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2.3.1.155: acetyl-CoA C-myristoyltransferase

This is an abbreviated version!
For detailed information about acetyl-CoA C-myristoyltransferase, go to the full flat file.

Word Map on EC 2.3.1.155

Reaction

myristoyl-CoA
+
acetyl-CoA
=
CoA
+
3-oxopalmitoyl-CoA

Synonyms

3-oxopalmitoyl-CoA hydrolase, 3-oxopalmitoyl-CoA-CoA acetyltransferase, peroxisomal 3-ketoacyl-CoA thiolase

ECTree

     2 Transferases
         2.3 Acyltransferases
             2.3.1 Transferring groups other than aminoacyl groups
                2.3.1.155 acetyl-CoA C-myristoyltransferase

Disease

Disease on EC 2.3.1.155 - acetyl-CoA C-myristoyltransferase

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
acetyl-coa c-myristoyltransferase deficiency
Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.
[Peroxisomal 3-ketoacyl-CoA thiolase deficiency]
Adrenoleukodystrophy
Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienes.
Carcinoma, Hepatocellular
trans-activation of PPARalpha and induction of PPARalpha target genes by perfluorooctane-based chemicals.
Chondrodysplasia Punctata, Rhizomelic
Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.
Peroxisomal 3-ketoacyl-CoA thiolase is partially processed in fibroblasts from patients with rhizomelic chondrodysplasia punctata.
Zellweger Syndrome
Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.