A kinetic analysis of substrate recognition by uracil-DNA glycosylase from herpes simplex virus type 1
S.R.W.Bellamy and G.S.Baldwin
Nucleic Acids Res. (2001) 29, 3857–3863
In this study the authors used a mutant of UDG to investigate the binding of the enzyme to DNA substrates. They stated in the original article that the D88N mutant was used. However, it was in fact a double mutant where both the catalytic residues Asp 88 and His 210 were mutated to Asn (D88N; H210N) that was used. This in no way affects the conclusions that were reached in the paper.