pI: 6.031 |
Length (AA): 704 |
MW (Da): 80447 |
Paralog Number:
2
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 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 |
---|---|---|---|---|---|---|---|---|---|
83 | 170 | 2vl7 (A) | 139 | 226 | 30.00 | 0.51 | 0.08 | 0.0377 | 1.66 |
200 | 379 | 4uvj (A) | 835 | 1047 | 24.00 | 0.84 | 0.93 | 0.457382 | -0.28 |
398 | 651 | 3crv (A) | 317 | 542 | 27.00 | 0.0081 | 1 | 0.445495 | 0.76 |
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_127294)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G20720 | RAD3-like DNA-binding helicase protein |
Arabidopsis thaliana | AT1G20750 | RAD3-like DNA-binding helicase protein |
Arabidopsis thaliana | AT1G79950 | RAD3-like DNA-binding helicase protein |
Babesia bovis | BBOV_III006210 | hypothetical protein |
Babesia bovis | BBOV_III008820 | DNA repair helicase (rad3) family protein |
Brugia malayi | Bm1_16815 | BRCA1-binding helicase-like protein BACH1 |
Brugia malayi | Bm1_30515 | DEAD_2 family protein |
Caenorhabditis elegans | CELE_F25H2.13 | Protein RTEL-1 |
Caenorhabditis elegans | CELE_F33H2.1 | Protein DOG-1 |
Cryptosporidium hominis | Chro.60307 | helicase, belonging to UvrD family |
Cryptosporidium parvum | cgd6_2660 | DNA repair helicase |
Dictyostelium discoideum | DDB_G0286621 | DEAD/DEAH box helicase |
Drosophila melanogaster | Dmel_CG4078 | CG4078 gene product from transcript CG4078-RB |
Echinococcus granulosus | EgrG_000640000 | regulator of telomere length splice variant |
Echinococcus granulosus | EgrG_000961200 | Fanconi anemia group J protein |
Echinococcus granulosus | EgrG_000961300 | Fanconi anemia group J protein |
Entamoeba histolytica | EHI_054240 | DNA repair helicase, putative |
Echinococcus multilocularis | EmuJ_000640000 | regulator of telomere length splice variant regulator of telomere elongation helicase |
Echinococcus multilocularis | EmuJ_000961200 | Fanconi anemia group J protein |
Giardia lamblia | GL50803_5631 | TFIIH basal transcription factor complex helicase subunit |
Homo sapiens | 83990 | BRCA1 interacting protein C-terminal helicase 1 |
Homo sapiens | ENSG00000258366 | regulator of telomere elongation helicase 1 |
Leishmania braziliensis | LbrM.29.2630 | helicase, putative |
Leishmania donovani | LdBPK_292770.1 | helicase, putative |
Leishmania infantum | LinJ.29.2770 | helicase, putative |
Leishmania major | LmjF.29.2660 | helicase, putative |
Leishmania mexicana | LmxM.08_29.2660 | helicase, putative |
Loa Loa (eye worm) | LOAG_05322 | hypothetical protein |
Loa Loa (eye worm) | LOAG_10252 | hypothetical protein |
Loa Loa (eye worm) | LOAG_11323 | hypothetical protein |
Mus musculus | ENSMUSG00000034329 | BRCA1 interacting protein C-terminal helicase 1 |
Mus musculus | ENSMUSG00000038685 | regulator of telomere elongation helicase 1 |
Neospora caninum | NCLIV_004030 | hypothetical protein |
Oryza sativa | 4326378 | Os01g0592900 |
Oryza sativa | 4347791 | Os09g0551800 |
Plasmodium berghei | PBANKA_1034100 | FANCJ-like helicase, putative |
Plasmodium falciparum | PF3D7_1408400 | FANCJ-like helicase, putative |
Plasmodium knowlesi | PKNH_1350000 | FANCJ-like helicase, putative |
Plasmodium vivax | PVX_086025 | DNA repair helicase, putative |
Plasmodium yoelii | PY06657 | DNA repair helicase, putative |
Schistosoma japonicum | Sjp_0309300 | Regulator of telomere elongation helicase 1, putative |
Schistosoma japonicum | Sjp_0310020 | Regulator of telomere elongation helicase 1, putative |
Schistosoma japonicum | Sjp_0309350 | ko:K01509 adenosinetriphosphatase [EC3.6.1.3], putative |
Schistosoma japonicum | Sjp_0045750 | Fanconi anemia group J protein homolog, putative |
Schistosoma mansoni | Smp_136280 | regulator of telomere elongation helicase 1 rtel1 |
Schistosoma mansoni | Smp_173440 | brca1 interacting protein C-terminal helicase 1 brip1 |
Schmidtea mediterranea | mk4.000667.07 | |
Schmidtea mediterranea | mk4.003032.00 | Fanconi anemia group J protein |
Schmidtea mediterranea | mk4.000667.08 | RTEL1 |
Schmidtea mediterranea | mk4.014273.00 | |
Schmidtea mediterranea | mk4.000667.06 | Regulator of telomere elongation helicase 1 homolog |
Schmidtea mediterranea | mk4.000996.00 | Fanconi anemia group J protein |
Schmidtea mediterranea | mk4.015556.01 | Fanconi anemia group J protein |
Schmidtea mediterranea | mk4.015556.00 | Fanconi anemia group J protein |
Schmidtea mediterranea | mk4.003032.01 | Fanconi anemia group J protein |
Schmidtea mediterranea | mk4.003032.02 | Fanconi anemia group J protein |
Trypanosoma brucei gambiense | Tbg972.3.3240 | helicase, putative |
Trypanosoma brucei | Tb927.3.3090 | helicase, putative |
Trypanosoma congolense | TcIL3000_3_2000 | helicase, putative |
Trypanosoma cruzi | TcCLB.508153.500 | helicase, putative |
Trypanosoma cruzi | TcCLB.506697.40 | helicase, putative |
Toxoplasma gondii | TGME49_209770 | helicase, putative |
Theileria parva | TP04_0785 | DNA repair helicase, putative |
Trichomonas vaginalis | TVAG_067090 | brca1 interacting protein C-terminal helicase 1 brip1, putative |
Trichomonas vaginalis | TVAG_013790 | regulator of telomere elongation helicase 1 rtel1, putative |
Trichomonas vaginalis | TVAG_288470 | regulator of telomere elongation helicase 1 rtel1, putative |
Trichomonas vaginalis | TVAG_390170 | DNA repair helicase rad3/xp-D, putative |
Trichomonas vaginalis | TVAG_445200 | regulator of telomere elongation helicase 1 rtel1, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.3.3090 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.3.3090 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.3.3090 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.3.3090 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_1034100 | Plasmodium berghei | Slow | plasmo |
TGME49_209770 | 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 |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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.