6YRC
Spectroscopically-validated structure of DtpB from Streptomyces lividans in the ferric state
6YRC の概要
エントリーDOI | 10.2210/pdb6yrc/pdb |
分子名称 | Putative iron-dependent peroxidase, PROTOPORPHYRIN IX CONTAINING FE, 2-(2-(2-(2-(2-(2-ETHOXYETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHOXY)ETHANOL, ... (6 entities in total) |
機能のキーワード | peroxidase; dye-decolourising; spectroscopically-validated, ferric, oxidoreductase |
由来する生物種 | Streptomyces lividans 1326 |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 212786.47 |
構造登録者 | Lucic, M.,Dworkowski, F.S.N.,Worrall, J.A.R.,Hough, M.A. (登録日: 2020-04-20, 公開日: 2021-01-13, 最終更新日: 2024-05-01) |
主引用文献 | Lucic, M.,Svistunenko, D.A.,Wilson, M.T.,Chaplin, A.K.,Davy, B.,Ebrahim, A.,Axford, D.,Tosha, T.,Sugimoto, H.,Owada, S.,Dworkowski, F.S.N.,Tews, I.,Owen, R.L.,Hough, M.A.,Worrall, J.A.R. Serial Femtosecond Zero Dose Crystallography Captures a Water-Free Distal Heme Site in a Dye-Decolorising Peroxidase to Reveal a Catalytic Role for an Arginine in Fe IV =O Formation. Angew.Chem.Int.Ed.Engl., 59:21656-21662, 2020 Cited by PubMed Abstract: Obtaining structures of intact redox states of metal centers derived from zero dose X-ray crystallography can advance our mechanistic understanding of metalloenzymes. In dye-decolorising heme peroxidases (DyPs), controversy exists regarding the mechanistic role of the distal heme residues aspartate and arginine in the heterolysis of peroxide to form the catalytic intermediate compound I (Fe =O and a porphyrin cation radical). Using serial femtosecond X-ray crystallography (SFX), we have determined the pristine structures of the Fe and Fe =O redox states of a B-type DyP. These structures reveal a water-free distal heme site that, together with the presence of an asparagine, imply the use of the distal arginine as a catalytic base. A combination of mutagenesis and kinetic studies corroborate such a role. Our SFX approach thus provides unique insight into how the distal heme site of DyPs can be tuned to select aspartate or arginine for the rate enhancement of peroxide heterolysis. PubMed: 32780931DOI: 10.1002/anie.202008622 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.99 Å) |
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