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  • Book
    editor-in-chief, Leonard G. Gomella, MD, FACS, ... Show More The Bernard W. Goodwin Professor of Prostate Cancer, Chairman, Department of Urology, Sidney Kimmel Medical College, Associate Director, Jefferson Sidney Kimmel Cancer Center, Clinical Director, Jefferson Sidney Kimmel Cancer Network, Thomas Jefferson University, Philadelphia, Pennsylvania ; associate editors, Gerald Andriole, MD, FACS, [and six others].
    Contents:
    Section I. Urologic diseases and conditions
    Section II. Short topics: A to Z
    Section III. Algorithms
    Section IV. Urinalyasis and urine studies
    Section V. Alternative and complementary urologic therapies
    Section VI. Urologic drug reference
    Section VII. Reference tables.
    Digital Access Ovid 2015
  • Article
    Goto Y, Shimizu J, Okazaki T, Shukuya R.
    J Biochem. 1979 Jul;86(1):71-8.
    Cytosol PEP carboxykinase has been purified to electrophoretic homogeneity from bullfrog liver homogenate. The enzyme is a single polypeptide chain with a molecular weight of approximately 72,000-75,000. The purified enzyme catalyzed oxaloacetate decarboxylation (nucleoside triphosphate-supported), phosphoenolpyruvate carboxylation, and an exchange reaction between oxaloacetate and [14C]HCO3-in the presence of ITP or CTP. Manganese is absolutely required for the enzyme-catalyzed phosphoenolpyruvate carboxylation, whereas it can be replaced by Mg2+ for the oxaloacetate decarboxylation and the exchange reaction. The optimal pH of each reaction is dependent on the divalent metal ion used. The dependence of the enzyme activity on Mn2+ is markedly different in the phosphoenolpyuvate carboxylation and the oxaloacetate decarboxylation reactions.
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