Improvement of hydrogen bond geometry in protein NMR structures by residual dipolar couplings - An assessment of the interrelation of NMR restraints

Journal of Biomolecular NMR

Volumn 28, Issue 1, 2004, Pages 31-41

  Jensen, Pernille Rose ^a   Axelsen, Jacob Bock ^a   Lerche, Mathilde Hauge ^a,b   Poulsen, Flemming M ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b Amersham Health R and D   (Sweden)

Author keywords

Chymotrypsin inhibitor 2; Hydrogen bonds; NMR structures; Residual dipolar couplings; Structure refinement

Indexed keywords

CARBON 13; HYDROGEN; NITROGEN 15;

ARTICLE; CALCULATION; COMPUTER PROGRAM; CONTROLLED STUDY; CROSS COUPLING REACTION; GEOMETRY; HYDROGEN BOND; MOLECULAR CLONING; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NUCLEAR OVERHAUSER EFFECT; PRIORITY JOURNAL; PROTEIN FOLDING; PROTEIN STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE;

DIAZEPAM BINDING INHIBITOR; HYDROGEN BONDING; MOLECULAR STRUCTURE; NEURAL CELL ADHESION MOLECULES; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PEPTIDES; PLANT PROTEINS; PROTEINS;

EID: 1242340497     PISSN: 09252738     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:JNMR.0000012865.35872.cc     Document Type: Article

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