Resolution of the diastereoisomers generated by the chemical reduction of the pyruvate-lysine schiff's base
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference19 articles.
1. The Mechanism of 2-Keto-3-deoxy-6-phosphogluconic Aldolase
2. Aldolase Catalysis: Single Base-Mediated Proton Activation
3. Confirmation of a Trimeric Subunit Arrangement for 2-Keto-3-deoxy-6-phosphogluconic Aldolase Using X-ray Crystallographic Methods
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1. N5-(1-Carboxyethyl) Ornithine and Related (n-Carboxyalkyl)-Amino Acids: Structure, Biosynthesis, and Function;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
2. N5-( -1-Carboxyethyl)- -Ornithine:NADP+ Oxidoreductase from Streptococcus lactis;Journal of Biological Chemistry;1989-06
3. N6-(1-carboxyethyl)lysine formation by Streptococcus lactis. Purification, synthesis, and stereochemical structure.;Journal of Biological Chemistry;1988-02
4. On the interaction of tritiated 2-ketobutyrate with 2-keto-3-deoxygluconate-6P aldolase ofPseudomonas putida. Evidence suggesting enzyme-mediated, uncatalyzed tritium exchange;Journal of Protein Chemistry;1983-10
5. Pyruvate-specific lyases as models of the aldolase reaction;Trends in Biochemical Sciences;1981-01
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