pI: 9.7634 |
Length (AA): 218 |
MW (Da): 25469 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 0
Targets have been classified into druggability groups (DG) according to their druggability score in network driven prioritizations. DGs range from 1 to 5; the higher the group number, the higher the chance of the target to be druggable
Modbase 3D models:
There are 2 models calculated for this protein. More info on
these models, including the
models themselves is available at:
Modbase
Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
---|---|---|---|---|---|---|---|---|---|
1 | 182 | 2pmi (B) | 23 | 217 | 29.00 | 0 | 1 | 1.21946 | -0.39 |
33 | 162 | 4krd (B) | 293 | 430 | 22.00 | 0.0003 | 1 | 0.90573 | -0.68 |
Help me make sense of these data.
A more detailed description of these scores is available at the Modbase Model Evaluation Help Pages, and in the papers referenced therein.
PDB Structures:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 80-100% percentile | Gametocyte, Ookinete, 22 hs Schizont, Female gametocyte, Male gametocyte. | Otto TD Yeoh LM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | 4 hs Ring, Erthyrocytic stages. | Otto TD Yeoh LM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 0-20% percentile | 16 hs Trophozoite. | Otto TD |
Yeoh LM | Comparative transcriptomics of female and male gametocytes in Plasmodium berghei and the evolution of sex in alveolates. |
Otto TD | A comprehensive evaluation of rodent malaria parasite genomes and gene expression. |
Ortholog group members (OG5_128496)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G44740 | 1 |
Arabidopsis thaliana | AT3G05327 | cyclin family protein |
Arabidopsis thaliana | AT3G21870 | 1 |
Babesia bovis | BBOV_II002730 | cyclin, N-terminal domain containing protein |
Candida albicans | CaO19.5755 | similar to S. cerevisiae Pho80p cyclin: negative regulator of PHO81 and PHO5 |
Candida albicans | CaO19.13178 | similar to S. cerevisiae Pho80p cyclin: negative regulator of PHO81 and PHO5 |
Cryptosporidium hominis | Chro.70422 | cyclin |
Cryptosporidium parvum | cgd7_3780 | cyclin |
Dictyostelium discoideum | DDB_G0295785 | cyclin-related 2 family protein |
Dictyostelium discoideum | DDB_G0286485 | hypothetical protein |
Dictyostelium discoideum | DDB_G0280425 | hypothetical protein |
Dictyostelium discoideum | DDB_G0286347 | hypothetical protein |
Dictyostelium discoideum | DDB_G0277481 | hypothetical protein |
Drosophila melanogaster | Dmel_CG42507 | CG42507 gene product from transcript CG42507-RB |
Leishmania braziliensis | LbrM.32.0910 | CYC2-like cyclin, putative |
Leishmania donovani | LdBPK_320870.1 | CYC2-like cyclin, putative |
Leishmania infantum | LinJ.32.0870 | CYC2-like cyclin, putative |
Leishmania major | LmjF.32.0820 | CYC2-like cyclin, putative |
Leishmania mexicana | LmxM.31.0820 | CYC2-like cyclin, putative |
Neospora caninum | NCLIV_043920 | hypothetical protein |
Neospora caninum | NCLIV_038600 | hypothetical protein |
Oryza sativa | 4338711 | Os05g0398000 |
Oryza sativa | 4349405 | Os10g0563900 |
Oryza sativa | 4336556 | Os04g0544200 |
Oryza sativa | 4328150 | Os02g0125400 |
Oryza sativa | 4330172 | Os02g0652000 |
Oryza sativa | 9266882 | Os02g0125450 |
Plasmodium berghei | PBANKA_1233200 | cyclin |
Plasmodium falciparum | PF3D7_0518400 | cyclin, putative |
Plasmodium knowlesi | PKNH_1014800 | cyclin, putative |
Plasmodium vivax | PVX_080325 | cyclin, putative |
Plasmodium yoelii | PY02686 | Cyclin, putative |
Saccharomyces cerevisiae | YOL001W | Pho80p |
Saccharomyces cerevisiae | YIL050W | Pcl7p |
Trypanosoma brucei gambiense | Tbg972.7.8450 | CYC2-like cyclin, putative |
Trypanosoma brucei gambiense | Tbg972.11.15710 | cyclin 2,G1 cyclin, putative |
Trypanosoma brucei | Tb927.11.14080 | cyclin 2 |
Trypanosoma brucei | Tb927.7.7170 | CYC2-like cyclin, putative |
Trypanosoma congolense | TcIL3000_0_08150 | CYC2-like cyclin, putative |
Trypanosoma cruzi | TcCLB.506791.10 | CYC2-like cyclin 4, putative |
Trypanosoma cruzi | TcCLB.511727.199 | CYC2-like cyclin 6, putative |
Trypanosoma cruzi | TcCLB.508385.30 | CYC2-like cyclin, putative |
Toxoplasma gondii | TGME49_267580 | cyclin2 related protein |
Toxoplasma gondii | TGME49_305330 | cyclin, N-terminal domain-containing protein |
Theileria parva | TP04_0316 | cyclin-related, putative |
Trichomonas vaginalis | TVAG_095210 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.7.7170 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.7.7170 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.7.7170 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.7.7170 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb11.01.5660 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.5660 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.5660 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb11.01.5660 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_1233200 this record | Plasmodium berghei | Dispensable | plasmo |
TGME49_267580 | Toxoplasma gondii | Probably essential | sidik |
TGME49_305330 | Toxoplasma gondii | Probably essential | sidik |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
In TDR Targets, information about phenotypes that are caused by drugs, or by genetic manipulation of cells (e.g. gene knockouts or knockdowns) is manually curated from the literature. These descriptions help to describe the potential of the target for drug development. If no information is available for this gene or if the information is incomplete, this may mean that i) the papers containing this information either appeared after the curation effort for this organism was carried out or they were inadvertently missed by curators; or that ii) the curation effort for this organism has not yet started.
In any case, if you have information about papers containing relevant validation data for this target, please contact us.
Species | Known druggable target | Linked compounds | Reference |
---|---|---|---|
Saccharomyces cerevisiae | Pho80p | Compounds | References |