Abstract
In this article the properties, assay, distribution, subcellular localization, deficiency in congenital peroxisomal disorders, purification and physiological functions of dihydroxyacetone phosphate acyltransferase (EC 2.3.1.42) are reviewed.
Publication types
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Research Support, U.S. Gov't, P.H.S.
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Review
MeSH terms
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Acyltransferases / deficiency
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Acyltransferases / isolation & purification
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Acyltransferases / metabolism*
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Animals
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Humans
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Membrane Proteins / isolation & purification
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Membrane Proteins / metabolism
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Peroxisomal Disorders / enzymology
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Saccharomyces cerevisiae / enzymology
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Subcellular Fractions / enzymology
Substances
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Membrane Proteins
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Acyltransferases
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glycerone-phosphate O-acyltransferase