Literature DB >> 9144769

Predicted structure of the extracellular region of ligand-gated ion-channel receptors shows SH2-like and SH3-like domains forming the ligand-binding site.

J E Gready1, S Ranganathan, P R Schofield, Y Matsuo, K Nishikawa.   

Abstract

Fast synaptic neurotransmission is mediated by ligand-gated ion-channel (LGIC) receptors, which include receptors for acetylcholine, serotonin, GABA, glycine, and glutamate. LGICs are pentamers with extracellular ligand-binding domains and form integral membrane ion channels that are selective for cations (acetylcholine and serotonin 5HT3 receptors) or anions (GABAA and glycine receptors and the invertebrate glutamate-binding chloride channel). They form a protein superfamily with no sequence similarity to any protein of known structure. Using a 1D-3D structure mapping approach, we have modeled the extracellular ligand-binding domain based on a significant match with the SH2 and SH3 domains of the biotin repressor structure. Refinement of the model based on knowledge of the large family of SH2 and SH3 structures, sequence alignments, and use of structure templates for loop building, allows the prediction of both monomer and pentamer models. These are consistent with medium-resolution electron microscopy structures and with experimental structure/function data from ligand-binding, antibody-binding, mutagenesis, protein-labeling and subunit-linking studies, and glycosylation sites. Also, the predicted polarity of the channel pore calculated from electrostatic potential maps of pentamer models of superfamily members is consistent with known ion selectivities. Using the glycine receptor alpha 1 subunit, which forms homopentamers, the monomeric and pentameric models define the agonist and antagonist (strychnine) binding sites to a deep crevice formed by an extended loop, which includes the invariant disulfide bridge, between the SH2 and SH3 domains. A detailed binding site for strychnine is reported that is in strong agreement with known structure/function data. A site for interaction of the extracellular ligand-binding domain with the activation of the M2 transmembrane helix is also suggested.

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Year:  1997        PMID: 9144769      PMCID: PMC2143702          DOI: 10.1002/pro.5560060504

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  52 in total

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Authors:  R B Russell; J Breed; G J Barton
Journal:  FEBS Lett       Date:  1992-06-08       Impact factor: 4.124

2.  Escherichia coli biotin holoenzyme synthetase/bio repressor crystal structure delineates the biotin- and DNA-binding domains.

Authors:  K P Wilson; L M Shewchuk; R G Brennan; A J Otsuka; B W Matthews
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-01       Impact factor: 11.205

3.  Assessment of protein models with three-dimensional profiles.

Authors:  R Lüthy; J U Bowie; D Eisenberg
Journal:  Nature       Date:  1992-03-05       Impact factor: 49.962

4.  A method to identify protein sequences that fold into a known three-dimensional structure.

Authors:  J U Bowie; R Lüthy; D Eisenberg
Journal:  Science       Date:  1991-07-12       Impact factor: 47.728

5.  Molecular recognition. Conformational analysis of limited proteolytic sites and serine proteinase protein inhibitors.

Authors:  S J Hubbard; S F Campbell; J M Thornton
Journal:  J Mol Biol       Date:  1991-07-20       Impact factor: 5.469

6.  Hierarchical method to align large numbers of biological sequences.

Authors:  W R Taylor
Journal:  Methods Enzymol       Date:  1990       Impact factor: 1.600

7.  Identification of two amino acid residues in the epsilon subunit that promote mammalian muscle acetylcholine receptor assembly in COS cells.

Authors:  Y Gu; P Camacho; P Gardner; Z W Hall
Journal:  Neuron       Date:  1991-06       Impact factor: 17.173

8.  Analysis of the conserved glycosylation site in the nicotinic acetylcholine receptor: potential roles in complex assembly.

Authors:  K W Rickert; B Imperiali
Journal:  Chem Biol       Date:  1995-11

9.  Agonist binding site of Torpedo electric tissue nicotinic acetylcholine receptor. A negatively charged region of the delta subunit within 0.9 nm of the alpha subunit binding site disulfide.

Authors:  C Czajkowski; A Karlin
Journal:  J Biol Chem       Date:  1991-11-25       Impact factor: 5.157

10.  Agonist pharmacology of neonatal and adult glycine receptor alpha subunits: identification of amino acid residues involved in taurine activation.

Authors:  V Schmieden; J Kuhse; H Betz
Journal:  EMBO J       Date:  1992-06       Impact factor: 11.598

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  4 in total

1.  Prediction of 5-HT3 receptor agonist-binding residues using homology modeling.

Authors:  David C Reeves; Muhammed F R Sayed; Pak-Lee Chau; Kerry L Price; Sarah C R Lummis
Journal:  Biophys J       Date:  2003-04       Impact factor: 4.033

2.  Improved secondary structure predictions for a nicotinic receptor subunit: incorporation of solvent accessibility and experimental data into a two-dimensional representation.

Authors:  N Le Novère; P J Corringer; J P Changeux
Journal:  Biophys J       Date:  1999-05       Impact factor: 4.033

3.  Fragment of GABA(A) receptor containing key ligand-binding residues overexpressed in Escherichia coli.

Authors:  H Xue; R Chu; J Hang; P Lee; H Zheng
Journal:  Protein Sci       Date:  1998-01       Impact factor: 6.725

4.  Identification of an inhibitory Zn2+ binding site on the human glycine receptor alpha1 subunit.

Authors:  R J Harvey; P Thomas; C H James; A Wilderspin; T G Smart
Journal:  J Physiol       Date:  1999-10-01       Impact factor: 5.182

  4 in total

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