pI: 6.2969 |
Length (AA): 849 |
MW (Da): 94918 |
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 is 1 model calculated for this protein. More info on
this model, including the
model itself is available at:
Modbase
Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
---|---|---|---|---|---|---|---|---|---|
26 | 158 | 4rgw (B) | 11 | 154 | 42.00 | 0 | 0.99 | 0.882824 | 0.5 |
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_128786)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G55300 | TBP-associated factor 7 |
Brugia malayi | Bm1_55960 | TAFII55 protein conserved region containing protein |
Candida albicans | CaO19.9147 | component of the TAF(II) complex |
Candida albicans | CaO19.1574 | component of the TAF(II) complex |
Caenorhabditis elegans | CELE_Y111B2A.16 | Protein TAF-7.2 |
Caenorhabditis elegans | CELE_F54F7.1 | Protein TAF-7.1 |
Dictyostelium discoideum | DDB_G0271338 | TFIID subunit |
Drosophila melanogaster | Dmel_CG2670 | TBP-associated factor 7 |
Echinococcus granulosus | EgrG_000514850 | transcription initiation factor tfiid 55 kD subunit-related |
Entamoeba histolytica | EHI_137090 | TFIID subunit, putative |
Echinococcus multilocularis | EmuJ_000514850 | transcription initiation factor tfiid 55 kD subunit-related |
Homo sapiens | ENSG00000178913 | TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 55kDa |
Homo sapiens | ENSG00000102387 | TAF7-like RNA polymerase II, TATA box binding protein (TBP)-associated factor, 50kDa |
Loa Loa (eye worm) | LOAG_03972 | hypothetical protein |
Mus musculus | ENSMUSG00000074734 | RIKEN cDNA 4933416C03 gene |
Mus musculus | ENSMUSG00000051316 | TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor |
Oryza sativa | 4338489 | Os05g0347000 |
Onchocerca volvulus | OVOC8551 | Transcription initiation factor TFIID subunit 7 homolog |
Saccharomyces cerevisiae | YMR227C | Taf7p |
Schistosoma japonicum | Sjp_0071650 | ko:K03132 transcription initiation factor TFIID subunit D6, putative |
Schistosoma mansoni | Smp_169300 | transcription initiation factor tfiid 55 kD subunit-related |
Schmidtea mediterranea | mk4.001917.05 | |
Schmidtea mediterranea | mk4.004390.02 | |
Trichomonas vaginalis | TVAG_040830 | transcription initiation factor TFIID subunit, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
YMR227C | Saccharomyces cerevisiae | inviable | yeastgenome |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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.