pI: 11.5664 |
Length (AA): 143 |
MW (Da): 16299 |
Paralog Number:
2
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 3 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 |
---|---|---|---|---|---|---|---|---|---|
6 | 123 | 1vq8 (T) | 1 | 119 | 37.00 | 0 | 1 | 1.36427 | -0.77 |
45 | 102 | 2jvv (A) | 126 | 179 | 22.00 | 0 | 0.32 | 0.595394 | -1.11 |
59 | 103 | 1aog (A) | 210 | 261 | 40.00 | 0.51 | 0.73 | 0.549085 | 0.79 |
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 | epimastigote, metacyclic. | Smircich P |
Smircich P | Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi. |
Ortholog group members (OG5_126931)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G49910 | 60S ribosomal protein L26-1 |
Arabidopsis thaliana | AT5G67510 | 60S ribosomal protein L26-2 |
Babesia bovis | BBOV_III008670 | ribosomal protein L24 family protein |
Brugia malayi | Bm1_47020 | 60S ribosomal protein L26 |
Caenorhabditis elegans | CELE_F28C6.7 | Protein RPL-26, isoform A |
Cryptosporidium hominis | Chro.60530 | ribosomal protein L26 |
Cryptosporidium parvum | cgd6_4620 | 60S ribosomal protein L26 |
Dictyostelium discoideum | DDB_G0283741 | S60 ribosomal protein L26 |
Drosophila melanogaster | Dmel_CG6846 | Ribosomal protein L26 |
Echinococcus granulosus | EgrG_000972500 | 60S ribosomal protein L26 |
Entamoeba histolytica | EHI_152570 | 60S ribosomal protein L26, putative |
Entamoeba histolytica | EHI_111570 | 60S ribosomal protein L26, putative |
Echinococcus multilocularis | EmuJ_000972500 | 60S ribosomal protein L26 |
Giardia lamblia | GL50803_15046 | Ribosomal protein L26 |
Homo sapiens | ENSG00000037241 | ribosomal protein L26-like 1 |
Homo sapiens | ENSG00000161970 | ribosomal protein L26 |
Leishmania braziliensis | LbrM.24.2130 | 60S ribosomal protein L26, putative |
Leishmania braziliensis | LbrM.34.1580 | 60S ribosomal protein L26, putative |
Leishmania infantum | LinJ.24.2140 | 60S ribosomal protein L26, putative |
Leishmania infantum | LinJ.35.1670 | 60S ribosomal protein L26, putative |
Leishmania major | LmjF.24.2050 | 60S ribosomal protein L26, putative |
Leishmania major | LmjF.35.1670 | 60S ribosomal protein L26, putative |
Leishmania mexicana | LmxM.24.2050 | 60S ribosomal protein L26, putative |
Leishmania mexicana | LmxM.34.1670 | 60S ribosomal protein L26, putative |
Loa Loa (eye worm) | LOAG_06690 | large subunit ribosomal protein 26 |
Mus musculus | ENSMUSG00000060938 | ribosomal protein L26 |
Neospora caninum | NCLIV_064360 | 50S ribosomal protein L24P, related |
Oryza sativa | 4349791 | Os11g0151300 |
Oryza sativa | 4351513 | Os12g0150100 |
Plasmodium berghei | PBANKA_0410600 | 60S ribosomal protein L26, putative |
Plasmodium falciparum | PF3D7_0312800 | 60S ribosomal protein L26, putative |
Plasmodium knowlesi | PKNH_0829400 | 60S ribosomal protein L26, putative |
Plasmodium vivax | PVX_119740 | 60S ribosomal protein L26, putative |
Plasmodium yoelii | PY04507 | ribosomal protein L24 |
Saccharomyces cerevisiae | YLR344W | ribosomal 60S subunit protein L26A |
Saccharomyces cerevisiae | YGR034W | ribosomal 60S subunit protein L26B |
Schistosoma japonicum | Sjp_0032430 | ko:K02898 large subunit ribosomal protein L26e, putative |
Schistosoma mansoni | Smp_098960 | 60S ribosomal protein L26 |
Schmidtea mediterranea | mk4.000892.05 | |
Trypanosoma brucei gambiense | Tbg972.9.9030 | 60S ribosomal protein L26, putative |
Trypanosoma brucei gambiense | Tbg972.8.6240 | 60S ribosomal protein L26, putative |
Trypanosoma brucei | Tb927.8.6180 | 60S ribosomal protein L26, putative |
Trypanosoma brucei | Tb927.9.14370 | 60S ribosomal protein L26, putative |
Trypanosoma congolense | TcIL3000_9_6170 | 60S ribosomal protein L26, putative |
Trypanosoma cruzi | TcCLB.510761.14 | 60S ribosomal protein L26, putative |
Trypanosoma cruzi | TcCLB.511903.130 | 60S ribosomal protein L26, putative |
Trypanosoma cruzi | TcCLB.511067.20 | 60S ribosomal protein L26, putative |
Toxoplasma gondii | TGME49_248390 | ribosomal protein RPL26 |
Theileria parva | TP04_0771 | 60S ribosomal protein L26, putative |
Trichomonas vaginalis | TVAG_389320 | 60S ribosomal protein L26, putative |
Trichomonas vaginalis | TVAG_237220 | 60S ribosomal protein L26, putative |
Trichomonas vaginalis | TVAG_038050 | 50S ribosomal protein L24p, putative |
Trichomonas vaginalis | TVAG_190230 | 60S ribosomal protein L26, putative |
Trichomonas vaginalis | TVAG_078160 | 50S ribosomal protein L24p, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.4850 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.4850 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.4850 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb09.211.4850 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb927.8.6180 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.8.6180 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.8.6180 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.8.6180 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F28C6.7 | Caenorhabditis elegans | embryonic arrest | wormbase |
CELE_F28C6.7 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F28C6.7 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_F28C6.7 | Caenorhabditis elegans | slow growth | wormbase |
CELE_F28C6.7 | Caenorhabditis elegans | sterile | wormbase |
TGME49_248390 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
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 |
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.