Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | glycogen phosphorylase | 0.0811 | 1 | 1 |
Trichomonas vaginalis | glycogen phosphorylase, putative | 0.0811 | 1 | 0.5 |
Schistosoma mansoni | glycogen phosphorylase | 0.0351 | 0.2034 | 0.2034 |
Schistosoma mansoni | glycogen phosphorylase | 0.0811 | 1 | 1 |
Onchocerca volvulus | Glycogen phosphorylase homolog | 0.0811 | 1 | 0.5 |
Entamoeba histolytica | glycogen phosphorylase, putative | 0.0811 | 1 | 1 |
Mycobacterium tuberculosis | Probable glycogen phosphorylase GlgP | 0.0351 | 0.2034 | 0.5 |
Mycobacterium ulcerans | glycogen phosphorylase GlgP | 0.0351 | 0.2034 | 0.5 |
Echinococcus granulosus | Glycosyl transferase family 35 | 0.0811 | 1 | 1 |
Schistosoma mansoni | glycogen phosphorylase | 0.0811 | 1 | 1 |
Chlamydia trachomatis | glycogen phosphorylase | 0.0811 | 1 | 0.5 |
Entamoeba histolytica | glycogen phosphorylase, putative | 0.0811 | 1 | 1 |
Echinococcus granulosus | glycogen phosphorylase | 0.0811 | 1 | 1 |
Loa Loa (eye worm) | glycogen phosphorylase | 0.0811 | 1 | 0.5 |
Giardia lamblia | Glycogen phosphorylase | 0.0811 | 1 | 0.5 |
Echinococcus multilocularis | Glycosyl transferase, family 35 | 0.0811 | 1 | 1 |
Trichomonas vaginalis | glycogen phosphorylase, putative | 0.0811 | 1 | 0.5 |
Echinococcus granulosus | glycogen phosphorylase | 0.0811 | 1 | 1 |
Echinococcus multilocularis | glycogen phosphorylase | 0.0811 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (binding) | 0 | Displacement of Eu-NDP-alpha-MSH from human melanocortin 4 receptor expressed in HEK293 cells at 1 pM to 10 uM | ChEMBL. | 17448660 |
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.