Biosynthesis of mannosylinositolphosphoceramide in Saccharomyces cerevisiae is dependent on genes controlling the flow of secretory vesicles from the endoplasmic reticulum to the Golgi.
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Synthesis of monohydroxylated inositolphosphorylceramide (IPC-C) in Saccharomyces cerevisiae requires Scs7p, a protein with both a cytochrome b5-like domain and a hydroxylase/desaturase domain.The VRG4 gene is required for GDP-mannose transport into the lumen of the Golgi in the yeast, Saccharomyces cerevisiaeHydroxylation of Saccharomyces cerevisiae ceramides requires Sur2p and Scs7p.Depletion of acyl-coenzyme A-binding protein affects sphingolipid synthesis and causes vesicle accumulation and membrane defects in Saccharomyces cerevisiaeLag1p and Lac1p are essential for the Acyl-CoA-dependent ceramide synthase reaction in Saccharomyces cerevisaeInositol phosphorylceramide synthase is located in the Golgi apparatus of Saccharomyces cerevisiae.Lipid rafts function in biosynthetic delivery of proteins to the cell surface in yeast.The Saccharomyces cerevisiae SEC20 gene encodes a membrane glycoprotein which is sorted by the HDEL retrieval system.A genomewide screen reveals a role of mitochondria in anaerobic uptake of sterols in yeast.Mutant analysis reveals complex regulation of sphingolipid long chain base phosphates and long chain bases during heat stress in yeast.Systematic analysis of yeast strains with possible defects in lipid metabolism.Phospholipid-synthesizing enzymes in Golgi membranes of the yeast, Saccharomyces cerevisiae.Deletion of GPI7, a yeast gene required for addition of a side chain to the glycosylphosphatidylinositol (GPI) core structure, affects GPI protein transport, remodeling, and cell wall integrity.MCD4 encodes a conserved endoplasmic reticulum membrane protein essential for glycosylphosphatidylinositol anchor synthesis in yeastThe Saccharomyces cerevisiae TSC10/YBR265w gene encoding 3-ketosphinganine reductase is identified in a screen for temperature-sensitive suppressors of the Ca2+-sensitive csg2Delta mutant.Electrospray ionization tandem mass spectrometry (ESI-MS/MS) analysis of the lipid molecular species composition of yeast subcellular membranes reveals acyl chain-based sorting/remodeling of distinct molecular species en route to the plasma membraneAlternative lipid remodelling pathways for glycosylphosphatidylinositol membrane anchors in Saccharomyces cerevisiaeLipid remodeling leads to the introduction and exchange of defined ceramides on GPI proteins in the ER and Golgi of Saccharomyces cerevisiae.Two different types of lipid moieties are present in glycophosphoinositol-anchored membrane proteins of Saccharomyces cerevisiae.The organizing potential of sphingolipids in intracellular membrane transport.Cumulative mutations affecting sterol biosynthesis in the yeast Saccharomyces cerevisiae result in synthetic lethality that is suppressed by alterations in sphingolipid profiles.Guanosine diphosphatase is required for protein and sphingolipid glycosylation in the Golgi lumen of Saccharomyces cerevisiae.Identification of six complementation classes involved in the biosynthesis of glycosylphosphatidylinositol anchors in Saccharomyces cerevisiae.Vesicular and nonvesicular transport of ceramide from ER to the Golgi apparatus in yeastThe Golgi-localization of yeast Emp47p depends on its di-lysine motif but is not affected by the ret1-1 mutation in alpha-COP.Following the flux of long-chain bases through the sphingolipid pathway in vivo using mass spectrometry.Suppressor gene analysis reveals an essential role for sphingolipids in transport of glycosylphosphatidylinositol-anchored proteins in Saccharomyces cerevisiae.An inducible ER-Golgi tether facilitates ceramide transport to alleviate lipotoxicityThe plasma membrane of Saccharomyces cerevisiae: structure, function, and biogenesis.Ceramide synthesis enhances transport of GPI-anchored proteins to the Golgi apparatus in yeast.Rustmicin, a potent antifungal agent, inhibits sphingolipid synthesis at inositol phosphoceramide synthase.Protein sorting in the late Golgi of Saccharomyces cerevisiae does not require mannosylated sphingolipids.Accumulation of long-chain bases in yeast promotes their conversion to a long-chain base vinyl ether.The long-chain sphingoid base of sphingolipids is acylated at the cytosolic surface of the endoplasmic reticulum in rat liver.The mitochondria-associated endoplasmic-reticulum subcompartment (MAM fraction) of rat liver contains highly active sphingolipid-specific glycosyltransferases.Endoplasmic reticulum-plasma membrane contact sites integrate sterol and phospholipid regulation.Association between the endoplasmic reticulum and mitochondria of yeast facilitates interorganelle transport of phospholipids through membrane contactThe yeast mic2 mutant is defective in the formation of mannosyl-diinositolphosphorylceramide 1Biosynthesis of Inositol Phosphoceramides and Remodeling of Glycosylphosphatidylinositol Anchors inSaccharomyces cerevisiaeAre Mediated by Different Enzymes
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Biosynthesis of mannosylinositolphosphoceramide in Saccharomyces cerevisiae is dependent on genes controlling the flow of secretory vesicles from the endoplasmic reticulum to the Golgi.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
1991年论文
@zh
1991年论文
@zh-cn
name
Biosynthesis of mannosylinosit ...... lasmic reticulum to the Golgi.
@ast
Biosynthesis of mannosylinosit ...... lasmic reticulum to the Golgi.
@en
type
label
Biosynthesis of mannosylinosit ...... lasmic reticulum to the Golgi.
@ast
Biosynthesis of mannosylinosit ...... lasmic reticulum to the Golgi.
@en
prefLabel
Biosynthesis of mannosylinosit ...... lasmic reticulum to the Golgi.
@ast
Biosynthesis of mannosylinosit ...... lasmic reticulum to the Golgi.
@en
P2093
P2860
P356
P1476
Biosynthesis of mannosylinosit ...... lasmic reticulum to the Golgi.
@en
P2093
P2860
P304
P356
10.1083/JCB.113.3.515
P407
P577
1991-05-01T00:00:00Z