Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | 5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target/s | Ortholog Group |
---|---|---|---|
Echinococcus multilocularis | tm gpcr rhodopsin gpcr rhodopsin superfamily | Get druggable targets OG5_145685 | All targets in OG5_145685 |
Echinococcus granulosus | tm gpcr rhodopsin | Get druggable targets OG5_145685 | All targets in OG5_145685 |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | serine:threonine protein kinase Chk2 | 0.0045 | 0.01 | 0.01 |
Trypanosoma cruzi | STE/STE20 serine/threonine-protein kinase, putative | 0.028 | 0.2133 | 1 |
Giardia lamblia | Kinase, STE STE20 | 0.028 | 0.2133 | 0.5 |
Echinococcus granulosus | leucine rich repeat serine:threonine protein | 0.0791 | 0.6568 | 0.6568 |
Entamoeba histolytica | protein kinase, putative | 0.0045 | 0.01 | 0.0285 |
Trichomonas vaginalis | STE family protein kinase | 0.028 | 0.2133 | 0.6073 |
Trichomonas vaginalis | STE family protein kinase | 0.0439 | 0.3513 | 1 |
Echinococcus multilocularis | serine threonine protein kinase | 0.0439 | 0.3513 | 0.3513 |
Brugia malayi | Protein kinase domain containing protein | 0.0353 | 0.2769 | 0.2769 |
Echinococcus multilocularis | serine:threonine protein kinase 3 | 0.1188 | 1 | 1 |
Echinococcus multilocularis | calcium:calmodulin dependent protein kinase I | 0.0045 | 0.01 | 0.01 |
Loa Loa (eye worm) | STE/STE20/MST protein kinase | 0.1188 | 1 | 1 |
Trypanosoma brucei | STE20-like serine/threonine-protein kinase 1, putative | 0.028 | 0.2133 | 1 |
Trichomonas vaginalis | STE family protein kinase | 0.0439 | 0.3513 | 1 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0045 | 0.01 | 0.0131 |
Echinococcus multilocularis | leucine rich repeat serine:threonine protein | 0.0786 | 0.6522 | 0.6522 |
Echinococcus multilocularis | myosin iiia | 0.028 | 0.2133 | 0.2133 |
Echinococcus granulosus | serine:threonine protein kinase 3 | 0.1188 | 1 | 1 |
Schistosoma mansoni | ste20-related kinase | 0.0915 | 0.7638 | 1 |
Plasmodium falciparum | protein kinase, putative | 0.0439 | 0.3513 | 1 |
Echinococcus multilocularis | tm gpcr rhodopsin gpcr rhodopsin superfamily | 0.1003 | 0.84 | 0.84 |
Echinococcus granulosus | tm gpcr rhodopsin | 0.1003 | 0.84 | 0.84 |
Entamoeba histolytica | protein kinase, putative | 0.0045 | 0.01 | 0.0285 |
Loa Loa (eye worm) | TKL/LRRK protein kinase | 0.0786 | 0.6522 | 0.6522 |
Onchocerca volvulus | 0.0033 | 0 | 0.5 | |
Echinococcus granulosus | calcium:calmodulin dependent protein kinase I | 0.0045 | 0.01 | 0.01 |
Onchocerca volvulus | Mitochondrial Rho GTPase homolog | 0.0033 | 0 | 0.5 |
Loa Loa (eye worm) | CAMK/CAMKL/CHK1 protein kinase | 0.0353 | 0.2769 | 0.2769 |
Entamoeba histolytica | serine/threonine protein kinase STE20, putative | 0.028 | 0.2133 | 0.6073 |
Entamoeba histolytica | serine/threonine-protein kinase 3, putative | 0.028 | 0.2133 | 0.6073 |
Leishmania major | protein kinase, putative | 0.028 | 0.2133 | 1 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0439 | 0.3513 | 0.4599 |
Echinococcus granulosus | serine threonine protein kinase | 0.0439 | 0.3513 | 0.3513 |
Plasmodium vivax | serine/threonine-specific protein kinase, putative | 0.0439 | 0.3513 | 1 |
Brugia malayi | Protein kinase domain containing protein | 0.0786 | 0.6522 | 0.6522 |
Entamoeba histolytica | protein kinase, putative | 0.0439 | 0.3513 | 1 |
Echinococcus multilocularis | serine:threonine protein kinase Chk2 | 0.0045 | 0.01 | 0.01 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0353 | 0.2769 | 0.3626 |
Loa Loa (eye worm) | STE/STE20/YSK protein kinase | 0.0439 | 0.3513 | 0.3513 |
Trypanosoma cruzi | STE/STE20 serine/threonine-protein kinase, putative | 0.028 | 0.2133 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 5.22 uM | Antagonist activity at human 5-HT6 receptor expressed in human HeLa cells assessed as inhibition of 5-HT-induced cAMP accumulation pretreated for 10 mins before 5-HT addition measured after 30 mins | ChEMBL. | 23820387 |
Inhibition (functional) | = 67.9 % | Antagonist activity at human 5-HT6 receptor expressed in human HeLa cells assessed as inhibition of 5-HT-induced cAMP accumulation at 10 uM pretreated for 10 mins before 5-HT addition measured after 30 mins | ChEMBL. | 23820387 |
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.