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利用天然产物靶向分枝杆菌蛋白水解复合物

Targeting mycobacterial proteolytic complexes with natural products.

作者信息

Parish Tanya

机构信息

TB Discovery Research, Infectious Disease Research Institute, Seattle, WA 98102, USA.

出版信息

Chem Biol. 2014 Apr 24;21(4):437-438. doi: 10.1016/j.chembiol.2014.04.002.

DOI:10.1016/j.chembiol.2014.04.002
PMID:24766844
Abstract

Controlled proteolysis is key to bacterial viability. In this issue of Chemistry & Biology, Gavrish and colleagues characterize a natural product, lassomycin, targeting the Mycobacterium tuberculosis caseinolytic (Clp) protease. Unusually, lassomycin activates ClpC1, inducing ATPase activity and decoupling it from proteolysis.

摘要

可控蛋白水解是细菌生存能力的关键。在本期《化学生物学》中,加夫里什及其同事对一种靶向结核分枝杆菌酪蛋白水解(Clp)蛋白酶的天然产物——拉索霉素进行了表征。不同寻常的是,拉索霉素激活ClpC1,诱导ATP酶活性并使其与蛋白水解解偶联。

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Targeting mycobacterial proteolytic complexes with natural products.利用天然产物靶向分枝杆菌蛋白水解复合物
Chem Biol. 2014 Apr 24;21(4):437-438. doi: 10.1016/j.chembiol.2014.04.002.
2
Lassomycin, a ribosomally synthesized cyclic peptide, kills mycobacterium tuberculosis by targeting the ATP-dependent protease ClpC1P1P2.拉索霉素是一种核糖体合成的环肽,通过作用于ATP依赖性蛋白酶ClpC1P1P2来杀死结核分枝杆菌。
Chem Biol. 2014 Apr 24;21(4):509-518. doi: 10.1016/j.chembiol.2014.01.014. Epub 2014 Mar 27.
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Rufomycin Targets ClpC1 Proteolysis in Mycobacterium tuberculosis and M. abscessus.利福霉素靶向结核分枝杆菌和脓肿分枝杆菌的 ClpC1 蛋白酶解。
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Mutation analysis of the interactions between Mycobacterium tuberculosis caseinolytic protease C1 (ClpC1) and ecumicin.结核分枝杆菌组织蛋白酶 C1(ClpC1)与埃库霉素相互作用的突变分析。
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Crystal structure of the N-terminal domain of MtClpC1 in complex with the anti-mycobacterial natural peptide Lassomycin.MtClpC1N 端结构域与抗结核天然肽 Lassomycin 的复合物的晶体结构
Int J Biol Macromol. 2023 Dec 31;253(Pt 2):126771. doi: 10.1016/j.ijbiomac.2023.126771. Epub 2023 Sep 6.
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Anti-tuberculosis lead molecules from natural products targeting Mycobacterium tuberculosis ClpC1.来自天然产物的靶向结核分枝杆菌ClpC1的抗结核先导分子。
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The cyclic peptide ecumicin targeting ClpC1 is active against Mycobacterium tuberculosis in vivo.靶向ClpC1的环肽ecumicin在体内对结核分枝杆菌具有活性。
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Substrate delivery by the AAA+ ClpX and ClpC1 unfoldases activates the mycobacterial ClpP1P2 peptidase.由AAA+ ClpX和ClpC1解折叠酶进行的底物传递激活了分枝杆菌的ClpP1P2肽酶。
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The antibiotic cyclomarin blocks arginine-phosphate-induced millisecond dynamics in the N-terminal domain of ClpC1 from .抗生素环玛琳阻断 ClpC1 N 端结构域中精氨酸-磷酸诱导的毫秒级动力学。
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Lassomycin and lariatin lasso peptides as suitable antibiotics for combating mycobacterial infections: current state of biosynthesis and perspectives for production.拉索霉素和拉里他汀拉索肽作为抗分枝杆菌感染的合适抗生素:生物合成的现状和生产前景。
Appl Microbiol Biotechnol. 2019 May;103(10):3931-3940. doi: 10.1007/s00253-019-09771-6. Epub 2019 Mar 26.

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