Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | phospholipase D | 0.0171 | 0.034 | 0.042 |
Toxoplasma gondii | phospholipase D active site domain-containing protein | 0.0315 | 0.2246 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0589 | 0.5848 | 0.7225 |
Onchocerca volvulus | Putative phospholipase D | 0.0171 | 0.034 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0171 | 0.034 | 0.042 |
Loa Loa (eye worm) | hypothetical protein | 0.0589 | 0.5848 | 0.7225 |
Loa Loa (eye worm) | hypothetical protein | 0.076 | 0.8094 | 1 |
Trypanosoma brucei | cardiolipin synthetase, putative | 0.0315 | 0.2246 | 1 |
Brugia malayi | Phospholipase D. Active site motif family protein | 0.0315 | 0.2246 | 0.2246 |
Loa Loa (eye worm) | hypothetical protein | 0.076 | 0.8094 | 1 |
Brugia malayi | Phospholipase D. Active site motif family protein | 0.0171 | 0.034 | 0.034 |
Trypanosoma cruzi | cardiolipin synthetase, putative | 0.0315 | 0.2246 | 0.5 |
Echinococcus multilocularis | phospholipase D | 0.0799 | 0.8611 | 0.8562 |
Echinococcus granulosus | phospholipase D | 0.0799 | 0.8611 | 0.8562 |
Trypanosoma cruzi | cardiolipin synthetase, putative | 0.0315 | 0.2246 | 0.5 |
Trypanosoma brucei | cardiolipin synthetase | 0.0315 | 0.2246 | 1 |
Leishmania major | phosphatidylglycerophosphate synthase, putative | 0.0171 | 0.034 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | Activation of Shh pathway in mouse Shh-Light II cells assessed as induction of gli1 expression at 1 uM after 48 hrs by renilla luminescence assay | ChEMBL. | 22985958 |
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.