Total chemical synthesis of HIV-1 protease using Fmoc/t-butyl protection strategy

This publication has 7 references indexed in Scilit:

• A cleavage method which minimizes side reactions following Fmoc solid phase peptide synthesis
  International Journal of Peptide and Protein Research, 1990
• Affinity purification of HIV-1 and HIV-2 proteases from recombinant E. coli strains using pepstatin-agarose
  Biochemical and Biophysical Research Communications, 1990
• Substrate analog inhibition and active site titration of purified recombinant HIV-1 protease
  Biochemistry, 1990
• Conserved Folding in Retroviral Proteases: Crystal Structure of Synthetic HIV-1 Protease
  Science, 1989
• Chemical synthesis and enzymatic activity of a 99-residue peptide with a sequence proposed for the human immunodeficiency virus protease.
  Proceedings of the National Academy of Sciences, 1988
• Active human immunodeficiency virus protease is required for viral infectivity.
  Proceedings of the National Academy of Sciences, 1988
• Enzymatic activity of a synthetic 99 residue protein corresponding to the putative HIV-1 protease
  Cell, 1988