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'''HIV-1 PROTEASE-INHIBITOR COMPLEX''' | '''HIV-1 PROTEASE-INHIBITOR COMPLEX''' | ||
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[[Category: Chen, Z.]] | [[Category: Chen, Z.]] | ||
[[Category: Munshi, S.]] | [[Category: Munshi, S.]] | ||
[[Category: | [[Category: Acid protease]] | ||
[[Category: | [[Category: Hydrolase]] | ||
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Revision as of 20:37, 3 May 2008
HIV-1 PROTEASE-INHIBITOR COMPLEX
OverviewOverview
The ability to replace an inhibitor bound to the HIV-1 protease in single crystals with other potent inhibitors offers the possibility of investigating a series of protease inhibitors rapidly and conveniently with the use of X-ray crystallography. This approach affords a fast turnaround of structural information for iterative rational drug designs and obviates the need for studying the complex structures by co-crystallization. The replacement approach has been successfully used with single crystals of the HIV-1 protease complexed with a weak inhibitor. The structures of the complexes obtained by the replacement method are similar to those determined by co-crystallization.
About this StructureAbout this Structure
2BPY is a Single protein structure of sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
ReferenceReference
Rapid X-ray diffraction analysis of HIV-1 protease-inhibitor complexes: inhibitor exchange in single crystals of the bound enzyme., Munshi S, Chen Z, Li Y, Olsen DB, Fraley ME, Hungate RW, Kuo LC, Acta Crystallogr D Biol Crystallogr. 1998 Sep 1;54(Pt 5):1053-60. PMID:9757136 Page seeded by OCA on Sat May 3 20:37:54 2008