Halogen Bonding in Nucleic Acid Complexes
Language English Country United States Media print-electronic
Document type Journal Article
- MeSH
- Bromouracil analogs & derivatives MeSH
- Phosphates chemistry MeSH
- Halogens chemistry MeSH
- Oxygen chemistry MeSH
- Ligands MeSH
- Nucleosides chemistry MeSH
- Nucleic Acids chemistry MeSH
- Uridine analogs & derivatives chemistry MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- 5-bromouridine MeSH Browser
- Bromouracil MeSH
- Phosphates MeSH
- Halogens MeSH
- Oxygen MeSH
- Ligands MeSH
- Nucleosides MeSH
- Nucleic Acids MeSH
- Uridine MeSH
Halogen bonding (X-bonding) has attracted notable attention among noncovalent interactions. This highly directional attraction between a halogen atom and an electron donor has been exploited in knowledge-based drug design. A great deal of information has been gathered about X-bonds in protein-ligand complexes, as opposed to nucleic acid complexes. Here we provide a thorough analysis of nucleic acid complexes containing either halogenated building blocks or halogenated ligands. We analyzed close contacts between halogens and electron-rich moieties. The phosphate backbone oxygen is clearly the most common halogen acceptor. We identified 21 X-bonds within known structures of nucleic acid complexes. A vast majority of the X-bonds is formed by halogenated nucleobases, such as bromouridine, and feature excellent geometries. Noncovalent ligands have been found to form only interactions with suboptimal interaction geometries. Hence, the first X-bonded nucleic acid binder remains to be discovered.
References provided by Crossref.org