PDR16 and PDR17, two homologous genes of Saccharomyces cerevisiae, affect lipid biosynthesis and resistance to multiple drugs.
about
A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress-induced membrane biogenesisDimeric Sfh3 has structural changes in its binding pocket that are associated with a dimer-monomer state transformation induced by substrate bindingStructural determinants for phosphatidylinositol recognition by Sfh3 and substrate-induced dimer-monomer transition during lipid transfer cyclesLem3p is essential for the uptake and potency of alkylphosphocholine drugs, edelfosine and miltefosine.Subcellular localization of yeast Sec14 homologues and their involvement in regulation of phospholipid turnover.Transcriptional response to deletion of the phosphatidylserine decarboxylase Psd1p in the yeast Saccharomyces cerevisiae.The yeast ABC transporter Pdr18 (ORF YNR070w) controls plasma membrane sterol composition, playing a role in multidrug resistanceCompartment-specific synthesis of phosphatidylethanolamine is required for normal heavy metal resistance.A novel membrane protein, Ros3p, is required for phospholipid translocation across the plasma membrane in Saccharomyces cerevisiae.Pse1/Kap121-dependent nuclear localization of the major yeast multidrug resistance (MDR) transcription factor Pdr1.Identification of a novel family of nonclassic yeast phosphatidylinositol transfer proteins whose function modulates phospholipase D activity and Sec14p-independent cell growth.A new gene involved in the transport-dependent metabolism of phosphatidylserine, PSTB2/PDR17, shares sequence similarity with the gene encoding the phosphatidylinositol/phosphatidylcholine transfer protein, SEC14.Roles of phosphoinositides and of Spo14p (phospholipase D)-generated phosphatidic acid during yeast sporulationGenome-wide fitness test and mechanism-of-action studies of inhibitory compounds in Candida albicansCharacterization of the chromosome 4 genes that affect fluconazole-induced disomy formation in Cryptococcus neoformansyMGV: helping biologists with yeast microarray data mining.cDNA microarray analysis of differential gene expression in Candida albicans biofilm exposed to farnesol.Energy-dependent flip of fluorescence-labeled phospholipids is regulated by nutrient starvation and transcription factors, PDR1 and PDR3.Functional genomic analysis of fluconazole susceptibility in the pathogenic yeast Candida glabrata: roles of calcium signaling and mitochondria.A multi-level study of recombinant Pichia pastoris in different oxygen conditions.Loss of Aip1 reveals a role in maintaining the actin monomer pool and an in vivo oligomer assembly pathwayCellular and molecular biology of Candida albicans estrogen response.Systematic profiling of cellular phenotypes with spotted cell microarrays reveals mating-pheromone response genesNew perspectives on the regulation of intermembrane glycerophospholipid traffic.Genetic analysis of intracellular aminoglycerophospholipid traffic.A Yeast Mutant Deleted of GPH1 Bears Defects in Lipid MetabolismMetabolome and transcriptome of the interaction between Ustilago maydis and Fusarium verticillioides in vitroAn update on antifungal targets and mechanisms of resistance in Candida albicans.Yeast viral killer toxins: lethality and self-protection.H3K4 methyltransferase Set1 is involved in maintenance of ergosterol homeostasis and resistance to Brefeldin A.Specific sterols required for the internalization step of endocytosis in yeastMultidrug resistance in fungiEnhancing drug accumulation in Saccharomyces cerevisiae by repression of pleiotropic drug resistance genes with chimeric transcription repressors.Relative contributions of the Candida albicans ABC transporters Cdr1p and Cdr2p to clinical azole resistanceCoordinate control of lipid composition and drug transport activities is required for normal multidrug resistance in fungi.Harnessing genetic diversity in Saccharomyces cerevisiae for fermentation of xylose in hydrolysates of alkaline hydrogen peroxide-pretreated biomassPhosphatidylinositol transfer proteins: negotiating the regulatory interface between lipid metabolism and lipid signaling in diverse cellular processes.Lipid transport between the endoplasmic reticulum and mitochondria.Multidrug resistance in fungi: regulation of transporter-encoding gene expression.Transport of phosphatidylserine from the endoplasmic reticulum to the site of phosphatidylserine decarboxylase2 in yeast.
P2860
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P248
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P2860
PDR16 and PDR17, two homologous genes of Saccharomyces cerevisiae, affect lipid biosynthesis and resistance to multiple drugs.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@ast
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@en
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@nl
type
label
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@ast
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@en
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@nl
prefLabel
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@ast
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@en
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@nl
P2093
P2860
P921
P356
P1476
PDR16 and PDR17, two homologou ...... resistance to multiple drugs.
@en
P2093
H B van den Hazel
M A do Valle Matta
P2860
P304
P356
10.1074/JBC.274.4.1934
P407
P577
1999-01-22T00:00:00Z