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利用假酶探究酶的进化设计原理。

Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes.

作者信息

Sharir-Ivry Avital, Xia Yu

机构信息

Department of Bioengineering, McGill University, Montreal, QC, Canada.

出版信息

Evol Bioinform Online. 2019 Jun 13;15:1176934319855937. doi: 10.1177/1176934319855937. eCollection 2019.

Abstract

Enzymes are governed by unique evolutionary design principles as their catalytic sites were shown to induce long-range evolutionary conservation gradients. We have recently used a comparative bioinformatics approach to disentangle structural determinants from other possible determinants of the evolutionary conservation gradients. The approach is based on comparing the evolutionary patterns of enzymes to those of pseudoenzymes with the same tertiary structure where the catalytic functionality is turned off. This approach provides a way to evaluate several hypotheses regarding the origin of the observed evolutionary conservation gradient in enzymes. The conclusions from such comparative analyses are important for a better understanding of the unique evolutionary design principles of enzymes, which can in turn potentially guide the design of new and improved enzymes.

摘要

酶受独特的进化设计原则支配,因为它们的催化位点显示出诱导远距离进化保守梯度。我们最近使用了一种比较生物信息学方法,将结构决定因素与进化保守梯度的其他可能决定因素区分开来。该方法基于将酶的进化模式与具有相同三级结构但催化功能关闭的假酶的进化模式进行比较。这种方法提供了一种评估关于酶中观察到的进化保守梯度起源的几种假设的方法。此类比较分析得出的结论对于更好地理解酶的独特进化设计原则很重要,这反过来又可能指导新型和改良酶的设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/023e/6572901/91935de8b230/10.1177_1176934319855937-fig1.jpg

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