Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | protein kinase C, alpha | Starlite/ChEMBL | References |
Homo sapiens | protein kinase C, epsilon | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | atypical protein kinase C | 0.0035 | 0.1446 | 0.1446 |
Echinococcus granulosus | protein kinase C gamma type | 0.0071 | 0.5017 | 0.5017 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Trypanosoma brucei | rac serine-threonine kinase, putative | 0.0021 | 0 | 0.5 |
Echinococcus multilocularis | protein kinase c iota type | 0.0035 | 0.1446 | 0.1446 |
Echinococcus granulosus | protein kinase c epsilon type | 0.0122 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0062 | 0.4117 | 0.4117 |
Echinococcus multilocularis | telomerase reverse transcriptase subunit | 0.0048 | 0.2671 | 0.2671 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0048 | 0.2671 | 0.2671 |
Echinococcus multilocularis | RNA directed DNA polymerase | 0.0048 | 0.2671 | 0.2671 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Echinococcus granulosus | protein kinase c iota type | 0.0035 | 0.1446 | 0.1446 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Entamoeba histolytica | PH domain containing protein kinase, putative | 0.0084 | 0.6253 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0122 | 1 | 1 |
Echinococcus granulosus | serine:threonine protein kinase N2 | 0.0084 | 0.6253 | 0.6253 |
Toxoplasma gondii | AGC kinase | 0.0021 | 0 | 0.5 |
Brugia malayi | Protein kinase c protein 2 | 0.0066 | 0.4462 | 0.4462 |
Echinococcus multilocularis | serine threonine protein kinase | 0.0071 | 0.5017 | 0.5017 |
Trichomonas vaginalis | AGC family protein kinase | 0.0021 | 0 | 0.5 |
Loa Loa (eye worm) | AGC/PKC/ALPHA protein kinase | 0.0051 | 0.3016 | 0.3016 |
Loa Loa (eye worm) | AGC/PKC/ETA protein kinase | 0.0122 | 1 | 1 |
Echinococcus granulosus | Protein kinase C brain isozyme | 0.0086 | 0.6463 | 0.6463 |
Echinococcus multilocularis | Protein kinase C, brain isozyme | 0.0086 | 0.6463 | 0.6463 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0086 | 0.6463 | 0.6463 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0086 | 0.6463 | 0.6463 |
Echinococcus multilocularis | protein kinase c epsilon type | 0.0122 | 1 | 1 |
Echinococcus granulosus | RNA directed DNA polymerase | 0.0048 | 0.2671 | 0.2671 |
Echinococcus multilocularis | serine:threonine protein kinase N2 | 0.0104 | 0.8254 | 0.8254 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 15.2 nM | Displacement of [20-3H] phorbol 12, 13-dibutylate from recombinant PKCepsilon (unknown origin) in presence of 100 ug/ml 100% phosphatidylserine | ChEMBL. | 25437619 |
Ki (binding) | = 33.1 nM | Displacement of [20-3H] phorbol 12, 13-dibutylate from recombinant PKCalpha (unknown origin) in presence of 100 ug/ml 100% phosphatidylserine | ChEMBL. | 25437619 |
Ki (binding) | = 58.8 nM | Displacement of [20-3H] phorbol 12, 13-dibutylate from recombinant PKCepsilon (unknown origin) in presence of nuclear membrane mimetic lipid mixture | ChEMBL. | 25437619 |
Ki (binding) | = 73 nM | Displacement of [20-3H] phorbol 12, 13-dibutylate from recombinant PKCalpha (unknown origin) in presence of nuclear membrane mimetic lipid mixture | ChEMBL. | 25437619 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.