Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | beta adrenergic receptor kinase | 0.0515 | 0.722 | 1 |
Echinococcus multilocularis | G protein coupled receptor kinase 6 | 0.0455 | 0.278 | 0.3851 |
Loa Loa (eye worm) | AGC/GRK/BARK protein kinase | 0.0515 | 0.722 | 0.6149 |
Echinococcus granulosus | beta-adrenergic receptor kinase | 0.0515 | 0.722 | 1 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0553 | 1 | 1 |
Echinococcus granulosus | [G-protein-coupledreceptor] kinase | 0.0455 | 0.278 | 0.3851 |
Loa Loa (eye worm) | AGC/GRK/GRK protein kinase | 0.0553 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | Antimicrobial activity against Escherichia coli AB734 by broth microdilution method | ChEMBL. | 23786712 | |
Activity (functional) | Antimicrobial activity against Escherichia coli 1411 by broth microdilution method | ChEMBL. | 23786712 |
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.