pI: 4.5327 |
Length (AA): 514 |
MW (Da): 58630 |
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 2 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 |
---|---|---|---|---|---|---|---|---|---|
255 | 393 | 3nfq (A) | 9 | 153 | 39.00 | 0 | 1 | 0.865028 | -1.99 |
268 | 395 | 2xpp (A) | 67 | 193 | 34.00 | 0 | 1 | 0.892627 | -2.09 |
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_128599)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G19000 | INTERACTS WITH SPT6-like protein IWS2 |
Arabidopsis thaliana | AT1G32130 | IWS1-like protein |
Babesia bovis | BBOV_II003510 | conserved hypothetical protein |
Brugia malayi | Bm1_13230 | IWS1 C-terminus family protein |
Candida albicans | CaO19.13630 | similar to S. cerevisiae YPR133C |
Candida albicans | CaO19.6252 | similar to S. cerevisiae YPR133C |
Caenorhabditis elegans | CELE_F13B12.1 | Protein F13B12.1 |
Cryptosporidium hominis | Chro.50270 | hypothetical protein |
Cryptosporidium parvum | cgd5_1150 | iwsip-like protein |
Dictyostelium discoideum | DDB_G0274327 | IWS1 family protein |
Drosophila melanogaster | Dmel_CG9915 | CG9915 gene product from transcript CG9915-RC |
Echinococcus granulosus | EgrG_000246900 | protein iws1 |
Echinococcus multilocularis | EmuJ_000246900 | protein iws1 |
Homo sapiens | ENSG00000163166 | IWS1 homolog (S. cerevisiae) |
Loa Loa (eye worm) | LOAG_11637 | IWS1 family protein |
Mus musculus | ENSMUSG00000024384 | IWS1 homolog (S. cerevisiae) |
Neospora caninum | NCLIV_045710 | hypothetical protein |
Oryza sativa | 4325206 | Os01g0147200 |
Plasmodium berghei | PBANKA_0938900 | IWS1-like protein, putative |
Plasmodium falciparum | PF3D7_1108000 | IWS1-like protein, putative |
Plasmodium knowlesi | PKNH_0905600 | IWS1-like protein, putative |
Plasmodium vivax | PVX_091080 | hypothetical protein, conserved |
Plasmodium yoelii | PY03357 | unnamed protein product, putative |
Saccharomyces cerevisiae | YPR133C | Spn1p |
Schistosoma japonicum | Sjp_0215200 | IWS1 homolog, putative |
Schistosoma mansoni | Smp_008500.1 | Transcription factor IWS1 |
Schistosoma mansoni | Smp_008500.2 | Transcription factor IWS1 |
Schmidtea mediterranea | mk4.004659.02 | Protein IWS1 homolog |
Schmidtea mediterranea | mk4.000188.13 | Protein IWS1 homolog |
Schmidtea mediterranea | mk4.001435.02 | Protein IWS1 homolog |
Schmidtea mediterranea | mk4.003340.00 | Protein IWS1 homolog |
Schmidtea mediterranea | mk4.001214.02 | Protein IWS1 homolog |
Schmidtea mediterranea | mk4.004572.00 | Protein IWS1 homolog |
Toxoplasma gondii | TGME49_227560 | IWS1 transcription factor, putative |
Theileria parva | TP04_0233 | hypothetical protein |
Trichomonas vaginalis | TVAG_267140 | transcription factor IWS1, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_F13B12.1 | Caenorhabditis elegans | sterile | wormbase |
YPR133C | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0938900 | Plasmodium berghei | Slow | plasmo |
TGME49_227560 | Toxoplasma gondii | Essentiality uncertain | sidik |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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 |
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.