Halogen Bonding in Nucleic Acid Complexes
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
- MeSH
- bromouracil analogy a deriváty MeSH
- fosfáty chemie MeSH
- halogeny chemie MeSH
- kyslík chemie MeSH
- ligandy MeSH
- nukleosidy chemie MeSH
- nukleové kyseliny chemie MeSH
- uridin analogy a deriváty chemie MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- 5-bromouridine MeSH Prohlížeč
- bromouracil MeSH
- fosfáty MeSH
- halogeny MeSH
- kyslík MeSH
- ligandy MeSH
- nukleosidy MeSH
- nukleové kyseliny MeSH
- uridin 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.
Citace poskytuje Crossref.org