pI: 9.7456 |
Length (AA): 702 |
MW (Da): 81733 |
Paralog Number:
1
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 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 |
---|---|---|---|---|---|---|---|---|---|
123 | 619 | 2qsh (A) | 125 | 630 | 22.00 | 0 | 1 | 0.773377 | 1.16 |
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_128561)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G16630 | DNA repair protein Rad4 |
Brugia malayi | Bm1_35290 | DNA repair protein Rad4 containing protein |
Brugia malayi | Bm1_03115 | DNA repair protein Rad4 containing protein |
Candida albicans | CaO19.14014 | similar to S. cerevisiae repairosome nucleotide excision repair protein. |
Candida albicans | CaO19.6722 | similar to S. cerevisiae repairosome nucleotide excision repair protein. |
Caenorhabditis elegans | CELE_Y76B12C.2 | Protein XPC-1 |
Dictyostelium discoideum | DDB_G0292296 | DNA repair protein Rad4 family protein |
Drosophila melanogaster | Dmel_CG8153 | mutagen-sensitive 210 |
Echinococcus granulosus | EgrG_000642500 | nucleotide excision repair protein |
Echinococcus multilocularis | EmuJ_000642500 | nucleotide excision repair protein |
Homo sapiens | ENSG00000154767 | xeroderma pigmentosum, complementation group C |
Leishmania braziliensis | LbrM.34.3360 | DNA-repair protein, putative |
Leishmania donovani | LdBPK_353500.1 | DNA-repair protein, putative |
Leishmania infantum | LinJ.35.3500 | DNA-repair protein, putative |
Leishmania major | LmjF.35.3450 | DNA-repair protein, putative |
Leishmania mexicana | LmxM.34.3450 | DNA-repair protein, putative |
Loa Loa (eye worm) | LOAG_03859 | DNA repair protein Rad4 containing protein |
Loa Loa (eye worm) | LOAG_10204 | hypothetical protein |
Loa Loa (eye worm) | LOAG_01614 | DNA repair protein Rad4 containing protein |
Mus musculus | ENSMUSG00000030094 | xeroderma pigmentosum, complementation group C |
Neospora caninum | NCLIV_012740 | DNA repair protein, putative |
Oryza sativa | 4345619 | Os08g0427500 |
Onchocerca volvulus | OVOC11468 | Alkylated DNA repair protein alkB homolog |
Saccharomyces cerevisiae | YER162C | Rad4p |
Schistosoma japonicum | Sjp_0001750 | DNA-repair protein complementing XP-C cells homolog, putative |
Schistosoma mansoni | Smp_021550 | DNA repair protein xp-C / rad4 |
Schmidtea mediterranea | mk4.003016.04 | Putative dna repair protein xp-C / rad4 |
Schmidtea mediterranea | mk4.002462.01 | Putative dna repair protein xp-C / rad4 |
Trypanosoma brucei gambiense | Tbg972.9.7210 | DNA-repair protein, putative |
Trypanosoma brucei | Tb927.9.11930 | DNA-repair protein, putative |
Trypanosoma congolense | TcIL3000_9_4920 | DNA-repair protein, putative |
Trypanosoma cruzi | TcCLB.507011.140 | DNA-repair protein, putative |
Trypanosoma cruzi | TcCLB.510665.40 | DNA-repair protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.3040 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.3040 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.3040 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb09.211.3040 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
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.