pI: 8.4717 |
Length (AA): 267 |
MW (Da): 30045 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 8
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 2 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 |
---|---|---|---|---|---|---|---|---|---|
70 | 102 | 2m6x (A) | 30 | 62 | 30.00 | 0 | 0.02 | 0.0168955 | 3.95 |
77 | 197 | 3rze (A) | 32 | 152 | 31.00 | 0.13 | 0.03 | 0.450384 | 1.68 |
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_129169)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G36305 | CAAX prenyl protease 2 |
Brugia malayi | Bm1_12350 | CAAX amino terminal protease family protein |
Candida albicans | CaO19.11306 | ras and a-factor terminal proteolysis |
Candida albicans | CaO19.3825 | ras and a-factor terminal proteolysis |
Caenorhabditis elegans | CELE_F48F5.5 | Protein FCE-2 |
Dictyostelium discoideum | DDB_G0292570 | hypothetical protein |
Drosophila melanogaster | Dmel_CG4852 | severas |
Echinococcus granulosus | EgrG_000535900 | CAAX prenyl protease 2 |
Entamoeba histolytica | EHI_187200 | CAAX prenyl protease family |
Echinococcus multilocularis | EmuJ_000535900 | CAAX prenyl protease 2 |
Giardia lamblia | GL50803_7029 | Hypothetical protein |
Homo sapiens | ENSG00000173653 | Ras converting CAAX endopeptidase 1 |
Leishmania braziliensis | LbrM.26.2620 | CAAX prenyl protease 2, putative,peptidase with unknown catalytic mechanism (family U48) |
Leishmania donovani | LdBPK_262720.1 | CAAX prenyl protease 2, putative |
Leishmania infantum | LinJ.26.2720 | CAAX prenyl protease 2, putative,peptidase with unknown catalytic mechanism (family U48) |
Leishmania major | LmjF.26.2690 | CAAX prenyl protease 2, putative,peptidase with unknown catalytic mechanism (family U48) |
Leishmania mexicana | LmxM.26.2690 | CAAX prenyl protease 2, putative,peptidase with unknown catalytic mechanism (family U48) |
Loa Loa (eye worm) | LOAG_09521 | hypothetical protein |
Mus musculus | ENSMUSG00000024889 | RCE1 homolog, prenyl protein peptidase (S. cerevisiae) |
Oryza sativa | 9268853 | Os05g0357700 |
Saccharomyces cerevisiae | YMR274C | Rce1p |
Schistosoma japonicum | Sjp_0201200 | ko:K08658 prenyl protein peptidase, putative |
Schistosoma japonicum | Sjp_0308190 | expressed protein |
Schistosoma mansoni | Smp_017650.2 | family U48 unassigned peptidase (U48 family) |
Schistosoma mansoni | Smp_017650.1 | family U48 unassigned peptidase (U48 family) |
Trypanosoma brucei gambiense | Tbg972.3.1300 | CAAX prenyl protease 2, putative,peptidase with unknown catalytic mechanism (family U48), putative |
Trypanosoma brucei | Tb927.3.1540 | CAAX amino terminal protease, putative |
Trypanosoma congolense | TcIL3000_0_31320 | CAAX amino terminal protease, putative |
Trypanosoma cruzi | TcCLB.510421.29 | CAAX prenyl protease 2, putative |
Trypanosoma cruzi | TcCLB.510089.39 | peptidase with unknown catalytic mechanism (family U48) |
Trichomonas vaginalis | TVAG_226550 | Clan U, family U48, CaaX prenyl peptidase 2-like |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.3.1540 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.3.1540 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.3.1540 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.3.1540 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
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 |
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 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
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 |
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.
Species | Known druggable target | Linked compounds | Reference |
---|---|---|---|
Saccharomyces cerevisiae | Rce1p | Compounds | References |
Homo sapiens | Ras converting CAAX endopeptidase 1 | Compounds | References |