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Protein Science, Vol 7, Issue 11 2472-2475, Copyright © 1998 by Cold Spring Harbor Laboratory Press
FOR THE RECORD |
J. WOUTERS
Facultes Universitaires N.-D. de la Paix, 61 Rue de Bruxelles, B-5000 Namur, Belgium
Experimental evidence of a cation-{pi} interaction between a sodium cation (Na(+)) and the indole ring of residue Trp123 in a structure (2.0 A) of hen egg-white lysozyme is presented. The geometry of the metal ion-{pi} interaction observed in the protein structure (distance between the aromatic plane and the cation ~4 A) is consistent with geometries observed among small molecules crystal structures and quantum chemistry ab initio calculations. The present crystal structure of lysozyme provides unique structural information about the geometry of binding of cations to {pi} systems in proteins. It shows that the metal ion-{pi} interaction within proteins is not significantly different from similar bindings found in small molecules and that it can be modeled by theoretical methods.
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