Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | family S9 non-peptidase homologue (S09 family) | 0.0138 | 1 | 1 |
Onchocerca volvulus | Matrix metalloproteinase homolog | 0.0047 | 0.1561 | 1 |
Echinococcus multilocularis | carboxylesterase 5A | 0.0138 | 1 | 1 |
Plasmodium falciparum | choline kinase | 0.0123 | 0.8627 | 0.5 |
Loa Loa (eye worm) | choline/ethanolamine kinase | 0.0123 | 0.8627 | 0.8373 |
Loa Loa (eye worm) | matrixin family protein | 0.0051 | 0.1951 | 0.0462 |
Echinococcus granulosus | acetylcholinesterase | 0.0138 | 1 | 1 |
Brugia malayi | Matrixin family protein | 0.0051 | 0.1951 | 0.1951 |
Loa Loa (eye worm) | hypothetical protein | 0.0138 | 1 | 1 |
Brugia malayi | Carboxylesterase family protein | 0.0138 | 1 | 1 |
Loa Loa (eye worm) | acetylcholinesterase 1 | 0.0138 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0138 | 1 | 1 |
Toxoplasma gondii | phosphotransferase enzyme family protein | 0.0123 | 0.8627 | 0.5 |
Brugia malayi | Choline/ethanolamine kinase family protein | 0.0123 | 0.8627 | 0.8627 |
Echinococcus multilocularis | choline:ethanolamine kinase | 0.0123 | 0.8627 | 0.758 |
Echinococcus multilocularis | acetylcholinesterase | 0.0138 | 1 | 1 |
Echinococcus granulosus | acetylcholinesterase | 0.0138 | 1 | 1 |
Schistosoma mansoni | matrix metallopeptidase-9 (M10 family) | 0.005 | 0.1867 | 0.1867 |
Onchocerca volvulus | Matrilysin homolog | 0.0047 | 0.1561 | 1 |
Echinococcus multilocularis | acetylcholinesterase | 0.0138 | 1 | 1 |
Echinococcus granulosus | choline:ethanolamine kinase | 0.0123 | 0.8627 | 0.758 |
Echinococcus granulosus | carboxylesterase 5A | 0.0138 | 1 | 1 |
Plasmodium vivax | choline kinase, putative | 0.0123 | 0.8627 | 0.5 |
Loa Loa (eye worm) | carboxylesterase | 0.0138 | 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.
1 literature reference was collected for this gene.