Common and specific properties of herpesvirus UL34/UL31 protein family members revealed by protein complementation assay. - Wikidata - awgldk - TriplyDB

Common and specific properties of herpesvirus UL34/UL31 protein family members revealed by protein complementation assay.

Common and specific properties of herpesvirus UL34/UL31 protein family members revealed by protein complementation assay.

http://www.wikidata.org/entity/Q39321803

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Evolutionarily conserved herpesviral protein interaction networks The Herpes Simplex Virus Protein pUL31 Escorts Nucleocapsids to Sites of Nuclear Egress, a Process Coordinated by Its N-Terminal Domain.Random screening for dominant-negative mutants of the cytomegalovirus nuclear egress protein M50 Yeast two hybrid analyses reveal novel binary interactions between human cytomegalovirus-encoded virion proteins.Herpesvirus BACs: past, present, and future.Cytomegalovirus downregulates IRE1 to repress the unfolded protein response.A modified screening system for loss-of-function and dominant negative alleles of essential MCMV genes.Selection of HSV capsids for envelopment involves interaction between capsid surface components pUL31, pUL17, and pUL25 Emerin is hyperphosphorylated and redistributed in herpes simplex virus type 1-infected cells in a manner dependent on both UL34 and US3.Interactions of the Kaposi's Sarcoma-associated herpesvirus nuclear egress complex: ORF69 is a potent factor for remodeling cellular membranes Effects of lamin A/C, lamin B1, and viral US3 kinase activity on viral infectivity, virion egress, and the targeting of herpes simplex virus U(L)34-encoded protein to the inner nuclear membrane Control of cytoplasmic maturation events by cytomegalovirus tegument protein pp150.Herpesvirus interactions with the host cytoskeleton.Biochemical, biophysical, and mutational analyses of subunit interactions of the human cytomegalovirus nuclear egress complex.Expression and characterization of the UL31 protein from duck enteritis virus The U(L)31 and U(L)34 gene products of herpes simplex virus 1 are required for optimal localization of viral glycoproteins D and M to the inner nuclear membranes of infected cells HVint: A Strategy for Identifying Novel Protein-Protein Interactions in Herpes Simplex Virus Type 1 The human cytomegalovirus nuclear egress complex unites multiple functions: Recruitment of effectors, nuclear envelope rearrangement, and docking to nuclear capsids.Functional characterization of nuclear trafficking signals in pseudorabies virus pUL31.Intragenic and extragenic suppression of a mutation in herpes simplex virus 1 UL34 that affects both nuclear envelope targeting and membrane budding.A physical link between the pseudorabies virus capsid and the nuclear egress complex.Human cytomegalovirus UL50 and UL53 recruit viral protein kinase UL97, not protein kinase C, for disruption of nuclear lamina and nuclear egress in infected cells Characterization of conserved region 2-deficient mutants of the cytomegalovirus egress protein pM53.Herpes simplex virus 1 pUL34 plays a critical role in cell-to-cell spread of virus in addition to its role in virus replication Varicella zoster virus ORF25 gene product: an essential hub protein linking encapsidation proteins and the nuclear egress complex.Analysis of a charge cluster mutation of herpes simplex virus type 1 UL34 and its extragenic suppressor suggests a novel interaction between pUL34 and pUL31 that is necessary for membrane curvature around capsids.Identification and characterization of the product encoded by ORF69 of Kaposi's sarcoma-associated herpesvirus Herpesvirus Nuclear Egress.The Herpesvirus Nuclear Egress Complex Component, UL31, Can Be Recruited to Sites of DNA Damage Through Poly-ADP Ribose Binding.The m74 gene product of murine cytomegalovirus (MCMV) is a functional homolog of human CMV gO and determines the entry pathway of MCMV.Extragenic Suppression of a Mutation in Herpes Simplex Virus 1 UL34 That Affects Lamina Disruption and Nuclear Egress.A single herpesvirus protein can mediate vesicle formation in the nuclear envelope Proteomic analysis of the multimeric nuclear egress complex of human cytomegalovirus.Dominant negative mutants of the murine cytomegalovirus M53 gene block nuclear egress and inhibit capsid maturation.Functional homologies between avian and human alphaherpesvirus VP22 proteins in cell-to-cell spreading as revealed by a new cis-complementation assay.Temporal profiling of the coding and noncoding murine cytomegalovirus transcriptomes.Venture from the Interior-Herpesvirus pUL31 Escorts Capsids from Nucleoplasmic Replication Compartments to Sites of Primary Envelopment at the Inner Nuclear Membrane.

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P2860

Common and specific properties of herpesvirus UL34/UL31 protein family members revealed by protein complementation assay.

http://www.wikidata.org/entity/Q39321803

description

2006 nî lūn-bûn

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2006年の論文

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年學術文章

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2006年學術文章

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2006年學術文章

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name

Common and specific properties ...... protein complementation assay.

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Common and specific properties ...... protein complementation assay.

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type

label

Common and specific properties ...... protein complementation assay.

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Common and specific properties ...... protein complementation assay.

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prefLabel

Common and specific properties ...... protein complementation assay.

@en

Common and specific properties ...... protein complementation assay.

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Common and specific properties ...... protein complementation assay.

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P2093

Anja Bubeck

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Margit Schnee

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Ulrich H Koszinowski

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Zsolt Ruzsics

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P2860

Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate

A novel genetic system to detect protein-protein interactions

Monitoring protein-protein interactions in intact eukaryotic cells by beta-galactosidase complementation

Inhibition of herpes simplex virus replication by a 2-amino thiazole via interactions with the helicase component of the UL5-UL8-UL52 complex

The interacting UL31 and UL34 gene products of pseudorabies virus are involved in egress from the host-cell nucleus and represent components of primary enveloped but not mature virions.

Comprehensive mutational analysis of a herpesvirus gene in the viral genome context reveals a region essential for virus replication

The equine herpesvirus 1 UL34 gene product is involved in an early step in virus egress and can be efficiently replaced by a UL34-GFP fusion protein.

Detecting protein-protein interactions with a green fluorescent protein fragment reassembly trap: scope and mechanism.

Beta-lactamase protein fragment complementation assays as in vivo and in vitro sensors of protein protein interactions.

Capturing protein interactions in the secretory pathway of living cells.

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10.1128/JVI.01662-06

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23

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