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Qu'est-ce (qui) est Xanthan ketal pyruvate transferase - définition
Xanthan ketal pyruvate transferase
CLASS OF ENZYMES
EC 2.5.1.95; Phosphoenolpyruvate:D-Man-beta-(1-4)-GlcA-beta-(1-2)-D-Man-alpha-(1-3)-D-Glc-beta-(1-4)-D-Glc-alpha-1-diphospho-ditrans,octacis-undecaprenol 4,6-O-(1-carboxyethan-1,1-diyl)transferase
Xanthan ketal pyruvate transferase (, KPT) is an enzyme with systematic name phosphoenolpyruvate:D-Man-beta-(1->4)-GlcA-beta-(1->2)-D-Man-alpha-(1->3)-D-Glc-beta-(1->4)-D-Glc-alpha-1-diphospho-ditrans,octacis-undecaprenol 4,6-O-(1-carboxyethan-1,1-diyl)transferase. This enzyme catalyses the following chemical reaction
Pyruvate dehydrogenase deficiency
CARBOHYDRATE METABOLIC DISORDER CHARACTERIZED BY THE BUILDUP OF LACTIC ACID IN THE BODY AND A VARIETY OF NEUROLOGICAL PROBLEMS AND CAUSED BY A DEFICIENCY OF ONE OF THE THREE ENZYMES IN THE PYRUVATE DEHYDROGENASE COMPLEX
Pyruvate dehydrogenase complex deficiency disease; Deficiency of pyruvate dehydrogenase
Pyruvate dehydrogenase deficiency (also known as pyruvate dehydrogenase complex deficiency or PDCD) is a rare neurodegenerative disorders associated with abnormal mitochondrial metabolism. PDCD is a genetic disease resulting from mutations in one of the components of the pyruvate dehydrogenase complex (PDC).
Lysine—pyruvate 6-transaminase
CLASS OF ENZYMES
Lysine--pyruvate 6-transaminase; Lysine-pyruvate 6-transaminase; EC 2.6.1.71; L-lysine:pyruvate aminotransferase
In enzymology, a lysine-pyruvate 6-transaminase () is an enzyme that catalyzes the chemical reaction
