3BDJ
Crystal Structure of Bovine Milk Xanthine Dehydrogenase with a Covalently Bound Oxipurinol Inhibitor
Summary for 3BDJ
Entry DOI | 10.2210/pdb3bdj/pdb |
Descriptor | Xanthine dehydrogenase/oxidase, CALCIUM ION, FE2/S2 (INORGANIC) CLUSTER, ... (10 entities in total) |
Functional Keywords | oxypurinol, oxipurinol, alloxanthine, allopurinol, covalently bound inhibitor, xanthine oxidase, xanthine oxidoreductase, xanthine dehydrogenase, fad, flavoprotein, iron-sulfur, molybdopterin, peroxisome, oxidoreductase |
Biological source | Bos taurus (Bovine) |
Cellular location | Cytoplasm (By similarity): P80457 |
Total number of polymer chains | 2 |
Total formula weight | 298490.44 |
Authors | Eger, B.T.,Okamoto, K.,Nishino, T.,Pai, E.F.,Nishino, T. (deposition date: 2007-11-14, release date: 2008-11-25, Last modification date: 2023-08-30) |
Primary citation | Okamoto, K.,Eger, B.T.,Nishino, T.,Pai, E.F.,Nishino, T. Mechanism of inhibition of xanthine oxidoreductase by allopurinol: crystal structure of reduced bovine milk xanthine oxidoreductase bound with oxipurinol. Nucleosides Nucleotides Nucleic Acids, 27:888-893, 2008 Cited by PubMed Abstract: Inhibitors of xanthine oxidoreductase block conversion of xanthine to uric acid and are therefore potentially useful for treatment of hyperuricemia or gout. We determined the crystal structure of reduced bovine milk xanthine oxidoreductase complexed with oxipurinol at 2.0 A resolution. Clear electron density was observed between the N2 nitrogen of oxipurinol and the molybdenum atom of the molybdopterin cofactor, indicating that oxipurinol coordinated directly to molybdenum. Oxipurinol forms hydrogen bonds with glutamate 802, arginine 880, and glutamate 1261, which have previously been shown to be essential for the enzyme reaction. We discuss possible differences in the hypouricemic effect of inhibitors, including allopurinol and newly developed inhibitors, based on their mode of binding in the crystal structures. PubMed: 18600558DOI: 10.1080/15257770802146577 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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