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Centre for Chemical Biology, Department of Chemistry, Krebs Institute, University of Sheffield, Sheffield, UK
E-mail: j.a.grasby@sheffield.ac.uk
; Tel: +44 (0)1142229478
Chem. Commun., 2012,48, 8895-8897
DOI:
10.1039/C2CC33400C
Received
10 May 2012,
Accepted
10 Jul 2012
First published online
11 Jul 2012
Flap endonucleases (FENs) are proposed to select their target phosphate diester by unpairing the two terminal nucleotides of duplex. Interstrand disulfide crosslinks, introduced by oxidation of thiouracil and thioguanine bases, abolished the specificity of human FEN1 for hydrolysis one nucleotide into the 5′-duplex.
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