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Protein Sci. 1994 Jun;3(6):866-75. doi: 10.1002/pro.5560030601.
2
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Structural alignment of globins, phycocyanins and colicin A.球蛋白、藻蓝蛋白和大肠杆菌素A的结构比对。
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Families and the structural relatedness among globular proteins.家族与球状蛋白质之间的结构相关性。
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Relation between structure and function of alpha/beta-proteins.α/β 蛋白的结构与功能之间的关系。
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Molecular structure of the bilin binding protein (BBP) from Pieris brassicae after refinement at 2.0 A resolution.在2.0埃分辨率下精修后的粉纹夜蛾胆色素结合蛋白(BBP)的分子结构。
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非同源蛋白质中局部空间相似性的生物学意义、统计学显著性及分类

Biological meaning, statistical significance, and classification of local spatial similarities in nonhomologous proteins.

作者信息

Alexandrov N N, Go N

机构信息

Protein Engineering Research Institute, Osaka, Japan.

出版信息

Protein Sci. 1994 Jun;3(6):866-75. doi: 10.1002/pro.5560030601.

DOI:10.1002/pro.5560030601
PMID:8069217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2142880/
Abstract

We have completed an exhaustive search for the common spatial arrangements of backbone fragments (SARFs) in nonhomologous proteins. This type of local structural similarity, incorporating short fragments of backbone atoms, arranged not necessarily in the same order along the polypeptide chain, appears to be important for protein function and stability. To estimate the statistical significance of the similarities, we have introduced a similarity score. We present several locally similar structures, with a large similarity score, which have not yet been reported. On the basis of the results of pairwise comparison, we have performed hierarchical cluster analysis of protein structures. Our analysis is not limited by comparison of single chains but also includes complex molecules consisting of several subunits. The SARFs with backbone fragments from different polypeptide chains provide a stable interaction between subunits in protein molecules. In many cases the active site of enzyme is located at the same position relative to the common SARFs, implying a function of the certain SARFs as a universal interface of the protein-substrate interaction.

摘要

我们已经对非同源蛋白质中主链片段(SARFs)的常见空间排列进行了详尽的搜索。这种局部结构相似性,包含主链原子的短片段,它们在多肽链上的排列顺序不一定相同,似乎对蛋白质的功能和稳定性很重要。为了估计这些相似性的统计显著性,我们引入了一个相似性得分。我们展示了几个具有高相似性得分的局部相似结构,这些结构尚未见报道。基于成对比较的结果,我们对蛋白质结构进行了层次聚类分析。我们的分析不仅限于单链比较,还包括由多个亚基组成的复杂分子。来自不同多肽链的带有主链片段的SARFs在蛋白质分子的亚基之间提供了稳定的相互作用。在许多情况下,酶的活性位点相对于常见的SARFs位于相同位置,这意味着某些SARFs作为蛋白质 - 底物相互作用的通用界面发挥作用。