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Mechanism of specific site location and DNA cleavage by EcoR I endonuclease.

作者信息

Terry B J, Jack W E, Modrich P

机构信息

Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Gene Amplif Anal. 1987;5:103-18.

PMID:3333364
Abstract
摘要

相似文献

1
Mechanism of specific site location and DNA cleavage by EcoR I endonuclease.EcoR I核酸内切酶对特定位点的定位及DNA切割机制。
Gene Amplif Anal. 1987;5:103-18.
2
Label-free monitoring of site-specific DNA cleavage by EcoRI endonuclease using cyclic voltammetry and electrochemical impedance.使用循环伏安法和电化学阻抗对EcoRI核酸内切酶位点特异性DNA切割进行无标记监测。
Anal Chim Acta. 2009 Feb 16;634(1):44-8. doi: 10.1016/j.aca.2008.12.005. Epub 2008 Dec 7.
3
Molecular recognition mediated by bound water. A mechanism for star activity of the restriction endonuclease EcoRI.由结合水介导的分子识别。限制性内切酶EcoRI星号活性的一种机制。
J Mol Biol. 1993 Nov 20;234(2):302-6. doi: 10.1006/jmbi.1993.1586.
4
Structure and function of the EcoR I restriction endonuclease.
Gene Amplif Anal. 1987;5:119-45.
5
Linkage of EcoRI dissociation from its specific DNA recognition site to water activity, salt concentration, and pH: separating their roles in specific and non-specific binding.EcoRI从其特定DNA识别位点解离与水活性、盐浓度和pH值的关联：区分它们在特异性和非特异性结合中的作用。
J Mol Biol. 2001 Jul 20;310(4):801-16. doi: 10.1006/jmbi.2001.4781.
6
Sequence context influencing cleavage activity of the K130E mutant of the restriction endonuclease EcoRI identified by a site selection assay.通过位点选择分析鉴定的影响限制性内切酶EcoRI的K130E突变体切割活性的序列背景。
Biochemistry. 1997 Aug 5;36(31):9478-85. doi: 10.1021/bi970076g.
7
Bending and flexibility of methylated and unmethylated EcoRI DNA.甲基化和未甲基化的EcoRI DNA的弯曲与柔韧性。
J Mol Biol. 2002 Feb 8;316(1):7-17. doi: 10.1006/jmbi.2001.5247.
8
Differential DNA recognition and cleavage by EcoRI dependent on the dynamic equilibrium between the two forms of the malondialdehyde-deoxyguanosine adduct.EcoRI对DNA的差异性识别与切割取决于丙二醛-脱氧鸟苷加合物两种形式之间的动态平衡。
Biochemistry. 2005 Apr 5;44(13):5024-33. doi: 10.1021/bi0472898.
9
Contribution of facilitated diffusion and processive catalysis to enzyme efficiency: implications for the EcoRI restriction-modification system.易化扩散和持续性催化对酶效率的贡献：对EcoRI限制修饰系统的启示
Biochemistry. 1996 Feb 20;35(7):2201-8. doi: 10.1021/bi951883n.
10
Changes in solvation during DNA binding and cleavage are critical to altered specificity of the EcoRI endonuclease.DNA结合和切割过程中溶剂化作用的变化对于EcoRI核酸内切酶特异性的改变至关重要。
Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2186-91. doi: 10.1073/pnas.95.5.2186.

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Type II restriction endonucleases--a historical perspective and more.II型限制性核酸内切酶——历史回顾及更多内容。
Nucleic Acids Res. 2014 Jul;42(12):7489-527. doi: 10.1093/nar/gku447. Epub 2014 May 30.
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Uracil DNA glycosylase uses DNA hopping and short-range sliding to trap extrahelical uracils.尿嘧啶DNA糖基化酶利用DNA跳跃和短程滑动来捕获螺旋外尿嘧啶。
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Recombination by resolvase to analyse DNA communications by the SfiI restriction endonuclease.通过解离酶进行重组以分析SfiI限制性内切核酸酶的DNA通讯。
EMBO J. 1996 Mar 15;15(6):1460-9.
6
Cloning and characterization of the MboII restriction-modification system.MboII 限制修饰系统的克隆与特性分析
Nucleic Acids Res. 1991 Mar 11;19(5):1007-13. doi: 10.1093/nar/19.5.1007.