5M22
Crystal structure of hydroquinone 1,2-dioxygenase from Sphingomonas sp. TTNP3
Summary for 5M22
Entry DOI | 10.2210/pdb5m22/pdb |
Descriptor | Hydroquinone dioxygenase small subunit, Hydroquinone dioxygenase large subunit, FE (III) ION, ... (4 entities in total) |
Functional Keywords | oxidoreductase |
Biological source | Sphingomonas sp. TTNP3 More |
Total number of polymer chains | 8 |
Total formula weight | 227465.77 |
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 citation | Ferraroni, 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: 28232026DOI: 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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