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本文引用的文献

1
Evolution based on domain combinations: the case of glutaredoxins.基于结构域组合的进化:谷氧还蛋白的实例
BMC Evol Biol. 2009 Mar 25;9:66. doi: 10.1186/1471-2148-9-66.
2
Nuclear activity of ROXY1, a glutaredoxin interacting with TGA factors, is required for petal development in Arabidopsis thaliana.ROXY1是一种与TGA因子相互作用的谷氧还蛋白,其核活性是拟南芥花瓣发育所必需的。
Plant Cell. 2009 Feb;21(2):429-41. doi: 10.1105/tpc.108.064477. Epub 2009 Feb 13.
3
Structure-function relationship of the chloroplastic glutaredoxin S12 with an atypical WCSYS active site.具有非典型WCSYS活性位点的叶绿体谷氧还蛋白S12的结构-功能关系
J Biol Chem. 2009 Apr 3;284(14):9299-310. doi: 10.1074/jbc.M807998200. Epub 2009 Jan 21.
4
STRING 8--a global view on proteins and their functional interactions in 630 organisms.STRING 8——关于630种生物中蛋白质及其功能相互作用的全局视图。
Nucleic Acids Res. 2009 Jan;37(Database issue):D412-6. doi: 10.1093/nar/gkn760. Epub 2008 Oct 21.
5
Comparison of the thiol-dependent antioxidant systems in the ectomycorrhizal Laccaria bicolor and the saprotrophic Phanerochaete chrysosporium.外生菌根双色蜡蘑和腐生黄孢原毛平革菌中硫醇依赖性抗氧化系统的比较。
New Phytol. 2008;180(2):391-407. doi: 10.1111/j.1469-8137.2008.02498.x. Epub 2008 May 28.
6
The role of glutathione in photosynthetic organisms: emerging functions for glutaredoxins and glutathionylation.谷胱甘肽在光合生物中的作用:谷氧还蛋白和谷胱甘肽化的新功能
Annu Rev Plant Biol. 2008;59:143-66. doi: 10.1146/annurev.arplant.59.032607.092811.
7
A glutaredoxin-fused thiol peroxidase acts as an important player in hydrogen peroxide detoxification in late-phased growth of Anabaena sp. PCC7120.一种谷氧还蛋白融合的硫醇过氧化物酶在鱼腥藻PCC7120生长后期的过氧化氢解毒过程中起着重要作用。
Arch Biochem Biophys. 2008 Jul 1;475(1):42-9. doi: 10.1016/j.abb.2008.04.006. Epub 2008 Apr 13.
8
Chloroplast monothiol glutaredoxins as scaffold proteins for the assembly and delivery of [2Fe-2S] clusters.叶绿体单硫醇谷氧还蛋白作为用于组装和传递[2Fe-2S]簇的支架蛋白。
EMBO J. 2008 Apr 9;27(7):1122-33. doi: 10.1038/emboj.2008.50. Epub 2008 Mar 20.
9
Identification of FRA1 and FRA2 as genes involved in regulating the yeast iron regulon in response to decreased mitochondrial iron-sulfur cluster synthesis.鉴定FRA1和FRA2为参与调控酵母铁调节子以响应线粒体铁硫簇合成减少的基因。
J Biol Chem. 2008 Apr 18;283(16):10276-86. doi: 10.1074/jbc.M801160200. Epub 2008 Feb 15.
10
Biochemical characterization of glutaredoxins from Chlamydomonas reinhardtii reveals the unique properties of a chloroplastic CGFS-type glutaredoxin.莱茵衣藻谷氧还蛋白的生化特性揭示了叶绿体CGFS型谷氧还蛋白的独特性质。
J Biol Chem. 2008 Apr 4;283(14):8868-76. doi: 10.1074/jbc.M709567200. Epub 2008 Jan 23.

光合生物中谷氧还蛋白的进化与多样性

Evolution and diversity of glutaredoxins in photosynthetic organisms.

作者信息

Couturier Jérémy, Jacquot Jean-Pierre, Rouhier Nicolas

机构信息

Interactions Arbres Microorganismes, IFR 110 Génomique Ecophysiologie et Ecologie Fonctionnelles, Unité Mixte de Recherches 1136 INRA-Nancy Université, 54506 Vandoeuvre-lès-Nancy Cedex, France.

出版信息

Cell Mol Life Sci. 2009 Aug;66(15):2539-57. doi: 10.1007/s00018-009-0054-y. Epub 2009 Jun 9.

DOI:10.1007/s00018-009-0054-y
PMID:19506802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11115520/
Abstract

The genome sequencing of prokaryotic and eukaryotic photosynthetic organisms enables a comparative genomic study of the glutaredoxin (Grx) family. The analysis of 58 genomes, using a specific motif composed of the active site sequence and of amino acids involved in glutathione binding, led to an updated classification of Grxs into six classes. Only two classes (I and II) are common to all photosynthetic organisms. Eukaryotes and cyanobacteria have two specific Grx classes (classes III and IV and classes V and VI, respectively). The classes IV, V and VI have not yet been identified and contain multimodular Grx fusions. In addition, putative Grx partners were identified from the presence of fusion proteins, the conservation of gene order in bacterial operons, and the gene co-occurrence. The genes encoding class II Grxs and BolA/YrbA proteins are frequently adjacent, in the same transcriptional orientation in prokaryote genomes and present in the same organisms.

摘要

对原核生物和真核生物光合生物体进行基因组测序,有助于对谷氧还蛋白(Grx)家族开展比较基因组研究。利用由活性位点序列和参与谷胱甘肽结合的氨基酸组成的特定基序,对58个基因组进行分析,从而将Grx更新分类为六个类别。所有光合生物体都共有仅两个类别(I和II)。真核生物和蓝细菌分别有两个特定的Grx类别(III和IV类以及V和VI类)。IV、V和VI类尚未得到鉴定,且包含多模块Grx融合体。此外,通过融合蛋白的存在、细菌操纵子中基因顺序的保守性以及基因共现情况,鉴定出了假定的Grx伙伴。编码II类Grx和BolA/YrbA蛋白的基因常常相邻,在原核生物基因组中具有相同的转录方向,且存在于相同的生物体中。