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2
30S ribosomal subunits can be assembled in vivo without primary binding ribosomal protein S15.30S核糖体亚基在体内可以在没有核糖体蛋白S15初级结合的情况下进行组装。
RNA. 2006 Jul;12(7):1229-39. doi: 10.1261/rna.2262106. Epub 2006 May 8.
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Comparison of different torsion angle approaches for NMR structure determination.用于核磁共振结构测定的不同扭转角方法的比较。
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Binding of helix-threading peptides to E. coli 16S ribosomal RNA and inhibition of the S15-16S complex.
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Molecular dynamics simulations of the 136 unique tetranucleotide sequences of DNA oligonucleotides. II: sequence context effects on the dynamical structures of the 10 unique dinucleotide steps.DNA寡核苷酸136个独特四核苷酸序列的分子动力学模拟。II:序列环境对10个独特二核苷酸步动态结构的影响。
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Sequence to Structure (S2S): display, manipulate and interconnect RNA data from sequence to structure.序列到结构(S2S):展示、操作并连接从序列到结构的RNA数据。
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RECOORD: a recalculated coordinate database of 500+ proteins from the PDB using restraints from the BioMagResBank.RECOORD:一个使用来自生物磁共振数据库(BioMagResBank)的约束条件,对蛋白质数据银行(PDB)中500多种蛋白质重新计算得到的坐标数据库。
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Role of N-terminal helix in interaction of ribosomal protein S15 with 16S rRNA.
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RNA tertiary structure and cooperative assembly of a large ribonucleoprotein complex.大型核糖核蛋白复合体的RNA三级结构与协同组装
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核糖体蛋白S15的构象景观及其对该蛋白与16S RNA相互作用的影响。

The conformational landscape of the ribosomal protein S15 and its influence on the protein interaction with 16S RNA.

作者信息

Créty Thomas, Malliavin Thérèse E

机构信息

Laboratoire de Biochimie Théorique, CNRS UPR 9080, Institut de Biologie Physico-Chimique, 75 005 Paris, France.

出版信息

Biophys J. 2007 Apr 15;92(8):2647-65. doi: 10.1529/biophysj.106.092601. Epub 2007 Jan 26.

DOI:10.1529/biophysj.106.092601
PMID:17259282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1831693/
Abstract

The interaction between the ribosomal protein S15 and its binding sites in the 16S RNA was examined from two points of view. First, the isolated protein S15 was studied by comparing NMR conformer sets, available in the PDB and recalculated using the CNS-ARIA protocol. Molecular dynamics (MD) trajectories were then recorded starting from a conformer of each set. The recalculation of the S15 NMR structure, as well as the recording of MD trajectories, reveals that several orientations of the N-terminal alpha-helix alpha1 with respect to the structure core are populated. MD trajectories of the complex between the ribosomal protein S15 and RNA were also recorded in the presence and absence of Mg(2+) ions. The Mg(2+) ions are hexacoordinated by water and RNA oxygens. The coordination spheres mainly interact with the RNA phosphodiester backbone, reducing the RNA mobility and inducing electrostatic screening. When the Mg(2+) ions are removed, the internal mobility of the RNA and of the protein increases at the interaction interface close to the RNA G-U/G-C motif as a result of a gap between the phosphate groups in the UUCG capping tetraloop and of the disruption of S15-RNA hydrogen bonds in that region. On the other hand, several S15-RNA hydrogen bonds are reinforced, and water bridges appear between the three-way junction region and S15. The network of hydrogen bonds observed in the loop between alpha1 and alpha2 is consequently reorganized. In the absence of Mg(2+), this network has the same pattern as the network observed in the isolated protein, where the helix alpha1 is mobile with respect to the protein core. The presence of Mg(2+) ions may thus play a role in stabilizing the orientation of the helix alpha1 of S15.

摘要

从两个角度研究了核糖体蛋白S15与其在16S RNA中的结合位点之间的相互作用。首先,通过比较PDB中可用的并使用CNS-ARIA协议重新计算的NMR构象集来研究分离出的蛋白S15。然后从每组的一个构象开始记录分子动力学(MD)轨迹。S15 NMR结构的重新计算以及MD轨迹的记录表明,N端α螺旋α1相对于结构核心存在几种取向。还记录了在有和没有Mg(2+)离子的情况下核糖体蛋白S15与RNA之间复合物的MD轨迹。Mg(2+)离子由水和RNA氧原子进行六配位。配位球主要与RNA磷酸二酯主链相互作用,降低RNA的流动性并引发静电屏蔽。当去除Mg(2+)离子时,由于UUCG封端四环中磷酸基团之间的间隙以及该区域中S15-RNA氢键的破坏,RNA和蛋白质在靠近RNA G-U/G-C基序的相互作用界面处的内部流动性增加。另一方面,一些S15-RNA氢键得到加强,并且在三岔区和S15之间出现了水桥。因此,在α1和α2之间的环中观察到的氢键网络发生了重组。在没有Mg(2+)的情况下,该网络具有与在分离蛋白中观察到的网络相同的模式,其中螺旋α1相对于蛋白核心是可移动的。因此,Mg(2+)离子的存在可能在稳定S15的螺旋α1的取向上起作用。