1xf0

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1xf0, resolution 2.00Å

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Crystal structure of human 17beta-hydroxysteroid dehydrogenase type 5 (AKR1C3) complexed with delta4-androstene-3,17-dione and NADP

Overview

Human type 5 17beta-hydroxysteroid dehydrogenase (17beta-HSD5;AKR1C3), plays a major role in the metabolism of androgens in peripheral tissues., In prostate basal cells, this enzyme is involved in the transformation of, dehydroepiandrosterone into dihydrotestosterone, the most potent androgen., It is thus a potential target for prostate cancer therapy because it is, understood that the testosterone formation by this enzyme is an important, factor, particularly in patients who have undergone surgical or medical, castration. Here we report the first structure of a human type 5, 17beta-HSD in two ternary complexes, in which we found that the, androstenedione molecule has a different binding position from that of, testosterone. The two testosterone-binding orientations in the, substrate-binding site demonstrate the structural basis of the alternative, binding and multispecificity of the enzyme. Phe306 and Trp227 are the key, residues involved in ligand recognition as well as product release. A, safety belt in the cofactor-binding site enhances nicotinamide adenine, dinucleotide phosphate binding and accounts for its high affinity as, demonstrated by kinetic studies. These structures have provided a dynamic, view of the enzyme reaction converting androstenedione to testosterone as, well as valuable information for the development of potent enzyme, inhibitors.

About this Structure

1XF0 is a Single protein structure of sequence from Homo sapiens with ACT, NAP and ASD as ligands. The following page contains interesting information on the relation of 1XF0 with [Anabolic Steroids]. Full crystallographic information is available from OCA.

Reference

Crystal structures of the multispecific 17beta-hydroxysteroid dehydrogenase type 5: critical androgen regulation in human peripheral tissues., Qiu W, Zhou M, Labrie F, Lin SX, Mol Endocrinol. 2004 Jul;18(7):1798-807. Epub 2004 Apr 15. PMID:15087468

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