Hoogsteen base pair: Difference between revisions

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==History==
Ten years after [[James Watson]] and [[Francis Crick]] published their model of the DNA double helix,<ref name="Watson">{{cite journal |title=Molecular Structure of Nucleic Acids: A Structure for Deoxyribose Nucleic Acid|vauthors=Watson JD, Crick FH |journal=Nature|year=1953|volume=171|issue=4356|pages=737–738|doi=10.1038/171737a0|pmid=13054692|bibcode=1953Natur.171..737W|s2cid=4253007 }}</ref> [[Karst Hoogsteen]] reported <ref>{{cite journal |title=The crystal and molecular structure of a hydrogen-bonded complex between 1-methylthymine and 9-methyladenine|author=Hoogsteen K|journal=Acta Crystallographica|year=1963|volume=16|issue=9|pages=907–916|doi=10.1107/S0365110X63002437|doi-access=free}}</ref> a crystal structure of a complex in which analogues of A and T formed a base pair that had a different geometry from that described by Watson and Crick. Similarly, an alternative base-pairing geometry can occur for G•C pairs. Hoogsteen pointed out that if the alternative hydrogen-bonding patterns were present in DNA, then the double helix would have to assume a quite different shape. Hoogsteen base pairs are observed in alternative structures such as the four-stranded [[G-quadruplex]] structures that form in DNA and RNA.
 
==Chemical properties==