FOG02066
EOG870S0G
sce:TAZ1
Genes: 32
SGD DescriptionLyso-phosphatidylcholine acyltransferase; required for normal phospholipid content of mitochondrial membranes; major determinant of the final acyl chain composition of the mitochondrial-specific phospholipid cardiolipin; mutations in human ortholog tafazzin cause Barth syndrome, a rare X-linked disease characterized by skeletal and cardiomyopathy and bouts of cyclic neutropenia
AspGD DescriptionOrtholog(s) have 1-acylglycerophosphocholine O-acyltransferase activity
References
Richard MG, et al. (1998 Dec). Lysophosphatidylcholine acyltransferase activity in Saccharomyces cerevisiae: regulation by a high-affinity Zn2+ binding site.
Sickmann A, et al. (2003 Nov 11). The proteome of Saccharomyces cerevisiae mitochondria.
Gu Z, et al. (2004 Jan). Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome.
Testet E, et al. (2005 May 1). Ypr140wp, 'the yeast tafazzin', displays a mitochondrial lysophosphatidylcholine (lyso-PC) acyltransferase activity related to triacylglycerol and mitochondrial lipid synthesis.
Brandner K, et al. (2005 Nov). Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome.
FOG02067
EOG870S0G
EOG8ZS7KX
sce:absent
Genes: 3
AspGD DescriptionOrtholog of Aspergillus carbonarius ITEM 5010 : Acar5010_512192
FOG02068
EOG8ZS7KX
sce:absent
Genes: 1