蛋白质工程
离子通道
结构生物学
计算机科学
化学
生物系统
材料科学
生物物理学
纳米技术
生物
生物化学
受体
酶
作者
Jan Brezovský,Barbora Kozlíková,Jiřı́ Damborský
标识
DOI:10.1007/978-1-4939-7366-8_3
摘要
Protein tunnels connecting the functional buried cavities with bulk solvent and protein channels, enabling the transport through biological membranes, represent the structural features that govern the exchange rates of ligands, ions, and water solvent. Tunnels and channels are present in a vast number of known proteins and provide control over their function. Modification of these structural features by protein engineering frequently provides proteins with improved properties. Here we present a detailed computational protocol employing the CAVER software that is applicable for: (1) the analysis of tunnels and channels in protein structures, and (2) the selection of hot-spot residues in tunnels or channels that can be mutagenized for improved activity, specificity, enantioselectivity, or stability.
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