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2f3k
From Proteopedia
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'''Substrate envelope and drug resistance: crystal structure of r01 in complex with wild-type hiv-1 protease''' | '''Substrate envelope and drug resistance: crystal structure of r01 in complex with wild-type hiv-1 protease''' | ||
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[[Category: Prabu-Jeyabalan, M.]] | [[Category: Prabu-Jeyabalan, M.]] | ||
[[Category: Schiffer, C A.]] | [[Category: Schiffer, C A.]] | ||
| - | [[Category: | + | [[Category: Drug resistance]] |
| - | [[Category: | + | [[Category: Hiv protease]] |
| - | [[Category: | + | [[Category: Ro1]] |
| - | [[Category: | + | [[Category: Substrate envelope]] |
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Revision as of 00:25, 4 May 2008
Substrate envelope and drug resistance: crystal structure of r01 in complex with wild-type hiv-1 protease
Overview
In our previous crystallographic studies of human immunodeficiency virus type 1 (HIV-1) protease-substrate complexes, we described a conserved "envelope" that appears to be important for substrate recognition and the selection of drug-resistant mutations. In this study, the complex of HIV-1 protease with the inhibitor RO1 was determined and comparison with the substrate envelope provides a rationale for mutational patterns.
About this Structure
2F3K is a Single protein structure of sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
Substrate envelope and drug resistance: crystal structure of RO1 in complex with wild-type human immunodeficiency virus type 1 protease., Prabu-Jeyabalan M, King NM, Nalivaika EA, Heilek-Snyder G, Cammack N, Schiffer CA, Antimicrob Agents Chemother. 2006 Apr;50(4):1518-21. PMID:16569872 Page seeded by OCA on Sun May 4 03:25:25 2008
