S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase - Test2 - elhamkhani - TriplyDB

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

http://www.wikidata.org/entity/Q35018619

about

Identification and Characterization of Novel Broad-Spectrum Inhibitors of the Flavivirus Methyltransferase Novel Broad Spectrum Inhibitors Targeting the Flavivirus Methyltransferase A conformational switch high-throughput screening assay and allosteric inhibition of the flavivirus NS2B-NS3 protease.A convergent synthesis of carbocyclic sinefungin and its C5 epimer.5'-Silylated 3'-1,2,3-triazolyl Thymidine Analogues as Inhibitors of West Nile Virus and Dengue Virus Existing drugs as broad-spectrum and potent inhibitors for Zika virus by targeting NS2B-NS3 interaction.Refolding of a fully functional flavivirus methyltransferase revealed that S-adenosyl methionine but not S-adenosyl homocysteine is copurified with flavivirus methyltransferase.Erythrosin B is a potent and broad-spectrum orthosteric inhibitor of the flavivirus NS2B-NS3 protease.

P2860

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P2860

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

http://www.wikidata.org/entity/Q35018619

description

2013 nî lūn-bûn

@nan

2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

@ast

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

@en

type

label

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

@ast

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

@en

prefLabel

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

@ast

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

@en

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JOURNAL.PONE.0076900

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P1476

S-adenosyl-homocysteine is a weakly bound inhibitor for a flaviviral methyltransferase

@en

P2093

Arun K Ghosh

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

Bing Zhou

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

Dilip Nag

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

Hui Chen

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

Jing Zhang

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

Susan A Jones

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

Zhong Li

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

P2860

Molecular targets for flavivirus drug discovery

Structure and functionality in flavivirus NS-proteins: perspectives for drug design

Structural and Functional Analyses of a Conserved Hydrophobic Pocket of Flavivirus Methyltransferase

Sinefungin derivatives as inhibitors and structure probes of protein lysine methyltransferase SETD2

CHARMM general force field: A force field for drug-like molecules compatible with the CHARMM all-atom additive biological force fields

CHARMM: the biomolecular simulation program

Comparison of simple potential functions for simulating liquid water

trans-Complementation of flavivirus RNA polymerase gene NS5 by using Kunjin virus replicon-expressing BHK cells.

An RNA cap (nucleoside-2'-O-)-methyltransferase in the flavivirus RNA polymerase NS5: crystal structure and functional characterization

West Nile Virus 5'-Cap Structure Is Formed by Sequential Guanine N-7 and Ribose 2'-O Methylations by Nonstructural Protein 5

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e76900

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scholarly article

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10

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8

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Nilesh Banavali

Matthew Brecher

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2013-10-09T00:00:00Z

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257839977

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24130807

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3793912

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