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首页> 外文期刊>Journal of Molecular Biology >Protein-Protein Interactions: Hot Spots and Structurally Conserved Residues often Locate in Complemented Pockets that Pre-organized in the Unbound States: Implications for Docking.
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Protein-Protein Interactions: Hot Spots and Structurally Conserved Residues often Locate in Complemented Pockets that Pre-organized in the Unbound States: Implications for Docking.

机译:蛋白质-蛋白质相互作用:热点和结构保守的残基通常位于未结合状态下预组织的互补口袋中:对接的影响。

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摘要

Energetic hot spots account for a significant portion of the total binding free energy and correlate with structurally conserved interface residues. Here, we map experimentally determined hot spots and structurally conserved residues to investigate their geometrical organization. Unfilled pockets are pockets that remain unfilled after protein-protein complexation, while complemented pockets are pockets that disappear upon binding, representing tightly fit regions. We find that structurally conserved residues and energetic hot spots are strongly favored to be located in complemented pockets, and are disfavored in unfilled pockets. For the three available protein-protein complexes with complemented pockets where both members of the complex were alanine-scanned, 62% of all hot spots (DeltaDeltaG>2kcal/mol) are within these pockets, and 60% of the residues in the complemented pockets are hot spots. 93% of all red-hot residues (DeltaDeltaG>/=4kcal/mol) either protrude into or are located in complemented pockets. The occurrence of hot spots and conserved residues in complemented pockets highlights the role of local tight packing in protein associations, and rationalizes their energetic contribution and conservation. Complemented pockets and their corresponding protruding residues emerge among the most important geometric features in protein-protein interactions. By screening the solvent, this organization shields backbone hydrogen bonds and charge-charge interactions. Complemented pockets often pre-exist binding. For 18 protein-protein complexes with complemented pockets whose unbound structures are available, in 16 the pockets are identified to pre-exist in the unbound structures. The root-mean-squared deviations of the atoms lining the pockets between the bound and unbound states is as small as 0.9A, suggesting that such pockets constitute features of the populated native state that may be used in docking.
机译:高能热点占总结合自由能的很大一部分,并且与结构保守的界面残基相关。在这里,我们绘制了实验确定的热点和结构保守的残基,以调查其几何结构。未填充的口袋是蛋白质-蛋白质复合后仍未填充的口袋,而互补的口袋是在结合后消失的口袋,表示紧密贴合的区域。我们发现,结构上保守的残基和高能热点被强烈推荐位于互补袋中,而在未填充的袋中则不受欢迎。对于三种具有互补口袋的可用蛋白质-蛋白质复合物,其中复合物的两个成员均进行了丙氨酸扫描,所有热点中的62%(DeltaDeltaG> 2kcal / mol)位于这些口袋中,而60%的残留物位于互补口袋中是热点。所有炽热残渣中的93%(DeltaDeltaG> / = 4kcal / mol)伸入或位于互补袋中。互补口袋中热点和保守残基的出现凸显了局部紧密堆积在蛋白质缔合中的作用,并使它们的能量贡献和保存合理化。互补的口袋及其相应的突出残基出现在蛋白质-蛋白质相互作用的最重要的几何特征中。通过筛选溶剂,该组织可屏蔽主链氢键和电荷-电荷相互作用。互补的口袋通常预先存在约束力。对于18个具有互补袋的未结合结构可用的蛋白质-蛋白质复合物,在16个袋中被鉴定为预先存在于未结合结构中。排列在绑定状态和未绑定状态之间的口袋中的原子的均方根偏差小至0.9A,这表明此类口袋构成了可用于对接的填充原始状态的特征。

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