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5M22

Crystal structure of hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3

Summary for 5M22
Entry DOI10.2210/pdb5m22/pdb
DescriptorHydroquinone dioxygenase small subunit, Hydroquinone dioxygenase large subunit, FE (III) ION, ... (4 entities in total)
Functional Keywordsoxidoreductase
Biological sourceSphingomonas sp. TTNP3
More
Total number of polymer chains8
Total formula weight227465.77
Authors
Ferraroni, M.,Da Vela, S.,Scozzafava, A.,Kolvenbach, B.,Corvini, P.F.X. (deposition date: 2016-10-11, release date: 2017-09-27, Last modification date: 2024-01-17)
Primary citationFerraroni, M.,Da Vela, S.,Kolvenbach, B.A.,Corvini, P.F.,Scozzafava, A.
The crystal structures of native hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3 and of substrate and inhibitor complexes.
Biochim. Biophys. Acta, 1865:520-530, 2017
Cited by
PubMed Abstract: The crystal structure of hydroquinone 1,2-dioxygenase, a Fe(II) ring cleaving dioxygenase from Sphingomonas sp. strain TTNP3, which oxidizes a wide range of hydroquinones to the corresponding 4-hydroxymuconic semialdehydes, has been solved by Molecular Replacement, using the coordinates of PnpCD from Pseudomonas sp. strain WBC-3. The enzyme is a heterotetramer, constituted of two subunits α and two β of 19 and 38kDa, respectively. Both the two subunits fold as a cupin, but that of the small α subunit lacks a competent metal binding pocket. Two tetramers are present in the asymmetric unit. Each of the four β subunits in the asymmetric unit binds one Fe(II) ion. The iron ion in each β subunit is coordinated to three protein residues, His258, Glu264, and His305 and a water molecule. The crystal structures of the complexes with the substrate methylhydroquinone, obtained under anaerobic conditions, and with the inhibitors 4-hydroxybenzoate and 4-nitrophenol were also solved. The structures of the native enzyme and of the complexes present significant differences in the active site region compared to PnpCD, the other hydroquinone 1,2-dioxygenase of known structure, and in particular they show a different coordination at the metal center.
PubMed: 28232026
DOI: 10.1016/j.bbapap.2017.02.013
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

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