Effect of sterically demanding substituents on the conformational stability of the collagen triple helix

Journal of the American Chemical Society

Volumn 134, Issue 41, 2012, Pages 17117-17124

  Erdmann, Roman S ^a   Wennemers, Helma ^a  

^a ETH ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TRIPLE HELIX; COLLAGEN-MODEL PEPTIDE; CONFORMATIONAL STABILITIES; FUNCTIONALIZED; PROLINE RESIDUES; STERICALLY DEMANDING; STRUCTURAL STUDIES; TERT-BUTYL GROUP; TRIPLE HELIXES; TRIPLE-HELICES;

AMINO ACIDS; STABILITY;

COLLAGEN;

COLLAGEN; HYDROXYPROLINE; METHYL GROUP; PROLINE;

AMINO ACID SEQUENCE; ARTICLE; CIRCULAR DICHROISM; CRYSTAL STRUCTURE; MOLECULAR MODEL; PEPTIDE SYNTHESIS; PROTEIN CONFORMATION; PROTEIN DENATURATION; PROTEIN STABILITY; STRUCTURE ANALYSIS; THERMOSTABILITY; TRIPLE HELIX;

COLLAGEN; MODELS, MOLECULAR; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN CONFORMATION; PROTEIN STABILITY; THERMODYNAMICS;

EID: 84867514299     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja3066418     Document Type: Article

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