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. 2018 Jul 19;46(15):8010–8022. doi: 10.1093/nar/gky621

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© The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 4. — (A) Comparison of the (6-4)PP damaged duplex DNA binding to D. melanogaster (6-4) photolyase (3CVU) and CraCRY (6FN0). Electrostatic potentials were calculated with APBS (c = 0.1 M, solvent radius = 1.4 Å). The DNA ends were prolonged by regular B-type DNA using PyMOL and the overall binding angles of the DNA therefrom derived. (B) Detailed view of the (6-4)PP binding depicting the flipping of R413 upon DNA binding. The side chain of R413 in the unbound CraCRY structure is shown in blue.