5KWF
Joint X-ray Neutron Structure of Cholesterol Oxidase
5KWF の概要
| エントリーDOI | 10.2210/pdb5kwf/pdb |
| 分子名称 | Cholesterol oxidase, FLAVIN-ADENINE DINUCLEOTIDE (3 entities in total) |
| 機能のキーワード | oxidoreductase, isomerase |
| 由来する生物種 | Streptomyces sp. (strain SA-COO) |
| 細胞内の位置 | Secreted: P12676 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 56584.09 |
| 構造登録者 | Golden, E.,Vrielink, A.,Meilleur, F.,Blakeley, M. (登録日: 2016-07-18, 公開日: 2017-02-01, 最終更新日: 2024-03-06) |
| 主引用文献 | Golden, E.,Yu, L.J.,Meilleur, F.,Blakeley, M.P.,Duff, A.P.,Karton, A.,Vrielink, A. An extended N-H bond, driven by a conserved second-order interaction, orients the flavin N5 orbital in cholesterol oxidase. Sci Rep, 7:40517-40517, 2017 Cited by PubMed Abstract: The protein microenvironment surrounding the flavin cofactor in flavoenzymes is key to the efficiency and diversity of reactions catalysed by this class of enzymes. X-ray diffraction structures of oxidoreductase flavoenzymes have revealed recurrent features which facilitate catalysis, such as a hydrogen bond between a main chain nitrogen atom and the flavin redox center (N5). A neutron diffraction study of cholesterol oxidase has revealed an unusual elongated main chain nitrogen to hydrogen bond distance positioning the hydrogen atom towards the flavin N5 reactive center. Investigation of the structural features which could cause such an unusual occurrence revealed a positively charged lysine side chain, conserved in other flavin mediated oxidoreductases, in a second shell away from the FAD cofactor acting to polarize the peptide bond through interaction with the carbonyl oxygen atom. Double-hybrid density functional theory calculations confirm that this electrostatic arrangement affects the N-H bond length in the region of the flavin reactive center. We propose a novel second-order partial-charge interaction network which enables the correct orientation of the hydride receiving orbital of N5. The implications of these observations for flavin mediated redox chemistry are discussed. PubMed: 28098177DOI: 10.1038/srep40517 主引用文献が同じPDBエントリー |
| 実験手法 | NEUTRON DIFFRACTION (2.214 Å) X-RAY DIFFRACTION (1.499 Å) |
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