Publication | Closed Access
Synthesis and Peptide Binding Properties of Methoxypyrrole Amino Acids (MOPAS)
27
Citations
3
References
2004
Year
Bioorganic ChemistryPeptide EngineeringMolecular BiologyPeptide ScienceChemistryChemical BiologyNmr TitrationProtein FoldingSmall PeptidesProtein ChemistryBiochemistryBioconjugationHairpin StructuresSolution Nmr SpectroscopyMolecular ModelingStructural BiologyBiomolecular EngineeringNatural SciencesPeptide LibraryPeptide TherapeuticPeptide Binding PropertiesPeptide SynthesisMedicine
[structure: see text] Methoxypyrrole amino acids (MOPAS) have been prepared and were introduced into small peptides with hairpin structures. The intra- and intermolecular binding properties of this heterocyclic amino acid mimicking a dipeptido beta-strand was investigated by NMR titration and X-ray crystal structure analysis. The data reveal a hydrogen bonding pattern that is complementary to a peptide beta-sheet.
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