7vpw

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m (Protected "7vpw" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 7vpw is ON HOLD
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==Crystal structure of Transportin-1 in complex with BAP1 PY-NLS (residues 706-724)==
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<StructureSection load='7vpw' size='340' side='right'caption='[[7vpw]], [[Resolution|resolution]] 3.76&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7vpw]] 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=7VPW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7VPW 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]] 3.76&#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=7vpw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7vpw OCA], [https://pdbe.org/7vpw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7vpw RCSB], [https://www.ebi.ac.uk/pdbsum/7vpw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7vpw ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/BAP1_HUMAN BAP1_HUMAN] Pleural mesothelioma;Non-specific syndromic intellectual disability;Meningioma;BAP1-related tumor predisposition syndrome;Uveal melanoma;Familial melanoma. The gene represented in this entry is involved in disease pathogenesis. The disease is caused by variants affecting the gene represented in this entry. Disease susceptibility is associated with variants affecting the gene represented in this entry. 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/BAP1_HUMAN BAP1_HUMAN] Deubiquitinating enzyme that plays a key role in chromatin by mediating deubiquitination of histone H2A and HCFC1 (PubMed:12485996, PubMed:18757409, PubMed:20436459, PubMed:25451922, PubMed:35051358). Catalytic component of the PR-DUB complex, a complex that specifically mediates deubiquitination of histone H2A monoubiquitinated at 'Lys-119' (H2AK119ub1) (PubMed:20436459, PubMed:25451922, PubMed:35051358). Does not deubiquitinate monoubiquitinated histone H2B (PubMed:20436459). Acts as a regulator of cell growth by mediating deubiquitination of HCFC1 N-terminal and C-terminal chains, with some specificity toward 'Lys-48'-linked polyubiquitin chains compared to 'Lys-63'-linked polyubiquitin chains (PubMed:19188440, PubMed:19815555). Deubiquitination of HCFC1 does not lead to increase stability of HCFC1 (PubMed:19188440, PubMed:19815555). Interferes with the BRCA1 and BARD1 heterodimer activity by inhibiting their ability to mediate ubiquitination and autoubiquitination (PubMed:19117993). It however does not mediate deubiquitination of BRCA1 and BARD1 (PubMed:19117993). Able to mediate autodeubiquitination via intramolecular interactions to couteract monoubiquitination at the nuclear localization signal (NLS), thereby protecting it from cytoplasmic sequestration (PubMed:24703950). Acts as a tumor suppressor (PubMed:9528852).<ref>PMID:12485996</ref> <ref>PMID:18757409</ref> <ref>PMID:19117993</ref> <ref>PMID:19188440</ref> <ref>PMID:19815555</ref> <ref>PMID:20436459</ref> <ref>PMID:24703950</ref> <ref>PMID:25451922</ref> <ref>PMID:35051358</ref> <ref>PMID:9528852</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: Hsu STD]]
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[[Category: Yang TJ]]

Current revision

Crystal structure of Transportin-1 in complex with BAP1 PY-NLS (residues 706-724)

PDB ID 7vpw

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