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1
Hexameric ring structure of human MCM10 DNA replication factor.人类MCM10 DNA复制因子的六聚体环状结构。
EMBO Rep. 2007 Oct;8(10):925-30. doi: 10.1038/sj.embor.7401064. Epub 2007 Sep 7.
2
Mcm10 coordinates the timely assembly and activation of the replication fork helicase.Mcm10协调复制叉解旋酶的适时组装与激活。
Nucleic Acids Res. 2016 Jan 8;44(1):315-29. doi: 10.1093/nar/gkv1260. Epub 2015 Nov 17.
3
An intact Mcm10 coiled-coil interaction surface is important for origin melting, helicase assembly and the recruitment of Pol-α to Mcm2-7.完整的Mcm10卷曲螺旋相互作用表面对于起始点解链、解旋酶组装以及将Pol-α招募至Mcm2-7至关重要。
Nucleic Acids Res. 2017 Jul 7;45(12):7261-7275. doi: 10.1093/nar/gkx438.
4
The Mcm2-7-interacting domain of human mini-chromosome maintenance 10 (Mcm10) protein is important for stable chromatin association and origin firing.人类微小染色体维持蛋白10(Mcm10)的Mcm2-7相互作用结构域对于稳定的染色质结合和复制起点激活很重要。
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Mcm10 plays a role in functioning of the eukaryotic replicative DNA helicase, Cdc45-Mcm-GINS.Mcm10 在真核复制 DNA 解旋酶 Cdc45-Mcm-GINS 的功能中发挥作用。
Curr Biol. 2012 Feb 21;22(4):343-9. doi: 10.1016/j.cub.2012.01.023. Epub 2012 Jan 26.
6
Recruitment of Mcm10 to Sites of Replication Initiation Requires Direct Binding to the Minichromosome Maintenance (MCM) Complex.将Mcm10招募至复制起始位点需要与微小染色体维持(MCM)复合体直接结合。
J Biol Chem. 2016 Mar 11;291(11):5879-5888. doi: 10.1074/jbc.M115.707802. Epub 2015 Dec 30.
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Mcm10 and the MCM2-7 complex interact to initiate DNA synthesis and to release replication factors from origins.Mcm10与MCM2 - 7复合物相互作用,启动DNA合成并从起始点释放复制因子。
Genes Dev. 2000 Apr 15;14(8):913-26.
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Budding yeast mcm10/dna43 mutant requires a novel repair pathway for viability.出芽酵母mcm10/dna43突变体需要一种新的修复途径来维持生存能力。
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A novel zinc finger is required for Mcm10 homocomplex assembly.
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Pre-initiation complex assembly functions as a molecular switch that splits the Mcm2-7 double hexamer.起始前复合物组装功能作为分子开关,分裂 Mcm2-7 双六聚体。
EMBO Rep. 2017 Oct;18(10):1752-1761. doi: 10.15252/embr.201744206. Epub 2017 Aug 17.

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Single-molecule characterization of SV40 replisome and novel factors: human FPC and Mcm10.SV40 复制体及其新因子的单分子特征:人 FPC 和 Mcm10。
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A critical threshold of MCM10 is required to maintain genome stability during differentiation of induced pluripotent stem cells into natural killer cells.在诱导多能干细胞分化为自然杀伤细胞的过程中,需要达到一个关键的 MCM10 阈值,以维持基因组的稳定性。
Open Biol. 2024 Jan;14(1):230407. doi: 10.1098/rsob.230407. Epub 2024 Jan 24.
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The Mcm2-7-interacting domain of human mini-chromosome maintenance 10 (Mcm10) protein is important for stable chromatin association and origin firing.人类微小染色体维持蛋白10(Mcm10)的Mcm2-7相互作用结构域对于稳定的染色质结合和复制起点激活很重要。
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An intact Mcm10 coiled-coil interaction surface is important for origin melting, helicase assembly and the recruitment of Pol-α to Mcm2-7.完整的Mcm10卷曲螺旋相互作用表面对于起始点解链、解旋酶组装以及将Pol-α招募至Mcm2-7至关重要。
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Mcm10: A Dynamic Scaffold at Eukaryotic Replication Forks.Mcm10:真核生物复制叉处的动态支架蛋白
Genes (Basel). 2017 Feb 17;8(2):73. doi: 10.3390/genes8020073.
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Xenopus Mcm10 is a CDK-substrate required for replication fork stability.非洲爪蟾Mcm10是复制叉稳定性所需的一种细胞周期蛋白依赖性激酶底物。
Cell Cycle. 2016 Aug 17;15(16):2183-2195. doi: 10.1080/15384101.2016.1199305. Epub 2016 Jun 21.
7
Mcm10 coordinates the timely assembly and activation of the replication fork helicase.Mcm10协调复制叉解旋酶的适时组装与激活。
Nucleic Acids Res. 2016 Jan 8;44(1):315-29. doi: 10.1093/nar/gkv1260. Epub 2015 Nov 17.
8
The N-terminus of Mcm10 is important for interaction with the 9-1-1 clamp and in resistance to DNA damage.Mcm10的N端对于与9-1-1夹子的相互作用以及对DNA损伤的抗性很重要。
Nucleic Acids Res. 2014 Jul;42(13):8389-404. doi: 10.1093/nar/gku479. Epub 2014 Jun 27.
9
MCM10: one tool for all-Integrity, maintenance and damage control.MCM10:适用于完整性、维护和损害控制的通用工具。
Semin Cell Dev Biol. 2014 Jun;30:121-30. doi: 10.1016/j.semcdb.2014.03.017. Epub 2014 Mar 21.
10
Mcm10 self-association is mediated by an N-terminal coiled-coil domain.Mcm10 自我缔合是由 N 端卷曲螺旋结构域介导的。
PLoS One. 2013 Jul 23;8(7):e70518. doi: 10.1371/journal.pone.0070518. Print 2013.

本文引用的文献

1
Fission yeast Mcm10p contains primase activity.裂殖酵母Mcm10p含有引发酶活性。
J Biol Chem. 2006 Aug 4;281(31):22248-22260. doi: 10.1074/jbc.M512997200. Epub 2006 May 23.
2
A conserved Hsp10-like domain in Mcm10 is required to stabilize the catalytic subunit of DNA polymerase-alpha in budding yeast.在芽殖酵母中,Mcm10 中一个保守的类 Hsp10 结构域对于稳定 DNA 聚合酶α的催化亚基是必需的。
J Biol Chem. 2006 Jul 7;281(27):18414-25. doi: 10.1074/jbc.M513551200. Epub 2006 May 4.
3
MCM proteins and DNA replication.微小染色体维持蛋白与DNA复制
Curr Opin Cell Biol. 2006 Apr;18(2):130-6. doi: 10.1016/j.ceb.2006.02.006. Epub 2006 Feb 21.
4
Localization of MCM2-7, Cdc45, and GINS to the site of DNA unwinding during eukaryotic DNA replication.真核生物DNA复制过程中MCM2-7、Cdc45和GINS在DNA解旋位点的定位。
Mol Cell. 2006 Feb 17;21(4):581-7. doi: 10.1016/j.molcel.2006.01.030.
5
DNA replication and progression through S phase.DNA复制及S期进程。
Oncogene. 2005 Apr 18;24(17):2827-43. doi: 10.1038/sj.onc.1208616.
6
Structural polymorphism of Methanothermobacter thermautotrophicus MCM.嗜热自养甲烷杆菌MCM的结构多态性
J Mol Biol. 2005 Feb 18;346(2):389-94. doi: 10.1016/j.jmb.2004.11.076. Epub 2005 Jan 8.
7
Mcm10 regulates the stability and chromatin association of DNA polymerase-alpha.Mcm10调节DNA聚合酶α的稳定性和与染色质的结合。
Mol Cell. 2004 Oct 22;16(2):173-85. doi: 10.1016/j.molcel.2004.09.017.
8
Mcm10 and Cdc45 cooperate in origin activation in Saccharomyces cerevisiae.Mcm10与Cdc45在酿酒酵母的起始点激活过程中协同作用。
J Mol Biol. 2004 Jul 2;340(2):195-202. doi: 10.1016/j.jmb.2004.04.066.
9
Localization of human Mcm10 is spatially and temporally regulated during the S phase.人类Mcm10的定位在S期受到时空调控。
J Biol Chem. 2004 Jul 30;279(31):32569-77. doi: 10.1074/jbc.M314017200. Epub 2004 May 10.
10
Primer utilization by DNA polymerase alpha-primase is influenced by its interaction with Mcm10p.DNA聚合酶α-引发酶对引物的利用受其与Mcm10p相互作用的影响。
J Biol Chem. 2004 Apr 16;279(16):16144-53. doi: 10.1074/jbc.M400142200. Epub 2004 Feb 6.

人类MCM10 DNA复制因子的六聚体环状结构。

Hexameric ring structure of human MCM10 DNA replication factor.

作者信息

Okorokov Andrei L, Waugh Alastair, Hodgkinson Julie, Murthy Andal, Hong Hye Kyung, Leo Elisabetta, Sherman Michael B, Stoeber Kai, Orlova Elena V, Williams Gareth H

机构信息

Department of Pathology, University College London, London WC1E 6JJ, UK.

出版信息

EMBO Rep. 2007 Oct;8(10):925-30. doi: 10.1038/sj.embor.7401064. Epub 2007 Sep 7.

DOI:10.1038/sj.embor.7401064
PMID:17823614
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2002553/
Abstract

The DNA replication factor minichromosome maintenance 10 (MCM10) is a conserved, abundant nuclear protein crucial for origin firing. During the transition from pre-replicative complexes to pre-initiation complexes, MCM10 recruitment to replication origins is required to provide a physical link between the MCM2-7 complex DNA helicase and DNA polymerases. Here, we report the molecular structure of human MCM10 as determined by electron microscopy and single-particle analysis. The MCM10 molecule is a ring-shaped hexamer with large central and smaller lateral channels and a system of inner chambers. This structure, together with biochemical data, suggests that this important protein uses its architecture to provide a docking module for assembly of the molecular machinery required for eukaryotic DNA replication.

摘要

DNA复制因子微小染色体维持蛋白10(MCM10)是一种保守的、丰富的核蛋白,对起始点激发至关重要。在从复制前复合物向起始前复合物转变的过程中,MCM10募集到复制起始点是在MCM2-7复合物DNA解旋酶与DNA聚合酶之间建立物理连接所必需的。在此,我们报告了通过电子显微镜和单颗粒分析确定的人MCM10的分子结构。MCM10分子是一个环形六聚体,具有大的中央通道和较小的侧向通道以及一个内腔系统。这种结构与生化数据一起表明,这种重要的蛋白质利用其结构为真核DNA复制所需分子机器的组装提供一个对接模块。