Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | lysosomal alpha glucosidase | 0.0296 | 0.5142 | 0.3037 |
Brugia malayi | O-Glycosyl hydrolase family 30 protein | 0.0252 | 0.3414 | 0.0561 |
Brugia malayi | Glycosyl hydrolases family 31 protein | 0.0296 | 0.5142 | 0.3037 |
Onchocerca volvulus | 0.0268 | 0.4052 | 1 | |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0252 | 0.3414 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0252 | 0.3414 | 1 |
Schistosoma mansoni | alpha-l-fucosidase | 0.0419 | 1 | 1 |
Echinococcus multilocularis | lysosomal alpha glucosidase | 0.0296 | 0.5142 | 0.3037 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0252 | 0.3414 | 1 |
Loa Loa (eye worm) | alpha-L-fucosidase | 0.0419 | 1 | 1 |
Loa Loa (eye worm) | glycosyl hydrolase family 31 protein | 0.0296 | 0.5142 | 0.3037 |
Schistosoma mansoni | alpha-glucosidase | 0.0268 | 0.4052 | 0.1475 |
Echinococcus multilocularis | fucosidase, alpha L 1, tissue | 0.0419 | 1 | 1 |
Onchocerca volvulus | Ceramide glucosyltransferase homolog | 0.0242 | 0.3023 | 0.7461 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0252 | 0.3414 | 1 |
Trichomonas vaginalis | alpha-L-fucosidase, putative | 0.0184 | 0.073 | 0.2139 |
Mycobacterium ulcerans | alpha-L-fucosidase | 0.0419 | 1 | 0.5 |
Echinococcus multilocularis | lysosomal alpha glucosidase | 0.0296 | 0.5142 | 0.3037 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0174 | 0.0351 | 0.1027 |
Echinococcus granulosus | fucosidase alpha L 1 tissue | 0.0419 | 1 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0252 | 0.3414 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0252 | 0.3414 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0174 | 0.0351 | 0.1027 |
Schistosoma mansoni | alpha-glucosidase | 0.0268 | 0.4052 | 0.1475 |
Loa Loa (eye worm) | O-glycosyl hydrolase family 30 protein | 0.0252 | 0.3414 | 0.0561 |
Trichomonas vaginalis | alpha-L-fucosidase, putative | 0.0184 | 0.073 | 0.2139 |
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.
1 literature reference was collected for this gene.