6lvs

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'''Unreleased structure'''
 
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The entry 6lvs is ON HOLD until Mar 03 2021
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==USP14 catalytic domain mutant C114S==
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<StructureSection load='6lvs' size='340' side='right'caption='[[6lvs]], [[Resolution|resolution]] 2.73&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6lvs]] 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=6LVS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6LVS 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]] 2.73&#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=BME:BETA-MERCAPTOETHANOL'>BME</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=FMT:FORMIC+ACID'>FMT</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</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=6lvs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6lvs OCA], [https://pdbe.org/6lvs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6lvs RCSB], [https://www.ebi.ac.uk/pdbsum/6lvs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6lvs ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/UBP14_HUMAN UBP14_HUMAN] Proteasome-associated deubiquitinase which releases ubiquitin from the proteasome targeted ubiquitinated proteins. Ensures the regeneration of ubiquitin at the proteasome. Is a reversibly associated subunit of the proteasome and a large fraction of proteasome-free protein exists within the cell. Required for the degradation of the chemokine receptor CXCR4 which is critical for CXCL12-induced cell chemotaxis. Serves also as a physiological inhibitor of endoplasmic reticulum-associated degradation (ERAD) under the non-stressed condition by inhibiting the degradation of unfolded endoplasmic reticulum proteins via interaction with ERN1. Indispensable for synaptic development and function at neuromuscular junctions (NMJs).<ref>PMID:18162577</ref> <ref>PMID:19135427</ref> <ref>PMID:19106094</ref>
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Authors: Lin, H.C., Lin, T.H., Chou, C.Y.
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==See Also==
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*[[Thioesterase 3D structures|Thioesterase 3D structures]]
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Description: USP14 catalytic domain mutant C114S
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Chou, C.Y]]
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__TOC__
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[[Category: Lin, H.C]]
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</StructureSection>
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[[Category: Lin, T.H]]
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Chou CY]]
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[[Category: Lin HC]]
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[[Category: Lin TH]]

Current revision

USP14 catalytic domain mutant C114S

PDB ID 6lvs

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