Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | acetylcholinesterase | 0.0269 | 1 | 1 |
Plasmodium falciparum | choline kinase | 0.0082 | 0.0952 | 0.5 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0185 | 0.5899 | 0.5468 |
Echinococcus granulosus | small conductance calcium activated potassium | 0.0185 | 0.5899 | 0.5468 |
Toxoplasma gondii | phosphotransferase enzyme family protein | 0.0082 | 0.0952 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0269 | 1 | 1 |
Echinococcus granulosus | acetylcholinesterase | 0.0269 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0269 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0185 | 0.5899 | 0.5899 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0185 | 0.5899 | 0.4361 |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.0269 | 1 | 1 |
Loa Loa (eye worm) | carboxylesterase | 0.0269 | 1 | 1 |
Echinococcus multilocularis | carboxylesterase 5A | 0.0269 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0269 | 1 | 1 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0269 | 1 | 1 |
Echinococcus granulosus | acetylcholinesterase | 0.0269 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0185 | 0.5899 | 0.4361 |
Echinococcus granulosus | carboxylesterase 5A | 0.0269 | 1 | 1 |
Loa Loa (eye worm) | choline/ethanolamine kinase | 0.0082 | 0.0952 | 0.0952 |
Plasmodium vivax | choline kinase, putative | 0.0082 | 0.0952 | 0.5 |
Echinococcus multilocularis | acetylcholinesterase | 0.0269 | 1 | 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.