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3alpha-hydroxysteroid dehydrogenase (B-specific)

Enzyme From Wikipedia, the free encyclopedia

3alpha-hydroxysteroid dehydrogenase (B-specific)
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In enzymology, a 3alpha-hydroxysteroid dehydrogenase (B-specific) (EC 1.1.1.50) is an enzyme that catalyzes the chemical reaction

 
 
 
H+
Reversible left-right reaction arrow with minor forward product(s) to top right and minor reverse substrate(s) from bottom right
 
H+
 
Thumb
5α-Androstane-3,17-dione
 
Quick facts 3-alpha-hydroxysteroid dehydrogenase (B-specific), Identifiers ...

The two substrates of this enzyme are androsterone and oxidised nicotinamide adenine dinucleotide (NAD+). Its products are 5α-androstane-3,17-dione, reduced NADH, and a proton. The alternative cofactor nicotinamide adenine dinucleotide phosphate is also used by this enzyme.[1][2][3][4][5]

The enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor, more specifically it is part of the group of hydroxysteroid dehydrogenases. The systematic name of this enzyme class is 3alpha-hydroxysteroid:NAD(P)+ oxidoreductase (B-specific). Other names in common use include hydroxyprostaglandin dehydrogenase, 3alpha-hydroxysteroid oxidoreductase, and sterognost 3alpha. This enzyme participates in 3 metabolic pathways: bile acid biosynthesis, c21-steroid hormone metabolism, and androgen and estrogen metabolism.

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Structural studies

As of late 2007, 7 structures have been solved for this class of enzymes, with PDB accession codes 1AFS, 1FJH, 1FK8, 1LWI, 1RAL, 2DKN, and 2FVL.

References

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