共价键
连接器
化学
酶
基质(水族馆)
分子机器
催化作用
底物特异性
活动站点
立体化学
组合化学
生物物理学
生物化学
纳米技术
生物
材料科学
计算机科学
有机化学
生态学
操作系统
标识
DOI:10.1146/annurev.biochem.69.1.961
摘要
▪ Abstract Multistep chemical reactions are increasingly seen as important in a growing number of complex biotransformations. Covalently attached prosthetic groups or swinging arms, and their associated protein domains, are essential to the mechanisms of active-site coupling and substrate channeling in a number of the multifunctional enzyme systems responsible. The protein domains, for which the posttranslational machinery in the cell is highly specific, are crucially important, contributing to the processes of molecular recognition that define and protect the substrates and the catalytic intermediates. The domains have novel folds and move by virtue of conformationally flexible linker regions that tether them to other components of their respective multienzyme complexes. Structural and mechanistic imperatives are becoming apparent as the assembly pathways and the coupling of multistep reactions catalyzed by these dauntingly complex molecular machines are unraveled.
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