Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | GABA-A receptor; anion channel | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | matrix metallopeptidase-9 (M10 family) | 0.0081 | 0.0197 | 0.0566 |
Leishmania major | ubiquitin-conjugating enzyme e2, putative | 0.0121 | 0.3474 | 0.5 |
Trypanosoma cruzi | ubiquitin-conjugating enzyme E2, putative | 0.0121 | 0.3474 | 0.5 |
Loa Loa (eye worm) | matrixin family protein | 0.0134 | 0.4509 | 1 |
Trichomonas vaginalis | ubiquitin-conjugating enzyme E2, putative | 0.0121 | 0.3474 | 0.5 |
Trichomonas vaginalis | ubiquitin-conjugating enzyme E2, putative | 0.0121 | 0.3474 | 0.5 |
Plasmodium vivax | ubiquitin-conjugating enzyme E2 N, putative | 0.0121 | 0.3474 | 0.5 |
Onchocerca volvulus | Matrilysin homolog | 0.0123 | 0.3607 | 1 |
Brugia malayi | Matrixin family protein | 0.0134 | 0.4509 | 1 |
Loa Loa (eye worm) | matrixin family protein | 0.0123 | 0.3607 | 0.1288 |
Brugia malayi | Ubiquitin conjugating enzyme protein 13 | 0.0121 | 0.3474 | 0.7705 |
Onchocerca volvulus | Matrix metalloproteinase homolog | 0.0123 | 0.3607 | 1 |
Trypanosoma cruzi | ubiquitin-conjugating enzyme E2, putative | 0.0121 | 0.3474 | 0.5 |
Echinococcus multilocularis | matrix metallopeptidase 7 (M10 family) | 0.0201 | 1 | 1 |
Plasmodium falciparum | ubiquitin-conjugating enzyme E2 N, putative | 0.0121 | 0.3474 | 0.5 |
Toxoplasma gondii | ubiquitin-conjugating enzyme subfamily protein | 0.0121 | 0.3474 | 0.5 |
Trypanosoma brucei | ubiquitin-protein ligase, putative | 0.0121 | 0.3474 | 0.5 |
Entamoeba histolytica | ubiquitin-conjugating enzyme family protein | 0.0121 | 0.3474 | 0.5 |
Brugia malayi | ubiquitin conjugating enzyme protein 13 | 0.0121 | 0.3474 | 0.7705 |
Schistosoma mansoni | ubiquitin conjugating enzyme 13 | 0.0121 | 0.3474 | 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.
1 literature reference was collected for this gene.