Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Serotonin 7 (5-HT7) receptor | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target/s | Ortholog Group |
---|---|---|---|
Schistosoma mansoni | biogenic amine (5HT) receptor | Get druggable targets OG5_133074 | All targets in OG5_133074 |
Echinococcus multilocularis | biogenic amine (5HT) receptor | Get druggable targets OG5_133074 | All targets in OG5_133074 |
Echinococcus granulosus | biogenic amine 5HT receptor | Get druggable targets OG5_133074 | All targets in OG5_133074 |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Echinococcus granulosus | g protein coupled receptor | Serotonin 7 (5-HT7) receptor | 448 aa | 396 aa | 19.9 % |
Echinococcus multilocularis | g protein coupled receptor | Serotonin 7 (5-HT7) receptor | 448 aa | 422 aa | 21.1 % |
Echinococcus granulosus | g protein coupled receptor | Serotonin 7 (5-HT7) receptor | 448 aa | 420 aa | 21.2 % |
Schistosoma japonicum | ko:K04136 adrenergic receptor, alpha 1b, putative | Serotonin 7 (5-HT7) receptor | 448 aa | 362 aa | 32.3 % |
Echinococcus multilocularis | neuropeptides capa receptor | Serotonin 7 (5-HT7) receptor | 448 aa | 428 aa | 19.2 % |
Echinococcus multilocularis | g protein coupled receptor | Serotonin 7 (5-HT7) receptor | 448 aa | 396 aa | 19.9 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.0748 | 0.1585 | 0.3431 | |
Loa Loa (eye worm) | matrixin family protein | 0.117 | 0.4621 | 0.859 |
Mycobacterium leprae | PROBABLE HYDROLASE | 0.0642 | 0.0827 | 0.5 |
Brugia malayi | Putative carbonic anhydrase 5 precursor | 0.0747 | 0.1582 | 0.2941 |
Leishmania major | carbonic anhydrase-like protein | 0.0747 | 0.1582 | 0.5 |
Trypanosoma cruzi | carbonic anhydrase-like protein, putative | 0.0747 | 0.1582 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0642 | 0.0827 | 0.1537 |
Brugia malayi | Matrixin family protein | 0.1275 | 0.5379 | 1 |
Echinococcus multilocularis | matrix metallopeptidase 7 (M10 family) | 0.1917 | 1 | 1 |
Schistosoma mansoni | carbonic anhydrase II (carbonate dehydratase II) | 0.0747 | 0.1582 | 0.9978 |
Schistosoma mansoni | carbonic anhydrase II (carbonate dehydratase II) | 0.0747 | 0.1582 | 0.9978 |
Brugia malayi | Hemopexin family protein | 0.0748 | 0.1585 | 0.2947 |
Trypanosoma brucei | carbonic anhydrase-like protein | 0.0747 | 0.1582 | 0.5 |
Trypanosoma cruzi | carbonic anhydrase-like protein, putative | 0.0747 | 0.1582 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0748 | 0.1585 | 1 |
Brugia malayi | Eukaryotic-type carbonic anhydrase family protein | 0.0747 | 0.1582 | 0.2941 |
Brugia malayi | Matrix metalloprotease, N-terminal domain containing protein | 0.0642 | 0.0827 | 0.1537 |
Loa Loa (eye worm) | matrixin family protein | 0.1275 | 0.5379 | 1 |
Onchocerca volvulus | Matrilysin homolog | 0.117 | 0.4621 | 1 |
Mycobacterium ulcerans | hydrolase | 0.0642 | 0.0827 | 0.5 |
Loa Loa (eye worm) | carbonic anhydrase 3 | 0.0747 | 0.1582 | 0.2941 |
Onchocerca volvulus | Matrix metalloproteinase homolog | 0.117 | 0.4621 | 1 |
Loa Loa (eye worm) | eukaryotic-type carbonic anhydrase | 0.0747 | 0.1582 | 0.2941 |
Wolbachia endosymbiont of Brugia malayi | extracellular metallopeptidase | 0.1264 | 0.5301 | 0.5 |
Mycobacterium tuberculosis | Probable peptidoglycan hydrolase | 0.0642 | 0.0827 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | < -5 | Binding affinity towards 5-hydroxytryptamine receptor 7 on rat hypothalamus membranes using [3H]-5-CT as radioligand. | ChEMBL. | 14667218 |
Log Ki (binding) | < 5 | Binding affinity towards 5-hydroxytryptamine receptor 7 on rat hypothalamus membranes using [3H]-5-CT as radioligand. | ChEMBL. | 14667218 |
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.