Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | TKL/MLK/ILK protein kinase | 0.1345 | 1 | 1 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.0757 | 0.4683 | 0.4683 |
Loa Loa (eye worm) | hypothetical protein | 0.0518 | 0.2515 | 0.2515 |
Echinococcus granulosus | integrin linked protein kinase | 0.1345 | 1 | 1 |
Schistosoma mansoni | protein kinase | 0.1345 | 1 | 1 |
Schistosoma mansoni | protein kinase | 0.1345 | 1 | 1 |
Echinococcus multilocularis | integrin linked protein kinase | 0.1345 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0757 | 0.4683 | 0.4683 |
Schistosoma mansoni | hypothetical protein | 0.0518 | 0.2515 | 0.2515 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.0757 | 0.4683 | 0.4683 |
Brugia malayi | latrophilin 2 splice variant baaae | 0.0518 | 0.2515 | 0.2515 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.0757 | 0.4683 | 0.4683 |
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.