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醛糖还原酶和醛脱氢酶抑制剂结合位点的结构特征。

Structural features of the aldose reductase and aldehyde reductase inhibitor-binding sites.

作者信息

El-Kabbani O, Wilson D K, Petrash M, Quiocho F A

机构信息

Department of Medicinal Chemistry, Victorian College of Pharmacy, Monash University, Parkville, Victoria, Australia.

出版信息

Mol Vis. 1998 Sep 29;4:19.

PMID:9756955
Abstract

The three-dimensional structures of aldose reductase and aldehyde reductase, members of the aldo-keto reductase superfamily, are composed of similar alpha/beta TIM-barrels. However, examination of the structures reveals that the inhibitor-binding site of aldose reductase differs from that of aldehyde reductase due to the participation of non-conserved residues in its formation. This information will be useful in the design of inhibitors to prevent or delay diabetic retinopathy. A review of the structures of the inhibitor-binding sites is presented.

摘要

醛糖还原酶和醛还原酶属于醛酮还原酶超家族,它们的三维结构由相似的α/β桶状结构组成。然而,对这些结构的研究表明,醛糖还原酶的抑制剂结合位点与醛还原酶的不同,这是由于非保守残基参与了其形成过程。这些信息将有助于设计预防或延缓糖尿病视网膜病变的抑制剂。本文对抑制剂结合位点的结构进行了综述。

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