饱和突变
化学
蛋白质工程
基质(水族馆)
活动站点
裂解酶
立体化学
催化循环
酶
过渡状态
结合位点
催化作用
过渡态模拟
突变
蛋白质结构
构象异构
变构调节
构象变化
酶催化
血浆蛋白结合
蛋白质设计
劈理(地质)
组合化学
底物特异性
分子动力学
功能(生物学)
生物物理学
衬底模拟
酶动力学
合理设计
生物催化
作者
Yu‐Cong Zheng,Yong Mao,Qiang Geng,Fulong Li,Xu‐Dong Kong,Yizhou Qi,Lin Zhang,Qi Chen,Zhi‐Jun Zhang,Rong Ran,Yi‐Lei Zhao,Hui‐Lei Yu,Jian‐He Xu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-24
卷期号:64 (52): e202515778-e202515778
被引量:1
标识
DOI:10.1002/anie.202515778
摘要
, that destabilizes the non-productive substrate binding state thereby facilitating its transition to the catalytically productive conformation and significantly enhancing catalytic efficiency. Crystallographic studies provide a structural description of the factors that stabilize versus destabilize the different binding conformers in the different enzyme variants and thus the differing catalytic efficiencies. These findings demonstrate that destabilizing unfavorable substrate binding conformations within an enzyme active site can improve functionality and provide a promising strategy for designing efficient biocatalysts.
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