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2
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本文引用的文献

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Heterogeneity and clonality among isolates of Mycobacterium kansasii: implications for epidemiological and pathogenicity studies.堪萨斯分枝杆菌分离株之间的异质性和克隆性:对流行病学和致病性研究的启示。
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Crystal structure of PI-SceI, a homing endonuclease with protein splicing activity.PI-SceI的晶体结构,一种具有蛋白质剪接活性的归巢内切酶。
Cell. 1997 May 16;89(4):555-64. doi: 10.1016/s0092-8674(00)80237-8.
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Compilation and analysis of intein sequences.内含肽序列的汇编与分析。
Nucleic Acids Res. 1997 Mar 15;25(6):1087-93. doi: 10.1093/nar/25.6.1087.
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The mechanism of protein splicing and its modulation by mutation.蛋白质剪接机制及其突变调控
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A new intein in cyanobacteria and its significance for the spread of inteins.蓝藻中的一种新型内含肽及其对内含肽传播的意义。
Trends Genet. 1996 Aug;12(8):287-8. doi: 10.1016/0168-9525(96)20005-8.
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Homing events in the gyrA gene of some mycobacteria.一些分枝杆菌gyrA基因中的归巢事件。
Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3410-5. doi: 10.1073/pnas.93.8.3410.
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Structure and mechanism of DNA topoisomerase II.DNA拓扑异构酶II的结构与机制。
Nature. 1996 Jan 18;379(6562):225-32. doi: 10.1038/379225a0.
8
The comings and goings of homing endonucleases and mobile introns.归巢内切核酸酶和移动内含子的来来去去。
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9
Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis.通过聚合酶链反应和限制性酶切分析快速鉴定分枝杆菌至种水平
J Clin Microbiol. 1993 Feb;31(2):175-8. doi: 10.1128/jcm.31.2.175-178.1993.
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In vitro protein splicing of purified precursor and the identification of a branched intermediate.纯化前体的体外蛋白质剪接及分支中间体的鉴定。
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蟾分枝杆菌GyrA蛋白剪接元件:最小内含肽的特性

The Mycobacterium xenopi GyrA protein splicing element: characterization of a minimal intein.

作者信息

Telenti A, Southworth M, Alcaide F, Daugelat S, Jacobs W R, Perler F B

机构信息

Institut für Medizinische Mikrobiologie, Universität Bern, Switzerland.

出版信息

J Bacteriol. 1997 Oct;179(20):6378-82. doi: 10.1128/jb.179.20.6378-6382.1997.

DOI:10.1128/jb.179.20.6378-6382.1997
PMID:9335286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC179553/
Abstract

The 198-amino-acid in-frame insertion in the gyrA gene of Mycobacterium xenopi is the smallest known naturally occurring active protein splicing element (intein). Comparison with other mycobacterial gyrA inteins suggests that the M. xenopi intein underwent a complex series of events including (i) removal of 222 amino acids that encompass most of the central intein domain, and (ii) addition of a linker of unrelated residues. This naturally occurring genetic rearrangement is a representative characteristic of the taxon. The deletion process removes the conserved motifs involved in homing endonuclease activity. The linker insertion represents a structural requirement, as its mutation resulted in failure to splice. The M. xenopi GyrA intein thus provides a paradigm for a minimal protein splicing element.

摘要

蟾分枝杆菌gyrA基因中198个氨基酸的框内插入是已知最小的天然存在的活性蛋白质剪接元件(内含肽)。与其他分枝杆菌gyrA内含肽的比较表明,蟾分枝杆菌内含肽经历了一系列复杂事件,包括:(i)去除包含大部分中央内含肽结构域的222个氨基酸,以及(ii)添加不相关残基的连接子。这种天然发生的基因重排是该分类单元的一个代表性特征。缺失过程去除了归巢内切核酸酶活性所涉及的保守基序。连接子插入代表一种结构要求,因为其突变导致剪接失败。因此,蟾分枝杆菌GyrA内含肽为最小蛋白质剪接元件提供了一个范例。