Chemical shifts provide fold populations and register of β hairpins and β sheets

Journal of Biomolecular NMR

Volumn 33, Issue 4, 2005, Pages 213-231

  Fesinmeyer, R Matthew ^a   Hudson, F Michael ^a   Olsen, Katherine A ^a   White, George W N ^a   Euser, Anna ^a   Andersen, Niels H ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Chemical shift deviations; CSD; Hairpin fold population; Hairpin register; Turn signatures; Two state folding

Indexed keywords

GLYCINE; PROLINE; SOLVENT;

ANISOTROPY; AQUEOUS SOLUTION; ARTICLE; BETA SHEET; BINDING SITE; CONTROLLED STUDY; CORRELATION FUNCTION; HYDROGEN BOND; PRIORITY JOURNAL; PROTEIN FOLDING; PROTEIN SECONDARY STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; TEMPERATURE DEPENDENCE;

AMINO ACID SEQUENCE; AMINO ACIDS; HYDROGEN BONDING; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PEPTIDES; PROTEIN DENATURATION; PROTEIN FOLDING; PROTEIN STRUCTURE, SECONDARY; PROTEINS;

EID: 31044434259     PISSN: 09252738     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10858-005-3731-7     Document Type: Article

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