pI: 9.5539 |
Length (AA): 229 |
MW (Da): 26024 |
Paralog Number:
2
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:
PDB Structures:
Ortholog group members (OG5_132068)
Species | Accession | Gene Product |
---|---|---|
Dictyostelium discoideum | DDB_G0293034 | hypothetical protein |
Dictyostelium discoideum | DDB_G0286197 | hypothetical protein |
Drosophila melanogaster | Dmel_CG6012 | CG6012 gene product from transcript CG6012-RA |
Entamoeba histolytica | EHI_118210 | estradiol 17-beta-dehydrogenase, putative |
Leishmania braziliensis | LbrM.33.1860 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_331690.1 | 3-ketoacyl-CoA reductase, putative |
Leishmania infantum | LinJ.33.1690 | hypothetical protein, conserved |
Leishmania major | LmjF.33.1590 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.32.1590 | hypothetical protein, conserved |
Oryza sativa | 4350399 | Os11g0432600 |
Trypanosoma brucei gambiense | Tbg972.10.14760 | short-chain dehydrogenase, putative |
Trypanosoma brucei | Tb927.10.12240 | 3-ketoacyl-CoA reductase, putative |
Trypanosoma congolense | TcIL3000_10_10470 | 3-ketoacyl-CoA reductase, putative |
Trypanosoma cruzi | TcCLB.509213.100 | 3-ketoacyl-CoA reductase, putative |
Trypanosoma cruzi | TcCLB.510257.60 | 3-ketoacyl-CoA reductase, putative |
Trichomonas vaginalis | TVAG_041000 | short-chain dehydrogenase, putative |
Trichomonas vaginalis | TVAG_174570 | steroid dehydrogenase, putative |
Trichomonas vaginalis | TVAG_429960 | estradiol 17 beta-dehydrogenase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.12240 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.12240 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.12240 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.12240 | Trypanosoma brucei | significant loss 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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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.