Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | intermediate filament protein | 0.0027 | 0.2772 | 0.2561 |
Brugia malayi | TAR-binding protein | 0.0063 | 1 | 1 |
Echinococcus multilocularis | musashi | 0.0027 | 0.2772 | 0.2772 |
Echinococcus granulosus | lamin | 0.0027 | 0.2772 | 0.2772 |
Loa Loa (eye worm) | hypothetical protein | 0.0026 | 0.2674 | 0.2674 |
Onchocerca volvulus | 0.0027 | 0.2772 | 0.5 | |
Schistosoma mansoni | tar DNA-binding protein | 0.0063 | 1 | 1 |
Loa Loa (eye worm) | RNA binding protein | 0.0063 | 1 | 1 |
Schistosoma mansoni | tar DNA-binding protein | 0.0063 | 1 | 1 |
Echinococcus granulosus | lamin dm0 | 0.0027 | 0.2772 | 0.2772 |
Loa Loa (eye worm) | TAR-binding protein | 0.0063 | 1 | 1 |
Loa Loa (eye worm) | intermediate filament protein | 0.0027 | 0.2772 | 0.2772 |
Echinococcus granulosus | intermediate filament protein | 0.0027 | 0.2772 | 0.2772 |
Loa Loa (eye worm) | hypothetical protein | 0.0027 | 0.2772 | 0.2772 |
Loa Loa (eye worm) | intermediate filament tail domain-containing protein | 0.0027 | 0.2772 | 0.2772 |
Onchocerca volvulus | 0.0027 | 0.2772 | 0.5 | |
Echinococcus multilocularis | lamin dm0 | 0.0027 | 0.2772 | 0.2772 |
Loa Loa (eye worm) | RNA recognition domain-containing protein domain-containing protein | 0.0063 | 1 | 1 |
Schistosoma mansoni | tar DNA-binding protein | 0.0063 | 1 | 1 |
Echinococcus multilocularis | lamin | 0.0027 | 0.2772 | 0.2772 |
Echinococcus granulosus | tar DNA binding protein | 0.0063 | 1 | 1 |
Schistosoma mansoni | tar DNA-binding protein | 0.0063 | 1 | 1 |
Schistosoma mansoni | tar DNA-binding protein | 0.0063 | 1 | 1 |
Brugia malayi | RNA recognition motif domain containing protein | 0.0063 | 1 | 1 |
Echinococcus multilocularis | tar DNA binding protein | 0.0063 | 1 | 1 |
Brugia malayi | Intermediate filament tail domain containing protein | 0.0027 | 0.2772 | 0.2561 |
Loa Loa (eye worm) | cytoplasmic intermediate filament protein | 0.0014 | 0.0285 | 0.0285 |
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.