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. 2021 Feb 22;49(5):2959–2972. doi: 10.1093/nar/gkab076

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© The Author(s) 2021. 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-NonCommercial 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. — The dimeric interface of p204 HINa domain. (A) HINa dimer in p204 HINa crystal. Two HINa molecules are related by a 2-fold rotational asymmetry and coloured differently. The secondary structure components involved in the dimeric interface were labeled. (B) HINa dimer in p204 HINab:dsDNA complex crystal. (C) FP assay of the dimeric interface of p204 HINab and HINa binding to 30 mer dsDNA. The apparent Kd values (Kd^a) are shown for p204 HINab, HINa and mutants. (D) Structural comparison of HINa dimer from p204 HINab:DNA and IFI16 HINa:DNA complexes. HINa dimer from IFI16 HINa: DNA complex is shown in yellow orange. HINa dimer from p204 HINab:DNA is shown in orange and pink. (E) Structural comparison of HINa dimer from p204 HINa and HINab:dsDNA complex. HINa dimer from p204 HINa structure is shown in violet and slate. HINa dimer from p204 HINab:dsDNA complex is shown in orange and pink.