7liq
From Proteopedia
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<StructureSection load='7liq' size='340' side='right'caption='[[7liq]], [[Resolution|resolution]] 1.98Å' scene=''> | <StructureSection load='7liq' size='340' side='right'caption='[[7liq]], [[Resolution|resolution]] 1.98Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'> | + | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7LIQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7LIQ FirstGlance]. <br> |
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.98Å</td></tr> |
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7liq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7liq OCA], [https://pdbe.org/7liq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7liq RCSB], [https://www.ebi.ac.uk/pdbsum/7liq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7liq ProSAT]</span></td></tr> | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7liq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7liq OCA], [https://pdbe.org/7liq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7liq RCSB], [https://www.ebi.ac.uk/pdbsum/7liq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7liq ProSAT]</span></td></tr> | ||
</table> | </table> | ||
- | == Function == | ||
- | [[https://www.uniprot.org/uniprot/SPOP_HUMAN SPOP_HUMAN]] Inhibits IPF1/PDX1 transactivation of established target promoters, such as insulin, may be by recruiting a repressor complex (By similarity). In complex with CUL3, involved in ubiquitination of BMI1, H2AFY and DAXX, and probably also in ubiquitination and proteasomal degradation of Gli2 or Gli3.<ref>PMID:14528312</ref> <ref>PMID:15897469</ref> <ref>PMID:16524876</ref> | ||
- | <div style="background-color:#fffaf0;"> | ||
- | == Publication Abstract from PubMed == | ||
- | 53BP1 activates nonhomologous end joining (NHEJ) and inhibits homologous recombination (HR) repair of DNA double-strand breaks (DSBs). Dissociation of 53BP1 from DSBs and consequent activation of HR, a less error-prone pathway than NHEJ, helps maintain genome integrity during DNA replication; however, the underlying mechanisms are not fully understood. Here, we demonstrate that E3 ubiquitin ligase SPOP promotes HR during S phase of the cell cycle by excluding 53BP1 from DSBs. In response to DNA damage, ATM kinase-catalyzed phosphorylation of SPOP causes a conformational change in SPOP, revealed by x-ray crystal structures, that stabilizes its interaction with 53BP1. 53BP1-bound SPOP induces polyubiquitination of 53BP1, eliciting 53BP1 extraction from chromatin by a valosin-containing protein/p97 segregase complex. Our work shows that SPOP facilitates HR repair over NHEJ during DNA replication by contributing to 53BP1 removal from chromatin. Cancer-derived SPOP mutations block SPOP interaction with 53BP1, inducing HR defects and chromosomal instability. | ||
- | + | ==See Also== | |
- | + | *[[Speckle-type POZ protein 3D structures|Speckle-type POZ protein 3D structures]] | |
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: Human]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Botuyan | + | [[Category: Botuyan MV]] |
- | [[Category: Cui | + | [[Category: Cui G]] |
- | [[Category: Mer | + | [[Category: Mer G]] |
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Current revision
X-ray structure of SPOP MATH domain (S119A)
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