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与 6-磷酸葡萄糖酸脱氢酶(来自大肠杆菌和肺炎克雷伯菌)的辅因子/底物结合相关的构象变化:对酶机制的影响。

Conformational changes associated with cofactor/substrate binding of 6-phosphogluconate dehydrogenase from Escherichia coli and Klebsiella pneumoniae: Implications for enzyme mechanism.

机构信息

Institute of Biological Chemistry, Academia Sinica, Taipei 115, Taiwan; Institute of Biochemical Sciences, National Taiwan University, Taipei 106, Taiwan.

出版信息

J Struct Biol. 2010 Jan;169(1):25-35. doi: 10.1016/j.jsb.2009.08.006. Epub 2009 Aug 15.

Abstract

6-Phosphogluconate dehydrogenase (6PGDH), the third enzyme of the pentose phosphate pathway, catalyzes the oxidative decarboxylation of 6-phosphogluconate, making ribulose 5-phosphate, along with the reduction of NADP(+) to NADPH and the release of CO(2). Here, we report the first apo-form crystal structure of the pathogenic Klebsiella pneumoniae 6PGDH (Kp6PGDH) and the structures of the highly homologous Escherichia coli K12 6PGDH (Ec6PGDH) complexed with substrate, substrate/NADPH and glucose at high resolution. The binding of NADPH to one subunit of the homodimeric structure triggered a 10 degrees rotation and resulting in a 7A movement of the coenzyme-binding domain. The coenzyme was thus trapped in a closed enzyme conformation, in contrast to the open conformation of the neighboring subunit. Comparison of our Ec/Kp6PGDH structures with those of other species illustrated how the domain conformation can be affected upon binding of the coenzyme, which in turn gives rise to concomitant movements of two important NADP(+)-interacting amino acids, M14 and N102. We propose that the catalysis follows an ordered binding mechanism with alternating conformational changes in the corresponding subunits, involving several related amino acid residues.

摘要

6-磷酸葡萄糖酸脱氢酶(6PGDH)是戊糖磷酸途径的第三酶,催化 6-磷酸葡萄糖的氧化脱羧,生成核酮糖 5-磷酸,同时将 NADP(+)还原为 NADPH,并释放 CO(2)。在这里,我们报告了第一个致病性肺炎克雷伯氏菌 6PGDH(Kp6PGDH)的apo 形式晶体结构,以及高度同源的大肠杆菌 K12 6PGDH(Ec6PGDH)与底物、底物/NADPH 和葡萄糖结合的结构,分辨率很高。NADPH 与同源二聚体结构的一个亚基结合,引发了 10 度的旋转,导致辅酶结合域移动了 7A。辅酶因此被捕获在封闭的酶构象中,与相邻亚基的开放构象形成对比。比较我们的 Ec/Kp6PGDH 结构与其他物种的结构表明,辅酶结合如何影响结构域构象,进而导致两个重要的 NADP(+)相互作用氨基酸 M14 和 N102 的伴随运动。我们提出,该催化遵循有序结合机制,相应亚基的构象交替变化,涉及几个相关的氨基酸残基。

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