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蛋白质内部堆积中粗粒度规则性的起源与范围。

The origin and extent of coarse-grained regularities in protein internal packing.

作者信息

Bagci Zerrin, Kloczkowski Andrzej, Jernigan Robert L, Bahar Ivet

机构信息

Center for Computational Biology & Bioinformatics, and Department of Molecular Genetics & Biochemistry, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.

出版信息

Proteins. 2003 Oct 1;53(1):56-67. doi: 10.1002/prot.10435.

Abstract

Despite the suitability of various lattice geometries for coarse-grained modeling of proteins, the actual packing geometry of residues in folded structures has remained largely unexplored. A strong tendency to assume a regular packing geometry is shown here by optimally reorienting and superimposing clusters of neighboring residues from databank structures examined on a coarse-grained (single-site-per-residue) scale. The orientation function (or order parameter) of the examined coordination clusters with respect to fcc lattice directions is found to be 0.82. The observed geometry, which may be termed an incomplete distorted face-centered cubic (fcc) packing, is apparently favored by the drive to maximize packing density, in a fashion analogous to the way identical spheres pack densely and follow fcc geometry. About 2/3 of all residues obey this packing geometry, while the remainder occupy other context-dependent positions. The preferred coordination directions show relatively small variations over the various amino acid types, consistent with uniform residue viewpoint. Both the extremes of solvent-exposed and completely buried residue neighborhoods approximate the same generic packing, the only difference being in the numbers (and not the orientations) of coordination sites that are occupied (or left void for solvent occupancy). We observe the prevalence of a rather uniform (tight) residue packing density throughout the structure, including even the residues packed near solvent-exposed regions. The observed orientation distribution reveals an underlying, intrinsic orientation lattice for proteins.

摘要

尽管各种晶格几何结构适用于蛋白质的粗粒度建模,但折叠结构中残基的实际堆积几何结构在很大程度上仍未得到探索。通过在粗粒度(每个残基一个位点)尺度上对数据库结构中相邻残基簇进行最佳重新定向和叠加,显示出一种强烈的假设规则堆积几何结构的趋势。所研究的配位簇相对于面心立方晶格方向的取向函数(或序参量)为0.82。观察到的几何结构,可称为不完全扭曲的面心立方(fcc)堆积,显然受到最大化堆积密度驱动力的青睐,其方式类似于相同球体紧密堆积并遵循fcc几何结构的方式。大约2/3的所有残基遵循这种堆积几何结构,而其余残基占据其他依赖于上下文的位置。首选的配位方向在各种氨基酸类型上显示出相对较小的变化,这与残基观点一致。溶剂暴露和完全埋藏的残基邻域的极端情况都近似相同的通用堆积,唯一的区别在于被占据(或留作溶剂占据的空位)的配位点数量(而非取向)。我们观察到在整个结构中存在相当均匀(紧密)的残基堆积密度,甚至包括靠近溶剂暴露区域堆积的残基。观察到的取向分布揭示了蛋白质潜在的、内在的取向晶格。

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