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CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
bifunctional LKR/SDH cDNA and monofunctional LKR cDNA are cloned, expression in Saccharomyces cerevisiae mutant lys1, but LKR cannot complement yeast LKR null mutant because of its uni-directional catabolic activity, overexpression in wild type yeast
cloning of cDNA encoding the bifunctional protein with lysine 2-oxoglutarate reductase EC 1.5.1.8 and saccharopine dehydrogenase EC 1.5.1.9 activities, expression of the single gene is subject to spatial and developmental controls, expression in Escherichia coli produces no active LKR, perhaps because of a missing post-translational modification in prokaryotes, expression in Saccharomyces cerevisiae mutant lys1
gene LKR/SDH, transcriptomic profiling of Arabidopsis thaliana under biotic and abiotic stresses. In Arabidopsis, a monofunctional SDH probably produced from the same gene encoding the bifunctional enzyme localizes in the mitochondria
isolation and cloning of the cDNA and single copy gene encoding bifunctional enzyme with lysine-ketoglutarate reductase EC 1.5.1.8 and saccharopine dehydrogenase EC 1.5.1.9, no expression in Escherichia coli, gene product with amino domain corresponding to LKR and carboxy domain corresponding to SDH
isolation of the cDNA and gene encoding bifunctional enzyme with lysine-ketoglutarate reductase EC 1.5.1.8 and saccharopine dehydrogenase EC 1.5.1.9 activities