pI: 4.763 |
Length (AA): 1307 |
MW (Da): 141199 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
233 | 325 | 5gjk (A) | 446 | 538 | 84.00 | 0 | 1 | 1.04636 | -1.73 |
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_127525)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G34430 | SWI/SNF complex subunit SWI3D |
Arabidopsis thaliana | AT1G21700 | SWI/SNF complex subunit SWI3C |
Arabidopsis thaliana | AT2G33610 | switch subunit 3 |
Arabidopsis thaliana | AT2G47620 | SWI/SNF complex subunit SWI3A |
Brugia malayi | Bm1_20550 | SWIRM domain containing protein |
Candida albicans | CaO19.4488 | General RNA polymerase II transcription factor |
Candida albicans | CaO19.11964 | General RNA polymerase II transcription factor |
Candida albicans | CaO19.7234 | similar to eighth largest subunit (RSC8) of S. cerevisiae nucleosome remodeling complex |
Caenorhabditis elegans | CELE_Y113G7B.23 | Protein SWSN-1, isoform B |
Cryptosporidium hominis | Chro.20189 | erythrocyte membrane protein PFEMP3 |
Cryptosporidium parvum | cgd2_1740 | RSC8 ortholog with a swirm domain, ZZ finger and Myb |
Dictyostelium discoideum | DDB_G0277033 | SWIRM domain-containing protein |
Drosophila melanogaster | Dmel_CG18740 | moira |
Echinococcus granulosus | EgrG_001118700 | SWI:SNF complex subunit SMARCC2 |
Echinococcus multilocularis | EmuJ_001118700 | SWI:SNF complex subunit SMARCC2 |
Homo sapiens | ENSG00000139613 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 |
Homo sapiens | ENSG00000173473 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 |
Loa Loa (eye worm) | LOAG_04430 | hypothetical protein |
Mus musculus | ENSMUSG00000032481 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 |
Mus musculus | ENSMUSG00000025369 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 |
Neospora caninum | NCLIV_013840 | hypothetical protein |
Oryza sativa | 4336176 | Os04g0480300 |
Oryza sativa | 4349954 | Os11g0183700 |
Oryza sativa | 4328597 | Os02g0194000 |
Oryza sativa | 9266524 | Os12g0176600 |
Oryza sativa | 4334928 | Os04g0110300 |
Saccharomyces cerevisiae | YFR037C | Rsc8p |
Saccharomyces cerevisiae | YJL176C | Swi3p |
Schistosoma japonicum | Sjp_0076870 | SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily C member 2, putative |
Schistosoma mansoni | Smp_152650 | SWI/SNF complex-related |
Schmidtea mediterranea | mk4.002006.06 | Brahma associated protein 155 kDa |
Schmidtea mediterranea | mk4.035810.01 | Brahma associated protein 155 kDa |
Schmidtea mediterranea | mk4.034641.00 | Brahma associated protein 155 kDa |
Schmidtea mediterranea | mk4.035810.02 | Brahma associated protein 155 kDa |
Schmidtea mediterranea | mk4.034641.01 | Brahma associated protein 155 kDa |
Schmidtea mediterranea | mk4.002752.01 | SWI/SNF complex subunit SMARCC-1 |
Toxoplasma gondii | TGME49_286920 | SWIRM domain-containing protein |
Theileria parva | TP03_0714 | hypothetical protein |
Trichomonas vaginalis | TVAG_288520 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_002270 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_153470 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_Y113G7B.23 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_Y113G7B.23 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_Y113G7B.23 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_Y113G7B.23 | Caenorhabditis elegans | slow growth | wormbase |
CELE_Y113G7B.23 | Caenorhabditis elegans | sterile | wormbase |
YFR037C | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_286920 | Toxoplasma gondii | Probably essential | sidik |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
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 |
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 |
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.