Literature DB >> 8289290

Planar stacking interactions of arginine and aromatic side-chains in proteins.

M M Flocco1, S L Mowbray.   

Abstract

A parallel stacking arrangement of the guanidinium groups of arginines directly over the center of the rings of aromatic side-chains is observed much more frequently in proteins than would be expected by chance. This type of interaction, which is often found in locations critical to the function, apparently serves to orient the arginine side-chain without interfering with its ability to form hydrogen bonds elsewhere. It is distinct from the interactions which involve the side-chains of asparagine or glutamine, which do frequently assume a nearly planar relationship to the ring, but at a position at or beyond the ring edge.

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Year:  1994        PMID: 8289290     DOI: 10.1006/jmbi.1994.1022

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  58 in total

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3.  Crystal structure of the yeast cytochrome bc1 complex with its bound substrate cytochrome c.

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4.  Do guanidinium and tetrapropylammonium ions specifically interact with aromatic amino acid side chains?

Authors:  Bei Ding; Debopreeti Mukherjee; Jianxin Chen; Feng Gai
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Review 5.  Cation-pi bonding and amino-aromatic interactions in the biomolecular recognition of substituted ammonium ligands.

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7.  Conformational preferences of 1-amino-2-phenylcyclohexanecarboxylic acid, a phenylalanine cyclohexane analogue.

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8.  An arginine switch in the species B adenovirus knob determines high-affinity engagement of cellular receptor CD46.

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9.  Contribution of the tyrosines to the structure and function of the human U1A N-terminal RNA binding domain.

Authors:  J K Kranz; J Lu; K B Hall
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10.  Trp fluorescence reveals an activation-dependent cation-pi interaction in the Switch II region of Galphai proteins.

Authors:  Heidi E Hamm; Scott M Meier; Guihua Liao; Anita M Preininger
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