pI: 9.9134 |
Length (AA): 267 |
MW (Da): 30487 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
72 | 220 | 2cqm (A) | 21 | 141 | 36.00 | 0 | 1 | 0.738352 | 0.42 |
113 | 143 | 5kpe (A) | 2 | 32 | 39.00 | 0.13 | 0.23 | 0.624305 | -1.02 |
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_127423)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G54210 | 50S ribosomal protein L17 |
Arabidopsis thaliana | AT5G64650 | large subunit ribosomal protein L17 |
Arabidopsis thaliana | AT5G09770 | ribosomal protein L17 family protein |
Babesia bovis | BBOV_III003930 | 50S ribosomal subunit protein L17, putative |
Brugia malayi | Bm1_42730 | hypothetical protein |
Candida albicans | CaO19.6129 | likely mitochondrial ribosomal protein similar to S. cerevisiae MRPL8 (YJL063C) large subunit protein L8 (E. coli L17) |
Candida albicans | CaO19.13548 | likely mitochondrial ribosomal protein similar to S. cerevisiae MRPL8 (YJL063C) large subunit protein L8 (E. coli L17) |
Caenorhabditis elegans | CELE_Y54E10A.7 | Protein MRPL-17 |
Chlamydia trachomatis | CT_506 | 50S ribosomal protein L17 |
Dictyostelium discoideum | DDB_G0281435 | ribosomal protein L17, mitochondrial |
Drosophila melanogaster | Dmel_CG13880 | mitochondrial ribosomal protein L17 |
Escherichia coli | b3294 | 50S ribosomal subunit protein L17 |
Homo sapiens | ENSG00000158042 | mitochondrial ribosomal protein L17 |
Loa Loa (eye worm) | LOAG_03663 | hypothetical protein |
Mycobacterium leprae | ML1956c | PROBABLE 50S RIBOSOMAL PROTEIN L17 RPLQ |
Mus musculus | 27397 | mitochondrial ribosomal protein L17 |
Mycobacterium tuberculosis | Rv3456c | 50S ribosomal protein L17 RplQ |
Mycobacterium ulcerans | MUL_0849 | 50S ribosomal protein L17 |
Neospora caninum | NCLIV_062370 | At5g09770, related |
Oryza sativa | 4327382 | Os01g0839300 |
Oryza sativa | 4334555 | Os03g0815400 |
Plasmodium berghei | PBANKA_1237200 | 50S ribosomal protein L17, apicoplast, putative |
Plasmodium falciparum | PF3D7_0522500 | 50S ribosomal protein L17, apicoplast, putative |
Plasmodium knowlesi | PKNH_1010400 | 50S ribosomal protein L17, apicoplast, putative |
Plasmodium yoelii | PY00041 | ribosomal protein L17, putative |
Saccharomyces cerevisiae | YJL063C | mitochondrial 54S ribosomal protein YmL8 |
Schistosoma japonicum | Sjp_0217230 | IPR000456,Ribosomal protein L17,domain-containing |
Schistosoma mansoni | Smp_174980 | mitochondrial ribosomal protein L17 |
Schmidtea mediterranea | mk4.020572.00 | 39S ribosomal protein L17, mitochondrial |
Toxoplasma gondii | TGME49_217590 | 50S ribosomal protein L17, putative |
Treponema pallidum | TP0213 | 50S ribosomal protein L17 |
Theileria parva | TP03_0011 | 40S ribosomal protein L17, putative |
Wolbachia endosymbiont of Brugia malayi | Wbm0317 | 50S ribosomal protein L17 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
b3294 | Escherichia coli | essential | goodall |
CELE_Y54E10A.7 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_Y54E10A.7 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_Y54E10A.7 | Caenorhabditis elegans | slow growth | wormbase |
PBANKA_1237200 | Plasmodium berghei | Essential | plasmo |
TGME49_217590 | 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 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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.