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Solution structure of the cyclic-nucleotide binding homology domain of a KCNH channel. | LitMetric

Solution structure of the cyclic-nucleotide binding homology domain of a KCNH channel.

J Struct Biol

Experimental Therapeutics Centre, Agency for Science, Technology and Research (A∗STAR), Singapore 138669, Singapore. Electronic address:

Published: April 2014

AI Article Synopsis

Article Abstract

The carboxy-terminal region of the KCNH family of potassium channels contains a cyclic-nucleotide binding homology domain (CNBHD) that is important for channel gating and trafficking. The solution structure of the CNBHD of the KCNH potassium of zebrafish was determined using solution NMR spectroscopy. This domain exists as a monomer under solution conditions and adopts a similar fold to that determined by X-ray crystallography. The CNBHD does not bind cAMP because residue Y740 blocks the entry of cyclic-nucleotide to the binding pocket. Relaxation results show that the CNBHD is rigid except that some residues in the loop between β6 and β7 are flexible. Our results will be useful to understand the gating mechanism of KCNH family members through the CNBHD.

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Source
http://dx.doi.org/10.1016/j.jsb.2014.03.008DOI Listing

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