pI: 10.9165 |
Length (AA): 179 |
MW (Da): 20807 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
17 | 132 | 5cqc (A) | 186 | 319 | 28.00 | 0 | 0.02 | 0.547545 | 1.75 |
70 | 145 | 2jxt (A) | 2 | 76 | 15.00 | 0 | 0.05 | 0.540081 | -0.01 |
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_127130)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G14600 | 60S ribosomal protein L18a-3 |
Arabidopsis thaliana | AT1G29970 | 60S ribosomal protein L18a-1 |
Arabidopsis thaliana | AT2G34480 | 60S ribosomal protein L18a-2 |
Arabidopsis thaliana | AT1G29965 | ribosomal protein L18ae/LX family protein |
Babesia bovis | BBOV_III004630 | 60S ribosomal protein L18ae, putative |
Brugia malayi | Bm1_23030 | 60S ribosomal protein L18a |
Candida albicans | CaO19.12102 | likely cytosolic ribosomal protein similar to S. cerevisiae RPL20B (YOR312C) large subunit protein L20 (L18) |
Candida albicans | CaO19.4632 | likely cytosolic ribosomal protein similar to S. cerevisiae RPL20B (YOR312C) large subunit protein L20 (L18) |
Cryptosporidium hominis | Chro.70045 | 60S ribosomal protein L18a |
Cryptosporidium parvum | cgd7_320 | putative 60S ribosomal protein L18A |
Dictyostelium discoideum | DDB_G0285881 | S60 ribosomal protein L18a |
Drosophila melanogaster | Dmel_CG6510 | Ribosomal protein L18A |
Echinococcus granulosus | EgrG_000581100 | ribosomal protein L18a |
Entamoeba histolytica | EHI_163670 | ribosomal protein L18a, putative |
Entamoeba histolytica | EHI_035600 | ribosomal protein L18a, putative |
Entamoeba histolytica | EHI_090020 | ribosomal protein L18a, putative |
Entamoeba histolytica | EHI_131940 | ribosomal protein L18a, putative |
Echinococcus multilocularis | EmuJ_000581100 | ribosomal protein L18a |
Giardia lamblia | GL50803_16387 | Ribosomal protein L18a |
Homo sapiens | ENSG00000105640 | ribosomal protein L18a |
Leishmania braziliensis | LbrM.34.0600 | 60S ribosomal protein L18a, putative |
Leishmania donovani | LdBPK_350600.1 | 60S ribosomal protein L18a, putative |
Leishmania infantum | LinJ.32.0930 | 60S ribosomal protein L18a, putative |
Leishmania infantum | LinJ.35.0600 | 60S ribosomal protein L18a, putative |
Leishmania major | LmjF.32.0880 | 60S ribosomal protein L18a, putative |
Leishmania major | LmjF.35.0600 | 60S ribosomal protein L18a, putative |
Leishmania mexicana | LmxM.31.0880 | 60S ribosomal protein L18a, putative |
Leishmania mexicana | LmxM.34.0600 | 60S ribosomal protein L18a, putative |
Loa Loa (eye worm) | LOAG_10387 | 60S ribosomal protein L18a |
Mus musculus | ENSMUSG00000045128 | ribosomal protein L18A |
Neospora caninum | NCLIV_025190 | LOC549444 protein, related |
Oryza sativa | 4327004 | Os01g0752300 |
Oryza sativa | 4326865 | Os01g0666900 |
Oryza sativa | 4339625 | Os05g0565000 |
Plasmodium berghei | PBANKA_1354400 | 60S ribosomal protein L18, putative |
Plasmodium falciparum | PF3D7_1341200 | 60S ribosomal protein L18, putative |
Plasmodium knowlesi | PKNH_1260200 | 60S ribosomal subunit protein L18, putative |
Plasmodium vivax | PVX_082965 | 60S ribosomal protein L18a, putative |
Plasmodium yoelii | PY01391 | Ribosomal L18ae protein family |
Saccharomyces cerevisiae | YMR242C | ribosomal 60S subunit protein L20A |
Saccharomyces cerevisiae | YOR312C | ribosomal 60S subunit protein L20B |
Schistosoma japonicum | Sjp_0201600 | ko:K02882 large subunit ribosomal protein L18Ae, putative |
Schistosoma mansoni | Smp_185810 | 60S ribosomal protein L18a |
Schistosoma mansoni | Smp_191540 | 60S ribosomal protein L18a |
Schmidtea mediterranea | mk4.001900.07 | 60S ribosomal protein L18a |
Trypanosoma brucei gambiense | Tbg972.10.4760 | 60S ribosomal protein L18a, putative |
Trypanosoma brucei gambiense | Tbg972.11.15790 | ribosomal protein L18, putative |
Trypanosoma brucei | Tb927.11.14130 | ribosomal protein L18, putative |
Trypanosoma brucei | Tb927.10.3840 | 60S ribosomal protein L18a, putative |
Trypanosoma brucei | Tb427tmp.01.5720 | ribosomal protein L18, putative |
Trypanosoma congolense | TcIL3000_10_3180 | ribosomal protein L18, putative |
Trypanosoma congolense | TcIL3000.11.14430 | ribosomal protein L18, putative |
Trypanosoma cruzi | TcCLB.511727.129 | ribosomal protein L18, putative |
Trypanosoma cruzi | TcCLB.506957.90 | 60S ribosomal protein L18a, putative |
Trypanosoma cruzi | TcCLB.511001.120 | 60S ribosomal protein L18a, putative |
Toxoplasma gondii | TGME49_262670 | ribosomal protein RPL18A |
Theileria parva | TP02_0803 | 60S ribosomal protein L18, putative |
Trichomonas vaginalis | TVAG_347250 | 60S ribosomal protein L18a, putative |
Trichomonas vaginalis | TVAG_416010 | 60S ribosomal protein L18a, putative |
Trichomonas vaginalis | TVAG_263760 | 60S ribosomal protein L18a, putative |
Trichomonas vaginalis | TVAG_061890 | 60S ribosomal protein L18a, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.01.5720 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.5720 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.5720 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb11.01.5720 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb927.10.3840 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.3840 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.3840 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.3840 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_1354400 | Plasmodium berghei | Essential | plasmo |
TGME49_262670 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
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 |
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.