Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | peroxisome proliferator-activated receptor gamma | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Echinococcus granulosus | ecdysone induced protein 78C | peroxisome proliferator-activated receptor gamma | 477 aa | 447 aa | 28.2 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Entamoeba histolytica | protein kinase domain containing protein | 0.0055 | 0.0489 | 1 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0099 | 0.2348 | 0.2348 |
Brugia malayi | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Echinococcus granulosus | semaphorin 1A | 0.0099 | 0.2348 | 0.2348 |
Loa Loa (eye worm) | hypothetical protein | 0.0139 | 0.3991 | 0.3991 |
Schistosoma mansoni | hypothetical protein | 0.0099 | 0.2348 | 0.2874 |
Brugia malayi | Sema domain containing protein | 0.0099 | 0.2348 | 0.2348 |
Onchocerca volvulus | 0.0238 | 0.8169 | 1 | |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0044 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Entamoeba histolytica | tyrosin kinase, putative | 0.0055 | 0.0489 | 1 |
Schistosoma mansoni | plexin | 0.0238 | 0.8169 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0044 | 0 | 0.5 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0044 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0044 | 0 | 0.5 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0044 | 0 | 0.5 |
Brugia malayi | Plexin repeat family protein | 0.0238 | 0.8169 | 0.8169 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0044 | 0 | 0.5 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0044 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0044 | 0 | 0.5 |
Echinococcus multilocularis | semaphorin 5B | 0.0099 | 0.2348 | 0.2348 |
Echinococcus multilocularis | plexin a4 | 0.0282 | 1 | 1 |
Schistosoma mansoni | semaphorin 5-related | 0.0099 | 0.2348 | 0.2874 |
Echinococcus granulosus | plexin a4 | 0.0282 | 1 | 1 |
Echinococcus multilocularis | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Schistosoma mansoni | hypothetical protein | 0.0139 | 0.3991 | 0.4885 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0044 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0238 | 0.8169 | 0.8169 |
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Echinococcus granulosus | semaphorin 5B | 0.0099 | 0.2348 | 0.2348 |
Schistosoma mansoni | plexin | 0.0139 | 0.3991 | 0.4885 |
Brugia malayi | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0044 | 0 | 0.5 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0099 | 0.2348 | 0.2348 |
Schistosoma mansoni | hypothetical protein | 0.0099 | 0.2348 | 0.2874 |
Brugia malayi | Sema domain containing protein | 0.0099 | 0.2348 | 0.2348 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0044 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0044 | 0 | 0.5 |
Loa Loa (eye worm) | plexin A | 0.0282 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.2348 | 0.2348 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 3657 nM | Binding affinity to human PPARgamma by scintillation proximity assay | ChEMBL. | 22070604 |
IC50 (binding) | > 50 uM | Binding affinity to human PPARalpha expressed in COS-1 by scintillation proximity assay | ChEMBL. | 22070604 |
IC50 (binding) | > 50 uM | Binding affinity to PPARdelta by scintillation proximity assay | ChEMBL. | 22070604 |
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.