pI: 7.8093 |
Length (AA): 138 |
MW (Da): 16490 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 4
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:
PDB Structures:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
NA% percentile | intra-erythrocytic - 32 hs. | Otto TD |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 16 hs, Female Gametocyte. | Otto TD Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 0 hs, intra-erythrocytic - 8 hs. | Otto TD |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Oocyst, Sporozoite, Male Gametocyte. | Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 0-20% percentile | intra-erythrocytic - 24 hs, intra-erythrocytic - 40 hs, intra-erythrocytic - 48 hs, Ring. | Otto TD Zanghi G |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
Ortholog group members (OG5_129756)
Species | Accession | Gene Product |
---|---|---|
Brugia malayi | Bm1_36185 | Hypothetical 23.7 kDa protein in CYR1-OST1 intergenic region |
Candida albicans | CaO19_7128 | hypothetical protein |
Candida albicans | CaO19.7128 | similar to mammalian SPC12 |
Caenorhabditis elegans | CELE_T03F1.12 | Protein T03F1.12 |
Dictyostelium discoideum | DDB_G0269368 | hypothetical protein |
Drosophila melanogaster | Dmel_CG11753 | CG11753 gene product from transcript CG11753-RC |
Echinococcus granulosus | EgrG_000464000 | protein sys1 |
Echinococcus multilocularis | EmuJ_000464000 | protein sys1 |
Homo sapiens | ENSG00000204070 | Sys1 golgi trafficking protein |
Loa Loa (eye worm) | LOAG_02701 | hypothetical protein |
Mus musculus | ENSMUSG00000045503 | SYS1 Golgi-localized integral membrane protein homolog (S. cerevisiae) |
Neospora caninum | NCLIV_047210 | hypothetical protein, conserved |
Oryza sativa | 4326384 | Os01g0593600 |
Onchocerca volvulus | OVOC539 |
|
Plasmodium falciparum | PF3D7_0621350 | protein SYS1, putative |
Saccharomyces cerevisiae | YJL004C | Sys1p |
Schistosoma japonicum | Sjp_0014570 | Protein SYS1 homolog, putative |
Schistosoma mansoni | Smp_038410 | hypothetical protein |
Schmidtea mediterranea | mk4.000994.00 | Protein SYS1 homolog |
Toxoplasma gondii | TGME49_225500 | hypothetical protein |
Trichomonas vaginalis | TVAG_266030 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
TGME49_225500 | Toxoplasma gondii | Probably non-essential | sidik |
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 |
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 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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.