Probing the molecular environment of membrane proteins in vivo.
about
The yeast split-ubiquitin membrane protein two-hybrid screen identifies BAP31 as a regulator of the turnover of endoplasmic reticulum-associated protein tyrosine phosphatase-like BTopological and mutational analysis of Saccharomyces cerevisiae Ste14p, founding member of the isoprenylcysteine carboxyl methyltransferase familyIdentification of novel ErbB3-interacting factors using the split-ubiquitin membrane yeast two-hybrid systemIdentification of protein interactions involved in cellular signalingInteractions between co-expressed Arabidopsis sucrose transporters in the split-ubiquitin systemTechniques for the Analysis of Protein-Protein Interactions in VivoPhenotypes on demand via switchable target protein degradation in multicellular organisms.Identification of novel protein-protein interactions at the cytosolic surface of the Sec63 complex in the yeast ER membrane.Modulation of sterol homeostasis by the Cdc42p effectors Cla4p and Ste20p in the yeast Saccharomyces cerevisiae.Ssh4, Rcr2 and Rcr1 affect plasma membrane transporter activity in Saccharomyces cerevisiae.Membrane topology and function of Der3/Hrd1p as a ubiquitin-protein ligase (E3) involved in endoplasmic reticulum degradation.Srb7p is a physical and physiological target of Tup1p.Cell growth-dependent coordination of lipid signaling and glycosylation is mediated by interactions between Sac1p and Dpm1p.Cdc48/p97 and Shp1/p47 regulate autophagosome biogenesis in concert with ubiquitin-like Atg8Large-scale identification of yeast integral membrane protein interactionsThe Cdc42 effectors Ste20, Cla4, and Skm1 down-regulate the expression of genes involved in sterol uptake by a mitogen-activated protein kinase-independent pathway.Recognition of a subset of signal sequences by Ssh1p, a Sec61p-related protein in the membrane of endoplasmic reticulum of yeast Saccharomyces cerevisiae.A Split-Ubiquitin Based Strategy Selecting for Protein Complex-Interfering MutationsA fluorescent reporter for mapping cellular protein-protein interactions in time and space.Signaling of human frizzled receptors to the mating pathway in yeast.Utilizing the split-ubiquitin membrane yeast two-hybrid system to identify protein-protein interactions of integral membrane proteins.A new screen for protein interactions reveals that the Saccharomyces cerevisiae high mobility group proteins Nhp6A/B are involved in the regulation of the GAL1 promoter.An optimized split-ubiquitin cDNA-library screening system to identify novel interactors of the human Frizzled 1 receptor.Functional association of cell death suppressor, Arabidopsis Bax inhibitor-1, with fatty acid 2-hydroxylation through cytochrome b₅.Association of cytochrome b5 with ETR1 ethylene receptor signaling through RTE1 in Arabidopsis.Isolation of compensatory inhibitor domain mutants to novel activation domain variants using the split-ubiquitin screen.Diversity in genetic in vivo methods for protein-protein interaction studies: from the yeast two-hybrid system to the mammalian split-luciferase system.Phosphatidylethanolamine deficiency disrupts α-synuclein homeostasis in yeast and worm models of Parkinson diseaseAnalysis of Sec61p and Ssh1p interactions in the ER membrane using the split-ubiquitin system.The post-genomic era of interactive proteomics: facts and perspectives.Yeast two-hybrid, a powerful tool for systems biologyGenetic approaches to the identification of interactions between membrane proteins in yeast.Physical interaction between RRS1-R, a protein conferring resistance to bacterial wilt, and PopP2, a type III effector targeted to the plant nucleusStudying the interactome with the yeast two-hybrid system and mass spectrometry.TOR-induced resistance to toxic adenosine analogs in Leishmania brought about by the internalization and degradation of the adenosine permease.A Novel Interacting Protein SERP1 Regulates the N-Linked Glycosylation and Function of GLP-1 Receptor in the Liver.Plant sphingolipid fatty acid 2-hydroxylases have unique characters unlike their animal and fungus counterparts.Split-ubiquitin and the split-protein sensors: chessman for the endgame.Functional genomics in the study of yeast cell polarity: moving in the right direction.A new method for the selection of protein interactions in mammalian cells.
P2860
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P2860
Probing the molecular environment of membrane proteins in vivo.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Probing the molecular environment of membrane proteins in vivo.
@en
type
label
Probing the molecular environment of membrane proteins in vivo.
@en
prefLabel
Probing the molecular environment of membrane proteins in vivo.
@en
P2093
P2860
P356
P1476
Probing the molecular environment of membrane proteins in vivo.
@en
P2093
P2860
P304
P356
10.1091/MBC.10.8.2519
P577
1999-08-01T00:00:00Z