Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 7-Day Trial for You or Your Team.

Learn More →

The Use of Chemical Double‐Mutant Cycles in Biomolecular Recognition Studies: Application to HCV NS3 Protease Inhibitors

The Use of Chemical Double‐Mutant Cycles in Biomolecular Recognition Studies: Application to HCV... Things don′t always add up: Our understanding of biomolecular recognition processes is often complicated by the fact that the binding contributions of individual ligand–protein subcontacts do not add up in a linear fashion. Chemical double‐mutant cycles are useful analyses to quantify the degree of nonadditivity in such binding phenomena, and peptidyl inhibitors of hepatitis C virus NS3 protease are used to exemplify this. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png ChemMedChem Wiley

The Use of Chemical Double‐Mutant Cycles in Biomolecular Recognition Studies: Application to HCV NS3 Protease Inhibitors

Loading next page...
 
/lp/wiley/the-use-of-chemical-double-mutant-cycles-in-biomolecular-recognition-peJKfAaUB0

References (29)

Publisher
Wiley
Copyright
Copyright © 2008 Wiley Subscription Services
ISSN
1860-7179
eISSN
1860-7187
DOI
10.1002/cmdc.200800214
pmid
18942693
Publisher site
See Article on Publisher Site

Abstract

Things don′t always add up: Our understanding of biomolecular recognition processes is often complicated by the fact that the binding contributions of individual ligand–protein subcontacts do not add up in a linear fashion. Chemical double‐mutant cycles are useful analyses to quantify the degree of nonadditivity in such binding phenomena, and peptidyl inhibitors of hepatitis C virus NS3 protease are used to exemplify this.

Journal

ChemMedChemWiley

Published: Jan 17, 2008

Keywords: ; ; ; ;

There are no references for this article.