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Titlebook: Biochemistry of Vitamin B6; Proceedings of the 7 Timo K. Korpela,Philipp Christen Conference proceedings 1987 Birkhäuser Verlag Basel 1987

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https://doi.org/10.1007/978-3-663-13222-6fe in vivo. Components of ai hepatic system that reversibly inactivates TyrAT in the presence of L-cysteine are described. An additional, soluble factor irreversibly inactivates TyrAT during incubation at pH 8.
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Closing Remarksthe blue and white shirts have charmed us all. Their efforts, the friendliness of the people of Turku, and the beautiful midsummer nights have combined to make our week of work together here unforgettable.
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Anlagenauswahl und Dimensionierung,ic acid. Instead, she observed the accumulation of succinate. She had surmised that “possibly a combination of the amino group with some reactive carbohydrate residue takes place; then when splitting and oxidation occur the amino group is retained in the form of a new amino acid”.
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Tarife der Kraftfahrtversicherung,oxal 5′-phosphate was determined from the nucleotide sequence of the gene and the amino acid sequences of tryptic peptides. The primary structure of D- amino acid aminotransferase shows high sequence homology with that of branched-chain amino acid aminotransferase of .. . (the . gene product).
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Genes, Biosynthesis, and Intracellular Processing of the Iso-Enzymes of Aspartate Aminotransferaseurs with t. ∼0.5 min; it can be blocked by dissipating the mitochondrial membrane potential. The ensuing accumulation of the precursor in the cytosol is limited by its rapid proteolytic degradation (t. ∼5 min). Extensive inhibitor studies indicated that the bulk of accumulated pre-mAspAT is degraded
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