The analysis of desensitizing CNGA1 channels reveals molecular interactions essential for normal gating

Journal of General Physiology

Volumn 133, Issue 4, 2009, Pages 375-386

  Mazzolini, Monica ^a   Anselmi, Claudio ^a,b   Torre, Vincent ^a  

^a SISSA   (Italy)

^b MAX PLANCK INSTITUTE OF BIOPHYSICS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; CYCLIC GMP; CYCLIC NUCLEOTIDE GATED A1 CHANNEL; CYCLIC NUCLEOTIDE GATED CHANNEL; GLUTAMINE; LEUCINE; NUCLEOTIDE BINDING PROTEIN; PHENYLALANINE; POTASSIUM CHANNEL; PROLINE; PROTEIN SUBUNIT; THREONINE; UNCLASSIFIED DRUG; CNGA1 PROTEIN, BOVINE; CYCLIC NUCLEOTIDE;

ANIMAL CELL; ARTICLE; CHANNEL GATING; CONFORMATIONAL TRANSITION; DESENSITIZATION; INDUCED MUTATION; ION CHANNEL DESENSITIZATION; MEMBRANE CURRENT; MOLECULAR INTERACTION; NONHUMAN; OOCYTE; PROTEIN DOMAIN; PROTEIN PROTEIN INTERACTION; XENOPUS LAEVIS; AMINO ACID SEQUENCE; ANIMAL; COMPARATIVE STUDY; FEMALE; GENETICS; METABOLISM; MOLECULAR GENETICS; PHYSIOLOGY; POINT MUTATION; PROTEIN SECONDARY STRUCTURE; PROTEIN TERTIARY STRUCTURE;

AMINO ACID SEQUENCE; ANIMALS; CYCLIC GMP; CYCLIC NUCLEOTIDE-GATED CATION CHANNELS; FEMALE; ION CHANNEL GATING; MOLECULAR SEQUENCE DATA; NUCLEOTIDES, CYCLIC; POINT MUTATION; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; XENOPUS LAEVIS;

EID: 64549158922     PISSN: 00221295     EISSN: 15407748     Source Type: Journal    
DOI: 10.1085/jgp.200810157     Document Type: Article

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