Requirement of STE50 for osmostress-induced activation of the STE11 mitogen-activated protein kinase kinase kinase in the high-osmolarity glycerol response pathway.
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SAM domain-based protein oligomerization observed by live-cell fluorescence fluctuation spectroscopyPtc1, a type 2C Ser/Thr phosphatase, inactivates the HOG pathway by dephosphorylating the mitogen-activated protein kinase Hog1Liprin phosphorylation regulates binding to LAR: evidence for liprin autophosphorylationStructure of the sterile alpha motif (SAM) domain of the Saccharomyces cerevisiae mitogen-activated protein kinase pathway-modulating protein STE50 and analysis of its interaction with the STE11 SAMRequirement for the polarisome and formin function in Ssk2p-mediated actin recovery from osmotic stress in Saccharomyces cerevisiae.Yeast Cdc42 GTPase and Ste20 PAK-like kinase regulate Sho1-dependent activation of the Hog1 MAPK pathway.Functional characterization of the interaction of Ste50p with Ste11p MAPKKK in Saccharomyces cerevisiae.The transcriptional response of Saccharomyces cerevisiae to osmotic shock. Hot1p and Msn2p/Msn4p are required for the induction of subsets of high osmolarity glycerol pathway-dependent genes.The filamentous growth MAPK Pathway Responds to Glucose Starvation Through the Mig1/2 transcriptional repressors in Saccharomyces cerevisiaeThe MAPK Hog1p modulates Fps1p-dependent arsenite uptake and tolerance in yeast.Rck1 and Rck2 MAPKAP kinases and the HOG pathway are required for oxidative stress resistance.Hyperosmotic stress response and regulation of cell wall integrity in Saccharomyces cerevisiae share common functional aspects.Role of Ptc2 type 2C Ser/Thr phosphatase in yeast high-osmolarity glycerol pathway inactivationOsmotic stress-induced gene expression in Saccharomyces cerevisiae requires Msn1p and the novel nuclear factor Hot1p.Scaffold Protein Ahk1, Which Associates with Hkr1, Sho1, Ste11, and Pbs2, Inhibits Cross Talk Signaling from the Hkr1 Osmosensor to the Kss1 Mitogen-Activated Protein KinaseA protein interaction map for cell polarity development.Adaptor functions of Cdc42, Ste50, and Sho1 in the yeast osmoregulatory HOG MAPK pathway.A signaling mucin at the head of the Cdc42- and MAPK-dependent filamentous growth pathway in yeast.Heat stress activates the yeast high-osmolarity glycerol mitogen-activated protein kinase pathway, and protein tyrosine phosphatases are essential under heat stressThe signaling mucins Msb2 and Hkr1 differentially regulate the filamentation mitogen-activated protein kinase pathway and contribute to a multimodal response.Nuclear sequestration of the exchange factor Cdc24 by Far1 regulates cell polarity during yeast mating.Adaptor protein Ste50p links the Ste11p MEKK to the HOG pathway through plasma membrane association.Rck2 kinase is a substrate for the osmotic stress-activated mitogen-activated protein kinase Hog1.Osmotic stress signaling and osmoadaptation in yeasts.Yeast osmosensors Hkr1 and Msb2 activate the Hog1 MAPK cascade by different mechanisms.Insertional mutagenesis combined with an inducible filamentation phenotype reveals a conserved STE50 homologue in Cryptococcus neoformans that is required for monokaryotic fruiting and sexual reproduction.Ste50 adaptor protein governs sexual differentiation of Cryptococcus neoformans via the pheromone-response MAPK signaling pathwayThe ubc2 gene of Ustilago maydis encodes a putative novel adaptor protein required for filamentous growth, pheromone response and virulence."Mutagenesis" by peptide aptamers identifies genetic network members and pathway connections.Unravelling the functional interaction structure of a cellular network from temporal slope information of experimental data.Integrated cellular network of transcription regulations and protein-protein interactionsSpecialization of the HOG pathway and its impact on differentiation and virulence of Cryptococcus neoformansThe RA domain of Ste50 adaptor protein is required for delivery of Ste11 to the plasma membrane in the filamentous growth signaling pathway of the yeast Saccharomyces cerevisiae.Cdc42p-interacting protein Bem4p regulates the filamentous-growth mitogen-activated protein kinase pathway.Selective regulation of MAP kinase signaling by an endomembrane phosphatidylinositol 4-kinase.The casein kinase I protein Cck1 regulates multiple signaling pathways and is essential for cell integrity and fungal virulence in Cryptococcus neoformansUnique and redundant roles for HOG MAPK pathway components as revealed by whole-genome expression analysis.MAP kinases and the adaptive response to hypertonicity: functional preservation from yeast to mammals.Phosphorylation of the MAPKKK regulator Ste50p in Saccharomyces cerevisiae: a casein kinase I phosphorylation site is required for proper mating functionComparative genomics of the environmental stress response in ascomycete fungi.
P2860
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P248
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P2860
Requirement of STE50 for osmostress-induced activation of the STE11 mitogen-activated protein kinase kinase kinase in the high-osmolarity glycerol response pathway.
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@ast
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@en
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@nl
type
label
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@ast
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@en
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@nl
prefLabel
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@ast
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@en
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@nl
P2093
P2860
P356
P1476
Requirement of STE50 for osmos ...... ity glycerol response pathway.
@en
P2093
P2860
P304
P356
10.1128/MCB.18.10.5788
P407
P577
1998-10-01T00:00:00Z