首页> 外文期刊>Journal of Molecular Biology >Improved structural characterizations of the drkN SH3 domain unfolded state suggest a compact ensemble with native-like and non-native structure.
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Improved structural characterizations of the drkN SH3 domain unfolded state suggest a compact ensemble with native-like and non-native structure.

机译:drkN SH3结构域的未折叠状态的改进的结构特征表明具有天然样和非天然结构的紧凑的整体。

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Due to their dynamic ensemble nature and a deficiency of experimental restraints, disordered states of proteins are difficult to characterize structurally. Here, we have expanded upon our previous work on the unfolded state of the Drosophila drk N-terminal (drkN) SH3 domain with our program ENSEMBLE, which assigns population weights to pregenerated conformers in order to calculate ensembles of structures whose properties are collectively consistent with experimental measurements. The experimental restraint set has been enlarged with newly measured paramagnetic relaxation enhancements from Cu(2+) bound to an amino terminal Cu(2+)-Ni(2+) binding (ATCUN) motif as well as nuclear Overhauser effect (NOE) and hydrogen exchange data from recent studies. In addition, two new pseudo-energy minimization algorithms have been implemented that have dramatically improved the speed of ENSEMBLE population weight assignment. Finally, we have greatly improved our conformational sampling by utilizing a variety of techniques to generate both random structures and structures that are biased to contain elements of native-like or non-native structure. Although it is not possible to uniquely define a representative structural ensemble, we have been able to assess various properties of the drkN SH3 domain unfolded state by performing ENSEMBLE minimizations of different conformer pools. Specifically, we have found that the experimental restraint set enforces a compact structural distribution that is not consistent with an overall native-like topology but shows preference for local non-native structure in the regions corresponding to the diverging turn and the beta5 strand of the folded state and for local native-like structure in the region corresponding to the beta6 and beta7 strands. We suggest that this approach could be generally useful for the structural characterization of disordered states.
机译:由于它们的动态集合性质和缺乏实验约束,蛋白质的无序状态很难在结构上表征。在这里,我们使用程序ENSEMBLE扩展了以前关于果蝇drk N末端(drkN)SH3域的未折叠状态的工作,该程序将种群权重分配给预生成的构象子,以计算其性质与实验测量。实验的约束集已经扩大,新测量的顺磁弛豫增强从结合到氨基末端Cu(2 +)-Ni(2+)结合(ATCUN)图案的Cu(2+)以及核Overhauser效应(NOE)和最新研究中的氢交换数据。此外,已经实现了两种新的伪能量最小化算法,这些算法极大地提高了ENSEMBLE总体权重分配的速度。最终,我们通过利用各种技术来生成随机结构和偏向于包含天然或非天然结构元素的结构,大大改善了构象采样。尽管不可能唯一定义一个代表性的结构集合,但是我们已经能够通过执行不同构象库的ENSEMBLE最小化来评估drkN SH3域未折叠状态的各种属性。具体来说,我们发现实验约束集强制执行紧凑的结构分布,该结构分布与整体的类似自然的拓扑结构不一致,但是在与折叠的分叉转向和beta5链相对应的区域中显示出对局部非本地结构的偏爱状态和对应于beta6和beta7链的区域中的本地天然样结构。我们建议这种方法通常可用于无序状态的结构表征。

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