Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | Pyruvate dehydrogenase (lipoamide) kinase | 0.0373 | 1 | 0.5 |
Toxoplasma gondii | ATPase/histidine kinase/DNA gyrase B/HSP90 domain-containing protein | 0.0151 | 0.0855 | 1 |
Schistosoma mansoni | pyruvate dehydrogenase | 0.0373 | 1 | 1 |
Leishmania major | developmentally regulated phosphoprotein-like protein | 0.0373 | 1 | 1 |
Trypanosoma cruzi | developmentally regulated phosphoprotein, putative | 0.0373 | 1 | 1 |
Echinococcus granulosus | Pyruvate dehydrogenase lipoamide kinase | 0.0373 | 1 | 0.5 |
Echinococcus multilocularis | Pyruvate dehydrogenase (lipoamide) kinase | 0.0373 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0373 | 1 | 0.5 |
Trypanosoma brucei | developmentally regulated phosphoprotein | 0.0373 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (functional) | = 1100 nM | Antagonist potency against human histamine H3 receptor expressed in CHO cells was determined by GTPgamma[S]-assay | ChEMBL. | 15139761 |
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.