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首页> 外文期刊>The Journal of Chemical Physics >CALCULATION OF NUCLEAR MAGNETIC RESONANCE ORDER PARAMETERS IN PROTEINS BY NORMAL MODE ANALYSIS .2. CONTRIBUTION FROM LOCALIZED HIGH FREQUENCY MOTIONS
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CALCULATION OF NUCLEAR MAGNETIC RESONANCE ORDER PARAMETERS IN PROTEINS BY NORMAL MODE ANALYSIS .2. CONTRIBUTION FROM LOCALIZED HIGH FREQUENCY MOTIONS

机译:用正常模式分析计算蛋白质中核磁共振级参数2。局部高频运动的贡献

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摘要

Nuclear magnetic resonance (NMR) order parameter (S) over tilde(2) for spin pairs in protein is an important quantity for deducing protein static and dynamic three-dimensional structures from NMR experimental data. In the previous paper it has been shown that contribution from low frequency motions to the order parameter can be calculated reliably from normal mode analysis carried out in dihedral angle space for spin pairs for which a number of intervening dihedral angles (NIVDA) is 10 or less. However, it has been known that for spin pairs with NIVDA=0, high frequency motions also affect the value of the order parameter. In this paper we show that the effect of high frequency motions can be accounted for by a correction term to be added to the value obtained from normal mode analysis in dihedral angle space. A factor of the correction term determined by high frequency motions can be calculated by the usual normal mode analysis for a small peptide fragment which has the same local conformation as in protein. (C) 1996 American Institute of Physics. [References: 12]
机译:蛋白质中自旋对在波浪号(2)上的核磁共振(NMR)顺序参数(S)是从NMR实验数据推导蛋白质静态和动态三维结构的重要量。在先前的论文中,已经表明,对于中间对二面角(NIVDA)小于等于10的自旋对,可以通过在二面角空间中进行的正态分析可靠地计算出低频运动对阶次参数的贡献。但是,已知对于NIVDA = 0的自旋对,高频运动也会影响阶数参数的值。在本文中,我们证明了高频运动的影响可以由一个校正项来解释,该校正项要添加到二面角空间中从正常模式分析获得的值中。由高频运动确定的校正项的因子可以通过通常的正常模式分析来计算,该小肽片段具有与蛋白质相同的局部构象。 (C)1996年美国物理研究所。 [参考:12]

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