| Literature DB >> 23043109 |
Lavanya Krishnan1, Alan Engelman.
Abstract
Retroviral integrases catalyze two reactions, 3'-processing of viral DNA ends, followed by integration of the processed ends into chromosomal DNA. X-ray crystal structures of integrase-DNA complexes from prototype foamy virus, a member of the Spumavirus genus of Retroviridae, have revealed the structural basis of integration and how clinically relevant integrase strand transfer inhibitors work. Underscoring the translational potential of targeting virus-host interactions, small molecules that bind at the host factor lens epithelium-derived growth factor/p75-binding site on HIV-1 integrase promote dimerization and inhibit integrase-viral DNA assembly and catalysis. Here, we review recent advances in our knowledge of HIV-1 DNA integration, as well as future research directions.Entities:
Mesh:
Substances:
Year: 2012 PMID: 23043109 PMCID: PMC3510789 DOI: 10.1074/jbc.R112.397760
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157