Internalization and trafficking of guanylyl (guanylate) cyclase/natriuretic peptide receptor A is regulated by an acidic tyrosine-based cytoplasmic motif GDAY

Biochemical Journal

Volumn 388, Issue 1, 2005, Pages 103-113

  Pandey, Kailash N ^a   Nguyen, Huong T ^a   Garg, Renu ^a   Khurana, Madan L ^a   Fink, Jude ^a  

^a TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Cytoplasmic motif; Guanylyl cylcase (guanylate cyclase) natriuretic peptide receptor A; Human embryonic kidney 293 cells (HEK 293 cells); Ligand binding; Receptor internalization and trafficking; Site directed mutagenesis

Indexed keywords

LIGANDS; MUTANTS; MUTATION; NATRIURETIC PEPTIDE RECEPTOR A (NPRA) SEQUENCE;

BIOCHEMISTRY; CELL CULTURE; DNA SEQUENCES; GENETIC ENGINEERING; MOLECULAR STRUCTURE; RECYCLING;

ENZYMES;

ALANINE; ASPARTIC ACID; COMPLEMENTARY DNA; GLYCINE; GUANYLATE CYCLASE; NATRIURETIC FACTOR; PROTEIN NATRIURETIC PEPTIDE RECEPTOR A; TYROSINE; UNCLASSIFIED DRUG;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DOWN REGULATION; ENDOCYTOSIS; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; INTERNALIZATION; LIGAND BINDING; MUTATION; PRIORITY JOURNAL; PROTEIN MOTIF; SITE DIRECTED MUTAGENESIS;

AMINO ACID MOTIFS; ATRIAL NATRIURETIC FACTOR; CELL LINE; DOWN-REGULATION; HUMANS; MUTAGENESIS, SITE-DIRECTED; MUTATION; PROTEIN TRANSPORT; RECEPTORS, ATRIAL NATRIURETIC FACTOR; TYROSINE;

EID: 19544384364     PISSN: 02646021     EISSN: None     Source Type: Journal    
DOI: 10.1042/BJ20041250     Document Type: Article

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