pI: 7.5236 |
Length (AA): 302 |
MW (Da): 34664 |
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 |
---|---|---|---|---|---|---|---|---|---|
2 | 131 | 2hcm (A) | 11 | 148 | 30.00 | 0 | 1 | 0.915164 | -1.93 |
2 | 150 | 1yz4 (A) | 5 | 155 | 32.00 | 0.0000000029 | 1 | 0.959077 | -1.64 |
2 | 148 | 4ki9 (A) | 27 | 185 | 37.00 | 0 | 1 | 1.03245 | -1.64 |
2 | 130 | 4jmk (A) | 161 | 298 | 40.00 | 0.00000000042 | 1 | 0.966852 | -1.58 |
2 | 130 | 4yr8 (G) | 159 | 296 | 36.00 | 0 | 1 | 0.953852 | -1.67 |
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_127982)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G18593 | dual specificity protein phosphatase-like protein |
Babesia bovis | BBOV_III006280 | dual specificity phosphatase, catalytic domain containing protein |
Brugia malayi | Bm1_24660 | Dual specificity phosphatase, catalytic domain containing protein |
Candida albicans | CaO19.11879 | potential dual specificity phosphatase similar to S. cerevisiae YVH1 (YIR026C) nitrogen starvation-induced tyrosine phosphatase |
Candida albicans | CaO19.4401 | potential dual specificity phosphatase similar to S. cerevisiae YVH1 (YIR026C) nitrogen starvation-induced tyrosine phosphatase |
Caenorhabditis elegans | CELE_C24F3.2 | Protein C24F3.2 |
Cryptosporidium hominis | Chro.20172 | dual-specificity protein phosphatase |
Cryptosporidium parvum | cgd2_1580 | conserved hypothetical protein |
Dictyostelium discoideum | DDB_G0281963 | hypothetical protein |
Drosophila melanogaster | Dmel_CG14211 | MAPK Phosphatase 4 |
Echinococcus granulosus | EgrG_000507100 | dual specificity protein phosphatase 12 |
Entamoeba histolytica | EHI_153220 | dual specificity protein phosphatase, putative |
Echinococcus multilocularis | EmuJ_000507100 | dual specificity protein phosphatase 12 |
Giardia lamblia | GL50803_36315 | Dual specificity protein phosphatase 12 |
Homo sapiens | ENSG00000081721 | dual specificity phosphatase 12 |
Leishmania braziliensis | LbrM.09.1300 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_091310.1 | hypothetical protein, conserved |
Leishmania infantum | LinJ.09.1310 | hypothetical protein, conserved |
Leishmania major | LmjF.09.1250 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.09.1250 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_10521 | dual specificity phosphatase |
Mus musculus | 102643029 | dual specificity protein phosphatase 12-like |
Mus musculus | ENSMUSG00000026659 | dual specificity phosphatase 12 |
Neospora caninum | NCLIV_050170 | hypothetical protein |
Oryza sativa | 4328898 | Os02g0251700 |
Oryza sativa | 4351431 | Os12g0133700 |
Oryza sativa | 4349715 | Os11g0136800 |
Onchocerca volvulus | OVOC2320 |
|
Plasmodium berghei | PBANKA_0407200 | dual specificity protein phosphatase |
Plasmodium falciparum | PF3D7_0309000 | dual specificity protein phosphatase |
Plasmodium knowlesi | PKNH_0833700 | dual specificity protein phosphatase, putative |
Plasmodium vivax | PVX_119565 | dual specificity protein phosphatase, putative |
Plasmodium yoelii | PY03455 | putative dual-specificity protein phosphatase |
Saccharomyces cerevisiae | YIR026C | Yvh1p |
Schistosoma japonicum | Sjp_0059170 | ko:K01090 protein phosphatase [EC3.1.3.16], putative |
Schistosoma mansoni | Smp_081510 | hypothetical protein |
Schmidtea mediterranea | mk4.002546.00 | LD31102p |
Schmidtea mediterranea | mk4.001002.16 | LD31102p |
Trypanosoma brucei gambiense | Tbg972.11.14950 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.11.13390 | hypothetical protein, conserved |
Trypanosoma congolense | TcIL3000.11.13760 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.510359.140 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.506755.130 | hypothetical protein, conserved |
Toxoplasma gondii | TGME49_235890 | dual-specificity protein phosphatase |
Theileria parva | TP02_0369 | dual-specificity protein phosphatase, putative |
Trichomonas vaginalis | TVAG_306000 | hyvh1 dual specificity phosphatase, putative |
Trichomonas vaginalis | TVAG_484590 | hyvh1 dual specificity phosphatase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.01.4990 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.4990 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.4990 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb11.01.4990 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_C24F3.2 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_0407200 | Plasmodium berghei | Slow | plasmo |
TGME49_235890 | Toxoplasma gondii | Probably essential | sidik |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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.