| Literature DB >> 16575941 |
Patricia A Khuu1, Andrea Regier Voth1, Franklin A Hays1, P Shing Ho1.
Abstract
The crystal structure of the four-stranded DNA Holliday junction has now been determined in the presence and absence of junction binding proteins, with the extended open-X form of the junction seen in all protein complexes, but the more compact stacked-X structure observed in free DNA. The structures of the stacked-X junction were crystallized because of an unexpected sequence dependence on the stability of this structure. Inverted repeat sequences that contain the general motif NCC or ANC favor formation of stacked-X junctions, with the junction cross-over occurring between the first two positions of the trinucleotides. This review focuses on the sequence dependent structure of the stacked-X junction and how it may play a role in structural recognition by a class of dimeric junction resolving enzymes that themselves show no direct sequence recognition. Copyright 2006 John Wiley & Sons, Ltd.Entities:
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Year: 2006 PMID: 16575941 PMCID: PMC4537160 DOI: 10.1002/jmr.765
Source DB: PubMed Journal: J Mol Recognit ISSN: 0952-3499 Impact factor: 2.137