Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.0389 | 0.488 | 0.3874 | |
Brugia malayi | hypothetical protein | 0.052 | 0.8919 | 0.8706 |
Onchocerca volvulus | 0.0555 | 1 | 1 | |
Mycobacterium ulcerans | chitinase/cellulase | 0.0231 | 0 | 0.5 |
Loa Loa (eye worm) | cuticular endochitinase | 0.0284 | 0.1642 | 0.1642 |
Mycobacterium ulcerans | chitinase/cellulase | 0.0231 | 0 | 0.5 |
Brugia malayi | Endochitinase | 0.0306 | 0.2315 | 0.0805 |
Brugia malayi | endochitinase | 0.0306 | 0.2315 | 0.0805 |
Onchocerca volvulus | Putative endochitinase | 0.0306 | 0.2315 | 0.0805 |
Loa Loa (eye worm) | hypothetical protein | 0.0555 | 1 | 1 |
Toxoplasma gondii | PAN domain-containing protein | 0.0346 | 0.3571 | 0.5 |
Onchocerca volvulus | Putative endochitinase | 0.0306 | 0.2315 | 0.0805 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0555 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0555 | 1 | 1 |
Onchocerca volvulus | Putative endochitinase | 0.0306 | 0.2315 | 0.0805 |
Loa Loa (eye worm) | hypothetical protein | 0.052 | 0.8919 | 0.8919 |
Loa Loa (eye worm) | chitinase I | 0.0284 | 0.1642 | 0.1642 |
Brugia malayi | sulfakinin receptor protein | 0.052 | 0.8919 | 0.8706 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0555 | 1 | 0.5 |
Leishmania major | chitinase | 0.0284 | 0.1642 | 0.5 |
Mycobacterium tuberculosis | Possible chitinase | 0.0231 | 0 | 0.5 |
Loa Loa (eye worm) | microfilarial chitinase | 0.0253 | 0.0672 | 0.0672 |
Entamoeba histolytica | chitinase, putative | 0.0284 | 0.1642 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.0346 | 0.3571 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 0.1 nM | Inhibition of binding of [125I]-Bolton-Hunter labeled CCK-8 to cholecystokinin type A receptor in the rat pancreas. | ChEMBL. | 7684452 |
IC50 (binding) | = 31 nM | Inhibition of binding of [125I]-Bolton-Hunter labeled CCK-8 to cholecystokinin type B receptor in the mouse cerebral cortex | ChEMBL. | 7684452 |
Ratio (binding) | = 0.0032 | Selectivity ratio is IC50 value of CCK-A receptor to that of CCK-B receptor | ChEMBL. | 7684452 |
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.