Vaccinia virus virulence factor N1L is a novel promising target for antiviral therapeutic intervention. - Wikidata - wikimedia - TriplyDB

Vaccinia virus virulence factor N1L is a novel promising target for antiviral therapeutic intervention.

Vaccinia virus virulence factor N1L is a novel promising target for antiviral therapeutic intervention.

http://www.wikidata.org/entity/Q39707773

about

Specific small molecule inhibitors of Skp2-mediated p27 degradation Incorporation of protein flexibility and conformational energy penalties in docking screens to improve ligand discovery Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes.Viral infection: an evolving insight into the signal transduction pathways responsible for the innate immune response Structural revisions of small molecules reported to cross-link G-quadruplex DNA in vivo reveal a repetitive assignment error in the literature Pd(0)-catalyzed 1,1-diarylation of ethylene and allylic carbonates.Viral interference with innate immunity by preventing NF-κB activity.The Bcl-2 family: structures, interactions and targets for drug discovery.Resveratrol, sirtuins, and viruses.The vaccinia virus-encoded Bcl-2 homologues do not act as direct Bax inhibitors.Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters.Nickel-catalyzed cross couplings of benzylic ammonium salts and boronic acids: stereospecific formation of diarylethanes via C-N bond activation.A General, Simple Catalyst for Enantiospecific Cross Couplings of Benzylic Ammonium Triflates and Boronic Acids: No Phosphine Ligand Required Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.Aldimine-directed branched-selective hydroarylation of styrenes.Nickel(0)-Catalyzed Hydroarylation of Styrenes and 1,3-Dienes with Organoboron Compounds.Suppression of Poxvirus Replication by Resveratrol.Enantioselective Intermolecular C-O Bond Formation in the Desymmetrization of Diarylmethines Employing a Guanidinylated Peptide-Based Catalyst.Direct cross-coupling of benzyl alcohols to construct diarylmethanes via palladium catalysis.Phosphine-catalyzed Friedel-Crafts reaction of naphthols with para-quinone methides: expedient access to triarylmethanes.Organocatalyzed Asymmetric Conjugate Addition of Heteroaryl and Aryl Trifluoroborates: a Synthetic Strategy for Discoipyrrole D.

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P2860

Vaccinia virus virulence factor N1L is a novel promising target for antiviral therapeutic intervention.

http://www.wikidata.org/entity/Q39707773

description

2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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2010年學術文章

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2010年學術文章

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name

Vaccinia virus virulence facto ...... iral therapeutic intervention.

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Vaccinia virus virulence facto ...... iral therapeutic intervention.

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type

label

Vaccinia virus virulence facto ...... iral therapeutic intervention.

@en

Vaccinia virus virulence facto ...... iral therapeutic intervention.

@nl

prefLabel

Vaccinia virus virulence facto ...... iral therapeutic intervention.

@en

Vaccinia virus virulence facto ...... iral therapeutic intervention.

@nl

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Journal of Medicinal Chemistry

P1476

Vaccinia virus virulence facto ...... iral therapeutic intervention.

@en

P2093

Alexander Aleshin

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

Andrey A Bobkov

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

Anton V Cheltsov

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

Dayong Zhai

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

Eric Chi-Wang Yu

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

John C Reed

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

Mika Aoyagi

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Robert C Liddington

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

Taylor Gilliland

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P2860

Functional and structural studies of the vaccinia virus virulence factor N1 reveal a Bcl-2-like anti-apoptotic protein

Vaccinia virus N1L protein resembles a B cell lymphoma-2 (Bcl-2) family protein

Vaccinia virus anti-apoptotic F1L is a novel Bcl-2-like domain-swapped dimer that binds a highly selective subset of BH3-containing death ligands

Flexible ligand docking to multiple receptor conformations: a practical alternative

Complete sequence and genomic analysis of murine gammaherpesvirus 68

Web-based toolkits for topology prediction of transmembrane helical proteins, fold recognition, structure and binding scoring, folding-kinetics analysis and comparative analysis of domain combinations

Structural and functional analysis of the actin binding domain of plectin suggests alternative mechanisms for binding to F-actin and integrin beta4

The structure of a Bcl-xL/Bim fragment complex: implications for Bim function

Humanin binds and nullifies Bid activity by blocking its activation of Bax and Bak

Glide: a new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy

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3899-3906

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10.1021/JM901446N

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