Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | RNA recognition domain-containing protein domain-containing protein | 0.0067 | 0.1331 | 0.1331 |
Echinococcus multilocularis | musashi | 0.0029 | 0.0369 | 0.0369 |
Schistosoma mansoni | tar DNA-binding protein | 0.0067 | 0.1331 | 0.2095 |
Loa Loa (eye worm) | hypothetical protein | 0.01 | 0.2147 | 0.2147 |
Loa Loa (eye worm) | intermediate filament tail domain-containing protein | 0.0029 | 0.0369 | 0.0369 |
Loa Loa (eye worm) | DnaJ domain-containing protein | 0.0065 | 0.1275 | 0.1275 |
Echinococcus granulosus | lamin | 0.0029 | 0.0369 | 0.0369 |
Schistosoma mansoni | tar DNA-binding protein | 0.0067 | 0.1331 | 0.2095 |
Echinococcus granulosus | dnaJ subfamily C 6 | 0.0065 | 0.1275 | 0.1275 |
Brugia malayi | intermediate filament protein | 0.0029 | 0.0369 | 0.0332 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.01 | 0.2147 | 0.3874 |
Brugia malayi | DnaJ domain containing protein | 0.0065 | 0.1275 | 0.1242 |
Loa Loa (eye worm) | cytoplasmic intermediate filament protein | 0.0015 | 0.0038 | 0.0038 |
Schistosoma mansoni | tar DNA-binding protein | 0.0067 | 0.1331 | 0.2095 |
Loa Loa (eye worm) | hypothetical protein | 0.01 | 0.2147 | 0.2147 |
Echinococcus multilocularis | muscleblind protein | 0.0159 | 0.3605 | 0.3605 |
Echinococcus multilocularis | tar DNA binding protein | 0.0067 | 0.1331 | 0.1331 |
Loa Loa (eye worm) | hypothetical protein | 0.0028 | 0.0356 | 0.0356 |
Echinococcus granulosus | tar DNA binding protein | 0.0067 | 0.1331 | 0.1331 |
Schistosoma mansoni | hypothetical protein | 0.0065 | 0.1275 | 0.1975 |
Loa Loa (eye worm) | TAR-binding protein | 0.0067 | 0.1331 | 0.1331 |
Echinococcus granulosus | intermediate filament protein | 0.0029 | 0.0369 | 0.0369 |
Onchocerca volvulus | 0.0094 | 0.1985 | 0.9087 | |
Brugia malayi | Muscleblind-like protein | 0.0159 | 0.3605 | 0.3581 |
Onchocerca volvulus | 0.01 | 0.2147 | 1 | |
Loa Loa (eye worm) | intermediate filament protein | 0.0029 | 0.0369 | 0.0369 |
Brugia malayi | Trypsin family protein | 0.01 | 0.2147 | 0.2117 |
Echinococcus multilocularis | muscleblind protein 1 | 0.0159 | 0.3605 | 0.3605 |
Loa Loa (eye worm) | hypothetical protein | 0.0159 | 0.3605 | 0.3605 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0212 | 0.4927 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0159 | 0.3605 | 0.3605 |
Brugia malayi | RNA binding protein | 0.0067 | 0.1331 | 0.1298 |
Schistosoma mansoni | tar DNA-binding protein | 0.0067 | 0.1331 | 0.2095 |
Echinococcus granulosus | lamin dm0 | 0.0029 | 0.0369 | 0.0369 |
Schistosoma mansoni | tar DNA-binding protein | 0.0067 | 0.1331 | 0.2095 |
Echinococcus multilocularis | lamin | 0.0029 | 0.0369 | 0.0369 |
Brugia malayi | TAR-binding protein | 0.0067 | 0.1331 | 0.1298 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription | 0.0038 | 0.0607 | 0.0607 |
Trichomonas vaginalis | serine threonine-protein kinase, putative | 0.0212 | 0.4927 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0038 | 0.0607 | 0.0519 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0214 | 0.4959 | 1 |
Brugia malayi | hypothetical protein | 0.0038 | 0.0607 | 0.0571 |
Echinococcus multilocularis | dnaJ subfamily C 6 | 0.0065 | 0.1275 | 0.1275 |
Schistosoma mansoni | transcription factor LCR-F1 | 0.0038 | 0.0607 | 0.0519 |
Loa Loa (eye worm) | RNA binding protein | 0.0067 | 0.1331 | 0.1331 |
Loa Loa (eye worm) | hypothetical protein | 0.0029 | 0.0369 | 0.0369 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.01 | 0.2147 | 0.3874 |
Brugia malayi | RNA recognition motif domain containing protein | 0.0067 | 0.1331 | 0.1298 |
Echinococcus multilocularis | lamin dm0 | 0.0029 | 0.0369 | 0.0369 |
Echinococcus granulosus | muscleblind protein | 0.0159 | 0.3605 | 0.3605 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription | 0.0038 | 0.0607 | 0.0607 |
Brugia malayi | Intermediate filament tail domain containing protein | 0.0029 | 0.0369 | 0.0332 |
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.