International journal of peptide & protein research · 1988 · 398 citations · 21 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignMolecular PharmacologyStructure-activity RelationshipsAmino Acid ChemistryAmino Acid PropertiesAmino Acid StructurePeptide ChemistryPeptide Drug DiscoveryStructure-activity Relationship AnalysisAmino Acid AnaloguesAmino AcidsCross-correlation StudiesPeptide HydrophobicityPeptide Medicinal ChemistryPrincipal ComponentsSide-chain ModelingSteric Properties
Fifteen physicochemical descriptors of side chains of the 20 natural and of 26 non-coded amino acids are compiled and simple methods for their evaluation described. The relevance of these parameters to account for hydrophobic, steric, and electric properties of the side chains is assessed and their intercorrelation analyzed. It is shown that three principal components, one steric, one bulk, and one electric (electronic), account for 66% of the total variance in the available set. These parameters may prove to be useful for correlation studies in series of bioactive peptide analogues.
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Solvation energy in protein folding and binding
David Eisenberg, Andrew D. McLachlan · Nature · 1986 · 1.9K citations
NMR in biological research: Peptides and proteins
G. K. Radda · Trends in Biochemical Sciences · 1977 · 529 citations