tailieunhanh - Báo cáo y học: " Flexible catalytic site conformations implicated in modulation of HIV-1 protease autoprocessing reactions"

Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Respiratory Research cung cấp cho các bạn kiến thức về ngành y đề tài: Flexible catalytic site conformations implicated in modulation of HIV-1 protease autoprocessing reactions. | Retrovirology BioMed Central Vz The Open Access Publisher This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text HTML versions will be made available soon. Flexible catalytic site conformations implicated in modulation of HIV-1 protease autoprocessing reactions Retrovirology 2011 8 79 doi 1742-4690-8-79 Liangqun Huang Yanfei Li Chaoping Chen chaoping@ ISSN 1742-4690 Article type Research Submission date 27 April 2011 Acceptance date 10 October 2011 Publication date 10 October 2011 Article URL http content 8 1 79 This peer-reviewed article was published immediately upon acceptance. It can be downloaded printed and distributed freely for any purposes see copyright notice below . Articles in Retrovirology are listed in PubMed and archived at PubMed Central. For information about publishing your research in Retrovirology or any BioMed Central journal go to http authors instructions For information about other BioMed Central publications go to http 2011 Huang etal. licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Flexible catalytic site conformations implicated in modulation of HIV-1 protease autoprocessing reactions Liangqun Huang Y anfei Li Chaoping Chen Department of Biochemistry and Molecular Biology Colorado State University Fort Collins Colorado 80523-1870 USA Corresponding author Email addresses LH YL CC Chaoping@ 1 Abstract Background The HIV-1 protease is initially synthesized as part of the Gag-Pol polyprotein in the infected cell. Protease autoprocessing .