J Green

X-ray crystallographic structure of a complex between a synthetic protease of human immunodeficiency virus 1 and a substrate-based hydroxyethylamine inhibitor.

A Wlodawer, A. Wlodawer, S. Kent, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Hydroxyethylamine analogues of the p17/p24 substrate cleavage site are tight-binding inhibitors of HIV protease.

G R Marshall, G. Marshall, S. Kent, 1990, Journal of medicinal chemistry.

Measurement of the binding of tyrosyl phosphopeptides to SH2 domains: a reappraisal.

J. Schlessinger, J. Ladbury, M. Lemmon, 1995, Proceedings of the National Academy of Sciences of the United States of America.