Heptad repeat 2-based peptides inhibit avian sarcoma and leukosis virus subgroup a infection and identify a fusion intermediate - Wikidata - awgldk - TriplyDB

Heptad repeat 2-based peptides inhibit avian sarcoma and leukosis virus subgroup a infection and identify a fusion intermediate

Heptad repeat 2-based peptides inhibit avian sarcoma and leukosis virus subgroup a infection and identify a fusion intermediate

http://www.wikidata.org/entity/Q30448708

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Imaging single retrovirus entry through alternative receptor isoforms and intermediates of virus-endosome fusion Characterization of a Structural Intermediate of Flavivirus Membrane Fusion Structures and Mechanisms of Viral Membrane Fusion Proteins: Multiple Variations on a Common Theme Receptor Binding and Low pH Coactivate Oncogenic Retrovirus Envelope-Mediated Fusion Fusion of Enveloped Viruses in Endosomes.Receptor-induced thiolate couples Env activation to retrovirus fusion and infection Visualization of the two-step fusion process of the retrovirus avian sarcoma/leukosis virus by cryo-electron tomography.Studies of the "chain reversal regions" of the avian sarcoma/leukosis virus (ASLV) and ebolavirus fusion proteins: analogous residues are important, and a His residue unique to EnvA affects the pH dependence of ASLV entry.A charged second-site mutation in the fusion peptide rescues replication of a mutant avian sarcoma and leukosis virus lacking critical cysteine residues flanking the internal fusion domain.Cysteines flanking the internal fusion peptide are required for the avian sarcoma/leukosis virus glycoprotein to mediate the lipid mixing stage of fusion with high efficiency.Receptor-induced conformational changes in the SU subunit of the avian sarcoma/leukosis virus A envelope protein: implications for fusion activation.Imaging individual retroviral fusion events: from hemifusion to pore formation and growth.Fluorescent protein-tagged Vpr dissociates from HIV-1 core after viral fusion and rapidly enters the cell nucleus.Inhibition of Nipah virus infection in vivo: targeting an early stage of paramyxovirus fusion activation during viral entry Inhibitors of cathepsin L prevent severe acute respiratory syndrome coronavirus entry.Kinetic analyses of the surface-transmembrane disulfide bond isomerization-controlled fusion activation pathway in Moloney murine leukemia virus Na+/H+ exchanger type 1 is a receptor for pathogenic subgroup J avian leukosis virus.Inhibition of Ebola virus entry by a C-peptide targeted to endosomes.Inhibition of hendra virus fusion.Chemical and Structural Aspects of Ebola Virus Entry Inhibitors.Quantitative imaging of endosome acidification and single retrovirus fusion with distinct pools of early endosomes Heptad repeat-derived peptides block protease-mediated direct entry from the cell surface of severe acute respiratory syndrome coronavirus but not entry via the endosomal pathway Stabilization of TM trimer interactions during activation of moloney murine leukemia virus Env.Kinetic dependence of paramyxovirus entry inhibition.Common principles and intermediates of viral protein-mediated fusion: the HIV-1 paradigm.pH regulation in early endosomes and interferon-inducible transmembrane proteins control avian retrovirus fusion.Receptor-triggered but alkylation-arrested env of murine leukemia virus reveals the transmembrane subunit in a prehairpin conformation.Spring-loaded model revisited: paramyxovirus fusion requires engagement of a receptor binding protein beyond initial triggering of the fusion protein.The six-helix bundle of human immunodeficiency virus Env controls pore formation and enlargement and is initiated at residues proximal to the hairpin turn Retroviral host range extension is coupled with Env-activating mutations resulting in receptor-independent entry.The hr1 and fusion peptide regions of the subgroup B avian sarcoma and leukosis virus envelope glycoprotein influence low pH-dependent membrane fusion.Expanded tropism and altered activation of a retroviral glycoprotein resistant to an entry inhibitor peptide.Conserved leucines in N-terminal heptad repeat HR1 of envelope fusion protein F of group II nucleopolyhedroviruses are important for correct processing and essential for fusogenicity.

P2860

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P2860

Heptad repeat 2-based peptides inhibit avian sarcoma and leukosis virus subgroup a infection and identify a fusion intermediate

http://www.wikidata.org/entity/Q30448708

description

2004 nî lūn-bûn

@nan

2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2004年の論文

@ja

2004年学术文章

@wuu

2004年学术文章

@zh-cn

2004年学术文章

@zh-hans

2004年学术文章

@zh-my

2004年学术文章

@zh-sg

2004年學術文章

@yue

name

Heptad repeat 2-based peptides ...... identify a fusion intermediate

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Heptad repeat 2-based peptides ...... identify a fusion intermediate

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type

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Heptad repeat 2-based peptides ...... identify a fusion intermediate

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Heptad repeat 2-based peptides ...... identify a fusion intermediate

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prefLabel

Heptad repeat 2-based peptides ...... identify a fusion intermediate

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Heptad repeat 2-based peptides ...... identify a fusion intermediate

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P1433

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P356

JVI.78.24.13430-13439.2004

P1433

Journal of Virology

P1476

Heptad repeat 2-based peptides ...... identify a fusion intermediate

@en

P2093

Arwen Vermeulen

http://www.w3.org/2001/XMLSchema#string

John W Balliet

http://www.w3.org/2001/XMLSchema#string

Judith M White

http://www.w3.org/2001/XMLSchema#string

Laurie J Earp

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Mark J Biscone

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Robert C Netter

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Sean M Amberg

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P2860

Mutational analysis of the subgroup A avian sarcoma and leukosis virus putative fusion peptide domain.

The viral transmembrane superfamily: possible divergence of Arenavirus and Filovirus glycoproteins from a common RNA virus ancestor

The Coronavirus Spike Protein Is a Class I Virus Fusion Protein: Structural and Functional Characterization of the Fusion Core Complex

Core structure of the envelope glycoprotein GP2 from Ebola virus at 1.9-A resolution

Crystal structure of the Ebola virus membrane fusion subunit, GP2, from the envelope glycoprotein ectodomain

The structural biology of type I viral membrane fusion

A synthetic peptide inhibitor of human immunodeficiency virus replication: correlation between solution structure and viral inhibition

Membrane fusion machines of paramyxoviruses: capture of intermediates of fusion

Peptides corresponding to a predictive alpha-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection

Determinants of human immunodeficiency virus type 1 resistance to gp41-derived inhibitory peptides.

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13430-13439

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scholarly article

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10.1128/JVI.78.24.13430-13439.2004

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24

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78

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P577

2004-12-01T00:00:00Z

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P698

15564453

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P921

membrane fusion involved in viral entry into host cell

P932

533931

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