Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | glutamate receptor, metabotropic 4 | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | glutamate receptor | 0.0061 | 0.0045 | 0.6249 |
Schistosoma mansoni | dipeptidyl-peptidase I (C01 family) | 0.5261 | 1 | 1 |
Entamoeba histolytica | hypothetical protein | 0.004 | 0.0004 | 0.5 |
Schistosoma mansoni | neuropeptide receptor | 0.0114 | 0.0146 | 0.0146 |
Echinococcus multilocularis | G protein coupled receptor 139 | 0.0114 | 0.0146 | 0.5224 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.0055 | 0.0033 | 0.462 |
Plasmodium falciparum | dipeptidyl aminopeptidase 2 | 0.5261 | 1 | 1 |
Brugia malayi | metabotropic glutamate receptor subtype 5a (mGluR5a), putative | 0.0055 | 0.0034 | 0.7558 |
Schistosoma mansoni | transcription factor LCR-F1 | 0.004 | 0.0004 | 0.0004 |
Brugia malayi | hypothetical protein | 0.004 | 0.0004 | 0.089 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.0055 | 0.0033 | 0.7394 |
Plasmodium vivax | dipeptidyl aminopeptidase 1, putative | 0.5261 | 1 | 1 |
Echinococcus multilocularis | neuropeptide receptor | 0.0114 | 0.0146 | 0.5224 |
Entamoeba histolytica | hypothetical protein | 0.004 | 0.0004 | 0.5 |
Plasmodium vivax | dipeptidyl aminopeptidase 2, putative | 0.5261 | 1 | 1 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.0055 | 0.0033 | 0.7394 |
Toxoplasma gondii | cathepsin CPC1 | 0.5261 | 1 | 1 |
Toxoplasma gondii | preprocathepsin c precursor, putative | 0.5261 | 1 | 1 |
Echinococcus granulosus | geminin | 0.0182 | 0.0276 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0182 | 0.0276 | 0.0276 |
Schistosoma mansoni | hypothetical protein | 0.004 | 0.0004 | 0.0004 |
Plasmodium falciparum | dipeptidyl aminopeptidase 1 | 0.5261 | 1 | 1 |
Entamoeba histolytica | hypothetical protein | 0.004 | 0.0004 | 0.5 |
Schistosoma mansoni | metabotropic glutamate receptor | 0.0051 | 0.0026 | 0.0026 |
Schistosoma mansoni | metabotropic glutamate receptor 2 3 (mglur group 2) | 0.0069 | 0.0061 | 0.0061 |
Echinococcus multilocularis | metabotropic glutamate receptor 2 | 0.0051 | 0.0026 | 0.0811 |
Trichomonas vaginalis | Clan CA, family C1, cathepsin B-like cysteine peptidase | 0.3265 | 0.6178 | 0.5 |
Echinococcus granulosus | neuropeptide receptor | 0.0114 | 0.0146 | 0.5224 |
Loa Loa (eye worm) | hypothetical protein | 0.0055 | 0.0033 | 0.462 |
Schistosoma mansoni | hypothetical protein | 0.0182 | 0.0276 | 0.0276 |
Entamoeba histolytica | hypothetical protein | 0.004 | 0.0004 | 0.5 |
Brugia malayi | Metabotropic glutamate receptor precursor. | 0.0061 | 0.0045 | 1 |
Echinococcus multilocularis | metabotropic glutamate receptor 5 | 0.0075 | 0.0072 | 0.2505 |
Loa Loa (eye worm) | hypothetical protein | 0.0075 | 0.0072 | 1 |
Echinococcus granulosus | metabotropic glutamate receptor 5 | 0.0075 | 0.0072 | 0.2505 |
Echinococcus multilocularis | geminin | 0.0182 | 0.0276 | 1 |
Echinococcus granulosus | metabotropic glutamate receptor 2 | 0.0051 | 0.0026 | 0.0811 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
EC50 (binding) | = 2900 nM | Positive allosteric modulation of human mGlu4 receptor expressed in BHK cells assessed as potentiation of glutamate-induced calcium mobilization by FLIPR analysis | ChEMBL. | 22465637 |
Emax (binding) | = 110 % | Positive allosteric modulation of human mGlu4 receptor expressed in BHK cells assessed as potentiation of glutamate-induced calcium mobilization by FLIPR analysis relative to PHCCC | ChEMBL. | 22465637 |
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.