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1
The bacterial cell-division protein ZipA and its interaction with an FtsZ fragment revealed by X-ray crystallography.通过X射线晶体学揭示的细菌细胞分裂蛋白ZipA及其与FtsZ片段的相互作用。
EMBO J. 2000 Jul 3;19(13):3179-91. doi: 10.1093/emboj/19.13.3179.
2
ZipA-induced bundling of FtsZ polymers mediated by an interaction between C-terminal domains.由C端结构域之间的相互作用介导的ZipA诱导的FtsZ聚合物成束。
J Bacteriol. 2000 Sep;182(18):5153-66. doi: 10.1128/JB.182.18.5153-5166.2000.
3
Solution structure of ZipA, a crucial component of Escherichia coli cell division.大肠杆菌细胞分裂关键组分ZipA的溶液结构
Biochemistry. 2000 Aug 8;39(31):9146-56. doi: 10.1021/bi0009690.
4
ZipA is a MAP-Tau homolog and is essential for structural integrity of the cytokinetic FtsZ ring during bacterial cell division.ZipA是一种微管相关蛋白Tau同源物,在细菌细胞分裂过程中,对细胞分裂的FtsZ环的结构完整性至关重要。
EMBO J. 1999 May 4;18(9):2372-83. doi: 10.1093/emboj/18.9.2372.
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Peptide Linkers within the Essential FtsZ Membrane Tethers ZipA and FtsA Are Nonessential for Cell Division.必需的 FtsZ 膜栓蛋白 ZipA 和 FtsA 中的肽接头对于细胞分裂不是必需的。
J Bacteriol. 2020 Feb 25;202(6). doi: 10.1128/JB.00720-19.
6
ZipA Uses a Two-Pronged FtsZ-Binding Mechanism Necessary for Cell Division.ZipA 使用一种双叉 FtsZ 结合机制,这对于细胞分裂是必要的。
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Development of a fluorescence polarization assay to screen for inhibitors of the FtsZ/ZipA interaction.开发一种荧光偏振测定法以筛选FtsZ/ZipA相互作用的抑制剂。
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8
Genetic analysis of the Escherichia coli FtsZ.ZipA interaction in the yeast two-hybrid system. Characterization of FtsZ residues essential for the interactions with ZipA and with FtsA.酵母双杂交系统中大肠杆菌FtsZ与ZipA相互作用的遗传分析。鉴定与ZipA和FtsA相互作用所必需的FtsZ残基。
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FtsZ Polymers Tethered to the Membrane by ZipA Are Susceptible to Spatial Regulation by Min Waves.由ZipA锚定在细胞膜上的FtsZ聚合物易受Min波的空间调控。
Biophys J. 2015 May 5;108(9):2371-83. doi: 10.1016/j.bpj.2015.03.031.

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Cell division protein CdpA organises and anchors the midcell ring in haloarchaea.细胞分裂蛋白CdpA在嗜盐古菌中组织并锚定细胞中部环。
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High-throughput discovery of inhibitory protein fragments with AlphaFold.利用AlphaFold进行抑制性蛋白质片段的高通量发现。
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AAp-MSMD: Amino Acid Preference Mapping on Protein-Protein Interaction Surfaces Using Mixed-Solvent Molecular Dynamics.AAp-MSMD:使用混合溶剂分子动力学在蛋白质-蛋白质相互作用表面上进行氨基酸偏好映射。
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Anchors: A way for FtsZ filaments to stay membrane bound.锚定蛋白:保持 FtsZ 丝膜结合的一种方式。
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The structural integrity of the membrane-embedded bacterial division complex FtsQBL studied with molecular dynamics simulations.利用分子动力学模拟研究膜嵌入细菌分裂复合体FtsQBL的结构完整性。
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本文引用的文献

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[27] Maximum-likelihood heavy-atom parameter refinement for multiple isomorphous replacement and multiwavelength anomalous diffraction methods.[27] 用于多同晶置换和多波长反常衍射方法的最大似然重原子参数精修
Methods Enzymol. 1997;276:472-494. doi: 10.1016/S0076-6879(97)76073-7.
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Phase combination and cross validation in iterated density-modification calculations.迭代密度修正计算中的相位组合与交叉验证
Acta Crystallogr D Biol Crystallogr. 1996 Jan 1;52(Pt 1):43-8. doi: 10.1107/S090744499500761X.
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The CCP4 suite: programs for protein crystallography.CCP4软件包:用于蛋白质晶体学的程序。
Acta Crystallogr D Biol Crystallogr. 1994 Sep 1;50(Pt 5):760-3. doi: 10.1107/S0907444994003112.
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Bacterial cell division.细菌细胞分裂
Annu Rev Genet. 1999;33:423-48. doi: 10.1146/annurev.genet.33.1.423.
5
Genetic and functional analyses of the conserved C-terminal core domain of Escherichia coli FtsZ.大肠杆菌FtsZ保守C端核心结构域的遗传与功能分析
J Bacteriol. 1999 Dec;181(24):7531-44. doi: 10.1128/JB.181.24.7531-7544.1999.
6
ZipA is a MAP-Tau homolog and is essential for structural integrity of the cytokinetic FtsZ ring during bacterial cell division.ZipA是一种微管相关蛋白Tau同源物,在细菌细胞分裂过程中,对细胞分裂的FtsZ环的结构完整性至关重要。
EMBO J. 1999 May 4;18(9):2372-83. doi: 10.1093/emboj/18.9.2372.
7
Recruitment of ZipA to the division site by interaction with FtsZ.通过与FtsZ相互作用将ZipA招募到分裂位点。
Mol Microbiol. 1999 Mar;31(6):1853-61. doi: 10.1046/j.1365-2958.1999.01322.x.
8
Recruitment of ZipA to the septal ring of Escherichia coli is dependent on FtsZ and independent of FtsA.ZipA募集到大肠杆菌的隔膜环上依赖于FtsZ且不依赖于FtsA。
J Bacteriol. 1999 Jan;181(1):167-76. doi: 10.1128/JB.181.1.167-176.1999.
9
Crystallography & NMR system: A new software suite for macromolecular structure determination.晶体学与核磁共振系统:用于大分子结构测定的新软件套件。
Acta Crystallogr D Biol Crystallogr. 1998 Sep 1;54(Pt 5):905-21. doi: 10.1107/s0907444998003254.
10
Dominant C-terminal deletions of FtsZ that affect its ability to localize in Caulobacter and its interaction with FtsA.FtsZ的显性C末端缺失会影响其在柄杆菌中的定位能力及其与FtsA的相互作用。
Mol Microbiol. 1998 Mar;27(5):1051-63. doi: 10.1046/j.1365-2958.1998.00752.x.

通过X射线晶体学揭示的细菌细胞分裂蛋白ZipA及其与FtsZ片段的相互作用。

The bacterial cell-division protein ZipA and its interaction with an FtsZ fragment revealed by X-ray crystallography.

作者信息

Mosyak L, Zhang Y, Glasfeld E, Haney S, Stahl M, Seehra J, Somers W S

机构信息

Biological Chemistry, Wyeth Research, 87 Cambridge Park Drive, Cambridge, MA 02140, USA.

出版信息

EMBO J. 2000 Jul 3;19(13):3179-91. doi: 10.1093/emboj/19.13.3179.

DOI:10.1093/emboj/19.13.3179
PMID:10880432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC313961/
Abstract

In Escherichia coli, FtsZ, a homologue of eukaryotic tubulins, and ZipA, a membrane-anchored protein that binds to FtsZ, are two essential components of the septal ring structure that mediates cell division. Recent data indicate that ZipA is involved in the assembly of the ring by linking FtsZ to the cytoplasmic membrane and that the ZipA-FtsZ interaction is mediated by their C-terminal domains. We present the X-ray crystal structures of the C-terminal FtsZ-binding domain of ZipA and a complex between this domain and a C-terminal fragment of FtsZ. The ZipA domain is a six-stranded beta-sheet packed against three alpha-helices and contains the split beta-alpha-beta motif found in many RNA-binding proteins. The uncovered side of the sheet incorporates a shallow hydrophobic cavity exposed to solvent. In the complex, the 17-residue FtsZ fragment occupies this entire cavity of ZipA and binds as an extended beta-strand followed by alpha-helix. An alanine-scanning mutagenesis analysis of the FtsZ fragment was also performed, which shows that only a small cluster of the buried FtsZ side chains is critical in binding to ZipA.

摘要

在大肠杆菌中,FtsZ(真核微管蛋白的同源物)和ZipA(一种与FtsZ结合的膜锚定蛋白)是介导细胞分裂的隔膜环结构的两个必需成分。最近的数据表明,ZipA通过将FtsZ连接到细胞质膜而参与环的组装,并且ZipA与FtsZ的相互作用由它们的C末端结构域介导。我们展示了ZipA的C末端FtsZ结合结构域以及该结构域与FtsZ的C末端片段之间复合物的X射线晶体结构。ZipA结构域是由三条α螺旋堆积而成的六股β折叠,并且包含许多RNA结合蛋白中发现的分裂β-α-β基序。折叠的未覆盖面包含一个暴露于溶剂的浅疏水腔。在复合物中,17个残基的FtsZ片段占据ZipA的整个腔,并作为延伸的β链随后是α螺旋结合。还对FtsZ片段进行了丙氨酸扫描诱变分析,结果表明只有一小簇埋藏的FtsZ侧链在与ZipA结合中起关键作用。