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1QJE

Isopenicillin N synthase from Aspergillus nidulans (IP1 - Fe complex)

1QJE の概要
エントリーDOI10.2210/pdb1qje/pdb
関連するPDBエントリー1BK0 1QJF
分子名称ISOPENICILLIN N SYNTHASE, SULFATE ION, ISOPENICILLIN N, ... (6 entities in total)
機能のキーワードb-lactam antibiotic, oxygenase, penicillin biosynthesis, enzyme-product complex
由来する生物種Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) (Aspergillus nidulans)
タンパク質・核酸の鎖数1
化学式量合計38438.57
構造登録者
Burzlaff, N.I.,Clifton, I.J.,Rutledge, P.J.,Roach, P.L.,Adlington, R.M.,Baldwin, J.E. (登録日: 1999-06-23, 公開日: 2000-06-29, 最終更新日: 2024-05-08)
主引用文献Burzlaff, N.I.,Rutledge, P.J.,Clifton, I.J.,Hensgens, C.M.H.,Pickford, M.,Adlington, R.M.,Roach, P.L.,Baldwin, J.E.
The Reaction Cycle of Isopenicillin N Synthase Observed by X-Ray Diffraction
Nature, 401:721-, 1999
Cited by
PubMed Abstract: Isopenicillin N synthase (IPNS), a non-haem iron-dependent oxidase, catalyses the biosynthesis of isopenicillin N (IPN), the precursor of all penicillins and cephalosporins. The key steps in this reaction are the two iron-dioxygen-mediated ring closures of the tripeptide delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-valine (ACV). It has been proposed that the four-membered beta-lactam ring forms initially, associated with a highly oxidized iron(iv)-oxo (ferryl) moiety, which subsequently mediates closure of the five-membered thiazolidine ring. Here we describe observation of the IPNS reaction in crystals by X-ray crystallography. IPNS Fe2+ substrate crystals were grown anaerobically, exposed to high pressures of oxygen to promote reaction and frozen, and their structures were elucidated by X-ray diffraction. Using the natural substrate ACV, this resulted in the IPNS x Fe2+ x IPN product complex. With the substrate analogue, delta-(L-alpha-aminoadipoyl)-L-cysteinyl-L-S-methylcysteine (ACmC) in the crystal, the reaction cycle was interrupted at the monocyclic stage. These mono- and bicyclic structures support our hypothesis of a two-stage reaction sequence leading to penicillin. Furthermore, the formation of a monocyclic sulphoxide product from ACmC is most simply explained by the interception of a high-valency iron-oxo species.
PubMed: 10537113
DOI: 10.1038/44400
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.35 Å)
構造検証レポート
Validation report summary of 1qje
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2026-04-22に公開中

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