Low pH overrides the need of calcium ions for the shape-function relationship of calmodulin: Resolving prevailing debates

Journal of Physical Chemistry B

Volumn 118, Issue 19, 2014, Pages 5059-5074

  Pandey, Kalpana ^a   Dhoke, Reema R ^a   Rathore, Yogendra Singh ^a   Nath, Samir K ^a   Verma, Neha ^a   Bawa, Simranjot ^a   Ashish, ^a  

^a INSTITUTE OF MICROBIAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; CAMS; CRYSTAL STRUCTURE; IONS; MOLECULES; PEPTIDES;

ANALYTICAL ULTRACENTRIFUGATION; CELLULAR FUNCTION; GLOBAL SHAPES; ION CONCENTRATIONS; NMR STRUCTURES; PEPTIDE BINDING; SEDIMENTATION COEFFICIENTS; WEIGHTED AVERAGES;

CALMODULIN;

APOPROTEIN; CALCIUM; CALMODULIN; DIVALENT CATION; PEPTIDE; PROTEIN BINDING; RECOMBINANT PROTEIN;

CHEMICAL STRUCTURE; CHEMISTRY; ESCHERICHIA COLI; GENE EXPRESSION; GENETICS; HUMAN; KINETICS; METABOLISM; PH; PROTEIN SECONDARY STRUCTURE; PROTEIN TERTIARY STRUCTURE; STATIC ELECTRICITY; THERMODYNAMICS;

APOPROTEINS; CALCIUM; CALMODULIN; CATIONS, DIVALENT; ESCHERICHIA COLI; GENE EXPRESSION; HUMANS; HYDROGEN-ION CONCENTRATION; KINETICS; MODELS, MOLECULAR; PEPTIDES; PROTEIN BINDING; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; RECOMBINANT PROTEINS; STATIC ELECTRICITY; THERMODYNAMICS;

EID: 84900525415     PISSN: 15206106     EISSN: 15205207     Source Type: Journal    
DOI: 10.1021/jp501641r     Document Type: Article

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