pI: 10.5038 |
Length (AA): 317 |
MW (Da): 36275 |
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 4 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 |
---|---|---|---|---|---|---|---|---|---|
18 | 84 | 1tif () | 7 | 78 | 21.00 | 0.0000000000047 | 0.02 | 0.42 | -0.26 |
31 | 232 | 1giy (E) | 40 | 318 | 26.00 | 0 | 0.91 | 0.84 | 1.94 |
94 | 296 | 5dm6 (B) | 1 | 203 | 33.00 | 0 | 1 | 0.923379 | 0.88 |
95 | 296 | 4wfa (B) | 3 | 216 | 36.00 | 0 | 1 | 0.945224 | 0.93 |
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 | intra-erythrocytic - 24 hs, intra-erythrocytic - 32 hs, intra-erythrocytic - 40 hs, intra-erythrocytic - 48 hs. | Otto TD |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 8 hs, gametocyte, merozoite, sporozoite, early ring, early schizont, early trophozoite, late ring, late schizont, late trophozoite, Oocyst, Sporozoite. | Otto TD PlasmoDB Zanghi G |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 0 hs, intra-erythrocytic - 16 hs, Ring, Female Gametocyte. | Otto TD Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Male Gametocyte. | Lasonder E |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
Ortholog group members (OG5_127133)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G17465 | 50S ribosomal protein L3-2 |
Arabidopsis thaliana | AT2G43030 | 50S ribosomal protein L3-1 |
Babesia bovis | BBOV_III008320 | 50S ribosomal protein L3, putative |
Babesia bovis | BBOV_I004730 | ribosomal protein L3 domain containing protein |
Brugia malayi | Bm1_56120 | Mitochondrial 39S ribosomal protein L3 |
Candida albicans | CaO19.7485 | likely mitochondrial ribosomal protein similar to S. cerevisiae MRPL9 (YGR220C) large subunit protein (E. coli L3) |
Caenorhabditis elegans | CELE_C26E6.6 | Protein MRPS-18C |
Chlamydia trachomatis | CT_528 | 50S ribosomal protein L3 |
Dictyostelium discoideum | DDB_G0288983 | ribosomal protein L3, mitochondrial |
Drosophila melanogaster | Dmel_CG8288 | mitochondrial ribosomal protein L3 |
Escherichia coli | b3320 | 50S ribosomal subunit protein L3 |
Echinococcus granulosus | EgrG_000927800 | 39S ribosomal protein L3 mitochondrial |
Echinococcus multilocularis | EmuJ_000927800 | 39S ribosomal protein L3, mitochondrial |
Homo sapiens | ENSG00000114686 | mitochondrial ribosomal protein L3 |
Leishmania braziliensis | LbrM.29.0040 | ribosomal protein L3-like protein |
Leishmania donovani | LdBPK_290030.1 | ribosomal protein L3-like protein |
Leishmania infantum | LinJ.29.0030 | ribosomal protein L3-like protein |
Leishmania major | LmjF.29.0030 | ribosomal protein L3-like protein |
Leishmania mexicana | LmxM.08_29.0030 | ribosomal protein L3-like protein |
Mycobacterium leprae | ML1863c | PROBABLE 50S RIBOSOMAL PROTEIN L3 RPLC |
Mus musculus | 94062 | mitochondrial ribosomal protein L3 |
Mycobacterium tuberculosis | Rv0701 | 50S ribosomal protein L3 RplC |
Mycobacterium ulcerans | MUL_0790 | 50S ribosomal protein L3 |
Neospora caninum | NCLIV_018210 | 50S ribosomal protein L3, putative |
Neospora caninum | NCLIV_030720 | ribosomal protein L3p, putative |
Oryza sativa | 4327104 | Os01g0251100 |
Oryza sativa | 4328236 | Os02g0137200 |
Plasmodium berghei | PBANKA_1458600 | mitochondrial ribosomal protein L3 precursor, putative |
Plasmodium berghei | PBANKA_0819200 | 50S ribosomal protein L3, apicoplast, putative |
Plasmodium falciparum | PF3D7_1245400 | mitochondrial ribosomal protein L3 precursor, putative |
Plasmodium falciparum | PF3D7_0918200 | 50S ribosomal protein L3, apicoplast, putative |
Plasmodium knowlesi | PKNH_1465100 | 50S ribosomal protein L3, putative |
Plasmodium knowlesi | PKNH_0716200 | 50S ribosomal protein L3, apicoplast, putative |
Plasmodium vivax | PVX_099330 | 50S ribosomal protein L3, apicoplast, putative |
Plasmodium vivax | PVX_101165 | 50S ribosomal protein L3, putative |
Plasmodium yoelii | PY07001 | ribosomal protein L3, putative |
Plasmodium yoelii | PY04814 | ribosomal protein L3, putative |
Saccharomyces cerevisiae | YGR220C | mitochondrial 54S ribosomal protein YmL9 |
Schistosoma japonicum | Sjp_0212870 | ko:K02906 large subunit ribosomal protein L3, putative |
Schistosoma mansoni | Smp_087440 | 50S ribosomal protein L3 |
Schmidtea mediterranea | mk4.000669.05 | Putative 39S ribosomal protein L3, mitochondrial |
Trypanosoma brucei gambiense | Tbg972.3.6310 | ribosomal protein L3 mitochondrial, putative |
Trypanosoma brucei | Tb927.3.5610 | Mitochondrial ribosomal protein L3 |
Trypanosoma congolense | TcIL3000_3_3550 | ribosomal protein L3 mitochondrial, putative |
Trypanosoma cruzi | TcCLB.510645.49 | ribosomal protein L3 mitochondrial, putative |
Trypanosoma cruzi | TcCLB.507795.100 | mitochondrial ribosomal protein L3, putative |
Toxoplasma gondii | TGME49_230050 | 50S ribosomal protein L3, putative |
Toxoplasma gondii | TGME49_243480 | 50S ribosomal protein L3, putative |
Treponema pallidum | TP0189 | 50S ribosomal protein L3 |
Theileria parva | TP03_0514 | 50S ribosomal protein L3, putative |
Theileria parva | TP04_0733 | 60S ribosomal protein L3, putative |
Wolbachia endosymbiont of Brugia malayi | Wbm0341 | 50S ribosomal protein L3 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu713 | Mycobacterium tuberculosis | essential | nmpdr |
Tb927.3.5610 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.3.5610 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.3.5610 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.3.5610 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b3320 | Escherichia coli | essential | goodall |
CELE_C26E6.6 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_C26E6.6 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_C26E6.6 | Caenorhabditis elegans | slow growth | wormbase |
CELE_C26E6.6 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_0819200 | Plasmodium berghei | Essential | plasmo |
PBANKA_1458600 | Plasmodium berghei | Essential | plasmo |
TGME49_230050 | Toxoplasma gondii | Probably essential | sidik |
TGME49_243480 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
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.