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单点突变对疏水-极性晶格蛋白的影响。

Effect of single-site mutations on hydrophobic-polar lattice proteins.

作者信息

Shi Guangjie, Vogel Thomas, Wüst Thomas, Li Ying Wai, Landau David P

机构信息

Center for Simulational Physics, The University of Georgia, Athens, Georgia 30602, USA.

Theoretical Division (T-1), Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2014 Sep;90(3):033307. doi: 10.1103/PhysRevE.90.033307. Epub 2014 Sep 15.

Abstract

We developed a heuristic method for determining the ground-state degeneracy of hydrophobic-polar (HP) lattice proteins, based on Wang-Landau and multicanonical sampling. It is applied during comprehensive studies of single-site mutations in specific HP proteins with different sequences. The effects in which we are interested include structural changes in ground states, changes of ground-state energy, degeneracy, and thermodynamic properties of the system. With respect to mutations, both extremely sensitive and insensitive positions in the HP sequence have been found. That is, ground-state energies and degeneracies, as well as other thermodynamic and structural quantities, may be either largely unaffected or may change significantly due to mutation.

摘要

我们基于王-朗道算法和多正则采样,开发了一种用于确定疏水-极性(HP)晶格蛋白质基态简并度的启发式方法。该方法应用于对具有不同序列的特定HP蛋白质单点突变的全面研究中。我们感兴趣的效应包括基态的结构变化、基态能量的变化、简并度以及系统的热力学性质。关于突变,在HP序列中发现了极其敏感和不敏感的位置。也就是说,基态能量和简并度,以及其他热力学和结构量,可能基本不受影响,也可能因突变而发生显著变化。

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