Titlebook: Alpha-Keto Acid Dehydrogenase Complexes; Mulchand S. Patel,Thomas E. Roche,Robert A. Harris Book 1996 Birkhäuser Verlag 1996 Molekularbiol

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978-3-0348-9853-9Birkhäuser Verlag 1996

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https://doi.org/10.1007/978-3-7091-5835-7 reactions: the thiamin pyrophosphate (TPP)-dependent decarboxylation of pyruvic acid to 2-hydroxyethylidene-TPP (HETPP) [Eq. 1] and reductive acetylation of lipoic acid residues covalently linked to the second catalytic component — dihydrolipoamide acetyltransferase (E2) [Eq. 2] (Reed, 1974): . Mam

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https://doi.org/10.1007/978-3-7091-5835-7s execute the overall reaction through a series of steps linked by cofactor-mediated active site coupling: the pyruvate dehydrogenase component (E1); the dihydrolipoyl acetyltransferase component (E2); the dihydrolipoyl dehydrogenase component (E3); and the E3-binding component (E3BP, previously pro

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,Some Exact Results on π π Scattering,uirements have led to increasing diversity between these two classes of eukaryotes. Analyses of the pyruvate dehydrogenase complex (PDC) in plant cells serve to illustrate both the similarities inherent in pyruvate metabolism and differences dictated by the need to respond to diverse external stimul

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Lectures on Regge Phenomenology,ita, 1992; Komuniecki and Komuniecki, 1995). Adult ascarid muscle mitochondria use unsaturated organic acids, instead of oxygen, as terminal electron-acceptors and acetate, propionate, succinate, and the 2-methyl branched-chain fatty acids, 2-methylbutyrate and 2-methylvalerate, accumulate as end pr