Abstract Conformation of a tetradecapeptide with a RXVRG consensus sequence, Arg
s-Asp-Val-Arg-Gly
9, found in several precursors of antibacterian peptides, was investigated in dimethylsulfoxide solution by proton NMR spectroscopy. Complete resonance assignments and conformational parameters were obtained through correlated (COSY) and nuclear Overhauser (NOESY) techniques. The
3J(αH, βH) coupling constants and the intramolecular NOE, NH…βH, were used to analyse the conformers around the Cα-Cβ bond and, in four cases, to obtain stereospecific assignments. Use of restraints derived from NOE connectivities and
3J(NH, αH) coupling constants allows the determination of a range of φ and ψ dihedral angles for all the residues in the sequence. The present NMR results provide favourable evidence for the formation of two bends in the consensus sequence of the tetradecapeptide. The first one has most of the features of a Glu
4- Val
7 β–turn (low temperature coefficient of the Val
7NH chemical shift, Arg
5αH…Val
7NH and Asp
6NH.-.Val
7NH NOE correlations). The second one exhibits only the Asp
6αH…Arg
7NH and Val
7NH…Arg
8NH NOE interactions. These consensus sequence organizations proposed were confirmed by molecular modeling based on low potential energy structure on the [4–9] fragment with high agreement of NOE data. Overall, the substitution of Ser
12 by Ala
12 shifts the conformation of the hydrophobic moiety [10–14] towards a quite random coil structure in this fragment and strongly destabilizes the folded structures of the consensus domain where only one NH (Val
7) is solvent-shielded opposed to three (Asp
6 to Arg
8) in the [Ser
12] tetradecapeptide. These conformational changes could be related to the processing enzyme activities on these model oligopeptides.
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