Phospholipase C-β3 and -β1 form homodimers, but not heterodimers, through catalytic and carboxyl-terminal domains

Molecular Pharmacology

Volumn 70, Issue 3, 2006, Pages 860-868

  Zhang, Yong ^a   Vogel, Walter K ^a   McCullar, Jennifer S ^a   Greenwood, Jeffrey A ^a   Filtz, Theresa M ^a  

^a OREGON STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE NUCLEOTIDE BINDING PROTEIN; HETERODIMER; HOMODIMER; ISOENZYME; MONOMER; PHOSPHOLIPASE C BETA1; PHOSPHOLIPASE C BETA3; HYBRID PROTEIN; PHOSPHOLIPASE C; PHOSPHOLIPASE C BETA;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DIMERIZATION; ENZYME ACTIVE SITE; FLUORESCENCE RESONANCE ENERGY TRANSFER; GEL PERMEATION CHROMATOGRAPHY; HUMAN; HUMAN CELL; IMMUNOPRECIPITATION; PRIORITY JOURNAL; ANIMAL; CELL CULTURE; CHEMISTRY; GEL CHROMATOGRAPHY; ISOLATION AND PURIFICATION; METABOLISM; PROTEIN TERTIARY STRUCTURE; RAT;

ANIMALS; CATALYTIC DOMAIN; CELLS, CULTURED; CHROMATOGRAPHY, GEL; DIMERIZATION; FLUORESCENCE RESONANCE ENERGY TRANSFER; HUMANS; IMMUNOPRECIPITATION; ISOENZYMES; PHOSPHOLIPASE C; PROTEIN STRUCTURE, TERTIARY; RATS; RECOMBINANT FUSION PROTEINS;

EID: 33747603007     PISSN: 0026895X     EISSN: 15210111     Source Type: Journal    
DOI: 10.1124/mol.105.021923     Document Type: Article

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