Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0052 | 0.7003 | 0.7677 |
Schistosoma mansoni | tar DNA-binding protein | 0.0059 | 0.9121 | 0.9121 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.0042 | 0.4036 | 0.4425 |
Loa Loa (eye worm) | TAR-binding protein | 0.0059 | 0.9121 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.3471 | 0.3806 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.0042 | 0.4036 | 0.4036 |
Loa Loa (eye worm) | hypothetical protein | 0.004 | 0.3471 | 0.3806 |
Schistosoma mansoni | tar DNA-binding protein | 0.0059 | 0.9121 | 0.9121 |
Schistosoma mansoni | tar DNA-binding protein | 0.0059 | 0.9121 | 0.9121 |
Echinococcus granulosus | phospholipase D1 | 0.0062 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0042 | 0.4036 | 0.4425 |
Echinococcus multilocularis | phospholipase D1 | 0.0062 | 1 | 1 |
Echinococcus granulosus | tar DNA binding protein | 0.0059 | 0.9121 | 0.5978 |
Loa Loa (eye worm) | RNA recognition domain-containing protein domain-containing protein | 0.0059 | 0.9121 | 1 |
Schistosoma mansoni | phospholipase D | 0.0062 | 1 | 1 |
Echinococcus multilocularis | tar DNA binding protein | 0.0059 | 0.9121 | 0.5978 |
Schistosoma mansoni | tar DNA-binding protein | 0.0059 | 0.9121 | 0.9121 |
Brugia malayi | RNA recognition motif domain containing protein | 0.0059 | 0.9121 | 0.9121 |
Brugia malayi | TAR-binding protein | 0.0059 | 0.9121 | 0.9121 |
Loa Loa (eye worm) | RNA binding protein | 0.0059 | 0.9121 | 1 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.0042 | 0.4036 | 0.4036 |
Entamoeba histolytica | phospholipase D, putative | 0.0062 | 1 | 1 |
Brugia malayi | RNA binding protein | 0.0059 | 0.9121 | 0.9121 |
Loa Loa (eye worm) | hypothetical protein | 0.0052 | 0.7003 | 0.7677 |
Schistosoma mansoni | tar DNA-binding protein | 0.0059 | 0.9121 | 0.9121 |
Entamoeba histolytica | phospholipase D, putative | 0.0062 | 1 | 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.