALNQQTHEIVAIKKMKRKYYIWEECINLREVKSL	1163	2545
		RKLNHPNIIKLKEVIRENNELFFIFEYMECNLYQIMKERSTPFSETAIIKFCYQ
		ILQGLSYMHRNGYFHRDLKPENLLVTSDLIKIADFGLAREVLTSPPYTDYVSTR
		WYRAPEVLLQSPTYTTAIDMWAVGAILAELFTLHPLFPGESELDEIYKICGVLG
		TPDYETWPDGMQLAAFRNFIFPQFLPVNLSVLIPHASPEAIDLITRLCSWDPQK
		RPTAEQALHHPFFRIGMSIPLSLGGHFQDNTCAAEVDTNFHSKKACKGRGMGEK
		ESSLECFLGLSLGLKPSLGHLGAMGSQGVGAVKQEVGSSPGCQSNPKQSLFQVL
		NSRAILPLFSSSPNLNVVPVKSSLPSAYTVNSQVMWPTIAGPPAAAVTVSTLQP
		SILGDFKIFGKSMGLASQYAGKEASPFS
385	CDK type A	MGEMGRGINNSSNNNNSNRPAWLQHYDLVGKIGEGTYGLVFLARSKLPNNRGLR	152	1582
		IAIKKFKQSKDGDGVSPTAIREIMLLREFSHENVVKLVNVHINHVDMSLYLAFD
		YAEHDLYEIIRHHREKLNHHNINQYTVKSLLWQLLNGLNYLHSNWIVHRDLKPS
		NILVMGEGEEHGVVKIADFGLARIYQAPLKPLSDNGVVVTIWYRAPELLLGAKH
		YTSAVDMWAVGCIFAELITLKPLFQGVEVKASPNPFQLDQLDKIFKVLGHPTIE
		KWPTLMNLPHWSKNLQQIQQHKYDNAGLHIGPIPAKSPAYDLLSKMLEYDPRKR
		ITAAQALEHEYFRIDPQPGRNALVPSQPGEKAINYPPRLVDANTDFDGTIAPQP
		SQVSSGNAPSGSIASAAVPAVRPLPQQMQLMGMQRMQNPGMAAFNLGAQASMSG
		LNHNNIALQRGSSQQQAHQQVRRKEPNSGFPNTGYPPPPKSRRL
386	CDK type B-1	MDKYEKLEKVGEGTYGKVYKARDKMTGQLVALKKTRLEMDEEGVPPSSLREISL	389	1297
		LQMLSQSIYVVRLLCVEHVTKKGKPLLYLVFEYLDTDLKKFIDYRRSVNAGPLP
		QNVIQSFMYQLLKGVAHCHSHGVLHRDLKPQNLLVDKSKGLLKVGDLGLGRAFT
		VPLKCYTHEVVTLWYRAPEVLLGSTHYSTPVDIWSVGCIFAEMVRRQPLFPGDC
		EIQQLLHIFTLLGTPTEEMWPGVKRLRDWHEYPQWKPENLARAVPNLSPTGLDL
		ISKMLQCDPAKRISAKAAMNHPYFDDLDKSQF;
387	CDK type B-1	MDGYEKMDKVGEGTYGKVYMARDKKTGQLVALKKTRLENDGEGIPPTALREISL	38	946
		LQMLSQDIYIVRLLDVKHTENKLGKPLLYLVFEYMESDLKKYIDSYRRSHTKMP
		PSMIKSFMYQLCRGVAYCHSRGVMHRDLKPHNLLVDKEKGVLKIADLGLSRAFT
		VPVKKYTHEIVTLWYRAPEVLLGATHYSLPVDIWSVGCIFAEMSRMQALFTGDS
		EVQQLMNIFRFLGTPNEEVWPGVTKLKDWHIYPEWKPQDISHAVPDLEPSGLDL
		LSQMLVYEPSKRISAKKALEHPYFDDLDKSQF
388	CDK type B-1	MDAYEKLEKVGEGTYGKVYKAKDKNTGQLVALKKTRLESDDEGIPPTALREISL	180	1088
		LQMLSQDIHIVRLLDVEHTENKNGKPLLYLVFEYMDSDLKKYIDGYRRSHTKVP
		PNIIKSFMYQLCQGVAYCHSRGVMHRDLKPHNLLVDKQRGVVKIADLGLGRAFT
		IPIKKYTHEIVTLWYRAPEVLLGATHYSTPVDIWSVGCIFAEMVRLQALFIGDS
		EVQQLFKIFSFLGTPNEEIWPGVTKFRDWHIYPQWKPQDISSAVPDLEPSGVDL
		LSKMLVYEPSKRISAKKALEHPYFDDLDKSQF
389	CDK type B-1	MDSYEKLEKVGEGTYGKVYKAKDKKTGKLVALKKTRLENDGEGIPPTALREISL	40	948
		LQMLSQDMNIVRLLDVEHTENKNGKPLLYLVFEYMDSDLKKYVDGYRRSHTKMP
		PKIIKSFMYQLCQGVAYCHSRGVMHRDLKPHNLLVDKQRGVLKIADLGLGRAFT
		VPIKKYTHEIVTLWYRAPEVLLGATHYSTPVDIWSVGCIFAEMSRMHALFCGDS
		EVQQLMSIFKFLGTPNEGVWPGVTKLKDWHIYPEWRPQDLSRAVPDLEPSGVDL
		LTKMLVYEPSKRISAKKALQHPYFDDLDKSQF
390	CDK type B-1	MEKYEKLEKVGEGTYGKVYKGRDKRTGRLVALKKTPFHQEEGIPPTAIREISLL	299	1134
		KSLSQCIYIVKLLDVKASFNGKGKHVLFMVFEYADSDLKKHIDAHRQCNTKLSP
		RSIQSYMFQLCKGIAYCHSHGVLHRDLKPQNILVDQKIGLLKIADLGLGRACTV
		PIKSYTFEVVTLWYRAPEVLLGAKRYSMALDIWSLGCIFAELCNLQALFAGDSQ
		IQQLINIFRLLGTPNEQLWPGVTQLSDWHEFPQWRPQDLSKVVFNLDPNGVDLL
		SKMLQYDPAKRISAKEALDHPYFDSLDKSQF
391	CDK type C	MGCVCGKPSARAADYVESPAEKGASSNSRSSSMASRRLVAPAVMDQGIDAENGH	105	2642
		EGDYRTKLRGKQSNGADPVSLLSDDAEKQRHSRHHQHQQHHPIRPHHLRPQGEF
		VPNANSNPRFGNPPRHIEGEQVAAGWPAWLTAVAGEAIKGWIPRRADSFEKLDK
		IGQGTYSNVYKARDLDTGKIVALKKVRFDNLEPESVRFMAREIQVLRRLDHPNV
		VKLEGLVTSRMSCSLYLVFEYMDHDLAGLAACPGIKFTEPQVKCYMQQLLRGLD
		HCHSRGVLHRDIKGSNLLIDNGGILKIADFGLATFFHPDQRQPLTSRVVTLWYR
		PPELLLGATEYGVAVDLWSTGCILAELLAGKPIMPGRTEVEQLHKIFKLCGSPS
		EDYWKKSKLPHATIFKPQQPYKRCVAETFKDFPPSALALMEVLLAIEPADRGTA
		TSALKSDFFTTKPLACDPSSLPKYPPSKEFDAKIRDEEARRQRAAGGRGRDAAR
		RPSRESRAIPAPEANAELAISIQKRRLSSQGPSKSKSEKFNPQQEDGAVGFPIE
		PPRPMHIGIDAGATSRMYSQQFGPSHSGPLSNQISSSIWGKNQKEDEIQMAPGR
		PSRSSKATISDFRKPGACAPQPGADLSHLSSLVATARSNAGIDTHKDRSGMWQH
		NRIDAIDGVHNNGKHEFLEVPEHPNRQDWTRFQQPESFKGLDNYHLQDLPATHH
		RKDERVASKEATMNWQGYGGQGGDKIHYSGPLLPPSGNIDEILKEHERHIQHAV
		RRARQDKGRPQRSNLSQNERKAFEHRSFVSGVNGNAGYSDLVNELPISVGSNRL
		KVSKTRGTEEIVELRELEREPLSSVMEKYEREHEM
392	CDK type C	MGCVCAKQSDILGEPESPKVKGSNLASSRWSVSSETKQLPQHSDSGILHHQHYY	187	2580
		HPRDESDEAKLKESNYGGSKRRTRQGRDPADLDMGIFVRTPSSQSEAELVAAGW
		PAWMAAFAGEAIHGWIPRRAESFEKLYKIGQGTYSNVYKARDLDNGKIVALKKV
		RFDSLDAESVRFMAREILVLRKLDHPNIVKLEGLVTSEVSSSLYLVFEYMEHDL
		AGLAACPGIKFTEPQVKCYMQQLLQGLDHCHRHGVLHRDIKGSNLLIDNGGILK
		IADFGLATFFYPDQKQLLTSRVVTLWYRPPELLLGATDYGVAVDIWSAGCILAE
		LLAGKPILPGRTEVEQLHKTFKLCGSPSEDYWKESKLPHATIFKPQHPYKSCIA
		EAFKDFSPSALALLETLLAIEPGHRGEASGALKSEFFTTEPLSCDPSSLPKYPP
		SKEFDAKLRAQETRRQRDVGVRGHGSEAARRTSRLSRAGPTPNEGAELTALTQK
		QHSTSHATSNIGSEKPSTKKEDYTAGLHIDPPRPVNHSYETTGVSRAYDAIRGV
		AYSGPLSQTHVSGSTSGKKPKRDHVKGLSGQSSLQPSKPFIVSDSRSERIYEKS
		HVTDLSNHSRLAVGRNRDTTDPHKSLSTLMQQIQDGTLDGIDIGTHEYARAPVS
		STKQKSAQLQRPSALKYVDNVQLQNTRVGSRQSDERPANKESDMVSHRQGQRIH
		CSGPLLHPSANIEDLLQKHEQQIQQAVRRAHHGKREALSNKSSLPGKKPVDHRA
		WVSSGKGNKESPYFKGKGNKELSDLKGGPTAKVTNFRQKVM
393	CDK type C	MAVANPGQLNLQEAPSWGSRSVNCFEKLEQIGEGTYGQVYMAKEIETGEIVALK	220	1749
		KIRMDNEREGFPITAIREIKLLKKLQHENVIKLKEIVTSPGPEKDEQGKSDGNK
		YNGSIYMVFEYMDHDLTGLAERPGMRFSVPQIKCYMKQLLIGLHYCHINQVLHR
		DIKGSNLLIDNNGILKLADFGLARSFCSDQNGNLTNRVITLWYRPPELLLGSTK
		YGPAVDMWSVGCIFAELLYGKPILPGKNEPEQLTKIFELCGSPDESNWPGVSKL
		PWYSNFKPQRQMKRRVRESFKNFDRHALDLVEKMLTLDPSQRISAKDALDAEYF
		WTDPVPCAPSSLPRYEPSHDFQTKRKRQQQRQHDEMTKRQKISQHPPQQHVRLP
		PIQNAGQGHLPLRPGPNPTMHNPPPQFPVGPSHYTGGPRGAGGQNRHPQNIRPL
		HAAQGGGYNANRGYGGPPQQQGGGYPPHGMGNQGPRGGQFGGRGAGYSQGGPYG
		GPVGGRGPNVGGGNRGPQFWSEQ
394	CDK type D	MQNMEDNVQSSWSLHGNKEICARYEILERVGSGTYSDVYRGRRKADGLIVALKE	438	1748
		VHDYQSSWREIEALQRLCGCPNVVRLYEWFWRENEDAVLVLEFLPSDLYSVIKS
		GKNKGENGIPEAEVKAWMIQILQGLADCHANWVIHRDLKPSNLLISADGILKLA
		DFGQARILEEPEAIYEVEYELPQEDIVADAPGERLMEEDDSVKGVRNEGEEDSS
		TAVETNFGDMAETANLDLSWKNEGDMVMQGFTSGVGTRWYRAPELLYGATIYGK
		EIDLWSLGCILGELLILEPLFSGTSDIDQLSRLVKVLGTPTEENWPGCSNLPDY
		RKLCFPGDGSPVGLKNHVPSCSDSVFSILERLVCYDPAARLNAKEVLENKYFVE
		DPYPVLTHELRVPSPLREENNFSEDWAKWKDMEADSDLENIDEFNVVHSSDGFC
		IKFS
395	CDK type D	MDLNQYPEDLNPELPEGTDNVDNPDNNKGSPVPSPHPPLKPLDPSERYRKGITL	240	1631
		GQGTYGIVYKAFDTVTNKTVAVKKIHLGKAKEGVNVTALREIKLLKELSHPNII
		QLIDAYPHKQNLHIVFEFMETDLEAVIKDRNLVFSPADIKSYLQMTLKGLAVCH
		KKWVLHRDMKPNNLLIAADGQLKLGDFGLARLFGSPDRKFTHQVFAVWYRAPEL
		LFGAKQYGPAVDIWATGCIFAELLLRKPFLQGVSDLDQIGKIFAAFGTPRQSQW
		PDVASLPDFVEFQFVPAPSLRSLFPMASEDALDLLSKMFTLDPKNRITAQQALE
		HRYFSSVPAPTRPDLLPKPSKVDSSRPPKHASPDGPVVLSPSKARRVMLFPNNL
		AGILPKQVSQSTTGGTPIEFDMPTQKLREVCPRSRITESGKKHLKRKTMDMSAA
		LDECAREQEGQEGKTILDPDHQRSAKKEKHM
396	Cyclin A	MAGGQENCVRITRARAACVSKASAPVIQSQVDEKKSRKRAPKRAAVDDLAANAS	252	1604
		GSQPKRRAVLGDVTNLHAAATDCLSTAEDQVDAPNPSIKGRARNKKKEARTSTK
		VVKDEIHPESNPLADHSSNLSECQKPPAAKLAEQRSLRGVPSKAKQGGSSNSQS
		CSKHTDIDKDHTDPQMCTTYVEDIYEYLRNAELKNRPSANFMETAQNDITPNMR
		AILVDWLVEVSEEYKLVPDTLYLTVSYIDRYLSANPTSRHKLQLLGVSCMLIAS
		KYEEVCPPHVEEFCYITDNTYTRDEMLSMERKILIFLNFEMTKPTTKSFLRRFV
		RASQAGNKAPSLHMEFLANYLAELTLMECSFLQYLPSLIAASTVFLSRLTLDFL
		TNPWNPTLAHYTGYKASQLKDCVMAIYNVQMNRKGSTLVAIREKYQQHKFKCVA
		SLPPPPFIAERFFEDTPN
397	Cyclin A	MTGTQASNVRITRARAAKSTLNNALPPLPPAQGKPRGKRAATESNISGFSVAAE	261	1817
		PLKRRAVLSDVSNICKEAAAVDCLKKPKAVKVVSQNANAKGRGRGIPRNNKKIT
		QEAEIKKETSPAICNVDDASAGNAIGDDKQNNNVNPLKEVQDNPKELNPIAEQI
		SVHPHCKQSVEKPNEKEIVVSDNKAAIASLKQQSTLQSLRIPKQPKYSLKQGNP
		VPLANLHEDVGRSSCSDFIDIDSEYKDPQMCTAYVTDIYANMRVVELKRRPLPN
		FMETTQRDINANMRSVLIDWLVEVSEEYKLVPDTLYLTVSYIDRFLSANVVNRQ
		RLQLLGVSCMLVASKYEEICAPPVEEFCYITDNTYKKEEVLEMEISVLNRLQYD
		LTTPTTKTFLRRFIRAAQASCKVSSLHLEFMGNYLAELTLVEYDFLKYLPSLIA
		AAAVFVARMTLDPMVHPWNSTLQHYTGYKVSDMRDCICAIHDLQLNRKGCTLAA
		IREKYNQPKFKCVANLFPPPIISPQFLIDNEV
398	Cyclin B	MAAPNQNALLINNNNRRPLVDIGNLVGALNAQCNISKNGARKRAFGDIGNLVED	167	1576
		LDAKCTISKYWVRKRPRTNFGVNANKGASSSTQGQGIVVRGEQKAWDRIVWGNK
		QSCAIKMNAQHVTATQRGTAISISDIIDSSVQDGGIKAPSQLKARKQTVRTVTA
		TLTARSEDSLRDVLEVPPGIDDGDRDNPLAVVEYVEDIYHFYRKIEVRSCVPPD
		YMTRQLEIKDSMRGVIIDWLIEVHRTFLLMPETLYLTVNIIDRYLSIQSVTRNE
		LQLMGITAMFIASKYEEISPPKINDLVYITKDAYTSKQIVNMEHTILNRLKFKL
		TVPTPYVFLVRFLKAAGPDKVMKNLAFFLVDLCLLHYKMIKYSPSMLAAAAVYT
		AQCTLKKHPYWNKTLILHIGYSEAHLRECAHLMADLHLKAEGSNLKSVYKKYSY
		PIFGSVAFLSPAKIPAGTVAAPAIDKCAHQIYLRNLR
399	Cyclin B	MFPNKQTQGLVQNKKMASKAAQPKAMVPPQRVPPAANNRRALGDIGNIVADVGG	183	1598
		KCNVTKDGVNGKPLAQVSRPITRSFGAQLLAQAAANKGISAANNQTQVPVVIPK
		ADVRGNKQRRTSKSKDIPPTTVVTNESDDCVIIEQAQRIKPTCNHNVGAVGNKE
		KPQLLTAKPKSLTASLTSRSAVALRGFRFDDEMTEAEEDPLPNIDVGDRDNQLA
		VVEYVEDIYKFYRRTEQMSCVPDYMPRQQEINPKMRAVLINWLIEVHYRFGLMP
		ETLYLTTNLIDRYLATQLVSRSNYQLVGATAMLLASKYEEIWAPEMNDFLDILE
		NKFERKHVLVMEKAMLNKLKFHLTVPTPYVFLVRFLKAAASDEEMENLVFFLME
		LSLMQYVMIKFPPSMLAAAAVYTAQITLKKTTVWNDVLKRHTGYSEIDLKECTR
		LMVAFHQSSEESKLNVVFKKYSMPEYDSVALIKPAKLPA
400	Cyclin D	MAPSFDCVANAYIESCEDQEKLRQNAQILAQSGENDVDEPVSMLVQRETHYMLP	98	1126
		EDYLQRLRNRTLDVNVRREAVGWILKVHSFYNFGAPTAYLAVNYLDRFLSRHRM
		PQGVKAWMIQLMAVACLSLAAKMEETQVPLPSDLQREDARFIFDARTIQRMELL
		ILSTLQWGMRSITPFSFIDYFAYRAVQGHGHGHDATPKAVMSRAIELILSTTEE
		IDFMEYRPSAIAAAALLCAAEEVVPLQAVHYKRALSSSITDVDKDKMFGCYNLI
		QETIIEGGCYWTPMSLQSTEKTPVGVLDAAACLSNTPTSSYSVKPYASVTAAKR
		RKLNEICSALLVSQAHPC
401	Cyclin D	MAANFWTSSHCKELLDAEKVGIVHPLDKDQGLTQEDVKIIKINMSNCIRTLAQY	148	894
		VKLRQRVVATAITYCRRVYTRKSFTEYDPQLVAPTCLYLASKAEESTVQAKLVI
		FYMKKYSKHRYEIKDMLEMEMKLLEALDYYLVIYHPYRPLIQFLQDAGLNDLKV
		TAWALVNDTYRTDLILTYPPYMIALACIYFACIMEEKDAQAWFEELRVDMNEIK
		NISMEIVDYYDNYRVIPDEKMNSALNKLPHRF
402	Cyclin D	MAPALSSSYECLSHLLCAEDASNVVGCWDEDESKIFCEEEEGFGIQHFPDFPVP	287	1363
		DDDEIRVLVRKESQYMPGKSYVQSYQNLGLDFTARQNAIGWILKVHGSYNFGPL
		TAYLSINYLDRFLSRNPLPKAKVWMLQLLSVACLSLAAKMEETQVPLLLDLQAE
		EPDFLFEPRTIQRMELLVLSTLEWRMLSVTPFSFVDYFLQGGGGRKPPPRAMVA
		RANELIFNTHTVLDFLEHRPSAIAAAAVICAAEEVLPLEAAQYKETILSCSLVD
		KEWVFGSYNLIQEVLIEKFSTPKKAKSASSSIPQSPVGVLDAFCLSNNSNNTSL
		EASLSVNLYASVAAKRRKLNDYCNTWRMFQHSTC
403	Cyclin D	MAPNCIDCAPSDLFCAEDAFGVVEWGDAETGSLYGDEDQLHYNLDICDQHDEHL	251	1348
		WDDGELVAFAEKETLYVPNPVEKNSAEAKARQDAVDWILKVHAHYGFGPVTAVL
		SINYLDRFLSANQLQQDKPWMTQLAAVACLSLAAKMDETEVPLLLDFQVEEAKY
		IFESRTIQRMELLVLSTLEWRMSPVTPLSYIDHASRMIGLENHHCWIFTMRCKE
		ILLNTLRDAKFLGLLPSVVAAAIMLHVIKETELVNPCEYENRLLSAMKVNKDMC
		ERCIGLLIAPESSSLGSFSLGLKRKSSTINIPVPGSPDGVLDATFSCSSSSCGS
		GQSTPGSYDSNNSSILCISPAVIKKRKLNYEFCSDLHCLED
404	Cyclin-	MPQIQYSEKYTDDTYEYRHVVLPPETAKLLPKNRLLNENEWRAIGVQQSRGWVH	229	510
	dependent	YAIHRPEPHIMLFRRPLNYQQNQQQQAGAQSQPMGLKAQ
	kinase
	regulatory
	subunit
405	Cyclin-	MDQIEYSEKYYDDTYEYRHVELPPDVARLLPKNRLLTENEWRGIGVQQSRGWVH	92	409
	dependent	YAIHCSEPHIMLFRRPLNYEQNHQHPEPHIMLFRRPLNCQPNHQPQAHHPT
	kinase
	regulatory
	subunit
406	Cyclin-	MDQIEYSEKYYDDTYEYRHVELPPDVARLLPKNRLLTENEWRGIGVQQSRGWVH	64	381
	dependent	YAIHCSEPHIMLFRRPLNYEQNHQHPEPHIMLFRRPLNCQPNHQPQAHHPT
	kinase
	regulatory
	subunit
407	Cyclin-	MPQIQYSEKYYDDTYEYRHVVLPPDVARLLPKNRLLNENEWRGIGVQQSRGWVH	68	349
	dependent	YAIHRPEPHIMLFRRHLNYQQNQQQQAQQQPAQAMGLQA
	kinase
	regulatory
	subunit
408	Histone	MALVETEPVTLIHPEEPKKFKKKPTPGRGGVISHGLTEEEARVKAIAEIVGAMV	125	1849
	acetyltransferase	EGCRKGEDVDLNALKAAACRRYGLSRAPKLVEMIAALPDGERAAVLPKLKAKPV
		RTASGIAVVAVMSKPHRCPHIATTGNICVYCPGGPDSDFEYSTQSYTGYEPTSM
		RAIRARYNPYVQTRSRIDQLKRLGHTVDKVEFILMGGTFMSLPADYRDYFIRNL
		HDALSGHTSSNVEEAVCYSEHSATKCTGLTIETRPDYCLGPHLRQMLSYGCTRL
		EIGVQSTYEDVARDTNRGHTVAAVADCFCLAKDAGFKVVAHMMPDLPNVGVERD
		MESFREFFENPAFRADGLKIYPTLVIRGTGLYELWKTGRYRNYPPEQLVDIIAR
		VLALVPPWTRVYRVQRDIPMPLVTSGVEKGNLRELALARMDDLGLKCRDVRTRE
		AGIQDIHHKIRPEVVELVRRDYCANEGWETFLSYEDTRQDILVGLLRLRKCGHN
		TTCPELKGRCSIVRELHVYGTAVPVHGRDADKLQHQGYGTLLMEQAERIAWKEH
		RSIKIAVISGVGTRHYYRKLGYELEGPYMMKYLN
409	Histone	MLGFRDLYTSICEHLQRASGRLPIIAAATSLISTPEIAAVEKENKAPNSVDKMG	70	1602
	acetyltransferase	MGSADESGRFSTSNGQFMNMNNGVVKEEWKGGVPVVPSAPTTVPVITNVKLETP
		SSPDHDMARKRKLGFLPLEVGTRVLCKWRDGKFHPVKIIERRKLPNGATNDYEY
		YVHYTEFNRRLDEWVKLEQLELDSVETDADEKVDDKAGSLKMTRHQKRKIDETH
		VEGNEELDAASLREHEEFTKVKNITKIELGRYEIETWYFSPFPSEYNNCEKLYF
		CEFCLNFMKRKEQLQRHMRKCDLKHPPGDEIYRSGTLSMFEVDGKKNKVYAQNL
		CYLAKLFLDHKTLYYDVDLFLFYILCECDERGCHMVGYFSKEKHSEESYNLACI
		LTLPPYQRKGYGKFLISFSYELSKKEGKVGTPERPLSDLGLLSYRGYWTRVLLD
		ILKKHKSNISIKELSDMTAIKADDVLSTLQGLDLIQYRKGQHAICADPKVLDRH
		LKAVGRGGLEVDVCKLIWTPYKEQ
410	Histone	MGSLDESTCSEEIRDEGKDSIRTKFKVESTVNNAQNGGNDNSKKKRAAGLPLEV	140	1465
	acetyltransferase	GIRLLCKWRDSKLHPVKIIERRKLPNGFPQDYEYYVHYTEFNRRLDEWVKLEQF
		ELDSVETDADEKIEDKGGSLKMTRHQKRKIDEIHVEEGQGHEDFDPASLREHEE
		FTKVKNIAKVELGRYEIETWYFSPFPPEYSHCEKLFFCEFCLNFMKRKEQLQRH
		MRKCDLKHPPGDEIYRNGTLSMFEVDGKKNKIYGQNLCYLAKLFLDHKTLYYDV
		DLFLFYVLCECDDRGCHVVGYFSKEKHSDEAYNLACILTLPPYQRKGYGKFLIA
		FSYELSKKEGKVGTPERPLSDLGLLSYRGYWTRILLDILKKQRGNISIKELSDM
		TAIKVEDVISTLQVLDLIQYRKGQHVICADPKVLDRHLKAAGIAGLEVDVSKLI
		WTPYKEQCG
411	Histone	MASAPMVGCDDSRDKHRWVESKVYMRKGHGKGSKGNAGFNAQNSTAQVRRENDN	628	2565
	acetyltransferase	MGNSIADNGKSEAASEGLSSLSRKQITVNQDHPPNETSSMPAVGGLQNIDTHVT
		FKLEGCSKQEIWELRKKLTNELEQVRGTFKKLEARELQLRGYSVSAGVNTSYSA
		SQFSGNDMRNNGGKEVTSEVASGGAITPKQAQRESNPPRQLSISLMENNQAASD
		MGEKGKRTPKANQYYRNSEFVLGKDKFPPAESKKSKSTGNKKISQSKVFSKETM
		QVGKEFMPQKSVNEVFKQCSLLLTKLMKHKYGWVFNLPVDAQALGLHDYHTIIK
		RPMDLGTVKSKLEKNLYNSPASFAEDVKLTFSNAMTYNPKGHEVHTMAEQLLQL
		FEERWKTIYEEHLDGKMRFGSGQGLGASSSTKKLPFQDSKKNIKKSEPAGGPSP
		PKPKSTNHHASRTPSAKKPKAKDPHKRDMTYEEKQKLSTNLQNLPQERLELIVQ
		IIKKRNPSLCQHDEEIEVDIDSFDTETLWELDRFVTNYKKSLSKNKKKALLADQ
		AKRASEHGSARNKHPMIGRELPMNNKKGEQGEKVVEIDHMPPVNPPVVEVEKDG
		VYAKRSSSSSSSSSDSGSSSSDSDSGSSSGSESDAYAATSPPAGSNTSARG
412	Histone	MEGHSGALGFGQGFSRSSQSPNLSPSPSHSASASVTSSGQKRKRNEVEHAGVAS	55	1818
	acetyltransferase	NSTGMFAVPPSHIYSHLHPMSMSMPMPMHNSHPSSLSESRDGALTSNDDDDNLT
		GGNQSQLDSMSAGNTDGREDFDDEDDDDDDEEDDDEVEGDEEDQDHDPDADDDS
		DDGHDSMRTFTAARLDNGAPNSRNLKPKADAAGVAIAPTVKTEPILDTVKEEKV
		SGNNNNNSVSANNAQVAPSGSAVLLSAVKEEANKPTSTDHIQTSGAYCAREESL
		KREEDADRLKFVCFGNDGIDQHMIWLIGLKNIFARQLPNMPKEYIVRLVMDRSH
		KSVMIIKQNQVVGGITYRPYLSQKFGEIAFCAITADEQVKGYGTRLMNHLKQHA
		RDVDGLTHFLTYADNNAVGYFIKQDFTKEIKLEKERWHGYIKDYDGGILMECKI
		DPKLPYTDLPAMIRWQRQTIDEKIRELSNCHIVYSGIDIQKKEAGIPRKPIKVE
		DIPGLKEAGWTTDQWGHSRFRLLNSPSEGLPNRQVLHAFMRSLHKAMVEHADAW
		PFKEPVDPRDVPDYYDIIKDPMDVKRMFTNARTYNTHETIYYKCANR
413	Histone	MEESGNSLTSGPDGSKRRVSYFYDSDIGNYYYSQGHPMKPHRIRMAHSLIVHYA	259	1710
	deacetylase	LDEKMEVCRPNLLQSRELRVFHADDYISFLQSVTPETQHEQLRQLKRFNVGEDC
		PVFDGLYNFCQTYAGGSVGAAIKLNNKEADIAINWSGGLHHAKKCEASGFCYVN
		DIVLAILELLKVHQRVLYIDIDIHHGDGVEEAFYSTDRVMSVSFHKFGDYFPGT
		GHLKDVGYGKGKYYSLNVPLNDGIDDESYKNLFRPIIQKVMEIYQPEAVVLQCG
		ADSLSGDRLGCFNLSVKGHADCVRFLRSFNVPLVLVGGGGYTIRNVARCWCYET
		AVAVGVEPQDKLPYNEYYEYFGPDYTLHVAPSNMENQNSAKELAKIRNTLLEQL
		KRIQHVPSVPFQERPPDTKFPEEDEEDYEKRPKGHKWGGEYFGSESDEEQKPQN
		RDIDISDKPGIRRQSPPNVEAAKKIKVEEEDGDIGIVNENDGAKWPLGEAG
414	Histone	MEESGNSLTSGPDGSKRRVSYFYDSDIGNYYYSQGHPMKPHRIRMAHSLIVHYA	356	1807
	deacetylase	LDEKMEVCRPNLLQSRELRVFHADDYISFLQSVTPETQHEQLRQLKRFNVGEDC
		PVFDGLYNFCQTYAGGSVGAAIKLNNKEADIAINWSGGLHHAKKCEASGFCYVN
		DIVLAILELLKVHQRVLYIDIDIHHGDGVEEAFYSTDRVMSVSFHKFGDYFPGT
		GHLKDVGYGKGKYYSLNVPLNDGIDDESYKNLFRPIIQKVMEIYQPEAVVLQCG
		ADSLSGDRLGCFNLSVKGHADCVRFLRSFNVPLVLVGGGGYTIRNVARCWCYET
		AVAVGVEPQDKLPYNEYYEYFGPDYTLHVAPSNMENQNSAKELAKIRNTLLEQL
		KRIQHVPSVPFQERPPDTKFPEEDEEDYEKRPKGHKWGGEYFGSESDEEQKPQN
		RDIDISDKPGIRRQSPPNVEAAKKIKVEEEDGDIGIVNENDGAKWPLGEAG
415	Histone	MEFWGVEVKPGEALTCDPGDERYLHMSQAAIGDKEGAKENERVSLYVHVDGKKF	261	1298
	deacetylase	VLGTLSRGKCDQIGLDLVFEKEFKLSHTSQTGSVFVSGYTTVDHEALDGFPDDE
		DLESSEDEEEELAQITTLTAKENGGKTGAKPVKPESKSSVTDKAAAKGKPEVKP
		PVKKQEDDSDSDEDEDEDEDEDEDDDDEDDEDMKDASASDDGDEEDDSDEESDD
		DEEEDEETPKPAAGKKRPMPASDNKSPATDKKAKITTPAGGQKPGADKGKKTEH
		IATPYPKHGAKGPASGVKGKETPLGSKQTPGSKVKNSSTPESGKKSGQFKCQSC
		SRDFATEGALSSHNAAKHGGK
416	Histone	MMETGGNSLPSGPDGVKRKVAYFYDPEVGNYYYGQGHPMKPHRIRMTHALLVQY	365	2251
	deacetylase	GLHKEMQILKPYPARDRDLCRFHADDYVAFLRGITPETIQDQVKALKRFNVGDD
		CPVFDGLYQYCQTYAGGSVGGAVKLNHKLCDIAINWAGGLHHAKKCEASGFCYV
		NDIVLAILELLKYHKRVLYVDIDIHHGDGVEEAFYTTDRVMTVSFHKFGDYFPG
		TGDIRDIGCGKGKYYAVNVPLDDGIDDESFQSLFKPIIQQVMLVYNPEAIVLQC
		GADSLSGDRLGCFNLSVKGHAECVRYMRSFNVPLLMVGGGGYTVRNVARCWCYE
		TGVAVGVEIDDKMPQHEYYEYFGPDYTVHVAPSNMENKNTKQYLDKIRSKILEN
		INSLPCAPSAQFQVQPPDTDFPELEEEDYDERTRSHKWDGASCDSDSENGDLKH
		RNHDVEESAFPRHNLANISYNTKIKLEGVGTGGLDMAAGTDTKKNDESFEAMDY
		ESGEELRQDHFASTINASQPCDPALLTGVQNQLQSTDTVKPIEQSGNAPGIPPP
		SVATVSTGTRPSSISRTSSLNSMSSVKQGSILGPNPPQGLNASGLQFPVPTSNS
		PIRQGGSYSITVQAPDKQGLQNHMKGPQNMPGNS
417	Histone	MPPKDRVAYFYDGDVGSVYFGPNHPMKPHRLCMTHHLVLSYELHKKMEIYRPHK	156	1454
	deacetylase	AYPVELAQFHSADYVEFLHRITPDTQHLFTKELVKYNMGEDCPVFENLFEFCQI
		YAGGTIDAAHRLNNQICDIAINWSGGLHHAKKCEASGFCYINDLVLGILELLKH
		HARVLYVDIDVHHGDGVEEAFYFTDRVMTVSFHKYGDMFFPGTGDVKEVGEREG
		KYYAINVPLKDGIDDASFTRLFKTIITKVVDIYQPGAIVLQCGADSLAGDRLGC
		FNLSIDGHAQCVRIVKKFNLPLLVTGGGGYTKENVARCWSVETGVLLDTELPNE
		IPDNDYIKYFAPDYSLKINTAGNMENLNSKTYLSAIKVQVMENLRAIQHAPSVQ
		MHEVPPDFYIPDIDEDELNPDERMDQHTQDRQIQRDDEYYDGDNDIDHDMEEAS
418	Histone	MDSSKSEEANILHVFWHEGMLNHDLGTGVFDTLEDPGFLEVLEKHPENADRVRN	203	1348
	deacetylase	MLSILRKGPIAPYTEWHTGRAAYLSELYSFHRPDYVDMLAKTSTAGGKTLCHGT
		RLNPGSWEAALLAAGTTLEAMRYILDGHGKLSYALVRPPGHHAQPTQADGYCFL
		NNAGLAVELAVASGCKRVAVVDIDVHYGNGTAEGFYERDDVLTISLHMNHGSWG
		PSHPQTGFHDEVGRGKGLGFNLNVPLPNGTGDKGYEHAMHELVVPAISKFMPEM
		IVLVIGQDSSAFDPNGRECLTMEGYRKIGQIMRQQADQFSGGRLVVVQEGGYHI
		TYAAYCLHATLEGVLCLPHPLLSDPIAYYPEHDIYSERVTFIKNYWQGIISTTD
		KRN
419	Histone	MEESGNALVSGPDGSKRRVTYFYDADIGNYYYGQGHPMKPHRMRMAHNLIVHYG	229	1644
	deacetylase	LHQRMEVCRPHLAQSKDIRAFHTDDYIHFLSSVAPDTQQEQLRQLKRFNVGEDC
		PVFDGLFNFCQSSAGGSIGAALKLNRKDADIAINWAGGLHHAKKCEASGFCYVN
		DIVLGILELLKVHQRVLYIDIDIHHGDGVEEAFYTTDRVMTVSFHKFGDYFPGT
		GHIKDVGYGKGKYYALNVPLNDGIDDESYKHLFRPIIQKVMEVYQPEAVVLQCG
		ADSLSGDRLGCFNLSVKGHADCVRFVRSFNIPLMLVGGGGYTIRNVARCWCYET
		AVAVGVEPQDKLPYNEYYEYFGPDYTLYVAPSNMENLNTEKDLEKMRNVLLEQL
		SKIQHTPSVPFQERPPDTEFNDEEEEDMEKRSKCRIWDGEYVGSEPEEDGKLPR
		FDADTYERSVLKHENKRLVPVSNVEPLKRIKQEEDGAAV
420	Histone	MPPKDRVAYFYDGDVGSVYFGPNHPMKPHRLCMTHHLVLSYELHKKMEIYRPHK	156	1454
	deacetylase	AYPVELAQFHSADYVEFLHRITPDTQHLFTKELVKYNMGEDCPVFENLFEFCQI
		YAGGTIDAAHRLNNQICDIAINWSGGLHHAKKCEASGFCYINDLVLGILELLKH
		HARVLYVDIDVHHGDGVEEAFYFTDRVMTVSFHKYGDMFFPGTGDVKEVGEREG
		KYYAINVPLKDGIDDASFTRLFKTIITKVVDIYQPGAIVLQCGADSLAGDRLGC
		FNLSIDGHAQCVRIVKKFNLPLLVTGGGGYTKENVARCWSVETGVLLDTELPNE
		IPDNDYIKYFAPDYSLKINTAGNMENLNSKTYLSAIKVQVMENLRAIQHAPSVQ
		MHEVPPDFYIPDIDEDELNPDERMDQHTQDRQIQRDDEYYDGDNDIDHDMEEAS
421	Histone	MDLNLVSHGEEEEGVRRRKVGIVYDERMCKHATPEDQPHPEQPDRIRVIWDKLN	27	2222
	deacetylase	SAGVLHKCVMVEAKEASEEQLAGVHSRKHIEVMKSIGTARYNKKKRDKLAASYS
		SIYFSQGSSEAALLAAGSVVEISEKVASGELDAGVAIVRPPGHHAEADKAMGFC
		LFNNIAIAAKHLVHERPELGVQEVLIVDWDVHHGNGTQHMFWTDPHVLYFSVHR
		FDAGTFYPGGDDGFYDKIGEGKGAGYNINVPWEQGKCGDADYLAVWDHVLVPVA
		KSYDPDMVLISGGFDAALGDPLGGCRLTPYGYSLMTKKLMEFAGGKIVLALEGG
		YNLKSLADSFLACVEALLKDGPSRSSVLTHPFGSTWRVIQAVRKELSSFWPALN
		EELQLPRLLKDASESFDKLSSSSSDESSASEDEKKIAEVTSIMEVSPDPSSILA
		LTAEDIAQPLAGLKIEEAGTDSQRSSDHTLLDLTNDDTQKLKQFEGEIFVMIGD
		EESVPSASSSKDQNESTVVLSKSNIKAHSWRLTFSSIYVWYASYGSNMWNPRFL
		CYIEGGQVEGMAKRCCGSEDKTPPQRIQWKVVPHRMFFGRSYTNTWGSGGVSFL
		DPNCSDTSEAHVCLYKITLAQFNDLLLQENNLNCGTEHPLVDLSSIDAIRNGNS
		ILELIKDSWYGTLIYLGMEGGLPIVTFTCSVCDVEKFKHGQLPLCPPSSRYENI
		LIRGLVQGKKLSEDDATAYIRAASTSPLL
422	Peptidylprolyl	MADEDLDLSDVGEVEDEPGEEIESTPPLAVGQEKEINSLALKKKLLKVGTRWET	71	1759
	isomerase	PENGDEVTVHYTGTLPDGTKFDSSRDRGEPFTFKLGQGQVIKGWDQGIVTMKKG
		ERALFTIPPELAYGSSGVRPTIPPNATLQFDVELLSWTNIVDVCNDGGILKRII
		SEGEKYERPKDPDEVTVKYEAKLEDGTLVAKSPEEGVEFYVNDGHFCPAIAKAV
		KTMKRGESVILTIKPTYAFGERGKDAEEGFAAIPPNATLTTSLELVSFKAVIAV
		TEDKKVIKKILKEADGYDKPSDGTVVQIRYTAKLQDGTIFEKKGYEGEEPFQFV
		VDEEQVIAGLDKAVETMKTGEIALITIGAEYGFGNFETQRDLAVIPPNSTLIYE
		VEMISFTKEKESWDMDTTEKIEASKQKKEQGNSLFKVGKYQRAAKKYEKAAKYI
		EHDSSFSAEEKKQSKVLKVSCNLNHAACRLKLKDFKEAVKLCSKVLELESQNVK
		ALYRRAQAYIETADLDLAEFDIKKALEIEPQNREVQLEYKILKQKQIEYNKKDA
		KLYGNMFAKLNKLEAFEGKVLS
423	Peptidylprolyl	MADEGLELSDVAEVEDEPGEEFESAPPLVVGQEKELNSSGLKKKLLKAGTRCET	358	2040
	isomerase	PENGDEVTVHYTGTLLDGTKFDSSRDRGEPFTFNIGQGQVIKGWDQGIVTMKKR
		EHALFTIPPELAYGASGMPPTIPPNATLQFDVELLSWTNIVDVCKDGGILKRII
		SDGEKYERPKDPDEVTVKYEAKLEDGMLVAKSPEEGVEFYVNDGNFCPAIVKAV
		KTMKKGENVTLTIKPAYAFGEQGKDAEEGFAAIPPNATITINLQLVSFKAVKEV
		TEDKKVIKKILKEADGYDKPSDGTVVQIRYTAKLQDGTIFEKKGYAGEEPFQFV
		VDEEQVIAGLDKAVETMKTGEVALITIGPEYGFGNIETQRDLAVIPPYSTLIYE
		VEMVSFTKEKESWDMNTTENIEASKQKKEQGNSLFKVGKYLRAAKKYDKAAKYI
		EHDNSFSAEEKKQSKVLKVSCNLNHAACCLKLKDFKKAVKLCSKVLELESQNVK
		ALYRRAQAYIETADLDLAEFDIKKALEIEPQNREVRLEYLILKQKQIEYNKKDA
		KLYGNMFARQNKLEAIEGKD
424	Peptidylprolyl	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRALCTGEKGTGRSGKPLH	238	756
	isomerase	FKGSSFHRVIPGFMCQGGDFTRGNGTGGESIYGEKFADENFVKKHTGPGILSMA
		NAGPNTNGSQFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGSGRTSKP
		VVIADSGQLA
425	Peptidylprolyl	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRALCTGEKGNGRSGKPLH	238	756
	isomerase	FKGSSFHRVIPGFMCQGGDFTRGNGTGGESIYGEKFADENFVKKHTGPGILSMA
		NAGPNTNGSQFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGSGRTSKP
		VVIADSGQLA
426	Peptidylprolyl	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRALCTGEKGTGRSGKPLH	238	756
	isomerase	FKGSSFHRVIPGFMCQGGDFTRGNGTGGESIYGEKFADENFVKKHTGPGILSMA
		NAGPNTNGSQFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGSGRTSKP
		VVIADSGQLA
427	Peptidylprolyl	MPNPKVFFDMQVGGAPAGRIVMELYADVVPKTAENFRALCTGEKGTGRSGKPLH	238	756
	isomerase	FKGSSFHRVIPGFMCQGGDFTRGNGTGGESIYGEKFADENFVKKHTGPGILSMA
		NAGPNTNGSQFFICTAQTSWLDGKHVVFGQVVEGLEVVRDIEKVGSGSGRTSKP
		VVIADSGQLA
428	Peptidylprolyl	MADDFELPESAGMMENEDFGDTVFKVGEEKEIGKQGLKKLLVKEGGSWETPETG	176	1912
	isomerase	DEVEVHYTGTLLDGTKFDSSRDRGTPFKFKLGQGQVIKGWDQGIATMKKGENAV
		FTIPPDLAYGESGSQPTIPPNATLKFDVELLSWASVKDICKDGGIFKKIIKEGE
		KWEHPKEADEVLVKYEARLEDGTVVSKSEEGVEFYVKDGYFCPAFAIAVKTMKK
		GEKVLLTVKPQYGFGHQGREAIGNDVARSTNATLLVDLELVSWKVVDEVTDDKK
		VLKKILKQGEGYERPNDGAVVKVKYTGKLEDGTIFEEKGSDEEPFEFMAGEEQV
		VDGLDRAVMTMKKGEVALVSVAAEYGYQTEIKTDLAVVPPKSTLIYEVELVSFV
		KEKESWDMNTAEKIEAAGKKKEEGNALFKVGKYFRASKKYEKATKYIEYDTSFS
		EEEKKQSKPLKVTCNLNNAACKLKLKDYTQAEKLCTKVLEVESQNVKALYRRAQ
		AYIQTADLELAELDIKKALEIDPNNRDVKLEYRALKEKQKEYNKKEAKFYGNMF
		ARMSKLEELESRKSGSQKVETANKEEGSDAMAVDGESA
429	Peptidylprolyl	MAASLTPLGAGLAYATIYDQAKVRKLEPTKRSLIALCQHSDSQHRRFITRKYHV	64	765
	isomerase	NVQILNRRDAIRLIGLAAGLCIDLSLMYDARGAGLPPQENAKLCDTTCEKELEN
		APMITTESGLQYKDIKIGNGPSPPIGFQVAANYVAMVPSGQVFDSSLDKGQPYI
		FRVGSGQVIKGLDEGLLSMKVGGKRRLYIPGPLAFPKGLNSAPGRPRVAPSSPV
		IFDVSLEFIPGLESEEE
430	Peptidylprolyl	MSAASLSADMAIRGTILGKTALHVLGPQVVSQCRQPVMFKCPPHTLRKMRFSAQ	93	881
	isomerase	DLQSKNFYSGFTPFKSVFISTSKRSWQAGSARAMSQDAAFQSKVTTKCFLDIEI
		GGDPAGRIVLGLFGEDVPKTAENFRALCTGEKGFGYKGSSFHRIIKDFMLQGGD
		FDRGDGTGGKSIYGRTFEDENFKLAHVGPGVLSMANAGPNTNGSQFFICTVKTP
		WLDKRHVVFGQVIEGMEIVKKLESEETNRTDRPKRPCRIVDCGELP
431	Peptidylprolyl	MGRIKPQTLLQQSKKKKVPGRISVSTIIVCNLIIIFLMFSLVGIYRQRAKRNRA	372	1070
	isomerase	TSRSDGDEEMENFGRSKINSVPHQAIVNTTKGLITLELFGKSSAHTVEKFVEWS
		ERGYFNGLPFYRVIKHFVIQVGDPKFAGNREDWTVGGQLNVQLEFSPKHEAFML
		GTSKLEDQGDGFELFITTAPIPDLNDKLNVFGRVIKGQDVVQEIEEVDTDEHFQ
		PKSPIIINDVRLKDEL
432	Peptidylprolyl	MARQSTLLLFWSLVFLGAIVFTQAKHEELEEVTHKVYFDVDIAGKPAGRVVIGL	28	594
	isomerase	FGKAVPKTVENFRALCTGEKGVGKSGKPLHYKGSFFHRIIPSFMIQGGDFTLGD
		GRGGESIYGTKFADENFKLKHTGPVFITTVTTDWLDGRHVVFGKIISGMDVVYK
		VEAEGRQSGQPKRKVKIADSGELSMD
433	Peptidylprolyl	MARQSTLLLFWSLVFLGAIVFTQAKHEELEEVTHKVYFDVDIAGKPAGRVVIGL	34	648
	isomerase	FGKAVPKTVENFRALCTGEKGVGKSGKPLHYKGSFFHRIIPSFMIQGGDFTLGD
		GRGGESIYGTKFADENFKLKHTGPGFLSMANAGPDTNGSQFFITTVTTDWLDGR
		HVVFGKIISGMDVVYKVEAEGRQSGQPKRKVKIADSGELSMD
434	Peptidylprolyl	MEMDEIQEQSQPQSSEKQDISQESDTGNDKTINAEKITSENAEVEEDDMLPPKV	481	1611
	isomerase	NTEVEVLHDKVTKQIIKEGSGNKPSRNSTCFLHYRAWAESTMHKFQDTWQEQQP
		LELVLGREKKELSGFAIGVAGMKAGERALLHVDWQLGYGEEGNFSFPNVPPRAN
		LIYEAELIGFEEAKEGKARSDMTVEERIEAADRRRQQGNELFKEDKLAEAMQQY
		EMALAYMGDDFMFQLFGKYKDMANAVKNPCHLNMAQCLLKLNRYEEAIGQCNMV
		LAEDEKNIKALFRRGKARATLGQTDDAREDFQKVRKFSPEDKAVIRELRLLAEH
		DKQVYQKQKEMFKGLFGQKPEQKPKKLHWFVVFWQWLLSMIRTIFRMRSKTD
435	Peptidylprolyl	MAGAGEGTPEVTLETSMGPITVELYHKHAPKTCRNFLELSRRGYYNNVKFHRVI	93	584
	isomerase	KDFMVQGGDPTGTGRGGESIYGPRFEDEITRDLKHTGAGILSMANAGPNTNGSQ
		FFISLAPTPWLDEKHTIFGRVCKGMDVVKRLGNVQTDKNDRPIHDVKILRTTVKD
436	Peptidylprolyl	MMDPELMRLAQEQMSKISPDELMKMQRQIMANPDLMRMASENMKNLKPEDIRFA	250	1869
	isomerase	AEQMKNVRKEEMAEISERISRASPEEIEAMKARANLQSAYQLQVAQNLKDQGNQ
		LHARMKYSEAAEKYLQARNNLTGIPFSEAKSLLLASSSNLMSCYLKTGQYEECV
		QTGSEVLAYDAMNVKALYRRGQAYKQIGKLELAVADLRKAVEVSPEDETIAQAL
		REASTELMEKGGTQDQNGPRIEEIIEEEAVQPTAEKYPQSAPMVTSVTEDVSDD
		EQGSEDQNGFSRDSFQATNAPDGQMYAESLRNLTENPDMLRTMQSLMKNVDPDS
		LVALSGGKLSPDMVKTVSGMFGRMSPEEIQNMMKMSSTLSRQNPSTSSRFDDIT
		RGHSNMDSSPQSVSVDNDLFEENQNRVGESSTNLSSSAAFSGMPNFSAEMQEQV
		RNQMNDPATRQMFTSMIQNMSPEMMASMSEQFGVKLSPEDAVKAQNAMASLSPN
		DLDRLMNWATRLQTAIDYARKIKNWILGRPGLIFAISMLLLAIILHRFGYIGD
437	Peptidylprolyl	MGVEKEILRPGNGPKPRPGQSVTVHCTGYGKNEDLSQKFWSTKDPGQKPFTFTI	84	422
	isomerase	GQGRVIKGWDEGVLDMQLGEIFKLRCSPDYGYGSNGFPAWGIRPNSVLVFEIEV
		LSVN
438	Peptidylprolyl	MPNPRCYLDITIGEELEGRILVELYSDVVPKTAENFRALCTGEKGIGPHTGVPL	128	1213
	isomerase	HYKGLPFHRVIKGFMIQGGDISAQNGTGGESIYGLKFDDENFQLKHERRGMLSM
		ANSGPNTNGSQFFITTTRTSHLDGKHVVFGKVIKGMGVVRGIEHTPTESNDRPS
		LDVVISDCGEIPEGSDDGIANFFKDGDLYPDWPADLDEKSAEISWWMNAVDSAK
		CFGNENYKKGDYKMALRKYRKALRYLDICWEKEEIDEEKSNHLRKTKSQIFTNS
		SACKLKLGDLKGALLDTEFAMRDGEDNVKALFRQGQAYMALKDVDSAVASFKKA
		LQLEPNDAGIRKELAVATKMINDRRDQERRAYARMFQ
439	Peptidylprolyl	MGDVIDLNGDGGVLKTIIRSAKPGAMQPTEDLPNVDVHYEGTLADTGEVFDTTR	265	837
	isomerase	EDNTLFSFELGKGTVIKAWDIAVKTMKVGEVARITCKPEYAYGSAGSPPDIPEN
		ATLIFEVELVACKPRKGSTFGSVSDEKARLEELKKQREIAAASKEEEKKRREEA
		KATAAARVQAKLEAKKGQGRGKGKSKGK
440	Peptidylprolyl	MGLGLKIASASFLPIFNIMATRSLCILLVCFIPVLAHVLSLQDPELGTVRVYFQ	38	781
	isomerase	TTYGDIEFGFFPHVAPKTVEHIYKLVRLGCYNSNHFFRVDKGFVAQVADVVGGR
		EVPLNSEQRKEGEKTIVGEFSEVKHVRGILSMGRYSDPDSASSSFSILLGNAPH
		LDGQYAVFGKVTKGDDTLKRLEEVPTRQEGIFVMPLERIRILSTYYYDTNERES
		NLTCDHEVSILKRRLVESAYEIEYQRRKCLP
441	Peptidylprolyl	MASKRSLRTMNVWPTLPPLVLLLLLCFSSMSSSVVAKKSDVSELQIGVKHKPKS	38	526
	isomerase	CDIQAHKGDRIKVHYRGSLTDGTVFDSSFERGDPIEFELGSGQVIKGWDQGLLG
		MCVGEKRKLRIPSKLGYGAQGSPPKIPGGATLIFDTELVAVNGKGISNDGDSDL
442	Peptidylprolyl	MSGAPAERPISYFDITIGGKPIGRIVFSLYADLVPKTAENFRALCTGEKGIGKS	37	1158
	isomerase	GKPLCYAGSGFHRVIKGFMCQGGDFTAGNGTGGESIYGEKFEDEAFPVKHTKPF
		LLSMANAGKDTNGSQFFITVSQTPHLDDKHVVFGEVIKGKSIVRAIENYPTASG
		DVPTSPIIISACGVLSPDDPSLAASEETIGDSYEDYPEDDDSDVQNPEVALDIA
		RKIRELGNKLFKEGQIELALKKYLKSIRYLDVHPVLPDDSPPELKDSYDALLAP
		LLLNSALAALRTQPADAQTAVKNATRALERLELSDADKAKALYREASAHVILKQ
		EDEAEEDLVAASQLSPEDMAISSKLKEVKDEKKKKREKEKKAFKKMFSS
443	Peptidylprolyl	MASSLRSSLFSSWALDSKSVCSLFNLNPGKMGLPSISTPLNWRTCCCSHSSELL	61	768
	isomerase	ELNEGLQSSRRKTVMGLSTVIALSLVYCDEVGAVSTSKRALRSQKVPEDEYTTL
		PNGLKYYDLKVGSGTEAVKGSRVAVHYVAKWKGITFMTSRQGMGITGGTPYGFD
		VGASERGAVLKGLDLGVQGMRVGGQRILIVPPELAYGNTGIQEIPPNATLEFDV
		ELISIKQSPEGSSVKIVEG
444	WD40 repeat	MGAIEDEEPPLKRLKVSSPGLRRGLEEEAPSLSVGSVSILMAKSLSLEEGETVG	421	2172
	protein	SKGLIRRVEFVRIITQALYSLGYQKAGALLEEESGILLQSSNVALFRKQILDGK
		WDESVVTLRGIDQVEVEGNTLKAASFLILQQKFFELLDKGNIPEAMKTLRLEIS
		PMQLNTKRVHELASCIVFPSRCEELGYSKQGNPKSSQRMKVLQEIQQLLPPSIM
		IPEKRLERLVEQALNVQREACIFHNSLDPALSLYTDHQCGRDQIPTTTLQVLES
		HKNEVWFLQFSNNGKYLASASKDCSAIIWEITEGDSFSMKHRLSAHQKPVSFVA
		WSPDDKLLLTCGIEEVVKLWNVETGECKLTYDKANSGFTSCGWFPDGERFISGG
		VDKCIYIWDLEGKELDSWKGQGMPKISDLAVTSDGKEIISICGDNAIVMYNLDT
		KTERLIEEESGITSLCVSKDSRFLLLNLANQEIHLWDIGARSKLLLKYKGHRQG
		RYVIRSCFGGSDLAFVVSGSEDSQVYIWHRGNGELLAVLPGHSGTVNCVSWNPV
		NPHVFASASDDYTIRIWGVNRNTFRSKNASSSNGVVHLANGGP
445	WD40 repeat	MPGTTAGAGIEPIEPQSLKKLSLKSLKRSFDLFASLHGEPQPPDQRSQRIRIAC	163	1647
	protein	KVRAEYEVVKNLPTLPQREVGSSVSNSNVGETHSSLTTNQAQGFPTDTSGDLSK
		DEGKEITSIAVHLQPQTGLIDGKAGAIAGTSTAISSVGSSDRYQPSAAIMKRLP
		SKWPRPIWHPPWKNYRVISGHLGWVRSVAFDPGNEWFCTGSADRTIKIWEVATG
		KLKLTLTGHIEQIRGLAVSSRHPYLFSAGDDKQVKCWDLEYNKAIRSYHGHLSG
		VYCLALHPTLDILCTGGRDSVCRVWDIRTKAQIFALSGHENTVCSVFTQAIDPQ
		VVTGSHDTTIKLWDLAAGKTMSTLTYHKKSVRAIAKHPFEHTFASASADNIKKF
		KLPKGEFLHNMLSQQKTIVNAMAINEDNVLVSAGDNGSLWFWDWKSGHNFQQAQ
		TIVQPGSLDSEAGIYALQYDITGSRLVSCEADKTIKMWKEDETATPESHPINFK
		APKDIRRF
446	WD40 repeat	MRPILMKGHERPLTFLKYNRDGDLLFSCAKDHTPTVWYGHNGERLGTYRGHNGA	192	1172
	protein	VWCCDVSRDSTRLITSSADQTAKLWNVETGAQLFSFNFESPARAVDLAIGDKLV
		VITTDPFMELPSAIHIKRIEKDLSKQTADSVLTITGIKGRINRAVWGPLNSTII
		SGGEDSVVRIWDSETGKLLRESDKETGHQKPITSLCKSADGSHFLTGSLDKSAR
		LWDIRTLTLIKTYVTERPVNAVAISPLLDHVVIGGGQEASHVTTTDRRAGKFEA
		KFFHKILEEEIGGVKGHFGPINSLAFNPDGRSFASGGEDGYVRLHHFDPDYFHI
		KM
447	WD40 repeat	MRPILMKGHERPLTFLKYNRDGDLLFSCAKDHTPTVWYGHNGERLGTYRGHNGA	131	1111
	protein	VWCCDVSRDSTRLITSSADQTAKLWNVETGNQLFSFNFESPARAVDLAIGDKLV
		VITTDPFMELPSAIHIKRIEKDLSKQTADSVLTITGIKGRINRAVWGPLNSTII
		SGGEDSVVRIWDSETGKLLRESDKETGHQKAITSLCKSADGSHFLTGSLDKSAR
		LWDIRTLTLIKTYVTERPVNAVAISPLLDHVVIGGGQEASHVTTTDRRAGKFEA
		KFFHKILEEEIGGVKGHFGPINSLAFNPDGRSFASGGEDGYVRLHHFDPDYFHI
		KM
448	WD40 repeat	MAENNVGDFIPLDRQEYPSKPAPGAVDSSFWKSFKKKEVSRQIAGVTCINFCPE	149	1726
	protein	PPHDFAVTSSTRVHIYDGKSCELKKTITKFKDVAYSGVFRSDSQIIAAGGETGV
		IQVFNAKSQMVLRQLKGHGRPVRVVRYSPQDKLHLLSGGDDSMVKWWDITTQEE
		LLNLEGHKDYVRCGAASPSSVNLWATGSYDHTVRLWDLRNSKTVLQLKHGKPLE
		DVLFFPSGGLLATAGGNVVKVWDILGGGRPIHTMETHQKTVMAMCISKVPRSGQ
		ALGDAPSRLVTASLDGYMKVFDLDHFKVTHSARYPAPILSMGISSLCRTMAVGT
		SSGLLFIRQRKGQIEDKIHSDSSGLQVNPVNDEKDSAVLKPNQYRYYLRGRSEK
		PSEGDYVVKRMAKVYFQEYDKDLRHFNHSKALVSALKAADSKGTVAVIEELVAR
		KRLIQTLSILNLDELELLINFLSRFILVPKYSRFLISLTDRVLDARAVDLGKSE
		NLKKQIADLKGIVVQELRVQQSMQELQGIIEPLIRASAR
449	WD40 repeat	MDVETSGKPTGNKRTYTRLPRQVCVFWQEGRCTRESCNFLHVDEPGSVKRGGAT	948	2228
	protein	NGFAPKRSYNGSDERDTLAAGPPGGSRRNISARWGRGRGGIFISDERQKIRNKV
		CNYWLAGNCQRGEECKYLHSFVMGSDVKFLTQLSGHVKAIRGIAFPSDSGKLYS
		GGQDKKVIVWDCQTGQGTDIPLNDEVGCLMSEGPWIFVGLPNAVKAWNILTSTE
		LSLVGPRGQVHALAVGNGMLFAGTHDGSILAWKFSPASNTFEPAASLVGHTQAV
		VSLVSGADRLYSGSMDKTIRVWDLGTFQCLQTLRDHTSVVMSLLCWDQFLLSCS
		LDNTVKVWVATSSGALEVTYTHNEEHGVLALCGMNDEQAKPVLLCSCNDNTVRL
		YDLPSFSERGRIFSRNEVRTFQIAPGGLFFTGDATGELKVWNWATQKS
450	WD40 repeat	MSVQELRERHAAATAKVNALRERIKAKRLQLLDTDVATYASSNGRTPISFSFTD	332	1465
	protein	LVCCRTLQGHTGKVYSLDWTSEKNRIVSASQDGRLIVWNALTSQKTHAIKLPCA
		WVMTCAFSPSGQAVACGGLDSVCSIFQLNNQLDRDGHLPVSRILSGHRSYVSSC
		QYVPDGDTHVITGSGDRTCIQWDVTTGQRIAIFGGEFPLGHTADVMSVSISAAN
		PKEFVSGSCDTTTRLWDTRIASRAIRTFHGHEADVNTVKFFPDGLRFGSGSDDG
		TCRLFDIRTGHQLQVYRQPPRENQSPTVTAIAFSFSGRLLFAGYSNGDCFVWDT
		ILEKVVLNLGELQNTHNGRISCLGLSADGSALCTGSWDKNLKIWAFGGHRKIV
451	WD40 repeat	MKVKIISRSTDEFTRERSNDLQRVFRNFDPNLHTQARAQEYVRALNAAKLDKIF	232	1590
	protein	AKPFLAAMSGHIDGISAMAKSPRHLKSIFSGSVDGDIRLWDIAARRTVQQFPGH
		RGAVRGLTVSTEGGRLISCGDDCTVRLWDIPVAGIGESSYGSENVQKPLATYVG
		KNSFRAVDYQWDSNVFATGGAQVDIWDHDRSEPTNSFAWGSDTVISVRFNPAEK
		DIFATTASDRSIVLYDLRMASPLNKLIMQTRNNAIAWNPREPMNFTAANEDCNC
		YSYDMRRMNISTCVHQDHVSAVMDIDYSPSGREFVTGSYDRTVRIFPYNAGHSR
		EIYHTKRMQRVFCVKFSGDATYVVSGSDDANIRLWKAKASEQLGVLLPRERKRH
		EYLDAVKERFKHLPEIKRIERHRHLPKPIYKAALLRHTVNAAAKRKEERKRAHS
		APGSVVTNPLRKKRIVAQLE
452	WD40 repeat	MDHYYQDDFDYLVDDEMVDFADDVEDDVRTRRRSDIDSDSENDFDLNNKSPDTT	207	1550
	protein	ALQAKRGKDIQGIPWNRLNFTREKYRETRLQQYKNYENLPRPRRSRNLDKECTN
		FERGSSFYDFRHNTRSVKATIVHFQLRNLVWATSKHNVYLMQNYSIMHWSSLKQ
		KGEEVLNVAGPIVPSVKHPGSSPQGLTRVQVSAMSVKDNLVVAGGFQGELICKY
		LDKPGVSFCTKISHDENGITNAVEIYNDASGATRLMTANNDLAVRVFDTEKFTV
		LERFSFPWSVNHTSVSPDGKLVAVLGDNADCLLADCKTGKTVGTLRGHLDYSFA
		AAWHPDGYILATGNQDTTCRLWDVRKLSSSLAVLKGRMGAIRSIRFSSDGRFMA
		MAEPADFVHLYDTRQNYTKSQEIDLFGEIAGISFSPDTEAFFVGVADRTYGSLL
		EFNRRRMNYYLDSIL
453	WD40 repeat	MAEALVLRGTMEGHTDAVTAIATPIDNSDMIVSSSRDKSILLWNLTKEPEKYGV	221	1171
	protein	PRRRLTGHSHFVQDVVISSDGQFALSGSWDSELRLWDLNTGLTTRRFVGHTKDV
		LSVAFSIDNRQIVSASRDRTIKLWNTLGECKYTIQPDAEGHSNWISCVRFSPSA
		TNPTIVSCSWDRTVKVWNLTNCKLRNTLVGHGGYVNTAAVSPDGSLCASGGKDG
		VTMLWDLAEGKRLYSLDAGDIIYALCFSPNRYWLCAATQQCVKIWDLESKSIVA
		DLRPDFIPNKKAQIPYCTSLSWSADGSTLFSGYTDGKIRVWGIGHV
454	WD40 repeat	MAAIKSTSRSASVAFAPDAPLLAAGTMAGAIDLSFSSLANLEIFKLDFQSDDPE	221	3679
	protein	LPVVGECPSNERLNRLSWGSAGGSFGIIAGGLVDGTINIWNPATLINSEDNGDA
		LIARLEQHTGPVRGLEFNTISTNLLASGAEDGELCIWDLANPTAPTHFPPLKGV
		GSGAQGEISFLAWNRKVQHILASTSYSGTTVVWDLRRQKPIISFPDATRRRCSV
		LQWNPDASTQLIVASDDDNSPTLRAWDLRNTISPYKEFVGHSRGVIAMSWCPSD
		SLFLLTCAKDNRTLCWDTGSGEIVCELPAGANWNFDVQWSPKIPGILSTSSFDG
		KIGIHNIEACSRNVSGEVEFGGAIVRGGPSALLKAPKWLERPAGVSFGFGGKLA
		SFRPSTVAQAADHRHSEVFIHNLVTEDNLVIRSTEFEAAIADGEKVSLRALCDR
		KAEESQSDEEKETWNFLRVMFEDEGTARTKLLEHLGFKVQSEENGDLQETHSSK
		IDDIGSEIGKTLTLDDKTEEDVLPQLKGGQDAAIPQDNGEDFFDNLHSPKEEVS
		LSHVGNDFVGEKDKDMVVNGAEIEHETEDLTEYSDWNEAIQHSLVVGDYKGAVL
		QCLSANRMADALIIAHLGGNSLWEKTRDEYLKKAKSSYLKVVSAMVNNDLTGLV
		NSRPLKSWKETLAMLCTYSQREEWTVLCDMLASRLIAAGNVMAATLCYICAGNI
		EKTVEIWSRSLKYDYDGRSFVDHLQDVMEKTVVLALATGQKRVSPSLSKLVENY
		AELLASQGLLTTAMEYLKLLGTEESSHELSILRDRLYLSGTDNKVEASSFPFET
		RQDLTESQYNMHQTGFGAPETQKNYQENVHQVLPSGSYTDNYQPTANTHYIAGY
		QPAPQQQPSFQNYFTPASYQPAPSPNVFYPSQVSQAEQSNFAPPVNQPPMKTFV
		PSTPPILRNVDQYQTPSLNPQLYQGVSSATVETHPYQTGAPASVSVGTTPGQPS
		VVPNFMVPGPVTAPTVTPRGFMPVTTPTQHPLGSANPPVQPQSPQSSQVQSVTA
		ATTPPPTIQNVDTSNVAAEIRPVIGTLRRLYDETSEALGGARANPAKRREIEDN
		SRKIGSLFAKLNSGDISSNAASKLVHLCQALESRDYATAFQIQVGLTTSDWDEC
		SFWLAALKRMIKVKQNMR
455	WD40 repeat	MAGAADSQLQTLSERDSTPNFKNLHTREYAAHKKKVHSVAWNCTGTKLASGSVD	269	1252
	protein	QTARVWNIEPHGHSKTKDLELKGHADSVDQLCWDPKHSELLATASGDRTVRLWD
		ARSGKCSQQVELSGENINITFKPDGTHIAVGNRDDELTIIDVRKFKPLHKRKFS
		YEVNEIAWNTTGELFFLTTGNGTVEVLSYPSLQVLHTLVAHTAGCYCIAIDPIG
		RYFAVGSADALVSLWDLSEMLCVRTFTKLEWPVRTISFNHDGQYIASASEDLFI
		DIADVQTGRTVHQISCRAAMNSVEWNPKYNLLAFAGDDKNKYMQDEGVFRVFGF
		ETP
456	WD40 repeat	MAATSPVGAGSGRELANPPTDGISNLRFSNHSDHLLVSSWDRKVRLYDASANSL	214	1242
	protein	KGQFVHGGPVLDCCFHDDASGFSGSADNTVRRYDFSTRKEDILGRHEAPVRCVE
		YSYAAGQVITGSWDKTLKCWDPRGASGQEKTLVGTYSQLERVYSMSLVGHRLVV
		ATAGRHINVYDLRNMSQPEQRRESSLKYQTRCVRCYPNGTGFALSSVEGRVAME
		FFDLSEAGQAKKYAFKCHRKSEAGRDTVYPVNAIAFHPIYGTFATGGCDGYVNV
		WDGNNKKRLYQYSKYPTSIAALSFSRDGRLLAVASSYTFEEGEKPHEPDAVFVR
		SVNEAEVKPKPKVYAAPP
457	WD40 repeat	MASDDEEGFKNEEAPGVVDEAEVQEGLRACFPLSFGKQEKKQAPLESIHSATKR	119	2065
	protein	PEDPRPRRQLGPPRPPPSILAEQEDSDRFVGPPRPPQFVRDDNDDGEAEIMIGP
		PRPPAQYSDDHDNEETIGPPKPSYLEKGEETDQMVGPSKRGSDDETSGDSDDGD
		DAVDFRVPLSNEIVLRGHTKVVSALAIDQTGSRVLTGSYDYSVRMYDFQGMTSQ
		LKSFRQLEPAEGHQVRSLSWSPTSDRFLCVTGSAQAKIFDRDGLTLGEFVKGDM
		YLRDLKNTKGHISGLTCGEWHPKEKQTILTCSEDGSLRIWDVNDFNTQKQVIKP
		KLAKPGRVPVTACAWGRDGKCIAGGVGDGSIQVWNLKPGWGSRPDLYVAKGHDD
		DITGLQFSADGNILLTRSTDETLKVWDLRKAITPLQVFRDLPNNYAQTNVAFSP
		DERLIFTGTSVERDGNSGGLLCFYDRQTLELVLRIGVSPVHSVVRCTWHPRHNQ
		VFATVGDKKEGGAHILYDPALSERGALVCVARAPRKKSLDDFEAKPVIHNPHAL
		PLFRDEPSRKRQREKARMDPMKSQRPDLPVTGPGFGGRVGSTKGSLLTQYLLKE
		GGLIKETWMEEDPREAILKYADVAAKDPKFIAPAYAQTQPETVFAETDSEEEQK
458	WD40 repeat	MKERGQSHAGQPSVDERYTQWKSLVPVLYDWLANHNLVWPSLSCRWGPQMHQAT	186	1550
	protein	YKNSQRLYLSEQTDGTVPNTLVIATCEVVKPRVAAAEHISQFNEEARSPFVKKF
		KTIIHPGEVNRIRELPQNSKIVATHTDGPDVLIWDVDTQPNRQATLGAADSRPD
		LVLTGHKDNAEFALAMSPSAPFVLSGGKDKCVLLWSIQDHISAATEPSSAKASK
		TPSSAHGEKVPKIPSIGPRGVYKGHKDTVEDVQFCPSNAQEFCSVGDDSALILW
		DARNGNEPVIKVEKAHNADLHCVDWNPHDENLILTGSADNSVRMFDRRNLTSSG
		VGSPVHKFEGHSAPVLCVQWCPDKASVFGSAAEDSYLNVWDYEKVGKNVGKKTP
		PGLFFQHAGHRDKVVDFHWNSFDPWTIVSVSDDGESTGGGGTLQIWRMSDLIYR
		PEDEVLAELERFRAHILSCQNK
459	WD40 repeat	MSSLSRELVFLILQFLDEEKFKESVHKLEQESGFFFNMKYFDEKAQAGEWDEVE	244	3671
	protein	RYLSGFTKVDDNRYSMKIFFEIRKQKYLEALDRQDRAKAVDILVKDLKVFSTFN
		EELYKEITQLLTLDNFRENEQLSKYGDTKSARTIMMSELKKLIEANPLFREKLI
		YPNLKASRLRTLINQSLNWQHQLCKNPRPNPDIKTLFTDHACGPPNGARTPTQP
		TASLGVLPKATTFTPIGPHGPFPSSSTATSGLASWMSNPNMVTSPQAPVAVGPS
		VPVPPNQATLLKRPRTPPGSSSVVDYQTADSEQLIKRLRPVSQSIDEATYPGPT
		LRVPWSTDDLPKTLARALNEPYPVTSIDFHPSQQTFLLVGTKNGEITLWEVGSR
		EKLATRSFKIWDNANCSNHLEAAFVKDSSVSINRVLWSPDGTLIGIAFTKHLVH
		TYTFQGLDLRQHLEIDAHVGGVNDLAFSHPNKQLCVVTCGDDKMIKVWDAVTGR
		KLYNFEGHDAPVYSVCPHHKENIQFIFSTAVDGKIKAWLYDHLGSRVDYDAPGH
		SCTTMMYSADGTRLFSCGTSKEGESFLVEWNESEGAIKRTYSGLRKKGSGVVQF
		DTTQNHFLAVGDEHLIKFWDMDSTNMLTSCDAEGGLLNLPRLRFNKEGSLLAVT
		TVNGIKILANADGQKLLKTMENRTFDLPSRAHIDAASATSSPATGRMERIERTS
		SANTVSGINGVDPAQSSEKLRLSDDLSEKTKIWKLTEITDSIQCRCITLPENAA
		EPASKVSRLLYTNSGVGLLALGSNAVHKLWKWNRSEQNPSGKATASVHPQRWQP
		TSGLLMTNDITDINPEEAVPCIALSKNDSYVMSASGGKVSLFNMMTFKVMTTFM
		PPPPASTFLAFHPQDNNIIAIGMEDSTIHIYNVRVDEVKTKLKGHQKRITGLAF
		SSTQNILVSSGADAQLCVWNTETWEKRKSKTIQMPVGKTVSGDTRVQFHSDQLH
		ILVVHETQLAIYDAYKLERQYQWVPQDALSAPILYATYSCNRQLIYATFSDGNI
		GVYDAEILRPRCRIAPTTYLSSGTSSSTSLPLVVAAHPHEPNQFAIGLSDGAVQ
		VLEPSESEGKWGVSPPPENGVVPAVVAGPSTSNQGSEQAPR
460	WD40 repeat	MAKDEEEFRGEMEERLVNEEYKIWKKNTPFLYDLVITHALEWPSLTVQWLPDRE	163	1431
	protein	EPPGKDYSVQKMILGTHTSDNEPNYLMLAQVQLPLEDAENDARQYDDERGEIGG
		FGCANGKVQVIQQINHDGEVNRARYMPQNPFIIATKTVSAEVYVFDYSKHPSKP
		PQDGGCHPDLRLRGHNTEGYGLSWSPFKHGHLLSGSDDAQICLWDINVPAKNKV
		LEAQQIFKVHEGVVEDVAWHLRHEYLFGSVGDDRHLLIWDLRTSATNKPLHSVV
		AHQGEVNCLAFNPFNEWVLATGSADRTVKLFDLRKISSALHTFSCHKEEVFQIG
		WSPKNETILASCSADRRLMVWDLSRIDEFQTPEDALDGPPELLFIHGGHTSKIS
		DFSWNPCEDWVIASVAEDNILQIWQMAENIYHDEEDDMPPEEVV
461	WD40 repeat	MSPGVKQTGSQKFESGHQDVVHDVTMDYYGKRIATCSADRTIKLFGLNASDTPS	155	1081
	protein	LLASLTGHEGPVWQVAWAHPKFGSMLASCSYDGRVIIWREGQQENEWSQVQVFK
		EHEASVNSISWAPNELGLCLACGSSDGSITVFTCREDGSWDKTKIDQAHQVGVT
		AVSWAPASAPGSLVGQPSDPIQKLVSGGCDNTAKVWKFYNGSWKLDCFPPLQMH
		TDWVRDVAWAPNLGLPKSTIASCSQDGKVVIWTQGKEGDKWEGRILNDFKIPVW
		RVNWSLTGNILAVADGNNSVTLWKEAVDGDWNQVTTVQ
462	WD40 repeat	MSSGVKQTGSQKFESGHQDVVHDVTMDYYGKRIATCSADRTIKLFGMNTSDTPT	537	1463
	protein	LLASLTGHEGPVWQVAWAHPKFGSMLASCSYDRRVIIWREGQQENEWSQVQVFK
		EHEASVNSISWAPHELGLCLACGSSDGSITVFTGREDGSWDKTKIDQAHQVGVT
		AVSWAPASAPGSLVGQPSDPVQKLVSGGCDNTAKVWKFYNGSWKLDCFPPLQMH
		TDWVRDVAWAPNLGLPKSTIASCSQDGRVVIWTQGKEGDKWEGKILNDFKTPVW
		RISWSLTGNILAVADGNNNVTLWKEAVDGEWNQVTTVQ
463	WD40 repeat	MKKRSRPSNGHLSTAAKNKSRKTAPITKDPFFDSAHNRNKSKGKGKSRGKGEEI	284	1909
	protein	FSSDEDDDAIGRDAPAEEEEEIAEEERETADEKRLRVAKAYLDKIRAITKANEE
		DNEEEAGEDEETEAERRGKRDSLVAEILQQEQLEESGRVQRQLASRVVTPSKLV
		ECRVVKRHKQSVTAVALTEDDLRGFSASKDGTIIHWDVETGASEKYEWPSQAVS
		VSSSNEVSKTQKGKGSKKQGSKHVLSMAVSSDGRYLATGGLDRYIHLWDTRTQK
		HIQAFRGHRGAVSCLAFRQGTQQLISGSFDRTIKLWSAEDRAYMDTLYGHQSEI
		LAVDCLRKERVLSVGRDHTLRLWKVPEETQLVFRGHAASLECCCFINNEDFLSG
		SDDGSIELWSMLRKKPVFMAKNAHGHAIVENLSEDTSTREEPDEEVTTRQLPNG
		NSIGNGMTNQMGITPSVESWVGAVTVCRGTDLAASGAGNGVVRLWAIENSSKSL
		RALHDIPLTGFVNSLTFARSGRFLIAGVGQEPRLGRWGRIQAARNGVTLCPIELS
464	WD40 repeat	MAATFGTINTATSPHNPNKSFEIVQPPNDSISSLSFSPKANYLVATSWDNQVRC	610	1659
	protein	WEVLQTGASMPKAAMSHDQPVLCSTWKDDGTAVFSAGCDKQAKMWPLLTGGQPV
		TVAMHDAPIKDIAWIPEMNLLATGSWDKTLKYWDTRQSNPVHTQQLPERCFALS
		VRHPLMVVGTADRNLIIFNLQNPQTEFKRISSPLKYQTRCVAAFPDKQGFLVGS
		IEGRVGVHHVEEAQQSKNFTFKCHRDSNDIYAVNSLNFHPVHQTFATAGSDGAF
		NFWDKDSKQRLKAMARSNQPTPCSTFNSDGSLYAYAVSYDWSKGAENHNPATAK
		HHILLHVPQESEIKGKPRVTTSGRK
465	WD40 repeat	MVVMDKGTHQTNEDESESEFIDEDDVIDEISIDEEDLPDADVEGEDVQEDNKRS	241	1452
	protein	EPDENSSSLDDAIHTFEGHEDTLFAVACSPVDATWVASGGGDDKAFMWRIGHAT
		PFFELKGHTDSVVALSFSNDGLLLASGGLDGVVRIWDASTGNLIHVLDGPGGGI
		EWVRWHPKGHLVLAGSEDYSTWMWNADLGKCLSVYTGHCESVTCGDFTPDGKAI
		CTGSADGSLRVWNPQTQESKLTVKGYPYHTEGLTCLSISSDSTLVVSGSTDGSV
		HVVNIKNGKVVASLVGHSGSIECVRFSPSLTWVATGGMDKKLMIWELQSSSLRC
		TCQHEEGVMRLSWSLSSQHIITSSLDGIVRLWDSRSGVCERVFEGHNDSIQDMV
		VTVDQRFILTGSDDTTAKVFEIGAF
466	WD40 repeat	MPVFRTAFNGYAVKFSPFVETRLAVATAQNFGIIGNGRQHVLELTPNGIVEVCA	223	1173
	protein	FDSSDGLYDCTWSEANENLVVSASGDGSVKIWDIALPPVANPIRSLEEHAREVY
		SVDWNLVRKDCFLSASWDDTIRLWTIDRPQSMRLFKEHTYCIYAAVWNPRHADV
		FASASGDCTVRIWDVREPNATIIIPAHEHEILSCDWNKYNDCMLVTGSVDKLIK
		VWDIRTYRTPMTVLEGHTYAIRRVKFSPHQESLIASCSYDMTTCMWDYRAPEDA
		LLARYDHHTEFAVGIDISVLVEGLLASTGWDETVYVWQHGMDPRAC
467	WD40 repeat	MDSRNRRSRLNLPPGMSPSSLHLETTAGSPGLSRVNSSPSTPSPSRTTTYSDRF	251	1777
	protein	IPSRTGSRLNGFALIDKQPQPLPSPTRSAAEGRDDASSSSASAYSTLLRNELFG
		EDVVGPATPATPEKSTGLYGGSRDSIKSPMSPSRNLFRFKNDHGGNSPGSPYSA
		STVGSEGLFSSNVGTPPKPARKITRSPYKVLDAPALQDDFYLNLVDWSSNNVLA
		VGLGTCVYLWSACTSKVTKLCDLGVNDSVCSVGWTPQGTHLAVGTNIGEVQIWD
		TSRCKKVRTMGGHCTRAGALAWSSYILSSGSRDRNILHRDIRVQDDFIRKLVGH
		KSEVCGLKWSYDDRELASGGNDNQLLVWNQQSAQPLLRFNEHTAAVKAIAWSPH
		QHGILASGGGTADRCLRFWNTATDTRLNCVDTGSQVCNLVWCKNVNELVSTHGY
		SQNQIMVWRYPSMSKLATLTGHTLRVLYLAISPDGQTIVTGAGDETLRFWSIFP
		SPKSQSAVHDSGLWSLGRTHIR
468	WD40 repeat	MEKKKVVVPIVCHGHSRPIVDLFYSPVTPDGLFLISASKDSSTMLRNGETGDWI	367	1419
	protein	GTFEGHKGAVWSCCLDNRALRAASGSADFSAKIWDALTGDELHCFVHKHIVRAC
		AFSESTSLLLTGGHEKILRIFDLNRPDAPPKEVDNSPGSIRTVAWLHSDQTILS
		SNSDAGGVRLWDLRTEKIVRVLETKSPVTSAEVSQDGRYITTADGNSVKFWDAN
		HFGMVKSYTMPCMVESASLEPTMGNMFVAGGEDMWVRLFDFHTGEEIACNKGHH
		GPVHCVRFAPGGESYSSGSEDGTIRIWQTLNMNSEENESYGVNGLSGKVRVGVD
		DVVQKVEGFQITADGHLNDKPEKPNP
469	WD40 repeat	MERYSQGTQKKSEIYTYEAPWQIYGMNWSVRKDKKFRLGIGSFLEEYNNRVEII	284	1303
	protein	ELDEESGEFKSDPRLAFDHPYPTTKIMFVPDKECQRPDLLATTGDYLRIWQVCE
		DRVEPKSLLNNNKNSEFCAPLTSFDWNDADPKRIGTSSIDTTCTIWDIEKEVVD
		TQLIAHDKEVYDIAWGEVGVFASVSADGSVRVFDLRDKEHSTIIYESSQPETPL
		LRLGWNKQDPRFIATILMDSCKVVILDIRFPTLPVAELQRHQASVNTIAWAPHS
		PCHICTAGDDSQALIWELSSVSQPLVEGGGLDPILAYTAAAEINQLQWSSMQPD
		WVAIAFSNEVQILRV
470	WD40 repeat	MQSENNLDESLHLREVQELQGHTDTVWAVAWNPVTGIDGAPSMLASCSGDKTVR	684	1784
	protein	IWENTHTLNSTSPSWACKAVLEETHTRTVRSCAWSPNGKLLATASFDATTAIWE
		NVGGEFECIASLEGHENEVKSVSWSASGMLLATCGRDKSVWIWDVQPGNEFECV
		SVLQGHTQDVKMVQWHPNRDILVSASYDNSIKVWAEDGDGDDWACMQTLGNSVS
		GHTSTVWAVSFNSSGDRMVSCSDDLTLMVWDTSINPAERSGNAGPWKHLCTISG
		YHDRTIFSVHWSRSGLIASGASDDCIRLFSESTDDSVTPVDGTSYKLILKKEKA
		HSMDVNSVQWHPSEPQLLASASDDGRIKIWEVTRINGLANSH
471	WD40 repeat	MKRAYKLQEFVAHASNVNCLKIGKKSSRVLVTGGEDHKVNMWAIGKPNAILSLS	336	2738
	protein	GHSSAVESVTFDSAEALVVAGAASGTIKLWDLEEAKIVRTLTGHRSNCISVDFH
		PFGEFFASGSLDTNLKIWDIRRKGCIHTYKGHTRGVNSIRFSPDGRWVVSGGED
		NIVKLWDLTAGKLMHDFKCHEGQIQCMDFHPQEFLLATGSADRTVKFWDLETFE
		LIGSAGPETTGVRAMIFNPDGRTLLTGLHESLKVFSWEPLRCYDAVDVGWSKLA
		DLNIHEGKLLGCSYNQSCVGVWVVDISRVGPYAAGNVSRTNGHNEAKLASSGHP
		SVQQLDNNLKTNMARLSLSHSTESGIKEPKTTTSLTTTEGLSSTPQRAGIAFSS
		KNLPASSGPPSYVSTPKKNSTSRVQPTTNFQTLSRPDIVPVIVPRSNSLRPETT
		SDVKKEMNNFGRVVPSTVSTKSTDVIKSGSNRDESDKIDSINQKRMTGNDKTDL
		NIARAEQHVSSRLDNTNTSSVVCDGNQPAARWIGAAKFRRNSPVDPVVSPHDRS
		PTFPWSATDDGVTCQPDRQVTAPELSKRVVEPGRARALVASWETREKALTADTP
		VLVSGRPPTSPGVDMNSFIPRGSHGTSESDLTVSDDNSAIEELMQQHNAFTSIL
		QARLTKLQVIRRFWQRNDLKGAIDATGKMGDHSVSADVISVLIERSEIFTLDIC
		TVILPLLTRLLQSETDRHLTVAMETLLVLVKTFGDVIRATISATPTIGVDLQAE
		QRLERCNLCYVELENIKQILVPLIRRGGAVAKSAQELSLALQEV
472	WD40 repeat	MSTLEIEARDVIKIVLQFCKENSLHQTFQTLQNECQVSLNTVDSLETFVADINS	81	1622
	protein	GRWDVILPQVAQLKLPRKKLEDLYEQIVLEMIELRELDTARAILRQTQAMGFMK
		QEQPERYLRLEHLLVRTYFDPREAYHESSKEKRRSQIAQALASEVTVVPPSRLM
		ALIGQSLKWQQHQGLLPPGTQFDLFRGTAAVKADEEEMYPTTLAHTIKFGKQSH
		PECARFSPDGQYLVSCSVDGFIEVWDYISGKLKKDLQYQADDSFMMHDDAVLCV
		DFSRDSEMLASGSQDGKIKVWRIRTGQCLRRLERAHSQGVTSLSFSRDGSQLLS
		TSFDSTARIHGLKSGKALKEFRGHTSYVNDAIFTSDGGRVITASSDCTVKVWDV
		KTTDCIQTFKPPPPLKGGDVSVNSVHLFPKNSEHIVVCNKASSIYIMTLQGQVV
		KSFSSGKREGGDFVAACISPKGEWIYCVGEDRNIYCFSQQSGKLEHLMKAHDKD
		IIGVTPHPHRNLLVTYSEDSTMKIWKP
473	WD40 repeat	MDIELEDQPFDLDFHPSAPIVAVALITGRLQLFRYVDISSEPERLWTVTAHTES	399	1460
	protein	CRAARFINAGSSVLTASPDCSILATNVETGQPVARLDNAHGAAINCLTNLTEST
		IASGDENGIIKVWDTRQNSCCNKFKAHEDYISDMEFVPDTMQLLGTSGDGTLSV
		CNLRKNKVHARSEFSEDELLSVALMKNGKKVVCGSQEGVLLLYSWGYFKDCSDR
		FVGHPHSVDALLKLDEDTVLTGSSDGIIRVVSILPNKMIGVIGEHSSYPIERLA
		FSHDRNVLGSASHDQILKLWDIHYLHEDDEPETNKQEAVNDENVDMDLDVDTEK
		RPRGSKRKKRAEKGQTSSQKQSSDFFADI
474	WD40 repeat	MDRIQQIPHTCVARKINLPLGMSKESLALNLPANLAPTMSPPSITYSDRFIPSR	207	1673
	protein	KASNFEEFALPDKTSPSPNSAGGQSSSTNGEGRDDACAAYSALLRTELFPATPD
		KTEGCRRPVIGSPSGNVFRFKSQQCKSQSPFSLCPVGEDGDLSETGAVARKTTR
		KIPRSPFKVLDAPALQDDFYLNLVDWSSHNILAVGLSACVYLWSASSSKVTKLC
		DLGLDDNVCSVAWTQRGTYLAVGTNNGGVQIWDAAHCKQVRTMEGHCTRVGTLA
		WNSHILSSGGRDRNILQRDIRAQDDFVSKFSGHKSEVCGLKWSYDNRELASGGN
		DNQLFVWNQQSQQPVLKYNEHTAAVKAIAWSPHQHGLLASGGGTADRCIRFWNT
		ATNTSLNCVDTGSQVCNLVWSKNVNELVSTHGYSQNQIIVWRYPTMSKLATLTG
		HTLRVLYLAISPDGQTIVTGAGDETLRFWNVFPSSKTQQNTIRDMGVWSSGRTH
		IR
475	WD40 repeat	MAGGQGEGEEKVDKLSMELTEDVMKSMEIGAVFKDYNGKINSLDFHRTNNYLVT	263	1309
	protein	ASDDEAIRLFDTASATWQKTSYSKKYGVDLICFTNHQTSVLYSSKNGWDESLRH
		LSLMDNKYLRYFKGHHDRVVSLCMSPKGECFMSGSLDRTVLLWDLRIDKCQGLI
		RVRGRPAVAYDEQGLVFAISNEGGLIKMFDARLYDKGPFDTFVVEGDKSEASGI
		KFSNDGKLILLSTMDSNIHVLDAYQGTTVHSFSVEAVPNGGEAVPNGGTLEASF
		SPDGKFVISGSGNGNIHAWSVNSGKEVACWTTEGVIPAVVKWAPRRLMFASGSS
		VLSLWVPDLSKLASLTGSNSNSAY
476	WD40 repeat	MHRVGSTGNTSNSSRPRREKRLTYVLNDANDSRHCSGINCLVISKLSLLGGNDY	232	2529
	protein	LFSGSRDGTLKRWELADDSAVCSATFESHVDWVNDAVLTGETLVSCSSDTTLKT
		WRPFSDGVCTRTLRQHSDYVTCLAAASKNSNIVASGGLGREVFIWDIEAAMAPV
		SRTSEAMDDDTSNGVLSSGNSVLSTTVRSTNATNSASLHTSQLQGYTPIAAKGH
		KESVYALAMNDVGTLLVSGGTEKVVRVWDPRSGAKQMKLRGHTDNVRALILDST
		GRFCLSGSSDSIIRLWDLGQQRCVHSYAVHTDSVWALASTPNFSHVYSGGRDLS
		LYLTDLTTRESLLLCMEKHPLLRLTLQDDSIWVATTDSSLHRWPAEGQNPPKMF
		QRGGSFLAGNLSFTRARACLEGSAPVPVNTQPSFVIPGSPGIVQHEILNNRRHV
		LTKDAEGTVKLWEITRGAVLDDYGKVSFEEKKEELFEMVSIPAWFTMDTRLGSM
		SVHLDTPQCFTAEMYAVDLNVPDAPEEQKINLAQETLRGLLAHWLSRRRQRLAT
		QASANGDFPAGQENALRNHISSRIDVHDDAETHIAGILPAFDFSTTSPPSIITE
		GSQGGPWRKKITDLDGTEDEKDFPWWCLECVLHGRLSPRESLKCSFYLHPYEGT
		TVQVLTQGKLSAPRILRIQKVINYVLEKMVLDRPLDSSNSETTFTPGLSGNQSH
		AAVVGDGSLRSGARVWQQKAKPLVEILCNNQVLSPDMSLATVRTYIWKKPDDLY
		LYYRLVQNR
477	WD40 repeat	MMKGKTIQMQAAHQNHDGETSVACVLWDWHAKHLITAGADNTILIHSYPSSSSS	56	2950
	protein	KPITLRHHKNAVTALAINSNVRSLASGSVDHSVKLYSYPGGEFQSNVTRFTLPI
		RSLAFNKSGELLAAAGDDEGIKLISTIDNSIARVLKGHNGPVTSISFDPKNEFL
		ASSDSDGTVIYWELSTGKPVHTLKKIAPNTTSNPTSLNQISWRPDGEMLAVPGR
		KSEVSMYDRDTAEKLFSLKGGHSDTICSLAWSPNGKYIATAGTDRQVMVWDADR
		RQDIDKQRFDNPICSVAWKPSDNALAVIDVLGRFGVWESPIASHMKSPADGAER
		YDNMEDEEPLMARYEEELEDSVSGSLNEIINDDDDDDEMGKIPRKILQKKPSVK
		VEKGKEESNAKAFKSGQDSFKLKSAMQEAFQPGATQRQSGKRNFLAYNMLGSVI
		TFDNDGFSHIEVDFHDIGKGCRVPSMTDYFGFTMASLSESGSVFGSPQKGEKNP
		STLMYRPFSSWANNSEWSMRFPMGEEVKAVALGSGWVAAVTSLNFLRVFSEGGL
		QKFVLSMDGPVVTAAGYENLLVVVSHASNPLLSGDQVLSFTVYDISQKTCPLSG
		RLPLSPGSHLTWLGFSEEGLLSSYDSEGNLRVFTNDYNGCWVPIFSAARERKSE
		TESIWMVGLNSTQVFCVVCKLPDTYPQVAPKPVLSVLNLSLPLACSDLGADDLE
		NEYLRGSLLLSQMQKKAEDAVACGRESNMEEDSIFKMEAALDRCLLRLIANCCK
		GDKLVRATELARLLSLEKSLQGAIKLVSAMKLPMLAERFNTILEEKILQENMET
		ISCRRLTSEAQDMDTPISISVKQVSYGANLGDSPFLPNRQVEPKHSTPVFSKPD
		TKIEVDTSEAIAKGCDAQNGNIKSGDAEVQPASHNDSIQKPSNPFAKASNTSAN
		QAVQRNASLLSSIKQMKTATENEGKRKERARSGSLPQKPAKQSKIS
478	WD40 repeat	MKQKRKGHQVDDPKYSVQTPQEDDTPNESGPASEEVESSDEEGGNSSNIEDDII	193	2577
	protein	YSSSEEDPVVSSDYEEDEDAESDAEGVTAEQELEGDIDNALQNYMGTLTVLSNF
		HGENLKNAEGEDTSGDDDDEEEMPKRAEESDSPEDENDERPKRAEESDFSEDED
		EERPKRAEESDSSEDEVPSRNTVGDVPLRWYKDEQHIGYDIKGKKIKKQPKKDQ
		LDSFLASTDDSSDWRKVYDEYNDEEVELTKDEIKFISRLRKGTIPHADVNPYEP
		YVDWFDWKDKGHPLSNAPEPKRRFIPSKWEAKKVVKLVRAIRKGWITFQKAEEK
		PRFYLMWGDDLKPSEKMANGLSYIPAPKPKLPGHEESYNPPPEYIPTQEEINSY
		QLMYEEDRPKFIPKRFDSLRNVPAYDRFLSEIFERCLDLYLCPRTRKKRINIDP
		ESLIPKLPKPKDLQPFPSICFLEYKGHTGAVSCISPESSGQWLASGSKDGTVRI
		WEVETARCLKVWDIGRPIQHIAWNPVSQLSILAVAVDEEVLVLNTGLGSEDSQE
		KVAELLHVKSKPVSADDLGDNTSLTKWIKHEKFDGIKLTHLKPVHLISWHHKGD
		YFATVAPDGNTRAVLVHQLSKQQTQNPFKKMQGRVVHVLFHPSRAIFFVATKTH
		VRVYDLVKQQLVKRLVTGLHEVSSMAVHHKGDNLLVGSKEGKVCWFDMDLSTQP
		YKTLKNHSKDIHSVAFHDSYPLFASCSDDCKAYVFYGLVYSDLLQNPLIVPLKV
		LQGHQSVNGMGVLDCQFHPKQPWLFTAGADSVVKLYCN
479	WD40 repeat	MMSLKRGFEESLVPAKRQKTELSTVTYGDGPRRTSSLESPIMLLTGHHAAIYTM	187	1233
	protein	KFNPTGTVIASGSHEREIFLWNVHGDCKNFMVLKGHKNAVLDLHWTTDGCQIIS
		ASPDKTLRAWDVETGKQIKKMAEHSSFVNSCCPSRRGPPLVVSGSDDGTAKLWD
		LRHRGAIQTFPDKYQITAVGFSDAADKIYSGGIDNEIKVWDLRRGEVTMRLQGH
		TDTITGMQLSSDGSYLLTNSMDCSLRIWDMRPYAPQNRCVKILTGHQHNFEKNL
		LKCSWSSDGSKVTAGSADRMVYIWDTTTRRILYKLPGHTGSVNETGFHPTQPII
		GSCSSDKQIYLGEIEPNVGYQAVI
480	WD40 repeat	MEFSDTYKHTGPCCFSPDARYLAIAVDYRLVIRDVVTLKVVQLYSCMDKISNIE	51	1436
	protein	WALDSEYILCGLYKRAMVQAWSLSQPEWTCKIDEGPAGIAHARWSPDSRHIITT
		SDFQLRLTVWSLVNTACIHIQWPKHASKGVSFTQDGKFAAIATRRDCKDYVNLL
		SCHTWEVMGTFTVDTIDLADLEWSPNDSAIVVWDSPLEYKVLIYSPDGRCLFKY
		QAYDSWLGVKTVAWSPCSQFLAVGSYDQTLRTLNHLTWKPFAEFVHVSTVRGPA
		SAVVFKEVEEPWNLDVSGLHLNDDNAHDIQDGKPAEGHSRVRYKVVEFPVNVSS
		QKHPVDKPNPKQGIGLLAWSRDSQYLFTRNDNMPTALWIWDICRLELAALLIQK
		EPIRAAAWDPVYPRVALCTGSSHLYMWTPSGACCVNIPLPQFVVSDLKWNPDGT
		SMLLKDRESFCCTFVPMLPEFNDDETNEE
481	WD40 repeat	MAKLIETHSCVPSTERGRGILIAGDAKTNSIIYCNGRSVIMRNLDNPLEASVYG	525	2351
	protein	EHSYPATVARFSPNGEWVASGDTSGTVRIWGRGSDHTLKYEYKALAGRIDDLEW
		SADGQRIVVCGDSKGKSMVRAFMWDSGTNVGEFDGHSRRVLSCSFKPTRPFRVA
		TCGEDFLVNFYEGPPFRFKTSHRDHSNYVNCVRFAPDGSKFITVGSDRKGVIFD
		GKMGEKIGELSKEGGHTGSIYAASWSPDSKQVLTVSADKSAKIWEISETGNGTV
		KKTLTFGSQGGADDMLVGCLWLNDYLITVSLGGIVSLLSAVDPDKPPKTISGHM
		KSINAIALSLQSGQSEVCSSSYDGVIVRWILGVGYAGRVERKDSTQIKCLATIE
		GELVTCGFDNKVRRVPLLSEQHKESEPIDIGAQPKDLDVAVGCPELTFVSTDAG
		IIIIRASKIVSTTNVGYAVTAAAISPDGTEAVVGGQDGKLRVYSIKGDTLLEES
		VLERHRGPINAIRFSPDGSMFASGDLNREAVVWDRITREVKLKNMVYHTARINC
		IAWSPDSSKVATGSLDTCILIYEVGKPASSRITIKGAHLGGVYGLAFSDQSTVI
		SAGEDACVRVWSLP
482	WD40 repeat	MPQPSVILATAGYDHTVRFWEATSGRCYRTLQYPDSQVNHLEITPDKQYLAAAG	152	1099
	protein	NPHIRLFEVNSNNPQPVISYDSHTNNVTAVGFQCDGKWMYSGSEDGTVKIWDLR
		APGFQREYESRAAVNTVVLHPNQTELISGDQNGNIRVWDLNANSCSCELVPEDT
		AVRSLTVMWDGSLVVAANNHGTCYVWRLMRGTQTMTNFEPLHKLQAHNSYILKC
		LLSPEFCEHHRYLATTSSDQTVKIWNVDGFTLERTLTGHQRWVWDCVFSVDGAF
		LVTASSDSTARLWDLSTGEAIRTYQGHHKATVCCALHDGTDGASC
483	WD40 repeat	MLTKFETKSNRVKGLSFHPKRPWILASLHSGVIQLWDYRMGTLIDKFDEHDGPV	470	4114
	protein	RGVHFHKTQPLFVSGGDDYKIKVWNYKMRQCLFTFVGHLDYIRTVHFHNEYPWI
		VSASDDQTIRLWNWQSRVCISVLTGHNHYVMSASFHPKEDLVVSASLDQTVRVW
		DISGLRKKTVSPADDLSRLAQMNTDLFGGGDVVVKYVLEGHDRGVNWAAFGTSL
		PLIVSGADRQVGKLWRMNDTKAWEVDTLRGHTNNVSCVIFHARQDIIVSNSEDK
		SIRVWDMSKRTSVQTFRREHDRFWILAAHPEMNLLAAGHDSGMIVFKLERERPA
		YVVYGGSLLYVKDRYLRTYEFATQKDNPLIPIRKPGSIGPNQGPRSLSYSPTEN
		AILICSDADGGAYELYAVPKDSHGRSDTVQEAKKGLGGSAVGVARNRFAVLDKN
		HNQVTIKNLKNEVTKKFDLPVTADALFYAGTGNLLCRSEDSVFLFDMQQRTVLG
		EIQTPNVRYVVWSNDMENVALLSKHTIIIASKKLSSTCSLHETIRVKSGAWDDN
		GIFMYSTLNHIKYCLPNGDSGIIKTLDVPVYITKVSGKSLYCLDRDGKNRVIQI
		DITECLFKLALSKKKYDYVINMIRNSQLCGQAIIAYLQQKGFPEVALHFVRDER
		TRFNLAVESGNIEIAVASAKEIDEKDHWYRLGVEALRQGNAGIVEYAYQRTKNF
		ERLSFLYLITGNLDKLSKMLRIAEMKNDVMGQFHNALYLGDIQERIKILEESGH
		LHLAYATASLHGLADIADRLAADLGGNIPVLPPGKKSSLLMPPAPILHGGDWPL
		LRVTKGIFEGGLENSTSAAYEEEDEEAAADWGEDIDIENIEGENGEATVLDDQE
		VKGGEDDEGGWDMEDLELPPDVAAANVGTNQKTLFVAPTLGMPVSQIWMQKSSL
		AGEHAAAGNFETALRLLTRQLGIKNFSPLKPLFLELYMGSHTFLPSFASVPAFS
		LALQRGWSESASPNIRGPPALVYRLSVLEEKLTVAYRATTEGRFSEALRLFLNI
		LHTIPVIVVDSRKEIDEVKELIGIAKEYVLGLRMEVKRKEIRDDAVRQQELAAY
		FTHCNLQKAHLKLALLNAMGISYRCKNYNTAANFARRLLETDPSSNHATKARQV
		LQVCERNLQDATQLNYDFRNPFVVCGATFTPIYRGQKEVSCPYCMARFVPDIAG
		KLCSICDLAIVGSDASGLFCFATQTR
484	WD40 repeat	MDLLQNYQDDSEDSNPELRNHPPLEDATATSAPAGVENETSSSPDSSPLRLALP	196	2007
	protein	AKSCAPDVDETLMALGVPGSEKKNNHNKPIDPTQHSVTFNPSYDQLWAPLYGPA
		HPYAKDGIAQGMRNHKLGFVEDSAIEPFMFDEQYNTFHRYGYAADPSASLGSHI
		VGDLESLKKNDGASVYNLPKREHKRQKLEKKMIQKDENEEEEKEVGEEVDNPST
		EEWLKKNRKSPWAGKKEGLQTELTEEQKKYAQEHAEKKGDREKGEKVEIVDKTT
		FHGKEERDYQGRSWIDPPKDAKATNDHCYIPKRWVHTWSGHTKGVSAIRFFPKY
		GHLLLSAGMDTKVKIWDVFNSGKCMRTYMGHSKAVRDISFSNDGSRFLSAGYDR
		NIKLWDTETGKVISTFSTGKIPYVVKLHPDEDKQNVLLAGMSDKKIVQWDMNSG
		EITQEYDQHLGAVNTITFVDNNRRFVTSSDDKSLRVWEFGIPVVIKYISEPHMH
		SMPSISLHPNTNWLAAQSLDNQILIYSTRERFQLNKKKRFAGHIAAGYACQVNF
		SPDGRFVMSGDGEGRCWFWDWKTCKVFRTLKCHDNVCIGCEWHPLEQSKVATCG
		WDGMIKYWD
485	WD40 repeat	MARKGLGTDPAIGSLMSSKKRKEYKVTNRFQEGKRPLYAIAFNFIDARYHNIFA	214	1323
	protein	TAGGTRVTIYQCLEGGAISVLQAYVDDDKDESFYTLSWACDVNGSPLLVAGGHN
		GIIRVLDVANEKVHKSFVGHGDSVNEIRTQALKPSLILSASKDESVRLWNVQTG
		ICILIFAGAGGHRNEVLSVDFHPSDVYRIASCGMDNTVKIWSMKEFWTYVEKSF
		TWTDLPSKFPTKYVQFPVFIAAVHSNYVDCTRWLGNFILSKSVDNEVVLWEPYS
		KEQSTSDGVVDILQKYPVPECDIWFIKFSCDFHYNSMAVGNREGKVYVWELQSS
		PPNLIARLSHAHCKNPIRQTAISHDGSTILCCCDDGSMWRWDVVQ
486	WD40 repeat	MESGAGGSVGARVPSAKPEMLQQPPYSNGDDDNDMERGTAPVPSSNPNTVSKWE	68	2146
	protein	LDKDFLCPICMQTMKDAFLTACGHSFCYMCIMTHLNNKSNCPCCSLYLTNNQLF
		PNFLLNKLLKKTSACQMASTASPVENLCLSLQQGAEVSVKELDFLLTLLAEKKR
		KMEQEEAETNMEILLDFLQRLRQQKQAELNEVQADLHYIKDDILALEKRRLELS
		RARERYSRKLHMLLDDPMDTTLGHAAIDDGNNVRTAFVRGGQGDAISGKFQQKK
		AEIKAQASSQGMQKRANFCHSDSQVLPTLSGLTIARKRRVLAQFDDLQECYLQK
		RRRWATQLRKQCDGGLRKERDGNSISREGYHAGLEEFQSILTTFTRYSRLRVIS
		ELRHGDLFHSANIVSSIEFDRDDELFATAGVSRRIKVFDFATVVNEPADVHCPV
		VEMSTRSKLSCLSWNKCIKSQIASSDYEGIVTVWDVNTRQSVMMYEEHEKRAWS
		VDFSRTEPTRLISGSDDGKVKVWCTRQETSVLNIDMKANICCVKYNPGSSYYVA
		VGSADHHIHYYDLRNPSVPLYEFNGHRKTVSYVKFISTNELASASTDSTLRLWD
		VRDNCLVRTFKGHTNEKNFVGLTVNSEYIACGSETNGVFVYHKAISKPAAWHQF
		GSPDLDDSDDDTSHFISAVCWKSESPTMLAANSQGTIKVLVLAP
487	WD40 repeat	MANYVDSKKNFKCVPALQQFYTGGPFRLSSDGSFLVCACNDEVKVVDLATGSVK	874	3705
	protein	NTLEGDSELIVALALTPDNKYLFSASRSTQIKRWDLSSATCKRTWKAHNGPVAD
		MACDASGGLLATAGADRSILVWDVDGGYCTHSFRGHQGVVTTVIFHPDPHCLLL
		FSGSDDATVRIWDLVAKKCISVLEKHFSTVTSLAISENGWNLLSAGRDKVVNIW
		DLRDYHCRATIPTYEPLEAVCVLPTGSRLVSVMNQSRALPENRKKSGAAPVYFL
		TVGERGIVRIWYSEGALCLYEQKSSDAIISSDKDELKGGFVSAVLLPLTQGVMC
		VTADQRFLFYNLDESDEGKCDLKVSKRLIGYNEEIVDLKFLGDEEKFLAVATNL
		EQVRMYDLSSMTCVYELSGHTDIVLCLDTVVFSGHSLLASGSKDHTVRIWDTES
		KSCICVAAGHMGAVGAVAFSKKAKNFFVSGSSDRTIKVWSFASVLDFGGISKSI
		KLSSQAAVAAHDKDINSVAVAPNDSLICTGSQDRTARIWRLPDLVPVLVLRGHK
		RGVWCVEFSPVDQCVMTASGDKTIKIWALSDGSCLKTFEGHTASVLRASFLTRG
		TQFVSSGADGLLKLWTIKSNECIATFDQHEDKIWAMAVGKKTEMLATGGSDSLV
		NLWHDCTTTDEEEALLKEEEAALKDQELLNALADTDYVKAIQLAFELRRPYKLL
		NVFTELYSKGHAQDQIQKVIRELGNEELRLLLEYVREWNTKPKFAHVAQFVLFQ
		LFNVLPPKEIIEVQGISELLEGLIPYAQRHYSRIDRLMRSTFLLDYTLSSMSVL
		SPTETDLSSSNLLARTADPLHAQIDQFHPTHFPEPNLTPIQSLLDSGNTDSVEV
		TARRAKKKRVSGNDSEKTTVAEVKIGDMENAFDEPDVADQGSSRKHKPASSKKR
		KSIAVGNASIKRIASGNAVTIALQV
488	WD40 repeat	MESSCSSMNSNRHSTEKRCLRPLQKQGASMNKHSSDRFIPARGSIDLDVARFMV	360	1754
	protein	TQKQKDNNDIHALSPSPSPSKKAYQKEMADTLLKNAGAADNNCRILSFNGKSST
		VSQGSQENVLANLSISRRARRYIPQSADRTLDAPDLLDDYYLNLLDWSSTNVLS
		TALGNTVYLWDASNSSISELLIADEEEGPVTSVSWAPDGSQIAVGLNNSVVQLW
		DSQSNKKLRALKGHHDRVGALSWNGPILTTGGLDGIIINHDVRTRDHIVQTYKG
		HTQEVCGLKWSPSGQQLASGGNDNLLYIWDKSMASHNPSSQYFHQLDEHCAAVK
		ALAWCPFQTNLLASGGGTSDGSIKFWNTQTGACLNTVDTHSQVCSLLWNRHERE
		LLSSHGLNQNQLTLWKYPSMVKITELTGHTARVLHMAQSPDGYTVASAAADETL
		KFWQVFGAPDASKKTKTKDTKGAFNMFHMHIR
489	WD40 repeat	MLDEIVADEEEEFNIWKKNTPLLYDVVITHALEWPSLTVQWLPDRHQSPTKDYS	185	1384
	protein	LQKMIVGTHTSGDEPNYLMIAEVQMPLQYSEDGNVGGFESTEAKVHIIQQINHE
		GEVNRAQYMPQNSFIIATKTVSSDVYVFDYTKHSSNAPQERVCNPELILKGHTN
		EGYSLSWSPLKEGQLLSGSNDAQICFWDINAASGRKVVEAKQIFKVHEGAVEDV
		SWHLKHEYLFGSVGDDCHLLIWDTRTAAPNKPQHSVVAHESEVNSLAFNPFNEW
		LLATGSADKTVKLFKLRKLSCSLFTFSNHTEEVFQIEWSPMNETILASSGGDRR
		LMVWDLRRIGDEQTSEDAEDGPPELIFIHGGHTSKISDFSWNLHDDWLIASSAE
		DNILQIWQMAENIYHDDADIL
490	WD40 repeat	MTKEDHGESRDEMGERMVNEEYKLWKKNTPFLYDLVITHALEWPSLTVQWLPPS	241	1533
	protein	CKQQQDIIKDDDIDHPNTQMVILGTHTSDNEPNYLILAEVQLHDGTEDEDGDGD
		VKRPQDKMKPGTSGGAMGKVRILQQINHQKEVNRARYMPQKPTIIATKTVNADV
		YVFDYSKHPSKPPQEGRCNPELRLQGHESEGYGLSWSPLKEGHLLSASDDAQIC
		LWDITAATKAPKVVEANQIFRYHDGPVEDVAWHAIHDHLFGSVGDDHHLLLWDI
		RNDSEKPLHIVEAHQAEVNCLAFNPFNEWIVATGSADRTVALHDIRKLDKVLHT
		CAHHMEEVFQIGWSPQNGAILASCGSDRRLMVWDLSRIGDEQNPEDAEEAPPEL
		LFIHGGHTSKISDFSWNPAEEWVIASVAEDNILQVWQMSEHIYNDDNDSPTA
491	WD40 repeat	MAMAMGDENAADPVEEFNIWKKNTPFLYDLVITHALEWPSLTVQWLPDRHQSST	230	1435
	protein	ADYSLQKMIVGTHTSEDEPNYLMIAEVQIPLQNSSEDNIIGGFESTEAKVQIIQK
		INHEGEVNKARYMPQNSFVIATKTVSSDVYVFDYSKHPSKAPQERVCNPELILK
		GHSNEGYGLSWSPLKEGYLLSGSNDAQICLWDINAAFGKKVLEANQIFKVHEGA
		VGDVSWHLKHEYLFGSVGDDCHLLIWDMRTAAPNKPQQSVIAHQSEVNSLAFNP
		FNEWLLATGSMDKTVKLFDLRKLSCSLHTFSNHSTDQVFQIEWSPMNETILASSG
		ADRRLMVWDLARIGETPEDEEDGPPELLFVHGGHTSKISDFSWNLNDDRVIASV
		AEDNILQIWQMAENIYHDDEDML
492	WD40 repeat	MGLFEPFRALGYITDGVPFAVQRRGIETFVTLSVGKAWQIYNCAKLIPVLVGPQ	101	2857
	protein	MDKKIRALACWRDFTFAATGHDIAVFRRAHQVATWSGHKAKVTLLLSFGQHVLS
		VDLEGCLFIWAVAEVNQNKPPIGQIQLGEKFSPSCIMHPDTYLNKVLIGSEEGT
		LQLWNVNTRKKLYEFKGWGSSIRCCVSSPALDVVGIGCSDGKIHVHNLRYDEEI
		VTFMHSTRGAVTALSFRTDGQPLLAAGGSSGVISIWNLEKKKLQSVIKDAHDSS
		VCSLHFFANEPVLMSSATDNSIKMWIFDTTDGEARLLKYRSGHSAPPMCIRYYG
		KGRHILSAGQDRAFRIFSVIQDQQSRELSQGHVGKRAKKLKVKDEEIKLPPVIA
		FDAAEIRERDWCNVVTCHLDDPCAYTWRLQNFVIGEHILKPCLEDPTPVKSCSI
		SACGNFAVLGTEGGWLERFNLQSGISRGTYIDIGEKRQCAHNGAVVGLACDATN
		TLLISGGYNGDIKVWDFKGRELKFRWEIEVPLIKIVYHPGNGILATAADDMILR
		LFDVTAMRLVRIFVGHMDRVTDLCFSGDGKWLLSSSMDGTIRVWDIISSRQLNA
		MHMDSAVTALSLSPGMDMLATTHVGHNGIYLWANRMIYSKATDIEPFISGKQVV
		KVSMPTVSSKRESEEGDEKRTIVAESNVNKSDVSGSLIGDSYSAQLTPELVTLA
		LLPKAQWQSLVNLDIIKMRNKPIEPPKKPEKAPFFLPSLPTLSGERIFIPSSMN
		GDGDQDETRNDKTVFEARGKKLGGESLSFMQLLQSCAKIKDFTTFTNYLKGLSP
		SAVDMELRLLQIVDNENISETEHSVELQGIGMLLDYFVNEVSCNNNFEFVQALI
		RLFLKIHGETIRCQVSLQEKARKLLEIQSSTWERLDTSFQNARCMITFLSSSQF
493	WD40 repeat	MIAAVCWVPKGVAKVLPDSAEPPTQEEIQELLKCNVVAESDDNEDSDEESEEMD	43	1548
	protein	TETDKNTDAVAKALAAANALGSQSSDFQRQHKVDDIANGLKELDMDHYDDEDEG
		IDIFGSGSLGNCYYPANDMDPYLVEQDDDDEDEIEDMTIKPSDLIILSARNEDD
		VSHLEVWIYEEETEEGGSNMYVHHDIILPAFPLSLAWLDCNLKGGEKGNFVAVG
		TMQPEIELWDLDVLDEVEPAVVLGGAVKDEASGKTTKLKKKKKNKQAVNFKEGS
		HTDAVLGLAWNMEYRNVLASASADKSVKIWDIVAEKCEHTMQPHTDKVQAVAWN
		PNQATVLLSGSFDRSVIMMDMRAPTHSGIRWPVPADVESLAWDPHTDHSFMVSA
		EDGTVRGFDIRAAASTADFDGKPMFILHAHDKAVCAISYNPAAPSLLTTGSTDK
		MVKLWDITNNQPSCIASTNPNVGAVFSAAFSKNSPFLLATGGSKGILHVWDTLD
		NSEVARRFGKFRPQN
494	WEE1-like	MIMDENEFCDIFSLRKRLCLLSSQEGEEEEELEAMSQLDAGEFTVTGNEEVVAI	206	1657
	protein	AEDDVNTGILSQDLFSSQDYCTPSQPQDSTDLDSKDKAPCPLSPVKSTIQRKRC
		RPELLSNPPDSIQFSFQRLERVRSEESIQSSSQQLARVRSEVSSSDDFKTPKIT
		ASGQKNYVSQSALALRARVMSPPCIKNPYLDENEELNEKIQRSTRRSPACVTPI
		QSGACLSRYRADFHELEEIGRGNFSRVYKALNRLDGCCYAVKCSQSELRLDTER
		KVALMEVQSLAALGPHKNIVGYHTAWFENDHLYIQMELCDHNLTTANDRGILRT
		DTDFLEAVYQIAQALEFIHGRGVAHLDVKPENIYVRDGTYKLGDFGRATLINGT
		LHVEEGDARYMSREILNDNYEHLDKVDMFSLGATFFELLMRKQYPGSGKRIDRD
		TEIKIPILPGFSIYFQKLLQDLVSNDPGKRPSAKDVLKNPIFNKVRGAKEV
495	WD40 repeat	MLAPALEMEPVEPQSLKKLSFKSLKRALDLFSPVHGQIAPPDPESKKMRISYSL	117	1580
	protein	NFEYGGGSGSEDQVPKRKESGAAQNQGQQAAGASNALALPGPEGSKIPPMEKSQ
		NALTVGPSLRPQGLNDVGLHGKGTAIISASGSSDRNLSTASAIMERLPSRWPRPV
		WHPPWKNYRVISGHLGWVRSIAFDPSNQWFCTGSADRTIKIWDLASGRLKLTLT
		GHIEQIRGLAVSSKHTYMFSAGDDKQVKCWDLEQNKVIRSYHGHLSGRLKLTLT
		PTIDILLTGGRDSVCRVWDIRSKMQIFALSGHDNTVCSVFARPTDPQVVTGSHD
		TTIKFWDLRHGKTMTTLTNHKKSVRAMAQHPKENCFASASADNIKKFQLPRGEF
		LHNMLSQQKTIINTMAVNEEGVMATGGDNGSLWFWDWKSGHNGQQAHTIVQPGS
		LESEAGIYALSYDLTGSRLVSCEADKTIKMWKEDELATPETHPLNFKPPKDIRRF
496	WD40 repeat	MEEAAKEQSAGSGKPKLLRYGLRSAAKPKEDKKEEQLHQPPPPPPPQQQAAPAP	111	1700
	protein	APAATRSSTSGSAGGRDRRPQQQHAVDEKYARWKSLVPVLYDWLANHNLLWPSL
		SCRWGPQLEQATYKNRQRLYISEQTDGSVPNTLVIANCEVVKPRVAAAEHVSQF
		NEEARSPFIRKYKTIIHPGEVNRIRELPQNPNIVATHTDSPDVLIWDVESQPNR
		HAVYGATASRPNLILTGHQENAEFALAMCPAEPFVLSGGKDKTVVLWSIQDHIT
		ASATDQTTNKSPGSGGSIIKKTGEGNEETGNGPSVGPRGIYCGHEDTVEDVAFC
		PSTAQEFCSVGDDSCLILWDARIGTNPVAKVEKAHNGDLHCVDWNPHDNNLILT
		GSADNSVNMFDRRNLTSNGVGSPVYKFEGHKAAVLCVQWSPDKPSVFGSSAEDG
		LLNIWDYERVDKKVDRAPNAPAGLFFQHAGHRDKIVDFHWNTADPWTMVSVSDD
		CDTAGGGGTLQIWRMSDLIYRPEEEVLAELENGKAHVLECSKA
497	WD40 repeat	MAKDEEEFRGEMEERLVNEEYKIWKKNTPFLYDLVITHALEWPSLTVQWLPDRE	144	1412
	protein	EPPGKDYSVQKMILGTHTSDNEPNYLMLAQVQKOKEDAENDARQYDDERGEIGG
		EGCANGKVQVTQQTNHDGEVNEARYYIPQNPETTATKTVSAEVYVEDYSKHPSKP
		PQDGGCHPDLRLRGHNTEGYGLSWSPFKHGHLLSGSDDAQICLWDINVPAKNKV
		LEAQQIFKVHEGVVEDVAWHLRHEYLFGSVGDDRHLLIWDLRTSATNKPLHSVV
		AHQGEVNCLAFNPFNEWVLATGSADRTVKLFDLRKISSALHTFSCHKEEVFQIG
		WSPKNETILASCSADRRLMVWDLSRIDEFQTPEDALDGPPELLFIHGGHTSKIS
		DFSWNPCEDWVIASVAEDNILQIWQMAENIYHDEEDDMPPEEVV
498	Cyclin-	MGKYMRKGKGVGEVAVMEVSQGSLGVRTRARTLAAASSQKDHRRLGASKSVTTK	793	1683
	dependant	HQSSAPPASPCVESSMHTCYLELRSRKLEKFSRCYHSAHGATSHGESKRSLSLS
	kinase	EPSRLAVSEEARVASDKSSHRVLQQQSSVAHSRNNASATFSHNAKPAKAAQRKER
	inhibitor	RDDDHTSARPSEAPHEDEDGMEVEASFGENVMDLDSRERRTRETTPSSYTRDVE
		TMETPGSTTRPPSNAGRRRFQTEGGHGTRNQFHVPTTNEIEEFFAGAEQQEQRR
		FTDRYNYDPVSDSPLPGRFEWVRLRP
499	CDK type D	MQNMEENVQSSWSLHGNKEICARYEILKRVSSGTYLDVYRGRRKEDGLIVALKE	415	2196
		VHDYQSSWREIEALQRLCGCPNVVRLYEVILEFLTSDLYSVIKSAKKNKGENGIP
		EAEVKAWMIQILQGLANCHANWVIHRDLKPSNMLISAYGILKLADFGSMSFLKR
		AIYEVEYELPQEDILADAPGERLMDEDDSVKGVWNEGEEDSSTAVETNFDDMAE
		TANLDLSWKNEGDMVMQGFTSGVGTRWYRAPDFLYGATIYGKEIDLWSLGCILG
		ELLILEPLFSGTSNIDOLSRLVKVLGLQQKKNWPGCSNLPDYRKLCFPGDGSPV
		GLKNHVPNCSDNMFSILERLVCYDPAARLNAKEIVENKYFVEDPYPVLTHELRV
		PSPLREENNFSEDWAKWKDMEVDSDLENIDEFNVVHSSDGFCIKFS
500	Histone	MAPVKRIEPEKTKANEGKPKRRKVAFAIDTGIEANDCISLHLVSTPEEMRDAEG	109	1653
	acetyltransferase	VEDQSLSFNPEYMQHFVGEHGKIYGYKGLKIDVWLNALSFHAYVDIQYESKVEE
		GKSEKEATDLTDIMKRIFGRGLVEDRNAFIQSFSSNSQSIESMIHNEGERIATR
		EILTDKGLSAQGDSERLGVSNEIFRLELSDPQIREWHARLEPLVLLFVEGSQPI
		EQDDPKWEMYIRVQRESLSGGSAVCRLLGFCTVYRFYHYPDTTRLRISQILVFP
		PYQGKGHGLLLLEAVNKTAVSRDSYDVTVEEPSESLQELRDCMDTIRISQILVFP
		MPAVKSAVQKLKEANPSDKGAADHCLEGNVNNETVTTSSTKPKNKSGWFPPPGL
		VEEVRKHLKISKKQFKRCWEILLYLNLDRSDSQCEDKYHISLMEQIMSELFDKS
		SEKSAKGKRVIDIDNEYDNSKTFIMVRTRNPGNGEGFLPEALEGGMEVSQEDQL
		KSLFEERLEEIAQIAEKVPSLCKALQMP
501	Histone	MPEDRKKILEALAAKRKAEAESGEKKPRQKSSLNPAKPVSKPVSKPVGGIGSKG	343	1023
	deacetylase	KSTSAPISSTKAKSKHKEEVKAKRVTKMDRYETDEDDESEEEEDLDSESDDDEL
		SDEDSEDDIKSKSVKKLPPQSKGKAPVKGISSSNGKGRDEKGKGIMKDKGKAKA
		KVEESSSDAEGDSDDDGGDLSDDPLQEVDPSNILPSKTRREASQPTNYQFANMS
		GDDDDDDDSD
502	Histone	MADVPESLQQEKDEQGTDKNCCDGKFQKEIDIDDMEEEYNESSIDDEEENLSDN	417	2351
	deacetylase	VATNNMGTIPQGQACMAVTVEGIEHANSVGCGRNGREGSEEVTAAEDMGHVSIE
		NIREQGRNRKSSEQLLALYEQEGLLEDDEDDDDVDWEPFEGVTVQMKWYCTNCT
		MANSDDSVHCDSCGEHRNSDILRQGFLASPYLPAESPSSSDVPDERLEESKCVM
		TTLTPSISPMIGVCCSSLQSERRTVVGFDERMLLHSEIQMETYPHPERPDRLRA
		IAASLRAAGLFPGKCFSIPAREATCEELQTIHSLEHVNAVESTSCGMLSHLSPD
		TYANEHSSLAARLAAGLCADLAKAIMTGQAQNGFALVRPPGHHAGVKDSMGFCL
		HNNAAIAVSASRVVGAKKVLIVDWDVHHGNGTQEIFEADQSVLYISLHRHGEGF
		YPGSGAVTEVGSSKGEGYSVNIPWKCGGVGDNDYIFAFQHAVLPIAEQFEPDLT
		IISAGFDAAKGDPLGRCEVTPDGFAHMAQMLSCLSKGKMLVILEGGYNLRSISA
		SATAVIKVLLGDNPKALPIDIQPSKGGLQTLLEVFEIQSKYWSSLKGHDQKLRS
		QWEAQYGSKKRKVIRKRHMHIVGGPVWWKWGRKRVVYYHWFARVSSRKHL
503	Peptidylprolyl	MASGAGAAGVVEWHQKPPNPKNPVVFFDVTIGTIPAGRIKMELFADIVPRTAEN	69	641
	isomerase	FRQFCTGEYRKAGIPIGYKGCHFHRVIKDFMIQAGDFVKGDGSGCISIYGSKFE
		DENFIAKHTGPGLLSMANSGPNTNGCQFFLTCAKCDWLDNKHVVFGRVLGEGLL
		VLRKIENVQTGQHNRPKLPCVIAECGEM
504	Peptidylprolyl	MAKLVSSVCAFSCQQRHPHSRPRFLSNRDHYNHYHNHSHYHNVCYFPPMMMMQQ	172	1623
	isomerase	QLQKQKRMTTKTITSLFKCNSSNHTLLKGLKEFMGFKFRLQAAMLSCEMSILGR
		VFAIFFIVHQAAAPFPFNHFDNWLVPPASAVLYSPNTKVPRTGEVALRKSIPAN
		PAMKSIQDFLEDIYYLLRFPQRKPYGTMEGDVKSALQIAINEKDSILGSVPLDM
		KERGLQLYNFLIDGQGGLQVLIEYIKEKDPDKVSVNLSSSLDTIAQLELLQAPG
		LPYLLPEEYQQYPRLNGRATIEFTMEKGDNSMFSVSSGGGLQKTATIQVVLDGY
		SAPLTAGNFTKLVIDGAYNGLKLKTTEQAVISDNERAEAGFNLPIEILPAGGFE
		PLYRTTLSVQDGELPVLPLSVYGAIAMAHNTISEDYSSPSQFFFYLYDKRNAGL
		GGLSFDEGQFSVFGYTTVGKEILPQLKTGDIIKSAKLVDGFDHLVLPSSST
505	WD40 repeat	MDHYYQDDFDYLVDDEMVDFADDVEDDVRTRRRSDIDSDSENDFDSNNKSPDTT	231	1768
	protein	ALQAKRGKDIQGIPWNRLNFTREKYRETRLQQYKNYENLPRPRRSRNLDKECTN
		FERGSSFYDFRHNTRSVKATIVHFQLRNLVWATSKHNVYLMQNYSIMHWSSLKQ
		KGEEVLNVAGPIIPSVKHPGSSPQGLTRVQVSAMSVKDNLVVAGGFQGELICKY
		LDKPGVSFCTKISHDENGITNAVEIYNDASGATRLMTANNDLAVRVFDTEKFTV
		LERFSFPWSVNHTSVSPDGKLVAVLGDNADCLLADCKTGKTVGTLRGHLDYSFA
		AAWHPDGYILATGNQDTTCRLWDVRKLSSSLAVLKGRMGAIRSIRFSSDGRFMA
		MAEPADFVHLYDTRQNYTKSQEIDLFGEIAGISFSPDTEAFFVGVADRTYGSLL
		EFNRRRMNYYLDSIL
506	WD40 repeat	MDCSGDEEEEQFFESLEEMLSPSDSGSEAADNETGCRNADARSKYEIWKRAPSS	376	2943
	protein	IQERRQRFLVRMGLANPSELGNQVNSTSAESTCSTETANIPNGIERLRENSGAV
		LRTAGSSGRKTHCKNVINIGLREGSVRSSSSSNGTPDVGEDNGEFGGTIFSRSG
		GTWECMCKIKNLDSGKEFVVDELGQDGLWNKLREVGTDRQLTMDEFERSLGLSP
		LVQELMRRESGVAQADCNGVHHHDAEISSSKRRSWLKALKSAAYSMRRPKEDQS
		NYDSERSGRRSGSFDVPWGKPQWTKVRHYRKRYKEFTALYMGQEIEAHEGSIWT
		MKFSLDGRYLASAGQDCVIHVREVIESMRTFGADTPDLYASSAYFSMNGLQELV
		PLSIEDHANKMKRGKIIGSKKSSNSDCIVLPNKVFQLSEEPVCSFHGHLLDVFD
		LSWSPSQYLLSSSMDKTVRLWKLGHESCLKVFSHNDIVTCIQFNPVDERYFISG
		SLDGKARIWSIPDRQVVDWSDLREMVTAVCYTPDGQGGLVGSIKGSCRFYNTSG
		NKLQLENQLNVRSKKKKSSGKKITGFQFAPGGDSQKVLITSADSRVRVYNGSEL
		VCKYKGFRNTCSQISASFAPNGQHFVCASEDSRVYIWNHESPRGSGARHEKSSW
		SHEHFLSQGVSVAIPWSGMKLQPPVWNSPEFMLGQRHNLLSLQGGKDVGCQNGL
		LSREAGEGQESETPLHYISQVSHSCGSQNMVDRDGQDDLSRYSACISDSRLSSF
		MAFPESPGNPDDLNSKVFFSDSSSKGSATWPEEKLPPTRKQSRSNSTSSHYDTL
		KTHLGNTIQGQSGASAAVAWGLVIVTAGHGGEIRSFQNYGLPVRL
507	WD40 repeat	MPSIPAIGEFTVCEINRELLTTKDESDTQAKDAYAKILGLVFPPISFQIEEGFG	107	1498
	protein	SASRQQFDQDLDREDTIVTPSTSEGTNALQEGGLLLKGVSVLKNILASSFGPIF
		SPNDTKVLKKVELLQGISWHRHKHILAFISGSNQVTVHDFQDPEWRESSLLVSE
		SQRGIEALEWRPNGGTTLSVACRGGICIWSASYPGSVAPVRSGVASFLGTSTRG
		SSVRWTLVDFLQIPGGKAVTALSWSPTGRLLASASREDSSFTIWDVAQGVGTPL
		RRGLGGISLLKWSPTGDYLFSAKPNGTFYLWETNTWTLEQWSSSGGCVISATWG
		PDGRMLFMAFSESTTLGSLHFAGRPPSLDAHLLPMELPEIGSITGGFGNIEKMA
		WDGCGERLAVSYTGGDLMYVGLIAIYDTRRTPFISASLVGFIRGPGEQVKPLAF
		AFHDKFKQGPLLSVCWSSGLCCTYPLIFRAH
508	WD40 repeat	MEEENAKHTEETRQVQVRFTTKLQPALRVPTTSIAIPAHLTRYGLSDIVNTLLG	118	1425
	protein	NDKPQPFDFLVESELVRTSLEKLLLIKGISAEKILNIEYILAVVPPKQEEPSLH
		DDWVSVVDGSYPNFIFSGSFDSIGRIWKGEGLCTHVLEGHRDAITSAAFIMPSD
		SSDSFINLATASKDRTLRLWQFKPNEHMTNGKMVRPYKLLKGHTSSVQTVSACP
		RRNLICSGSWDCSIKIWQTAGEMDIESNAGSVKKRKLEDSTEQIISQIEASRTL
		EGHSQCVSSVVWLEKDTIYSASWDHSVRSWDVETGVNSLTVGCRKALHCLSIGG
		EGSALIAAGGADSVLRIWDPRMPGTFTPILQLSSHKSWITACKWHPKSRHHLIS
		ASHDGTLKLWDVRSKVPLTTLEAHKDKVLCADWWKEDCVISGGADSTLQIFSNL
		NLT
509	WD40 repeat	MNRLRSKRNHILELRLGQSEPEKEATLASNRSRGTNAPIVVEDDDDVVVSSPRS	186	797
	protein	FALARSSVSQRSSRIPIVNEEDLELRLGLAVTGRTSAEHNPRRRHGRVPPNKPI
		VLCDDAGEADQSSSKKRRTGQQLSSDVQSDESKEVKLTCAICISTMEEETSTIC
		GHIFCKKCITNAIHRWKRCPTCRKKLAINNIHRIYISSSTG
510	WD40 repeat	MEEPPPPAVLPSSEDTSIVSSHSFVNAPPTVPVGLDASIPQISTPGINQPGLTI	387	2456
	protein	PVPPEAAPLTASLVAASAGMPPAVVPSFVRPAIVAHPSVMPPPSMPLAALPMPV
		ASAVPVAAPHFPPSTPNDNSITPSMPVPTPIVASSSVPPSVTIPGIAPLPFIAP
		IPVPSSRPVAPSPFMPPARPLGASVSVAMDVDNTDEQDQDADNKGESPSSSPDH
		PEDPSAAEYEITEESRKVRERQEQAIQELLLRRRAYALAVPTNDSSVRARLRRL
		NEPITLFGEREMERRDRLRALMAKLDAEGQLEKLMKVQEEEEAAANVDAEEVQE
		MEGPQVYPFYTEGSQELLKARTEITKFSLPRAVSRLQRARRKREDPDEDEDEEL
		KCVLQQSAQINMDCSEIGDDRPLSGCAFSSDGTLLATSAWSGVTKLWSVPNINK
		VATLKGHTERVTDVAFSPTNCHLATACADRTAMLWNSEGVLMKTYEGHLDRLAR
		LAFHPSGLYLGTASFDKTWRLWDVNTGIELLLQEGHSRSVYGIAFQCDGSLAAT
		CGLDGLARIWDLRTGRSILALEGHVKPVLGIDFSPNGYHLATGSEDHTCRIWDL
		RKRQSVYIIPAHSHLVSQVKFEPQEGYFLVTASYDSTAKVWSARDFKSIKVLAG
		HEAKVTSVDITADGQYIATVSHDRTIKLWSSKNSTNDMNIG
511	WD40 repeat	MKRAYKLQEFVAHASNVNCLKIGKKSSRVLVTGGEDHKVNMWAIGKPNAILSLS	359	2761
	protein	GHSSAVESVTFDSAEALVVAGAASGTIKLWDLEEAKIVRTLTGHRSNCISVDFH
		PFGEFFASGSLDTNLKIWDIRRKGCIHTYKGHTRGVNSIRFSPDGRWVVSGGED
		NIVKLWDLTAGKLMHDFKCHEGQIQCMDFHPQEFLLATGSADRTVKFWDLETFE
		LIGSAGPETTGVRAMIFNPDGRTLLTGLHESLKVFSWEPLRCYDAVDVGWSKLA
		DLNIHEGKLLGCSYNQSCVGVWVVDISRVGPYAAGNVSRTNGHNEAKLASSGHP
		SVQQLDNNLKTNMARLSLSHSTESGIKEPKTTTSLTTTEGLSSTPQRAGIAFSS
		KNLPASSGPPSYVSTPKKNSTSRVQPTTNFQTLSRPDIVPVIVPRSNSLRPETT
		SDAKKEMNNFGRVVPSTVSTKSTDVIKSGSNRDESDKIDSINQKRMTGNDKTDL
		NIARAEQHVSSRLDNTNTSSVVCDGNQPAARWIGAAKFRRNSPVDPVVSPHDRS
		PTFPWSATDDGVTCQPDRQVTAPELSKRVVEPGRARALVASWETREKALTADTP
		VLVSGRPPTSPGVDMNSFIPRGSHGTSESDLTVSDDNSAIEELMQQHNAFTSIL
		QARLTKLQVIRRFWQRNDLKGAIDATGKMGDHSVSADVISVLIERSEIFTLDIC
		TVILPLLTRLLQSETDRHLTVAMETLLVLVKTFGDVIRATISATPTIGVDLQAE
		QRLERCNLCYVELENIKQILVPLIRRGGAVAKSAQELSLALQEV
512	Cyclin B	MAGSDENNPGVVGGAHVQEGLRVGAGKMGAGNVQQRRALSNINSNIIGAPPYPC	238	1648
		AVNKRVLSEKNVNSENDLLNAAHRPITRQFAAQMAYKQQLRPEENKRTTQSVSN
		PSKSEDCAILDVDDDKMADDFPVPMFVQHTEAMLEEIDRMEEVEMEDVAEEPVT
		DIDSGDKENQLAVVEYIDDLYMFYQKAEASSCVPPNYMDRQQDINERMRGILID
		WLIEVHYKFELMDETLYLTVNLIDRFLAVQPVVKKKLQLVGVTAMLLACKYEEV
		SVPVVEDLILISDRAYSRKEVLEMERLMVNTLHFNMSVPTPYVFMRRFLKAAQS
		DKKLELLSFFIIELSLVEYDMLKFPPSLLAASAIYTALSTITRTKQWSTTCEWH
		TSYSEEQLLECARLMVTFHQRAGSGKLTGVHRKYSTSKFGHAARTEPANFLLDF
		RL
513	Cyclin-	MQAPREGKSAAAIVGMGKYMKKSKAIPRDVSLLEASPRSPSATGVRTRAKTLAS	59	859
	dependant	RRLRRASQRRPPPPAAAAAAAAPSLDASPCPFSYLQLRSRRLRRPRLAPSPEAR
	kinase	IDEGPAGSGSRGSRDASCSARTASSSGGVEGEGACVGRGDRGNGGECVRDAAVD
	inhibitor	ASYGENDLEIEDRDRSTRESTPCSLIRDSNANTPPGSTTRQQSSCTAHRTQMSI
		LRSIPTSDEMEEFFAYAEQRQQRSFIEKYNFDIVKDRPLPGRFEWVQVIP
514	Histone	MDGHSSHLAAQNRSRGSQTPSPSHSAASASATSSIHLKRKLSAANASAASAAAA	44	1829
	acetyltransferase	AAAAAAAADDHAPPFPPSSISADTRDGALTSNDDLESISARGGGAGDDSDDDSD
		DEEEDDGDNDGGSSLRTFTAARLENVGPAAARNRKIKAESNATVKVEKEDSAKD
		GGNGAGVGALGPAATSGAGSGSGTVPKEDAVKIFTENLQASGAYSAREENLKRE
		EEAGRLKFECLSNDGVDDHMVWLIGLKNIFARQLPNMPKEYIVRLVMDRNHKSV
		MVIRRNLVVGGITYRPYASQKFGEIAFCAIKADEQVKGYGTRLMNHLKQHARDV
		DGLTHFLTYADNNAVGYFIKQGFTKEIYLDKDRWHGYIKDYDGGILMECKIDPK
		LPYTDLSTMVRRQRQAIDEKIRELSNCHIVYQGIDFQKRDAGVPQNTIKMEDIP
		GLREAGWTPDQWGYSRFRGLSDQKRLTFFIRQLLKVLNDHSDAWPFKEPVDARE
		VPDYYDIIKDPMDLKTMTKRVESEQYYVTLEMFIADVKRMFANARTYNSPDTIY
		FKIATRLEAHFQSKVQSNLQSGAGKIQQ
515	Peptidylprolyl	MFNGMMDPELFKLAQEQMNRMSPAELAKIQQQMMSNPELMRMASESMKNMRPED	109	1866
	isomerase	LRQAAEQLKHVRPEEMAEIGEKMANASPEEIAAVRARADAQMTYEINAAKILKK
		EGNELHSQGRFKDASQKYLRAKNNLKGIPSSEGKNLLLACSLNLMSCYLKTRQY
		EECIKEGSEALACEEKNLKAFYRRGQAYRELGQLKDAVSDLRKAHEISPDDETI
		AQVLRDTEESLTKEGGSAPRGVVIEEITEEDETLASVNHESPSEYSEKRHQESE
		DAHKGPINGDIMGQMTNSESLKALKGDPDAIRSFQNFISNADPTTLAAMGAGNA
		GEVSPDLIKTASSMIGKMSAEELQKMIQLASSFPGENPYVTRNSDSNSNSFGNG
		SIPNVSPDMLKTASDMMSKMSPDDLQRMFEMASSSRGKDPSLDANHASSSSGAN
		LAANLNHILGESEPSSSYHIPSSSRNISSSPLSNFPSSPGDMQEQIRNQMKDPA
		MRQMFTSMMKNMSPEMMANMGKQFGLELSPEDAAKAQEAMSSLSPEMLDKMMRW
		ADRAQRGVETAKKTKNWLLGRPGMILAICMLLLAVILHRLGFIGS
516	WD40 repeat	MIAAISWVPRGASKAVPEVAEPPSKEEIEEILKSGVVERSGDSDGEEDDENMDA	212	1815
	protein	VASEKADEVSTALSAADALGRISKVTKAGSGFEDIADGLRELDMDNYDEEDEDV
		KLFSTGLGDLYYPSNDMDPYLKDKDDDDDTEEIEDLSIKPMDSLIVCARTDDEV
		NLLEVYLLEPSLSDESNMYVHHEVVISEFPLCTAWLDCPIKGGDKGNFIAVGSM
		EPAIEIWDLDIIDAVEPCLVLGGQEELKKKKKKGKKASIKYKEGSHTDSVLGLA
		WNKEFRNILASASADRQVKIWDVAAGKCNITMEHHTDKVQAVAWNHHAPQVLLS
		GSFDHSVVMKDGRIPSHSGYRWSVTADVESLAWDPHSEHFFVVSLEDGTVRGFD
		VRAAISNSASQSLPSFTLHAHEKAVSTISYNPAAPNLLATGSTDKMVKLWDLSN
		NQPSCIASRNPKAGAVFSVSFSEDSPLLLAIGGSKGRLEVWDTSSDAAVSRRFG
		KHGKPKTAEPGS
517	WD40 repeat	MKFCKKYQEYMQGQEGKKLPGLGFKKLKKILKRCRRRDSLHSQKALQAVQNPRT	207	1193
	protein	CPAHCSVCDGSFFPSLLEEMSAVLGCFNKQAQKLLELHLASGFQKYLMWFKGKL
		RGNHVALIQEGKDLVTYALINAIAIRKILKKYDKIHLSTQGQAFKSQVQRMHME
		ILQSPWLCELIAFHINVRETKANSGKGHALFEGCSLVVDDGKPSLSCELFDSIK
		LDIDLTCSICLDTVFDSVSLTCGHIYCYMCACSAASVTIVDGLKAAEPKEKCPL
		CREARVFEGAVHLDELNILLSRSCPEYWAERLQTERVERVRQAKEHWESQCRAF
		MGVE
518	WD40 repeat	MVSTQSTRENPSIFFPPPLKPWLLPVVLSLSLSRQLGMAAAAAASLPFKKNYRS	6	2786
	protein	SQALQQFYAGGPFAVSSDGSFIACNCGDSIKIVDSSNASLRPSIDCGSDTITAL
		SLSPDGKLLFSAGHSRQIRVWDLSTSTCLRSWKGHDGPVMSMACPVSGGLLATG
		GADRKVMVWDVDGGFCTHFFKGHDGVVSTVLFHPDSNRSLLFSGSDDGTIRVWD
		LLAKKCASTLRGHDSTVTSLAFSEDGLTLLAAGRDKVVSLWDLHNYACKKTIPM
		YEVLESVCVIHSGTVLASQLGLDDQLKVTKESAQNIHFITVGERGILRIWKSEG
		SVCLFKQEHSDVTVISDEDDSRSGFTAAVMLPLDQGLLCVTADQQFLFYYPEKH
		PEGIFSLTLCRRLVGYNEEIVDMKFLGEEENFLAVATNLEQVRVYELASMSCSY
		VLAGHTETVLCLDTCISSSGRTLIVTGSKDNSVRLWDSESRHCIGVGVGHMGAV
		GAVAFSRKRQDFFVSGSSDRTLKVWSLDGISEDGVDSTNLKAKAVVAAHDKDIN
		SVAVAPNDSLVCSGSQDRTACVWRLPDLVSVVVLKGHKRGIWSVEFSPVDQCVL
		TASGDKTVKIWAISDGSCLKTFEGHVSSVLRASFLTRGTQFVSCGADGLVKLWT
		VRTNECIATYDQHSDKVWALAVGKKTEMLATGGSDAVVNLWYDSTASDKEDAFR
		KEEEGVLKGQELENAVSDADYTKAIELALELRRPHKLFELFSELCRTREVGDRV
		ERILSALSGEEVCLLLEYIREWNAKPKLCHVAQSVLSQVFRILSPTEIVEIKGI
		GELLEGLIPYSQRHFSRIDRLVRSTYLLDYTLTGMSVIEPEADRSAVNDGSPDK
		SGLEKLEDGLLGENVGEEKIQNKEELESSAYKKRKLPRSKDRSKKKSKNVVYAD
		AAAISFRA
519	WD40 repeat	MDSAPRRKSGGINLPSGMSETSLRLDGFSGSSSSFRAISNLTSPSKSSSISDRF	213	1726
	protein	IPCRSSSRLHTFGLVERGSPVKEGGNEAYSRLLKAELFGSDFGSLSPAGQGSPM
		SPSKNMLRFKTESSGPNSPFSPSILRQDSGFSSEASTPPKPPRKVPKTPHKVLD
		APSLQDDFYLNLVDWSSQNTLAVGLGTCVYLWSASNSKVTKLCDLGPNDGVCAV
		QWTREGSYISIGTSLGQVQIWDGTQCKRVRTMGGHQTRTGVLAWNSRILASGSR
		DRVILQHDLRVPNEFIGKLVGHKSEVCGLKWSHDDRELASGGNDNQLLVWNQHS
		QQPVLKLTEHTAAVKAIAWSPHQNGLLASGGGTADRCIRFWNTTNGHQTSSVDT
		GSQVCNLAWSKNVNELVSTHGYSQNQIMVWKYPSMAKVATLTGHSLRVLYLAMS
		PDGQTIVTGAGDETLRFWNVFPSAKAPAPVKDTGLWSLGRTHIR
520	WD40 repeat	MEDEAEIYDGVRAQFPLTFGKQSKPQTSLESVHSATRRGGPAPAPAPASSSSLP	101	2110
	protein	STTSPSAAGGAGKSSGLPSLSSSSTAWLEGLRAGNPRAGREAGIGSRGGDGEDG
		GRAMIGPPRPPPGFSANDDGGGEDDDDDGDGVMVGPPPPPPGNLGDGDDDEEEE
		EAMIGPPRPPVVDSDEEEEEEEEENRYRLPLSNEIVLKGHNKIVSALAVDPTGS
		RVLSGSYDYTVRMFDFQSMNSRLSSFRDFEPVEGHQVRNLSWSPTADRFLCVTG
		SAQAKIYDRDGLTLGEFVKGDMYIRDLKNTKGHITGLTWGEWHPKTKETILTSS
		EDGSLRIWDVNDFKSQKQVIKPKLARPGRVPVTTCTWDREGKCIAGGIGDGSIQ
		IWNLKPGWGSRPDIHVEQAHADDITGLKFSSDGKILLTRSFDDSLKVWDLRLMK
		NPLKVFEDLPNHYAQTNIACSPDEQLFLTGTSVERESTIGGLLCFFDRSKLELV
		SRIGISPTCSVVQCAWHPRLNQIFATSGDKSQGGTHVLYDPTLSERGALVCVAR
		APRKKSVDDFELKPVIHNPHALPLFRDQPSRKRQREKILKDPLKSHKPELPMNG
		PGHGGRVGASKGSLLTQYLLKQGGMIKETWMDEDPREAILKHADAAEKNPKFTR
		AYAETQPDPVFAKSDSEDEDK

TABLE 16
BLAST Sequence Alignment Table.

			BlastX top		BlastX e	BlastX	BlastX
SEQ ID	Target	Patent Identifier	hit	Gene name	value	identities	overlap

1	CDK type A	eucalyptusSpp_003910	Q9FRN5	PUTATIVE	0	367	492
				SERINE/THREONINE
				KINASE
2	CDK type A	eucalyptusSpp_019213	O44000	CDC2-LIKE	e−160	217	290
				PROTEIN
				KINASE TPK2
3	CDK type A	eucalyptusSpp_036800	Q40789	PROTEIN	0	259	294
				KINASE
				P34CDC2
4	CDK type A	eucalyptusSpp_040260	Q27168	CDC2	e−156	208	304
5	CDK type A	eucalyptusSpp_041965	Q43361	CDC2PA mRNA.	e−159	274	294
				SPTREMBL
6	CDK type B-1	eucalyptusSpp_002906	Q9FYT9	Cyclin-	e−159	269	305
				dependent
				kinase B1-1
7	CDK type B-2	eucalyptusSpp_001518	Q9FSH4	B2-TYPE	0	270	315
				CYCLIN
				DEPENDENT
				KINASE
8	CDK type C	eucalyptusSpp_008078	Q9LDC1	CRK1 protein	0	415	558
9	CDK type C	eucalyptusSpp_009826	Q9LNN0	F8L10.9	0	392	716
				protein.
				SPTREMBL
10	CDK type C	eucalyptusSpp_010364	Q8GZA7	Putative	e−172	309	499
				cyclin-
				dependent
				protein
				kinase.
11	CDK type C	eucalyptusSpp_011523	Q8W2N0	Cyclin-	e−165	273	405
				dependent
				kinase CDC2C
12	CDK type C	eucalyptusSpp_024358	P93320	CDC2MSC	0	448	523
				PROTEIN
13	CDK type C	eucalyptusSpp_039125	O80540	F14J9.26	0	418	743
				protein
14	CDK type D	eucalyptusSpp_005362	O80345	CDK-	e−180	305	483
				activating
				kinase 1AT
				(Cdk-
				activating
				kinase
				CAK1At)
15	CDK type D	eucalyptusSpp_044857	O80345	CDK-	e−177	302	477
				activating
				kinase 1AT
				(Cdk-
				activating
				kinase
				CAK1At)
16	Cyclin A	eucalyptusSpp_001743	Q39879	MITOTIC	0	360	508
				CYCLIN A2-
				TYPE
17	Cyclin A	eucalyptusSpp_012405	Q39878	MITOTIC	e−179	278	470
				CYCLIN A2-
				TYPE
18	Cyclin B	eucalyptusSpp_003739	Q9LDM4	F2D10.10	e−148	288	466
				(F5M15.6)
19	Cyclin B	eucalyptusSpp_022338	P93557	Mitotic	e−168	310	476
				cyclin
20	Cyclin B	eucalyptusSpp_028605	Q40337	B-like	e−158	300	439
				cyclin.
				SPTREMBL
21	Cyclin B	eucalyptusSpp_041006	Q40337	B-like	e−158	300	439
				cyclin
22	Cyclin D	eucalyptusSpp_006643	Q9SXN7	NtcycD3-1	1E−73	177	404
				protein
23	Cyclin D	eucalyptusSpp_045338	Q8LK74	Cyclin D3.1	e−101	190	332
				protein.
				SPTREMBL
24	Cyclin D	eucalyptusSpp_046486	Q9ZRX7	CYCLIN D3.2	e−126	196	373
				PROTEIN
25	Cyclin-	eucalyptusSpp_012070	CAB69358	SEQUENCE 1	8E−64	83	88
	dependent			FROM PATENT
	kinase			WO9841642
	regulatory
	subunit
26	Histone	eucalyptusSpp_006617	O80378	181	0	371	395
	acetyltransferase			(Fragment)
27	Histone	eucalyptusSpp_007827	Q9FJT8	Histone	e−148	260	465
	acetyltransferase			acetyltransferase
				HAT B
28	Histone	eucalyptusSpp_008036	Q9FJT8	Histone	e−149	262	465
	acetyltransferase			acetyltransferase
				HAT B.
				SPTREMBL
30	Histone	eucalyptusSpp_001596	Q9M4T5	Putative	7E−76	156	305
	deacetylase			histone
				deacetylase
				HD2
31	Histone	eucalyptusSpp_005870	Q9M4T4	Putative	7E−66	144	318
	deacetylase			histone
				deacetylase
				HD2c
				(AT5g03740/F17C15_160)
32	Histone	eucalyptusSpp_006901	HDAC_ARATH	Histone	0	405	499
	deacetylase			deacetylase
				(HD)
33	Histone	eucalyptusSpp_006902	AAM13152	HISTONE	0	427	499
	deacetylase			DEACETYLASE
34	Histone	eucalyptusSpp_007440	Q8W508	HISTONE	0	369	428
	deacetylase			DEACETYLASE
35	Histone	eucalyptusSpp_008994	Q8LD93	Histone	0	354	536
	deacetylase			deacetylase,
				putative
36	Histone	eucalyptusSpp_024580	Q94EJ2	At1g08460/T27G7_7	e−165	274	373
	deacetylase			(HDA8).
				SPTREMBL
37	Histone	eucalyptusSpp_037831	Q9FML2	Histone	0	356	464
	deacetylase			deacetylase.
				SPTREMBL
38	MAT1 CDK-	eucalyptusSpp_034958	Q8LES8	Hypothetical	4E−47	101	190
	activating			protein
	kinase
	assembly
	factor
39	Peptidylprolyl	001209EGXC004488HT	TL40_SPIOL	Peptidylprolyl	0	329	392
	isomerase			cis-
				trans
				isomerase,
				chloroplast
				precursor
40	Peptidylprolyl	010310EGXD012820HT	Q9FJL3	PEPTIDYLPROLYL	0	453	579
	isomerase			ISOMERASE
41	Peptidylprolyl	010310EGXD013036HT	O82646	HYPOTHETICAL	0	302	521
	isomerase			57.1 KDA
				PROTEIN (EC
				5.2.1.8)
42	Peptidylprolyl	010316EGXF999037HT	BAB39983	PUTATIVE	e−115	146	172
	isomerase			PEPTIDYLPROLYL
				CIS-
				TRANS
				ISOMERASE,
				CHLOROPLAST
43	Peptidylprolyl	010324EGXF002118HT	AAK32894	AT5G13120/T19L5_80	e−122	179	264
	isomerase
44	Peptidylprolyl	011019EGKA001923HT	AAM14253	HYPOTHETICAL	e−108	146	188
	isomerase			20.3 KDA
				PROTEIN
45	Peptidylprolyl	eucalyptusSpp_000966	Q8L5T1	Peptidylprolyl	1E−91	155	170
	isomerase			isomerase
				(Cyclophilin)
				(EC
				5.2.1.8)
46	Peptidylprolyl	eucalyptusSpp_001037	Q8VX73	CYCLOPHILIN	e−120	155	169
	isomerase			(EC 5.2.1.8)
47	Peptidylprolyl	eucalyptusSpp_004603	AAM14253	HYPOTHETICAL	e−108	146	188
	isomerase			20.3 KDA
				PROTEIN.
48	Peptidylprolyl	eucalyptusSpp_005465	Q9SP02	Cyclophilin	2E−93	172	204
	isomerase			ROC7 (EC
				5.2.1.8)
				(AT5g58710/mzn1_160)
				(Pepti . . .
49	Peptidylprolyl	eucalyptusSpp_006571	O49605	EC 5.2.1.8	9E−98	169	224
	isomerase			(Cyclophilin-
				like
				protein)
				(Peptidyl-
				prolyl
50	Peptidylprolyl	eucalyptusSpp_006786	Q93VG0	Cyclophilin	5E−82	142	164
	isomerase			(EC 5.2.1.8)
				(Peptidyl-
				prolyl cis-
				trans
51	Peptidylprolyl	eucalyptusSpp_007057	Q38901	Cytosolic	3E−84	144	172
	isomerase			cyclophilin
				(EC 5.2.1.8)
				(Peptidyl-
				prolyl
52	Peptidylprolyl	eucalyptusSpp_008670	Q9FJL3	PEPTIDYLPROLYL	0	423	596
	isomerase			ISOMERASE
53	Peptidylprolyl	eucalyptusSpp_009137	Q9C566	Cyclophilin-	e−168	285	361
	isomerase			40 (EC
				5.2.1.8)
				(Expressed
				protein)
54	Peptidylprolyl	eucalyptusSpp_010285	Q9LY75	Cyclophylin-	e−160	345	658
	isomerase			like protein
				(EC 5.2.1.8)
				(Peptidyl-
				prolyl
55	Peptidylprolyl	eucalyptusSpp_010600	Q93YQ8	HYPOTHETICAL	0	346	475
	isomerase			50.1 KDA
				PROTEIN
				(FRAGMENT)
56	Peptidylprolyl	eucalyptusSpp_011551	Q9ZVG4	T2P11.13	e−115	154	192
	isomerase			PROTEIN
57	Peptidylprolyl	eucalyptusSpp_020743	Q8VXA5	PUTATIVE	e−125	161	172
	isomerase			CYCLOSPORIN
				A-BINDING
				PROTEIN
58	Peptidylprolyl	eucalyptusSpp_023739	FK21_NEUCR	FK506-	3E−49	74	112
	isomerase			binding
				protein
				precursor
				(FKBP-21)
60	Peptidylprolyl	eucalyptusSpp_031985	Q8L8W5	Cyclophilin-	1E−82	155	229
	isomerase			like protein
				(EC 5.2.1.8)
				(Peptidyl-
				prolyl
61	Peptidylprolyl	eucalyptusSpp_032025	Q9LPC7	F22M8.7	1E−45	99	160
	isomerase			protein (EC
				5.2.1.8)
				(Peptidyl-
				prolyl cis-
				trans
62	Peptidylprolyl	eucalyptusSpp_032173	Q8L8W5	Cyclophilin-	4E−83	156	229
	isomerase			like protein
				(EC 5.2.1.8)
				(Peptidyl-
				prolyl
64	Retinoblastoma	eucalyptusSpp_009143	Q9SLZ4	Retinoblastoma-	0	704	1008
	related			related
	protein			protein
65	WD40 repeat	eucalyptusSpp_000349	AAK49947	TGF-BETA	0	291	326
	protein			RECEPTOR-
				INTERACTING
				PROTEIN 1
66	WD40 repeat	eucalyptusSpp_000575	Q9LW17	WD-40 repeat	e−168	282	341
	protein			protein-like
				(Expressed
				protein)
67	WD40 repeat	eucalyptusSpp_000804	GBLP_SOYBN	Guanine	0	291	326
	protein			nucleotide-
				binding
				protein beta
				subunit-like
68	WD40 repeat	eucalyptusSpp_000805	GBLP_MEDSA	Guanine	e−171	291	327
	protein			nucleotide-
				binding
				protein beta
69	WD40 repeat	eucalyptusSpp_000806	GBLP_MEDSA	Guanine	e−171	291	327
	protein			nucleotide-
				binding
				protein beta
				subunit-like
70	WD40 repeat	eucalyptusSpp_002248	AAL86002	HYPOTHETICAL	0	261	388
	protein			43.8 KDA
				PROTEIN
71	WD40 repeat	eucalyptusSpp_003203	Q9SY00	Putative WD-	e−144	236	317
	protein			repeat
				protein
				(AT4G02730/T5J8_2)
72	WD40 repeat	eucalyptusSpp_003209	AAM14986	HYPOTHETICAL	e−160	259	302
	protein			32.6 KDA
				PROTEIN
73	WD40 repeat	eucalyptusSpp_004429	Q9SZQ5	HYPOTHETICAL	0	260	322
	protein			34.3 KDA
				PROTEIN
74	WD40 repeat	eucalyptusSpp_004607	AAC27402	EXPRESSED	0	253	356
	protein			PROTEIN
75	WD40 repeat	eucalyptusSpp_004682	AAK00964	HYPOTHETICAL	0	264	313
	protein			35.3 KDA
				PROTEIN
76	WD40 repeat	eucalyptusSpp_005786	Q944S2	At2g47790/F17A22.18	e−155	264	396
	protein			(Expressed
				protein).
				SPTREMBL
77	WD40 repeat	eucalyptusSpp_005887	Q94AB4	AT3g13340/MDC11_13	0	332	446
	protein
78	WD40 repeat	eucalyptusSpp_005981	Q8L4X6	WD-repeat	0	315	348
	protein			protein
				GhTTG2.
				SPTREMBL
79	WD40 repeat	eucalyptusSpp_006766	Q8L4M1	Putative WD-	e−137	234	369
	protein			40 repeat
				protein
80	WD40 repeat	eucalyptusSpp_006769	Q9LJC6	RETINOBLASTOMA-	0	372	566
	protein			BINDING
				PROTEIN-LIKE
81	WD40 repeat	eucalyptusSpp_006907	Q94C94	Hypothetical	0	446	812
	protein			protein.
82	WD40 repeat	eucalyptusSpp_007518	Q93ZN5	AT4G00090/F6N15_8	0	311	436
	protein
83	WD40 repeat	eucalyptusSpp_007717	O82266	At2g47990	e−180	327	528
	protein			protein
				(Hypothetical
				58.9 kDa
				protein)
84	WD40 repeat	eucalyptusSpp_007718	Q8RWD8	Hypothetical	e−173	278	350
	protein			protein.
				SPTREMBL
85	WD40 repeat	eucalyptusSpp_007741	Q8LA40	Putative WD-	e−158	269	409
	protein			40 repeat
				protein,
				MSI2
86	WD40 repeat	eucalyptusSpp_007884	Q9FHY2	Similarity	e−149	316	765
	protein			to unknown
				protein
87	WD40 repeat	eucalyptusSpp_008258	Q9LHN3	EMB|CAB63739.1	0	524	758
	protein			(AT3G18860/MCB22_3)
88	WD40 repeat	eucalyptusSpp_008465	Q9FLS2	WD-repeat	0	366	460
	protein			protein-like
89	WD40 repeat	eucalyptusSpp_008616	Q9LYK6	Hypothetical	e−148	252	321
	protein			protein
90	WD40 repeat	eucalyptusSpp_008690	Q9SW94	G PROTEIN	0	326	376
	protein			BETA SUBUNIT
91	WD40 repeat	eucalyptusSpp_008708	Q8L862	Hypothetical	e−167	297	487
	protein			protein
92	WD40 repeat	eucalyptusSpp_008850	O22725	F11P17.7	0	402	853
	protein			protein.
				SPTREMBL
93	WD40 repeat	eucalyptusSpp_009072	Q9SAJ0	F23A5.2 (form	e−176	288	350
	protein			2) (mRNA
				export
				protein,
				putative)
94	WD40 repeat	eucalyptusSpp_009465	Q9FLX9	NOTCHLESS	0	384	475
	protein			PROTEIN
				HOMOLOG
95	WD40 repeat	eucalyptusSpp_009472	Q9SZA4	WD-REPEAT	0	374	457
	protein			PROTEIN-LIKE
				PROTEIN
96	WD40 repeat	eucalyptusSpp_009550	Q9FKT5	Gb|AAF54217.1	e−167	275	313
	protein			(Hypothetical
				protein)
97	WD40 repeat	eucalyptusSpp_010284	O22466	WD-40 repeat	0	397	423
	protein			protein MSI1
98	WD40 repeat	eucalyptusSpp_010595	Q94C94	Hypothetical	0	419	789
	protein			protein
99	WD40 repeat	eucalyptusSpp_010657	Q94AH2	HYPOTHETICAL	0	243	298
	protein			33.1 KDA
				PROTEIN
100	WD40 repeat	eucalyptusSpp_012636	Q8L611	Hypothetical	0	756	1133
	protein			protein
101	WD40 repeat	eucalyptusSpp_012748	AAD10151	PUTATIVE WD-	0	375	469
	protein			40 REPEAT
				PROTEIN,
				MSI4
102	WD40 repeat	eucalyptusSpp_012879	Q8VZY6	FERTILIZATION-	0	291	377
	protein			INDEPENDENT
				ENDOSPERM
				PROTEIN
103	WD40 repeat	eucalyptusSpp_015515	Q8LPI5	Putative WD-	0	360	493
	protein			repeat
				protein.
				SPTREMBL
104	WD40 repeat	eucalyptusSpp_015724	O22607	WD-40 repeat	0	395	522
	protein			protein MSI4
105	WD40 repeat	eucalyptusSpp_016167	Q93YS7	Putative WD-	0	663	917
	protein			repeat
				membrane
				protein
106	WD40 repeat	eucalyptusSpp_016633	Q9SUY6	HYPOTHETICAL	e−174	240	384
	protein			43.8 KDA
				PROTEIN
107	WD40 repeat	eucalyptusSpp_017485	Q8RXC4	Hypothetical	0	650	1348
	protein			144.7 kDa
				protein
108	WD40 repeat	eucalyptusSpp_018007	O94289	WD repeat-	e−129	302	794
	protein			containing
				protein
109	WD40 repeat	eucalyptusSpp_020775	Q8W403	Sec13p	e−150	242	304
	protein
110	WD40 repeat	eucalyptusSpp_023132	AAK52092	WD-40 REPEAT	0	458	515
	protein			PROTEIN
111	WD40 repeat	eucalyptusSpp_023569	Q9XIJ3	T10O24.21.	0	404	576
	protein			SPTREMBL
112	WD40 repeat	eucalyptusSpp_023611	Q8L4J2	Cleavage	e−174	301	438
	protein			stimulation
				factor 50K
				chain
				(Cleavage
				stimulation
113	WD40 repeat	eucalyptusSpp_024934	Q94AB4	AT3g13340/MDC11_13.	0	343	444
	protein			WD-
				repeat
				protein-like
				SPTREMBL
114	WD40 repeat	eucalyptusSpp_025546	O22212	Hypothetical	0	352	566
	protein			61.8 kDa
				Trp-Asp
				repeats
				containing
				protein
115	WD40 repeat	eucalyptusSpp_030134	Q9LVF2	Genomic DNA,	0	677	946
	protein			chromosome
				3, P1 clone:
				MIL23
116	WD40 repeat	eucalyptusSpp_031787	AAL91206	WD REPEAT	0	264	329
	protein			PROTEIN-LIKE
117	WD40 repeat	eucalyptusSpp_034435	Q9SAJ0	F23A5.2(form	e−178	290	349
	protein			2) (mRNA
				export
				protein,
				putative).
				SPTREMBL
118	WD40 repeat	eucalyptusSpp_034452	Q94BR4	Hypothetical	0	381	525
	protein			protein
				(Putative
				pre-mRNA
				splicing
				factor
119	WD40 repeat	eucalyptusSpp_035789	P93563	Guanine	3E−88	171	356
	protein			nucleotide-
				binding
				protein beta
				subunit
120	WD40 repeat	eucalyptusSpp_035804	Q9FNN2	WD-repeat	0	356	589
	protein			protein-
				like.
				SPTREMBL
121	WD40 repeat	eucalyptusSpp_043057	Q9LV35	WD40-repeat	0	472	610
	protein			protein.
				SPTREMBL
122	WD40 repeat	eucalyptusSpp_046741	Q93VK1	AT4g28450/F20O9_130	0	363	452
	protein
123	WD40 repeat	eucalyptusSpp_047161	Q9ZUN8	Putative WD-	0	350	473
	protein			40 repeat
				protein
124	CDK type A	pinusRadiata_001766	Q9M3W7	PUTATIVE	e−128	237	436
				CDC2-RELATED
				PROTEIN
				KINASE CRK2.459
				e−128
125	CDK type A	pinusRadiata_002927	Q9FRN5	PUTATIVE	0	349	470
				SERINE/THREONINE
				KINASE
126	CDK type B-1	990309PRCA009171HT	Q9FYT8	Cyclin-	e−145	244	303
				dependent
				kinase B1-2
127	CDK type B-1	pinusRadiata_013714	Q9FYT8	CYCLIN-	e−174	222	304
				DEPENDENT
				KINASE B1-2
128	CDK type B-1	pinusRadiata_016332	Q9FYT8	CYCLIN-	e−178	228	304
				DEPENDENT
				KINASE B1-2
129	CDK type B-1	pinusRadiata_021677	Q9FYT8	CYCLIN-	e−176	229	304
				DEPENDENT
				KINASE B1-2
130	CDK type B-1	pinusRadiata_027562	Q9FYT8	Cyclin-	e−118	211	304
				dependent
				kinase B1-2
131	CDK type C	pinusRadiata_001504	Q9LNN0	F8L10.9	0	434	790
				protein
132	CDK type C	pinusRadiata_015211	Q9LNN0	F8L10.9	0	371	746
				protein
133	CDK type C	pinusRadiata_020421	P93320	Cdc2MsC	0	318	432
				protein
134	CDK type D	pinusRadiata_003187	O80345	CDK-	e−137	226	485
				ACTIVATING
				KINASE 1AT
				(CDK-
				ACTIVATING
				KINASE
				CAK1AT)
135	CDK type D	pinusRadiata_015661	Q947K6	CDK-	0	266	407
				ACTIVATING
				KINASE.
136	Cyclin A	pinusRadiata_013874	Q96226	Cyclin	e−108	223	474
137	Cyclin A	pinusRadiata_014615	CAC27333	PUTATIVE A-	0	332	390
				LIKE CYCLIN
				(FRAGMENT)
138	Cyclin B	pinusRadiata_004578	O65064	Probable	9E−87	162	217
				G2/mitotic-
				specific
				cyclin
				(Fragment)
139	Cyclin B	pinusRadiata_023387	O04389	B-like	2E−98	220	466
				cyclin
140	Cyclin D	pinusRadiata_006970	P93103	CYCLIN-D	1E−75	135	293
				LIKE PROTEIN
141	Cyclin D	pinusRadiata_010322	CAC17049	SEQUENCE 33	e−131	171	254
				FROM PATENT
				WO0065040
142	Cyclin D	pinusRadiata_022721	P93103	CYCLIN-D	1E−76	137	289
				LIKE PROTEIN
143	Cyclin D	pinusRadiata_023407	Q9SMD5	CYCD3,2	8E−90	139	278
				PROTEIN
144	Cyclin-	pinusRadiata_001945	Q947Y1	PUTATIVE	5E−55	74	86
	dependent			CYCLIN-
	kinase			DEPENDENT
	regulatory			KINASE
	subunit			REGULATORY
				SUBUNIT
145	Cyclin-	pinusRadiata_008233	CAB69358	SEQUENCE 1	4E−49	65	86
	dependent			FROM PATENT
	kinase			WO9841642
	regulatory
	subunit
146	Cyclin-	pinusRadiata_008234	CAB69358	SEQUENCE 1	4E−49	65	86
	dependent			FROM PATENT
	kinase			WO9841642
	regulatory
	subunit
147	Cyclin-	pinusRadiata_022054	CAB69358	SEQUENCE 1	8E−55	70	82
	dependent			FROM PATENT
	kinase			WO9841642
	regulatory
	subunit
148	Histone	pinusRadiata_012137	Q9FK40	Histone	0	496	555
	acetyltransferase			acetyltransferase
				(AT5g50320/MXI22_3)
149	Histone	pinusRadiata_012582	O80378	181	0	354	402
	acetyltransferase			(Fragment)
				SPTREMBL
150	Histone	pinusRadiata_015285	O80378	181	0	342	401
	acetyltransferase			(Fragment)
151	Histone	pinusRadiata_017229	Q9LNC4	F9P14.9	e−118	268	585
	acetyltransferase			protein
152	Histone	pinusRadiata_020724	Q9AR19	Histone	e−177	355	639
	acetyltransferase			acetyltransferase
				GCN5
				(Expressed
				protein)
153	Histone	pinusRadiata_004555	AAM13152	HISTONE	0	331	488
	deacetylase			DEACETYLASE
154	Histone	pinusRadiata_004556	AAM13152	HISTONE	0	331	488
	deacetylase			DEACETYLASE
155	Histone	pinusRadiata_005729	Q9M4U5	Histone	9E−62	154	348
	deacetylase			deacetylase
				2 isoform b
156	Histone	pinusRadiata_007395	AAM13152	HISTONE	0	335	426
	deacetylase			DEACETYLASE
157	Histone	pinusRadiata_009503	Q8W508	Histone	0	365	427
	deacetylase			deacetylase
158	Histone	pinusRadiata_011283	AAM19887	AT1G08460/T27G7_7	0	255	366
	deacetylase
159	Histone	pinusRadiata_012322	Q9FML2	HISTONE	0	327	435
	deacetylase			DEACETYLASE
				(PUTATIVE
				HISTONE
				DEACETYLASE)
161	Histone	pinusRadiata_023236	Q8RX28	Putative	e−144	238	390
	deacetylase			histone
				deacetylase
162	Peptidylprolyl	pinusRadiata_000171	Q9FJL3	PEPTIDYLPROLYL	0	364	549
	isomerase			ISOMERASE
163	Peptidylprolyl	pinusRadiata_000172	Q38949	FK506	0	365	552
	isomerase			BINDING
				PROTEIN
				FKBP62
				(ROF1)
164	Peptidylprolyl	pinusRadiata_001480	Q8VXA5	PUTATIVE	e−125	161	172
	isomerase			CYCLOSPORIN
				A-BINDING
				PROTEIN
168	Peptidylprolyl	pinusRadiata_001692	FKB7_WHEAT	70 kDa	0	418	553
	isomerase			peptidylprolyl
				isomerase
				(EC 5.2.1.8)
169	Peptidylprolyl	pinusRadiata_005313	AAB64339	FKBP-TYPE	1E−97	135	175
	isomerase			PEPTIDYL-
				PROLYL CIS-
				TRANS
				ISOMERASE
170	Peptidylprolyl	pinusRadiata_006362	BAB39983	PUTATIVE	3E−77	129	168
	isomerase			PEPTIDYL-
				PROLYL CIS-
				TRANS
				ISOMERASE,
				CHLOROPLA . . .
				290 3e−77
171	Peptidylprolyl	pinusRadiata_006493	Q9C835	Hypothetical	2E−62	128	235
	isomerase			26.4 kDa
				protein (EC
				5.2.1.8)
				(Peptidyl-
				prol . . .
172	Peptidylprolyl	pinusRadiata_006983	AAK96784	CYCLOPHILIN	e−103	151	204
	isomerase
174	Peptidylprolyl	pinusRadiata_007665	Q9LDC0	FKBP-like	e−138	239	378
	isomerase			protein
				(Genomic
				DNA,
				chromosome
				3, P1 clone:
175	Peptidylprolyl	pinusRadiata_012196	Q93VG0	Cyclophilin	4E−74	132	160
	isomerase			(EC 5.2.1.8)
				(Peptidyl-
				prolyl cis-
				trans
176	Peptidylprolyl	pinusRadiata_013382	Q9C588	HYPOTHETICAL	0	288	581
	isomerase			60.2 KDA
				PROTEIN
177	Peptidylprolyl	pinusRadiata_016461	O04287	IMMUNOPHILIN	9E−66	88	109
	isomerase
178	Peptidylprolyl	pinusRadiata_017611	Q9C566	Cyclophilin-	e−163	276	360
	isomerase			40 (EC
				5.2.1.8)
				(Expressed
				protein)
179	Peptidylprolyl	pinusRadiata_019776	AAM14253	HYPOTHETICAL	e−110	146	190
	isomerase			20.3 KDA
				PROTEIN
180	Peptidylprolyl	pinusRadiata_020659	AAO63961	Hypothetical	7E−85	159	227
	isomerase			protein
				SPTREMBL
181	Peptidylprolyl	pinusRadiata_022559	AAK43974	PUTATIVE	2E−73	113	153
	isomerase			PEPTIDYL-
				PROLYL CIS-
				TRANS
				ISOMERASE
182	Peptidylprolyl	pinusRadiata_024188	Q9P3X9	PEPTIDYL-	e−122	210	379
	isomerase			PROLYL CIS-
				TRANS
				ISOMERASE
				(EC 5.2.1.8)
183	Peptidylprolyl	pinusRadiata_027973	Q9SR70	T22K18.11	3E−69	125	171
	isomerase			protein
				(AT3g10060/T22K18_11)
184	WD40 repeat	pinusRadiata_001353	Q9FNN2	WD-repeat	0	317	590
	protein			protein-
				likeSPTREMBL
185	WD40 repeat	pinusRadiata_001978	PRL1_ARATH	PP1/PP2A	0	341	502
	protein			phosphatases
				pleiotropic
				regulator
				PRL1
186	WD40 repeat	pinusRadiata_002810	AAK49947	TGF-BETA	0	273	326
	protein			RECEPTOR-
				INTERACTING
				PROTEIN 1
187	WD40 repeat	pinusRadiata_002811	AAK49947	TGF-BETA	0	273	326
	protein			RECEPTOR-
				INTERACTING
				PROTEIN 1
188	WD40 repeat	pinusRadiata_002812	AAM15129	HYPOTHETICAL	e−127	225	521
	protein			58.9 KDA
				PROTEIN
189	WD40 repeat	pinusRadiata_003514	Q9FJ94	Similarity	e−137	242	445
	protein			to myosin
				heavy chain
				kinaseSPTREMBL
190	WD40 repeat	pinusRadiata_004104	GBB_ORYSA	Guanine	0	294	378
	protein			nucleotide-
				binding
				protein beta
				subunit
191	WD40 repeat	pinusRadiata_005595	Q9FTT9	PUTATIVE	0	320	459
	protein			DKFZP564O0463
				PROTEIN
192	WD40 repeat	pinusRadiata_005754	Q94JT6	At1g78070/F28K19_28SPTREMBL	e−168	294	451
	protein
193	WD40 repeat	pinusRadiata_006463	GBLP_MEDSA	Guanine	e−152	261	324
	protein			nucleotide-
				binding
				protein beta
				subunit-like . . .
				538 e−152
194	WD40 repeat	pinusRadiata_006665	AAM20553	HYPOTHETICAL	0	655	1169
	protein			119.9 KDA
				PROTEIN.
				1229 0.0
195	WD40 repeat	pinusRadiata_006750	AAM13119	HYPOTHETICAL	e−158	264	312
	protein			35.4 KDA
				PROTEIN. 560
				e−158
196	WD40 repeat	pinusRadiata_007030	Q9LJN8	MITOTIC	e−169	284	335
	protein			CHECKPOINT
				PROTEIN. 595
				e−169
197	WD40 repeat	pinusRadiata_007854	Q8H919	Putative WD	0	429	644
	protein			domain
				containing
				protein
198	WD40 repeat	pinusRadiata_007917	AAD10151	PUTATIVE WD-	0	353	462
	protein			40 REPEAT
				PROTEIN,
				MSI4
199	WD40 repeat	pinusRadiata_007989	Q9LRZ0	Genomic DNA,	0	480	687
	protein			chromosome
				3, TAC
				clone: K20I9
200	WD40 repeat	pinusRadiata_008506	MSI1_LYCES	WD-40 repeat	0	364	420
	protein			protein MSI1
201	WD40 repeat	pinusRadiata_008692	Q8W403	Sec13p	e−134	218	301
	protein
202	WD40 repeat	pinusRadiata_008693	Q8W403	Sec13p	e−137	222	301
	protein
203	WD40 repeat	pinusRadiata_009170	Q9M0V4	U3 snoRNP-	e−127	244	524
	protein			associated-
				like
				protein.
				SPTREMBL
204	WD40 repeat	pinusRadiata_009408	Q9SAJ0	F23A5.2(FORM	e−171	282	350
	protein			2). 602 e−171
205	WD40 repeat	pinusRadiata_009522	Q8RXQ4	Hypothetical	e−129	231	395
	protein			43.8 kDa
				protein
206	WD40 repeat	pinusRadiata_009734	AAO27452	Peroxisomal	e−142	227	317
	protein			targeting
				signal type
				2 receptor.
				SPTREMBL
207	WD40 repeat	pinusRadiata_009815	AAM20433	CELL CYCLE	0	326	500
	protein			SWITCH
				PROTEIN
208	WD40 repeat	pinusRadiata_010670	AAN72058	Expressed	e−157	264	345
	protein			protein
209	WD40 repeat	pinusRadiata_011297	AAM13100	WD REPEAT	e−157	262	337
	protein			PROTEIN
				ATAN11
210	WD40 repeat	pinusRadiata_013098	AAM13153	HYPOTHETICAL	e−136	229	352
	protein			39.1 KDA
				PROTEIN. 487
				e−136
211	WD40 repeat	pinusRadiata_013172	Q8H0T9	Hypothetical	0	437	860
	protein			protein
212	WD40 repeat	pinusRadiata_013589	AAK52092	WD-40 REPEAT	0	448	512
	protein			PROTEIN
213	WD40 repeat	pinusRadiata_013608	AAC27402	EXPRESSED	e−141	202	358
	protein			PROTEIN
214	WD40 repeat	pinusRadiata_014299	Q9XED5	Cell cycle	0	335	488
	protein			switch
				proteinSPTREMBL
215	WD40 repeat	pinusRadiata_014498	Q9FH64	WD REPEAT	e−152	206	329
	protein			PROTEIN-LIKE
216	WD40 repeat	pinusRadiata_014548	Q93ZS6	HYPOTHETICAL	0	505	763
	protein			82.2 KDA
				PROTEIN
217	WD40 repeat	pinusRadiata_014610	Q9M298	Hypothetical	0	450	922
	protein			104.7 kDa
				protein
218	WD40 repeat	pinusRadiata_016090	Q9SIY9	Putative WD-	0	442	802
	protein			40 repeat
				proteinSPTREMBL
219	WD40 repeat	pinusRadiata_016722	O22826	Putative	e−159	257	310
	protein			splicing
				factorSPTREMBL
220	WD40 repeat	pinusRadiata_016785	AAG60193	PUTATIVE	0	344	464
	protein			WD40 PROTEIN
221	WD40 repeat	pinusRadiata_017094	Q9LV35	WD40-REPEAT	0	406	604
	protein			PROTEIN
222	WD40 repeat	pinusRadiata_017527	Q9AYE4	Hypothetical	e−154	254	314
	protein			35.3 kDa
				protein
223	WD40 repeat	pinusRadiata_017591	O80706	F8K4.21	0	905	1218
	protein			protein
224	WD40 repeat	pinusRadiata_017769	Q9XIJ3	T10O24.21	0	446	607
	protein
225	WD40 repeat	pinusRadiata_018047	Q8VZY6	FERTILIZATION-	0	285	373
	protein			INDEPENDENT
				ENDOSPERM
				PROTEIN
226	WD40 repeat	pinusRadiata_018414	Q947M8	COPI	0	455	638
	protein
227	WD40 repeat	pinusRadiata_018986	Q9LFE2	WD40-repeat	0	518	886
	protein			protein
228	WD40 repeat	pinusRadiata_019479	Q9SZA4	WD-repeat	e−156	276	454
	protein			protein-like
				protein
229	WD40 repeat	pinusRadiata_020144	Q8W514	MSI TYPE	0	288	413
	protein			NUCLEOSOME/CHROMATIN
				ASSEMBLY
				FACTOR C
230	WD40 repeat	pinusRadiata_022480	Q8W514	MSI type	e−167	287	426
	protein			nucleosome/chromatin
				assembly
				factor C
231	WD40 repeat	pinusRadiata_023079	Q8W514	MSI type	e−169	283	397
	protein			nucleosome/chromatin
				assembly
				factor C. SPTREMBL
232	WD40 repeat	pinusRadiata_026739	Q93YS7	Putative WD-	0	591	918
	protein			repeat
				membrane
				protein.
				SPTREMBL
233	WD40 repeat	pinusRadiata_026951	Q93VS5	AT4g18900/F13C5_70	e−163	290	503
	protein			(Hypothetical
				protein)
234	WEE1-like	pinusRadiata_026529	Q9SRY9	F22D16.3	e−122	209	451
	protein			PROTEIN
235	WD40 repeat	eucalyptusSpp_006366	Q8LF96	PRL1 protein	0	374	492
	protein
236	WD40 repeat	eucalyptusSpp_017378	O22607	WD-40 repeat	0	371	453
	protein			protein MSI4
237	WD40 repeat	pinusRadiata_000888	O22466	WD-40 repeat	0	364	420
	protein			protein MSI1
238	Cyclin-	pinusRadiata_014166	Q9FKB5	GENOMIC DNA,	5E−42	114	304
	dependant			CHROMOSOME
	kinase			5, TAC
	inhibitor			CLONE: K24G6
				(CYCLIN-
				DEPENDENT
239	CDK type D	pinusRadiata_003189	Q9M5G4	CDK-	8E−21	56	100
				activating
				kinase
240	Histone	pinusRadiata_009356	Q9FJT8	Histone	7E−85	187	510
	acetyltransferase			acetyltransferase
				HAT B
241	Histone	pinusRadiata_000065	Q9LPW6	F13K23.8	5E−18	71	209
	deacetylase			protein.
242	Histone	pinusRadiata_014197	Q8GXJ1	Putative	e−170	308	519
	deacetylase			histone
				deacetylase
243	Peptidylprolyl	pinusRadiata_009081	Q9ZRQ9	Cyclophilin	e−106	185	190
	isomerase			(EC 5.2.1.8)
				(Peptidyl-
				prolyl cis-
				trans
244	Peptidyprolyl	pinusRadiata_013417	Q8H4T0	Putative	e−140	235	345
	isomerase			peptidyl-
				prolycis-
				trans
				isomerase
				protein
245	WD40 repeat	pinusRadiata_005755	Q9SKW4	F5J5.6.	e−143	144	319
	protein
246	WD40 repeat	pinusRadiata_006670	Q9LDG7	WD-40 repeat	e−163	393	960
	protein			protein-like
				(MJK13.13
				protein)
247	WD40 repeat	pinusRadiata_007027	Q8GWR1	Hypothetical	e−157	276	470
	protein			protein.
248	WD40 repeat	pinusRadiata_007276	Q9LF27	Hypothetical	e−138	235	428
	protein			47.3 kDa
				protein
249	WD40 repeat	pinusRadiata_007390	Q94AH4	PUTATIVE	3E−17	53	158
	protein			RING ZINC
				FINGER
				PROTEIN. 91
				3e−17
250	WD40 repeat	pinusRadiata_012648	O22212	Hypothetical	0	324	561
	protein			61.8 kDa
				Trp-Asp
				repeats
				containing
				protein
251	WD40 repeat	pinusRadiata_013171	Q8H0T9	Hypothetical	0	437	860
	protein			protein.
252	Cyclin B	eucalyptusSpp_045414	Q9LDM4	F2D10.10	e−142	255	423
				(F5M15.6)
253	Cyclin-	eucalyptusSpp_044328	Q9FKB5	GENOMIC DNA,	1E−54	121	260
	dependant			CHROMOSOME
	kinase			5, TAC
	inhibitor			CLONE: K24G6
				(CYCLIN-
				DEPENDENT
254	Histone	eucalyptusSpp_015615	Q9AR19	Histone	0	390	563
	acetyltransferase			acetyltransferase
				GCN5
				(Expressed
				protein)
255	Peptidylprolyl	eucalyptusSpp_017239	Q8GWM6	Hypothetical	0	364	591
	isomerase			protein
256	WD40 repeat	eucalyptusSpp_018643	Q93VS5	AT4g18900/F13C5_70	0	229	327
	protein			(Hypothetical
				protein)
257	WD40 repeat	eucalyptusSpp_019127	Q9SRX9	F22D16.14	e−131	232	337
	protein			protein.
				SPTREMBL
258	WD40 repeat	eucalyptusSpp_022624	Q9LFE2	WD40-repeat	0	594	868
	protein			protein
259	WD40 repeat	eucalyptusSpp_032424	Q8LPL5	Cell cycle	0	255	327
	protein			switch
				protein
260	WD40 repeat	eucalyptusSpp_037472	Q9SK69	Putative WD-	0	461	677
	protein			40 repeat
				protein
				(AT2G20330/F11A3.12)