pI: 10.2046 |
Length (AA): 214 |
MW (Da): 24530 |
Paralog Number:
1
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 6 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 |
---|---|---|---|---|---|---|---|---|---|
1 | 213 | 1ad2 () | 11 | 224 | 20.00 | 0 | 1 | 1.11 | 0.13 |
4 | 213 | 1dwu (A) | 1 | 211 | 28.00 | 0 | 1 | 1.42 | -0.74 |
1 | 214 | 4reo (A) | 11 | 225 | 20.00 | 0 | 1 | 1.2457 | -0.23 |
4 | 214 | 1dwu (A) | 1 | 212 | 28.00 | 0 | 1 | 1.41698 | -0.71 |
4 | 213 | 4lq4 (A) | 1 | 211 | 22.00 | 0 | 1 | 1.36021 | -0.79 |
5 | 213 | 1mzp (A) | 4 | 215 | 26.00 | 0 | 1 | 1.36174 | -0.6 |
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:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 80-100% percentile | amastigotes, metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_127114)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G08360 | 60S ribosomal protein L10a-1 |
Arabidopsis thaliana | AT5G22440 | 60S ribosomal protein L10a-3 |
Arabidopsis thaliana | AT2G27530 | 60S ribosomal protein L10a-2 |
Babesia bovis | BBOV_III003180 | ribosomal protein L1, putative |
Brugia malayi | Bm1_01805 | 60S ribosomal protein L10a |
Candida albicans | CaO19.10969 | likely ribosomal protein L1 |
Candida albicans | CaO19.3465 | likely ribosomal protein L1 |
Caenorhabditis elegans | CELE_Y71F9AL.13 | Protein RPL-1, isoform B |
Cryptosporidium hominis | Chro.80334 | ribosomal protein L1 |
Cryptosporidium parvum | cgd8_2870 | 60S ribosomal protein L10A |
Dictyostelium discoideum | DDB_G0276871 | S60 ribosomal protein L10a |
Drosophila melanogaster | Dmel_CG7283 | Ribosomal protein L10Ab |
Echinococcus granulosus | EgrG_000776500 | 60S ribosomal protein L10a |
Entamoeba histolytica | EHI_135790 | 60S ribosomal protein L10a, putative |
Entamoeba histolytica | EHI_012480 | 60S ribosomal protein L10a-2, putative |
Echinococcus multilocularis | EmuJ_000776500 | 60S ribosomal protein L10a |
Giardia lamblia | GL50803_1345 | Ribosomal protein L10a |
Homo sapiens | ENSG00000198755 | ribosomal protein L10a |
Leishmania braziliensis | LbrM.35.4000 | 60S ribosomal protein L10a, putative |
Leishmania braziliensis | LbrM.18.0700 | 60S ribosomal protein L10a, putative |
Leishmania infantum | LinJ.36.3950 | 60S ribosomal protein L10a, putative |
Leishmania infantum | LinJ.18.0630 | 60S ribosomal protein L10a, putative |
Leishmania major | LmjF.18.0620 | 60S ribosomal protein L10a, putative |
Leishmania major | LmjF.36.3760 | 60S ribosomal protein L10a, putative |
Leishmania mexicana | LmxM.36.3760 | 60S ribosomal protein L10a, putative |
Leishmania mexicana | LmxM.18.0620 | 60S ribosomal protein L10a, putative |
Loa Loa (eye worm) | LOAG_12216 | 60S ribosomal protein L10a |
Mus musculus | ENSMUSG00000037805 | ribosomal protein L10A |
Neospora caninum | NCLIV_052390 | hypothetical protein |
Oryza sativa | 9268245 | Os08g0558000 |
Oryza sativa | 9266191 | Os08g0558800 |
Oryza sativa | 4329171 | Os02g0321900 |
Oryza sativa | 4325065 | Os01g0860300 |
Plasmodium berghei | PBANKA_1305100 | 60S ribosomal protein L1, putative |
Plasmodium falciparum | PF3D7_1441200 | 60S ribosomal protein L1, putative |
Plasmodium knowlesi | PKNH_1241100 | 60S ribosomal protein L1, putative |
Plasmodium vivax | PVX_118430 | 60S ribosomal protein L10a, putative |
Plasmodium yoelii | PY05328 | L1P family of ribosomal proteins |
Saccharomyces cerevisiae | YPL220W | ribosomal 60S subunit protein L1A |
Saccharomyces cerevisiae | YGL135W | ribosomal 60S subunit protein L1B |
Schistosoma japonicum | Sjp_0217590 | ko:K02865 large subunit ribosomal protein L10Ae, putative |
Schistosoma mansoni | Smp_042090.3 | 60S ribosomal protein L10a |
Schistosoma mansoni | Smp_042090.2 | 60S ribosomal protein L10a |
Schmidtea mediterranea | mk4.000514.13 | 60S ribosomal protein L10a |
Schmidtea mediterranea | mk4.001260.01 | 60S ribosomal protein L10a |
Schmidtea mediterranea | mk4.009045.00 | |
Trypanosoma brucei gambiense | Tbg972.11.10900 | 60S ribosomal protein L10a, putative |
Trypanosoma brucei gambiense | Tbg972.10.16300 | 60S ribosomal protein L10a, putative |
Trypanosoma brucei | Tb927.11.9710 | 60S ribosomal protein L10a, putative |
Trypanosoma brucei | Tb927.10.13500 | 60S ribosomal protein L10a |
Trypanosoma congolense | TcIL3000.11.10200 | 60S ribosomal protein L10a, putative |
Trypanosoma congolense | TcIL3000_0_35380 | 60S ribosomal protein L10a, putative |
Trypanosoma cruzi | TcCLB.511277.160 | 60S ribosomal protein L10a, putative |
Trypanosoma cruzi | TcCLB.511233.7 | 60S ribosomal protein L10a, putative |
Trypanosoma cruzi | TcCLB.506963.10 | 60S ribosomal protein L10a, putative |
Toxoplasma gondii | TGME49_215470 | ribosomal protein RPL10A |
Theileria parva | TP04_0125 | 60S ribosomal protein L1, putative |
Trichomonas vaginalis | TVAG_276180 | 60S ribosomal protein L10a, putative |
Trichomonas vaginalis | TVAG_144550 | 60S ribosomal protein L10a, putative |
Trichomonas vaginalis | TVAG_249740 | 60S ribosomal protein L10a, putative |
Trichomonas vaginalis | TVAG_107720 | 60S ribosomal protein L10a, putative |
Trichomonas vaginalis | TVAG_477470 | 60S ribosomal protein L10a, putative |
Trichomonas vaginalis | TVAG_074480 | 60S ribosomal protein L10a, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.13500 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.13500 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.13500 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.13500 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb11.01.1470 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.1470 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.1470 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb11.01.1470 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y71F9AL.13 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_Y71F9AL.13 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_Y71F9AL.13 | Caenorhabditis elegans | slow growth | wormbase |
CELE_Y71F9AL.13 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_1305100 | Plasmodium berghei | Essential | plasmo |
TGME49_215470 | 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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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.