Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0207 | 1 | 1 |
Schistosoma mansoni | inhibitor of apoptosis protein | 0.0207 | 1 | 1 |
Onchocerca volvulus | Deterin homolog | 0.0207 | 1 | 0.5 |
Plasmodium falciparum | diacylglycerol O-acyltransferase | 0.0153 | 0.3229 | 0.5 |
Toxoplasma gondii | acyl-CoA:cholesterol acyltransferase alpha ACAT1-alpha | 0.0153 | 0.3229 | 0.5 |
Toxoplasma gondii | acyl-CoA:diacylglycerol acyltransferase 1-related enzyme | 0.0153 | 0.3229 | 0.5 |
Loa Loa (eye worm) | diacylglycerol acyltransferase | 0.0153 | 0.3229 | 0.3229 |
Schistosoma mansoni | hypothetical protein | 0.0207 | 1 | 1 |
Onchocerca volvulus | 0.0207 | 1 | 0.5 | |
Plasmodium vivax | diacylglycerol O-acyltransferase, putative | 0.0153 | 0.3229 | 0.5 |
Echinococcus multilocularis | baculoviral IAP repeat containing protein | 0.0207 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0207 | 1 | 1 |
Brugia malayi | Inhibitor of Apoptosis domain containing protein | 0.0207 | 1 | 1 |
Echinococcus granulosus | inhibitor of apoptosis protein | 0.0207 | 1 | 1 |
Echinococcus multilocularis | inhibitor of apoptosis protein | 0.0207 | 1 | 1 |
Echinococcus granulosus | baculoviral IAP repeat containing protein | 0.0207 | 1 | 1 |
Schistosoma mansoni | inhibitor of apoptosis (iap) domain family member | 0.0207 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | = 27 % | Inhibition of human full length DGAT-1 expressed in insect sf9 cells using [14C]decanoylCoA as substrate at 3 uM after 1.5 hrs by scintillation spectrometry | ChEMBL. | 23871442 |
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.