pI: 9.8881 |
Length (AA): 109 |
MW (Da): 12263 |
Paralog Number:
1
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 1
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_130820)
Species | Accession | Gene Product |
---|---|---|
Brugia malayi | Bm1_30150 | hypothetical protein |
Caenorhabditis elegans | CELE_R13A5.9 | Protein R13A5.9 |
Dictyostelium discoideum | DDB_G0270720 | hypothetical protein |
Dictyostelium discoideum | DDB_G0290423 | hypothetical protein |
Dictyostelium discoideum | DDB_G0268230 | hypothetical protein |
Drosophila melanogaster | Dmel_CG12858 | CG12858 gene product from transcript CG12858-RB |
Echinococcus multilocularis | EmuJ_000573300 | major facilitator superfamily domain containing protein |
Homo sapiens | ENSG00000151690 | major facilitator superfamily domain containing 6 |
Loa Loa (eye worm) | LOAG_11482 | hypothetical protein |
Loa Loa (eye worm) | LOAG_09616 | hypothetical protein |
Mus musculus | ENSMUSG00000041439 | major facilitator superfamily domain containing 6 |
Onchocerca volvulus | OVOC8041 |
|
Schistosoma japonicum | Sjp_0101320 | Macrophage MHC class I receptor 2, putative |
Schistosoma japonicum | Sjp_0095840 | Macrophage MHC class I receptor 2 homolog, putative |
Schistosoma mansoni | Smp_145040 | hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_R13A5.9 | Caenorhabditis elegans | slow growth | wormbase |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
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.