Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | opiate receptor-like 1 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Echinococcus multilocularis | growth hormone secretagogue receptor type 1 | opiate receptor-like 1 | 370 aa | 349 aa | 22.1 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.0091 | 0.2517 | 0.2517 |
Loa Loa (eye worm) | proteasome A-type and B-type family protein | 0.0231 | 0.8137 | 0.8137 |
Trypanosoma cruzi | proteasome beta 6 subunit, putative | 0.0069 | 0.16 | 0.1966 |
Mycobacterium leprae | proteasome (beta subunit) PrcB | 0.0231 | 0.8137 | 0.5 |
Echinococcus granulosus | geminin | 0.0158 | 0.5211 | 0.6404 |
Plasmodium falciparum | proteasome subunit beta type-1, putative | 0.0069 | 0.16 | 0.1966 |
Schistosoma mansoni | hypothetical protein | 0.0158 | 0.5211 | 0.6404 |
Echinococcus granulosus | proteasome prosome macropain | 0.0231 | 0.8137 | 1 |
Toxoplasma gondii | proteasome subunit beta type 1, putative | 0.0069 | 0.16 | 0.1966 |
Brugia malayi | Proteasome A-type and B-type family protein | 0.0231 | 0.8137 | 0.8137 |
Echinococcus multilocularis | proteasome (prosome, macropain) subunit, beta | 0.0069 | 0.16 | 0.1966 |
Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0231 | 0.8137 | 1 |
Schistosoma mansoni | proteasome catalytic subunit 3 (T01 family) | 0.0231 | 0.8137 | 1 |
Entamoeba histolytica | proteasome subunit beta type 5 precursor, putative | 0.0231 | 0.8137 | 1 |
Brugia malayi | latrophilin 2 splice variant baaae | 0.0062 | 0.1351 | 0.1351 |
Plasmodium vivax | proteasome subunit beta type-1, putative | 0.0069 | 0.16 | 0.1966 |
Echinococcus granulosus | proteasome prosome macropain subunit beta | 0.0069 | 0.16 | 0.1966 |
Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0231 | 0.8137 | 1 |
Brugia malayi | proteasome subunit beta type 1 | 0.0069 | 0.16 | 0.16 |
Loa Loa (eye worm) | hypothetical protein | 0.0277 | 1 | 1 |
Echinococcus multilocularis | geminin | 0.0158 | 0.5211 | 0.6404 |
Loa Loa (eye worm) | hypothetical protein | 0.0062 | 0.1351 | 0.1351 |
Trypanosoma brucei | proteasome subunit beta type-5, putative | 0.0231 | 0.8137 | 1 |
Leishmania major | proteasome beta 6 subunit, putative,20S proteasome beta 6 subunit, putative | 0.0069 | 0.16 | 0.1966 |
Loa Loa (eye worm) | proteasome subunit beta type 1 | 0.0069 | 0.16 | 0.16 |
Plasmodium vivax | proteasome subunit beta type-5, putative | 0.0231 | 0.8137 | 1 |
Trypanosoma brucei | proteasome beta 6 subunit | 0.0069 | 0.16 | 0.1966 |
Giardia lamblia | Proteasome subunit beta type 5 precursor | 0.0231 | 0.8137 | 1 |
Plasmodium falciparum | proteasome subunit beta type-5 | 0.0231 | 0.8137 | 1 |
Mycobacterium tuberculosis | Proteasome beta subunit PrcB; assembles with alpha subunit PrcA. | 0.0231 | 0.8137 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0158 | 0.5211 | 0.6404 |
Trichomonas vaginalis | Family T1, proteasome beta subunit, threonine peptidase | 0.0231 | 0.8137 | 1 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.0091 | 0.2517 | 0.2517 |
Toxoplasma gondii | proteasome subunit beta type, putative | 0.0231 | 0.8137 | 1 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.0091 | 0.2517 | 0.2517 |
Leishmania major | proteasome beta 5 subunit, putative | 0.0231 | 0.8137 | 1 |
Trypanosoma cruzi | proteasome beta 6 subunit, putative | 0.0069 | 0.16 | 0.1966 |
Loa Loa (eye worm) | hypothetical protein | 0.0091 | 0.2517 | 0.2517 |
Echinococcus multilocularis | proteasome (prosome, macropain) | 0.0231 | 0.8137 | 1 |
Onchocerca volvulus | 0.0277 | 1 | 0.5 | |
Schistosoma mansoni | proteasome subunit beta 1 (T01 family) | 0.0069 | 0.16 | 0.1966 |
Schistosoma mansoni | hypothetical protein | 0.0062 | 0.1351 | 0.166 |
Mycobacterium ulcerans | proteasome PrcB | 0.0231 | 0.8137 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Kb (functional) | = 15.8 nM | Antagonist activity at human recombinant NOP receptor expressed in CHO cells assessed as inhibition of nociceptin-induced [35S]GTPgammaS binding after 2 hrs by scintillation proximity assay | ChEMBL. | 21438532 |
Ki (binding) | = 10.2 nM | Displacement of [3H]nociceptin from human recombinant NOP receptor expressed in CHO cells after 60 mins by microbeta scintillation counting | ChEMBL. | 21438532 |
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.