Cargando…
The Free Energy Landscape of Pseudorotation in 3′–5′ and 2′–5′ Linked Nucleic Acids
[Image: see text] The five-membered furanose ring is a central component of the chemical structure of biological nucleic acids. The conformations of the furanose ring can be analytically described using the concept of pseudorotation, and for RNA and DNA they are dominated by the C(2′)-endo and C(3′)...
Autores principales: | Li, Li, Szostak, Jack W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982932/ https://www.ncbi.nlm.nih.gov/pubmed/24499340 http://dx.doi.org/10.1021/ja412079b |
Ejemplares similares
-
Productive
Alkyne Metathesis with “Canopy Catalysts”
Mandates Pseudorotation
por: Haack, Alexander, et al.
Publicado: (2021) -
Interplay of Rotational and
Pseudorotational Motions in Flexible Cyclic Molecules
por: Paoloni, Lorenzo, et al.
Publicado: (2021) -
Revealing pseudorotation and ring-opening reactions in colloidal organic molecules
por: Swinkels, P. J. M., et al.
Publicado: (2021) -
Electrostatic free energy landscapes for nucleic acid helix assembly
por: Tan, Zhi-Jie, et al.
Publicado: (2006) -
Efficient and Rapid Template-Directed Nucleic Acid Copying Using 2′-Amino-2′,3′-dideoxyribonucleoside−5′-Phosphorimidazolide Monomers
por: Schrum, Jason P., et al.
Publicado: (2009)