Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trichomonas vaginalis | protein ssnA, putative | 0.0132 | 0.7422 | 1 |
Trypanosoma cruzi | imidazolonepropionase, putative | 0.0019 | 0.021 | 0.0284 |
Schistosoma mansoni | dihydropyrimidinase related protein-2 (M38 family) | 0.0019 | 0.021 | 0.021 |
Echinococcus multilocularis | dihydropyrimidinase protein 4 | 0.0019 | 0.021 | 0.021 |
Trypanosoma brucei | dihydroorotase, putative | 0.0019 | 0.021 | 0.0284 |
Plasmodium falciparum | isocitrate dehydrogenase [NADP], mitochondrial | 0.0016 | 0 | 0.5 |
Echinococcus multilocularis | imidazolonepropionase | 0.0019 | 0.021 | 0.021 |
Echinococcus multilocularis | dihydropyrimidinase 2 | 0.0019 | 0.021 | 0.021 |
Echinococcus granulosus | imidazolonepropionase | 0.0019 | 0.021 | 0.021 |
Brugia malayi | Amidohydrolase family protein | 0.0019 | 0.021 | 1 |
Toxoplasma gondii | isocitrate dehydrogenase | 0.0016 | 0 | 0.5 |
Leishmania major | N-acetylglucosamine-6-phosphate deacetylase-like protein | 0.0019 | 0.021 | 0.0284 |
Trypanosoma brucei | guanine deaminase, putative | 0.0132 | 0.7422 | 1 |
Schistosoma mansoni | dihydropyrimidinase (M38 family) | 0.0019 | 0.021 | 0.021 |
Trichomonas vaginalis | guanine deaminase, putative | 0.0132 | 0.7422 | 1 |
Mycobacterium tuberculosis | Conserved protein | 0.0019 | 0.021 | 1 |
Mycobacterium tuberculosis | Urease alpha subunit UreC (urea amidohydrolase) | 0.0019 | 0.021 | 1 |
Schistosoma mansoni | dihydropyrimidinase (M38 family) | 0.0019 | 0.021 | 0.021 |
Schistosoma mansoni | hypothetical protein | 0.0019 | 0.021 | 0.021 |
Echinococcus granulosus | dihydropyrimidinase | 0.0019 | 0.021 | 0.021 |
Wolbachia endosymbiont of Brugia malayi | dihydroorotase, PyrC | 0.0019 | 0.021 | 0.5 |
Trypanosoma cruzi | guanine deaminase, putative | 0.0132 | 0.7422 | 1 |
Trypanosoma cruzi | dihydroorotase, putative | 0.0019 | 0.021 | 0.0284 |
Leishmania major | guanine deaminase, putative | 0.0132 | 0.7422 | 1 |
Leishmania major | dihydroorotase, putative | 0.0019 | 0.021 | 0.0284 |
Schistosoma mansoni | hypothetical protein | 0.0172 | 1 | 1 |
Trypanosoma cruzi | dihydroorotase, putative | 0.0019 | 0.021 | 0.0284 |
Trypanosoma brucei | guanine deaminase, putative | 0.0132 | 0.7422 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0019 | 0.021 | 0.021 |
Entamoeba histolytica | guanine deaminase, putative | 0.0132 | 0.7422 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0172 | 1 | 1 |
Trypanosoma cruzi | guanine deaminase, putative | 0.0132 | 0.7422 | 1 |
Echinococcus granulosus | dihydropyrimidinase 2 | 0.0019 | 0.021 | 0.021 |
Toxoplasma gondii | isocitrate dehydrogenase | 0.0016 | 0 | 0.5 |
Trypanosoma cruzi | imidazolonepropienase, putative | 0.0019 | 0.021 | 0.0284 |
Echinococcus multilocularis | dihydropyrimidinase | 0.0019 | 0.021 | 0.021 |
Trichomonas vaginalis | protein ssnA, putative | 0.0132 | 0.7422 | 1 |
Loa Loa (eye worm) | amidohydrolase | 0.0019 | 0.021 | 1 |
Mycobacterium leprae | Probable dihydroorotase PyrC (DHOase) | 0.0019 | 0.021 | 0.5 |
Plasmodium vivax | dihydroorotase, putative | 0.0019 | 0.021 | 1 |
Schistosoma mansoni | dihydropyrimidinase related protein-1 (M38 family) | 0.0019 | 0.021 | 0.021 |
Trypanosoma cruzi | dihydroorotase, putative | 0.0019 | 0.021 | 0.0284 |
Trypanosoma cruzi | imidazolonepropionase, putative | 0.0019 | 0.021 | 0.0284 |
Echinococcus multilocularis | geminin | 0.0172 | 1 | 1 |
Echinococcus granulosus | dihydropyrimidinase protein 4 | 0.0019 | 0.021 | 0.021 |
Schistosoma mansoni | aspartate carbamoyltransferase | 0.0019 | 0.021 | 0.021 |
Mycobacterium ulcerans | hydroxydechloroatrazine ethylaminohydrolase | 0.0132 | 0.7422 | 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.