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On the relationships of substrate orientation, hydrogen abstraction, and product stereochemistry in single and double dioxygenations by soybean lipoxygenase-1 and its Ala542Gly mutant.

Coffa G, Imber AN, Maguire BC, Laxmikanthan G, Schneider C, Gaffney BJ, Brash AR
J Biol Chem. 2005 280 (46): 38756-66

PMID: 16157595 · PMCID: PMC1351262 · DOI:10.1074/jbc.M504870200

MeSH Terms (39)

Alanine Arachidonic Acid Binding Sites Catalysis Chromatography, Gas Chromatography, High Pressure Liquid Cloning, Molecular DNA Primers Dose-Response Relationship, Drug Electron Spin Resonance Spectroscopy Esters Glycine Hydrogen Hydrogen-Ion Concentration Iron Kinetics Leukotrienes Linoleic Acid Linoleic Acids Lipid Peroxides Lipoxygenase Magnetic Resonance Spectroscopy Magnetics Mass Spectrometry Models, Chemical Models, Molecular Mutagenesis Mutation Oxygen Plasmids Protein Binding Protein Conformation Protein Structure, Tertiary Software Soybeans Stereoisomerism Substrate Specificity Time Factors Ultraviolet Rays

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