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Volumn 12, Issue 7, 2011, Pages 1039-1042

The Combination of Prolinoamino Acids and Cyclopropylamino Acids Leads to Fully Functionalized, Stable β-Turns in Water

(9) Guitot, Karine a,b,c Larregola, Maud a,b,c Pradhan, Tarun K d Vasse, Jean Luc d Lavielle, Solange a,b,c Bertus, Philippe e Szymoniak, Jan d Lequin, Olivier a,b,c Karoyan, Philippe a,b,c

a SORBONNE UNIVERSITÉ (France)

b ECOLE NORMALE SUPÉRIEURE (France)

c CNRS (France)

d UNIVERSITÉ DE REIMS CHAMPAGNE ARDENNE (France)

e UNIVERSITÉ DU MAINE (France)

Author keywords

Beta turns; Cyclopropylamino acids; NMR spectroscopy; Peptidomimetics; Prolinoamino acid

Indexed keywords

AMINO ACID; BETA AMINO ACID; PEPTIDOMIMETIC AGENT; PROLINE DERIVATIVE; PROPYLAMINE;

ARTICLE; BETA TURN; BINDING AFFINITY; DIASTEREOISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN CONFORMATION; PROTEIN FOLDING; PROTEIN MOTIF; PROTEIN SECONDARY STRUCTURE; PROTEIN STRUCTURE;

CRYSTALLOGRAPHY, X-RAY; CYCLOPROPANES; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; OLIGOPEPTIDES; PROLINE; STEREOISOMERISM; WATER;

EID: 79955057486 PISSN: 14394227 EISSN: 14397633 Source Type: Journal
DOI: 10.1002/cbic.201000707 Document Type: Article

Times cited : (10)

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