8q0n
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==HACE1 in complex with RAC1 Q61L== | |
- | + | <StructureSection load='8q0n' size='340' side='right'caption='[[8q0n]], [[Resolution|resolution]] 4.20Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8q0n]] 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=8Q0N OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8Q0N FirstGlance]. <br> | |
- | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 4.2Å</td></tr> | |
- | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=04E:IODOACETIC+ACID'>04E</scene>, <scene name='pdbligand=GTP:GUANOSINE-5-TRIPHOSPHATE'>GTP</scene></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=8q0n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8q0n OCA], [https://pdbe.org/8q0n PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8q0n RCSB], [https://www.ebi.ac.uk/pdbsum/8q0n PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8q0n ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Disease == | ||
+ | [https://www.uniprot.org/uniprot/HACE1_HUMAN HACE1_HUMAN] Spastic paraplegia-severe developmental delay-epilepsy syndrome;Neuroblastoma. Defects in HACE1 are a cause of Wilms tumor (WT). WT is a pediatric malignancy of kidney and one of the most common solid cancers in childhood. HACE1 is epigenetically down-regulated in sporadic Wilms tumor. Moreover, a t(5;6)(q21;q21) translocation that truncates HACE1 has been found in a child with bilateral, young-onset Wilms tumor (PubMed:19948536).<ref>PMID:17694067</ref> <ref>PMID:19948536</ref> The disease is caused by variants affecting the gene represented in this entry. | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/HACE1_HUMAN HACE1_HUMAN] E3 ubiquitin-protein ligase involved in Golgi membrane fusion and regulation of small GTPases. Acts as a regulator of Golgi membrane dynamics during the cell cycle: recruited to Golgi membrane by Rab proteins and regulates postmitotic Golgi membrane fusion. Acts by mediating ubiquitination during mitotic Golgi disassembly, ubiquitination serving as a signal for Golgi reassembly later, after cell division. Specifically interacts with GTP-bound RAC1, mediating ubiquitination and subsequent degradation of active RAC1, thereby playing a role in host defense against pathogens. May also act as a transcription regulator via its interaction with RARB.<ref>PMID:15254018</ref> <ref>PMID:21988917</ref> <ref>PMID:22036506</ref> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Dienemann C]] | ||
+ | [[Category: Duering J]] | ||
+ | [[Category: Lorenz S]] | ||
+ | [[Category: Wolter M]] |
Revision as of 10:26, 10 January 2024
HACE1 in complex with RAC1 Q61L
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