Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1991243 | The Journal of Steroid Biochemistry and Molecular Biology | 2016 | 19 Pages |
•Known structures of androgen metabolizing enzymes are reviewed.•Structural analysis of enzyme-ligand complexes are included.•Structural insights used in inhibitor design are discussed.
Androgen-metabolizing enzymes convert cholesterol, a relatively inert molecule, into some of the most potent chemical messengers in vertebrates. This conversion involves thermodynamically challenging reactions catalyzed by P450 enzymes and redox reactions catalyzed by Aldo-Keto Reductases (AKRs). This review covers the structures of these enzymes with a focus on active site interactions and proposed mechanisms. Due to their role in a number of diseases, particularly in cancer, androgen-metabolizing enzymes have been targets of drug design. Hence we will also highlight how existing knowledge of structure is being used to this end.