Interaction of indole derivatives with biologically important aromatic compounds. Part 22. Importance of simultaneous co-operation of hydrogen-bond pairing and stacking interactions for recognition of guanine base by a peptide: X-ray crystal analysis of 7-methylguanosine-5′-phosphate–tryptophanylglutamic acid complex
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1991/P1/P19910001847
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1. Prominent stacking interaction with aromatic amino acid by N-quarternization of nucleic acid base: X-ray crystallographic characteristics and biological implications
2. Nucleotide base recognition: ditopic binding of guanine to a macrocyclic receptor containing naphthyridine and naphthalene units
3. Molecular recognition: hydrogen bonding and stacking interactions stabilize a model for nucleic acid structure
4. Molecular Recognition: Stacking Interactions Influence Watson-Crick vs. Hoogsteen Base-Pairing in a Model for Adenine Receptors
5. Nucleotide base recognition: a macrocyclic receptor for adenine employing hydrogen bonding and aromatic stacking interactions
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1. The first 3′:5′-cyclic nucleotide–amino acid complex:L-His–cIMP;Acta Crystallographica Section C Crystal Structure Communications;2012-07-13
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3. Nucleotide–amino acid interactions in theL-His–IMP·MeOH·H2O complex;Acta Crystallographica Section C Crystal Structure Communications;2010-05-08
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5. Aromatic interactions in tryptophan-containing peptides: crystal structures of model tryptophan peptides and phenylalanine analogs*;The Journal of Peptide Research;2008-12-05
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