1byy
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(New page: 200px<br /><applet load="1byy" size="450" color="white" frame="true" align="right" spinBox="true" caption="1byy" /> '''SODIUM CHANNEL IIA INACTIVATION GATE'''<br /...)
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Revision as of 09:54, 20 November 2007
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SODIUM CHANNEL IIA INACTIVATION GATE
Overview
The sodium channel initiates action potentials by opening in response to, membrane depolarization. Fast channel inactivation, which is required for, proper physiological function, is mediated by a cytoplasmic loop proposed, to occlude the ion pore via a hinged lid mechanism with the triad IFM, serving as a hydrophobic "latch". The NMR solution structure of the, isolated inactivation gate reveals a stably folded core comprised of an, alpha-helix capped by an N-terminal turn, supporting a model in which the, tightly folded core containing the latch motif pivots on a more flexible, hinge region to occlude the pore during inactivation. The structure, in, combination with substituted cysteine mutagenesis experiments, indicates, that the IFM triad and adjacent Thr are essential components of the latch, and suggests differing roles for the residues of the IFMT motif in fast, inactivation.
About this Structure
1BYY is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.
Reference
Solution structure of the sodium channel inactivation gate., Rohl CA, Boeckman FA, Baker C, Scheuer T, Catterall WA, Klevit RE, Biochemistry. 1999 Jan 19;38(3):855-61. PMID:9893979
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