Solution structure of calmodulin bound to the target peptide of endothelial nitric oxide synthase phosphorylated at Thr495

Biochemistry

Volumn 53, Issue 8, 2014, Pages 1241-1249

  Piazza, Michael ^a   Taiakina, Valentina ^a   Guillemette, Simon R ^a   Guillemette, J Guy ^a   Dieckmann, Thorsten ^a  

^a UNIVERSITY OF WATERLOO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM BINDING PROTEINS; CALCIUM CONCENTRATION; CONFORMATIONAL CHANGE; ELECTROSTATIC REPULSION; ENDOTHELIAL NITRIC OXIDE SYNTHASE; NITRIC-OXIDE SYNTHASE; PATHOLOGICAL PROCESS; PHOSPHORYLATION SITES;

AMINO ACIDS; CALCIUM; CAMS; ENZYMES; NITRIC OXIDE; PEPTIDES; PHOSPHORYLATION; PHYSIOLOGY;

CALMODULIN;

CALMODULIN; ENDOTHELIAL NITRIC OXIDE SYNTHASE; THREONINE;

ARTICLE; BIOPHYSICS; CHEMICAL STRUCTURE; CONFORMATIONAL TRANSITION; ELECTRON; FLUORESCENCE SPECTROSCOPY; ISOTHERMAL TITRATION CALORIMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; PROTEIN TARGETING;

AMINO ACID SEQUENCE; CALCIUM; CALMODULIN; HUMANS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NITRIC OXIDE SYNTHASE TYPE III; PEPTIDE FRAGMENTS; PHOSPHOPEPTIDES; PHOSPHORYLATION; PROTEIN BINDING; PROTEIN STRUCTURE, SECONDARY; SOLUTIONS; STATIC ELECTRICITY; THREONINE;

EID: 84896798577     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi401466s     Document Type: Article

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