Envelope glycoprotein interactions in coronavirus assembly - Wikidata - wikimedia - TriplyDB

Envelope glycoprotein interactions in coronavirus assembly

Envelope glycoprotein interactions in coronavirus assembly

http://www.wikidata.org/entity/Q36382749

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A transmembrane serine protease is linked to the severe acute respiratory syndrome coronavirus receptor and activates virus entry Severe acute respiratory syndrome coronavirus 3a protein is a viral structural protein Coronavirus particle assembly: primary structure requirements of the membrane protein.Assembly of the coronavirus envelope: homotypic interactions between the M proteins Mouse Hepatitis Coronavirus RNA Replication Depends on GBF1-Mediated ARF1 Activation Characterization of an Immunodominant Epitope in the Endodomain of the Coronavirus Membrane Protein Anti-SARS coronavirus agents: a patent review (2008 - present).Cryo-electron tomography of mouse hepatitis virus: Insights into the structure of the coronavirion.Interaction of the coronavirus infectious bronchitis virus membrane protein with beta-actin and its implication in virion assembly and budding A single tyrosine in the severe acute respiratory syndrome coronavirus membrane protein cytoplasmic tail is important for efficient interaction with spike protein Fish rhabdovirus cell entry is mediated by fibronectin.A structural analysis of M protein in coronavirus assembly and morphology.Retargeting of coronavirus by substitution of the spike glycoprotein ectodomain: crossing the host cell species barrier Characterization of the coronavirus mouse hepatitis virus strain A59 small membrane protein E.Characterization of the coronavirus M protein and nucleocapsid interaction in infected cells.Variations in disparate regions of the murine coronavirus spike protein impact the initiation of membrane fusion.Palmitoylation of SARS-CoV S protein is necessary for partitioning into detergent-resistant membranes and cell-cell fusion but not interaction with M protein.Virus maturation by budding.A major determinant for membrane protein interaction localizes to the carboxy-terminal domain of the mouse coronavirus nucleocapsid protein.Contribution of trafficking signals in the cytoplasmic tail of the infectious bronchitis virus spike protein to virus infection.The coronavirus nucleocapsid is a multifunctional protein.Intracellular targeting signals contribute to localization of coronavirus spike proteins near the virus assembly site.A conserved domain in the coronavirus membrane protein tail is important for virus assembly.Palmitoylations on murine coronavirus spike proteins are essential for virion assembly and infectivity.The cytoplasmic tail of infectious bronchitis virus E protein directs Golgi targeting.Antiviral drugs specific for coronaviruses in preclinical development Genetic evidence for a structural interaction between the carboxy termini of the membrane and nucleocapsid proteins of mouse hepatitis virus.Functional characterization of heptad repeat 1 and 2 mutants of the spike protein of severe acute respiratory syndrome coronavirus.Identification of functionally important negatively charged residues in the carboxy end of mouse hepatitis coronavirus A59 nucleocapsid protein.Switching species tropism: an effective way to manipulate the feline coronavirus genome.Incorporation of spike and membrane glycoproteins into coronavirus virions.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.Role of the coronavirus E viroporin protein transmembrane domain in virus assembly.Nucleocapsid-independent assembly of coronavirus-like particles by co-expression of viral envelope protein genes.Importance of the penultimate positive charge in mouse hepatitis coronavirus A59 membrane protein.Contributions of the structural proteins of severe acute respiratory syndrome coronavirus to protective immunity.Envelope protein palmitoylations are crucial for murine coronavirus assembly.Chimeric coronavirus-like particles carrying severe acute respiratory syndrome coronavirus (SCoV) S protein protect mice against challenge with SCoV Protein interactions during coronavirus assembly Identifying SARS-CoV membrane protein amino acid residues linked to virus-like particle assembly.

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Envelope glycoprotein interactions in coronavirus assembly

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1995 nî lūn-bûn

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Envelope glycoprotein interactions in coronavirus assembly

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Horzinek MC

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Opstelten DJ

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Raamsman MJ

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Rottier PJ

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Wolfs K

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P2860

Brefeldin A: insights into the control of membrane traffic and organelle structure

Formation and intracellular transport of a heterodimeric viral spike protein complex

Nucleocapsid-glycoprotein interactions required for assembly of alphaviruses

Spike protein-nucleocapsid interactions drive the budding of alphaviruses

Eukaryotic transient-expression system based on recombinant vaccinia virus that synthesizes bacteriophage T7 RNA polymerase

Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: evidence for membrane cycling from Golgi to ER

Microtubule-dependent retrograde transport of proteins into the ER in the presence of brefeldin A suggests an ER recycling pathway

In vitro reassembly of vesicular stomatitis virus skeletons.

Cytoplasmic expression system based on constitutive synthesis of bacteriophage T7 RNA polymerase in mammalian cells

The budding mechanisms of enveloped animal viruses.

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339-349

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2199982

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