1uw6

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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1uw6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1uw6 OCA], [http://www.ebi.ac.uk/pdbsum/1uw6 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1uw6 RCSB]</span>
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[[Category: Sixma, T K.]]
[[Category: Sixma, T K.]]
[[Category: Smit, A B.]]
[[Category: Smit, A B.]]
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[[Category: NCT]]
 
[[Category: acetylcholine]]
[[Category: acetylcholine]]
[[Category: glycoprotein]]
[[Category: glycoprotein]]
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[[Category: pentamer]]
[[Category: pentamer]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:16:05 2008''

Revision as of 21:16, 30 March 2008


PDB ID 1uw6

Drag the structure with the mouse to rotate
, resolution 2.2Å
Sites:
Ligands:
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



X-RAY STRUCTURE OF ACETYLCHOLINE BINDING PROTEIN (ACHBP) IN COMPLEX WITH NICOTINE


Overview

Nicotinic acetylcholine receptors are prototypes for the pharmaceutically important family of pentameric ligand-gated ion channels. Here we present atomic resolution structures of nicotine and carbamylcholine binding to AChBP, a water-soluble homolog of the ligand binding domain of nicotinic receptors and their family members, GABAA, GABAC, 5HT3 serotonin, and glycine receptors. Ligand binding is driven by enthalpy and is accompanied by conformational changes in the ligand binding site. Residues in the binding site contract around the ligand, with the largest movement in the C loop. As expected, the binding is characterized by substantial aromatic and hydrophobic contributions, but additionally there are close contacts between protein oxygens and positively charged groups in the ligands. The higher affinity of nicotine is due to a main chain hydrogen bond with the B loop and a closer packing of the aromatic groups. These structures will be useful tools for the development of new drugs involving nicotinic acetylcholine receptor-associated diseases.

About this Structure

1UW6 is a Single protein structure of sequence from Lymnaea stagnalis. Full crystallographic information is available from OCA.

Reference

Nicotine and carbamylcholine binding to nicotinic acetylcholine receptors as studied in AChBP crystal structures., Celie PH, van Rossum-Fikkert SE, van Dijk WJ, Brejc K, Smit AB, Sixma TK, Neuron. 2004 Mar 25;41(6):907-14. PMID:15046723

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