phospholipid acyltransferases

E coli enzyme transfers acyl group from diacylphospholids to 2-acyl-lysophospholipids, preference for palmitic acid on the 1 position of glycerol backbone as donor; does not use & acyl CoA or acylcarrier protein

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1.	Blanck, Thomas J J: 2 articles (12/2003 - 05/2002)
2.	DiMauro, Salvatore: 2 articles (12/2003 - 05/2002)
3.	Heerdt, Paul M: 2 articles (12/2003 - 05/2002)
4.	Schlame, Michael: 2 articles (12/2003 - 05/2002)
5.	Towbin, Jeffrey A: 2 articles (12/2003 - 05/2002)
6.	Feigenbaum, Annette: 1 article (12/2003)
7.	Kelley, Richard I: 1 article (12/2003)
8.	Schieble, Thomas: 1 article (12/2003)
9.	Wanders, Ronald J A: 1 article (12/2003)
10.	Jehle, Roswitha: 1 article (05/2002)

Related Diseases

1.	Barth Syndrome 05/01/2002 - "Barth syndrome may be due to lipid alterations because the product of the mutated gene is homologous to phospholipid acyltransferases. " 12/03/2003 - "Barth syndrome typically includes cardiomyopathy, skeletal myopathy, neutropenia, growth retardation, and 3-methylglutaconic aciduria, and it is commonly associated with mutations in the tafazzin (TAZ) gene, whose products are homologous to phospholipid acyltransferases. "
2.	Neutropenia 12/03/2003 - "Barth syndrome typically includes cardiomyopathy, skeletal myopathy, neutropenia, growth retardation, and 3-methylglutaconic aciduria, and it is commonly associated with mutations in the tafazzin (TAZ) gene, whose products are homologous to phospholipid acyltransferases. "
3.	Cardiomyopathies (Cardiomyopathy) 12/03/2003 - "Barth syndrome typically includes cardiomyopathy, skeletal myopathy, neutropenia, growth retardation, and 3-methylglutaconic aciduria, and it is commonly associated with mutations in the tafazzin (TAZ) gene, whose products are homologous to phospholipid acyltransferases. "
4.	Muscular Diseases (Myopathy) 12/03/2003 - "Barth syndrome typically includes cardiomyopathy, skeletal myopathy, neutropenia, growth retardation, and 3-methylglutaconic aciduria, and it is commonly associated with mutations in the tafazzin (TAZ) gene, whose products are homologous to phospholipid acyltransferases. "
5.	3-Methylglutaconic Aciduria 12/03/2003 - "Barth syndrome typically includes cardiomyopathy, skeletal myopathy, neutropenia, growth retardation, and 3-methylglutaconic aciduria, and it is commonly associated with mutations in the tafazzin (TAZ) gene, whose products are homologous to phospholipid acyltransferases. "

Related Drugs and Biologics

1.	Lipids