• ITs AP (apurinic/apyrimidinic) lyase activity introduces nicks in the DNA strand, cleaving the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates. (wikipedia.org)
  • Taken together, the data support a model in which spore resistance to solar UV results from a complex interplay of structural, photochemical, and DNA repair processes. (photobiology.com)
  • DNA glycosylase/AP lyase enzymes are involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. (wikipedia.org)
  • The two DNA-binding motifs (a zinc finger and the helix-two-turns-helix motifs) suggest that the oxidized base is flipped out from double-stranded DNA in the binding mode and excised by a catalytic mechanism similar to that of bifunctional base excision repair enzymes. (wikipedia.org)
  • ii) Spore DNA damage correction during spore germination is dependent upon nucleotide excision repair, recombination repair, and the SP-specific SP lyase repair systems. (photobiology.com)
  • 2000). The nucleotide excision repair (NER), recombinational repair (Rec), and spore photoproduct (SP) lyase DNA repair pathways are major determinants of spore resistance to 254-nm UV-C radiation in the laboratory ( Fig. 1 ). (photobiology.com)
  • UV resistance of spores and vegetative cells of B. subtilis DNA repair mutants. (photobiology.com)
  • Escherichia coli endonuclease III (EC 4.2.99.18 ) (gene nth) [ 1 ] is a DNA repair enzyme that acts both as a DNA N-glycosylase, removing oxidized pyrimidines from DNA, and as an apurinic/apyrimidinic (AP) endonuclease, introducing a single-strand nick at the site from which the damaged base was removed. (expasy.org)
  • Escherichia coli and related protein DNA repair protein mutY, which is an adenine glycosylase. (expasy.org)
  • In Escherichia coli , early studies indicated that the DNA glycosylase encoded by alkA gene could recognize and release hypoxanthine residues from DNA [ 1 ]. (biomedcentral.com)
  • and AP lyase activity EC 4.2.99.18. (wikipedia.org)
  • EC 3.2.2.23) and cleaves both the 3'- and 5'-phosphodiester bonds of the resulting apurinic/apyrimidinic site (AP lyase activity;EC 4.2.99.18). (wikipedia.org)
  • In molecular biology, the H2TH domain (helix-2turn-helix domain) is a DNA-binding domain found in DNA glycosylase/AP lyase enzymes, which are involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. (wikipedia.org)
  • These enzymes are primarily from bacteria, and have both DNA glycosylase activity EC 3.2.2. (wikipedia.org)
  • Micrococcus luteus ultraviolet N-glycosylase/AP lyase which initiates repair at cis-syn pyrimidine dimers. (expasy.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)
  • Atomic structure of the DNA repair [4Fe-4S] enzyme endonuclease III. (expasy.org)
  • Endonuclease V (EndoV) in E. coli is active upon DNA exposed to UV light, OsO4, acids, or X-rays [ 10 ]. (biomedcentral.com)
  • This enzyme was later characterized as 3′-deoxyinosine endonuclease that incises the DNA at the second phosphodiester bond 3′ to the dI lesion, leaving 3′-OH and 5′-P termini [ 13 ]. (biomedcentral.com)
  • Most damage to bases in DNA is repaired by the base excision repair pathway. (wikipedia.org)
  • The two DNA-binding motifs (a zinc finger and the H2TH (helix-two-turns-helix) motifs) suggest that the oxidised base is flipped out from double-stranded DNA in the binding mode and excised by a catalytic mechanism similar to that of bifunctional base excision repair enzymes. (wikipedia.org)
  • In mammalian cells, base excision repair (BER) was thought to be the major pathway for dI repair. (biomedcentral.com)
  • Wilson, S.H. and Kuff, E.L. A novel DNA polymerase activity found in association with intracisternal A-type particles. (nih.gov)
  • Moreover, judging from the repair requirements and sensitivity to specific polymerase inhibitors, there were overlapping repair activities in processing of dI in DNA. (biomedcentral.com)
  • From radionucleotide incorporation fine mapping, the resulting apurinic/apyrimidinic (AP) sites are further processed by both the short patch pathway (1-nucleotide gap filling) with DNA polymerase (Pol) β and the long patch pathway (2-6 nucleotide resynthesis) with Pol δ and PCNA [ 7 ]. (biomedcentral.com)
  • Deoxyinosine derived from deamination of deoxyadenosine in DNA is potentially mutagenic since it prefers to pair with dCTP during replication, yielding A:T to G:C transition mutations at sites of adenine deamination [ 5 ]. (biomedcentral.com)
  • The N-terminal catalytic domain and the C-terminal zinc finger straddle the DNA with the long axis of the protein oriented roughly orthogonal to the helical axis of the DNA. (wikipedia.org)
  • The 4Fe-4S cluster does not seem to be important for catalytic activity, but is probably involved in the proper positioning of the enzyme along the DNA strand [ 2 ]. (expasy.org)
  • Nfi homologues from Thermotoga maritima possess 3′-exonuclease activity that might be used for removal of damaged bases [ 14 ], but similar exonuclease activities were not found in EndoV from E. coli and mammalian cells. (biomedcentral.com)