机译:疏水核心柔韧性调节HIV-1蛋白酶中的酶活性。
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, United States;
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, United States;
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, United States;
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, United States;
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, United States;
机译:HIV-1蛋白酶中Asp催化二元构象的柔性:从头开始研究游离酶。
机译:对结构多样的HIV-1蛋白酶抑制剂的定量构效关系研究:构象柔韧性对抑制活性的贡献。
机译:膜转化HIV-1糖蛋白GP41环形区域的结构和功能性通过其固有疏水芯来调节
机译:HIV-1蛋白酶结合机制的粗粒模型:I.靶向蛋白酶襟翼的结构柔韧性和对药物设计的影响
机译:新型HIV-1蛋白酶抑制剂的核心结构中间体的设计与合成,新型20S蛋白酶体抑制剂的合成,生物学活性和分子建模。
机译:疏水核灵活性调制在HIV-1蛋白酶的酶活性
机译:疏水核心灵活性调节HIV-1蛋白酶中的酶活性