pI: 8.8063 |
Length (AA): 183 |
MW (Da): 20590 |
Paralog Number:
0
Signal peptide: N | 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:
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 |
---|---|---|---|---|---|---|---|---|---|
54 | 102 | 1b12 (B) | 84 | 147 | 33.00 | 0 | 0.55 | 0.46286 | 0.98 |
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_127356)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G52600 | peptidase S24/S26A/S26B/S26C family protein |
Arabidopsis thaliana | AT3G15710 | peptidase S24/S26A/S26B/S26C family protein |
Babesia bovis | BBOV_III000270 | signal peptidase, putative |
Brugia malayi | Bm1_48535 | Microsomal signal peptidase 21 kDa subunit |
Candida albicans | CaO19.10769 | signal peptidase subunit |
Candida albicans | CaO19.3259 | signal peptidase subunit |
Caenorhabditis elegans | CELE_Y54E10BR.5 | Protein Y54E10BR.5 |
Cryptosporidium parvum | cgd1_440 | hypothetical protein |
Dictyostelium discoideum | DDB_G0276359 | microsomal signal peptidase subunit |
Drosophila melanogaster | Dmel_CG2358 | twisted bristles roughened eye |
Echinococcus granulosus | EgrG_000341800 | signal peptidase complex catalytic subunit |
Entamoeba histolytica | EHI_197020 | signal peptidase, putative |
Echinococcus multilocularis | EmuJ_000341800 | signal peptidase complex catalytic subunit |
Giardia lamblia | GL50803_9174 | Microsomal signal peptidase 18 kDa subunit |
Homo sapiens | ENSG00000140612 | SEC11 homolog A (S. cerevisiae) |
Homo sapiens | ENSG00000166562 | SEC11 homolog C (S. cerevisiae) |
Leishmania donovani | LdBPK_080460.1 | signal peptidase type I, putative |
Leishmania infantum | LinJ.08.0460 | signal peptidase type I, putative |
Leishmania major | LmjF.08.0450 | signal peptidase type I, putative |
Leishmania mexicana | LmxM.08.0450 | signal peptidase type I, putative,serine peptidase, Clan SF, Family S26A |
Loa Loa (eye worm) | LOAG_03449 | microsomal signal peptidase 21 kDa subunit |
Mus musculus | ENSMUSG00000025724 | SEC11 homolog A (S. cerevisiae) |
Mus musculus | ENSMUSG00000024516 | SEC11 homolog C (S. cerevisiae) |
Neospora caninum | NCLIV_019450 | hypothetical protein |
Oryza sativa | 4338334 | Os05g0297900 |
Oryza sativa | 4340738 | Os06g0273800 |
Oryza sativa | 4331226 | Os02g0827900 |
Onchocerca volvulus | OVOC1066 |
|
Plasmodium berghei | PBANKA_1346200 | signal peptidase 21 kDa subunit, putative |
Plasmodium falciparum | PF3D7_1331300 | signal peptidase 21 kDa subunit |
Plasmodium knowlesi | PKNH_1269200 | signal peptidase 21 kDa subunit, putative |
Plasmodium vivax | PVX_082500 | signal peptidase 21 kDa subunit, putative |
Plasmodium yoelii | PY00480 | signal peptidase 18 subunit-related |
Saccharomyces cerevisiae | YIR022W | Sec11p |
Schistosoma japonicum | Sjp_0058200 | ko:K03100 signal peptidase I [EC3.4.21.89], putative |
Schistosoma mansoni | Smp_031730 | signalase (S26 family) |
Schmidtea mediterranea | mk4.000058.06 | GM04682p |
Trypanosoma brucei gambiense | Tbg972.5.4490 | signal peptidase type I, putative,serine peptidase, Clan SF, Family S26A |
Trypanosoma brucei | Tb927.5.3220 | signal peptidase type I, putative |
Trypanosoma congolense | TcIL3000_0_11990 | signal peptidase type I, putative |
Trypanosoma cruzi | TcCLB.511661.40 | signal peptidase type I, putative |
Trypanosoma cruzi | TcCLB.507809.74 | signal peptidase type I, putative |
Toxoplasma gondii | TGME49_280740 | signal peptidase |
Theileria parva | TP03_0804 | signal peptidase, putative |
Trichomonas vaginalis | TVAG_240820 | Clan SF, family S26, signal peptidase I-like serine peptidase |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.5.3220 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.5.3220 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.5.3220 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.5.3220 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y54E10BR.5 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_Y54E10BR.5 | Caenorhabditis elegans | slow growth | wormbase |
CELE_Y54E10BR.5 | Caenorhabditis elegans | sterile | wormbase |
YIR022W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_1346200 | Plasmodium berghei | Essential | plasmo |
TGME49_280740 | Toxoplasma gondii | Probably essential | sidik |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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.