2GAS
Crystal Structure of Isoflavone Reductase
2GAS の概要
| エントリーDOI | 10.2210/pdb2gas/pdb |
| 分子名称 | isoflavone reductase (2 entities in total) |
| 機能のキーワード | nadph-dependent reductase, oxidoreductase |
| 由来する生物種 | Medicago sativa |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 68601.77 |
| 構造登録者 | |
| 主引用文献 | Wang, X.,He, X.,Lin, J.,Shao, H.,Chang, Z.,Dixon, R.A. Crystal Structure of Isoflavone Reductase from Alfalfa (Medicago sativa L.) J.Mol.Biol., 358:1341-1352, 2006 Cited by PubMed Abstract: Isoflavonoids play important roles in plant defense and exhibit a range of mammalian health-promoting activities. Isoflavone reductase (IFR) specifically recognizes isoflavones and catalyzes a stereospecific NADPH-dependent reduction to (3R)-isoflavanone. The crystal structure of Medicago sativa IFR with deletion of residues 39-47 has been determined at 1.6A resolution. Structural analysis, molecular modeling and docking, and comparison with the structures of other NADPH-dependent enzymes, defined the putative binding sites for co-factor and substrate and potential key residues for enzyme activity and substrate specificity. Further mutagenesis has confirmed the role of Lys144 as a catalytic residue. This study provides a structural basis for understanding the enzymatic mechanism and substrate specificity of IFRs as well as the functions of IFR-like proteins. PubMed: 16600295DOI: 10.1016/j.jmb.2006.03.022 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.6 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






