pI: 9.6249 |
Length (AA): 185 |
MW (Da): 22209 |
Paralog Number:
0
Signal peptide: Y | GPI Anchor: N | Predicted trans-membrane segments: 1
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 |
---|---|---|---|
Upper 80-100% percentile | intra-erythrocytic - 24 hs, intra-erythrocytic - 32 hs, intra-erythrocytic - 40 hs, intra-erythrocytic - 48 hs, gametocyte, merozoite, early schizont, early trophozoite, late ring, late schizont, late trophozoite. | Otto TD PlasmoDB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | early ring, Oocyst, Female Gametocyte. | PlasmoDB Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 0 hs, intra-erythrocytic - 8 hs, Sporozoite, Male Gametocyte. | Otto TD Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | intra-erythrocytic - 16 hs, Ring. | Otto TD Zanghi G |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
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. |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Ortholog group members (OG5_128397)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G05230 | Signal peptidase complex subunit 3A |
Arabidopsis thaliana | AT5G27430 | Signal peptidase complex subunit 3B |
Babesia bovis | BBOV_III002870 | signal peptidase family protein |
Brugia malayi | Bm1_16935 | Signal peptidase subunit family protein |
Candida albicans | CaO19.12396 | signal peptidase subunit |
Candida albicans | CaO19.4930 | signal peptidase subunit |
Caenorhabditis elegans | CELE_K12H4.4 | Protein K12H4.4 |
Cryptosporidium hominis | Chro.30306 | hypothetical protein |
Cryptosporidium parvum | cgd3_2680 | possible signal peptidase subunit, signal peptide |
Dictyostelium discoideum | DDB_G0290851 | microsomal signal peptidase subunit |
Drosophila melanogaster | Dmel_CG5677 | Spase 22/23-subunit |
Echinococcus granulosus | EgrG_000866100 | signal peptidase complex subunit 3 |
Entamoeba histolytica | EHI_121860 | microsomal signal peptidase subunit, putative |
Echinococcus multilocularis | EmuJ_000866100 | signal peptidase complex subunit 3 |
Giardia lamblia | GL50803_2964 | hypothetical protein |
Homo sapiens | ENSG00000129128 | signal peptidase complex subunit 3 homolog (S. cerevisiae) |
Loa Loa (eye worm) | LOAG_03394 | signal peptidase subunit family protein |
Mus musculus | ENSMUSG00000048040 | adipocyte-related X-chromosome expressed sequence 2 |
Mus musculus | ENSMUSG00000054408 | signal peptidase complex subunit 3 homolog (S. cerevisiae) |
Mus musculus | ENSMUSG00000048355 | adipocyte-related X-chromosome expressed sequence 1 |
Neospora caninum | NCLIV_064640 | Probable signal peptidase complex subunit 3 (EC 3.4.-.-), related |
Oryza sativa | 4325792 | Os01g0131800 |
Oryza sativa | 4347817 | Os09g0556000 |
Onchocerca volvulus | OVOC9016 | Putative signal peptidase complex subunit 3 |
Plasmodium berghei | PBANKA_0417000 | signal peptidase complex subunit 3, putative |
Plasmodium falciparum | PF3D7_0904400 | signal peptidase complex subunit 3, putative |
Plasmodium knowlesi | PKNH_0702100 | signal peptidase complex subunit 3, putative |
Plasmodium vivax | PVX_098665 | signal peptidase complex subunit 3, putative |
Plasmodium yoelii | PY04820 | probable microsomal signal peptidase 22 kDa subunit, putative |
Saccharomyces cerevisiae | YLR066W | Spc3p |
Schistosoma japonicum | Sjp_0200670 | ko:K01423 Spase22-23; Spase 22/23-subunit [EC:3.4.-.-], putative |
Schistosoma mansoni | Smp_175420 | microsomal signal peptidase 23 kD subunit (spc22/23) |
Schmidtea mediterranea | mk4.001249.02 | Probable signal peptidase complex subunit 3 |
Toxoplasma gondii | TGME49_300060 | signal peptidase subunit protein |
Theileria parva | TP04_0108 | signal peptidase, putative |
Trichomonas vaginalis | TVAG_455170 | Signal peptidase complex subunit, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_K12H4.4 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_K12H4.4 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_K12H4.4 | Caenorhabditis elegans | slow growth | wormbase |
CELE_K12H4.4 | Caenorhabditis elegans | sterile | wormbase |
YLR066W | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_300060 | Toxoplasma gondii | Probably essential | sidik |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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.