3aul
From Proteopedia
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==Crystal structure of wild-type Lys48-linked diubiquitin in an open conformation== | ==Crystal structure of wild-type Lys48-linked diubiquitin in an open conformation== | ||
- | <StructureSection load='3aul' size='340' side='right' caption='[[3aul]], [[Resolution|resolution]] 2.39Å' scene=''> | + | <StructureSection load='3aul' size='340' side='right'caption='[[3aul]], [[Resolution|resolution]] 2.39Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[3aul]] is a 2 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[3aul]] 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=3AUL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3AUL FirstGlance]. <br> |
- | </td></tr><tr><td class="sblockLbl"><b>[[ | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.39Å</td></tr> |
- | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3aul FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3aul OCA], [https://pdbe.org/3aul PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3aul RCSB], [https://www.ebi.ac.uk/pdbsum/3aul PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3aul ProSAT]</span></td></tr> |
- | <table> | + | </table> |
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/UBC_HUMAN UBC_HUMAN] Ubiquitin exists either covalently attached to another protein, or free (unanchored). When covalently bound, it is conjugated to target proteins via an isopeptide bond either as a monomer (monoubiquitin), a polymer linked via different Lys residues of the ubiquitin (polyubiquitin chains) or a linear polymer linked via the initiator Met of the ubiquitin (linear polyubiquitin chains). Polyubiquitin chains, when attached to a target protein, have different functions depending on the Lys residue of the ubiquitin that is linked: Lys-6-linked may be involved in DNA repair; Lys-11-linked is involved in ERAD (endoplasmic reticulum-associated degradation) and in cell-cycle regulation; Lys-29-linked is involved in lysosomal degradation; Lys-33-linked is involved in kinase modification; Lys-48-linked is involved in protein degradation via the proteasome; Lys-63-linked is involved in endocytosis, DNA-damage responses as well as in signaling processes leading to activation of the transcription factor NF-kappa-B. Linear polymer chains formed via attachment by the initiator Met lead to cell signaling. Ubiquitin is usually conjugated to Lys residues of target proteins, however, in rare cases, conjugation to Cys or Ser residues has been observed. When polyubiquitin is free (unanchored-polyubiquitin), it also has distinct roles, such as in activation of protein kinases, and in signaling.<ref>PMID:16543144</ref> <ref>PMID:19754430</ref> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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Conformational Dynamics of Wild-type Lys-48-linked Diubiquitin in Solution.,Hirano T, Serve O, Yagi-Utsumi M, Takemoto E, Hiromoto T, Satoh T, Mizushima T, Kato K J Biol Chem. 2011 Oct 28;286(43):37496-502. Epub 2011 Sep 7. PMID:21900242<ref>PMID:21900242</ref> | Conformational Dynamics of Wild-type Lys-48-linked Diubiquitin in Solution.,Hirano T, Serve O, Yagi-Utsumi M, Takemoto E, Hiromoto T, Satoh T, Mizushima T, Kato K J Biol Chem. 2011 Oct 28;286(43):37496-502. Epub 2011 Sep 7. PMID:21900242<ref>PMID:21900242</ref> | ||
- | From | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> |
</div> | </div> | ||
+ | <div class="pdbe-citations 3aul" style="background-color:#fffaf0;"></div> | ||
+ | |||
+ | ==See Also== | ||
+ | *[[3D structures of ubiquitin|3D structures of ubiquitin]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Hirano | + | [[Category: Large Structures]] |
- | [[Category: Hiromoto | + | [[Category: Hirano T]] |
- | [[Category: Kato | + | [[Category: Hiromoto T]] |
- | [[Category: Mizushima | + | [[Category: Kato K]] |
- | [[Category: Olivier | + | [[Category: Mizushima T]] |
- | [[Category: Satoh | + | [[Category: Olivier S]] |
- | [[Category: Takemoto | + | [[Category: Satoh T]] |
- | [[Category: Yagi | + | [[Category: Takemoto E]] |
- | + | [[Category: Yagi M]] | |
- | + | ||
- | + |
Current revision
Crystal structure of wild-type Lys48-linked diubiquitin in an open conformation
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Categories: Homo sapiens | Large Structures | Hirano T | Hiromoto T | Kato K | Mizushima T | Olivier S | Satoh T | Takemoto E | Yagi M