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7b96

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'''Unreleased structure'''
 
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The entry 7b96 is ON HOLD
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==NHL domain of human TRIM2==
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<StructureSection load='7b96' size='340' side='right'caption='[[7b96]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7b96]] 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=7B96 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7B96 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">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=7b96 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7b96 OCA], [https://pdbe.org/7b96 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7b96 RCSB], [https://www.ebi.ac.uk/pdbsum/7b96 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7b96 ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/TRIM2_HUMAN TRIM2_HUMAN] Charcot-Marie-Tooth disease type 2R. The disease is caused by variants affecting the gene represented in this entry.
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== Function ==
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[https://www.uniprot.org/uniprot/TRIM2_HUMAN TRIM2_HUMAN] UBE2D1-dependent E3 ubiquitin-protein ligase that mediates the ubiquitination of NEFL and of phosphorylated BCL2L11. Plays a neuroprotective function. May play a role in neuronal rapid ischemic tolerance.[UniProtKB:Q9ESN6]
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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: Foot J]]
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[[Category: Hennig J]]
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[[Category: Murciano B]]
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[[Category: Williams FP]]

Current revision

NHL domain of human TRIM2

PDB ID 7b96

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