Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | SMAD family member 2 | Starlite/ChEMBL | No references |
Homo sapiens | APEX nuclease (multifunctional DNA repair enzyme) 1 | Starlite/ChEMBL | No references |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Brugia malayi | MH2 domain containing protein | SMAD family member 2 | 467 aa | 405 aa | 31.6 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Iron-sulfur cluster assembly accessory protein | 0.0058 | 0.0054 | 0.1756 |
Mycobacterium ulcerans | peptide deformylase | 0.893 | 1 | 1 |
Brugia malayi | MH2 domain containing protein | 0.0144 | 0.0151 | 0.4872 |
Giardia lamblia | Endonuclease/Exonuclease/phosphatase | 0.0023 | 0.0014 | 0.5 |
Mycobacterium tuberculosis | Probable polypeptide deformylase Def (PDF) (formylmethionine deformylase) | 0.893 | 1 | 1 |
Plasmodium vivax | peptide deformylase, putative | 0.893 | 1 | 1 |
Echinococcus multilocularis | DNA (apurinic or apyrimidinic site) lyase | 0.0023 | 0.0014 | 0.0467 |
Trypanosoma cruzi | Peptide deformylase 2, putative | 0.3407 | 0.3809 | 1 |
Trypanosoma brucei | Peptide deformylase 2 | 0.3407 | 0.3809 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0058 | 0.0054 | 1 |
Brugia malayi | hypothetical protein | 0.0286 | 0.0309 | 1 |
Schistosoma mansoni | survival motor neuron protein | 0.0058 | 0.0054 | 1 |
Trypanosoma cruzi | polypeptide deformylase-like protein, putative | 0.3407 | 0.3809 | 1 |
Mycobacterium leprae | PROBABLE POLYPEPTIDE DEFORMYLASE DEF (PDF) (FORMYLMETHIONINE DEFORMYLASE) | 0.893 | 1 | 0.5 |
Leishmania major | polypeptide deformylase-like protein, putative | 0.3407 | 0.3809 | 1 |
Schistosoma mansoni | ap endonuclease | 0.0023 | 0.0014 | 0.2662 |
Trypanosoma brucei | Polypeptide deformylase 1 | 0.3407 | 0.3809 | 1 |
Onchocerca volvulus | 0.0058 | 0.0054 | 0.5 | |
Loa Loa (eye worm) | MH2 domain-containing protein | 0.0144 | 0.0151 | 0.4872 |
Trypanosoma cruzi | polypeptide deformylase-like protein, putative | 0.3407 | 0.3809 | 1 |
Schistosoma mansoni | ap endonuclease | 0.0023 | 0.0014 | 0.2662 |
Trichomonas vaginalis | ap endonuclease, putative | 0.0023 | 0.0014 | 0.5 |
Trypanosoma cruzi | Peptide deformylase 2, putative | 0.3407 | 0.3809 | 1 |
Treponema pallidum | polypeptide deformylase (def) | 0.893 | 1 | 1 |
Echinococcus multilocularis | survival motor neuron protein 1 | 0.0286 | 0.0309 | 1 |
Entamoeba histolytica | exodeoxyribonuclease III, putative | 0.0023 | 0.0014 | 0.5 |
Wolbachia endosymbiont of Brugia malayi | peptide deformylase | 0.893 | 1 | 1 |
Brugia malayi | exodeoxyribonuclease III family protein | 0.0023 | 0.0014 | 0.0467 |
Loa Loa (eye worm) | hypothetical protein | 0.0286 | 0.0309 | 1 |
Loa Loa (eye worm) | exodeoxyribonuclease III family protein | 0.0023 | 0.0014 | 0.0467 |
Echinococcus granulosus | DNA apurinic or apyrimidinic site lyase | 0.0023 | 0.0014 | 0.0467 |
Toxoplasma gondii | hypothetical protein | 0.893 | 1 | 1 |
Echinococcus granulosus | survival motor neuron protein 1 | 0.0286 | 0.0309 | 1 |
Trichomonas vaginalis | ap endonuclease, putative | 0.0023 | 0.0014 | 0.5 |
Plasmodium falciparum | peptide deformylase | 0.893 | 1 | 1 |
Loa Loa (eye worm) | transcription factor SMAD2 | 0.0144 | 0.0151 | 0.4872 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | 0.2239 uM | PubChem BioAssay. qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1). (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 1.7783 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of TGF-b. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588856, AID588860] | ChEMBL. | No reference |
Potency (functional) | 50.1187 uM | PubChem BioAssay. qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 79.4328 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of Polymerase Iota. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588623] | ChEMBL. | No reference |
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.