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PDBsum entry 4cis

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Hydrolase PDB id
4cis
Contents
Protein chains
263 a.a.
DNA/RNA
Ligands
BU3
Metals
_ZN ×2
Waters ×135

References listed in PDB file
Key reference
Title Ribose-Protonated DNA base excision repair: a combined theoretical and experimental study.
Authors K.Sadeghian, D.Flaig, I.D.Blank, S.Schneider, R.Strasser, D.Stathis, M.Winnacker, T.Carell, C.Ochsenfeld.
Ref. Angew Chem Int Ed Engl, 2014, 53, 10044-10048. [DOI no: 10.1002/anie.201403334]
PubMed id 25065673
Abstract
Living organisms protect the genome against external influences by recognizing and repairing damaged DNA. A common source of gene mutation is the oxidized guanine, which undergoes base excision repair through cleavage of the glycosidic bond between the ribose and the nucleobase of the lesion. We unravel the repair mechanism utilized by bacterial glycosylase, MutM, using quantum-chemical calculations involving more than 1000 atoms of the catalytic site. In contrast to the base-protonated pathway currently favored in the literature, we show that the initial protonation of the lesion's ribose paves the way for an almost barrier-free glycosidic cleavage. The combination of theoretical and experimental data provides further insight into the selectivity and discrimination of MutM's binding site toward various substrates.
PROCHECK
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 Headers

 

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