Sequence and structural duality: Designing peptides to adopt two stable conformations

Journal of the American Chemical Society

Volumn 126, Issue 51, 2004, Pages 17016-17024

  Pandya, Maya J ^a   Cerasoli, Eleonora ^a   Joseph, Abbey ^a   Stoneman, Rhys G ^a   Waite, Eleanor ^a   Woolfson, Derek N ^a  

^a UNIVERSITY OF SUSSEX   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DIMERS; MONOMERS; PROTEINS; REDUCTION;

INTRAMOLECULES; PEPTIDES; SWITCH STRUCTURAL STATE;

CONFORMATIONS;

BRIDGED COMPOUND; DIMER; DISULFIDE; LEUCINE; MONOMER; PEPTIDE; REDUCING AGENT;

AMINO ACID SEQUENCE; ARTICLE; PROTEIN CONFORMATION; PROTEIN MOTIF; PROTEIN TARGETING;

AMINO ACID SEQUENCE; CIRCULAR DICHROISM; CYSTEINE; HYDROPHOBICITY; LEUCINE ZIPPERS; LYSINE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MOLECULAR WEIGHT; OLIGOPEPTIDES; PEPTIDES; PROTEIN CONFORMATION; PROTEIN ENGINEERING;

EID: 11244335621     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja045568c     Document Type: Article

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