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PilZ 结构域介导的 c-di-GMP 信号转导的新兴模式。

Emerging paradigms for PilZ domain-mediated C-di-GMP signaling.

机构信息

School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, S637551 Singapore.

School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, S637551 Singapore

出版信息

Biochem Soc Trans. 2019 Feb 28;47(1):381-388. doi: 10.1042/BST20180543. Epub 2019 Feb 1.

Abstract

PilZ domain-containing proteins constitute a large family of bacterial signaling proteins. As a widely distributed protein domain for the binding of the second messenger c-di-GMP, the canonical PilZ domain contains a set of motifs that define the binding site for c-di-GMP and an allosteric switch for propagating local conformational changes. Here, we summarize some new insights gathered from recent studies on the commonly occurring single-domain PilZ proteins, YcgR-like proteins and PilZ domain-containing cellulose synthases. The studies collectively illuminate how PilZ domains function as - or -regulatory domains that enable c-di-GMP to control the activity of its cellular targets. Overall, the review highlights the diverse protein structure, biological function and regulatory mechanism of PilZ domain-containing proteins, as well as the challenge of deciphering the function and mechanism of orphan PilZ proteins.

摘要

PilZ 结构域蛋白构成了细菌信号转导蛋白的一个大家族。作为第二信使 c-di-GMP 的结合的广泛分布的蛋白结构域,典型的 PilZ 结构域包含一组基序,这些基序定义了 c-di-GMP 的结合位点和用于传播局部构象变化的别构开关。在这里,我们总结了最近关于常见的单结构域 PilZ 蛋白、YcgR 样蛋白和 PilZ 结构域纤维素合酶的研究中获得的一些新见解。这些研究共同阐明了 PilZ 结构域如何作为调节域发挥作用,使 c-di-GMP 能够控制其细胞靶标的活性。总的来说,该综述强调了 PilZ 结构域蛋白的多样性的蛋白质结构、生物学功能和调节机制,以及阐明孤儿 PilZ 蛋白的功能和机制的挑战。

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