pI: 9.3689 |
Length (AA): 839 |
MW (Da): 90458 |
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 6 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 |
---|---|---|---|---|---|---|---|---|---|
359 | 827 | 1d2e (A) | 63 | 450 | 22.00 | 0 | 1 | 0.51 | 0.4 |
470 | 812 | 2c78 (A) | 64 | 405 | 21.00 | 0 | 1 | 0.67 | -0.48 |
15 | 173 | 5cwj (A) | 2 | 160 | 11.00 | 0.008 | 0.02 | 0.317811 | -0.52 |
353 | 694 | 1kk1 (A) | 10 | 285 | 30.00 | 0.00016 | 0.38 | 0.216928 | 1.31 |
360 | 811 | 4zv4 (A) | 19 | 398 | 28.00 | 0 | 1 | 0.549037 | 1.02 |
633 | 723 | 1d1n (A) | 150 | 237 | 24.00 | 0 | 0.5 | 0.309862 | 0.32 |
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 |
---|---|---|---|
Mid 40-60% percentile | amastigotes, metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_127896)
Species | Accession | Gene Product |
---|---|---|
Brugia malayi | Bm1_52050 | Elongation factor Tu GTP binding domain containing protein |
Brugia malayi | Bm1_40375 | GTP-binding protein AGP-1 |
Caenorhabditis elegans | CELE_T04H1.2 | Protein T04H1.2 |
Caenorhabditis elegans | CELE_Y38C9A.2 | Protein CGP-1 |
Dictyostelium discoideum | DDB_G0292538 | GTP-binding protein 1 |
Drosophila melanogaster | Dmel_CG5729 | CG5729 gene product from transcript CG5729-RB |
Drosophila melanogaster | Dmel_CG2017 | CG2017 gene product from transcript CG2017-RD |
Echinococcus granulosus | EgrG_001129300 | GTP binding protein 1 |
Echinococcus multilocularis | EmuJ_001129300 | GTP binding protein 1 |
Homo sapiens | ENSG00000100226 | GTP binding protein 1 |
Homo sapiens | ENSG00000172432 | GTP binding protein 2 |
Leishmania braziliensis | LbrM.33.3070 | GTP-binding protein, putative,GTP-binding elongation factor tu family protein, putative |
Leishmania donovani | LdBPK_332930.1 | GTP-binding protein, putative |
Leishmania infantum | LinJ.33.2930 | GTP-binding protein, putative,GTP-binding elongation factor tu family protein, putative |
Leishmania major | LmjF.33.2790 | GTP-binding protein, putative,GTP-binding elongation factor tu family protein, putative |
Leishmania mexicana | LmxM.32.2790 | GTP-binding protein, putative,GTP-binding elongation factor tu family protein, putative |
Loa Loa (eye worm) | LOAG_04708 | hypothetical protein |
Loa Loa (eye worm) | LOAG_04209 | GTP-binding protein AGP-1 |
Mus musculus | ENSMUSG00000023952 | GTP binding protein 2 |
Mus musculus | ENSMUSG00000042535 | GTP binding protein 1 |
Neospora caninum | NCLIV_010100 | hypothetical protein |
Schistosoma japonicum | Sjp_0300640 | GTP-binding protein 1, putative |
Schistosoma mansoni | Smp_169280 | GTP binding protein |
Schmidtea mediterranea | mk4.000088.07 | GTP-binding protein cgp-1 |
Trypanosoma brucei gambiense | Tbg.972.2.1970 | GTP-binding elongation factor Tu family, putative |
Trypanosoma brucei | Tb927.2.3620 | GTP-binding elongation factor Tu family, putative |
Trypanosoma cruzi | TcCLB.507715.40 | GTP-binding elongation factor Tu family, putative |
Trypanosoma cruzi | TcCLB.511115.20 | GTP-binding elongation factor Tu family, putative |
Toxoplasma gondii | TGME49_320150 | elongation factor Tu GTP binding domain-containing protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.2.3620 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.2.3620 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.2.3620 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.2.3620 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
TGME49_320150 | Toxoplasma gondii | Essentiality uncertain | sidik |
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 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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.