Functional chimeras of GLIC obtained by adding the intracellular domain of anion- and cation-conducting Cys-loop receptors

Biochemistry

Volumn 54, Issue 16, 2015, Pages 2670-2682

  Mnatsakanyan, Nelli ^a,c   Nishtala, Sita Nirupama ^a   Pandhare, Akash ^a   Fiori, Mariana C ^a   Goyal, Raman ^a   Pauwels, Jonathan E ^a,b   Navetta, Andrew F ^a   Ahrorov, Afzal ^a,b   Jansen, Michaela ^a  

^a TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER SCHOOL OF MEDICINE   (United States)

^b TEXAS TECH UNIVERSITY   (United States)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION ANALYSIS; AMINO ACIDS; IONS; LIGANDS; MODULATION; POSITIVE IONS; PROTEINS;

ACETYLCHOLINE-BINDING PROTEINS; INTRACELLULAR DOMAIN; LARGE-SCALE EXPRESSION; LIGAND-GATED ION CHANNELS; NICOTINIC ACETYLCHOLINE RECEPTORS; SEQUENCE CONSERVATION; STRUCTURAL STUDIES; TRANS-MEMBRANE DOMAINS;

ENZYME ACTIVITY;

ACETYLCHOLINE; ANION; CATION; CHAPERONE; CYSTEINE; LIGAND GATED ION CHANNEL; MEMBRANE RECEPTOR; NICOTINIC RECEPTOR; PROTEIN RIC 3; UNCLASSIFIED DRUG; BACTERIAL PROTEIN; BUNGAROTOXIN RECEPTOR; FISH PROTEIN; HYBRID PROTEIN;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; BACTERIUM; CHIMERA; CONTROLLED STUDY; CRYSTAL STRUCTURE; EUKARYOTE; GLOEOBACTER VIOLACEUS; GLYCOSYLATION; HYDROPHOBICITY; LIGAND BINDING; MOLECULAR SIZE; NONHUMAN; PECTOBACTERIUM CHRYSANTHEMI; PRIORITY JOURNAL; PROKARYOTE; PROTEIN ASSEMBLY; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN PURIFICATION; TORPEDO; ANIMAL; CHEMISTRY; GENETICS; PROTEIN SECONDARY STRUCTURE; PROTEIN TERTIARY STRUCTURE;

ERWINIA CHRYSANTHEMI; EUKARYOTA; GLOEOBACTER VIOLACEUS; PROKARYOTA;

ALPHA7 NICOTINIC ACETYLCHOLINE RECEPTOR; ANIMALS; BACTERIAL PROTEINS; FISH PROTEINS; PECTOBACTERIUM CHRYSANTHEMI; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; RECOMBINANT FUSION PROTEINS; TORPEDO;

EID: 84928663325     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/acs.biochem.5b00203     Document Type: Article

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