4.2 Article

5β-Reduced steroids and human Δ4-3-ketosteroid 5β-reductase (AKR1D1)

期刊

STEROIDS
卷 83, 期 -, 页码 17-26

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.steroids.2014.01.013

关键词

Bile acid biosynthesis; Steroid metabolism; Enzyme mechanism; Genetics

资金

  1. National Institutes of Health [R01-DK47015, P30-ES13508, F32 (F32-DK089827)]

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5 beta-Reduced steroids are non-planar steroids that have a 900 bend in their structure to create an A/B cis-ring junction. This novel property is required for bile-acids to act as emulsifiers, but in addition 5 beta-reduced steroids have remarkable physiology and may act as potent tocolytic agents, endogenous cardiac glycosides, neurosteroids, and can act as ligands for orphan and membrane bound receptors. In humans there is only a single 5 beta-reductase gene AKR1D1, which encodes Delta(4)-3-ketosteroid-5 beta-reductase (AKR1D1). This enzyme is a member of the aldo-keto reductase superfamily, but possesses an altered catalytic tetrad, in which GIu120 replaces the conserved His residue. This predominant liver enzyme generates all 5 beta-dihydrosteroids in the C-19-C-27 steroid series. Mutations exist in the AKR1D1 gene, which result in loss of protein stability and are causative in bile-acid deficiency. (C) 2014 Elsevier Inc. All rights reserved.

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