5MI2
The study of the X-ray induced enzymatic reduction of molecular oxygen to water for laccase from Steccherinum murashkinskyi.The 10-th structure of the series with total exposition time 273 min.
Summary for 5MI2
| Entry DOI | 10.2210/pdb5mi2/pdb |
| Descriptor | Laccase 2, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, COPPER (II) ION, ... (7 entities in total) |
| Functional Keywords | multi copper oxidase, laccase, complex with molecular oxygen, oxidoreductase |
| Biological source | Steccherinum murashkinskyi |
| Total number of polymer chains | 1 |
| Total formula weight | 59964.95 |
| Authors | Polyakov, K.M.,Gavryushov, S.,Fedorova, T.V.,Glazunova, O.A.,Popov, A.N. (deposition date: 2016-11-27, release date: 2017-05-10, Last modification date: 2024-10-23) |
| Primary citation | Polyakov, K.M.,Gavryushov, S.,Ivanova, S.,Fedorova, T.V.,Glazunova, O.A.,Popov, A.N.,Koroleva, O.V. Structural study of the X-ray-induced enzymatic reduction of molecular oxygen to water by Steccherinum murashkinskyi laccase: insights into the reaction mechanism. Acta Crystallogr D Struct Biol, 73:388-401, 2017 Cited by PubMed Abstract: The laccase from Steccherinum murashkinskyi is a member of the large family of multicopper oxidases that catalyze the oxidation of a wide range of organic and inorganic substrates, accompanied by the reduction of dioxygen to water. The reducing properties of X-ray radiation and the high quality of the laccase crystals allow the study of the catalytic reduction of dioxygen to water directly in a crystal. A series of diffraction data sets with increasing absorbed radiation dose were collected from a single crystal of Steccherinum murashkinskyi laccase at 1.35 Å resolution. Changes in the active-site structure associated with the reduction of molecular oxygen to water on increasing the absorbed dose of ionizing radiation were detected. The structures in the series are mixtures of different states of the enzyme-substrate complex. Nevertheless, it was possible to interpret these structures as complexes of various oxygen ligands with copper ions in different oxidation states. The results allowed the mechanism of oxygen reduction catalyzed by laccases to be refined. PubMed: 28471364DOI: 10.1107/S2059798317003667 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.35 Å) |
Structure validation
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