Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma brucei | S-adenosylmethionine decarboxylase proenzyme, putative | 0.0641 | 1 | 0.5 |
Echinococcus granulosus | S adenosylmethionine decarboxylase proenzyme | 0.0641 | 1 | 0.5 |
Leishmania major | S-adenosylmethionine decarboxylase | 0.0641 | 1 | 0.5 |
Trypanosoma brucei | S-adenosylmethionine decarboxylase | 0.0641 | 1 | 0.5 |
Plasmodium vivax | S-adenosylmethionine decarboxylase-ornithine decarboxylase, putative | 0.0312 | 0.2972 | 0.5 |
Trypanosoma cruzi | S-adenosylmethionine decarboxylase proenzyme, putative | 0.0641 | 1 | 0.5 |
Plasmodium falciparum | S-adenosylmethionine decarboxylase/ornithine decarboxylase | 0.0312 | 0.2972 | 0.5 |
Trypanosoma brucei | S-adenosylmethionine decarboxylase | 0.0641 | 1 | 0.5 |
Echinococcus multilocularis | S adenosylmethionine decarboxylase proenzyme | 0.0641 | 1 | 0.5 |
Loa Loa (eye worm) | S-adenosylmethionine decarboxylase proenzyme | 0.0641 | 1 | 1 |
Trypanosoma cruzi | S-adenosylmethionine decarboxylase proenzyme, putative | 0.0641 | 1 | 0.5 |
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.