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Figure 3
Effects of mutations at the interface of p202 HINa on the dsDNA-binding ability. Fluorescence polarization assays were performed to determine the DNA-bound fractions of the wild-type and mutant proteins (mean and standard error, n = 3). The assays were performed in the presence of 10 µM p202 HINa protein and 15 nM 5′-FAM-labelled dsDNA.

Journal logoSTRUCTURAL BIOLOGY
COMMUNICATIONS
ISSN: 2053-230X
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