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Crystal structures of complexes of a peptidic inhibitor with wild-type and two mutant HIV-1 proteases.
Hong L, Treharne A, Hartsuck JA, Foundling S, Tang J. Hong L, et al. Biochemistry. 1996 Aug 20;35(33):10627-33. doi: 10.1021/bi960481s. Biochemistry. 1996. PMID: 8718851
Comparison of the three crystal structures provides explanations which are consistent with the known kinetic properties of these mutant enzymes with the U-89360E inhibitor [Lin, Y., Lin, X., Hong, L., Foundling, S., Heinrikson, R. L., Thaisrivongs, S., Leelam …
Comparison of the three crystal structures provides explanations which are consistent with the known kinetic properties of these mutant enzy …
Active-site mobility in human immunodeficiency virus, type 1, protease as demonstrated by crystal structure of A28S mutant.
Hong L, Hartsuck JA, Foundling S, Ermolieff J, Tang J. Hong L, et al. Protein Sci. 1998 Feb;7(2):300-5. doi: 10.1002/pro.5560070209. Protein Sci. 1998. PMID: 9521105 Free PMC article.
Comparison of the mutant enzyme structure with that of the wild-type HIV-1 protease bound to the same inhibitor (Hong L, Treharne A, Hartsuck JA, Foundling S, Tang J, 1996, Biochemistry 35:10627-10633) revealed double occupancy for the Ser28 hydroxyl group, which fo …
Comparison of the mutant enzyme structure with that of the wild-type HIV-1 protease bound to the same inhibitor (Hong L, Treha …
Memapsin 2 (beta-secretase) as a therapeutic target.
Hong L, Turner RT 3rd, Koelsch G, Ghosh AK, Tang J. Hong L, et al. Biochem Soc Trans. 2002 Aug;30(4):530-4. doi: 10.1042/bst0300530. Biochem Soc Trans. 2002. PMID: 12196130 Review.
3,879 results