The N137 and P140 amino acids in the p51 and the P95 amino acid in the p66 subunit of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase are instrumental to maintain catalytic activity and to design new classes of anti-HIV-1 drugs

Author:

Auwerx Joeri,Van Nieuwenhove Joke,Rodríguez-Barrios Fátima,de Castro Sonia,Velázquez Sonsoles,Ceccherini-Silberstein Francesca,De Clercq Erik,Camarasa María-José,Perno Carlo-Federico,Gago Federico,Balzarini Jan

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Reference27 articles.

1. Antiviral drugs in current clinical use;De Clercq;J. Clin. Virol.,2004

2. Reverse transcriptase inhibitors as anti-HIV drugs;De Clercq,2000

3. Current status of the non-nucleoside reverse transcriptase inhibitors of human immunodeficiency virus type 1;Balzarini;Curr. Top. Med. Chem.,2004

4. Suppression of resistance to drugs targeted to human immunodeficiency virus reverse transcriptase by combination therapy;Balzarini;Biochem. Pharmacol.,1999

5. Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors;Pelemans;Mol. Pharmacol.,2000

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