Kinetic and mutational analysis of Zn2+ modulation of recombinant human inhibitory glycine receptors

Journal of Physiology

Volumn 522, Issue 2, 2000, Pages 215-230

  Laube, Bodo ^a   Kuhse, Jochen ^a,b   Betz, Heinrich ^a  

^a MAX PLANCK INSTITUTE FOR BRAIN RESEARCH   (Germany)

^b UNIVERSITY OF ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; ASPARTIC ACID; GLYCINE RECEPTOR; TAURINE; THREONINE; ZINC ION; GLYCINE; GLYCINE RECEPTOR ALPHA1; UNCLASSIFIED DRUG; ZINC;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; BINDING AFFINITY; BINDING SITE; CHANNEL GATING; FEMALE; HUMAN; HUMAN CELL; KIDNEY CELL; KINETICS; NONHUMAN; OOCYTE; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS; ALLOSTERISM; CONCENTRATION RESPONSE; CONTROLLED STUDY; HEK293 CELL LINE; HILL COEFFICIENT; MUTATIONAL ANALYSIS; PROBABILITY; RECEPTOR BINDING; RECEPTOR UPREGULATION; WILD TYPE; XENOPUS;

EID: 0034650875     PISSN: 00223751     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1469-7793.2000.t01-1-00215.x     Document Type: Article

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