9d36

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Current revision (08:10, 13 August 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9d36 is ON HOLD until Paper Publication
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==Structure of the C-terminal Domain of RAGE and Its Inhibitor==
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<StructureSection load='9d36' size='340' side='right'caption='[[9d36]]' scene=''>
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Authors: Theophall, G.G., Ramasamy, R., Schmidt, A.M., Manigrasso, M., Shekthman, A.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9d36]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9D36 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9D36 FirstGlance]. <br>
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Description: Structure of the C-terminal Domain of RAGE and Its Inhibitor
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 20 models</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=A1A2E:4-[(morpholin-4-yl)methyl]-2-{4-[(2R)-5-oxopyrrolidin-2-yl]phenyl}quinoline-7-carbonitrile'>A1A2E</scene></td></tr>
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[[Category: Manigrasso, M]]
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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=9d36 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9d36 OCA], [https://pdbe.org/9d36 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9d36 RCSB], [https://www.ebi.ac.uk/pdbsum/9d36 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9d36 ProSAT]</span></td></tr>
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[[Category: Ramasamy, R]]
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</table>
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[[Category: Schmidt, A.M]]
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== Function ==
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[[Category: Shekthman, A]]
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[https://www.uniprot.org/uniprot/RAGE_HUMAN RAGE_HUMAN] Mediates interactions of advanced glycosylation end products (AGE). These are nonenzymatically glycosylated proteins which accumulate in vascular tissue in aging and at an accelerated rate in diabetes. Acts as a mediator of both acute and chronic vascular inflammation in conditions such as atherosclerosis and in particular as a complication of diabetes. AGE/RAGE signaling plays an important role in regulating the production/expression of TNF-alpha, oxidative stress, and endothelial dysfunction in type 2 diabetes. Interaction with S100A12 on endothelium, mononuclear phagocytes, and lymphocytes triggers cellular activation, with generation of key proinflammatory mediators. Interaction with S100B after myocardial infarction may play a role in myocyte apoptosis by activating ERK1/2 and p53/TP53 signaling (By similarity). Receptor for amyloid beta peptide. Contributes to the translocation of amyloid-beta peptide (ABPP) across the cell membrane from the extracellular to the intracellular space in cortical neurons. ABPP-initiated RAGE signaling, especially stimulation of p38 mitogen-activated protein kinase (MAPK), has the capacity to drive a transport system delivering ABPP as a complex with RAGE to the intraneuronal space.<ref>PMID:19906677</ref>
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[[Category: Theophall, G.G]]
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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: Manigrasso M]]
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[[Category: Ramasamy R]]
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[[Category: Schmidt AM]]
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[[Category: Shekthman A]]
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[[Category: Theophall GG]]

Current revision

Structure of the C-terminal Domain of RAGE and Its Inhibitor

PDB ID 9d36

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