pI: 6.4255 |
Length (AA): 281 |
MW (Da): 31537 |
Paralog Number:
1
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 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 |
---|---|---|---|---|---|---|---|---|---|
2 | 276 | 3u0a (A) | 2 | 276 | 86.00 | 0 | 1 | 1.93765 | -0.74 |
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_129049)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G01710 | acyl-CoA thioesterase family protein |
Arabidopsis thaliana | AT4G00520 | acyl-CoA thioesterase family protein |
Candida albicans | CaO19.11605 | identical to nonallelic CaP19.5218, possible overlap with contig19-10221 |
Candida albicans | CaO19.12683 | one of five genes similar to acyl-CoA thioesterase |
Candida albicans | CaO19.5217 | one of five genes similar to acyl-CoA thioesterase |
Candida albicans | CaO19.12684 | one of five genes similar to acyl-CoA thioesterase |
Candida albicans | CaO19.4122 | one of five genes similar to acyl-CoA thioesterase |
Candida albicans | CaO19.5216 | one of five genes similar to acyl-CoA thioesterase |
Caenorhabditis elegans | CELE_C37H5.13 | Protein C37H5.13, isoform C |
Caenorhabditis elegans | CELE_C17C3.1 | Protein C17C3.1, isoform D |
Caenorhabditis elegans | CELE_F25E2.3 | Protein F25E2.3 |
Escherichia coli | b0452 | acyl-CoA thioesterase 2 |
Homo sapiens | ENSG00000101473 | acyl-CoA thioesterase 8 |
Loa Loa (eye worm) | LOAG_13498 | hypothetical protein |
Loa Loa (eye worm) | LOAG_13373 | hypothetical protein |
Mycobacterium leprae | ML1278 | Probable acyl-CoA thioesterase II TesB |
Mus musculus | ENSMUSG00000017307 | acyl-CoA thioesterase 8 |
Mycobacterium tuberculosis | Rv1618 | Probable acyl-CoA thioesterase II TesB1 |
Mycobacterium tuberculosis | Rv2605c | Probable acyl-CoA thioesterase II TesB2 (TEII) |
Mycobacterium ulcerans | MUL_1599 | acyl-CoA thioesterase II TesB1 |
Mycobacterium ulcerans | MUL_3249 | acyl-CoA thioesterase II TesB2 |
Oryza sativa | 4336637 | Os04g0558400 |
Onchocerca volvulus | OVOC10131 |
|
Saccharomyces cerevisiae | YJR019C | Tes1p |
Schistosoma japonicum | Sjp_0051990 | expressed protein |
Schistosoma japonicum | Sjp_0052000 | ko:K01068 palmitoyl-CoA hydrolase [EC3.1.2.2], putative |
Schistosoma mansoni | Smp_150820 | acyl-CoA thioesterase-related |
Schmidtea mediterranea | mk4.014754.02 | |
Trypanosoma cruzi | TcCLB.504149.55 | acyl-CoA thioesterase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
b0452 | Escherichia coli | non-essential | goodall |
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 |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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.