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Non-canonical H-bonds in β-lactamases: Importance of C-H···π interactions

机译:β-内酰胺酶中的非规范H键:C-H··π相互作用的重要性

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摘要

β-Lactamase production is the common mechanism of resistance of β-lactam antibiotics. Knowledge of inter-residue interactions in protein structures increases our understanding of protein structure and stability. We have systematically analysed the contribution of C-H···π interactions to the stability of β-lactamases. Most of the interactions are long range and most of the interacting residues are evolutionarily conserved. The occurrence of C-H···π interactions in active sites and metal binding sites is very low in β-lactamases. Hence, C-H···π interactions are important determinants of stability in β-lactamases and they may not play a significant role in specificity. The results from this study provide valuable insights for understanding the stability patterns of β-lactamases and their relation to various other environmental preferences.
机译:β-内酰胺酶的产生是β-内酰胺类抗生素耐药的常见机制。蛋白质结构中残基间相互作用的知识增加了我们对蛋白质结构和稳定性的了解。我们已经系统地分析了C-H··π相互作用对β-内酰胺酶稳定性的影响。大多数相互作用是长距离的,大多数相互作用残基在进化上是保守的。在β-内酰胺酶中,活性位点和金属结合位点的C-H···π相互作用的发生率非常低。因此,C-H···π相互作用是β-内酰胺酶稳定性的重要决定因素,它们在特异性中可能没有重要作用。这项研究的结果为了解β-内酰胺酶的稳定性模式及其与其他各种环境偏好的关系提供了宝贵的见解。

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