pI: 10.6135 |
Length (AA): 189 |
MW (Da): 21909 |
Paralog Number:
3
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 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 |
---|---|---|---|---|---|---|---|---|---|
1 | 86 | 2cql (A) | 1 | 88 | 40.00 | 0 | 0.97 | 0.952726 | -0.52 |
8 | 182 | 1vq8 (E) | 4 | 171 | 36.00 | 0 | 1 | 1.36243 | -0.28 |
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_126993)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G33120 | 60S ribosomal protein L9-1 |
Arabidopsis thaliana | AT1G33140 | 60S ribosomal protein L9-1 |
Arabidopsis thaliana | AT4G10450 | 60S ribosomal protein L9-2 |
Babesia bovis | BBOV_IV006070 | ribosomal protein L9, putative |
Brugia malayi | Bm1_57375 | 60S ribosomal protein L9 |
Candida albicans | CaO19.236 | likely cytosolic ribosomal protein similar to S. cerevisiae RPL9A (YGL147C) and RPL9B (YNL067W) large subunit protein L9 |
Candida albicans | CaO19.7866 | likely cytosolic ribosomal protein similar to S. cerevisiae RPL9A (YGL147C) and RPL9B (YNL067W) large subunit protein L9 |
Caenorhabditis elegans | CELE_R13A5.8 | Protein RPL-9 |
Cryptosporidium hominis | Chro.80052 | ribosomal protein |
Cryptosporidium parvum | cgd8_400 | 60S ribosomal protein L9 |
Dictyostelium discoideum | DDB_G0278959 | 60S ribosomal protein L9 |
Drosophila melanogaster | Dmel_CG6141 | Ribosomal protein L9 |
Echinococcus granulosus | EgrG_001076300 | ribosomal protein L9 |
Entamoeba histolytica | EHI_193080 | 60S ribosomal protein L9, putative |
Entamoeba histolytica | EHI_126140 | 60S ribosomal protein L9, putative |
Echinococcus multilocularis | EmuJ_001076300 | ribosomal protein L9 |
Giardia lamblia | GL50803_17056 | Ribosomal protein L9 |
Homo sapiens | ENSG00000163682 | ribosomal protein L9 |
Leishmania braziliensis | LbrM.21.1280 | 60S ribosomal protein L9, putative |
Leishmania braziliensis | LbrM.30.3380 | 60S ribosomal protein L9, putative |
Leishmania donovani | LdBPK_211290.1 | 60S ribosomal protein L9, putative |
Leishmania infantum | LinJ.30.3390 | 60S ribosomal protein L9, putative |
Leishmania infantum | LinJ.21.1290 | 60S ribosomal protein L9, putative |
Leishmania major | LmjF.30.3340 | 60S ribosomal protein L9, putative |
Leishmania major | LmjF.21.1050 | 60S ribosomal protein L9, putative |
Leishmania mexicana | LmxM.29.3340 | 60S ribosomal protein L9, putative |
Leishmania mexicana | LmxM.21.1050 | 60S ribosomal protein L9, putative |
Loa Loa (eye worm) | LOAG_09683 | hypothetical protein |
Loa Loa (eye worm) | LOAG_05986 | 60S ribosomal protein L9 |
Mus musculus | ENSMUSG00000047215 | ribosomal protein L9 |
Mus musculus | 102641773 | 60S ribosomal protein L9-like |
Mus musculus | 101056029 | 60S ribosomal protein L9-like |
Neospora caninum | NCLIV_015160 | hypothetical protein |
Oryza sativa | 4347422 | Os09g0485900 |
Oryza sativa | 4327999 | Os02g0103700 |
Plasmodium berghei | PBANKA_1338300 | 60S ribosomal protein L6, putative |
Plasmodium falciparum | PF3D7_1323100 | 60S ribosomal protein L6, putative |
Plasmodium knowlesi | PKNH_1205700 | 60S ribosomal protein L6, putative |
Plasmodium vivax | PVX_116715 | 60S ribosomal protein L9, putative |
Plasmodium yoelii | PY01587 | ribosomal protein L6, putative |
Saccharomyces cerevisiae | YGL147C | ribosomal 60S subunit protein L9A |
Saccharomyces cerevisiae | YNL067W | ribosomal 60S subunit protein L9B |
Schistosoma japonicum | Sjp_0075950 | ko:K02940 large subunit ribosomal protein L9e, putative |
Schistosoma mansoni | Smp_018990 | 60S ribosomal protein L9 |
Schmidtea mediterranea | mk4.007424.01 | 60S ribosomal protein L9 |
Schmidtea mediterranea | mk4.030660.00 | 60S ribosomal protein L9 |
Trypanosoma brucei gambiense | Tbg972.6.4510 | 60S ribosomal protein L9, putative |
Trypanosoma brucei gambiense | Tbg972.10.1300 | 60S ribosomal protein L9, putative |
Trypanosoma brucei | Tb927.10.1100 | 60S ribosomal protein L9, putative |
Trypanosoma congolense | TcIL3000_10_900 | 60S ribosomal protein L9, putative |
Trypanosoma congolense | TcIL3000_6_4130 | 60S ribosomal protein L9, putative |
Trypanosoma cruzi | TcCLB.509695.170 | 60S ribosomal protein L9, putative |
Trypanosoma cruzi | TcCLB.506835.30 | 60S ribosomal protein L9, putative |
Trypanosoma cruzi | TcCLB.511729.40 | 60S ribosomal protein L9, putative |
Trypanosoma cruzi | TcCLB.504181.10 | 60S ribosomal protein L9, putative |
Toxoplasma gondii | TGME49_284560 | ribosomal protein RPL9 |
Theileria parva | TP01_0413 | 60S ribosomal protein L6, putative |
Trichomonas vaginalis | TVAG_255140 | 60S ribosomal protein L9, putative |
Trichomonas vaginalis | TVAG_054500 | 50S ribosomal protein L6p, putative |
Trichomonas vaginalis | TVAG_318710 | 50S ribosomal protein L6p, putative |
Trichomonas vaginalis | TVAG_198960 | 60S ribosomal protein L9, putative |
Trichomonas vaginalis | TVAG_297470 | 60S ribosomal protein L9, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.1100 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.1100 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.1100 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.1100 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_R13A5.8 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_R13A5.8 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_R13A5.8 | Caenorhabditis elegans | slow growth | wormbase |
CELE_R13A5.8 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_1338300 | Plasmodium berghei | Essential | plasmo |
TGME49_284560 | Toxoplasma gondii | Probably essential | sidik |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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.