pI: 6.1677 |
Length (AA): 303 |
MW (Da): 33902 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: | 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 4 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 |
---|---|---|---|---|---|---|---|---|---|
15 | 109 | 2l3l (A) | 29 | 134 | 14.00 | 0.012 | 0.08 | 0.379831 | -0.47 |
46 | 107 | 2n9v (A) | 24 | 85 | 37.00 | 0.25 | 0.09 | 0.40402 | 0.73 |
143 | 297 | 2yuh (A) | 2 | 167 | 28.00 | 0 | 1 | 0.855751 | -0.52 |
150 | 296 | 3bh7 (B) | 38 | 192 | 22.00 | 0 | 1 | 0.821348 | -1.3 |
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:
Ortholog group members (OG5_128787)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G39920 | tubulin-folding cofactor C |
Brugia malayi | Bm1_53750 | hypothetical protein |
Caenorhabditis elegans | CELE_Y71H2AM.24 | Protein Y71H2AM.24 |
Cryptosporidium hominis | Chro.40275 | similar to RIKEN cDNA 2810055C19 |
Cryptosporidium parvum | cgd4_2450 | conserved hypothetical protein |
Dictyostelium discoideum | DDB_G0284313 | tubulin folding cofactor C |
Drosophila melanogaster | Dmel_CG31961 | CG31961 gene product from transcript CG31961-RA |
Echinococcus granulosus | EgrG_000413000 | tubulin specific chaperone C |
Echinococcus multilocularis | EmuJ_000413000 | tubulin specific chaperone C |
Giardia lamblia | GL50803_15906 | Tubulin specific chaperone D |
Homo sapiens | ENSG00000124659 | tubulin folding cofactor C |
Leishmania braziliensis | LbrM.35.3380 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_363310.1 | tubulin binding cofactor c, putative |
Leishmania infantum | LinJ.36.3310 | hypothetical protein, conserved |
Leishmania major | LmjF.36.3160 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.36.3160 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_06411 | hypothetical protein |
Mus musculus | ENSMUSG00000036430 | tubulin-specific chaperone C |
Neospora caninum | NCLIV_040280 | hypothetical protein, conserved |
Plasmodium berghei | PBANKA_1214100 | tubulin binding cofactor c, putative |
Plasmodium falciparum | PF3D7_1015700 | tubulin binding cofactor c, putative |
Plasmodium knowlesi | PKNH_0815800 | tubulin binding cofactor c, putative |
Plasmodium vivax | PVX_095005 | hypothetical protein |
Plasmodium yoelii | PY04613 | hypothetical protein |
Schistosoma japonicum | Sjp_0314470 | expressed protein |
Schistosoma mansoni | Smp_097710 | hypothetical protein |
Schmidtea mediterranea | mk4.005301.02 | Tubulin-specific chaperone C |
Trypanosoma brucei gambiense | Tbg972.11.10640 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.11.9480 | tubulin binding cofactor c, putative |
Trypanosoma congolense | TcIL3000.11.9950 | tubulin binding cofactor c, putative |
Trypanosoma cruzi | TcCLB.508851.140 | tubulin binding cofactor c, putative |
Trypanosoma cruzi | TcCLB.511589.80 | tubulin binding cofactor c, putative |
Toxoplasma gondii | TGME49_264950 | hypothetical protein |
Theileria parva | TP01_1194 | hypothetical protein |
Trichomonas vaginalis | TVAG_091930 | tubulin folding cofactor C, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.01.1240 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.1240 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.1240 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb11.01.1240 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_1214100 | Plasmodium berghei | Essential | plasmo |
TGME49_264950 | Toxoplasma gondii | Probably essential | sidik |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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.