In enzymology, 20-ñ-hydroxysteroid dehydrogenase () is an enzyme that catalyzes the chemical reaction
The two substrates of this enzyme are 17ñ,20ñ-dihydroxypregn-4-en-3-one and oxidised nicotinamide adenine dinucleotide phosphate (NADP<sup>+</sup>). Its products are 17ñ-hydroxyprogesterone, reduced NADPH, and a proton.
This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD<sup>+</sup> or NADP<sup>+</sup> as acceptor. The systematic name of this enzyme class is 20alpha-hydroxysteroid:NAD(P)<sup>+</sup> 20-oxidoreductase. Other names in common use include 20alpha-hydroxy steroid dehydrogenase, 20alpha-hydroxy steroid dehydrogenase, 20alpha-HSD, and 20alpha-HSDH. This enzyme participates in c21-steroid hormone metabolism.
20alpha-HSD has been initially described as a progesterone metabolizing enzyme of the ovary. On a functional level, ovarian 20alpha-HSD is actively involved in the control of progesterone homeostasis in pregnancy of rats and mice. While 20alpha-HSD expression and activity is downregulated in the corpus luteum of pregnancy, 24 hrs prior to parturition ovarian 20alpha-HSD activity is acutely stimulated. Accordingly, in mice with targeted deletion of the 20alpha-HSD gene, progesterone blood concentration remain high throughout pregnancy which results in a delay of 2âÂÂ4 days in parturition. Indicating that expression of 20alpha-HSD activity is mandatory for the induction of parturition through reduction of progesterone blood concentration. In mice, 20alpha-HSD is also expressed in the adrenals, kidneys, brain, thymus, T cells and bone marrow. Its induction in hematopoietic cells was used as an assay for the identification of T cell derived factor interleukin-3. In addition, the enzyme reduces and inactivates 17-deoxycorticosterone, the precursor of aldosterone and corticosterone.
As of late 2007, 3 structures have been solved for this class of enzymes, with PDB accession codes (AKR1C1), , and .
AKR1C1, AKR1C2, and AKR1C3
AKR1C1 has high catalytic efficiency as a 20ñ-HSD and AKR1C2 and AKR1C3 efficiently catalyze this reaction as well.