pI: 8.4698 |
Length (AA): 1177 |
MW (Da): 127793 |
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 8 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 |
---|---|---|---|---|---|---|---|---|---|
697 | 1172 | 2acx (A) | 14 | 471 | 21.00 | 0 | 1 | 0.56 | 0.06 |
874 | 1155 | 1phk () | 16 | 290 | 27.00 | 0 | 1 | 0.55 | -0.93 |
672 | 787 | 4bgj (A) | 507 | 641 | 21.00 | 0 | 0.91 | 0.326656 | -0.7 |
685 | 781 | 4bgj (A) | 520 | 630 | 25.00 | 0.23 | 1 | 0.352513 | -0.34 |
728 | 1164 | 1fmk (A) | 120 | 529 | 24.00 | 0 | 1 | 0.437383 | 1.1 |
875 | 1156 | 4krd (A) | 5 | 301 | 26.00 | 0 | 1 | 0.539692 | -0.54 |
883 | 1171 | 5kbr (A) | 276 | 538 | 38.00 | 0 | 1 | 0.43464 | 0.15 |
891 | 1157 | 1cm8 (A) | 41 | 322 | 25.00 | 0 | 1 | 0.489948 | -0.37 |
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_166679)
Species | Accession | Gene Product |
---|---|---|
Leishmania braziliensis | LbrM.07.1260 | protein kinase, putative |
Leishmania donovani | LdBPK_071050.1 | protein kinase, putative |
Leishmania infantum | LinJ.07.1050 | protein kinase, putative |
Leishmania major | LmjF.07.0880 | protein kinase, putative |
Leishmania mexicana | LmxM.07.0880 | protein kinase, putative |
Trypanosoma cruzi | TcCLB.503715.40 | STE/STE11 serine/threonine-protein kinase, putative |
Trypanosoma cruzi | TcCLB.509607.50 | STE/STE11 serine/threonine-protein kinase, putative |
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): 0.5
Species | Target | Length | Identity | Alignment span | Linked Drugs | Reference |
---|---|---|---|---|---|---|
Rattus norvegicus | Jak1 protein | 210 aa | 25.0% | 204 aa | Compounds | References |
Plasmodium falciparum (isolate 3D7) | Cell division control protein 2 homolog | 288 aa | 26.5% | 298 aa | Compounds | References |
Xenopus laevis | Aurora kinase B-A | 361 aa | 25.8% | 295 aa | Compounds | References |
Rattus norvegicus | Cell division protein kinase 5 | 292 aa | 27.5% | 306 aa | Compounds | References |
Rattus norvegicus | Serine/threonine-protein kinase pim-3 | 326 aa | 28.3% | 297 aa | Compounds | References |
Homo sapiens | Cyclin-dependent kinase 1/cyclin B1 | 297 aa | 28.2% | 309 aa | Compounds | References |
Schizosaccharomyces pombe 972h- | Casein kinase II subunit alpha | 332 aa | 22.0% | 291 aa | Compounds | References |
Patiria pectinifera | Cdc2 | 300 aa | 28.1% | 303 aa | Compounds | References |
Xenopus laevis | Aurora kinase B-B | 368 aa | 26.1% | 295 aa | Compounds | References |