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Results 1 - 2 of 2
EC Number Protein Variants Commentary Reference
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9S586A 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
Show all pathways known for 1.3.8.9Display the word mapDisplay the reaction diagram Show all sequences 1.3.8.9T409M the mutation is associated with partial carnitine palmitoyltransferase II deficiency 741034
Results 1 - 2 of 2