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本文引用的文献

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Motif-based search for a novel fructosyl peptide oxidase from genome databases.基于模体的新型果糖肽氧化酶的基因组数据库搜索。
Biotechnol Bioeng. 2010 Jun 15;106(3):358-66. doi: 10.1002/bit.22710.
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Molecular replacement with MOLREP.使用MOLREP进行分子置换。
Acta Crystallogr D Biol Crystallogr. 2010 Jan;66(Pt 1):22-5. doi: 10.1107/S0907444909042589. Epub 2009 Dec 21.
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Crystal structure of the deglycating enzyme fructosamine oxidase (amadoriase II).去糖化酶果糖胺氧化酶(氨基脱氧酮糖还原酶II)的晶体结构
J Biol Chem. 2008 Oct 3;283(40):27007-16. doi: 10.1074/jbc.M804885200. Epub 2008 Jul 30.
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Enhancement of thermostability of fungal deglycating enzymes by directed evolution.通过定向进化提高真菌去糖基化酶的热稳定性。
Appl Microbiol Biotechnol. 2008 Apr;78(5):775-81. doi: 10.1007/s00253-008-1363-z. Epub 2008 Feb 1.
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An enzymatic method for the determination of hemoglobinA(1C).一种测定糖化血红蛋白A1C的酶法。
Biotechnol Lett. 2005 Jul;27(14):963-8. doi: 10.1007/s10529-005-7832-x.
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Enzymes used for the determination of HbA1C.用于测定糖化血红蛋白A1C的酶。
FEMS Microbiol Lett. 2004 Jun 1;235(1):157-62. doi: 10.1016/j.femsle.2004.04.027.
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Molecular cloning and expression of novel fructosyl peptide oxidases and their application for the measurement of glycated protein.新型果糖基肽氧化酶的分子克隆、表达及其在糖化蛋白测定中的应用
Biochem Biophys Res Commun. 2003 Nov 7;311(1):104-11. doi: 10.1016/j.bbrc.2003.09.169.
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Candidate reference methods for hemoglobin A1c based on peptide mapping.基于肽图谱分析的糖化血红蛋白A1c候选参考方法。
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9
Comparative evaluation of three assay systems for automated determination of hemoglobin A1c.三种用于自动测定糖化血红蛋白A1c的检测系统的比较评估
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How to measure and predict the molar absorption coefficient of a protein.如何测量和预测蛋白质的摩尔吸收系数。
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两种真核果糖基肽氧化酶的结晶及初步晶体学分析

Crystallization and preliminary crystallographic analysis of two eukaryotic fructosyl peptide oxidases.

作者信息

Ichiyanagi Atsushi, Hirokawa Kozo, Gomi Keiko, Nakatsu Toru, Kato Hiroaki, Kajiyama Naoki

机构信息

Research and Development Division, Kikkoman Corporation, 399 Noda, Noda-shi, Chiba 278-0037, Japan.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2013 Feb 1;69(Pt 2):130-3. doi: 10.1107/S1744309112051445. Epub 2013 Jan 30.

DOI:10.1107/S1744309112051445
PMID:23385752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3564613/
Abstract

Fructosyl peptide oxidase (FPOX) catalyses the oxidation of α-glycated dipeptides such as N(α)-(1-deoxy-D-fructos-1-yl)-L-valyl-L-histidine (Fru-ValHis) and is used in the diagnosis of diabetes mellitus. Here, two thermostable mutants of FPOX, CFP-T7 and EFP-T5M, were crystallized by the sitting-drop vapour-diffusion method. The crystal of CFP-T7 belonged to the tetragonal space group P4(1)2(1)2, with unit-cell parameters a = b = 110.09, c = 220.48 Å, and that of EFP-T5M belonged to the monoclinic space group P2(1), with unit-cell parameters a = 43.00, b = 230.05, c = 47.27 Å, β = 116.99°. The crystals of CFP-T7 and EFP-T5M diffracted to 1.8 and 1.6 Å resolution, respectively.

摘要

果糖基肽氧化酶(FPOX)催化α-糖化二肽的氧化,如N(α)-(1-脱氧-D-果糖-1-基)-L-缬氨酰-L-组氨酸(Fru-ValHis),并用于糖尿病的诊断。在此,通过坐滴气相扩散法使FPOX的两个热稳定突变体CFP-T7和EFP-T5M结晶。CFP-T7的晶体属于四方晶系空间群P4(1)2(1)2,晶胞参数a = b = 110.09,c = 220.48 Å,EFP-T5M的晶体属于单斜晶系空间群P2(1),晶胞参数a = 43.00,b = 230.05,c = 47.27 Å,β = 116.99°。CFP-T7和EFP-T5M的晶体分别衍射至1.8 Å和1.6 Å的分辨率。