Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.0064 | 0.7323 | 1 | |
Toxoplasma gondii | calcium binding egf domain-containing protein | 0.0016 | 0 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0035 | 0.2875 | 0.3751 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0082 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0066 | 0.7665 | 1 |
Brugia malayi | hypothetical protein | 0.0035 | 0.2875 | 0.2875 |
Brugia malayi | hypothetical protein | 0.0064 | 0.7323 | 0.7323 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.2875 | 0.5 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0082 | 1 | 1 |
Echinococcus granulosus | jun protein | 0.0082 | 1 | 1 |
Schistosoma mansoni | transcription factor LCR-F1 | 0.0035 | 0.2875 | 0.3751 |
Echinococcus multilocularis | jun protein | 0.0082 | 1 | 1 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.2875 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.9658 | 1 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.2875 | 0.5 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription | 0.0035 | 0.2875 | 0.2875 |
Entamoeba histolytica | hypothetical protein | 0.0035 | 0.2875 | 0.5 |
Schistosoma mansoni | jun-related protein | 0.0066 | 0.7665 | 1 |
Toxoplasma gondii | calcium binding egf domain-containing protein | 0.0016 | 0 | 0.5 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription | 0.0035 | 0.2875 | 0.2875 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 360 nM | Inhibition of Coagulation factor Xa | ChEMBL. | 12061878 |
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.