Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | jun protein | 0.0183 | 0.6792 | 1 |
Leishmania major | hypothetical protein, conserved | 0.004 | 0.0163 | 0.5 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.004 | 0.0163 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0252 | 1 | 1 |
Schistosoma mansoni | jun-related protein | 0.0149 | 0.5202 | 1 |
Trypanosoma brucei | membrane transporter protein, putative | 0.004 | 0.0163 | 0.5 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.004 | 0.0163 | 0.5 |
Trypanosoma brucei | membrane transporter protein, putative | 0.004 | 0.0163 | 0.5 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription factor | 0.0183 | 0.6792 | 1 |
Leishmania major | hypothetical protein, conserved | 0.004 | 0.0163 | 0.5 |
Brugia malayi | bZIP transcription factor family protein | 0.0183 | 0.6792 | 0.3623 |
Onchocerca volvulus | 0.0144 | 0.497 | 0.5 | |
Trypanosoma cruzi | hypothetical protein, conserved | 0.004 | 0.0163 | 0.5 |
Trypanosoma cruzi | membrane transporter protein, putative | 0.004 | 0.0163 | 0.5 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.004 | 0.0163 | 0.5 |
Echinococcus multilocularis | jun protein | 0.0183 | 0.6792 | 1 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription factor | 0.0183 | 0.6792 | 1 |
Trypanosoma brucei | MATE efflux family protein, putative | 0.004 | 0.0163 | 0.5 |
Echinococcus multilocularis | multidrug and toxin extrusion protein 2 | 0.004 | 0.0163 | 0.024 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.004 | 0.0163 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0149 | 0.5202 | 1 |
Trypanosoma brucei | membrane transporter protein, putative | 0.004 | 0.0163 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ratio (functional) | = 52.1 | Mosquito repellent activity in white mouse assessed as ratio of number of biting mosquito in treated to untreated control at 1.5 hrs | ChEMBL. | 18424131 |
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.