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- W2053801105 abstract "Uracil-DNA glycosylase (UDG) functions as a sentry guarding against uracil in DNA. UDG initiates DNA base excision repair (BER) by hydrolyzing the uracil base from the deoxyribose. As one of the best studied DNA glycosylases, a coherent and complete functional mechanism is emerging that combines structural and biochemical results. This functional mechanism addresses the detection of uracil bases within a vast excess of normal DNA, the features of the enzyme that drive catalysis, and coordination of UDG with later steps of BER while preventing the release of toxic intermediates. Many of the solutions that UDG has evolved to overcome the challenges of policing the genome are shared by other DNA glycosylases and DNA repair enzymes, and thus appear to be general." @default.
- W2053801105 created "2016-06-24" @default.
- W2053801105 creator A5028696052 @default.
- W2053801105 creator A5045737800 @default.
- W2053801105 creator A5059713279 @default.
- W2053801105 date "2000-08-01" @default.
- W2053801105 modified "2023-10-16" @default.
- W2053801105 title "Lessons learned from structural results on uracil-DNA glycosylase" @default.
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- W2053801105 doi "https://doi.org/10.1016/s0921-8777(00)00026-4" @default.
- W2053801105 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10946228" @default.
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