نتایج جستجو برای: uracil and cytosine

تعداد نتایج: 16828814  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1973
J M Mackenzie M M Neville G E Wright N C Brown

The active forms of 6-(p-hydroxyphenylazo)-uracil and 6-(p-hydroxyphenylazo)-isocytosine were isolated and identified as their respective hydrazino derivatives. These arylhydrazino pyrimidines selectively inhibited a chromatographically distinct DNA polymerase from Bacillus subtilis. The actions of the reduced drugs on this polymerase were identical to those observed on ATP-dependent DNA synthe...

Journal: :The Journal of clinical investigation 2004
Matthias Endres Detlev Biniszkiewicz Robert W Sobol Christoph Harms Michael Ahmadi Andreas Lipski Juri Katchanov Philipp Mergenthaler Ulrich Dirnagl Samuel H Wilson Andreas Meisel Rudolf Jaenisch

Uracil-DNA glycosylase (UNG) is involved in base excision repair of aberrant uracil residues in nuclear and mitochondrial DNA. Ung knockout mice generated by gene targeting are viable, fertile, and phenotypically normal and have regular mutation rates. However, when exposed to a nitric oxide donor, Ung(-/-) fibroblasts show an increase in the uracil/cytosine ratio in the genome and augmented ce...

Journal: :Nucleic Acids Research 2006
Jens Georg Lars Schomacher James P. J. Chong Alan I. Majerník Monika Raabe Henning Urlaub Sabine Müller Elena Ciirdaeva Wilfried Kramer Hans-Joachim Fritz

The genome of Methanothermobacter thermautotrophicus, as a hitherto unique case, is apparently devoid of genes coding for general uracil DNA glycosylases, the universal mediators of base excision repair following hydrolytic deamination of DNA cytosine residues. We have now identified protein Mth212, a member of the ExoIII family of nucleases, as a possible initiator of DNA uracil repair in this...

Journal: :Nucleic acids research 2004
Mayumi Matsubara Tamon Tanaka Hiroaki Terato Eiji Ohmae Shunsuke Izumi Katsuo Katayanagi Hiroshi Ide

Single-strand selective monofunctional uracil-DNA glycosylase (SMUG1), previously thought to be a backup enzyme for uracil-DNA glycosylase, has recently been shown to excise 5-hydroxyuracil (hoU), 5-hydroxymethyluracil (hmU) and 5-formyluracil (fU) bearing an oxidized group at ring C5 as well as an uracil. In the present study, we used site-directed mutagenesis to construct a series of mutants ...

2016
Javier Abellón-Ruiz Sonoko Ishino Yoshizumi Ishino Bernard A Connolly

In Archaea repair of uracil and hypoxanthine, which arise by deamination of cytosine and adenine, respectively, is initiated by three enzymes: Uracil-DNA-glycosylase (UDG, which recognises uracil); Endonuclease V (EndoV, which recognises hypoxanthine); and Endonuclease Q (EndoQ), (which recognises both uracil and hypoxanthine). Two archaeal DNA polymerases, Pol-B and Pol-D, are inhibited by dea...

2008
Josephine Wardle Peter M. J. Burgers Isaac K. O. Cann Kate Darley Pauline Heslop Erik Johansson Li-Jung Lin Peter McGlynn Jonathan Sanvoisin Carrie M. Stith Bernard A. Connolly

Family B DNA polymerases from archaea such as Pyrococcus furiosus, which live at temperatures approximately 100 degrees C, specifically recognize uracil in DNA templates and stall replication in response to this base. Here it is demonstrated that interaction with uracil is not restricted to hyperthermophilic archaea and that the polymerase from mesophilic Methanosarcina acetivorans shows identi...

Journal: :The EMBO journal 1998
M A Schumacher D Carter D M Scott D S Roos B Ullman R G Brennan

Uracil phosphoribosyltransferase (UPRTase) catalyzes the transfer of a ribosyl phosphate group from alpha-D-5-phosphoribosyl-1-pyrophosphate to the N1 nitrogen of uracil. The UPRTase from the opportunistic pathogen Toxoplasma gondii is a rational target for antiparasitic drug design. To aid in structure-based drug design studies against toxoplasmosis, the crystal structures of the T.gondii apo ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Gemma Serrano-Heras Alicia Bravo Margarita Salas

Protein p56 encoded by the Bacillus subtilis phage phi29 inhibits host uracil-DNA glycosylase (UDG) activity. In previous studies, we suggested that this inhibition is likely a defense mechanism developed by phage phi29 to prevent the action of UDG if uracilation occurs in DNA either from deamination of cytosine or the incorporation of dUMP during viral DNA replication. In this work, we analyze...

Density functional theory (DFT) calculations were performed to investigate the effects of a carbon nanotube (CNT) on the properties of the fluorouracil (F-Uracil) anticancer drug. To achieve the purpose, a molecular model including both of F-Uracil and CNT molecules was created to represent the CNT@F-Uracil compound. The optimized parameters indicated that the new compound could show new proper...

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