Configurationally driven folding of model tetrapeptides containing L- or D-morpholine-3-carboxylic acids as β-turn nucleators

Chirality

Volumn 21, Issue 6, 2009, Pages 584-594

  Trabocchi, Andrea ^a   Sladojevich, Filippo ^a   Guarna, Antonio ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

Author keywords

Conformation analysis; NMR spectroscopy; Peptides; Peptidomimetics; Protein folding

Indexed keywords

AMIDE; DEXTRO MORPHOLINE 3 CARBOXYLIC ACID; HYDROGEN; LEVO MORPHOLINE 3 CARBOXYLIC ACID; MORPHOLINE; PROLINE; TETRAPEPTIDE; UNCLASSIFIED DRUG; VALINE; AMINO ACID; CARBOXYLIC ACID; PEPTIDE;

ARTICLE; BETA TURN; CHIRALITY; CIS ISOMER; HYDROGEN BOND; INFRARED RADIATION; NUCLEAR MAGNETIC RESONANCE; PEPTIDOMICS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN CONFORMATION; PROTEIN FOLDING; TRANS ISOMER; CHEMICAL STRUCTURE; CHEMISTRY; INFRARED SPECTROPHOTOMETRY; STEREOISOMERISM; SYNTHESIS;

AMINO ACIDS; CARBOXYLIC ACIDS; MODELS, MOLECULAR; PEPTIDES; PROTEIN CONFORMATION; PROTEIN FOLDING; SPECTROPHOTOMETRY, INFRARED; STEREOISOMERISM;

EID: 67649414746     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20647     Document Type: Article

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