The cytoplasmic tail of the severe acute respiratory syndrome coronavirus spike protein contains a novel endoplasmic reticulum retrieval signal that binds COPI and promotes interaction with membrane protein.
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Ezrin interacts with the SARS coronavirus Spike protein and restrains infection at the entry stageRole of Coatomer Protein I in Virus Replication.The M, E, and N structural proteins of the severe acute respiratory syndrome coronavirus are required for efficient assembly, trafficking, and release of virus-like particles.A single tyrosine in the severe acute respiratory syndrome coronavirus membrane protein cytoplasmic tail is important for efficient interaction with spike proteinPalmitoylation of SARS-CoV S protein is necessary for partitioning into detergent-resistant membranes and cell-cell fusion but not interaction with M protein.Arenavirus stable signal peptide is the keystone subunit for glycoprotein complex organization.The hydrophobic domain of infectious bronchitis virus E protein alters the host secretory pathway and is important for release of infectious virus.Evidence that TMPRSS2 activates the severe acute respiratory syndrome coronavirus spike protein for membrane fusion and reduces viral control by the humoral immune response.Identification of a Golgi complex-targeting signal in the cytoplasmic tail of the severe acute respiratory syndrome coronavirus envelope protein.Incorporation of spike and membrane glycoproteins into coronavirus virions.Proteomics analysis unravels the functional repertoire of coronavirus nonstructural protein 3.The transmembrane domain of the severe acute respiratory syndrome coronavirus ORF7b protein is necessary and sufficient for its retention in the Golgi complex.Transcriptional regulation of secretory capacity by bZip transcription factors.Persistent replication of severe acute respiratory syndrome coronavirus in human tubular kidney cells selects for adaptive mutations in the membrane protein.The contribution of the cytoplasmic retrieval signal of severe acute respiratory syndrome coronavirus to intracellular accumulation of S proteins and incorporation of S protein into virus-like particles.Analyses of Coronavirus Assembly Interactions with Interspecies Membrane and Nucleocapsid Protein ChimerasKinetically distinct sorting pathways through the Golgi exhibit different requirements for Arf1.Histone deacetylase 6 inhibits influenza A virus release by downregulating the trafficking of viral components to the plasma membrane via its substrate, acetylated microtubules.Different host cell proteases activate the SARS-coronavirus spike-protein for cell-cell and virus-cell fusion.Mutagenesis of the transmembrane domain of the SARS coronavirus spike glycoprotein: refinement of the requirements for SARS coronavirus cell entry.Studies on membrane topology, N-glycosylation and functionality of SARS-CoV membrane protein.The spike protein of infectious bronchitis virus is retained intracellularly by a tyrosine motif
P2860
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P2860
The cytoplasmic tail of the severe acute respiratory syndrome coronavirus spike protein contains a novel endoplasmic reticulum retrieval signal that binds COPI and promotes interaction with membrane protein.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
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2006年论文
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2006年论文
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name
The cytoplasmic tail of the se ...... raction with membrane protein.
@ast
The cytoplasmic tail of the se ...... raction with membrane protein.
@en
type
label
The cytoplasmic tail of the se ...... raction with membrane protein.
@ast
The cytoplasmic tail of the se ...... raction with membrane protein.
@en
prefLabel
The cytoplasmic tail of the se ...... raction with membrane protein.
@ast
The cytoplasmic tail of the se ...... raction with membrane protein.
@en
P2093
P2860
P356
P1433
P1476
The cytoplasmic tail of the se ...... raction with membrane protein.
@en
P2093
Carolyn E Machamer
Corrin E McBride
P2860
P304
P356
10.1128/JVI.02146-06
P407
P577
2006-12-13T00:00:00Z