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Viruses. 2010 Apr;2(4):900-26. doi: 10.3390/v2040900. Epub 2010 Mar 30.

HIV-1 Ribonuclease H: Structure, Catalytic Mechanism and Inhibitors.

Author information

  • 1Department of Microbiology and Immunology, McGill University, Lyman Duff Medical Building (D6), 3775 University St., Montreal, QC, H3A 2B4, Canada.

Abstract

Since the human immunodeficiency virus (HIV) was discovered as the etiological agent of acquired immunodeficiency syndrome (AIDS), it has encouraged much research into antiviral compounds. The reverse transcriptase (RT) of HIV has been a main target for antiviral drugs. However, all drugs developed so far inhibit the polymerase function of the enzyme, while none of the approved antiviral agents inhibit specifically the necessary ribonuclease H (RNase H) function of RT. This review provides a background on structure-function relationships of HIV-1 RNase H, as well as an outline of current attempts to develop novel, potent chemotherapeutics against a difficult drug target.

KEYWORDS:

HIV; RNase H; drug resistance; inhibitors; reverse transcriptase

PMID:
21994660
[PubMed]
PMCID:
PMC3185654
Free PMC Article
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