Enhancement of beta-sheet assembly by cooperative hydrogen bonds potential
Author(s) -
Ami LevyMoonshine,
El-ad David Amir,
Chen Keasar
Publication year - 2009
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btp449
Subject(s) - hydrogen bond , beta sheet , beta (programming language) , computer science , term (time) , chemistry , crystallography , algorithm , materials science , protein structure , combinatorics , physics , molecule , mathematics , biochemistry , organic chemistry , quantum mechanics , programming language
The roughness of energy landscapes is a major obstacle to protein structure prediction, since it forces conformational searches to spend much time struggling to escape numerous traps. Specifically, beta-sheet formation is prone to stray, since many possible combinations of hydrogen bonds are dead ends in terms of beta-sheet assembly. It has been shown that cooperative terms for backbone hydrogen bonds ease this problem by augmenting hydrogen bond patterns that are consistent with beta sheets. Here, we present a novel cooperative hydrogen-bond term that is both effective in promoting beta sheets and computationally efficient. In addition, the new term is differentiable and operates on all-atom protein models.
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