8jj0

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(New page: '''Unreleased structure''' The entry 8jj0 is ON HOLD Authors: Wang, H., Zhu, S. Description: Cryo-EM structure of GluN1-2A NMDAR in complex with human Fab5F6 in one fab bind conformati...)
Current revision (05:16, 5 June 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8jj0 is ON HOLD
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==Cryo-EM structure of GluN1-2A NMDAR in complex with human Fab5F6 in one fab bind conformation==
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<StructureSection load='8jj0' size='340' side='right'caption='[[8jj0]], [[Resolution|resolution]] 4.50&Aring;' scene=''>
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Authors: Wang, H., Zhu, S.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8jj0]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8JJ0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8JJ0 FirstGlance]. <br>
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Description: Cryo-EM structure of GluN1-2A NMDAR in complex with human Fab5F6 in one fab bind conformation
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 4.5&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
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[[Category: Wang, H]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8jj0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8jj0 OCA], [https://pdbe.org/8jj0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8jj0 RCSB], [https://www.ebi.ac.uk/pdbsum/8jj0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8jj0 ProSAT]</span></td></tr>
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[[Category: Zhu, S]]
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/NMDE1_HUMAN NMDE1_HUMAN] Landau-Kleffner syndrome;Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation;Continuous spikes and waves during sleep;Rolandic epilepsy;Rolandic epilepsy - speech dyspraxia. The disease is caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving GRIN2A has been found in a family with epilepsy and neurodevelopmental defects. Translocation t(16;17)(p13.2;q11.2). GRIN2A somatic mutations have been frequently found in cutaneous malignant melanoma, suggesting that the glutamate signaling pathway may play a role in the pathogenesis of melanoma.<ref>PMID:21499247</ref> <ref>PMID:24455489</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/NMDE1_HUMAN NMDE1_HUMAN] NMDA receptor subtype of glutamate-gated ion channels possesses high calcium permeability and voltage-dependent sensitivity to magnesium. Activation requires binding of agonist to both types of subunits.
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Wang H]]
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[[Category: Zhu S]]

Current revision

Cryo-EM structure of GluN1-2A NMDAR in complex with human Fab5F6 in one fab bind conformation

PDB ID 8jj0

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