Membrane vesiculation function and exocytosis of wild-type and mutant matrix proteins of vesicular stomatitis virus.
about
Overlapping motifs (PTAP and PPEY) within the Ebola virus VP40 protein function independently as late budding domains: involvement of host proteins TSG101 and VPS-4.Vacuolar protein sorting pathway contributes to the release of Marburg virusRhabdovirus Matrix Protein Structures Reveal a Novel Mode of Self-AssociationA PPxY motif within the VP40 protein of Ebola virus interacts physically and functionally with a ubiquitin ligase: implications for filovirus buddingRhabdoviruses and the cellular ubiquitin-proteasome system: a budding interaction.A proline-rich motif within the matrix protein of vesicular stomatitis virus and rabies virus interacts with WW domains of cellular proteins: implications for viral buddingLate domain function identified in the vesicular stomatitis virus M protein by use of rhabdovirus-retrovirus chimerasThe membrane-proximal stem region of vesicular stomatitis virus G protein confers efficient virus assembly.Detecting protein-protein interactions in vesicular stomatitis virus using a cytoplasmic yeast two hybrid systemThe morphology and composition of influenza A virus particles are not affected by low levels of M1 and M2 proteins in infected cells.Role of matrix and fusion proteins in budding of Sendai virusEbola virus VP40-induced particle formation and association with the lipid bilayer.Virus maturation by budding.Architecture and regulation of negative-strand viral enzymatic machineryRequirements for budding of paramyxovirus simian virus 5 virus-like particles.Ebola virus VP40 drives the formation of virus-like filamentous particles along with GPRoles for the cytoplasmic tails of the fusion and hemagglutinin-neuraminidase proteins in budding of the paramyxovirus simian virus 5.Molecular mechanism of arenavirus assembly and budding.Direct stimulation of T lymphocytes by immunosomes: virus-like particles decorated with T cell receptor/CD3 ligands plus costimulatory molecules.Quantitative analysis of Nipah virus proteins released as virus-like particles reveals central role for the matrix protein.Influenza virus hemagglutinin and neuraminidase, but not the matrix protein, are required for assembly and budding of plasmid-derived virus-like particlesPlasma membrane microdomains containing vesicular stomatitis virus M protein are separate from microdomains containing G protein and nucleocapsidsThe small RING finger protein Z drives arenavirus budding: implications for antiviral strategies.Multimerization of tegument protein pp28 within the assembly compartment is required for cytoplasmic envelopment of human cytomegalovirusMumps virus matrix, fusion, and nucleocapsid proteins cooperate for efficient production of virus-like particles.Foreign glycoproteins expressed from recombinant vesicular stomatitis viruses are incorporated efficiently into virus particles.Involvement of a bovine viral diarrhea virus NS5B locus in virion assembly.Influenza a viruses with mutations in the m1 helix six domain display a wide variety of morphological phenotypes.A leucine residue in the C terminus of human parainfluenza virus type 3 matrix protein is essential for efficient virus-like particle and virion release.Arenavirus budding resulting from viral-protein-associated cell membrane curvature.Generation and analysis of infectious virus-like particles of uukuniemi virus (bunyaviridae): a useful system for studying bunyaviral packaging and budding.Mutations in the PPPY motif of vesicular stomatitis virus matrix protein reduce virus budding by inhibiting a late step in virion releaseMatrix protein of rabies virus is responsible for the assembly and budding of bullet-shaped particles and interacts with the transmembrane spike glycoprotein G.Influenza virus matrix protein is the major driving force in virus budding.Formation of wild-type and chimeric influenza virus-like particles following simultaneous expression of only four structural proteinsNontransmissible virus-like particle formation by F-deficient sendai virus is temperature sensitive and reduced by mutations in M and HN proteins.A new Sendai virus vector deficient in the matrix gene does not form virus particles and shows extensive cell-to-cell spreadingThe glycoprotein cytoplasmic tail of Uukuniemi virus (Bunyaviridae) interacts with ribonucleoproteins and is critical for genome packaging.The YLDL sequence within Sendai virus M protein is critical for budding of virus-like particles and interacts with Alix/AIP1 independently of C protein.Multivesicular bodies as a platform for formation of the Marburg virus envelope.
P2860
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P2860
Membrane vesiculation function and exocytosis of wild-type and mutant matrix proteins of vesicular stomatitis virus.
description
1995 nî lūn-bûn
@nan
1995 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Membrane vesiculation function ...... of vesicular stomatitis virus.
@ast
Membrane vesiculation function ...... of vesicular stomatitis virus.
@en
type
label
Membrane vesiculation function ...... of vesicular stomatitis virus.
@ast
Membrane vesiculation function ...... of vesicular stomatitis virus.
@en
prefLabel
Membrane vesiculation function ...... of vesicular stomatitis virus.
@ast
Membrane vesiculation function ...... of vesicular stomatitis virus.
@en
P2093
P2860
P1433
P1476
Membrane vesiculation function ...... of vesicular stomatitis virus
@en
P2093
P2860
P304
P577
1995-05-01T00:00:00Z