Literature DB >> 40612

31P NMR studies on the interaction of deoxyuridylate with thymidylate synthase.

M J Beckage, M Blumenstein, R L Kisliuk.   

Abstract

The 31P nuclear magnetic resonance signal of deoxyuridylate was studied in the presence and absence of thymidlate synthase. In the absence of enzyme the chemical shift of deoxyuridylate is pH dependent with a pKa of 6.25. In the presence of enzyme, a peak corresponding to the dianioinc form of deoxyuridylate is observed which is independent of pH between pH 5.7 and pH 7.4. The pKa of the phosphate in the deoxyuridylate-thymidylate synthase complex is therefore less than 5. The release of inorganic phosphate from deoxyuridylate catalyzed by contaminating phosphatase was also observed.

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Year:  1979        PMID: 40612     DOI: 10.1016/0005-2744(79)90236-5

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  2 in total

1.  19F NMR studies of the binding of 5-fluoro-2'-deoxyuridylate to thymidylate synthase.

Authors:  M J Beckage; M Blumenstein; R L Kisliuk
Journal:  Mol Cell Biochem       Date:  1980-08-29       Impact factor: 3.396

2.  Thymidylate synthetase - substrate complex formation.

Authors:  P V Danenberg; A Lockshin
Journal:  Mol Cell Biochem       Date:  1982-03-05       Impact factor: 3.396

  2 in total

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