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6Y0N

Arginine hydroxylase VioC in complex with Arg, 2OG and Fe under anaerobic environment using FT-SSX methods

6Y0N の概要
エントリーDOI10.2210/pdb6y0n/pdb
関連するPDBエントリー2WBO 6ALR
分子名称Alpha-ketoglutarate-dependent L-arginine hydroxylase, ARGININE, 2-OXOGLUTARIC ACID, ... (5 entities in total)
機能のキーワードiron dependent oxygenase, penicillin biosynthesis, isopenicillin n, oxidoreductase
由来する生物種Streptomyces vinaceus
タンパク質・核酸の鎖数1
化学式量合計39858.35
構造登録者
主引用文献Rabe, P.,Beale, J.H.,Butryn, A.,Aller, P.,Dirr, A.,Lang, P.A.,Axford, D.N.,Carr, S.B.,Leissing, T.M.,McDonough, M.A.,Davy, B.,Ebrahim, A.,Orlans, J.,Storm, S.L.S.,Orville, A.M.,Schofield, C.J.,Owen, R.L.
Anaerobic fixed-target serial crystallography.
Iucrj, 7:901-912, 2020
Cited by
PubMed Abstract: Cryogenic X-ray diffraction is a powerful tool for crystallographic studies on enzymes including oxygenases and oxidases. Amongst the benefits that cryo-conditions (usually employing a nitro-gen cryo-stream at 100 K) enable, is data collection of di-oxy-gen-sensitive samples. Although not strictly anaerobic, at low temperatures the vitreous ice conditions severely restrict O diffusion into and/or through the protein crystal. Cryo-conditions limit chemical reactivity, including reactions that require significant conformational changes. By contrast, data collection at room temperature imposes fewer restrictions on diffusion and reactivity; room-temperature serial methods are thus becoming common at synchrotrons and XFELs. However, maintaining an anaerobic environment for di-oxy-gen-dependent enzymes has not been explored for serial room-temperature data collection at synchrotron light sources. This work describes a methodology that employs an adaptation of the 'sheet-on-sheet' sample mount, which is suitable for the low-dose room-temperature data collection of anaerobic samples at synchrotron light sources. The method is characterized by easy sample preparation in an anaerobic glovebox, gentle handling of crystals, low sample consumption and preservation of a localized anaerobic environment over the timescale of the experiment (<5 min). The utility of the method is highlighted by studies with three X-ray-radiation-sensitive Fe(II)-containing model enzymes: the 2-oxoglutarate-dependent l-arginine hy-droxy-lase VioC and the DNA repair enzyme AlkB, as well as the oxidase isopenicillin N synthase (IPNS), which is involved in the biosynthesis of all penicillin and cephalosporin antibiotics.
PubMed: 32939282
DOI: 10.1107/S2052252520010374
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.86 Å)
構造検証レポート
Validation report summary of 6y0n
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-01-15に公開中

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