Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0084 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0038 | 0.3986 | 0.4096 |
Loa Loa (eye worm) | hypothetical protein | 0.0044 | 0.4761 | 0.4898 |
Schistosoma mansoni | hypothetical protein | 0.0068 | 0.7926 | 1 |
Echinococcus multilocularis | RNA directed DNA polymerase | 0.0038 | 0.3986 | 0.3971 |
Entamoeba histolytica | protein kinase, putative | 0.0008 | 0.0024 | 0.5 |
Brugia malayi | hypothetical protein | 0.0066 | 0.7622 | 0.7616 |
Echinococcus granulosus | jun protein | 0.0084 | 1 | 1 |
Echinococcus multilocularis | telomerase reverse transcriptase subunit | 0.0038 | 0.3986 | 0.3971 |
Loa Loa (eye worm) | AGC/PKC/ALPHA protein kinase | 0.004 | 0.417 | 0.4287 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Loa Loa (eye worm) | AGC/PKC/ETA protein kinase | 0.0015 | 0.096 | 0.0968 |
Echinococcus granulosus | Protein kinase C brain isozyme | 0.0054 | 0.6019 | 0.6009 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0082 | 0.9696 | 1 |
Echinococcus granulosus | protein kinase C gamma type | 0.0048 | 0.5243 | 0.5232 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0084 | 1 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0015 | 0.096 | 0.1185 |
Echinococcus multilocularis | protein kinase c epsilon type | 0.0015 | 0.096 | 0.0939 |
Echinococcus granulosus | RNA directed DNA polymerase | 0.0038 | 0.3986 | 0.3971 |
Entamoeba histolytica | protein kinase, putative | 0.0008 | 0.0024 | 0.5 |
Echinococcus multilocularis | protein kinase c iota type | 0.0014 | 0.0799 | 0.0777 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0054 | 0.6019 | 0.7587 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Toxoplasma gondii | AGC kinase | 0.0008 | 0.0024 | 0.5 |
Onchocerca volvulus | 0.0066 | 0.7622 | 0.5 | |
Trypanosoma brucei | rac serine-threonine kinase, putative | 0.0008 | 0.0024 | 0.5 |
Entamoeba histolytica | protein kinase, putative | 0.0008 | 0.0024 | 0.5 |
Entamoeba histolytica | protein kinase, putative | 0.0008 | 0.0024 | 0.5 |
Echinococcus multilocularis | jun protein | 0.0084 | 1 | 1 |
Echinococcus multilocularis | serine threonine protein kinase | 0.0048 | 0.5243 | 0.5232 |
Brugia malayi | Protein kinase c protein 2 | 0.0046 | 0.4946 | 0.4934 |
Schistosoma mansoni | atypical protein kinase C | 0.0014 | 0.0799 | 0.0981 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Brugia malayi | protein kinase C II. | 0.0015 | 0.096 | 0.0939 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0054 | 0.6019 | 0.7587 |
Echinococcus granulosus | protein kinase c iota type | 0.0014 | 0.0799 | 0.0777 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Echinococcus multilocularis | Protein kinase C, brain isozyme | 0.0054 | 0.6019 | 0.6009 |
Echinococcus granulosus | protein kinase c epsilon type | 0.0015 | 0.096 | 0.0939 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Schistosoma mansoni | jun-related protein | 0.0068 | 0.7926 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.0008 | 0.0024 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 21 uM | In vitro inhibition of human recombinant IL-1beta-induced breakdown of bovine cartilage in a cartilage organ culture assay | ChEMBL. | 7932530 |
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.