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Conservation of structural fluctuations in homologous protein kinases and its implications on functional sites.同源蛋白激酶中结构波动的保守性及其对功能位点的影响。
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T test as a parametric statistic.T检验作为一种参数统计方法。
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ff14SB: Improving the Accuracy of Protein Side Chain and Backbone Parameters from ff99SB.ff14SB:提高源自ff99SB的蛋白质侧链和主链参数的准确性。
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Quantifying the stabilizing effects of protein-ligand interactions in the gas phase.量化气相中蛋白质-配体相互作用的稳定作用。
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6
A Gaussian network model study suggests that structural fluctuations are higher for inactive states than active states of protein kinases.一项高斯网络模型研究表明,蛋白激酶的非活性状态比活性状态具有更高的结构波动。
Mol Biosyst. 2015 Apr;11(4):1079-95. doi: 10.1039/c4mb00675e.
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Catalytic mechanisms and regulation of protein kinases.蛋白激酶的催化机制与调控
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Dynamic architecture of a protein kinase.一种蛋白激酶的动态结构
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Rational Design of Particle Mesh Ewald Compatible Lennard-Jones Parameters for +2 Metal Cations in Explicit Solvent.显式溶剂中 +2 金属阳离子的粒子网格埃瓦尔德兼容 Lennard-Jones 参数的合理设计。
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长程分子动力学表明,蛋白激酶 A 的非活性形式比活性形式更具动态性。

Long-range molecular dynamics show that inactive forms of Protein Kinase A are more dynamic than active forms.

机构信息

Molecular Biophysics Unit, Indian Institute of Science, Bangalore, 560012, India.

INSERM, U 1134, DSIMB, F-75739, Paris, France.

出版信息

Protein Sci. 2019 Mar;28(3):543-560. doi: 10.1002/pro.3556. Epub 2018 Dec 30.

DOI:10.1002/pro.3556
PMID:30468265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6371217/
Abstract

Many protein kinases are characterized by at least two structural forms corresponding to the highest level of activity (active) and low or no activity, (inactive). Further, protein dynamics is an important consideration in understanding the molecular and mechanistic basis of enzyme function. In this work, we use protein kinase A (PKA) as the model system and perform microsecond range molecular dynamics (MD) simulations on six variants which differ from one another in terms of active and inactive form, with or without bound ligands, C-terminal tail and phosphorylation at the activation loop. We find that the root mean square fluctuations in the MD simulations are generally higher for the inactive forms than the active forms. This difference is statistically significant. The higher dynamics of inactive states has significant contributions from ATP binding loop, catalytic loop, and αG helix. Simulations with and without C-terminal tail show this differential dynamics as well, with lower dynamics both in the active and inactive forms if C-terminal tail is present. Similarly, the dynamics associated with the inactive form is higher irrespective of the phosphorylation status of Thr 197. A relatively stable stature of active kinases may be better suited for binding of substrates and detachment of the product. Also, phosphoryl group transfer from ATP to the phosphosite on the substrate requires precise transient coordination of chemical entities from three different molecules, which may be facilitated by the higher stability of the active state.

摘要

许多蛋白激酶的结构至少有两种形式,分别对应于最高活性(活性)和低活性或无活性(非活性)。此外,蛋白质动力学是理解酶功能的分子和机制基础的重要考虑因素。在这项工作中,我们使用蛋白激酶 A(PKA)作为模型系统,并对六种变体进行了微秒范围内的分子动力学(MD)模拟,这些变体在活性和非活性形式、有无结合配体、C 末端尾部和激活环磷酸化方面彼此不同。我们发现,MD 模拟中的均方根波动通常对于非活性形式高于活性形式。这种差异具有统计学意义。非活性状态的高动力学主要来自于 ATP 结合环、催化环和αG 螺旋。有和没有 C 末端尾部的模拟也显示了这种差异动力学,并且如果存在 C 末端尾部,则活性和非活性形式的动力学都较低。同样,与 Thr197 的磷酸化状态无关,非活性形式的动力学更高。活性激酶的相对稳定状态可能更适合于与底物结合和产物释放。此外,从 ATP 向底物上的磷酸化位点转移磷酸基团需要来自三个不同分子的化学实体的精确瞬时协调,这可能通过活性状态的更高稳定性来促进。