pI: 5.0955 |
Length (AA): 796 |
MW (Da): 87942 |
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 |
---|---|---|---|---|---|---|---|---|---|
38 | 100 | 2dt6 (A) | 48 | 110 | 62.00 | 0 | 1 | 0.995546 | -2.03 |
112 | 195 | 2dt7 (B) | 135 | 217 | 72.00 | 0 | 1 | 0.916628 | -0.54 |
689 | 794 | 1we6 (A) | 9 | 108 | 34.00 | 0 | 1 | 0.490266 | -0.49 |
690 | 794 | 1we7 (A) | 8 | 112 | 43.00 | 0 | 1 | 0.67401 | -0.63 |
738 | 787 | 2bwf (A) | 19 | 71 | 38.00 | 0.29 | 1 | 0.490214 | -0.14 |
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_128430)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G14650 | probable splicing factor 3A subunit 1 |
Arabidopsis thaliana | AT1G14640 | SWAP (Suppressor-of-White-APricot)/surp domain-containing protein |
Babesia bovis | BBOV_III005810 | Surp module domain containing protein |
Brugia malayi | Bm1_01890 | Surp module family protein |
Candida albicans | CaO19.12129 | similar to S. pombe SWAP domain-containing SAP114 (SPAC22A12.09c ) pre-mRNA splicing factor |
Candida albicans | CaO19.4659 | similar to S. pombe SWAP domain-containing SAP114 (SPAC22A12.09c ) pre-mRNA splicing factor |
Caenorhabditis elegans | CELE_W07E6.4 | Protein PRP-21 |
Cryptosporidium hominis | Chro.70247 | splicing factor |
Cryptosporidium parvum | cgd7_2160 | Pre-mRNA splicing factor SF3a. 2xSWAP domain protein |
Dictyostelium discoideum | DDB_G0272676 | SWAP/Surp domain-containing protein |
Drosophila melanogaster | Dmel_CG16941 | CG16941 gene product from transcript CG16941-RA |
Echinococcus granulosus | EgrG_000627300 | splicing factor 3A subunit 1 |
Entamoeba histolytica | EHI_058680 | splicing factor, putative |
Entamoeba histolytica | EHI_198910 | splicing factor, putative |
Echinococcus multilocularis | EmuJ_000627300 | splicing factor 3A subunit 1 |
Homo sapiens | ENSG00000099995 | splicing factor 3a, subunit 1, 120kDa |
Loa Loa (eye worm) | LOAG_02673 | splicing factor 3a |
Mus musculus | ENSMUSG00000002129 | splicing factor 3a, subunit 1 |
Neospora caninum | NCLIV_063290 | hypothetical protein |
Oryza sativa | 4328860 | Os02g0245000 |
Plasmodium berghei | PBANKA_1301700 | splicing factor 3A subunit 1, putative |
Plasmodium falciparum | PF3D7_1474500 | splicing factor 3A subunit 1, putative |
Plasmodium knowlesi | PKNH_1244800 | splicing factor 3A subunit 1, putative |
Plasmodium vivax | PVX_118605 | hypothetical protein, conserved |
Plasmodium yoelii | PY02637 | splicing factor, putative |
Saccharomyces cerevisiae | YJL203W | Prp21p |
Schistosoma japonicum | Sjp_0128200 | Splicing factor 3 subunit 1, putative |
Schistosoma japonicum | Sjp_0021450 | Splicing factor 3 subunit 1, putative |
Schistosoma mansoni | Smp_120320.1 | spliceosome-associated protein |
Schmidtea mediterranea | mk4.000686.00 | Spliceosome-associated protein, putative |
Toxoplasma gondii | TGME49_246500 | surp module domain-containing protein |
Theileria parva | TP02_0389 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_285080 | spliceosome associated protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_W07E6.4 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_W07E6.4 | Caenorhabditis elegans | slow growth | wormbase |
CELE_W07E6.4 | Caenorhabditis elegans | sterile | wormbase |
YJL203W | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_246500 | Toxoplasma gondii | Probably essential | sidik |
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 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
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 |
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.