pI: 5.9472 |
Length (AA): 542 |
MW (Da): 59772 |
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 |
---|---|---|---|---|---|---|---|---|---|
108 | 514 | 5m52 (B) | 373 | 897 | 27.00 | 0.95 | 1 | 0.799523 | 0.84 |
351 | 540 | 4ern (A) | 502 | 696 | 34.00 | 0 | 1 | 0.824054 | -1.02 |
398 | 470 | 5lm7 (A) | 80 | 161 | 42.00 | 0.81 | 0.06 | 0.246286 | 1.57 |
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_127208)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G41360 | DNA repair helicase XPB2 |
Arabidopsis thaliana | AT5G41370 | DNA repair helicase XPB1 |
Babesia bovis | BBOV_III010030 | DNA repair helicase rad25 family protein |
Brugia malayi | Bm1_20800 | helicase |
Candida albicans | CaO19.2857 | DNA helicase |
Candida albicans | CaO19.10376 | DNA helicase |
Caenorhabditis elegans | CELE_Y66D12A.15 | Protein Y66D12A.15 |
Cryptosporidium hominis | Chro.80227 | hypothetical protein |
Cryptosporidium parvum | cgd8_1940 | RAD25, helicase involved in DNA repair |
Dictyostelium discoideum | DDB_G0278729 | transcription factor IIH subunit |
Drosophila melanogaster | Dmel_CG8019 | haywire |
Echinococcus granulosus | EgrG_000600500 | rad25:xp B DNA repair helicase |
Entamoeba histolytica | EHI_088430 | DNA repair helicase, putative |
Entamoeba histolytica | EHI_077260 | DNA repair helicase, putative |
Echinococcus multilocularis | EmuJ_000600500 | rad25:xp B DNA repair helicase |
Giardia lamblia | GL50803_16512 | DNA repair helicase TFIIH P90 |
Homo sapiens | ENSG00000163161 | excision repair cross-complementation group 3 |
Leishmania braziliensis | LbrM.29.0600 | DNA repair helicase, putative |
Leishmania braziliensis | LbrM.32.4160 | helicase, putative,DNA repair helicase, putative |
Leishmania donovani | LdBPK_290610.1 | tfiih basal transcription factor complex helicase xpb subunit |
Leishmania donovani | LdBPK_324070.1 | TFIIH basal transcription factor complex helicase XPB subunit, putative |
Leishmania infantum | LinJ.29.0610 | DNA repair helicase, putative |
Leishmania infantum | LinJ.32.4070 | helicase, putative,DNA repair helicase, putative |
Leishmania major | LmjF.32.3920 | helicase, putative,DNA repair helicase, putative |
Leishmania major | LmjF.29.0590 | DNA repair helicase, putative |
Leishmania mexicana | LmxM.08_29.0590 | DNA repair helicase, putative |
Leishmania mexicana | LmxM.31.3920 | helicase, putative,DNA repair helicase, putative |
Loa Loa (eye worm) | LOAG_00638 | helicase |
Mycobacterium leprae | ML2157 | PROBABLE DNA HELICASE ERCC3 |
Mus musculus | ENSMUSG00000024382 | excision repair cross-complementing rodent repair deficiency, complementation group 3 |
Mycobacterium tuberculosis | Rv0861c | DNA helicase Ercc3 |
Mycobacterium ulcerans | MUL_0289 | DNA helicase Ercc3 |
Neospora caninum | NCLIV_036860 | hypothetical protein |
Oryza sativa | 4325640 | Os01g0691600 |
Plasmodium berghei | PBANKA_0520500 | DNA repair helicase RAD25, putative |
Plasmodium falciparum | PF3D7_1037600 | DNA repair helicase RAD25, putative |
Plasmodium knowlesi | PKNH_0622100 | DNA repair helicase RAD25, putative |
Plasmodium vivax | PVX_110880 | DNA repair helicase RAD25, putative |
Plasmodium yoelii | PY04074 | RepB-related |
Saccharomyces cerevisiae | YIL143C | TFIIH/NER complex ATPase/helicase subunit SSL2 |
Schistosoma japonicum | Sjp_0116080 | ko:K01509 adenosinetriphosphatase [EC3.6.1.3], putative |
Schistosoma japonicum | Sjp_0104520 | TFIIH basal transcription factor complex helicase XPB subunit, putative |
Schistosoma mansoni | Smp_165580 | rad25/xp-B DNA repair helicase |
Schmidtea mediterranea | mk4.003577.00 | |
Schmidtea mediterranea | mk4.004232.06 | |
Schmidtea mediterranea | mk4.037825.00 | TFIIH basal transcription factor complex helicase XPB subunit |
Schmidtea mediterranea | mk4.039578.00 | TFIIH basal transcription factor complex helicase XPB subunit |
Trypanosoma brucei gambiense | Tbg972.3.5740 | DNA repair helicase and transcription factor protein, putative,Transcription factor II H complex, XPB subunit, putative homologu |
Trypanosoma brucei gambiense | Tbg972.11.18270 | DNA repair helicase and transcription factor protein, putative,DNA repair helicase, putative,transcription factor II H complex, |
Trypanosoma brucei | Tb927.3.5100 | tfiih basal transcription factor complex helicase xpb subunit |
Trypanosoma brucei | Tb927.11.16270 | TFIIH basal transcription factor complex helicase XPB subunit, putative |
Trypanosoma congolense | TcIL3000.11.16180 | TFIIH basal transcription factor complex helicase XPB subunit, putative |
Trypanosoma congolense | TcIL3000_3_3090 | tfiih basal transcription factor complex helicase xpb subunit |
Trypanosoma cruzi | TcCLB.508411.90 | tfiih basal transcription factor complex helicase xpb subunit |
Trypanosoma cruzi | TcCLB.511527.20 | DNA repair helicase and transcription factor protein, putative |
Trypanosoma cruzi | TcCLB.510149.50 | tfiih basal transcription factor complex helicase xpb subunit |
Toxoplasma gondii | TGME49_269660 | TFIIH basal transcription factor complex helicase XPB subunit |
Toxoplasma gondii | TGME49_302450 | TFIIH basal transcription factor complex helicase XPB subunit, putative |
Treponema pallidum | TP0380 | DNA repair helicase |
Theileria parva | TP02_0144 | DNA helicase, putative |
Trichomonas vaginalis | TVAG_167010 | rad25/xp-B DNA repair helicase, putative |
Trichomonas vaginalis | TVAG_044250 | rad25/xp-B DNA repair helicase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.3.5100 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.3.5100 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.3.5100 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.3.5100 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb11.01.7950 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.7950 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.7950 | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb11.01.7950 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y66D12A.15 | Caenorhabditis elegans | embryonic lethal | wormbase |
YIL143C | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0520500 | Plasmodium berghei | Essential | plasmo |
TGME49_302450 | Toxoplasma gondii | Probably essential | sidik |
TGME49_269660 | Toxoplasma gondii | Probably essential | sidik |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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.