Co-evolutionary constraints of globular proteins correlate with their folding rates

被引:8
|
作者
Mallik, Saurav
Kundu, Sudip
机构
[1] Univ Calcutta, Dept Biophys Mol Biol & Bioinformat, Kolkata 700009, India
[2] Univ Calcutta, Ctr Excellence Syst Biol & Biomed Engn, TEQIP Phase 2, Kolkata 700009, India
关键词
Protein folding; Co-evolution; Relative co-evolution order; Contact order; TRANSITION-STATE; MUTUAL INFORMATION; CONTACT ORDER; MECHANISMS; PREDICTION; SEARCH; COEVOLUTION; RESIDUES; SUBUNIT;
D O I
10.1016/j.febslet.2015.06.032
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
Folding rates (lnk(f)) of globular proteins correlate with their biophysical properties, but relationship between lnk(f) and patterns of sequence evolution remains elusive. We introduce 'relative co-evolution order' (rCEO) as length-normalized average primary chain separation of co-evolving pairs (CEPs), which negatively correlates with lnk(f). In addition to pairs in native 3D contact, indirectly connected and structurally remote CEPs probably also play critical roles in protein folding. Correlation between rCEO and lnk(f) is stronger in multi-state proteins than two-state proteins, contrasting the case of contact order (co), where stronger correlation is found in two-state proteins. Finally, rCEO, co and lnk(f) are fitted into a 3D linear correlation. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2179 / 2185
页数:7
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