pI: 9.8744 |
Length (AA): 269 |
MW (Da): 31240 |
Paralog Number:
0
Signal peptide: Y | GPI Anchor: N | Predicted trans-membrane segments: 6
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 |
---|---|---|---|---|---|---|---|---|---|
181 | 228 | 3hzq (A) | 38 | 88 | 33.00 | 0.48 | 0.05 | 0.139139 | 2.69 |
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:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intraerythrocytic - 6 hs, intraerythrocytic - 12 hs, intraerythrocytic - 18 hs, intraerythrocytic - 24 hs, intraerythrocytic - 30 hs, intraerythrocytic - 36 hs, intraerythrocytic - 40 hs, intraerythrocytic - 48 hs. | Zhu L |
Zhu L | New insights into the Plasmodium vivax transcriptome using RNA-Seq. |
Ortholog group members (OG5_131748)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G47640 | hypothetical protein |
Babesia bovis | BBOV_I002280 | membrane protein, putative |
Brugia malayi | Bm1_05455 | seven transmembrane domain protein |
Caenorhabditis elegans | CELE_ZK418.5 | Protein ZK418.5 |
Dictyostelium discoideum | DDB_G0293704 | seven transmembrane domain protein |
Drosophila melanogaster | Dmel_CG5861 | CG5861 gene product from transcript CG5861-RA |
Homo sapiens | ENSG00000105677 | transmembrane protein 147 |
Loa Loa (eye worm) | LOAG_08333 | hypothetical protein |
Loa Loa (eye worm) | LOAG_10170 | hypothetical protein |
Mus musculus | ENSMUSG00000006315 | transmembrane protein 147 |
Neospora caninum | NCLIV_046670 | AGAP008757-PA, related |
Oryza sativa | 4334226 | Os03g0766000 |
Onchocerca volvulus | OVOC9083 | Transmembrane protein 147 homolog |
Plasmodium berghei | PBANKA_1205200 | conserved membrane protein, unknown function |
Plasmodium falciparum | PF3D7_1007000 | conserved membrane protein, unknown function |
Plasmodium knowlesi | PKNH_0805800 | conserved membrane protein, unknown function |
Plasmodium vivax | PVX_094545 | conserved membrane protein, unknown function |
Plasmodium yoelii | PY01878 | hypothetical protein |
Schistosoma japonicum | Sjp_0216640 | Transmembrane protein 147, putative |
Schistosoma mansoni | Smp_071560 | small seven transmembrane domain-containing protein |
Schmidtea mediterranea | mk4.000585.02 | |
Toxoplasma gondii | TGME49_226270 | hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
PBANKA_1205200 | Plasmodium berghei | Dispensable | plasmo |
TGME49_226270 | Toxoplasma gondii | Probably non-essential | sidik |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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.