pI: 10.1815 |
Length (AA): 142 |
MW (Da): 15003 |
Paralog Number:
0
Signal peptide: Y | GPI Anchor: | 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 |
---|---|---|---|---|---|---|---|---|---|
5 | 142 | 5dm6 (F) | 2 | 139 | 64.00 | 0 | 1 | 1.68973 | 0.12 |
10 | 141 | 1mms (A) | 8 | 139 | 67.00 | 0 | 1 | 1.77958 | -0.9 |
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 60-80% percentile | Dormant phase. | murphy |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Dormant phase. | hasan |
hasan | Prioritizing genomic drug targets in pathogens: application to Mycobacterium tuberculosis. |
murphy | Identification of gene targets against dormant phase Mycobacterium tuberculosis infections. |
Ortholog group members (OG5_127103)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G35490 | mitochondrial ribosomal protein L11 |
Arabidopsis thaliana | AT1G32990 | plastid ribosomal protein l11 |
Babesia bovis | BBOV_IV009800 | ribosomal protein L11, putative |
Brugia malayi | Bm1_57015 | Ribosomal protein L11, N-terminal domain containing protein |
Candida albicans | CaO19.6231 | likely mitochondrial ribosomal protein similar to S. cerevisiae MRPL19 (YNL185C) large subunit protein (E. coli L11) |
Candida albicans | CaO19.13611 | likely mitochondrial ribosomal protein similar to S. cerevisiae MRPL19 (YNL185C) large subunit protein (E. coli L11) |
Caenorhabditis elegans | CELE_B0303.15 | Protein MRPL-11 |
Chlamydia trachomatis | CT_319 | 50S ribosomal protein L11 |
Dictyostelium discoideum | DidioMp20 | ribosomal protein L11 |
Drosophila melanogaster | Dmel_CG3351 | mitochondrial ribosomal protein L11 |
Escherichia coli | b3983 | 50S ribosomal subunit protein L11 |
Echinococcus granulosus | EgrG_000151100 | mitochondrial ribosomal protein l11 |
Echinococcus multilocularis | EmuJ_000151100 | mitochondrial ribosomal protein l11 |
Homo sapiens | ENSG00000174547 | mitochondrial ribosomal protein L11 |
Leishmania braziliensis | LbrM.27.2400 | ribosomal protein L11, putative |
Leishmania donovani | LdBPK_272140.1 | ribosomal protein L11, putative |
Leishmania infantum | LinJ.27.2140 | ribosomal protein L11, putative |
Leishmania major | LmjF.27.2220 | ribosomal protein L11, putative |
Leishmania mexicana | LmxM.27.2220 | ribosomal protein L11, putative |
Loa Loa (eye worm) | LOAG_05636 | ribosomal protein L11 domain-containing protein |
Mycobacterium leprae | ML1905c | PROBABLE 50S RIBOSOMAL PROTEIN L11 RPLK |
Mus musculus | ENSMUSG00000024902 | mitochondrial ribosomal protein L11 |
Mycobacterium tuberculosis | Rv0640 | 50S ribosomal protein L11 RplK |
Mycobacterium ulcerans | MUL_0726 | 50S ribosomal protein L11 |
Neospora caninum | NCLIV_008670 | ribosomal protein L11, putative |
Oryza sativa | 4348843 | Os10g0466200 |
Oryza sativa | 4331442 | Os03g0122200 |
Plasmodium berghei | PBANKA_0937000 | mitochondrial ribosomal protein L11 precursor, putative |
Plasmodium falciparum | PF3D7_1110600 | mitochondrial ribosomal protein L11 precursor, putative |
Plasmodium knowlesi | PKNH_0908300 | ribosomal protein L11, putative |
Plasmodium vivax | PVX_091180 | 50S ribosomal protein L11, putative |
Plasmodium yoelii | PY01745 | putative ribosomal protein L11 |
Saccharomyces cerevisiae | YNL185C | mitochondrial 54S ribosomal protein YmL19 |
Schistosoma japonicum | Sjp_0081140 | ko:K02867 large subunit ribosomal protein L11, putative |
Schistosoma mansoni | Smp_045190.2 | 50S robosomal protein L11 |
Schmidtea mediterranea | mk4.005202.03 | Probable 39S ribosomal protein L11, mitochondrial |
Trypanosoma brucei gambiense | Tbg.972.2.2910 | ribosomal protein L11, putative |
Trypanosoma brucei gambiense | Tbg.972.2.2760 | ribosomal protein L11, putative |
Trypanosoma brucei | Tb927.2.4740 | mitochondrial ribosomal protein l11 |
Trypanosoma brucei | Tb927.2.4890 | mitochondrial ribosomal protein l11 |
Trypanosoma cruzi | TcCLB.504741.160 | ribosomal protein L11, putative |
Trypanosoma cruzi | TcCLB.511621.200 | ribosomal protein L11, putative |
Trypanosoma cruzi | TcCLB.511621.70 | ribosomal protein L11, putative |
Trypanosoma cruzi | TcCLB.509317.40 | ribosomal protein L11, putative |
Toxoplasma gondii | TGME49_254380 | ribosomal protein L11, putative |
Treponema pallidum | TP0237 | 50S ribosomal protein L11 |
Theileria parva | TP01_0788 | 60S ribosomal protein L11, putative |
Wolbachia endosymbiont of Brugia malayi | Wbm0651 | 50S ribosomal protein L11 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu652 this record | Mycobacterium tuberculosis | essential | nmpdr |
Tb927.2.4740 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.2.4740 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.2.4740 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.2.4740 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b3983 | Escherichia coli | essential | goodall |
CELE_B0303.15 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_B0303.15 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_B0303.15 | Caenorhabditis elegans | slow growth | wormbase |
PBANKA_0937000 | Plasmodium berghei | Essential | plasmo |
TGME49_254380 | 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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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 |
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 |
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 |
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.