4ITT

Crystal structure of iron soaked (5 min) ferritin from Pseudo-nitzschia multiseries

4ITT の概要

• エントリーDOI: 10.2210/pdb4itt/pdb
• 関連するPDBエントリー: 4ISM 4ISP 4ITW 4IWJ 4IWK 4IXK
• 分子名称: Ferritin, FE (III) ION (3 entities in total)
• 機能のキーワード: ferritin, 4 helix bundle, iron storage, acetamido-cysteines, transport protein
• 由来する生物種: Pseudo-nitzschia multiseries
• タンパク質・核酸の鎖数: 8
• 化学式量合計: 151270.91

構造登録者

Pfaffen, S.,Murphy, M.E.P. (登録日: 2013-01-18, 公開日: 2013-03-20, 最終更新日: 2017-11-15)

主引用文献

Pfaffen, S.,Abdulqadir, R.,Le Brun, N.E.,Murphy, M.E.
Mechanism of ferrous iron binding and oxidation by ferritin from a pennate diatom.
J.Biol.Chem., 288:14917-14925, 2013

PubMed Abstract: A novel ferritin was recently found in Pseudo-nitzschia multiseries (PmFTN), a marine pennate diatom that plays a major role in global primary production and carbon sequestration into the deep ocean. Crystals of recombinant PmFTN were soaked in iron and zinc solutions, and the structures were solved to 1.65-2.2-Å resolution. Three distinct iron binding sites were identified as determined from anomalous dispersion data from aerobically grown ferrous soaked crystals. Sites A and B comprise the conserved ferroxidase active site, and site C forms a pathway leading toward the central cavity where iron storage occurs. In contrast, crystal structures derived from anaerobically grown and ferrous soaked crystals revealed only one ferrous iron in the active site occupying site A. In the presence of dioxygen, zinc is observed bound to all three sites. Iron oxidation experiments using stopped-flow absorbance spectroscopy revealed an extremely rapid phase corresponding to Fe(II) oxidation at the ferroxidase site, which is saturated after adding 48 ferrous iron to apo-PmFTN (two ferrous iron per subunit), and a much slower phase due to iron core formation. These results suggest an ordered stepwise binding of ferrous iron and dioxygen to the ferroxidase site in preparation for catalysis and a partial mobilization of iron from the site following oxidation.

PubMed: 23548912
DOI: 10.1074/jbc.M113.454496

実験手法

X-RAY DIFFRACTION (2.1 Å)