Multiple evolutionarily conserved di-leucine like motifs in the carboxyl terminus control the anterograde trafficking of NKCC2

Journal of Biological Chemistry

Volumn 287, Issue 51, 2012, Pages 42642-42653

  Zaarour, Nancy ^a,b,c,d   Demaretz, Sylvie ^a,b,c,d   Defontaine, Nadia ^a,b,c,d   Zhu, Yingying ^a,b,c,d   Laghmani, Kamel ^a,b,c,d  

^a CENTRE DE RECHERCHE DES CORDELIERS   (France)

^b CNRS   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYL TERMINUS; CELL SURFACE EXPRESSION; CO-TRANSPORTERS; COLOCALIZATION; COOH-TERMINAL; DOUBLE MUTATION; EXPRESSION SYSTEM; GLYCOSYLATED; HUMAN DISEASE; HYDROPHOBIC MOTIFS; KIDNEY DISEASE; NATURALLY OCCURRING; PULSE-CHASE ANALYSIS; RENAL CELL; SURFACE EXPRESSION; THERAPEUTIC DRUGS;

CELL MEMBRANES; CHLORINE COMPOUNDS;

AMINO ACIDS;

CALNEXIN; SODIUM CHLORIDE COTRANSPORTER; SODIUM POTASSIUM CHLORIDE COTRANSPORTER;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ANTEROGRADE TRAFFICKING; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL STRAIN HEK293; CELL SURFACE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DILEUCINE MOTIF; EMBRYO; ENDOPLASMIC RETICULUM; GENETIC CONSERVATION; HUMAN; HUMAN CELL; IN VIVO STUDY; INTRACELLULAR SIGNALING; MEMBRANE TRANSPORT; MOLECULAR DYNAMICS; NONHUMAN; OPOSSUM; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN MOTIF; PROTEIN PROCESSING; PROTEIN TRANSPORT; PULSE CHASE ANALYSIS; SEQUENCE ANALYSIS;

AMINO ACID MOTIFS; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMALS; CELL LINE; CELL MEMBRANE; CONSERVED SEQUENCE; ENDOPLASMIC RETICULUM; EVOLUTION, MOLECULAR; HUMANS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MICE; MOLECULAR SEQUENCE DATA; MUTANT PROTEINS; MUTATION; OPOSSUMS; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; SODIUM CHLORIDE SYMPORTERS; SODIUM-POTASSIUM-CHLORIDE SYMPORTERS; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84871148861     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.399162     Document Type: Article

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