نتایج جستجو برای: nucleotide related compound

تعداد نتایج: 1394814  

Journal: :Nucleic acids research 1980
A B Vartapetian Y F Drygin K M Chumakov A A Bogdanov

Two protein, VPgA and VPgB, are covalently bound to the virion RNA of encephalomyocarditis (EMC) virus. Their molecular weightrs, as determined by polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate are 10,000 and 8,000, respectively. A study of nucleotide-peptides isolated from VPg-RNA compound has shown that VPgA is bound to the 5'-terminal nucleotide of RNA by a phos...

Journal: :Molecular cancer therapeutics 2007
Konstantinos Kiakos Atsushi Sato Tetsuji Asao Peter J McHugh Moses Lee John A Hartley

AS-I-145 is a novel achiral seco-amino-cyclopropylbenz[e]indolone (seco-amino-CBI) analogue of duocarmycin that has evolved from an alternative strategy of designing CC-1065/duocarmycin agents lacking the characteristic chiral center of the natural agents. The sequence specificity of this compound was assessed by a Taq polymerase stop assay, identifying the sites of covalent modification on pla...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2015
Jennifer La Catherine F Latham Ricky N Tinetti Adam Johnson David Tyssen Kelly D Huber Nicolas Sluis-Cremer Jamie S Simpson Stephen J Headey David K Chalmers Gilda Tachedjian

Fragment-based screening methods can be used to discover novel active site or allosteric inhibitors for therapeutic intervention. Using saturation transfer difference (STD) NMR and in vitro activity assays, we have identified fragment-sized inhibitors of HIV-1 reverse transcriptase (RT) with distinct chemical scaffolds and mechanisms compared to nonnucleoside RT inhibitors (NNRTIs) and nucleosi...

Journal: :The Journal of biological chemistry 2010
Maria Novikova Teymur Kazakov Gaston H Vondenhoff Ekaterina Semenova Jef Rozenski Anastasija Metlytskaya Inna Zukher Anton Tikhonov Arthur Van Aerschot Konstantin Severinov

The heptapeptide-nucleotide microcin C (McC) is a potent inhibitor of enteric bacteria growth. McC is excreted from producing cells by the MccC transporter. The residual McC that remains in the producing cell can be processed by cellular aminopeptidases with the release of a non-hydrolyzable aspartyl-adenylate, a strong inhibitor of aspartyl-tRNA synthetase. Accumulation of processed McC inside...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Haiying Meng Shelley D Smith Karl Hager Matthew Held Jonathan Liu Richard K Olson Bruce F Pennington John C DeFries Joel Gelernter Thomas O'Reilly-Pol Stefan Somlo Pawel Skudlarski Sally E Shaywitz Bennett A Shaywitz Karen Marchione Yu Wang Murugan Paramasivam Joseph J LoTurco Grier P Page Jeffrey R Gruen

DYX2 on 6p22 is the most replicated reading disability (RD) locus. By saturating a previously identified peak of association with single nucleotide polymorphism markers, we identified a large polymorphic deletion that encodes tandem repeats of putative brain-related transcription factor binding sites in intron 2 of DCDC2. Alleles of this compound repeat are in significant disequilibrium with mu...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Laura J Terry Livia Vastag Joshua D Rabinowitz Thomas Shenk

Human cytomegalovirus (HCMV) modulates numerous cellular signaling pathways. Alterations in signaling are evident from the broad changes in cellular phosphorylation that occur during HCMV infection and from the altered activity of multiple kinases. Here we report a comprehensive RNAi screen, which predicts that 106 cellular kinases influence growth of the virus, most of which were not previousl...

2015
Mark Davies Nathan Dedman Anne Hersey George Papadatos Matthew D. Hall Lourdes Cucurull-Sanchez Phil Jeffrey Samiul Hasan Peter J. Eddershaw John P. Overington

MOTIVATION ADME SARfari is a freely available web resource that enables comparative analyses of drug-disposition genes. It does so by integrating a number of publicly available data sources, which have subsequently been used to build data mining services, predictive tools and visualizations for drug metabolism researchers. The data include the interactions of small molecules with ADME (absorpti...

A new series of N-(5-Mercapto-1,3,4-thiadiazol-2-yl)-2-phenylacetamide derivatives (3a-3j) were synthesized via an amidation reaction using EDC and HOBt in acetonitrile solvent at room temperature condition. Chemical structures were characterized by 1H NMR, IR and MS spectroscopic methods and related melting points were also determined. The anticancer activity was evaluated using MTT procedure ...

A new series of N-(5-Mercapto-1,3,4-thiadiazol-2-yl)-2-phenylacetamide derivatives (3a-3j) were synthesized via an amidation reaction using EDC and HOBt in acetonitrile solvent at room temperature condition. Chemical structures were characterized by 1H NMR, IR and MS spectroscopic methods and related melting points were also determined. The anticancer activity was evaluated using MTT procedure ...

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