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    Arch Biochem Biophys. 1990 Aug 15;281(1):124-31.

    Vanadyl(IV) complexes with pyruvate kinase: activation of the enzyme and electron paramagnetic resonance properties of ternary complexes with the protein.

    Source

    Institute for Enzyme Research, Graduate School, University of Wisconsin, Madison 53705.

    Abstract

    Complexes of the oxocation of vanadyl(IV), VO2+, with pyruvate kinase from rabbit muscle have been investigated by steady-state kinetic assays and by EPR spectroscopy. Pyruvate kinase requires 2 eq of divalent cation for activity. VO2+ alone is a poor activator of the normal physiological reaction catalyzed by the enzyme and of the enzyme-catalyzed exchange of the methyl protons of pyruvate with solvent. VO2+ alone is, however, an activator of the enzyme-catalyzed phosphorylation of glycolate by ATP. VO2+ is more effective than Mg2+ in activation of the bicarbonate-dependent ATPase reaction of pyruvate kinase, and in the enzyme-catalyzed hydrolysis of phosphoenolpyruvate. EPR data show that VO2+ binds to the divalent cation site on the protein competitively with respect to Mg2+. The VO2+-enzyme complex has a high affinity for bicarbonate. Direct coordination of pyruvate, oxalate, and glycolate to the enzyme-bound VO2+ has been established by EPR measurements with specifically 17O-labeled forms of these compounds.

    PMID:
    2166476
    [PubMed - indexed for MEDLINE]

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