Conformational exchange of aromatic side chains characterized by L-optimized TROSY-selected 13C CPMG relaxation dispersion

Journal of Biomolecular NMR

Volumn 54, Issue 1, 2012, Pages 9-14

  Weininger, Ulrich ^a   Respondek, Michal ^a   Akke, Mikael ^a  

^a LUND UNIVERSITY   (Sweden)

Author keywords

Aromatic side chain; Conformational exchange; Protein folding; Relaxation dispersion; TROSY

Indexed keywords

CARBON 13;

ACCURACY; ARTICLE; CONFORMATIONAL TRANSITION; HETERONUCLEAR SINGLE QUANTUM COHERENCE; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN FOLDING; PROTEIN UNFOLDING; PROTON NUCLEAR MAGNETIC RESONANCE;

AMINO ACIDS, AROMATIC; CARBON ISOTOPES; KINETICS; MODELS, MOLECULAR; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN CONFORMATION; PROTEINS;

EID: 84865633476     PISSN: 09252738     EISSN: 15735001     Source Type: Journal    
DOI: 10.1007/s10858-012-9656-z     Document Type: Article

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