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Effect of Flap Mutations on Structure of HIV-1 Protease and Inhibition by Saquinavir and Darunavir

HIV-1 protease (PR) and its mutants are important antiviral drug targets. The PR flap region is critical for binding substrates or inhibitors and catalytic activity. Hence, mutations of flap residues frequently contribute to reduced susceptibility to PR inhibitors in drug resistant HIV. Structural a...

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Detalhes bibliográficos
Main Authors: Liu, Fengling, Kovalevsky, Andrey Y., Tie, Yunfeng, Ghosh, Arun K, Harrison, Robert W., Weber, Irene T.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2754059/
https://ncbi.nlm.nih.gov/pubmed/18597780
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jmb.2008.05.062
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