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Results 1 - 10 of 14

EC Number	Natural Substrates	Commentary (Nat. Sub.)
1.3.8.6	glutaryl-CoA + acceptor	-
1.3.8.6	glutaryl-CoA + acceptor	involved in mitochondrial degradation of lysine, hydroxylysine, tryptophan
1.3.8.6	glutaryl-CoA + acceptor	analysis of mutations causing glutaric acidemia type I
1.3.8.6	glutaryl-CoA + acceptor	deficiency causes glutaric aciduria type I, study on activities in wild type and mutants
1.3.8.6	glutaryl-CoA + acceptor	part of the degradative pathway of the amino acids tryptophan, lysine, and hydroxylysine, enzyme deficiency leads to glutaric aciduria type I leading to nonspecific developmental delay, hypotonia, and macrocephaly with cerebral atrophyof prenatal onset
1.3.8.6	glutaryl-CoA + electron transfer flavoprotein	-
1.3.8.6	glutaryl-CoA + electron transfer protein	-
1.3.8.6	glutaryl-CoA + electron-transfer flavoprotein	overall reaction
1.3.8.6	glutaryl-CoA + FAD	-
1.3.8.6	glutaryl-CoA + FAD	via intermediate glutaconyl-CoA

Results 1 - 10 of 14

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Release 2023.1 (January 2023)