首页> 外文期刊>Biochemistry >Structure of the PLP Degradative Enzyme 2-Methyl-3-hydroxypyridine-5-carboxylic Acid Oxygenase from Mesorhizobium loti MAFF303099 and Its Mechanistic Implications
【24h】

Structure of the PLP Degradative Enzyme 2-Methyl-3-hydroxypyridine-5-carboxylic Acid Oxygenase from Mesorhizobium loti MAFF303099 and Its Mechanistic Implications

机译:地上根瘤菌MAFF303099的PLP降解酶2-甲基-3-羟基吡啶-5-羧酸加氧酶的结构及其机理研究

获取原文
获取原文并翻译 | 示例
           

摘要

A vitamin B6 degradative pathway has recently been identified and characterized in Mesorhizobium loti MAFF303099. One of the enzymes on this pathway, 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase (MHPCO), is a flavin-dependent enzyme and catalyzes the oxidative ring-opening of 2-methyl-3-hydroxypyridine-5-carboxylic acid to form E-2-(acetamino-methylene)succinate. The gene for this enzyme has been cloned, and the corresponding protein has been overexpressed in Escherichia coli and purified. The crystal structure of MHPCO has been solved to 2.1 Å using SAD phasing with and without the substrate MHPC bound. These crystal structures provide insight into the reaction mechanism and suggest roles for active site residues in the catalysis of a novel oxidative ring-opening reaction.
机译:最近已经在许多中生根瘤菌MAFF303099中鉴定并表征了维生素B6降解途径。该途径中的一种酶,即2-甲基-3-羟基吡啶-5-羧酸加氧酶(MHPCO),是一种黄素依赖性酶,可催化2-甲基-3-羟基吡啶-5-羧酸的氧化开环。酸形成E-2-(乙酰氨基-亚甲基)琥珀酸酯。该酶的基因已被克隆,相应的蛋白质已在大肠杆菌中过表达并纯化。在有和没有结合底物MHPC的情况下,使用SAD相位已将MHPCO的晶体结构解析为2.1。这些晶体结构提供了对反应机理的了解,并暗示了活性位点残基在新型氧化性开环反应的催化中的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号