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2QS1

Crystal structure of the GluR5 ligand binding core dimer in complex with UBP315 at 1.80 Angstroms resolution

Summary for 2QS1
Entry DOI10.2210/pdb2qs1/pdb
Related1TXF 2F34 2F35 2F36 2QS2 2QS3 2QS4
DescriptorGlutamate receptor, ionotropic kainate 1, CHLORIDE ION, PENTAETHYLENE GLYCOL, ... (5 entities in total)
Functional Keywordsmembrane protein, cell junction, glycoprotein, ion transport, ionic channel, phosphorylation, postsynaptic cell membrane, receptor, rna editing, synapse, transmembrane, transport
Biological sourceRattus norvegicus (rat)
More
Cellular locationCell membrane; Multi-pass membrane protein: P22756
Total number of polymer chains2
Total formula weight59992.81
Authors
Alushin, G.M.,Jane, D.E.,Mayer, M.L. (deposition date: 2007-07-30, release date: 2008-08-05, Last modification date: 2023-08-30)
Primary citationAlushin, G.M.,Jane, D.,Mayer, M.L.
Binding site and ligand flexibility revealed by high resolution crystal structures of GluK1 competitive antagonists.
Neuropharmacology, 60:126-134, 2011
Cited by
PubMed: 20558186
DOI: 10.1016/j.neuropharm.2010.06.002
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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