Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | folate hydrolase (prostate-specific membrane antigen) 1 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target/s | Ortholog Group |
---|---|---|---|
Schistosoma japonicum | ko:K01301 glutamate carboxypeptidase II [EC3.4.17.21], putative | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Schistosoma mansoni | NAALADASE L peptidase (M28 family) | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Candida albicans | similar to transferrin receptor | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Loa Loa (eye worm) | hypothetical protein | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Loa Loa (eye worm) | hypothetical protein | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Echinococcus multilocularis | n acetylated alpha linked acidic dipeptidase 2 | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Loa Loa (eye worm) | hypothetical protein | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Candida albicans | hypothetical protein | Get druggable targets OG5_128101 | All targets in OG5_128101 |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma cruzi | aspartyl aminopeptidase, putative | 0.0075 | 0.3032 | 0.5 |
Entamoeba histolytica | aminopeptidase, putative | 0.0075 | 0.3032 | 0.5 |
Entamoeba histolytica | aspartyl aminopeptidase, putative | 0.0075 | 0.3032 | 0.5 |
Brugia malayi | Aspartyl aminopeptidase | 0.0075 | 0.3032 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0111 | 0.5735 | 0.5282 |
Trichomonas vaginalis | Clan MH, family M18, aspartyl aminopeptidase-like metallopeptidase | 0.0075 | 0.3032 | 1 |
Trichomonas vaginalis | Clan MH, family M18, aspartyl aminopeptidase-like metallopeptidase | 0.0075 | 0.3032 | 1 |
Plasmodium falciparum | M18 aspartyl aminopeptidase | 0.0075 | 0.3032 | 0.5 |
Schistosoma mansoni | aspartyl aminopeptidase (M18 family) | 0.0075 | 0.3032 | 0.4632 |
Loa Loa (eye worm) | hypothetical protein | 0.0075 | 0.3032 | 0.2291 |
Trichomonas vaginalis | Clan MH, family M18, aspartyl aminopeptidase-like metallopeptidase | 0.0075 | 0.3032 | 1 |
Mycobacterium leprae | PROBABLE AMINOPEPTIDASE PEPC | 0.0075 | 0.3032 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0152 | 0.8874 | 0.8754 |
Plasmodium vivax | M18 aspartyl aminopeptidase, putative | 0.0075 | 0.3032 | 0.5 |
Schistosoma mansoni | NAALADASE L peptidase (M28 family) | 0.0107 | 0.5433 | 1 |
Echinococcus granulosus | aspartyl aminopeptidase | 0.0075 | 0.3032 | 1 |
Mycobacterium tuberculosis | Probable aminopeptidase PepC | 0.0075 | 0.3032 | 0.5 |
Loa Loa (eye worm) | aspartyl aminopeptidase | 0.0075 | 0.3032 | 0.2291 |
Schistosoma mansoni | aspartyl aminopeptidase (M18 family) | 0.0075 | 0.3032 | 0.4632 |
Echinococcus multilocularis | n acetylated alpha linked acidic dipeptidase 2 | 0.0163 | 0.9698 | 1 |
Trypanosoma cruzi | metallo-peptidase, Clan MH, Family M20 | 0.0075 | 0.3032 | 0.5 |
Echinococcus multilocularis | aspartyl aminopeptidase | 0.0075 | 0.3032 | 0.2371 |
Trypanosoma brucei | aspartyl aminopeptidase, putative | 0.0075 | 0.3032 | 0.5 |
Trypanosoma brucei | aspartyl aminopeptidase, putative | 0.0075 | 0.3032 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0075 | 0.3032 | 0.2291 |
Leishmania major | aspartyl aminopeptidase, putative,metallo-peptidase, Clan MH, Family M20 | 0.0075 | 0.3032 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 245 nM | Inhibition of [131I]DCIT from PSMA in human LNCAP cells | ChEMBL. | 19111054 |
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.