Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Loa Loa (eye worm) | carboxylesterase | 0.0308 | 0.1149 | 0.1149 |
Echinococcus granulosus | neuroligin | 0.0308 | 0.1149 | 0.0711 |
Loa Loa (eye worm) | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Echinococcus multilocularis | family S9 non peptidase ue (S09 family) | 0.0308 | 0.1149 | 0.0711 |
Trichomonas vaginalis | spcc417.12 protein, putative | 0.0308 | 0.1149 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1822 | 1 | 1 |
Echinococcus granulosus | family S9 non peptidase ue S09 family | 0.0308 | 0.1149 | 0.0711 |
Schistosoma mansoni | gliotactin | 0.0308 | 0.1149 | 0.0711 |
Echinococcus granulosus | para nitrobenzyl esterase | 0.0308 | 0.1149 | 0.0711 |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.1822 | 1 | 1 |
Echinococcus multilocularis | acetylcholinesterase | 0.1822 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Echinococcus granulosus | acetylcholinesterase | 0.1822 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Echinococcus multilocularis | carboxylesterase 5A | 0.1822 | 1 | 1 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0308 | 0.1149 | 0.0711 |
Mycobacterium tuberculosis | POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) | 0.0308 | 0.1149 | 0.5 |
Loa Loa (eye worm) | carboxylesterase | 0.1822 | 1 | 1 |
Mycobacterium tuberculosis | Carboxylesterase LipT | 0.0308 | 0.1149 | 0.5 |
Onchocerca volvulus | 0.0308 | 0.1149 | 0.5 | |
Echinococcus granulosus | acetylcholinesterase | 0.1822 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Mycobacterium ulcerans | carboxylesterase, LipT | 0.0308 | 0.1149 | 0.5 |
Onchocerca volvulus | 0.0308 | 0.1149 | 0.5 | |
Brugia malayi | Carboxylesterase family protein | 0.0308 | 0.1149 | 0.1149 |
Echinococcus multilocularis | acetylcholinesterase | 0.1822 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.1822 | 1 | 1 |
Mycobacterium tuberculosis | POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) | 0.0308 | 0.1149 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Brugia malayi | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Brugia malayi | Carboxylesterase family protein | 0.1822 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0308 | 0.1149 | 0.1149 |
Schistosoma mansoni | neuroligin 3 (S09 family) | 0.0308 | 0.1149 | 0.0711 |
Echinococcus multilocularis | atpase aaa+ type core atpase aaa type core | 0.0919 | 0.4721 | 0.4459 |
Brugia malayi | Carboxylesterase family protein | 0.0308 | 0.1149 | 0.1149 |
Brugia malayi | Carboxylesterase family protein | 0.0308 | 0.1149 | 0.1149 |
Trichomonas vaginalis | carboxylesterase domain containing protein, putative | 0.0308 | 0.1149 | 0.5 |
Onchocerca volvulus | 0.0308 | 0.1149 | 0.5 | |
Echinococcus multilocularis | BC026374 protein (S09 family) | 0.0308 | 0.1149 | 0.0711 |
Loa Loa (eye worm) | carboxylesterase | 0.0308 | 0.1149 | 0.1149 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0308 | 0.1149 | 0.0711 |
Onchocerca volvulus | 0.0308 | 0.1149 | 0.5 | |
Onchocerca volvulus | 0.0308 | 0.1149 | 0.5 | |
Echinococcus multilocularis | para nitrobenzyl esterase | 0.0308 | 0.1149 | 0.0711 |
Echinococcus multilocularis | neuroligin | 0.0308 | 0.1149 | 0.0711 |
Brugia malayi | Carboxylesterase family protein | 0.0308 | 0.1149 | 0.1149 |
Echinococcus granulosus | carboxylesterase 5A | 0.1822 | 1 | 1 |
Echinococcus granulosus | BC026374 protein S09 family | 0.0308 | 0.1149 | 0.0711 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0308 | 0.1149 | 0.0711 |
Schistosoma mansoni | acetylcholinesterase | 0.0308 | 0.1149 | 0.0711 |
Schistosoma mansoni | BC026374 protein (S09 family) | 0.0308 | 0.1149 | 0.0711 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.1822 | 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.