pI: 6.4987 |
Length (AA): 565 |
MW (Da): 63198 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
82 | 565 | 3mwu (A) | 0 | 384 | 27.00 | 0 | 1 | 0.517737 | 1.33 |
97 | 170 | 3llt (A) | 558 | 633 | 38.00 | 0.0067 | 0.94 | 0.463973 | 0.12 |
294 | 325 | 2y4i (B) | 762 | 793 | 53.00 | 0.004 | 0.38 | 0.548637 | 0.57 |
425 | 511 | 5vam (A) | 626 | 714 | 21.00 | 0 | 0.6 | 0.429282 | -0.88 |
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:
Ortholog group members (OG5_130490)
Species | Accession | Gene Product |
---|---|---|
Brugia malayi | Bm1_33235 | hypothetical protein |
Dictyostelium discoideum | DDB_G0283065 | PEK family protein kinase |
Echinococcus granulosus | EgrG_000183600 | eukaryotic translation initiation factor 2 alpha |
Entamoeba histolytica | EHI_035950 | protein kinase domain containing protein |
Entamoeba histolytica | EHI_109700 | protein kinase domain containing protein |
Echinococcus multilocularis | EmuJ_000183600 | eukaryotic translation initiation factor 2 alpha |
Homo sapiens | ENSG00000086232 | eukaryotic translation initiation factor 2-alpha kinase 1 |
Leishmania braziliensis | LbrM.19.0260 | protein kinase |
Leishmania donovani | LdBPK_110060.1 | protein kinase, putative |
Leishmania infantum | LinJ.11.0060 | protein kinase, putative |
Leishmania major | LmjF.11.0060 | protein kinase, putative |
Leishmania mexicana | LmxM.11.0060 | protein kinase, putative |
Loa Loa (eye worm) | LOAG_05819 | PEK/HRI protein kinase |
Mus musculus | 15467 | eukaryotic translation initiation factor 2 alpha kinase 1 |
Trypanosoma brucei gambiense | Tbg972.11.8150 | protein kinase, putative |
Trypanosoma brucei | Tb11.02.5050b | protein kinase, putative |
Trypanosoma brucei | Tb927.11.7210 | eukaryotic translation initiation factor 2-alpha kinase 1, putative |
Trypanosoma congolense | TcIL3000.11.7780 | protein kinase, putative |
Trypanosoma congolense | TcIL3000_0_47340 | protein kinase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.02.5050 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.02.5050 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb11.02.5050 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb11.02.5050 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 |
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.
Species | Known druggable target | Linked compounds | Reference |
---|---|---|---|
Homo sapiens | eukaryotic translation initiation factor 2-alpha kinase 1 | Compounds | References |
Species | Target | Length | Identity | Alignment span | Linked Drugs | Reference |
---|---|---|---|---|---|---|
Plasmodium falciparum (isolate 3D7) | Cell division control protein 2 homolog | 288 aa | 24.9% | 233 aa | Compounds | References |
Rattus norvegicus | Jak1 protein | 210 aa | 19.8% | 192 aa | Compounds | References |
Rattus norvegicus | Cell division protein kinase 5 | 292 aa | 22.5% | 271 aa | Compounds | References |
Homo sapiens | Cyclin-dependent kinase 1/cyclin B1 | 297 aa | 24.5% | 245 aa | Compounds | References |