Crystal structures of complexes of a peptidic inhibitor with wild-type and two mutant HIV-1 proteases.
Cellular origin, complementary deoxyribonucleic acid and N-terminal amino acid sequences of human seminal progastricsin.
A kinetic model for comparing proteolytic processing activity and inhibitor resistance potential of mutant HIV-1 proteases.
Mechanism of autoprocessing of a mini-precursor of the aspartic protease of human immunodeficiency virus type 1.
