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5KWF

Joint X-ray Neutron Structure of Cholesterol Oxidase

5KWF の概要
エントリーDOI10.2210/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: 28098177
DOI: 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)
構造検証レポート
Validation report summary of 5kwf
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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