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Accurate structure prediction of biomolecular interactions with AlphaFold 3.利用 AlphaFold 3 进行生物分子相互作用的精确结构预测。
Nature. 2024 Jun;630(8016):493-500. doi: 10.1038/s41586-024-07487-w. Epub 2024 May 8.
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Arf6 as a therapeutic target: Structure, mechanism, and inhibitors.Arf6作为治疗靶点:结构、机制及抑制剂
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Allosteric site variants affect GTP hydrolysis on Ras.变构位点变异会影响 Ras 的 GTP 水解。
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De novo design of protein structure and function with RFdiffusion.利用 RFdiffusion 从头设计蛋白质结构和功能。
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Self-assembly and structure of a clathrin-independent AP-1:Arf1 tubular membrane coat.一种不依赖网格蛋白的AP-1:Arf1管状膜包被的自组装与结构
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Arf核苷酸开关变构前后控制的序列决定因素

Sequence Determinants of Allosteric Back-to-front Control of the Arf Nucleotide Switch.

作者信息

Hantman Noam, Koduru Tejaswi, Peters Edgar V, Jaworek Michel W, McCallum Scott A, Gillilan Richard E, Winter Roland, Cherfils Jacqueline, Royer Catherine A

机构信息

Graduate Program in Biochemistry and Biophysics, Rensselaer Polytechnic Institute, Troy, NY 12180, United States.

Department of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY 12180, United States.

出版信息

J Mol Biol. 2025 Jul 26;437(19):169361. doi: 10.1016/j.jmb.2025.169361.

DOI:10.1016/j.jmb.2025.169361
PMID:40721149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12355652/
Abstract

Unlike AI-based protein structure prediction, the sequence determinants of protein dynamics, and thus function, remain elusive. The nucleotide switch in Arf GTPases involves a massive structural change, which we showed recently in Arf1 is facilitated by a dynamic molten globule ensemble. Here we investigate the unresolved sequence-dynamics paradigm by comparing Arf1 and Arf6 using a combination of high-pressure NMR and other biophysical methods. We show that, as for Arf1, the Arf6 nucleotide switch implicates a functional molten globule ensemble, suggesting that this mechanism is a general feature of Arf and Arf-like GTPases. Comparison of the local stability distributions identifies key sequence determinants for the differences in switching between Arf1 and Arf6. Remarkably, these determinants are distant from the nucleotide-binding site, revealing back-to-front allosteric coupling controlling the switch. Evolutionary covariance analysis suggests that this back-to-front allosteric coupling is a fundamental characteristic of the Arf and Arf-like family, and may extend to the entire small GTPase kingdom. Our study thus establishes notable sequence-dynamics relationships with implications for signaling and diseases.

摘要

与基于人工智能的蛋白质结构预测不同,蛋白质动力学以及功能的序列决定因素仍然难以捉摸。Arf GTPases中的核苷酸开关涉及大规模的结构变化,我们最近在Arf1中发现这种变化由动态熔球集合促进。在这里,我们结合高压核磁共振和其他生物物理方法,通过比较Arf1和Arf6来研究尚未解决的序列-动力学范式。我们表明,与Arf1一样,Arf6核苷酸开关涉及一个功能性熔球集合,这表明这种机制是Arf和Arf样GTPases的一个普遍特征。局部稳定性分布的比较确定了Arf1和Arf6之间开关差异的关键序列决定因素。值得注意的是,这些决定因素远离核苷酸结合位点,揭示了控制开关的从后到前的变构偶联。进化协方差分析表明,这种从后到前的变构偶联是Arf和Arf样家族的一个基本特征,并且可能扩展到整个小GTPase王国。因此,我们的研究建立了显著的序列-动力学关系,对信号传导和疾病具有重要意义。