Handedness control of peptide helices by amino acid side-chain chirality: Ile/alle peptides

Biopolymers - Peptide Science Section

Volumn 84, Issue 5, 2006, Pages 490-501

  Andreetto, Erika ^a   Peggion, Cristina ^a   Crisma, Marco ^a   Toniolo, Claudio ^a  

^a UNIVERSITY OF PADOVA   (Italy)

Author keywords

aminoisobutyric acid; 310 helix; C tetrasubstituted amino acid; Circular dichroism; Conformational analysis; Helical screw sense; IR absorption; NMR; Peptide synthesis; X ray diffraction

Indexed keywords

HELICAL STRUCTURES; HEXAPEPTIDE SEQUENCE; OLIGOPEPTIDES; SOLUTION ABSORPTION;

ABSORPTION; AMINO ACIDS; CRYSTALLINE MATERIALS; NUCLEAR MAGNETIC RESONANCE; SOLUTIONS; SYNTHESIS (CHEMICAL); X RAY DIFFRACTION ANALYSIS;

NITROGEN COMPOUNDS;

AMINO ACID; CARBON; HEXAPEPTIDE; PEPTIDE;

ARTICLE; CHEMICAL BOND; CHIRALITY; CHROMATOPHORE; CIRCULAR DICHROISM; CONFORMATION; CRYSTALLIZATION; DIASTEREOISOMER; INFRARED SPECTROSCOPY; ISOMERISM; MELTING POINT; PEPTIDE ANALYSIS; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; X RAY DIFFRACTION;

ISOLEUCINE; MAGNETIC RESONANCE SPECTROSCOPY; OLIGOPEPTIDES; PROTEIN STRUCTURE, SECONDARY; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; STEREOISOMERISM; X-RAY DIFFRACTION;

ALLE;

EID: 33749497842     PISSN: 00063525     EISSN: 10970282     Source Type: Journal    
DOI: 10.1002/bip.20534     Document Type: Article

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