pI: 8.2009 |
Length (AA): 863 |
MW (Da): 92104 |
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 5 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 |
---|---|---|---|---|---|---|---|---|---|
11 | 455 | 1jny (A) | 4 | 427 | 22.00 | 0 | 1 | 0.79 | 0.09 |
13 | 192 | 1d2e (A) | 57 | 216 | 34.00 | 0 | 1 | 0.46 | -0.74 |
9 | 733 | 5izl (A) | 3 | 508 | 48.00 | 0 | 1 | 0.687493 | 1.29 |
323 | 410 | 1xe1 (A) | 27 | 107 | 22.00 | 0 | 0.84 | 0.30887 | -0.3 |
715 | 808 | 2pjp (A) | 513 | 603 | 12.00 | 0.011 | 0.01 | 0.265522 | -0.89 |
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 | VEG Tachyzoite, ME49 Tachyzoite, ME49 merozoite, ME49 Bradyzoite. | Gregory Hehl AB Sibley/Greg |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | ME49 Oocyst. | Fritz HM |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
Sibley/Greg | 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. |
Gregory | ToxoDB |
Ortholog group members (OG5_130322)
Species | Accession | Gene Product |
---|---|---|
Brugia malayi | Bm1_55780 | Elongation factor Tu GTP binding domain containing protein |
Caenorhabditis elegans | CELE_C47B2.7 | Protein SELB-1, isoform B |
Dictyostelium discoideum | DDB_G0270386 | hypothetical protein |
Drosophila melanogaster | Dmel_CG9841 | CG9841 gene product from transcript CG9841-RA |
Echinococcus granulosus | EgrG_000516300 | selenocysteine specific elongation factor |
Echinococcus multilocularis | EmuJ_000516300 | selenocysteine specific elongation factor |
Homo sapiens | ENSG00000132394 | eukaryotic elongation factor, selenocysteine-tRNA-specific |
Leishmania braziliensis | LbrM.20.2460 | selenocysteine-specific elongation factor, putative |
Leishmania donovani | LdBPK_342700.1 | selenocysteine-specific elongation factor, putative |
Leishmania infantum | LinJ.34.2700 | selenocysteine-specific elongation factor, putative |
Leishmania major | LmjF.34.2840 | selenocysteine-specific elongation factor, putative |
Leishmania mexicana | LmxM.33.2840 | selenocysteine-specific elongation factor, putative |
Loa Loa (eye worm) | LOAG_00130 | hypothetical protein |
Mus musculus | ENSMUSG00000033216 | eukaryotic elongation factor, selenocysteine-tRNA-specific |
Neospora caninum | NCLIV_059360 | elongation factor Tu GTP-binding domain- containing protein, putative |
Plasmodium berghei | PBANKA_0203500 | selenocysteine-specific elongation factor selB homologue, putative |
Plasmodium falciparum | PF3D7_0110100 | selenocysteine-specific elongation factor selB homologue, putative |
Plasmodium knowlesi | PKNH_0203700 | selenocysteine-specific elongation factor selB homologue, putative |
Plasmodium vivax | PVX_081285 | selenocysteine-specific elongation factor selB homologue, putative |
Plasmodium yoelii | PY00420 | selenocysteine-specific elongation factor |
Schistosoma japonicum | Sjp_0082810 | ko:K03231 elongation factor EF-1 alpha subunit, putative |
Schistosoma mansoni | Smp_176630 | selenocysteine-specific elongation factor |
Schmidtea mediterranea | mk4.020493.00 | Selenocysteine-specific elongation factor |
Schmidtea mediterranea | mk4.001056.01 | Selenocysteine-specific elongation factor |
Schmidtea mediterranea | mk4.009144.00 | Selenocysteine-specific elongation factor |
Trypanosoma brucei gambiense | Tbg972.4.1730 | selenocysteine-tRNA-specific elongation factor, putative |
Trypanosoma brucei | Tb927.4.1820 | selenocysteine-specific elongation factor, putative |
Trypanosoma congolense | TcIL3000_4_1470 | selenocysteine-specific elongation factor, putative |
Trypanosoma cruzi | TcCLB.504013.50 | selenocysteine-specific elongation factor, putative |
Trypanosoma cruzi | TcCLB.510879.70 | selenocysteine-specific elongation factor, putative |
Toxoplasma gondii | TGME49_216960 | elongation factor Tu GTP binding domain-containing protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.4.1820 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.1820 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.1820 | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb927.4.1820 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_0203500 | Plasmodium berghei | Dispensable | plasmo |
TGME49_216960 this record | Toxoplasma gondii | Probably non-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 |
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 |
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.