Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trichomonas vaginalis | glycogen phosphorylase, putative | 0.0513 | 0.5 | 0.5 |
Echinococcus multilocularis | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Onchocerca volvulus | Glycogen phosphorylase homolog | 0.0513 | 0.5 | 0.5 |
Schistosoma mansoni | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Echinococcus granulosus | Glycosyl transferase family 35 | 0.0513 | 0.5 | 0.5 |
Entamoeba histolytica | glycogen phosphorylase, putative | 0.0513 | 0.5 | 0.5 |
Schistosoma mansoni | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Entamoeba histolytica | glycogen phosphorylase, putative | 0.0513 | 0.5 | 0.5 |
Chlamydia trachomatis | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Echinococcus granulosus | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Giardia lamblia | Glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Loa Loa (eye worm) | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Echinococcus multilocularis | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Echinococcus multilocularis | Glycosyl transferase, family 35 | 0.0513 | 0.5 | 0.5 |
Trichomonas vaginalis | glycogen phosphorylase, putative | 0.0513 | 0.5 | 0.5 |
Echinococcus granulosus | glycogen phosphorylase | 0.0513 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
k2 (binding) | = 0.01 min-1 | Kinetic constant of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy). | ChEMBL. | 1588558 |
k2 (binding) | = 0.01 min-1 | Kinetic constant of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy). | ChEMBL. | 1588558 |
k2/KI (binding) | = 0.00000015 nM-1 min-1 | Ratio of kinetic constant to inhibitory activity against bovine liver S-adenosyl-L-homocysteine hydrolase(AdoHcy). | ChEMBL. | 1588558 |
Ki (binding) | = 67600 nM | Inhibitory activity of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy). | ChEMBL. | 1588558 |
Ki (binding) | = 67600 nM | Inhibitory activity of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy). | ChEMBL. | 1588558 |
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.