pI: 11.8308 |
Length (AA): 204 |
MW (Da): 23956 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 0
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 3 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 |
---|---|---|---|---|---|---|---|---|---|
2 | 193 | 1jj2 (L) | 3 | 193 | 40.00 | 0 | 1 | 1.40178 | 0.1 |
2 | 196 | 1ffk (I) | 3 | 193 | 38.00 | 0 | 1 | 1.34848 | 0.53 |
3 | 193 | 1vq8 (M) | 4 | 193 | 41.00 | 0 | 1 | 1.40487 | 0.12 |
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_127033)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G16720 | 60S ribosomal protein L15-1 |
Arabidopsis thaliana | AT4G17390 | 60S ribosomal protein L15-2 |
Babesia bovis | BBOV_III000550 | ribosomal protein L15, putative |
Brugia malayi | Bm1_20955 | 60S ribosomal protein L15 |
Candida albicans | CaO19.8123 | likely cytosolic ribosomal protein similar to S. cerevisiae RPL15B (YMR121C) large subunit protein L15 |
Candida albicans | CaO19.493 | likely cytosolic ribosomal protein similar to S. cerevisiae RPL15B (YMR121C) large subunit protein L15 |
Caenorhabditis elegans | CELE_K11H12.2 | Protein RPL-15 |
Cryptosporidium hominis | Chro.20035 | 60S ribosomal protein L15-2 |
Cryptosporidium parvum | cgd2_280 | 60S ribosomal protein L15 |
Dictyostelium discoideum | DDB_G0272893 | S60 ribosomal protein L15 |
Dictyostelium discoideum | DDB_G0273983 | S60 ribosomal protein L15 |
Drosophila melanogaster | Dmel_CG17420 | Ribosomal protein L15 |
Echinococcus granulosus | EgrG_000252800 | ribosomal protein L15 |
Entamoeba histolytica | EHI_040800 | 60S ribosomal protein L15, putative |
Entamoeba histolytica | EHI_020300 | 60S ribosomal protein L15, putative |
Echinococcus multilocularis | EmuJ_000252800 | ribosomal protein L15 |
Giardia lamblia | GL50803_8001 | Ribosomal protein L15 |
Homo sapiens | ENSG00000174748 | ribosomal protein L15 |
Leishmania braziliensis | LbrM.34.1810 | ribosomal protein L15, putative |
Leishmania braziliensis | LbrM.30.3680 | ribosomal protein L15, putative |
Leishmania donovani | LdBPK_351890.1 | ribosomal protein L15, putative |
Leishmania donovani | LdBPK_303710.1 | ribosomal protein L15, putative |
Leishmania infantum | LinJ.30.3710 | ribosomal protein L15, putative |
Leishmania infantum | LinJ.35.1890 | ribosomal protein L15, putative |
Leishmania major | LmjF.35.1910 | ribosomal protein L15, putative |
Leishmania major | LmjF.30.3650 | ribosomal protein L15, putative |
Leishmania mexicana | LmxM.29.3650 | ribosomal protein L15, putative |
Leishmania mexicana | LmxM.34.1910 | ribosomal protein L15, putative |
Loa Loa (eye worm) | LOAG_12612 | hypothetical protein |
Mus musculus | ENSMUSG00000012405 | ribosomal protein L15 |
Mus musculus | 102641848 | 60S ribosomal protein L15-like |
Mus musculus | 100043670 | predicted gene 4581 |
Neospora caninum | NCLIV_045010 | hypothetical protein |
Oryza sativa | 9266562 | Os05g0274700 |
Oryza sativa | 4333387 | Os03g0598800 |
Plasmodium berghei | PBANKA_0717800 | 60S ribosomal protein L15, putative |
Plasmodium falciparum | PF3D7_0415900 | 60S ribosomal protein L15, putative |
Plasmodium knowlesi | PKNH_0507500 | 60S ribosomal protein L15, putative |
Plasmodium vivax | PVX_089750 | 60S ribosomal protein L15-1, putative |
Plasmodium yoelii | PY02811 | Ribosomal L15 |
Saccharomyces cerevisiae | YLR029C | ribosomal 60S subunit protein L15A |
Saccharomyces cerevisiae | YMR121C | ribosomal 60S subunit protein L15B |
Schistosoma japonicum | Sjp_0305630 | ko:K02877 large subunit ribosomal protein L15e, putative |
Schistosoma mansoni | Smp_032260 | ribosomal protein L15 |
Schmidtea mediterranea | mk4.001588.04 | Ribosomal protein L15 |
Trypanosoma brucei gambiense | Tbg972.9.9400 | ribosomal protein L15, putative |
Trypanosoma brucei gambiense | Tbg972.6.4840 | ribosomal protein L15, putative |
Trypanosoma brucei | Tb927.9.15190 | ribosomal protein L15, putative |
Trypanosoma congolense | TcIL3000_9_6350 | ribosomal protein L15, putative |
Trypanosoma congolense | TcIL3000_6_4470 | ribosomal protein L15, putative |
Trypanosoma cruzi | TcCLB.509671.70 | ribosomal protein L15, putative |
Trypanosoma cruzi | TcCLB.506945.290 | ribosomal protein L15, putative |
Trypanosoma cruzi | TcCLB.510767.10 | ribosomal protein L15, putative |
Toxoplasma gondii | TGME49_228470 | ribosomal protein RPL15 |
Theileria parva | TP03_0755 | 60S ribosomal protein L15, putative |
Trichomonas vaginalis | TVAG_200220 | 60S ribosomal protein L15, putative |
Trichomonas vaginalis | TVAG_159780 | 50S ribosomal protein L15e, putative |
Trichomonas vaginalis | TVAG_276360 | 60S ribosomal protein L15, putative |
Trichomonas vaginalis | TVAG_148950 | 50S ribosomal protein L15e, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.6.5040 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.6.5040 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.6.5040 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.6.5040 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_K11H12.2 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_K11H12.2 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_K11H12.2 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_K11H12.2 | Caenorhabditis elegans | slow growth | wormbase |
CELE_K11H12.2 | Caenorhabditis elegans | sterile | wormbase |
YLR029C | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0717800 | Plasmodium berghei | Essential | plasmo |
TGME49_228470 | Toxoplasma gondii | Probably essential | sidik |
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.