Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium ulcerans | aminopeptidase N PepN | 0.0321 | 0 | 0.5 |
Schistosoma mansoni | cytosol alanyl aminopeptidase (M01 family) | 0.0321 | 0 | 0.5 |
Trypanosoma brucei | Aminopeptidase M1, putative | 0.0321 | 0 | 0.5 |
Trichomonas vaginalis | Clan MA, family M1, aminopeptidase N-like metallopeptidase | 0.0321 | 0 | 0.5 |
Trypanosoma cruzi | metallo-peptidase, clan MA(E), family M1, putative | 0.0321 | 0 | 0.5 |
Trypanosoma cruzi | aminopeptidase, putative | 0.0321 | 0 | 0.5 |
Echinococcus multilocularis | aminopeptidase N | 0.1089 | 1 | 1 |
Trypanosoma brucei | Aminopeptidase M1, putative | 0.0321 | 0 | 0.5 |
Trypanosoma brucei | metallo-peptidase, Clan MA(E) Family M1 | 0.0321 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0977 | 0.8533 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0769 | 0.5828 | 0.683 |
Entamoeba histolytica | aminopeptidase, putative | 0.0321 | 0 | 0.5 |
Onchocerca volvulus | 0.1089 | 1 | 1 | |
Echinococcus granulosus | aminopeptidase N | 0.1089 | 1 | 1 |
Loa Loa (eye worm) | peptidase family M1 containing protein | 0.0881 | 0.7295 | 0.8549 |
Trypanosoma cruzi | Aminopeptidase M1, putative | 0.0321 | 0 | 0.5 |
Leishmania major | aminopeptidase-like protein,metallo-peptidase, Clan MA(E), Family M1 | 0.0321 | 0 | 0.5 |
Trichomonas vaginalis | Clan MA, family M1, aminopeptidase N-like metallopeptidase | 0.0321 | 0 | 0.5 |
Schistosoma mansoni | aminopeptidase PILS (M01 family) | 0.0321 | 0 | 0.5 |
Leishmania major | aminopeptidase, putative,metallo-peptidase, Clan MA(E), Family M1 | 0.0321 | 0 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | > 3 | Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counter | ChEMBL. | 22651858 |
IC50 (binding) | = 4.02 | Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counter | ChEMBL. | 22651858 |
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.
1 literature reference was collected for this gene.