Graduate School of Biomedical Sciences, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA.
Biosciences Division, University of California Riverside School of Medicine, Riverside, California, USA.
Protein Sci. 2022 Jul;31(7):e4325. doi: 10.1002/pro.4325.
Proteins sample a multitude of different conformations by undergoing small- and large-scale conformational changes that are often intrinsic to their functions. Information about these changes is often captured in the Protein Data Bank by the apparently redundant deposition of independent structural solutions of identical proteins. Here, we mine these data to examine the conservation of large-scale conformational changes between homologous proteins. This is important for both practical reasons, such as predicting alternative conformations of a protein by comparative modeling, and conceptual reasons, such as understanding the extent of conservation of different features in evolution. To study this question, we introduce a novel approach to compare conformational changes between proteins by the comparison of their difference distance maps (DDMs). We found that proteins undergoing similar conformational changes have similar DDMs and that this similarity could be quantified by the correlation between the DDMs. By comparing the DDMs of homologous protein pairs, we found that large-scale conformational changes show a high level of conservation across a broad range of sequence identities. This shows that conformational space is usually conserved between homologs, even relatively distant ones.
蛋白质通过经历小范围和大范围的构象变化来探索多种不同的构象,这些构象变化通常是其功能的内在特征。这些变化的信息通常通过明显冗余的相同蛋白质的独立结构解决方案的独立沉积在蛋白质数据银行中被捕获。在这里,我们挖掘这些数据,以检查同源蛋白质之间的大范围构象变化的保守性。这对于实践和概念上的原因都很重要,例如通过比较建模预测蛋白质的替代构象,以及理解进化中不同特征的保守程度。为了研究这个问题,我们通过比较它们的差异距离图(DDM)引入了一种比较蛋白质之间构象变化的新方法。我们发现,经历相似构象变化的蛋白质具有相似的 DDM,并且这种相似性可以通过 DDM 之间的相关性来量化。通过比较同源蛋白质对的 DDM,我们发现大范围构象变化在广泛的序列同一性范围内表现出高度的保守性。这表明构象空间在同源物之间通常是保守的,即使是相对较远的同源物也是如此。