The variation among sites of protein structure divergence is shaped by mutation and scaled by selection

Curr Res Struct Biol. 2020 Aug 26:2:156-163. doi: 10.1016/j.crstbi.2020.08.002. eCollection 2020.

Abstract

Protein structures do not evolve uniformly, but the degree of structure divergence varies among sites. The resulting site-dependent structure divergence patterns emerge from a process that involves mutation and selection, which may both, in principle, influence the emergent pattern. In contrast with sequence divergence patterns, which are known to be mainly determined by selection, the relative contributions of mutation and selection to structure divergence patterns is unclear. Here, studying 6 protein families with a mechanistic biophysical model of protein evolution, we untangle the effects of mutation and selection. We found that even in the absence of selection, structure divergence varies from site to site because the mutational sensitivity is not uniform. Selection scales the profile, increasing its amplitude, without changing its shape. This scaling effect follows from the similarity between mutational sensitivity and sequence variability profiles.

Keywords: Biophysical model; Mutation; Protein evolution; Selection; Sequence divergence; Structure divergence.