Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | neuroglian | 0.0054 | 1 | 1 |
Loa Loa (eye worm) | TK/KIN16 protein kinase | 0.0044 | 0.5018 | 0.5018 |
Echinococcus granulosus | twitchin | 0.0054 | 1 | 1 |
Schistosoma mansoni | nephrin | 0.0054 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0054 | 1 | 1 |
Brugia malayi | Immunoglobulin I-set domain containing protein | 0.0044 | 0.5018 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0054 | 1 | 1 |
Echinococcus granulosus | neuroglian | 0.0054 | 1 | 1 |
Echinococcus multilocularis | roundabout 2 | 0.0054 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 0.28 uM | Inhibition of recombinant VZV TK assessed as [CH3-H3]dThd phosphorylation | ChEMBL. | 17298046 |
IC50 (binding) | > 500 uM | Inhibition of recombinant HSV-1 TK assessed as [CH3-H3]dThd phosphorylation | ChEMBL. | 17298046 |
IC50 (binding) | > 500 uM | Inhibition of recombinant cytosolic TK-1 assessed as [CH3-H3]dThd phosphorylation | ChEMBL. | 17298046 |
IC50 (binding) | > 500 uM | Inhibition of recombinant HSV-1 TK assessed as [CH3-H3]dThd phosphorylation | ChEMBL. | 17298046 |
IC50 (binding) | > 500 uM | Inhibition of recombinant cytosolic TK-1 assessed as [CH3-H3]dThd phosphorylation | ChEMBL. | 17298046 |
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.