• 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

对泰国伯克霍尔德菌E264来源的D,D-庚糖-1,7-二磷酸磷酸酶的初步X射线研究。

A preliminary X-ray study of D,D-heptose-1,7-bisphosphate phosphatase from Burkholderia thailandensis E264.

作者信息

Kim Mi Sun, Shin Dong Hae

机构信息

College of Pharmacy, Division of Life and Pharmaceutical Sciences and Center for Cell Signaling and Drug Discovery Research, Ewha Womans University, Seoul 120-750, Republic of Korea.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 Feb 1;66(Pt 2):160-2. doi: 10.1107/S1744309109042614. Epub 2010 Jan 27.

DOI:10.1107/S1744309109042614
PMID:20124712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2815682/
Abstract

D,D-Heptose-1,7-bisphosphate phosphatase (GmhB), which is involved in the third step of the NDP-heptose biosynthesis pathway, converts D,D-heptose-1,7-bisphosphate to D,D-heptose-1-phosphate. This biosynthesis pathway is a target for new antibiotics or antibiotic adjuvants for Gram-negative pathogens. Burkholderia thailandensis is a useful surrogate organism for studying the pathogenicity of melioidosis owing to its extensive genomic similarity to B. pseudomallei. Melioidosis caused by B. pseudomallei is a serious invasive disease of animals and humans in tropical and subtropical areas. In this study, GmhB has been cloned, expressed, purified and crystallized. X-ray data have also been collected to 2.50 A resolution using synchrotron radiation. The crystal belonged to space group P6, with unit-cell parameters a = 243.2, b = 243.2, c = 41.1 A.

摘要

D,D-庚糖-1,7-二磷酸磷酸酶(GmhB)参与NDP-庚糖生物合成途径的第三步,将D,D-庚糖-1,7-二磷酸转化为D,D-庚糖-1-磷酸。这条生物合成途径是新型抗生素或革兰氏阴性病原体抗生素佐剂的作用靶点。泰国伯克霍尔德菌由于其与类鼻疽伯克霍尔德菌在基因组上具有广泛的相似性,是研究类鼻疽病致病性的有用替代生物。类鼻疽伯克霍尔德菌引起的类鼻疽病是热带和亚热带地区动物和人类的一种严重侵袭性疾病。在本研究中,GmhB已被克隆、表达、纯化并结晶。还利用同步辐射收集了分辨率为2.50 Å的X射线数据。晶体属于空间群P6,晶胞参数a = 243.2,b = 243.2,c = 41.1 Å。

相似文献

1
A preliminary X-ray study of D,D-heptose-1,7-bisphosphate phosphatase from Burkholderia thailandensis E264.对泰国伯克霍尔德菌E264来源的D,D-庚糖-1,7-二磷酸磷酸酶的初步X射线研究。
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 Feb 1;66(Pt 2):160-2. doi: 10.1107/S1744309109042614. Epub 2010 Jan 27.
2
A preliminary X-ray study of sedoheptulose-7-phosphate isomerase from Burkholderia pseudomallei.来自伯克霍尔德菌的景天庚酮糖-7-磷酸异构酶的初步X射线研究。
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 Nov 1;65(Pt 11):1110-2. doi: 10.1107/S174430910903259X. Epub 2009 Oct 30.
3
Structure and in silico substrate-binding mode of ADP-L-glycero-D-manno-heptose 6-epimerase from Burkholderia thailandensis.泰国伯克霍尔德菌ADP-L-甘油-D-甘露庚糖6-表异构酶的结构及计算机模拟底物结合模式
Acta Crystallogr D Biol Crystallogr. 2013 Apr;69(Pt 4):658-68. doi: 10.1107/S0907444913001030. Epub 2013 Mar 14.
4
A preliminary X-ray study of 3-deoxy-D-manno-oct-2-ulosonic acid 8-phosphate phosphatase (YrbI) from Burkholderia pseudomallei.对来自类鼻疽伯克霍尔德菌的3-脱氧-D-甘露-辛-2-酮糖酸8-磷酸磷酸酶(YrbI)的初步X射线研究。
Acta Crystallogr F Struct Biol Commun. 2015 Jun;71(Pt 6):790-3. doi: 10.1107/S2053230X15006135. Epub 2015 May 22.
5
Structural and kinetic characterization of the LPS biosynthetic enzyme D-alpha,beta-D-heptose-1,7-bisphosphate phosphatase (GmhB) from Escherichia coli.大肠杆菌脂多糖生物合成酶 D-α,β-D-庚糖-1,7-双磷酸磷酸酶(GmhB)的结构和动力学特征。
Biochemistry. 2010 Feb 9;49(5):1033-41. doi: 10.1021/bi901780j.
6
Divergence of biochemical function in the HAD superfamily: D-glycero-D-manno-heptose-1,7-bisphosphate phosphatase (GmhB).HAD 超家族中生化功能的差异:D-甘油-D-甘露庚糖-1,7-二磷酸磷酸酶(GmhB)。
Biochemistry. 2010 Feb 16;49(6):1072-81. doi: 10.1021/bi902018y.
7
Expression and crystallographic studies of D-glycero-β-D-manno-heptose-1-phosphate adenylyltransferase from Burkholderia pseudomallei.来自类鼻疽伯克霍尔德菌的D-甘油-β-D-甘露庚糖-1-磷酸腺苷酸转移酶的表达及晶体学研究
Acta Crystallogr F Struct Biol Commun. 2017 Feb 1;73(Pt 2):90-94. doi: 10.1107/S2053230X16020537. Epub 2017 Jan 19.
8
A preliminary X-ray study of transketolase from Burkholderia pseudomallei.对伯克霍尔德菌属类鼻疽杆菌转酮醇酶的初步X射线研究。
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Dec 1;68(Pt 12):1554-6. doi: 10.1107/S1744309112044375. Epub 2012 Nov 28.
9
Structural determinants of substrate recognition in the HAD superfamily member D-glycero-D-manno-heptose-1,7-bisphosphate phosphatase (GmhB) .HAD 超家族成员 D-甘油基-D-甘露庚糖-1,7-二磷酸磷酸酶(GmhB)中底物识别的结构决定因素。
Biochemistry. 2010 Feb 16;49(6):1082-92. doi: 10.1021/bi902019q.
10
GmhB enzyme involved in ADP-heptose biosynthesis pathway is essential for lipopolysaccharide biosynthesis and bacterial virulence.GmhB 酶参与 ADP-庚糖生物合成途径,对脂多糖生物合成和细菌毒力是必需的。
Virulence. 2021 Dec;12(1):1610-1628. doi: 10.1080/21505594.2021.1938449.

本文引用的文献

1
Processing of X-ray diffraction data collected in oscillation mode.振荡模式下收集的X射线衍射数据的处理。
Methods Enzymol. 1997;276:307-26. doi: 10.1016/S0076-6879(97)76066-X.
2
Structural snapshots of Escherichia coli histidinol phosphate phosphatase along the reaction pathway.大肠杆菌组氨醇磷酸磷酸酶沿反应途径的结构快照。
J Biol Chem. 2006 Dec 8;281(49):37930-41. doi: 10.1074/jbc.M604916200. Epub 2006 Sep 11.
3
Melioidosis: insights into the pathogenicity of Burkholderia pseudomallei.类鼻疽:对类鼻疽伯克霍尔德菌致病性的见解。
Nat Rev Microbiol. 2006 Apr;4(4):272-82. doi: 10.1038/nrmicro1385.
4
Structural genomics of minimal organisms and protein fold space.最小生物的结构基因组学与蛋白质折叠空间
J Struct Funct Genomics. 2005;6(2-3):63-70. doi: 10.1007/s10969-005-2651-9.
5
Biosynthesis pathway of ADP-L-glycero-beta-D-manno-heptose in Escherichia coli.大肠杆菌中ADP-L-甘油-β-D-甘露庚糖的生物合成途径。
J Bacteriol. 2002 Jan;184(2):363-9. doi: 10.1128/JB.184.2.363-369.2002.
6
Role of lipopolysaccharides in antibiotic resistance and bacteriophage adsorption of Escherichia coli K-12.脂多糖在大肠杆菌K-12抗生素抗性及噬菌体吸附中的作用
J Bacteriol. 1971 Mar;105(3):968-75. doi: 10.1128/jb.105.3.968-975.1971.
7
Molecular basis of bacterial outer membrane permeability.细菌外膜通透性的分子基础。
Microbiol Rev. 1985 Mar;49(1):1-32. doi: 10.1128/mr.49.1.1-32.1985.