4uqg

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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4uqg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4uqg OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4uqg RCSB], [http://www.ebi.ac.uk/pdbsum/4uqg PDBsum]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4uqg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4uqg OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4uqg RCSB], [http://www.ebi.ac.uk/pdbsum/4uqg PDBsum]</span></td></tr>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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We report the development of a new heterobase that is held together through reversible bonding. The so-formed cross-link adds strong stabilization to the DNA duplex. Despite this, the cross-link opens and closes through reversible imine bonding. Moreover, even enzymatic incorporation of the cross-link is possible. The new principle can be used to stabilize DNA duplexes and nanostructures that otherwise require high salt concentrations, which may hinder biological applications.
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"Post-It" Type Connected DNA Created with a Reversible Covalent Cross-Link.,Tomas-Gamasa M, Serdjukow S, Su M, Muller M, Carell T Angew Chem Int Ed Engl. 2014 Nov 28. doi: 10.1002/anie.201407854. PMID:25446281<ref>PMID:25446281</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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== References ==
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<references/>
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</StructureSection>
</StructureSection>

Revision as of 12:20, 10 December 2014

A new bio-isosteric base pair based on reversible bonding

4uqg, resolution 2.00Å

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