• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

结核分枝杆菌中 meso-二氨基庚二酸(DAP)生物合成酶的结构与功能。

Structure and function of Mycobacterium tuberculosis meso-diaminopimelic acid (DAP) biosynthetic enzymes.

机构信息

School of Biosciences, University of Birmingham, Birmingham, UK.

出版信息

FEMS Microbiol Lett. 2012 May;330(1):10-6. doi: 10.1111/j.1574-6968.2012.02527.x. Epub 2012 Mar 7.

DOI:10.1111/j.1574-6968.2012.02527.x
PMID:22339732
Abstract

Because of an increased emergence of resistance to current antitubercular drugs, there is a need for new antitubercular agents directed against novel targets. Diaminopimelic acid (DAP) biosynthetic enzymes are unique to bacteria and are absent in mammals and provide a rich source of essential targets for antitubercular chemotherapy. Herein, we review the structure and function of the mycobacterial DAP biosynthetic enzymes.

摘要

由于当前抗结核药物的耐药性不断增加,因此需要针对新靶标开发新的抗结核药物。二氨基庚二酸(DAP)生物合成酶是细菌所特有的,而在哺乳动物中不存在,为抗结核化疗提供了丰富的必需靶标来源。本文综述了分枝杆菌 DAP 生物合成酶的结构和功能。

相似文献

1
Structure and function of Mycobacterium tuberculosis meso-diaminopimelic acid (DAP) biosynthetic enzymes.结核分枝杆菌中 meso-二氨基庚二酸(DAP)生物合成酶的结构与功能。
FEMS Microbiol Lett. 2012 May;330(1):10-6. doi: 10.1111/j.1574-6968.2012.02527.x. Epub 2012 Mar 7.
2
The three-dimensional structure of N-succinyldiaminopimelate aminotransferase from Mycobacterium tuberculosis.结核分枝杆菌N-琥珀酰二氨基庚二酸转氨酶的三维结构
J Mol Biol. 2007 Mar 30;367(3):825-38. doi: 10.1016/j.jmb.2007.01.023. Epub 2007 Jan 12.
3
Catalytic mechanism of l,l-diaminopimelic acid with diaminopimelate epimerase by molecular docking simulations.通过分子对接模拟研究L,L-二氨基庚二酸与二氨基庚二酸差向异构酶的催化机制
J Mol Graph Model. 2008 Apr;26(7):1082-90. doi: 10.1016/j.jmgm.2007.09.005. Epub 2007 Oct 5.
4
Reconstruction of diaminopimelic acid biosynthesis allows characterisation of Mycobacterium tuberculosis N-succinyl-L,L-diaminopimelic acid desuccinylase.重建二氨基庚二酸生物合成可用于鉴定结核分枝杆菌 N-琥珀酰-L,L-二氨基庚二酸脱琥珀酰酶。
Sci Rep. 2016 Mar 15;6:23191. doi: 10.1038/srep23191.
5
Purification and characterization of anthranilate synthase component I (TrpE) from Mycobacterium tuberculosis H37Rv.结核分枝杆菌H37Rv邻氨基苯甲酸合酶组分I(TrpE)的纯化与鉴定
Protein Expr Purif. 2009 Mar;64(1):8-15. doi: 10.1016/j.pep.2008.09.020. Epub 2008 Oct 10.
6
Substrate and inhibitor binding sites in Corynebacterium glutamicum diaminopimelate dehydrogenase.谷氨酸棒杆菌二氨基庚二酸脱氢酶中的底物和抑制剂结合位点。
Biochemistry. 1998 Mar 10;37(10):3278-85. doi: 10.1021/bi9727949.
7
A novel inhibitor of indole-3-glycerol phosphate synthase with activity against multidrug-resistant Mycobacterium tuberculosis.一种新型吲哚-3-甘油磷酸合酶抑制剂,对耐多药结核分枝杆菌具有活性。
FEBS J. 2009 Jan;276(1):144-54. doi: 10.1111/j.1742-4658.2008.06763.x. Epub 2008 Nov 20.
8
[Development of antituberculous drugs: current status and future prospects].[抗结核药物的研发:现状与未来前景]
Kekkaku. 2006 Dec;81(12):753-74.
9
Structural studies of shikimate 5-dehydrogenase from Mycobacterium tuberculosis.结核分枝杆菌莽草酸5-脱氢酶的结构研究
Proteins. 2008 Aug;72(2):720-30. doi: 10.1002/prot.21953.
10
Structure of the diaminopimelate epimerase DapF from Mycobacterium tuberculosis.结核分枝杆菌中二氨基庚二酸差向异构酶DapF的结构
Acta Crystallogr D Biol Crystallogr. 2009 Apr;65(Pt 4):383-7. doi: 10.1107/S0907444909002522. Epub 2009 Mar 19.

引用本文的文献

1
Computational Modelling, Functional Characterization and Molecular Docking to Lead Compounds of Bordetella pertussis Diaminopimelate Epimerase.计算建模、功能表征和分子对接博德特氏菌二氨基庚二酸差向异构酶的先导化合物。
Appl Biochem Biotechnol. 2023 Nov;195(11):6675-6693. doi: 10.1007/s12010-023-04413-0. Epub 2023 Mar 13.
2
The MtZ Strain: Molecular Characteristics and Outbreak Investigation of the Most Successful Strain in Aragon Using Whole-Genome Sequencing.MtZ 株:使用全基因组测序对阿拉贡地区最成功的菌株进行分子特征和爆发调查。
Front Cell Infect Microbiol. 2022 May 24;12:887134. doi: 10.3389/fcimb.2022.887134. eCollection 2022.
3
IMB-XMA0038, a new inhibitor targeting aspartate-semialdehyde dehydrogenase of .
IMB-XMA0038,一种新型抑制剂,靶向. 的天冬氨酸半醛脱氢酶。
Emerg Microbes Infect. 2021 Dec;10(1):2291-2299. doi: 10.1080/22221751.2021.2006578.
4
Antibacterial Activity and Mechanism of Linalool against .芳樟醇对. 的抑菌活性及作用机制研究。
Molecules. 2021 Jan 5;26(1):245. doi: 10.3390/molecules26010245.
5
Hybrid Dynamic Pharmacophore Models as Effective Tools to Identify Novel Chemotypes for Anti-TB Inhibitor Design: A Case Study With Mtb-DapB.混合动态药效团模型作为鉴定抗结核抑制剂设计新化学型的有效工具:以结核分枝杆菌二氢蝶酸合酶为例的研究
Front Chem. 2020 Dec 2;8:596412. doi: 10.3389/fchem.2020.596412. eCollection 2020.
6
Cell wall peptidoglycan in Mycobacterium tuberculosis: An Achilles' heel for the TB-causing pathogen.结核分枝杆菌细胞壁肽聚糖:结核致病病原体的阿喀琉斯之踵。
FEMS Microbiol Rev. 2019 Sep 1;43(5):548-575. doi: 10.1093/femsre/fuz016.
7
Peptidoglycan in Mycobacteria: chemistry, biology and intervention.分枝杆菌中的肽聚糖:化学、生物学与干预。
Glycoconj J. 2018 Oct;35(5):421-432. doi: 10.1007/s10719-018-9842-7. Epub 2018 Sep 19.
8
Metabolic profiles of cysteine, methionine, glutamate, glutamine, arginine, aspartate, asparagine, alanine and glutathione in Streptococcus thermophilus during pH-controlled batch fermentations.在 pH 控制分批发酵过程中,嗜热链球菌中半胱氨酸、蛋氨酸、谷氨酸、谷氨酰胺、精氨酸、天冬氨酸、天冬酰胺、丙氨酸和谷胱甘肽的代谢谱。
Sci Rep. 2018 Aug 20;8(1):12441. doi: 10.1038/s41598-018-30272-5.
9
Data Intensive Genome Level Analysis for Identifying Novel, Non-Toxic Drug Targets for Multi Drug Resistant Mycobacterium tuberculosis.基于数据密集型基因组分析鉴定新型、非毒性抗多药耐药结核分枝杆菌药物靶标
Sci Rep. 2017 Apr 20;7:46595. doi: 10.1038/srep46595.
10
Identification and Validation of Aspartic Acid Semialdehyde Dehydrogenase as a New Anti-Mycobacterium Tuberculosis Target.天冬氨酸半醛脱氢酶作为新型抗结核靶点的鉴定与验证
Int J Mol Sci. 2015 Sep 30;16(10):23572-86. doi: 10.3390/ijms161023572.