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

被引:8
|
作者
Laura Marcos, Maria [1 ]
Echave, Julian [1 ]
机构
[1] Univ Nac Onal San Martin, Escuela Ciencia & Tecnol, Inst Ciencias Fis, Martin Irigoyen 3100, RA-1650 San Martin, Buenos Aires, Argentina
关键词
Protein evolution; Mutation; Selection; Biophysical model; Structure divergence; Sequence divergence; EVOLUTION; SEQUENCE; DYNAMICS; MODELS; CONSTRAINTS; DATABASE; HOMSTRAD; PACKING; RATES;
D O I
10.1016/j.crstbi.2020.08.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:156 / 163
页数:8
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