从人类UBR6重新审视UBR盒的结构。

IF 4.5 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Protein Science Pub Date : 2025-04-01 DOI:10.1002/pro.70092
Bokyung Kim, Sohae Lee, Bong Heon Kim, Leehyeon Kim, Hyun Kyu Song
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引用次数: 0

摘要

真核生物n -降解途径是一种蛋白质水解系统,具有识别底物蛋白特定n端残基的能力,这是其降解信号的重要组成部分。几种E3泛素连接酶的结构域(称为UBR盒)可以识别碱性n端残基为N-degrons。UBR6是包含UBR盒子结构域的七种哺乳动物UBR家族蛋白之一。然而,UBR6对基本1型N-degrons的识别仍不清楚。来自人类UBR6的UBR盒的晶体结构显示了锌介导的二聚化,这是一种不同于其他单体UBR盒的结构特征。此外,它的折叠模式与UBR褶皱不同,尽管序列与其他UBR盒子的序列一致。在这项研究中,我们重新确定了来自人类UBR6的UBR盒子的结构,以研究这种不寻常的结构域交换二聚体是否在结构上相关。新确定的UBR6在1.5 Å分辨率下的UBR盒是一个具有经典UBR折叠的单体。我们的结构与先前报道的UBR盒结构进行了比较,并使用N-degron结合试验进一步分析了其结构特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Revisiting the structure of UBR box from human UBR6.

Eukaryotic N-degron pathways are proteolytic systems with the ability to recognize specific N-terminal residues of substrate proteins, which are essential parts of their degradation signals. Domains, referred to as UBR boxes, of several E3 ubiquitin ligases can recognize basic N-terminal residues as N-degrons. UBR6 is among the seven mammalian UBR family proteins containing the UBR box domain. However, the recognition of basic type-1 N-degrons by UBR6 is still not well understood. The crystal structure of the UBR box from human UBR6 revealed zinc-mediated dimerization, a structural feature distinct from other monomeric UBR boxes. Furthermore, its folding pattern differed from that of the UBR fold, although the sequences aligned well with those of other UBR boxes. In this study, we re-determined the structure of the UBR box from human UBR6 to investigate whether the unusual domain-swapped dimer was structurally relevant. The newly determined UBR box of UBR6 at 1.5 Å resolution was a monomer with a classical UBR fold. Our structure was compared with previously reported structures of UBR boxes, and its structural features were further analyzed using N-degron binding assays.

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来源期刊
Protein Science
Protein Science 生物-生化与分子生物学
CiteScore
12.40
自引率
1.20%
发文量
246
审稿时长
1 months
期刊介绍: Protein Science, the flagship journal of The Protein Society, is a publication that focuses on advancing fundamental knowledge in the field of protein molecules. The journal welcomes original reports and review articles that contribute to our understanding of protein function, structure, folding, design, and evolution. Additionally, Protein Science encourages papers that explore the applications of protein science in various areas such as therapeutics, protein-based biomaterials, bionanotechnology, synthetic biology, and bioelectronics. The journal accepts manuscript submissions in any suitable format for review, with the requirement of converting the manuscript to journal-style format only upon acceptance for publication. Protein Science is indexed and abstracted in numerous databases, including the Agricultural & Environmental Science Database (ProQuest), Biological Science Database (ProQuest), CAS: Chemical Abstracts Service (ACS), Embase (Elsevier), Health & Medical Collection (ProQuest), Health Research Premium Collection (ProQuest), Materials Science & Engineering Database (ProQuest), MEDLINE/PubMed (NLM), Natural Science Collection (ProQuest), and SciTech Premium Collection (ProQuest).
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