5ums

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m (Protected "5ums" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5ums is ON HOLD until Paper Publication
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==Crystal structure of middle double PH domain of human FACT complex subunit SSRP1==
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<StructureSection load='5ums' size='340' side='right' caption='[[5ums]], [[Resolution|resolution]] 1.57&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5ums]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5UMS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5UMS FirstGlance]. <br>
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Description:
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5umr|5umr]], [[5umt|5umt]], [[5umu|5umu]], [[5umv|5umv]]</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'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5ums FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ums OCA], [http://pdbe.org/5ums PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5ums RCSB], [http://www.ebi.ac.uk/pdbsum/5ums PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5ums ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/SSRP1_HUMAN SSRP1_HUMAN]] Component of the FACT complex, a general chromatin factor that acts to reorganize nucleosomes. The FACT complex is involved in multiple processes that require DNA as a template such as mRNA elongation, DNA replication and DNA repair. During transcription elongation the FACT complex acts as a histone chaperone that both destabilizes and restores nucleosomal structure. It facilitates the passage of RNA polymerase II and transcription by promoting the dissociation of one histone H2A-H2B dimer from the nucleosome, then subsequently promotes the reestablishment of the nucleosome following the passage of RNA polymerase II. The FACT complex is probably also involved in phosphorylation of 'Ser-392' of p53/TP53 via its association with CK2 (casein kinase II). Binds specifically to double-stranded DNA and at low levels to DNA modified by the antitumor agent cisplatin. May potentiate cisplatin-induced cell death by blocking replication and repair of modified DNA. Also acts as a transcriptional coactivator for p63/TP63.<ref>PMID:9489704</ref> <ref>PMID:9566881</ref> <ref>PMID:9836642</ref> <ref>PMID:10912001</ref> <ref>PMID:11239457</ref> <ref>PMID:12374749</ref> <ref>PMID:12934006</ref> <ref>PMID:16713563</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: Botuyan, M V]]
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[[Category: Hu, Q]]
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[[Category: Mer, G]]
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[[Category: Su, D]]
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[[Category: Thompson, J R]]
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[[Category: Double ph domain]]
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[[Category: Fact]]
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[[Category: Histone chaperone]]
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[[Category: Transcription]]

Revision as of 05:50, 31 January 2018

Crystal structure of middle double PH domain of human FACT complex subunit SSRP1

5ums, resolution 1.57Å

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