Halabi Najeeb, Rivoire Olivier, Leibler Stanislas, Ranganathan Rama
Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9050, USA.
Cell. 2009 Aug 21;138(4):774-86. doi: 10.1016/j.cell.2009.07.038.
Proteins display a hierarchy of structural features at primary, secondary, tertiary, and higher-order levels, an organization that guides our current understanding of their biological properties and evolutionary origins. Here, we reveal a structural organization distinct from this traditional hierarchy by statistical analysis of correlated evolution between amino acids. Applied to the S1A serine proteases, the analysis indicates a decomposition of the protein into three quasi-independent groups of correlated amino acids that we term "protein sectors." Each sector is physically connected in the tertiary structure, has a distinct functional role, and constitutes an independent mode of sequence divergence in the protein family. Functionally relevant sectors are evident in other protein families as well, suggesting that they may be general features of proteins. We propose that sectors represent a structural organization of proteins that reflects their evolutionary histories.
蛋白质在一级、二级、三级及更高级别上呈现出结构特征的层次体系,这种组织方式引导着我们目前对其生物学特性和进化起源的理解。在此,我们通过对氨基酸之间的协同进化进行统计分析,揭示了一种与这种传统层次体系不同的结构组织。将该分析应用于S1A丝氨酸蛋白酶时,结果表明蛋白质可分解为三个准独立的氨基酸相关组,我们将其称为“蛋白质扇区”。每个扇区在三级结构中物理相连,具有独特的功能作用,并且构成了蛋白质家族中序列分歧的一种独立模式。功能相关的扇区在其他蛋白质家族中也很明显,这表明它们可能是蛋白质的普遍特征。我们提出,扇区代表了一种反映蛋白质进化历史的结构组织。