首页> 外文期刊>Bioinformatics >The ruggedness of protein-protein energy landscape and the cutoff for 1/r(n) potentials
【24h】

The ruggedness of protein-protein energy landscape and the cutoff for 1/r(n) potentials

机译:蛋白质-蛋白质能量格局的坚固性和1 / r(n)电位的截止

获取原文
获取原文并翻译 | 示例
           

摘要

MOTIVATION: Computational studies of the energetics of protein association are important for revealing the underlying fundamental principles and for designing better tools to model protein complexes. The interaction cutoff contribution to the ruggedness of protein-protein energy landscape is studied in terms of relative energy fluctuations for 1/r(n) potentials based on a simplistic model of a protein complex. This artificial ruggedness exists for short cutoffs and gradually disappears with the cutoff increase. RESULTS: The critical values of the cutoff were calculated for each of 11 popular power-type potentials with n=0/9, 12 and for two thresholds of 5% and 10%. The artificial ruggedness decreases to tolerable thresholds for cutoffs larger than the critical ones. The results showed that for both thresholds the critical cutoff is a non-monotonic function of the potential power n. The functions reach the maximum at n=3/4 and then decrease with the increase of the potential power. The difference between two cutoffs for 5% and 10% artificial ruggedness becomes negligible for potentials decreasing faster than 1/r(12). The analytical results obtained for the simple model of protein complexes agree with the analysis of artificial ruggedness in a dataset of 62 protein-protein complexes, with different parameterizations of soft Lennard-Jones potential and two types of protein representations: all-atom and coarse-grained. The results suggest that cutoffs larger than the critical ones can be recommended for protein-protein potentials.
机译:动机:蛋白质缔合能量学的计算研究对于揭示基本原理和设计更好的工具来模拟蛋白质复合物很重要。基于蛋白质复合物的简化模型,根据1 / r(n)电位的相对能量波动,研究了相互作用截止对蛋白质-蛋白质能量格局的坚固性的贡献。这种人为的坚固性存在于短的截止点,并且随着截止点的增加而逐渐消失。结果:分别计算了11个n = 0 / 9、12的流行功率型电势的临界值,以及两个阈值5%和10%的临界值。对于比临界值大的临界值,人为的坚固性会降低到可容忍的阈值。结果表明,对于两个阈值,临界截止值都是势能n的非单调函数。函数在n = 3/4处达到最大值,然后随着势能的增加而减小。对于5%和10%的人工粗糙度,两个截止之间的差异对于电势下降速度快于1 / r的影响可以忽略不计(12)。简单蛋白质复合物模型获得的分析结果与62种蛋白质-蛋白质复合物数据集中的人工坚固性分析相符,具有软Lennard-Jones势的不同参数化和两种蛋白质表示形式:全原子和粗粒状的。结果表明,对于蛋白质-蛋白质潜力,建议使用大于临界值的临界值。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号