pI: 7.1859 |
Length (AA): 136 |
MW (Da): 15514 |
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 3 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 |
---|---|---|---|---|---|---|---|---|---|
27 | 135 | 1hv2 (A) | 1 | 98 | 22.00 | 0 | 1 | 0.981771 | -0.61 |
30 | 136 | 4ajy (C) | 17 | 112 | 32.00 | 0 | 1 | 1.07666 | -0.85 |
31 | 136 | 2c9w (C) | 18 | 112 | 33.00 | 0 | 0.99 | 0.868712 | -0.21 |
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 |
---|---|---|---|
Mid 40-60% percentile | Procyclic. | Siegel TN |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Bloodstream Form. | Siegel TN |
Siegel TN | Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites. |
Ortholog group members (OG5_128120)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G59140 | BTB/POZ domain-containing protein |
Brugia malayi | Bm1_21630 | transcription elongation factor B polypeptide 1, putative |
Candida albicans | CaO19.14139 | transcriptional elongation factor |
Candida albicans | CaO19.6849 | transcriptional elongation factor |
Caenorhabditis elegans | CELE_Y82E9BR.15 | Protein ELC-1 |
Cryptosporidium hominis | Chro.60322 | hypothetical protein |
Dictyostelium discoideum | DDB_G0284201 | hypothetical protein |
Drosophila melanogaster | Dmel_CG9291 | Elongin C |
Echinococcus granulosus | EgrG_000040100 | transcription elongation factor b polypeptide 1 |
Entamoeba histolytica | EHI_152700 | hypothetical protein |
Echinococcus multilocularis | EmuJ_000040100 | transcription elongation factor b polypeptide 1 |
Homo sapiens | ENSG00000154582 | transcription elongation factor B (SIII), polypeptide 1 (15kDa, elongin C) |
Loa Loa (eye worm) | LOAG_01824 | ELC-1 protein |
Mus musculus | 102642819 | transcription elongation factor B polypeptide 1-like |
Mus musculus | 100503053 | predicted gene 14517 |
Mus musculus | ENSMUSG00000079658 | transcription elongation factor B (SIII), polypeptide 1 |
Mus musculus | 100504036 | predicted gene, 20026 |
Mus musculus | 102637110 | predicted gene, 34005 |
Mus musculus | 102631956 | predicted gene, 30155 |
Neospora caninum | NCLIV_042880 | elongin c, putative |
Oryza sativa | 4351227 | Os11g0707700 |
Onchocerca volvulus | OVOC2291 | Transcription elongation factor B polypeptide 1 homolog |
Saccharomyces cerevisiae | YPL046C | elongin C |
Schistosoma japonicum | Sjp_0074960 | ko:K03872 transcription elongation factor B, polypeptide 1, putative |
Schistosoma mansoni | Smp_009320.1 | hypothetical protein |
Schistosoma mansoni | Smp_009320.2 | hypothetical protein |
Schmidtea mediterranea | mk4.004810.02 | Transcription elongation factor B polypeptide 1 |
Trypanosoma brucei gambiense | Tbg972.11.8510 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.11.7430 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.508241.70 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.511151.39 | hypothetical protein, conserved |
Toxoplasma gondii | TGME49_291010 | hypothetical protein |
Trichomonas vaginalis | TVAG_482240 | elongin C protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.02.5330 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.02.5330 this record | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb11.02.5330 this record | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb11.02.5330 this record | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y82E9BR.15 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_Y82E9BR.15 | Caenorhabditis elegans | larval arrest | wormbase |
TGME49_291010 | Toxoplasma gondii | Probably essential | sidik |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
Affected Entity | Phenotypic quality | Occurs in | Occurs at | Evidence | Observed in | Drugs/Inhibitors |
---|---|---|---|---|---|---|
cell proliferation (GO:0008283) | normal (PATO:0000461) | bloodstream stage trypomastigotes (PLO:0027) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | normal cell proliferation (no significant loss or gain of fitness) in bloodstream forms (stage 3 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | decreased (PATO:0000468) | bloodstream stage trypomastigotes (PLO:0027) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | decreased cell proliferation (significant loss of fitness) in bloodstream forms (stage 6 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | decreased (PATO:0000468) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | decreased cell proliferation (significant loss of fitness) in differentiation of procyclic to bloodstream forms . | References: | 21363968 |
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 |
---|---|---|---|
Homo sapiens | transcription elongation factor B (SIII), polypeptide 1 (15kDa, elongin C) | Compounds | References |
1 literature reference was collected for this gene.