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9RO1

Atomic resolution (1.00 A) XFEL structure of as-isolated copper nitrite reductase from Bradyrhizobium sp. at high pH (7.3) determined by serial femtosecond rotation crystallography (SF-ROX) at 100 K

9RO1 の概要
エントリーDOI10.2210/pdb9ro1/pdb
関連するPDBエントリー9RLL 9RN0 9RNZ
分子名称Copper-containing nitrite reductase, COPPER (II) ION, alpha-D-glucopyranose, ... (6 entities in total)
機能のキーワードcopper-containing nitrite reductase, brjnir, sf-rox, as-isolated, sub-atomic resolution, oxidoreductase
由来する生物種Bradyrhizobium diazoefficiens USDA 110
タンパク質・核酸の鎖数1
化学式量合計37896.64
構造登録者
主引用文献Rose, S.L.,Antonyuk, S.,Ferroni, F.M.,Sugimoto, H.,Yamashita, K.,Hirata, K.,Ago, H.,Ueno, G.,Murakami, H.,Eady, R.R.,Tosha, T.,Yamamoto, M.,Hasnain, S.S.
Accurate atomic resolution XFEL structures of a metalloenzyme reveal key insights into its catalytic mechanism.
Nat Commun, 2026
Cited by
PubMed Abstract: Metalloproteins represent a major fraction of the protein kingdom and often exploit the redox chemistry of transition metals to drive key biological events involving proton and electron transfer. Copper is one of the most widely used transition metals whose redox properties are utilised in both electron transfer and catalysis of chemical substrates. Copper nitrite reductases (CuNiRs) utilise two types of copper centres and have become a model system for studying complex biological events that underpin the reaction mechanisms of redox enzymes, including proton-coupled electron transfer and substrate gating. We utilised the higher X-ray energy (13 keV) available at the SACLA X-ray Free Electron Laser (XFEL) and SHELXL refinement to obtain accurate atomic resolution structures of CuNiRs at ~1 Å from three organisms - in the oxidised (low and high pH), reduced and substrate-bound states. A consistent picture now emerges with the observation of a pentacoordinated oxidised catalytic type-2 Cu (T2Cu) centre in all cases. A tetracoordinated reduced T2Cu site with a single solvent ligand has also been captured, giving structural support to the random-sequential scheme with ordered pathway being dominant.
PubMed: 41794770
DOI: 10.1038/s41467-026-70261-1
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1 Å)
構造検証レポート
Validation report summary of 9ro1
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2026-04-15に公開中

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