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酰基辅酶A脱氢酶的结构与作用机制。

Structure and mechanism of action of the acyl-CoA dehydrogenases.

作者信息

Thorpe C, Kim J J

机构信息

Department of Chemistry and Biochemistry, University of Delaware, Newark 19716, USA.

出版信息

FASEB J. 1995 Jun;9(9):718-25. doi: 10.1096/fasebj.9.9.7601336.

Abstract

Mitochondrial beta-oxidation involves a family of flavoproteins that introduce a C-C double bond into their fatty acyl-CoA substrates. Deficiencies of these acyl-CoA dehydrogenases lead to fatty acid oxidation disorders involving life-threatening episodes of metabolic derangement. This review focuses on the medium chain acyl-CoA dehydrogenase as the best-understood member of its class. The crystal structure of the enzyme and salient features of its substrate specificity and mechanism of action are summarized. The surprising observation of a catalytically essential amino acid residue that nevertheless is not conserved in the acyl-CoA dehydrogenase family is discussed.

摘要

线粒体β-氧化涉及一族黄素蛋白,它们将碳-碳双键引入其脂肪酰辅酶A底物中。这些酰基辅酶A脱氢酶的缺陷会导致脂肪酸氧化紊乱,引发危及生命的代谢紊乱发作。本综述聚焦于中链酰基辅酶A脱氢酶,它是该家族中研究最为透彻的成员。总结了该酶的晶体结构及其底物特异性和作用机制的显著特征。讨论了一个催化必需的氨基酸残基在酰基辅酶A脱氢酶家族中却不保守这一惊人发现。

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