Random coil chemical shift for intrinsically disordered proteins: Effects of temperature and pH

Journal of Biomolecular NMR

Volumn 49, Issue 2, 2011, Pages 139-149

  Kjaergaard, Magnus ^a   Brander, Søren ^a   Poulsen, Flemming M ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Natively unfolded protein; NMR; Peptide; Protonation state; Secondary chemical shift analysis

Indexed keywords

CARBON 13; HISTIDINE; INTRINSICALLY DISORDERED PROTEIN; PEPTIDE; PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; PH; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTON NUCLEAR MAGNETIC RESONANCE; TEMPERATURE; TITRIMETRY;

HYDROGEN-ION CONCENTRATION; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN FOLDING; PROTEINS; TEMPERATURE;

EID: 79954427635     PISSN: 09252738     EISSN: 15735001     Source Type: Journal    
DOI: 10.1007/s10858-011-9472-x     Document Type: Article

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