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
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2.3.1.155
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beta-oxidation
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chondrodysplasia
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rhizomelic
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punctata
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acetoacetyl-coa
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presequence
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refsum
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very-long-chain
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phytanic
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straight-chain
- 2.3.1.155
-
beta-oxidation
-
chondrodysplasia
-
rhizomelic
- punctata
- acetoacetyl-coa
- presequence
-
refsum
-
very-long-chain
-
phytanic
-
straight-chain
Reaction
Synonyms
3-oxopalmitoyl-CoA hydrolase, 3-oxopalmitoyl-CoA-CoA acetyltransferase, peroxisomal 3-ketoacyl-CoA thiolase
ECTree
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Disease
Disease on EC 2.3.1.155 - acetyl-CoA C-myristoyltransferase
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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.
acetyl-coa c-myristoyltransferase deficiency
[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.
Chondrodysplasia Punctata, Rhizomelic
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.
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