Active‐site mobility in human immunodeficiency virus, type 1, protease as demonstrated by crystal structure of A28S mutant von Hong, Lin, Hartsuck, Jean A., Foundling, Steve, Ermoliefe, Jacques, Tang, Jordan

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Crystal Structures of Complexes of a Peptidic Inhibitor with Wild-Type and Two Mutant HIV-1 Proteases von Hong, Lin, Treharne, Annemarie, Hartsuck, Jean Ann, Foundling, Steve, Tang, Jordan

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Effect of Point Mutations on the Kinetics and the Inhibition of Human Immunodeficiency Virus Type 1 Protease: Relationship to Drug Resistance von Lin, Yingzhang, Lin, Xinli, Hong, Lin, Foundling, Steve, Heinrikson, Robert L, Thaisrivongs, Suvit, Leelamanit, Wichet, Raterman, Dan, Shah, Manish

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Stability and Activity of Human Immunodeficiency Virus Protease: Comparison of the Natural Dimer with a Homologous, Single-Chain Tethered Dimer von Cheng, Yih-Shyun E., Yin, Fay H., Foundling, Steve, Blomstrom, Dale, Kettner, Charles A.

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Structure of a G48H mutant of HIV-1 protease explains how glycine-48 replacements produce mutants resistant to inhibitor drugs von Hong, Lin, Zhang, Xue-Jun, Foundling, Steve, Hartsuck, Jean Ann, Tang, Jordan

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Recombinant canditropsin, an extracellular aspartic protease from yeast Candida tropicalis. Escherichia coli expression, purification, zymogen activation, and enzymic properties von Lin, X, Tang, J, Koelsch, G, Monod, M, Foundling, S

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Structure of a G48H mutant of HIV‐1 protease explains how glycine‐48 replacements produce mutants resistant to inhibitor drugs 1 von Hong, Lin, Zhang, Xue-Jun, Foundling, Steve, Hartsuck, Jean Ann, Tang, Jordan

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The structure of a synthetic pepsin inhibitor complexed with endothiapepsin von COOPER, Jon, FOUNDLING, Steve, HEMMINGS, Andrew, BLUNDELL, Tom, JONES, D. Michael, HALLETT, Allan, SZELKE, Michael

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