1UZW
ISOPENICILLIN N SYNTHASE WITH L-D-(A-AMINOADIPOYL)-L-CYSTEINYL-D-ISODEHYDROVALINE
1UZW の概要
| エントリーDOI | 10.2210/pdb1uzw/pdb |
| 関連するPDBエントリー | 1BK0 1BLZ 1HB1 1HB2 1HB3 1HB4 1IPS 1OBN 1OC1 1ODM 1ODN 1QIQ 1QJE 1QJF |
| 分子名称 | ISOPENICILLIN N SYNTHETASE, FE (II) ION, D-(L-A-AMINOADIPOYL)-L-CYSTEINYL-D-ISODEHYDROVALINE, ... (5 entities in total) |
| 機能のキーワード | b-lactam antibiotic, oxygenase, penicillin biosynthesis, antibiotic biosynthesis, oxidoreductase |
| 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 | 38077.16 |
| 構造登録者 | Grummitt, A.R.,Rutledge, P.J.,Clifton, I.J.,Baldwin, J.E. (登録日: 2004-03-17, 公開日: 2004-06-10, 最終更新日: 2024-05-08) |
| 主引用文献 | Grummitt, A.R.,Rutledge, P.J.,Clifton, I.J.,Baldwin, J.E. Active Site Mediated Elimination of Hydrogen Fluoride from a Fluorinated Substrate Analogue by Isopenicillin N Synthase Biochem.J., 382:659-, 2004 Cited by PubMed Abstract: Isopenicillin N synthase (IPNS) is a non-haem iron oxidase that catalyses the formation of bicyclic isopenicillin N from delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-valine (ACV). In this study we report a novel activity for the iron of the IPNS active site, which behaves as a Lewis acid to catalyse the elimination of HF from the fluorinated substrate analogue, delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-beta-fluorovaline (ACbetaFV). X-Ray crystallographic studies of IPNS crystals grown anaerobically with ACbetaFV reveal that the valinyl beta-fluorine is missing from the active site region, and suggest the presence of the unsaturated tripeptide delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-isodehydrovaline in place of substrate ACbetaFV. (19)F NMR studies confirm the release of fluoride from ACbetaFV in the presence of the active IPNS enzyme. These results suggest a new mode of reactivity for the IPNS iron centre, a mechanism of action that has not previously been reported for any of the iron oxidase enzymes. PubMed: 15175003DOI: 10.1042/BJ20040529 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.3 Å) |
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