Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | hypothetical protein | 0.0065 | 0.7409 | 0.7409 |
Schistosoma mansoni | jun-related protein | 0.0068 | 0.774 | 1 |
Echinococcus multilocularis | jun protein | 0.0083 | 1 | 1 |
Echinococcus granulosus | jun protein | 0.0083 | 1 | 1 |
Schistosoma mansoni | retinoblastoma-binding protein 4 (rbbp4) | 0.0014 | 0.0018 | 0.0023 |
Echinococcus multilocularis | Ankyrin | 0.0014 | 0.0018 | 0.0018 |
Echinococcus multilocularis | nuclear factor of activated T cells 5 | 0.0073 | 0.8515 | 0.8515 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0083 | 1 | 1 |
Echinococcus granulosus | nuclear factor of activated T cells 5 | 0.0073 | 0.8515 | 0.8515 |
Onchocerca volvulus | 0.0065 | 0.7409 | 0.5 | |
Schistosoma mansoni | hypothetical protein | 0.0068 | 0.774 | 1 |
Echinococcus granulosus | Ankyrin | 0.0014 | 0.0018 | 0.0018 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0083 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0081 | 0.9669 | 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.