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glycerone-phosphate O-acyltransferase activity

Known as: acyl-CoA:glycerone-phosphate O-acyltransferase activity, dihydroxyacetone phosphate acyltransferase activity 
Catalysis of the reaction: acyl-CoA + glycerone phosphate = 1-acylglycerone 3-phosphate + CoA. [EC:2.3.1.42, RHEA:17660]
National Institutes of Health

Papers overview

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2006
2006
Leishmania major Expresses a Single Dihydroxyacetone Phosphate Acyltransferase Localized in the Glycosome, Important for Rapid Growth and Survival at High Cell Density and Essential for Virulence*
Despite major advances in the understanding of pathogenesis of the human protozoan parasite Leishmania major, little is known… 
1996
1996
Late-onset generalized disorder of peroxisomes
We diagnosed a unique peroxisomal disorder in a 32-year-old man with profound mental retardation, mild facial dysmorphism… 
1993
1993
Pseudo Infantile Refsum's Disease: Catalase-Deficient Peroxisomal Particles with Partial Deficiency of Plasmalogen Synthesis and Oxidation of Fatty Acids
ABSTRACT: Zellweger syndrome, neonatal adrenoleuko-dystrophy, and infantile Refsum's disease are genetic disorders characterized… 
1992
1992
HMG-CoA reductase inhibitors perturb fatty acid metabolism and induce peroxisomes in keratinocytes.
Topical lovastatin stimulates epidermal fatty acid synthesis in vivo; therefore, studies were undertaken to examine the effects… 
Review
1988
Review
1988
A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).
In the present paper two siblings are presented with clinical manifestations very similar to those of patients affected by… 
Highly Cited
1988
Highly Cited
1988
Rhizomelic chondrodysplasia punctata: clinical, pathologic, and biochemical findings in two patients.
Review
1986
Review
1986
Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.
Patients with the cerebrohepatorenal syndrome of Zellweger lack peroxisomes and certain peroxisomal enzymes such as… 
1986
1986
Mutants of Saccharomyces cerevisiae defective in sn-glycerol-3-phosphate acyltransferase. Simultaneous loss of dihydroxyacetone phosphate acyltransferase indicates a common gene.
1986
1986
Partial deficiency of dihydroxyacetone phosphate acyltransferase activity in both classical and infantile Refsum's diseases
We measured the activity of dihydroxyacetone phosphate acyltransferase (DHAP-AT) in fibroblasts of controls and patients with… 
1981
1981
Effects of chronic modification of dietary fat and carbohydrate in rats.
1. Rats were fed on diets enriched with starch, sucrose, corn oil or beef tallow for 3 weeks and the activities of various… 
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