肺炎克雷伯氏菌未知功能域 1480 (DUF1480) 的晶体结构。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-09-26 DOI:10.1002/prot.26752
Dhruvin H Patel, Nobuhiko Watanabe, Alexei Savchenko, Cameron Semper
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引用次数: 0

摘要

未知功能域(DUFs)仍然是细菌蛋白质组的重要组成部分,超过 20% 的细菌蛋白质仍然被注释为 DUFs。对其分子结构的表征可以提供主序列分析无法捕捉到的有价值的见解,从而为鉴定 DUF 代表的分子功能提供一个切入点。在此,我们展示了肺炎克雷伯氏菌肺炎亚种中含有 DUF1480 结构域的蛋白质 KPN_02352 的晶体结构,其分辨率为 1.75 Å。DUF1480 家族的代表广泛存在于肠杆菌属中,以前曾被证明有助于抗生素反应。我们的结构分析表明,DUF1480 由一个六链分裂桶折叠组成,其特点是一个小的α螺旋位于分裂桶的一端。研究发现,DUF1480 在溶液中是单体,与反应调节因子的结构相似。DUF1480的晶体结构是对这一保守蛋白家族分子结构的首次实验性洞察,揭示了可能与功能相关的几个保守特征。
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The Crystal Structure of the Domain of Unknown Function 1480 (DUF1480) From Klebsiella pneumoniae.

Domains of unknown function (DUFs) continue to comprise a significant portion of bacterial proteomes, with more than 20% of bacterial proteins remaining annotated as DUFs. The characterization of their molecular structure can provide valuable insight that is not captured by the primary sequence analysis, thus providing a segue into the identification of the molecular function of DUF representatives. Here, we present the crystal structure of KPN_02352 from Klebsiella pneumoniae subsp. pneumoniae, a DUF1480 domain-containing protein, which was determined to be 1.75 Å resolution. Representatives of the DUF1480 family are found broadly across Enterobacterales and have been previously shown to contribute to the antibiotic response. Our structural analysis suggests that DUF1480 is comprised of a six-stranded split barrel fold featuring a small alpha helix that is positioned to cap one end of the split barrel. DUF1480 was found to be monomeric in solution, and harbors structural similarity to response regulators. The crystal structure of DUF1480 is the first experimental insight into the molecular structure of this conserved protein family, revealing several conserved features that may be functionally relevant.

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CiteScore
7.20
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4.30%
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567
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