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EC Number
Protein Variants
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Reference
1.3.8.9
S586A
naturally occuring mutation leading to phosphorylation of VLCAD at Ser586 is inhibited in myofibroblasts, resulting in a significant loss of enzyme activity coupled with lipid peroxidation. The S586A mutant shows a significant reduction in electron transfer activity
723908
1.3.8.9
T409M
the mutation is associated with partial carnitine palmitoyltransferase II deficiency
741034
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