pI: 6.8008 |
Length (AA): 441 |
MW (Da): 50116 |
Paralog Number:
0
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 5 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 |
---|---|---|---|---|---|---|---|---|---|
9 | 247 | 4n5a (A) | 332 | 558 | 9.00 | 0 | 0.02 | 0.58975 | -0.39 |
266 | 432 | 2hhl (A) | 6 | 168 | 42.00 | 0 | 1 | 0.858485 | -0.18 |
279 | 436 | 2ght (A) | 77 | 234 | 45.00 | 0 | 1 | 0.928177 | -0.56 |
283 | 435 | 2q5e (A) | 91 | 244 | 46.00 | 0 | 1 | 0.949739 | -0.84 |
285 | 379 | 4xpz (A) | 157 | 268 | 35.00 | 0.000000031 | 0.98 | 0.46422 | 0.22 |
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_130261)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G11860 | SCP1-like small phosphatase 5 |
Brugia malayi | Bm1_35985 | NLI interacting factor-like phosphatase family protein |
Caenorhabditis elegans | CELE_Y47D9A.2 | Protein SCPL-3, isoform B |
Cryptosporidium hominis | Chro.40368 | ENSANGP00000011443 |
Cryptosporidium parvum | cgd4_3240 | possible NLI interacting factor CTD-like phosphatase |
Dictyostelium discoideum | DDB_G0290365 | CTD small phosphatase-like protein 2 |
Echinococcus granulosus | EgrG_001061300 | CTD small phosphatase protein 2 |
Echinococcus multilocularis | EmuJ_001061300 | CTD small phosphatase protein 2 |
Homo sapiens | ENSG00000137770 | CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 |
Leishmania braziliensis | LbrM.26.0150 | nuclear lim interactor-interacting factor-like protein |
Leishmania donovani | LdBPK_260140.1 | nuclear lim interactor-interacting factor-like protein |
Leishmania infantum | LinJ.26.0140 | nuclear lim interactor-interacting factor-like protein |
Leishmania major | LmjF.26.0160 | nuclear lim interactor-interacting factor-like protein |
Leishmania mexicana | LmxM.26.0160 | nuclear lim interactor-interacting factor-like protein |
Loa Loa (eye worm) | LOAG_03651 | SCP small domain phosphatase |
Mus musculus | ENSMUSG00000033411 | CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 |
Neospora caninum | NCLIV_024550 | Zgc:77714, related |
Oryza sativa | 4334791 | Os03g0850100 |
Schistosoma japonicum | Sjp_0034690 | CTD small phosphatase-like protein 2, putative |
Schistosoma mansoni | Smp_159170 | nuclear lim interactor-interacting factor-related |
Schmidtea mediterranea | mk4.005794.00 | Nuclear lim interactor-interacting factor-related |
Toxoplasma gondii | TGME49_263380 | Dullard family phosphatase domain-containing protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
TGME49_263380 | Toxoplasma gondii | Probably non-essential | sidik |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
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.