Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | geminin | 0.0181 | 0.88 | 1 |
Onchocerca volvulus | 0.0156 | 0.6237 | 0.5 | |
Trypanosoma cruzi | sterol 24-c-methyltransferase, putative | 0.0193 | 1 | 0.5 |
Leishmania major | sterol 24-c-methyltransferase, putative | 0.0193 | 1 | 0.5 |
Trypanosoma cruzi | sterol 24-c-methyltransferase, putative | 0.0193 | 1 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0181 | 0.88 | 1 |
Trypanosoma brucei | sterol 24-c-methyltransferase, putative | 0.0193 | 1 | 1 |
Loa Loa (eye worm) | glycosyl hydrolase family 31 protein | 0.0156 | 0.6237 | 1 |
Trypanosoma brucei | sterol 24-c-methyltransferase, putative | 0.0193 | 1 | 1 |
Echinococcus granulosus | geminin | 0.0181 | 0.88 | 1 |
Brugia malayi | Glycosyl hydrolases family 31 protein | 0.0156 | 0.6237 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0181 | 0.88 | 1 |
Trypanosoma brucei | Sterol methyltransferase, putative | 0.0193 | 1 | 1 |
Trypanosoma cruzi | sterol 24-c-methyltransferase, putative | 0.0193 | 1 | 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.