β-Arrestin differentially regulates the chemokine receptor CXCR4- mediated signaling and receptor internalization, and this implicates multiple interaction sites between β-arrestin and CXCR4

Journal of Biological Chemistry

Volumn 275, Issue 4, 2000, Pages 2479-2485

  Cheng, Zhi Jie ^a   Zhao, Jian ^a   Sun, Yue ^a   Hu, Wei ^a   Wu, Ya Lan ^a   Cen, Bo ^a   Wu, Guo Xiang ^a   Pei, Gang ^a  

^a INSTITUTE OF BIOCHEMISTRY AND CELL BIOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BETA ARRESTIN; CHEMOKINE RECEPTOR CXCR4; CYCLIC AMP; GLUTATHIONE TRANSFERASE; GUANINE NUCLEOTIDE BINDING PROTEIN; MITOGEN ACTIVATED PROTEIN KINASE; MUTANT PROTEIN;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; ENZYME ACTIVATION; HUMAN; HUMAN CELL; INTERNALIZATION; PRIORITY JOURNAL; PROTEIN CROSS LINKING; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN PROTEIN INTERACTION; REACTION ANALYSIS; RECEPTOR BINDING; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; STRUCTURE ACTIVITY RELATION;

ARRESTINS; BINDING SITES; CELL LINE; ENDOCYTOSIS; HUMANS; MUTAGENESIS; RECEPTORS, CXCR4; SIGNAL TRANSDUCTION;

HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 0034723291     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.275.4.2479     Document Type: Article

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