Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | pyruvate dehydrogenase kinase, isozyme 2 | Starlite/ChEMBL | No references |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Trypanosoma brucei | pyruvate dehydrogenase (lipoamide) kinase, putative | pyruvate dehydrogenase kinase, isozyme 2 | 343 aa | 321 aa | 22.7 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trichomonas vaginalis | cyclin D, putative | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclin B, putative | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclins, putative | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclin B, putative | 0.0041 | 0.0873 | 0.5 |
Entamoeba histolytica | cyclin family protein | 0.0041 | 0.0873 | 0.5 |
Toxoplasma gondii | pyruvate dehydrogenase kinase, putative | 0.005 | 0.1711 | 0.7071 |
Toxoplasma gondii | ATPase/histidine kinase/DNA gyrase B/HSP90 domain-containing protein | 0.0058 | 0.242 | 1 |
Plasmodium falciparum | cyclin | 0.0041 | 0.0873 | 0.5 |
Schistosoma mansoni | pyruvate dehydrogenase | 0.0144 | 1 | 1 |
Echinococcus multilocularis | Pyruvate dehydrogenase (lipoamide) kinase | 0.0144 | 1 | 1 |
Trypanosoma brucei | pyruvate dehydrogenase (lipoamide) kinase, putative | 0.005 | 0.1711 | 0.0918 |
Trichomonas vaginalis | cyclins, putative | 0.0041 | 0.0873 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0144 | 1 | 1 |
Schistosoma mansoni | pyruvate dehydrogenase | 0.0136 | 0.9291 | 0.9223 |
Giardia lamblia | Cyclin A | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclins, putative | 0.0041 | 0.0873 | 0.5 |
Onchocerca volvulus | 0.0041 | 0.0873 | 0.5 | |
Trichomonas vaginalis | cyclin A, putative | 0.0041 | 0.0873 | 0.5 |
Echinococcus granulosus | Pyruvate dehydrogenase lipoamide kinase | 0.0144 | 1 | 1 |
Trypanosoma cruzi | developmentally regulated phosphoprotein, putative | 0.0144 | 1 | 1 |
Trichomonas vaginalis | cyclins, putative | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclin B, putative | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0041 | 0.0873 | 0.5 |
Schistosoma mansoni | pyruvate dehydrogenase | 0.0136 | 0.9291 | 0.9223 |
Trypanosoma brucei | developmentally regulated phosphoprotein | 0.0144 | 1 | 1 |
Giardia lamblia | G2/mitotic-specific cyclin B | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclin B, putative | 0.0041 | 0.0873 | 0.5 |
Trypanosoma cruzi | pyruvate dehydrogenase (lipoamide) kinase, putative | 0.005 | 0.1711 | 0.0918 |
Trichomonas vaginalis | cyclins, putative | 0.0041 | 0.0873 | 0.5 |
Entamoeba histolytica | cyclin, putative | 0.0041 | 0.0873 | 0.5 |
Echinococcus multilocularis | Pyruvate dehydrogenase (lipoamide) kinase | 0.0144 | 1 | 1 |
Leishmania major | pyruvate dehydrogenase (lipoamide) kinase, putative | 0.005 | 0.1711 | 0.0918 |
Trichomonas vaginalis | cyclin D, putative | 0.0041 | 0.0873 | 0.5 |
Entamoeba histolytica | cyclin, putative | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclin B, putative | 0.0041 | 0.0873 | 0.5 |
Entamoeba histolytica | cyclin family protein | 0.0041 | 0.0873 | 0.5 |
Leishmania major | developmentally regulated phosphoprotein-like protein | 0.0144 | 1 | 1 |
Giardia lamblia | Hypothetical protein | 0.0041 | 0.0873 | 0.5 |
Trichomonas vaginalis | cyclin B3, putative | 0.0041 | 0.0873 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 2402 nM | BindingDB_Patents: Inhibition Assay. The inhibitory action of PDHK activity was indirectly evaluated by performing a kinase reaction in the presence of a test compound and measuring the residual PDH activity. For expression of hPDHK2 activity, Escherichia coli strain BL21(DE3) cells (Novagen) were transformed with the pET17b vector containing modified hPDHK2 cDNA. Escherichia coli were grown to an optical density 0.6 (600 nmol/L) at 30C. Protein expression was induced by the addition of 500 umol/L isopropyl-beta-thiogalactopyranoside. Escherichia coli were cultured at 30 C. for 5 hr and harvested by centrifugation. Resuspension of the Escherichia coli paste was disrupted by a microfluidizer. FLAG-Tagged protein was separated using FLAG affinity gel (Sigma). The gel was washed with 20 mmol/L N-(2-hydroxyethyl)piperazine-N'-2-ethanesulfonic acid-sodium hydroxide (HEPES-NaOH), 500 mmol/L sodium chloride, 1% ethylene glycol, and 0.1% Pluronic F-68 (pH 8.0), and the binding protein was eluted with 20 mmol/L HEPES. | ChEMBL. | No reference |
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.