Amino acid residues 489-503 of dihydropyridine receptor (dhpr) β1a subunit are critical for structural communication between the skeletal muscle dhpr complex and type 1 Ryanodine Receptor

Journal of Biological Chemistry

Volumn 289, Issue 52, 2014, Pages 36116-36124

  Eltit, Jose M ^b   Franzini Armstrong, Clara ^c   Perez, Claudio F ^a  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; CELL MEMBRANES; MUSCLE; PYRIDINE;

ALANINE SUBSTITUTION; AMINO ACID RESIDUES; C-TERMINAL TAIL; CRITICAL DETERMINANT; DIHYDROPYRIDINE RECEPTORS; FUNCTIONAL INTERACTION; RYANODINE RECEPTORS; SKELETAL MUSCLE;

AMINO ACIDS;

1,4 DIHYDROPYRIDINE RECEPTOR; 1,4 DIHYDROPYRIDINE RECEPTOR SUBUNIT BETA 1A; AMINO ACID; CALCIUM CHANNEL L TYPE; GLUTAMINYLVALYLGLUTAMINYLVALYLLEUCYLTHREONYLSERYLLEUCYLARGINYLARGINYLASPARAGINYLLEUCYLSERYLPHENYLALANYLTRYPTOPHAN; RYANODINE RECEPTOR 1; UNCLASSIFIED DRUG; CACNB1 PROTEIN, MOUSE; PROTEIN SUBUNIT; RYANODINE RECEPTOR;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CALCIUM SIGNALING; CALCIUM TRANSPORT; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CONTROLLED STUDY; EXCITATION CONTRACTION COUPLING; FREEZE FRACTURE; MEMBRANE DEPOLARIZATION; MOLECULAR CLONING; MOUSE; MUSCLE CONTRACTION; NONHUMAN; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN MOTIF; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; ANIMAL; CELL CULTURE; CHEMICAL PHENOMENA; MEMBRANE POTENTIAL; METABOLISM; MOLECULAR GENETICS; PROTEIN SUBUNIT; PROTEIN TRANSPORT;

AMINO ACID MOTIFS; AMINO ACID SEQUENCE; ANIMALS; CALCIUM CHANNELS, L-TYPE; CELLS, CULTURED; EXCITATION CONTRACTION COUPLING; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MEMBRANE POTENTIALS; MICE; MOLECULAR SEQUENCE DATA; PROTEIN SUBUNITS; PROTEIN TRANSPORT; RYANODINE RECEPTOR CALCIUM RELEASE CHANNEL;

EID: 84919785088     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.615526     Document Type: Article

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