Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | family S9 non peptidase ue (S09 family) | 0.0103 | 0.1017 | 0.1017 |
Onchocerca volvulus | 0.0103 | 0.1017 | 1 | |
Schistosoma mansoni | BC026374 protein (S09 family) | 0.0103 | 0.1017 | 0.1017 |
Echinococcus granulosus | para nitrobenzyl esterase | 0.0103 | 0.1017 | 0.1017 |
Echinococcus granulosus | acetylcholinesterase | 0.0607 | 1 | 1 |
Mycobacterium tuberculosis | POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) | 0.0103 | 0.1017 | 0.5 |
Trichomonas vaginalis | spcc417.12 protein, putative | 0.0103 | 0.1017 | 0.5 |
Onchocerca volvulus | 0.0103 | 0.1017 | 1 | |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0103 | 0.1017 | 0.1017 |
Echinococcus multilocularis | BC026374 protein (S09 family) | 0.0103 | 0.1017 | 0.1017 |
Mycobacterium ulcerans | carboxylesterase, LipT | 0.0103 | 0.1017 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0607 | 1 | 1 |
Schistosoma mansoni | memapsin-2 (A01 family) | 0.0432 | 0.6886 | 0.6886 |
Mycobacterium tuberculosis | Carboxylesterase LipT | 0.0103 | 0.1017 | 0.5 |
Schistosoma mansoni | acetylcholinesterase | 0.0103 | 0.1017 | 0.1017 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0103 | 0.1017 | 0.1017 |
Echinococcus granulosus | family S9 non peptidase ue S09 family | 0.0103 | 0.1017 | 0.1017 |
Brugia malayi | Carboxylesterase family protein | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
Brugia malayi | Carboxylesterase family protein | 0.0103 | 0.1017 | 0.1017 |
Echinococcus granulosus | acetylcholinesterase | 0.0607 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
Echinococcus granulosus | neuroligin | 0.0103 | 0.1017 | 0.1017 |
Echinococcus multilocularis | carboxylesterase 5A | 0.0607 | 1 | 1 |
Echinococcus multilocularis | neuroligin | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
Echinococcus multilocularis | para nitrobenzyl esterase | 0.0103 | 0.1017 | 0.1017 |
Onchocerca volvulus | 0.0103 | 0.1017 | 1 | |
Onchocerca volvulus | 0.0103 | 0.1017 | 1 | |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.0607 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0607 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | hypothetical protein | 0.0607 | 1 | 1 |
Echinococcus granulosus | carboxylesterase 5A | 0.0607 | 1 | 1 |
Schistosoma mansoni | gliotactin | 0.0103 | 0.1017 | 0.1017 |
Onchocerca volvulus | 0.0103 | 0.1017 | 1 | |
Echinococcus multilocularis | acetylcholinesterase | 0.0607 | 1 | 1 |
Brugia malayi | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
Trichomonas vaginalis | carboxylesterase domain containing protein, putative | 0.0103 | 0.1017 | 0.5 |
Schistosoma mansoni | neuroligin 3 (S09 family) | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | carboxylesterase | 0.0607 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0103 | 0.1017 | 0.1017 |
Mycobacterium tuberculosis | POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) | 0.0103 | 0.1017 | 0.5 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0607 | 1 | 1 |
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | carboxylesterase | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | carboxylesterase | 0.0103 | 0.1017 | 0.1017 |
Echinococcus multilocularis | acetylcholinesterase | 0.0607 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0103 | 0.1017 | 0.1017 |
Echinococcus granulosus | BC026374 protein S09 family | 0.0103 | 0.1017 | 0.1017 |
Loa Loa (eye worm) | hypothetical protein | 0.0103 | 0.1017 | 0.1017 |
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.