6SV1

Crystal structure of Rhodospirillum rubrum Rru_A0973 E34A variant

6SV1 の概要

• エントリーDOI: 10.2210/pdb6sv1/pdb
• 分子名称: Encapsulated Ferritin, FE (III) ION, CALCIUM ION, ... (4 entities in total)
• 機能のキーワード: encapsulated ferritin, ferroxidase, ferritin, oxidoreductase
• 由来する生物種: Rhodospirillum rubrum
• タンパク質・核酸の鎖数: 30
• 化学式量合計: 401085.89

構造登録者

Marles-Wright, J.,He, D. (登録日: 2019-09-17, 公開日: 2020-09-23, 最終更新日: 2024-01-24)

主引用文献

Piergentili, C.,Ross, J.,He, D.,Gallagher, K.J.,Stanley, W.A.,Adam, L.,Mackay, C.L.,Basle, A.,Waldron, K.J.,Clarke, D.J.,Marles-Wright, J.
Dissecting the structural and functional roles of a putative metal entry site in encapsulated ferritins.
J.Biol.Chem., 295:15511-15526, 2020

PubMed Abstract: Encapsulated ferritins belong to the universally distributed ferritin superfamily, whose members function as iron detoxification and storage systems. Encapsulated ferritins have a distinct annular structure and must associate with an encapsulin nanocage to form a competent iron store that is capable of holding significantly more iron than classical ferritins. The catalytic mechanism of iron oxidation in the ferritin family is still an open question because of the differences in organization of the ferroxidase catalytic site and neighboring secondary metal-binding sites. We have previously identified a putative metal-binding site on the inner surface of the encapsulated ferritin at the interface between the two-helix subunits and proximal to the ferroxidase center. Here we present a comprehensive structural and functional study to investigate the functional relevance of this putative iron-entry site by means of enzymatic assays, MS, and X-ray crystallography. We show that catalysis occurs in the ferroxidase center and suggest a dual role for the secondary site, which both serves to attract metal ions to the ferroxidase center and acts as a flow-restricting valve to limit the activity of the ferroxidase center. Moreover, confinement of encapsulated ferritins within the encapsulin nanocage, although enhancing the ability of the encapsulated ferritin to undergo catalysis, does not influence the function of the secondary site. Our study demonstrates a novel molecular mechanism by which substrate flux to the ferroxidase center is controlled, potentially to ensure that iron oxidation is productively coupled to mineralization.

PubMed: 32878987
DOI: 10.1074/jbc.RA120.014502

実験手法

X-RAY DIFFRACTION (2.19 Å)