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蛋白质天然状态结构中的氨基酸特性。

Amino-Acid Characteristics in Protein Native State Structures.

机构信息

Department of Molecular Sciences and Nanosystems, Ca' Foscari University of Venice, Campus Scientifico, Via Torino 155, 30170 Venice Mestre, Italy.

Department of Physics and Institute for Fundamental Science, University of Oregon, Eugene, OR 97403, USA.

出版信息

Biomolecules. 2024 Jul 7;14(7):805. doi: 10.3390/biom14070805.

Abstract

The molecular machines of life, proteins, are made up of twenty kinds of amino acids, each with distinctive side chains. We present a geometrical analysis of the protrusion statistics of side chains in more than 4000 high-resolution protein structures. We employ a coarse-grained representation of the protein backbone viewed as a linear chain of C atoms and consider just the heavy atoms of the side chains. We study the large variety of behaviors of the amino acids based on both rudimentary structural chemistry as well as geometry. Our geometrical analysis uses a backbone Frenet coordinate system for the common study of all amino acids. Our analysis underscores the richness of the repertoire of amino acids that is available to nature to design protein sequences that fit within the putative native state folds.

摘要

生命的分子机器,蛋白质,由二十种氨基酸组成,每种氨基酸都有独特的侧链。我们对 4000 多个高分辨率蛋白质结构中侧链的突出统计进行了几何分析。我们采用了一种粗粒度的蛋白质骨架表示方法,将其视为一条线性的 C 原子链,并仅考虑侧链的重原子。我们基于基本的结构化学和几何形状研究了氨基酸的各种行为。我们的几何分析使用了一个骨架 Frenet 坐标系,以便对所有氨基酸进行共同研究。我们的分析强调了氨基酸的丰富性,这些氨基酸可以被自然界用来设计适合假定天然状态折叠的蛋白质序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d476/11274641/8ec63b488689/biomolecules-14-00805-g003.jpg

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