Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Muscle positioning protein 4 | 0.1586 | 0.423 | 0.1744 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.2503 | 0.9701 | 0.5 |
Brugia malayi | Trypsin family protein | 0.2133 | 0.7494 | 0.667 |
Loa Loa (eye worm) | hypothetical protein | 0.1586 | 0.423 | 0.4225 |
Echinococcus multilocularis | tissue type plasminogen activator | 0.2503 | 0.9701 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.2503 | 0.9701 | 0.9701 |
Echinococcus granulosus | tissue type plasminogen activator | 0.2503 | 0.9701 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1393 | 0.3074 | 0.3005 |
Toxoplasma gondii | kringle domain-containing protein | 0.2503 | 0.9701 | 0.5 |
Loa Loa (eye worm) | DOMON domain-containing protein | 0.1393 | 0.3074 | 0.3005 |
Onchocerca volvulus | 0.2503 | 0.9701 | 1 | |
Onchocerca volvulus | 0.1422 | 0.3248 | 0.0263 | |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.2503 | 0.9701 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.2133 | 0.7494 | 0.7671 |
Loa Loa (eye worm) | hypothetical protein | 0.2503 | 0.9701 | 1 |
Onchocerca volvulus | 0.2133 | 0.7494 | 0.667 | |
Loa Loa (eye worm) | TK/ROR protein kinase | 0.2503 | 0.9701 | 1 |
Schistosoma mansoni | hypothetical protein | 0.1393 | 0.3074 | 0.3074 |
Leishmania major | hypothetical protein, conserved | 0.2503 | 0.9701 | 0.5 |
Onchocerca volvulus | 0.1586 | 0.423 | 0.1744 | |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.2133 | 0.7494 | 0.7494 |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.2503 | 0.9701 | 0.5 |
Brugia malayi | Protein kinase domain containing protein | 0.2503 | 0.9701 | 1 |
Brugia malayi | Kringle domain containing protein | 0.2503 | 0.9701 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.2133 | 0.7494 | 0.7671 |
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.