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LPFC:蛋白质家族核心结构的互联网文库。

LPFC: an Internet library of protein family core structures.

作者信息

Schmidt R, Gerstein M, Altman R B

机构信息

Section on Medical Informatics, Stanford University, California 94305-5479, USA.

出版信息

Protein Sci. 1997 Jan;6(1):246-8. doi: 10.1002/pro.5560060127.

Abstract

As the number of protein molecules with known, high-resolution structures increases, it becomes necessary to organize these structures for rapid retrieval, comparison, and analysis. The Protein Data Bank (PDB) currently contains nearly 5,000 entries and is growing exponentially. Most new structures are similar structurally to ones reported previously and can be grouped into families. As the number of members in each family increases, it becomes possible to summarize, statistically, the commonalities and differences within each family. We reported previously a method for finding the atoms in a family alignment that have low spatial variance and those that have higher spatial variance (i.e., the "core" atoms that have the same relative position in all family members and the "non-core" atoms that do not). The core structures we compute have biological significance and provide an excellent quantitative and visual summary of a multiple structural alignment. In order to extend their utility, we have constructed a library of protein family cores, accessible over the World Wide Web at http:/ /www-smi.stanford.edu/projects/helix/LPFC/. This library is generated automatically with publicly available computer programs requiring only a set of multiple alignments as input. It contains quantitative analysis of the spatial variation of atoms within each protein family, the coordinates of the average core structures derived from the families, and display files (in bitmap and VRML formats). Here, we describe the resource and illustrate its applicability by comparing three multiple alignments of the globin family. These three alignments are found to be similar, but with some significant differences related to the diversity of family members and the specific method used for alignment.

摘要

随着已知高分辨率结构的蛋白质分子数量的增加,有必要对这些结构进行组织,以便快速检索、比较和分析。蛋白质数据库(PDB)目前包含近5000个条目,并且正在呈指数增长。大多数新结构在结构上与先前报道的结构相似,可以归为家族。随着每个家族成员数量的增加,从统计学上总结每个家族内部的共性和差异成为可能。我们之前报道了一种方法,用于在家族比对中找到空间方差低的原子和空间方差高的原子(即所有家族成员中相对位置相同的“核心”原子和相对位置不同的“非核心”原子)。我们计算出的核心结构具有生物学意义,并为多重结构比对提供了出色的定量和可视化总结。为了扩展其用途,我们构建了一个蛋白质家族核心库,可通过万维网在http:/ /www-smi.stanford.edu/projects/helix/LPFC/上访问。这个库是使用仅需要一组多重比对作为输入的公开可用计算机程序自动生成的。它包含每个蛋白质家族中原子空间变化的定量分析、从这些家族中推导出来的平均核心结构的坐标以及显示文件(位图和VRML格式)。在这里,我们描述这个资源,并通过比较球蛋白家族的三个多重比对来说明其适用性。发现这三个比对相似,但在与家族成员的多样性以及用于比对的具体方法相关的方面存在一些显著差异。

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