Journal ArticleDOI
C8-amino purine nucleosides. A well-defined steric determinant of glycosyl conformational preferences.
Frank Jordan,Haggai Niv +1 more
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TLDR
Temperature dependent behavior of chemical shifts and the difference in chemical shifts between the C1'-H and C2'-H resonances clearly indicated whether the nucleoside exists in a syn glycosyl conformation or as a flexible syn-anti mixture (the monomethylamino and amino derivatives).About:
This article is published in Biochimica et Biophysica Acta.The article was published on 1977-06-17. It has received 39 citations till now. The article focuses on the topics: Chemical shift & Conformational isomerism.read more
Citations
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Journal ArticleDOI
A non-empirical chromophoric interpretation of CD spectra of DNA G-quadruplex structures
Stefano Masiero,Roberta Trotta,Silvia Pieraccini,Stefano De Tito,Rosaria Carmela Perone,Antonio Randazzo,Gian Piero Spada +6 more
TL;DR: The case of quadruplexes formed by monomeric guanosine derivatives, where there is no strand connecting the adjacent quartets and the definition parallel/antiparallel strands cannot apply, will be discussed.
Journal ArticleDOI
Recognition of Thymine Adenine Base Pairs by Guanine in a Pyrimidine Triple Helix Motif
Linda C. Griffin,Peter B. Dervan +1 more
TL;DR: A study of 20 base triplets reveals that the triple helix can be extended from homopurine to mixed sequences, and Guanine contained within a pyrimidine oligonucleotide specifically recognizes thymine.
Book ChapterDOI
Circular dichroism of quadruplex structures.
TL;DR: In this chapter the CD spectral features characteristic of different folding topologies of G4-DNA are analyzed in terms of the sequence of the syn or anti glycosidic bond angle (GBA) within a quadruplex stem.
Journal ArticleDOI
DNA base modification: ionized base pairs and mutagenesis
TL;DR: The model presented in this study should be useful as DNA-sequence analysis becomes more commonly applied to the study of mutagenesis, and as DNA structure at and surrounding ionized base pairs may be altered.
Journal ArticleDOI
Effects of an 8-bromodeoxyguanosine incorporation on the parallel quadruplex structure [d(TGGGT)]4
Veronica Esposito,Antonio Randazzo,Gennaro Piccialli,Luigi Petraccone,Concetta Giancola,Luciano Mayol +5 more
TL;DR: The conformational features found in the three quadruplexes might, in principle, amplify the range of applicability of synthetic oligonucleotides as aptamers or catalysts, by providing novel structural motifs with different molecular recognition capabilities from those of native DNA sequences.
References
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Journal ArticleDOI
Conformational analysis of the sugar ring in nucleosides and nucleotides. A new description using the concept of pseudorotation.
C. Altona,M. Sundaralingam +1 more
Journal ArticleDOI
Conformational analysis of the sugar ring in nucleosides and nucleotides. Improved method for the interpretation of proton magnetic resonance coupling constants
C. Altona,M. Sundaralingam +1 more
Journal ArticleDOI
Studies on Polynucleotides. XIV.1 Specific Synthesis of the C3"-C5" Interribonucleotide Linkage. Syntheses of Uridylyl-(3"5")-Uridine and Uridylyl-(3"5")-Adenosine2
Journal ArticleDOI
Nuclear magnetic resonance studies of 5'-ribo- and deoxyribonucleotide structures in solution
Journal ArticleDOI
Probing the interrelation between the glycosyl torsion, sugar pucker, and the backbone conformation in C(8) substituted adenine nucleotides by 1H and 1H-(31P) fast Fourier transform nuclear magnetic resonance methods and conformational energy calculations.
Related Papers (5)
Carbon-13 magnetic resonance spectra of 8-substituted purine nucleosides. Characteristic shifts for the syn conformation.
Seiichi Uesugi,Morio Ikehara +1 more
Conformational analysis of the sugar ring in nucleosides and nucleotides. Improved method for the interpretation of proton magnetic resonance coupling constants
C. Altona,M. Sundaralingam +1 more