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1 that catalyzes the removal of adenine bases mispaired with 2'-deoxyguanosine and 7,8-dihydro-8-oxo-2
2 Y from Escherchia coli is removal of adenine mispaired with 7,8-dihydro-8-oxoguanine (8-oxoG), a comm
5 MutY homolog-dependent excision of adenines mispaired with 8-oxoguanine (G(O)) also act as MMR initi
14 easurements of the quantum yield of 8-DEA-tC mispaired with adenosine and, separately, opposite an ab
15 ity of PolB1 was the highest when 8-oxoG was mispaired with an incorrect nucleotide and could therefo
17 oximately 17-fold more efficiently than when mispaired with dA, which is misinserted by DNA polymeras
23 ed DNA glycosylase activity removing adenine mispaired with G, C or 8-oxoG and weakly removing guanin
26 as the base 5-fluorouracil (FU) in DNA) when mispaired with guanine, but not paired with adenine.
30 sion of 8-oxoguanine from thermally unstable mispairs with guanine or thymine, while excision from th
32 ota generates a variety of single and tandem mispairs with high frequency, implying that it may act a
33 2, +4, and +10 insertion/deletion loop (IDL) mispairs with K(d) values of 0.20, 0.25, 11, 3.2, and 0.
36 e mismatch repair complex MSH2-MSH6 binds to mispairs with only slightly higher affinity than to full
39 closed state is achieved for the A*G and G*G mispair with the incoming dGTP in anti conformation, whi
40 guingly, the simulations reveal that the G*G mispair with the incoming nucleotide in the syn configur
42 esentative oxidative DNA lesions, frequently mispairs with the incoming dAMP during mammalian DNA rep
43 t unrepaired O(6)-methyldeoxyguanine lesions mispaired with thymine during the first replication cycl
45 TMZ produces O6-methylguanine in DNA, which mispairs with thymine during the next cycle of DNA repli
46 ces O(6)-methylguanine in DNA, which in turn mispairs with thymine, triggering futile DNA mismatch re
47 e-specific differences were observed for one mispair, with WT RT preferentially resolving dC-rC pairs
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