2ojt: Difference between revisions

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|PDB= 2ojt |SIZE=350|CAPTION= <scene name='initialview01'>2ojt</scene>, resolution 1.95&Aring;
|PDB= 2ojt |SIZE=350|CAPTION= <scene name='initialview01'>2ojt</scene>, resolution 1.95&Aring;
|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=BR:BROMIDE+ION'>BR</scene>, <scene name='pdbligand=1PE:PENTAETHYLENE+GLYCOL'>1PE</scene> and <scene name='pdbligand=UBA:(S)-1-(2-AMINO-2-CARBOXYETHYL)-3(2-CARBOXYTHIOPHENE-3-YL-METHYL)-5-METHYLPYRIMIDINE-2,4-DIONE'>UBA</scene>
|LIGAND= <scene name='pdbligand=1PE:PENTAETHYLENE+GLYCOL'>1PE</scene>, <scene name='pdbligand=BR:BROMIDE+ION'>BR</scene>, <scene name='pdbligand=UBA:(S)-1-(2-AMINO-2-CARBOXYETHYL)-3(2-CARBOXYTHIOPHENE-3-YL-METHYL)-5-METHYLPYRIMIDINE-2,4-DIONE'>UBA</scene>
|ACTIVITY=  
|ACTIVITY=  
|GENE= Grik1, Glur5 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10116 Rattus norvegicus])
|GENE= Grik1, Glur5 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10116 Rattus norvegicus])
|DOMAIN=
|RELATEDENTRY=[[2f34|2F34]], [[2f36|2F36]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ojt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ojt OCA], [http://www.ebi.ac.uk/pdbsum/2ojt PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ojt RCSB]</span>
}}
}}


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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Mayer, M L.]]
[[Category: Mayer, M L.]]
[[Category: 1PE]]
[[Category: BR]]
[[Category: UBA]]
[[Category: membrane protein]]
[[Category: membrane protein]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 18:00:35 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:18:48 2008''

Revision as of 04:18, 31 March 2008

File:2ojt.jpg


PDB ID 2ojt

Drag the structure with the mouse to rotate
, resolution 1.95Å
Ligands: , ,
Gene: Grik1, Glur5 (Rattus norvegicus)
Related: 2F34, 2F36


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Structure and mechanism of kainate receptor modulation by anions


OverviewOverview

L-glutamate, the major excitatory neurotransmitter in the human brain, activates a family of ligand-gated ion channels, the major subtypes of which are named AMPA, kainate, and NMDA receptors. In common with many signal transduction proteins, glutamate receptors are modulated by ions and small molecules, including Ca(2+), Mg(2+), Zn(2+), protons, polyamines, and steroids. Strikingly, the activation of kainate receptors by glutamate requires the presence of both Na(+) and Cl(-) in the extracellular solution, and in the absence of these ions, receptor activity is abolished. Here, we identify the site and mechanism of action of anions. Surprisingly, we find that Cl(-) ions are essential structural components of kainate receptors. Cl(-) ions bind in a cavity formed at the interface between subunits in a dimer pair. In the absence of Cl(-), dimer stability is reduced, the rate of desensitization increases, and the fraction of receptors competent for activation by glutamate drops precipitously.

About this StructureAbout this Structure

2OJT is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.

ReferenceReference

Structure and mechanism of kainate receptor modulation by anions., Plested AJ, Mayer ML, Neuron. 2007 Mar 15;53(6):829-41. PMID:17359918

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