Specific inhibition of herpes simplex virus DNA polymerase by helical peptides corresponding to the subunit interface
about
Inhibition of Epstein-Barr virus replication by a benzimidazole L-riboside: novel antiviral mechanism of 5, 6-dichloro-2-(isopropylamino)-1-beta-L-ribofuranosyl-1H-benzimidazole.Enhanced delivery of exogenous peptides into the class I antigen processing and presentation pathway.Cloning, expression, and functional characterization of the equine herpesvirus 1 DNA polymerase and its accessory subunit.Protein-protein interactions as targets for antiviral chemotherapy.Novel strategies for targeting the dimerization interface of HIV protease with cross-linked interfacial peptides.Design and characterization of a photo-activatable hedgehog probe that mimics the natural lipidated form.Leading and lagging strand DNA synthesis in vitro by a reconstituted herpes simplex virus type 1 replisome.Mutations that specifically impair the DNA binding activity of the herpes simplex virus protein UL42The catalytic subunit of the DNA polymerase of herpes simplex virus type 1 interacts specifically with the C terminus of the UL8 component of the viral helicase-primase complex.Intranuclear delivery of an antiviral peptide mediated by the B subunit of Escherichia coli heat-labile enterotoxin.The carboxyl terminus of the bacteriophage T4 DNA polymerase is required for holoenzyme complex formation.Inhibition of herpes simplex virus type 1 infection by cationic beta-peptides.Cloning and functional analysis of Kaposi's sarcoma-associated herpesvirus DNA polymerase and its processivity factorIdentification of crucial hydrogen-bonding residues for the interaction of herpes simplex virus DNA polymerase subunits via peptide display, mutational, and calorimetric approaches.Inhibition of human cytomegalovirus DNA polymerase by C-terminal peptides from the UL54 subunit.Evidence that the C-terminal PB2-binding region of the influenza A virus PB1 protein is a discrete alpha-helical domain.A Small Covalent Allosteric Inhibitor of Human Cytomegalovirus DNA Polymerase Subunit Interactions.Residues of human cytomegalovirus DNA polymerase catalytic subunit UL54 that are necessary and sufficient for interaction with the accessory protein UL44Targeting herpetic keratitis by gene therapy.Peptides containing membrane-transiting motifs inhibit virus entry.Secondary structure and structure-activity relationships of peptides corresponding to the subunit interface of herpes simplex virus DNA polymerase.Differential susceptibility of Plasmodium falciparum versus yeast and mammalian enolases to dissociation into active monomers.dsDNA-specific fluorescent copper nanoparticles as a "green" nano-dye for polymerization-mediated biochemical analysis.Label-free molecular beacon for real-time monitoring of DNA polymerase activity.Interface Peptides
P2860
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P2860
Specific inhibition of herpes simplex virus DNA polymerase by helical peptides corresponding to the subunit interface
description
1995 nî lūn-bûn
@nan
1995 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի փետրվարին 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
Specific inhibition of herpes ...... nding to the subunit interface
@ast
Specific inhibition of herpes ...... nding to the subunit interface
@en
Specific inhibition of herpes ...... nding to the subunit interface
@nl
type
label
Specific inhibition of herpes ...... nding to the subunit interface
@ast
Specific inhibition of herpes ...... nding to the subunit interface
@en
Specific inhibition of herpes ...... nding to the subunit interface
@nl
prefLabel
Specific inhibition of herpes ...... nding to the subunit interface
@ast
Specific inhibition of herpes ...... nding to the subunit interface
@en
Specific inhibition of herpes ...... nding to the subunit interface
@nl
P2093
P2860
P356
P1476
Specific inhibition of herpes ...... nding to the subunit interface
@en
P2093
P2860
P304
P356
10.1073/PNAS.92.5.1456
P407
P50
P577
1995-02-01T00:00:00Z