NMR Studies of the Stability, Protonation States, and Tautomerism of 13C- and 15N-Labeled Aldimines of the Coenzyme Pyridoxal 5′-Phosphate in Water
Author:
Affiliation:
1. Institut für Chemie und Biochemie, Freie Universität Berlin, Takustrasse 3, D-14195 Berlin, Germany
2. Department of Chemistry, University of California-Davis, Davis, California 95616, United States
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi101061m
Reference45 articles.
1. Metzler, D. E. (1977) Biochemistry. The chemical reactions of living cells, Vol.1, pp444−461,Academic Press,New York.
2. The mechanism of the transamination reaction
3. Semicarbazone Formation from Pyridoxal, Pyridoxal Phosphate, and Their Schiff Bases
4. Kinetics and equilibriums of the reaction of pyridoxal 5'-phosphate with ethylenediamine to form Schiff bases and cyclic geminal diamines. Evidence for kinetically competent geminal diamine intermediates in transimination sequences
5. Serine transhydroxymethylase. Relaxation and transient kinetic study of the formation and interconversion of the enzyme-glycine complexes.
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