• This enzyme would therefore recognize and cut out both types of uracil - the one incorporated naturally, and the one formed due to cytosine deamination, which would trigger unnecessary and inappropriate repair processes. (wikipedia.org)
  • The N123D mutation generates an enzyme that excises cytosine. (ox.ac.uk)
  • In the first stage of the base excision repair pathway the enzyme uracil DNA glycosylase (UNG) recognizes and excises uracil (U) from DNA filaments. (sissa.it)
  • 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. (elsevierpure.com)
  • The enzyme hydrolyzes uracil glycosidic bonds at U-DNA in single- and double-stranded DNA excising uracil and creating alkali sensitive abasic sites in the DNA. (apslabs.in)
  • The enzyme is inactive on RNA and native, uracil-free DNA. (apslabs.in)
  • Uracil-DNA glycosylase excises uracil bases from double-stranded DNA. (wikipedia.org)
  • In the present study, we used site-directed mutagenesis to construct a series of mutants of human SMUG1 (hSMUG1), and tested their activity for uracil, hoU, hmU, fU and other bases to elucidate the catalytic and damage-recognition mechanism of hSMUG1. (elsevierpure.com)
  • This tends to occur with bases uracil and guanine, as the pairing is less specific. (ukessays.com)
  • Degradation of uracil produces the substrates β-alanine, carbon dioxide, and ammonia. (wikipedia.org)
  • This N123D:L191A mutant excises C when it is mispaired with A or opposite an abasic site, but not when it is paired with G. In contrast no cleavage is observed with any substrates that contain 5-methylcytosine. (ox.ac.uk)
  • Surprisingly, H109 in the loop was found to make a covalent bond to the abasic site to form a stable intermediate, while the excised uracil remained in the pocket of the active site. (kaist.ac.kr)
  • Uracil DNA glycosylase (UDG) efficiently removes uracil from DNA in a reaction in which the base is flipped into the enzyme's active site. (ox.ac.uk)
  • Subsequent PCR/LAMP reaction mixes must be pre-treated with Uracil-DNA Glycosylase (UNG), thermo labile prior to PCR/LAMP to degrade uracil containing DNA. (apslabs.in)
  • The structure of UdgX from Mycobacterium smegmatis in complex with DNA shows an overall similarity to that of family 4 UDGs except for a protruding loop at the entrance of the uracil-binding pocket. (kaist.ac.kr)
  • Belongs to the uracil-DNA glycosylase family. (abcam.cn)
  • So cells continue to use uracil in RNA, and not in DNA, because RNA is shorter-lived than DNA, and any potential uracil-related errors do not lead to lasting damage. (wikipedia.org)
  • Uracil is rarely found in DNA, and this may have been an evolutionary change to increase genetic stability. (wikipedia.org)
  • The excision of base damage is initiated by a specific DNA glycosylase: Hypoxanthine is bound and excised efficiently by human N -methylpurine-DNA glycosylase (MPG, also known as AAG, ANPG, APNG, or MDG) [ 6 ]. (biomedcentral.com)
  • 5. Stimulation of DNA glycosylase activity of OGG1 by NEIL1: functional collaboration between two human DNA glycosylases. (nih.gov)
  • 8. Catalytic and DNA-binding properties of the human Ogg1 DNA N-glycosylase/AP lyase: biochemical exploration of H270, Q315 and F319, three amino acids of the 8-oxoguanine-binding pocket. (nih.gov)
  • 9. Cloning and characterization of an ascidian homolog of the human 8-oxoguanine DNA glycosylase (Ogg1) that is involved in the repair of 8-oxo-7,8-dihydroguanine in DNA in Ciona intestinalis. (nih.gov)
  • 14. The C-terminal alphaO helix of human Ogg1 is essential for 8-oxoguanine DNA glycosylase activity: the mitochondrial beta-Ogg1 lacks this domain and does not have glycosylase activity. (nih.gov)
  • 15. The Ogg1 protein of Saccharomyces cerevisiae: a 7,8-dihydro-8-oxoguanine DNA glycosylase/AP lyase whose lysine 241 is a critical residue for catalytic activity. (nih.gov)
  • 16. Dimerization and opposite base-dependent catalytic impairment of polymorphic S326C OGG1 glycosylase. (nih.gov)
  • The mechanism requires a family of enzymes called glycosylases. (news-medical.net)
  • The putative AP-endonuclease (mvAPE) specifically cleaves at the abasic site created by the glycosylase while also exhibiting the 3'-5' exonuclease activity. (bvsalud.org)
  • 3. Specificity of stimulation of human 8-oxoguanine-DNA glycosylase by AP endonuclease. (nih.gov)
  • 10. Mechanism of interaction between human 8-oxoguanine-DNA glycosylase and AP endonuclease. (nih.gov)
  • 19. Coordination of MYH DNA glycosylase and APE1 endonuclease activities via physical interactions. (nih.gov)
  • 13. Adenine Glycosylase MutY of Corynebacterium pseudotuberculosis presents the antimutator phenotype and evidences of glycosylase/AP lyase activity in vitro. (nih.gov)
  • The process called BASE EXCISION REPAIR can be completed by a DNA -(APURINIC OR APYRIMIDINIC SITE) LYASE which excises the remaining RIBOSE sugar from the DNA . (nih.gov)
  • We found that AAG bound to a wide variety of purine and pyrimidine lesions but excised only a few of them. (nih.gov)
  • Therefore, additional enzymes are required to excise the dI lesions in the EndoV-mediated repair process. (biomedcentral.com)
  • 12. Recognition of the oxidized lesions spiroiminodihydantoin and guanidinohydantoin in DNA by the mammalian base excision repair glycosylases NEIL1 and NEIL2. (nih.gov)
  • C4H4N2O2→ H3NCH2CH2COO− + NH+4 + CO2 Oxidative degradation of uracil produces urea and maleic acid in the presence of H2O2 and Fe2+ or in the presence of diatomic oxygen and Fe2+. (wikipedia.org)
  • The human 3-methyladenine DNA glycosylase (AAG) recognizes and excises a broad range of purines damaged by alkylation and oxidative damage, including 3-methyladenine, 7-methylguanine, hypoxanthine (Hx), and 1,N(6)-ethenoadenine (epsilonA). (nih.gov)
  • Uracil is a common and naturally occurring pyrimidine derivative. (wikipedia.org)
  • In contrast to the purine nucleotides, the pyrimidine ring (orotidylic acid) that leads uracil is synthesized first and then linked to ribose phosphate, forming UMP. (wikipedia.org)
  • Complementary pathways, initiated by the uracil-DNA glycosylase (UNG) or the mismatch repair factor MSH2/MSH6, must process the deoxyuridine to initiate class-switch recombination (CSR) and somatic hypermutation. (aai.org)
  • Furthermore, we show that when reconstituted in vitro, mvUDG, mvAPE, and mvPolX function cohesively to repair a uracil-containing DNA predominantly by long patch BER and together, may participate in the BER pathway during the early phase of Mimivirus life-cycle. (bvsalud.org)
  • In addition, we found that both the full-length and truncated AAG excised 1,N(2)-ethenoguanine (1,N(2)-epsilonG), albeit weakly, from duplex DNA. (nih.gov)
  • Apparently, either there was no evolutionary pressure to replace uracil in RNA with the more complex thymine, or uracil has some chemical property that is useful in RNA, which thymine lacks. (wikipedia.org)
  • 2. A functional analysis of the DNA glycosylase activity of mouse MUTYH protein excising 2-hydroxyadenine opposite guanine in DNA. (nih.gov)
  • We believe that """"""""recognition"""""""" of damage by DNA glycosylases is not limited to interactions in the enzyme's active site but, rather, is part of a dynamic process involving a series of conformational changes, each of which may ultimately contribute to lesion specificity. (grantome.com)
  • 18. Catalytically Competent Conformation of the Active Site of Human 8-Oxoguanine-DNA Glycosylase. (nih.gov)
  • So cells continue to use uracil in RNA, and not in DNA, because RNA is shorter-lived than DNA, and any potential uracil-related errors do not lead to lasting damage. (wikipedia.org)
  • This problem is believed to have been solved in terms of evolution, that is by "tagging" (methylating) uracil. (wikipedia.org)