7tuo

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m (Protected "7tuo" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 7tuo is ON HOLD
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==Crystal structure analysis of human USP28 complex with a compound==
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<StructureSection load='7tuo' size='340' side='right'caption='[[7tuo]], [[Resolution|resolution]] 1.96&Aring;' scene=''>
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Authors: Seo, H.-S., Dhe-Paganon, S.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7tuo]] is a 1 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=7TUO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7TUO FirstGlance]. <br>
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Description: Crystal Structure Analysis of human USP28 complex with a compound
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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]] 1.96&#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=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=KL9:7-amino-N-(2-{4-[(1R,3s,5S)-8-azabicyclo[3.2.1]octan-3-yl]phenyl}ethyl)-3-methylthieno[2,3-b]pyrazine-6-carboxamide'>KL9</scene></td></tr>
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[[Category: Dhe-Paganon, S]]
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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=7tuo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7tuo OCA], [https://pdbe.org/7tuo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7tuo RCSB], [https://www.ebi.ac.uk/pdbsum/7tuo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7tuo ProSAT]</span></td></tr>
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[[Category: Seo, H.-S]]
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/UBP28_HUMAN UBP28_HUMAN] Deubiquitinase involved in DNA damage response checkpoint and MYC proto-oncogene stability. Involved in DNA damage induced apoptosis by specifically deubiquitinating proteins of the DNA damage pathway such as CLSPN. Also involved in G2 DNA damage checkpoint, by deubiquitinating CLSPN, and preventing its degradation by the anaphase promoting complex/cyclosome (APC/C). In contrast, it does not deubiquitinate PLK1. Specifically deubiquitinates MYC in the nucleoplasm, leading to prevent MYC degradation by the proteasome: acts by specifically interacting with isoform 1 of FBXW7 (FBW7alpha) in the nucleoplasm and counteracting ubiquitination of MYC by the SCF(FBW7) complex. In contrast, it does not interact with isoform 4 of FBXW7 (FBW7gamma) in the nucleolus, allowing MYC degradation and explaining the selective MYC degradation in the nucleolus.<ref>PMID:16901786</ref> <ref>PMID:17558397</ref> <ref>PMID:17873522</ref> <ref>PMID:18662541</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: Dhe-Paganon S]]
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[[Category: Seo H-S]]

Current revision

Crystal structure analysis of human USP28 complex with a compound

PDB ID 7tuo

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