The stereochemistry at carbon 3 of pyruvate lyase condensation products. 2-Keto-3-deoxygluconate-6-phosphate aldolase.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference19 articles.
1. The Mechanism of 2-Keto-3-deoxy-6-phosphogluconic Aldolase
2. Reaction of the substrate analog bromopyruvate with two active-site conformers of 2-keto-3-deoxy-6 phosphogluconic aldolase
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4. STUDIES ON THE MECHANISM OF THE ALDOLASE REACTION
5. The Absolute Configuration of Dihydroxyacetone Phosphate Tritiated by Aldolase Reaction1
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Chiral Methyl Groups;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
2. 7 Stereochemistry of Enzyme -Catalyzed Reactions at Carbon;The Enzymes;1990
3. On the interaction of 2-keto-3-deoxygalactonate-6P with 2-keto-3-deoxygluconate-6P aldolase ofPseudomonas putida. Evidence for enzyme-mediated, noncatalytic C-C bond turnover;Journal of Protein Chemistry;1983-10
4. Complete primary structure of 2-keto-3-deoxy-6-phosphogluconate aldolase.;Journal of Biological Chemistry;1980-04
5. Interaction of the chiral pyruvate analog, 2-keto-3-bromobutyrate, with pyruvate lyases. 2-Keto-3-deoxygluconate-6-phosphate aldolase of Pseudomonas putida.;Journal of Biological Chemistry;1979-08
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