Unphosphorylated calponin enhances the binding force of unphosphorylated myosin to actin

Biochimica et Biophysica Acta - General Subjects

Volumn 1830, Issue 10, 2013, Pages 4634-4641

  Roman, Horia Nicolae ^a,b   Zitouni, Nedjma B ^a   Kachmar, Linda ^a   Ijpma, Gijs ^a,b   Hilbert, Lennart ^a,b   Matusovsky, Oleg ^a,b   Benedetti, Andrea ^b,c   Sobieszek, Apolinary ^d   Lauzon, Anne Marie ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

^c MCGILL UNIVERSITY   (Canada)

^d ERICH SCHMID INSTITUTE OF MATERIALS SCIENCE   (Austria)

Author keywords

Actin regulatory proteins; In vitro motility assay; Laser trap; Latch state

Indexed keywords

ACTIN; CALPONIN; F ACTIN; MYOSIN;

ARTICLE; BINDING AFFINITY; CONTROLLED STUDY; IONIC STRENGTH; LATCH STATE; MUSCLE CHARACTERISTICS AND FUNCTIONS; PRIORITY JOURNAL; PROTEIN CROSS LINKING; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; SMOOTH MUSCLE;

ACTIN REGULATORY PROTEINS; IN VITRO MOTILITY ASSAY; LASER TRAP; LATCH-STATE;

ACTINS; ANIMALS; BLOTTING, WESTERN; CALCIUM-BINDING PROTEINS; MICROFILAMENT PROTEINS; MICROSPHERES; MYOSINS; PHOSPHORYLATION; PROTEIN BINDING; SWINE;

EID: 84879485770     PISSN: 03044165     EISSN: 18728006     Source Type: Journal    
DOI: 10.1016/j.bbagen.2013.05.042     Document Type: Article

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