NADH/NADPH bi-cofactor-utilizing and thermoactive ketol-acid reductoisomerase from Sulfolobus acidocaldarius
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Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-25361-4.pdf
Reference47 articles.
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2. Armstrong, F. B., Lipscomb, E. L., Crout, D. H. G., Mitchell, M. B. & Prakash, S. R. Biosynthesis of valine and isoleucine: synthesis and biological activity of (2S)-α-acetolactic acid (2-hydroxy-2-methyl-3-oxobutanoic acid), and (2R)- and (2S)-α-acetohydroxybutyric acid (2-ethyl-2-hydroxy-3-oxobutanoic acid). J Chem Soc Perkin Trans 1, 1197–1201 (1983).
3. Hill, R. K., Sawada, S. & Arfin, S. M. Stereochemistry of valine and isoleucine biosynthesis: IV. Synthesis, configuration, and enzymatic specificity of α-acetolactate and α-aceto-α-hydroxybutyrate. Bioorg Chem 8, 175–189 (1979).
4. Chunduru, S., Mrachko, G. & Calvo, K. Mechanism of ketol acid reductoisomerase. Steady-state analysis and metal ion requirement. Biochemistry 28, 486–493 (1989).
5. Dumas, R., Biou, V., Halgand, F., Douce, R. & Duggleby, R. G. Enzymology, structure, and dynamics of acetohydroxy acid isomeroreductase. Acc Chem Res 34, 399–408 (2001).
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