Dalton Transactions · 2009 · 12 citations · 22 references
Natural SciencesBiochemistryChemistryBiophysical ChemistryStructural BiologyStructural BiophysicsCoordination ChemistryLigand BindingLigand-based DesignMetal-ligand BondingPeptide ChemistryProtein StructureCopper ProteinsCopper(ii) RecognitionCopper-binding SitesCopper-sulfur InteractionsPeptide Medicinal ChemistryPeptide Structure - Activity RelationshipsPhysiological Ph EffectsPotentiometric Measurement
A replacement of both Cys residues by His in oxytocin (OXT) sequence allows for the formation of the stable complex with the {NH(2), N(Im), N(Im(macrochelate))} binding mode at the physiological pH. The detailed potentiometric and spectroscopic studies on the Cu(II) complexes of [His(1,6)]OXT, together with high resolution NMR investigations on 3D structures of Cu(II) complexes with [His(1,6)]OXT and [His(1,6)]AVP analogues are presented and discussed. Exchange of the Cys-S-S-Cys bridge by the His-Cu(II)-His motif is very promising, because the resulting complexes retain topological similarity to the native S-S bridged AVP and OXT at pH values corresponding to the physiological pH.
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Coordination Chemistry Reviews · 1996 · 262 citations
Alpha plus beta folds revisited: some favoured motifs
Christine Orengo, Janet M. Thornton · Structure · 1993 · 135 citations · Full text