4EB3
Crystal structure of IspH in complex with iso-HMBPP
4EB3 の概要
| エントリーDOI | 10.2210/pdb4eb3/pdb |
| 関連するPDBエントリー | 3DNF 3F7T 3KE8 |
| 分子名称 | 4-hydroxy-3-methylbut-2-enyl diphosphate reductase, IRON/SULFUR CLUSTER, 3-(hydroxymethyl)but-3-en-1-yl trihydrogen diphosphate, ... (4 entities in total) |
| 機能のキーワード | iron-sulfur protein, reductase, (e)-4-hydroxy-3-methylbut-2-enyl diphosphate (hmbpp), oxidoreductase |
| 由来する生物種 | Escherichia coli |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 73443.35 |
| 構造登録者 | Wang, W.,Wang, K.,Span, I.,Bacher, A.,Groll, M.,Oldfield, E. (登録日: 2012-03-23, 公開日: 2013-02-06, 最終更新日: 2023-09-13) |
| 主引用文献 | Wang, W.,Wang, K.,Span, I.,Jauch, J.,Bacher, A.,Groll, M.,Oldfield, E. Are free radicals involved in IspH catalysis? An EPR and crystallographic investigation. J.Am.Chem.Soc., 134:11225-11234, 2012 Cited by PubMed Abstract: The [4Fe-4S] protein IspH in the methylerythritol phosphate isoprenoid biosynthesis pathway is an important anti-infective drug target, but its mechanism of action is still the subject of debate. Here, by using electron paramagnetic resonance (EPR) spectroscopy and (2)H, (17)O, and (57)Fe isotopic labeling, we have characterized and assigned two key reaction intermediates in IspH catalysis. The results are consistent with the bioorganometallic mechanism proposed earlier, and the mechanism is proposed to have similarities to that of ferredoxin, thioredoxin reductase, in that one electron is transferred to the [4Fe-4S](2+) cluster, which then performs a formal two-electron reduction of its substrate, generating an oxidized high potential iron-sulfur protein (HiPIP)-like intermediate. The two paramagnetic reaction intermediates observed correspond to the two intermediates proposed in the bioorganometallic mechanism: the early π-complex in which the substrate's 3-CH(2)OH group has rotated away from the reduced iron-sulfur cluster, and the next, η(3)-allyl complex formed after dehydroxylation. No free radical intermediates are observed, and the two paramagnetic intermediates observed do not fit in a Birch reduction-like or ferraoxetane mechanism. Additionally, we show by using EPR spectroscopy and X-ray crystallography that two substrate analogues (4 and 5) follow the same reaction mechanism. PubMed: 22687151DOI: 10.1021/ja303445z 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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