Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Loa Loa (eye worm) | glutaminase 2 | 0.0269 | 1 | 1 |
Echinococcus granulosus | diuretic hormone 44 receptor GPRdih2 | 0.0167 | 0.5037 | 0.9809 |
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Loa Loa (eye worm) | glutaminase | 0.0269 | 1 | 1 |
Mycobacterium ulcerans | 5'-methylthioadenosine phosphorylase | 0.0169 | 0.5134 | 0.1302 |
Giardia lamblia | Purine nucleoside phosphorylase lateral transfer candidate | 0.0153 | 0.4406 | 0.5 |
Onchocerca volvulus | Purine nucleoside phosphorylase homolog | 0.0153 | 0.4406 | 0.5 |
Brugia malayi | purine nucleoside phosphorylase I, inosine and guanosine-specific family protein | 0.0153 | 0.4406 | 0.4406 |
Schistosoma mansoni | methylthioadenosine phosphorylase | 0.0169 | 0.5134 | 0.5134 |
Loa Loa (eye worm) | S-methyl-5'-thioadenosine phosphorylase MTAP | 0.0169 | 0.5134 | 0.5134 |
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Trypanosoma cruzi | methylthioadenosine phosphorylase, putative | 0.0169 | 0.5134 | 0.5 |
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Schistosoma mansoni | glutaminase | 0.0269 | 1 | 1 |
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Trypanosoma cruzi | methylthioadenosine phosphorylase, putative | 0.0169 | 0.5134 | 0.5 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0101 | 0.186 | 0.3622 |
Schistosoma mansoni | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.4406 |
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus multilocularis | diuretic hormone 44 receptor GPRdih2 | 0.0167 | 0.5037 | 0.9809 |
Brugia malayi | MTAP | 0.0169 | 0.5134 | 0.5134 |
Schistosoma mansoni | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.4406 |
Trypanosoma brucei | methylthioadenosine phosphorylase, putative | 0.0169 | 0.5134 | 0.5 |
Mycobacterium leprae | Probable purine nucleoside phosphorylase DeoD (INOSINE PHOSPHORYLASE) (PNP) | 0.0153 | 0.4406 | 0.5 |
Schistosoma mansoni | methylthioadenosine phosphorylase | 0.0169 | 0.5134 | 0.5134 |
Leishmania major | methylthioadenosine phosphorylase, putative | 0.0169 | 0.5134 | 0.5 |
Trichomonas vaginalis | glutaminase, putative | 0.0269 | 1 | 1 |
Echinococcus granulosus | methylthioadenosine phosphorylase | 0.0169 | 0.5134 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.02 | 0.6659 | 0.6659 |
Mycobacterium ulcerans | glutaminase | 0.0269 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0101 | 0.186 | 0.186 |
Echinococcus granulosus | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0101 | 0.186 | 0.3622 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Mycobacterium tuberculosis | Probable purine nucleoside phosphorylase DeoD (inosine phosphorylase) (PNP) | 0.0153 | 0.4406 | 1 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.02 | 0.6659 | 0.6659 |
Echinococcus granulosus | inosine guanosine and xanthosine phosphorylase | 0.0101 | 0.186 | 0.3622 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus multilocularis | purine nucleoside phosphorylase | 0.0153 | 0.4406 | 0.8582 |
Echinococcus multilocularis | methylthioadenosine phosphorylase | 0.0169 | 0.5134 | 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.