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Curr Med Chem ; 13(3): 313-24, 2006.
Article in English | MEDLINE | ID: mdl-16475939

ABSTRACT

Human Immunodeficiency Virus type 1 Reverse Transcriptase (HIV-1 RT) is one of the most important targets for treatment of Acquired Immune Deficiency Syndrome (AIDS). It catalyzes the reverse transcription of HIV-RNA into a double stranded DNA, and the knowledge of its substrate specificity and catalytic mechanism has guided the development of several inhibitors widely used on current HIV/AIDS therapy. However, mutations in HIV-1 RT structure can lead to the emergence of drug-resistant virus strains. The goal of this review is to summarize relevant structural features of HIV-1 RT and its inhibitors in such a way that this cost-effective target in the development of new antiretroviral drugs is particularly highlighted.


Subject(s)
HIV Reverse Transcriptase/drug effects , HIV-1/enzymology , Drug Resistance, Viral , HIV Infections/drug therapy , HIV Reverse Transcriptase/chemistry , HIV Reverse Transcriptase/genetics , HIV-1/genetics , HIV-1/physiology , Humans , Models, Molecular , Protein Conformation , Reverse Transcriptase Inhibitors/pharmacology , Reverse Transcriptase Inhibitors/therapeutic use , Virus Replication
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