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JVI Accepts, published online ahead of print on 23 April 2008
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J. Virol. doi:10.1128/JVI.00018-08
Copyright (c) 2008, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Structural Analysis of HIV-1 CRF01_AE Protease in Complex with the Substrate p1-p6

Rajintha M. Bandaranayake, Moses Prabu-Jeyabalan, Junko Kakizawa, Wataru Sugiura, and Celia A. Schiffer*

Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, 364 Plantation Street, Worcester, MA 01605, USA; Laboratory of Therapeutic Research and Clinical Science, AIDS Research Center, National Institute of Infectious Diseases, 4-7-1 Gakuenn Musashimurayama, Tokyo 208-0011, Japan

* To whom correspondence should be addressed. Email: Celia.Schiffer{at}umassmed.edu.


   Abstract

The effect of amino acid variability between human immunodeficiency virus type-1 (HIV-1) clades on structure and the emergence of resistance mutations in HIV-1 protease has become an area of significant interest in recent years. We determined the first crystal structure of HIV-1 CRF01_AE protease in complex with the p1-p6 substrate determined to a resolution of 2.8 Å. Hydrogen bonding between the flap hinge and protease core regions show significant structural rearrangements in CRF01_AE protease when compared to the clade B protease structure.







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