Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | protein kinase C, beta | Starlite/ChEMBL | References |
Homo sapiens | protein kinase C, epsilon | Starlite/ChEMBL | References |
Homo sapiens | protein kinase C, alpha | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | Protein kinase C, brain isozyme | 0.0153 | 1 | 1 |
Echinococcus multilocularis | protein kinase c epsilon type | 0.0141 | 0.9022 | 0.9022 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Echinococcus granulosus | protein kinase c iota type | 0.0053 | 0.18 | 0.18 |
Echinococcus granulosus | RNA directed DNA polymerase | 0.0095 | 0.5281 | 0.5281 |
Loa Loa (eye worm) | AGC/PKC/ALPHA protein kinase | 0.01 | 0.571 | 0.6329 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Echinococcus granulosus | protein kinase C gamma type | 0.0131 | 0.82 | 0.82 |
Echinococcus multilocularis | serine:threonine protein kinase N2 | 0.0114 | 0.6848 | 0.6848 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0141 | 0.9022 | 0.9022 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Trypanosoma brucei | rac serine-threonine kinase, putative | 0.0031 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0153 | 1 | 1 |
Schistosoma mansoni | atypical protein kinase C | 0.0053 | 0.18 | 0.18 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0153 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0117 | 0.7081 | 0.7849 |
Brugia malayi | Protein kinase c protein 2 | 0.0122 | 0.751 | 0.8324 |
Entamoeba histolytica | PH domain containing protein kinase, putative | 0.0084 | 0.4358 | 1 |
Echinococcus granulosus | protein kinase c epsilon type | 0.0141 | 0.9022 | 0.9022 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Echinococcus multilocularis | telomerase reverse transcriptase subunit | 0.0095 | 0.5281 | 0.5281 |
Echinococcus multilocularis | serine threonine protein kinase | 0.0131 | 0.82 | 0.82 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Echinococcus multilocularis | RNA directed DNA polymerase | 0.0095 | 0.5281 | 0.5281 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Echinococcus granulosus | serine:threonine protein kinase N2 | 0.0084 | 0.4358 | 0.4358 |
Echinococcus multilocularis | protein kinase c iota type | 0.0053 | 0.18 | 0.18 |
Trichomonas vaginalis | AGC family protein kinase | 0.0031 | 0 | 0.5 |
Toxoplasma gondii | AGC kinase | 0.0031 | 0 | 0.5 |
Brugia malayi | protein kinase C II. | 0.0141 | 0.9022 | 1 |
Loa Loa (eye worm) | AGC/PKC/ETA protein kinase | 0.0141 | 0.9022 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0095 | 0.5281 | 0.5854 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 7.38 | Inhibition of PKCbeta2 (unknown origin) | ChEMBL. | No reference |
IC50 (binding) | = 41 nM | Inhibitory concentration against recombinant human Protein kinase C beta 2 | ChEMBL. | 15380221 |
IC50 (binding) | = 41 nM | Inhibitory concentration against recombinant human Protein kinase C beta 2 | ChEMBL. | 15380221 |
IC50 (binding) | = 41 nM | Inhibition of PKCbeta2 (unknown origin) | ChEMBL. | No reference |
IC50 (binding) | = 2232 nM | Inhibitory concentration against recombinant human Protein kinase C alpha | ChEMBL. | 15380221 |
IC50 (binding) | = 2232 nM | Inhibitory concentration against recombinant human Protein kinase C alpha | ChEMBL. | 15380221 |
IC50 (binding) | = 3905 nM | Inhibitory concentration against recombinant human Protein kinase C epsilon | ChEMBL. | 15380221 |
IC50 (binding) | = 3905 nM | Inhibitory concentration against recombinant human Protein kinase C epsilon | ChEMBL. | 15380221 |
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.