The Solution Conformation of a Carbocyclic Analog of the Dickerson-Drew Dodecamer: Comparison with its own X-ray Structure and that of the NMR Structure of the Native Counterpart-Reference-Cited by-同舟云学术

The Solution Conformation of a Carbocyclic Analog of the Dickerson-Drew Dodecamer: Comparison with its own X-ray Structure and that of the NMR Structure of the Native Counterpart

Published:1998-12 Issue:3 Volume:16 Page:547-568
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Denisov Aleksej Yu.,Zamaratski E. V.,Maltseva Tatiana V.,Sandström Anders,Bekiroglu Somer,Altmann Karl-Heinz,Egli Martin,Chattopadhyaya Jyoti

Publisher

Informa UK Limited

Subject

Molecular Biology,General Medicine,Structural Biology

Link

http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883

Reference51 articles.

1. 6′-Carbon-substituted carbocyclic analogs of 2′-deoxyribonucleosides — Synthesis and effect on DNA/RNA duplex stability

2. Crystal Structures of Oligodeoxyribonucleotides Containing 6‘-α-Methyl and 6‘-α-Hydroxy Carbocyclic Thymidines

3. Solution Structure of a DNA Dodecamer Containing the Anti-Neoplastic Agent Arabinosylcytosine: Combined Use of NMR, Restrained Molecular Dynamics, and Full Relaxation Matrix Refinement

4. Structure and Dynamics of a DNA.cntdot.RNA Hybrid Duplex with a Chiral Phosphorothioate Moiety: NMR and Molecular Dynamics with Conventional and Time-Averaged Restraints

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