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Literature summary extracted from

  • Law, L.K.; Tang, N.L.; Tong, M.K.; Mak, T.W.; Wanders, R.J.; Lam, C.W.
    Novel missense mutations in the first Chinese patient with very-long-chain acyl-CoA dehydrogenase deficiency (2007), Clin. Chim. Acta, 375, 173-174.
    View publication on PubMed

Protein Variants

EC Number Protein Variants Comment Organism
1.3.8.8 K259M missense mutation leading to VLCAD deficiency Homo sapiens
1.3.8.8 L462Q missense mutation leading to VLCAD deficiency Homo sapiens

Organism

EC Number Organism UniProt Comment Textmining
1.3.8.8 Homo sapiens P49748
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.3.8.8 fibroblast
-
Homo sapiens
-
1.3.8.8 leukocyte
-
Homo sapiens
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.3.8.8 palmitoyl-CoA + electron-transfer flavoprotein
-
Homo sapiens (2E)-2-hexadecenoyl-CoA + reduced electron-transfer flavoprotein
-
?

Synonyms

EC Number Synonyms Comment Organism
1.3.8.8 very-long-chain acyl-CoA dehydrogenase
-
Homo sapiens
1.3.8.8 VLCAD
-
Homo sapiens