Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | plexin | 0.029 | 0.3682 | 0.2822 |
Loa Loa (eye worm) | hypothetical protein | 0.0557 | 0.9327 | 0.9163 |
Entamoeba histolytica | protein kinase domain containing protein | 0.0116 | 0 | 0.5 |
Echinococcus multilocularis | plexin a4 | 0.0589 | 1 | 1 |
Brugia malayi | Plexin repeat family protein | 0.0498 | 0.8075 | 0.7608 |
Entamoeba histolytica | tyrosin kinase, putative | 0.0116 | 0 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.029 | 0.3682 | 0.2822 |
Onchocerca volvulus | Bile acid receptor homolog | 0.0557 | 0.9327 | 1 |
Loa Loa (eye worm) | plexin A | 0.0589 | 1 | 1 |
Echinococcus granulosus | plexin a4 | 0.0589 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.029 | 0.3682 | 0.2147 |
Loa Loa (eye worm) | hypothetical protein | 0.0498 | 0.8075 | 0.7608 |
Brugia malayi | ecdysteroid receptor | 0.0557 | 0.9327 | 0.9163 |
Onchocerca volvulus | 0.0498 | 0.8075 | 0.8302 | |
Schistosoma mansoni | plexin | 0.0498 | 0.8075 | 1 |
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.