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5tpa

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(New page: '''Unreleased structure''' The entry 5tpa is ON HOLD Authors: Wallweber, H.J.A., Lupardus, P.J. Description: Structure of the human GluN1/GluN2A LBD in complex with compound 9 (GNE3500...)
Current revision (15:42, 6 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5tpa is ON HOLD
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==Structure of the human GluN1/GluN2A LBD in complex with compound 9 (GNE3500)==
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<StructureSection load='5tpa' size='340' side='right'caption='[[5tpa]], [[Resolution|resolution]] 2.48&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5tpa]] is a 2 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=5TPA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5TPA FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.48&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=7H2:(1R,2R)-2-(2-{[5-CHLORO-3-(TRIFLUOROMETHYL)-1H-PYRAZOL-1-YL]METHYL}-7-METHYL-4-OXO-4H-PYRIDO[1,2-A]PYRIMIDIN-6-YL)CYCLOPROPANE-1-CARBONITRILE'>7H2</scene>, <scene name='pdbligand=GLU:GLUTAMIC+ACID'>GLU</scene>, <scene name='pdbligand=GLY:GLYCINE'>GLY</scene></td></tr>
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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=5tpa FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5tpa OCA], [https://pdbe.org/5tpa PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5tpa RCSB], [https://www.ebi.ac.uk/pdbsum/5tpa PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5tpa ProSAT]</span></td></tr>
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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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Authors: Wallweber, H.J.A., Lupardus, P.J.
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==See Also==
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*[[Glutamate receptor 3D structures|Glutamate receptor 3D structures]]
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Description: Structure of the human GluN1/GluN2A LBD in complex with compound 9 (GNE3500)
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Wallweber, H.J.A]]
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__TOC__
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[[Category: Lupardus, P.J]]
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Lupardus PJ]]
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[[Category: Wallweber HJA]]

Current revision

Structure of the human GluN1/GluN2A LBD in complex with compound 9 (GNE3500)

PDB ID 5tpa

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