pI: 5.8984 |
Length (AA): 586 |
MW (Da): 63550 |
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 7 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 |
---|---|---|---|---|---|---|---|---|---|
126 | 583 | 1r5b (A) | 215 | 661 | 45.00 | 0 | 1 | 1.21 | -0.09 |
145 | 584 | 1f60 (A) | 3 | 441 | 39.00 | 0 | 1 | 1.19 | -1.09 |
52 | 583 | 3mmp (A) | 177 | 1392 | 24.00 | 0 | 1 | 0.89165 | 1.11 |
145 | 583 | 1r5b (A) | 234 | 661 | 48.00 | 0 | 1 | 1.16495 | -0.01 |
147 | 582 | 3vmf (A) | 4 | 427 | 39.00 | 0 | 1 | 1.27063 | -0.94 |
147 | 584 | 1f60 (A) | 5 | 441 | 42.00 | 0 | 1 | 1.29404 | -0.64 |
147 | 582 | 1jny (A) | 4 | 427 | 40.00 | 0 | 1 | 1.22463 | -0.58 |
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 | VEG Tachyzoite, ME49 Tachyzoite, ME49 merozoite, ME49 Bradyzoite. | Gregory Hehl AB Sibley/Greg |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | ME49 Oocyst. | Fritz HM |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
Gregory | ToxoDB |
Hehl AB | Asexual expansion of Toxoplasma gondii merozoites is distinct from tachyzoites and entails expression of non-overlapping gene families to attach, invade, and replicate within feline enterocytes. |
Sibley/Greg | ToxoDB |
Ortholog group members (OG5_127225)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G18070 | translation elongation factor EF1A/initiation factor IF2gamma family protein |
Babesia bovis | BBOV_II000640 | translation elongation factor EF-1, subunit alpha protein, putative |
Brugia malayi | Bm1_24170 | Elongation factor Tu C-terminal domain containing protein |
Candida albicans | CaO19.1378 | translation release factor 3 |
Candida albicans | CaO19.8958 | translation release factor 3 |
Caenorhabditis elegans | CELE_H19N07.1 | Protein ERFA-3, isoform B |
Cryptosporidium parvum | cgd2_2070 | translation elongation factor EF-1, subunit alpha, putative |
Dictyostelium discoideum | DDB_G0277919 | hypothetical protein |
Drosophila melanogaster | Dmel_CG6382 | Ef1alpha-like factor |
Echinococcus granulosus | EgrG_000136000 | g1 to s phase transition protein |
Entamoeba histolytica | EHI_004230 | guanine nucleotide regulatory protein, putative |
Echinococcus multilocularis | EmuJ_000136000 | g1 to s phase transition protein |
Giardia lamblia | GL50803_17460 | G1 to S phase transition protein 1, putative |
Homo sapiens | ENSG00000103342 | G1 to S phase transition 1 |
Homo sapiens | ENSG00000189369 | G1 to S phase transition 2 |
Leishmania braziliensis | LbrM.11.0970 | eukaryotic release factor 3, putative |
Leishmania donovani | LdBPK_111160.1 | eukaryotic release factor 3, putative |
Leishmania infantum | LinJ.11.1160 | eukaryotic release factor 3, putative |
Leishmania major | LmjF.11.1170 | eukaryotic release factor 3, putative |
Leishmania mexicana | LmxM.11.1170 | eukaryotic release factor 3, putative |
Loa Loa (eye worm) | LOAG_04858 | elongation factor Tu domain-containing protein |
Mus musculus | ENSMUSG00000071723 | G1 to S phase transition 2 |
Mus musculus | 14852 | G1 to S phase transition 1 |
Neospora caninum | NCLIV_009700 | Elongation factor 1-alpha, related |
Oryza sativa | 4335338 | Os04g0270100 |
Plasmodium berghei | PBANKA_0924900 | translation elongation factor EF-1, subunit alpha, putative |
Plasmodium falciparum | PF3D7_1123400 | translation elongation factor EF-1, subunit alpha, putative |
Plasmodium knowlesi | PKNH_0921200 | translation elongation factor EF-1, putative |
Plasmodium vivax | PVX_091785 | translation elongation factor EF-1, subunit alpha, putative |
Plasmodium yoelii | PY04385 | Elongation factor Tu family, putative |
Saccharomyces cerevisiae | YDR172W | translation termination factor GTPase eRF3 |
Schistosoma japonicum | Sjp_0215560 | ko:K03267 G1 to S phase transition protein, putative |
Schistosoma japonicum | Sjp_0128460 | Eukaryotic peptide chain release factor GTP-binding subunit ERF3A, putative |
Schistosoma mansoni | Smp_005180 | hypothetical protein |
Schmidtea mediterranea | mk4.000515.13 | |
Trypanosoma brucei gambiense | Tbg972.11.6940 | eukaryotic release factor 3, putative |
Trypanosoma brucei | Tb927.11.6160 | eukaryotic release factor 3, putative |
Trypanosoma congolense | TcIL3000_0_08320 | eukaryotic release factor 3, putative |
Trypanosoma congolense | TcIL3000.11.6690 | eukaryotic release factor 3, putative |
Trypanosoma cruzi | TcCLB.506297.300 | eukaryotic release factor 3, putative |
Trypanosoma cruzi | TcCLB.508041.60 | eukaryotic release factor 3, putative |
Toxoplasma gondii | TGME49_320570 | elongation factor Tu, putative |
Theileria parva | TP04_0514 | translation elongation factor EF-1, subunit alpha, putative |
Trichomonas vaginalis | TVAG_133120 | sulfate adenylyltransferase subunit, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.02.4030 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb11.02.4030 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb11.02.4030 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb11.02.4030 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_H19N07.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_H19N07.1 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_H19N07.1 | Caenorhabditis elegans | slow growth | wormbase |
CELE_H19N07.1 | Caenorhabditis elegans | sterile | wormbase |
YDR172W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0924900 | Plasmodium berghei | Essential | plasmo |
TGME49_320570 this record | Toxoplasma gondii | Probably essential | sidik |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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 |
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.
Druggability index (range: 0 to 1): 0.2
Species | Known druggable target | Linked compounds | Reference |
---|---|---|---|
Saccharomyces cerevisiae | translation termination factor GTPase eRF3 | Compounds | References |
Species | Target | Length | Identity | Alignment span | Linked Drugs | Reference |
---|---|---|---|---|---|---|
Leishmania major | elongation factor 1-alpha | 449 aa | 38.4% | 438 aa | Compounds | References |