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8oj5
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==60S ribosomal subunit bound to the E3-UFM1 complex - state 3 (in-vitro reconstitution)== | |
| + | <StructureSection load='8oj5' size='340' side='right'caption='[[8oj5]], [[Resolution|resolution]] 2.90Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[8oj5]] is a 10 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=8OJ5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8OJ5 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]] 2.9Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=8oj5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8oj5 OCA], [https://pdbe.org/8oj5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8oj5 RCSB], [https://www.ebi.ac.uk/pdbsum/8oj5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8oj5 ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/UFL1_HUMAN UFL1_HUMAN] E3 protein ligase that mediates ufmylation, the covalent attachment of the ubiquitin-like modifier UFM1 to lysine residues on target proteins, and which plays a key role in reticulophagy (also called ER-phagy) induced in response to endoplasmic reticulum stress (PubMed:20018847, PubMed:20164180, PubMed:20228063, PubMed:25219498, PubMed:32160526). In response to endoplasmic reticulum stress, recruited to the endoplasmic reticulum membrane by DDRGK1, and mediates ufmylation of proteins such as RPN1 and RPL26/uL24, thereby promoting reticulophagy of endoplasmic reticulum sheets (PubMed:32160526). Ufmylation-dependent reticulophagy inhibits the unfolded protein response (UPR) via ERN1/IRE1-alpha (PubMed:23152784, PubMed:32160526). Ufmylation in response to endoplasmic reticulum stress is essential for processes such as hematopoiesis, blood vessel morphogenesis or inflammatory response (PubMed:32050156). Regulates inflammation in response to endoplasmic reticulum stress by promoting reticulophagy, leading to inhibit the activity of the NF-kappa-B transcription factor (By similarity). Mediates ufmylation of DDRGK1 and CDK5RAP3; the role of these modifications is however unclear: as both DDRGK1 and CDK5RAP3 act as substrate adapters for ufmylation, it is uncertain whether ufmylation of these proteins is a collateral effect or is required for ufmylation (PubMed:20531390, PubMed:20018847). Catalyzes ufmylation of various subunits of the ribosomal complex or associated components, such as RPS3/uS3, RPS20/uS10, RPL10/uL16, RPL26/uL24 and EIF6 (By similarity). Anchors CDK5RAP3 in the cytoplasm, preventing its translocation to the nucleus which allows expression of the CCND1 cyclin and progression of cells through the G1/S transition (PubMed:20531390). Also involved in the response to DNA damage: recruited to double-strand break sites following DNA damage and mediates monoufmylation of histone H4 (PubMed:30886146). Catalyzes ufmylation of TRIP4, thereby playing a role in nuclear receptor-mediated transcription (PubMed:25219498). Required for hematopoietic stem cell function and hematopoiesis (By similarity). Required for cardiac homeostasis (By similarity).[UniProtKB:A1A4I9][UniProtKB:Q8CCJ3]<ref>PMID:20018847</ref> <ref>PMID:20164180</ref> <ref>PMID:20228063</ref> <ref>PMID:20531390</ref> <ref>PMID:23152784</ref> <ref>PMID:25219498</ref> <ref>PMID:30886146</ref> <ref>PMID:32050156</ref> <ref>PMID:32160526</ref> | ||
| - | + | ==See Also== | |
| - | + | *[[Ubiquitin-fold modifier 3D structures|Ubiquitin-fold modifier 3D structures]] | |
| - | + | == References == | |
| - | [[Category: | + | <references/> |
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Becker T]] | ||
| + | [[Category: Beckmann R]] | ||
| + | [[Category: DaRosa PA]] | ||
| + | [[Category: Kopito R]] | ||
| + | [[Category: Kulathu Y]] | ||
| + | [[Category: Penchev I]] | ||
| + | [[Category: Peter JJ]] | ||
Current revision
60S ribosomal subunit bound to the E3-UFM1 complex - state 3 (in-vitro reconstitution)
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Categories: Homo sapiens | Large Structures | Becker T | Beckmann R | DaRosa PA | Kopito R | Kulathu Y | Penchev I | Peter JJ
