Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.033 | 0.3907 | 0.0935 |
Brugia malayi | Voltage-gated potassium channel, KCNQ (Kv7-like) alpha-subunit. C. elegans kqt-1 ortholog | 0.012 | 0.0012 | 0.5 |
Trypanosoma cruzi | ion transport protein, putative | 0.0557 | 0.8124 | 0.5 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0659 | 1 | 1 |
Leishmania major | ion transport protein-like protein | 0.0557 | 0.8124 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0659 | 1 | 1 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0659 | 1 | 1 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0626 | 0.9404 | 0.9404 |
Loa Loa (eye worm) | hypothetical protein | 0.0659 | 1 | 1 |
Trypanosoma cruzi | ion transport protein, putative | 0.0557 | 0.8124 | 0.5 |
Mycobacterium ulcerans | ion transport protein | 0.012 | 0 | 0.5 |
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.