9dqd

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m (Protected "9dqd" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 9dqd is ON HOLD
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==cryo-EM structure of human Cereblon/DDB1 in complex with a non-traditional CRBN binder==
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<StructureSection load='9dqd' size='340' side='right'caption='[[9dqd]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9dqd]] 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=9DQD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9DQD FirstGlance]. <br>
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Description:
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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]] 3&#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=A1BEP:(3~{R})-3-[1-methyl-6-(piperidin-4-ylamino)indazol-3-yl]piperidine-2,6-dione'>A1BEP</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=9dqd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9dqd OCA], [https://pdbe.org/9dqd PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9dqd RCSB], [https://www.ebi.ac.uk/pdbsum/9dqd PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9dqd ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/CRBN_HUMAN CRBN_HUMAN] Autosomal recessive nonsyndromic intellectual deficit;Distal monosomy 3p. The disease is caused by mutations affecting the gene represented in this entry.
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== Function ==
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[https://www.uniprot.org/uniprot/CRBN_HUMAN CRBN_HUMAN] Component of some DCX (DDB1-CUL4-X-box) E3 protein ligase complex, a complex that mediates the ubiquitination and subsequent proteasomal degradation of target proteins and is required for limb outgrowth and expression of the fibroblast growth factor FGF8. In the complex, may act as a substrate receptor. Regulates the assembly and neuronal surface expression of large-conductance calcium-activated potassium channels in brain regions involved in memory and learning via its interaction with KCNT1.<ref>PMID:18414909</ref> <ref>PMID:20223979</ref>
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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: Pagarigan B]]
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[[Category: Zhu J]]

Revision as of 09:32, 25 December 2024

cryo-EM structure of human Cereblon/DDB1 in complex with a non-traditional CRBN binder

PDB ID 9dqd

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