| Literature DB >> 31603676 |
F Xavier Ruiz, Anthony Hoang, Kalyan Das1,2, Eddy Arnold.
Abstract
HIV-1 reverse transcriptase (RT) is an essential enzyme, targeting half of approved anti-AIDS drugs. While nucleoside RT inhibitors (NRTIs) are DNA chain terminators, the nucleotide-competing RT inhibitor (NcRTI) INDOPY-1 blocks dNTP binding to RT. Lack of structural information hindered INDOPY-1 improvement. Here we report the HIV-1 RT/DNA/INDOPY-1 crystal structure, revealing a unique mode of inhibitor binding at the polymerase active site without involving catalytic metal ions. The structure may enable new strategies for developing NcRTIs.Entities:
Mesh:
Substances:
Year: 2019 PMID: 31603676 PMCID: PMC7737671 DOI: 10.1021/acs.jmedchem.9b01289
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446