| Literature DB >> 29800515 |
Ilaria Silvestri1, Haining Lyu2, Francesca Fata1, Giovanna Boumis3, Adriana E Miele3,4, Matteo Ardini1, Rodolfo Ippoliti1, Andrea Bellelli3, Ajit Jadhav5, Wendy A Lea5, Anton Simeonov5, Qing Cheng6, Elias S J Arnér6, Gregory R J Thatcher7, Pavel A Petukhov7, David L Williams2, Francesco Angelucci1.
Abstract
Members of the FAD/NAD-linked reductase family are recognized as crucial targets in drug development for cancers, inflammatory disorders, and infectious diseases. However, individual FAD/NAD reductases are difficult to inhibit in a selective manner with off-target inhibition reducing usefulness of identified compounds. Thioredoxin glutathione reductase (TGR), a high molecular weight thioredoxin reductase-like enzyme, has emerged as a promising drug target for the treatment of schistosomiasis, a parasitosis afflicting more than 200 million people. Taking advantage of small molecules selected from a high-throughput screen and using X-ray crystallography, functional assays, and docking studies, we identify a critical secondary site of the enzyme. Compounds binding at this site interfere with well-known and conserved conformational changes associated with NADPH reduction, acting as a doorstop for cofactor entry. They selectively inhibit TGR from Schistosoma mansoni and are active against parasites in culture. Since many members of the FAD/NAD-linked reductase family have similar catalytic mechanisms, the unique mechanism of inhibition identified in this study for TGR broadly opens new routes to selectively inhibit homologous enzymes of central importance in numerous diseases.Entities:
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Year: 2018 PMID: 29800515 DOI: 10.1021/acschembio.8b00349
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100