8bfh
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 8bfh is ON HOLD Authors: Basquin, J., Ozgur, S., Conti, E. Description: CNOT11 Category: Unreleased Structures Category: Conti, E [[Categor...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==CNOT11== | |
| + | <StructureSection load='8bfh' size='340' side='right'caption='[[8bfh]], [[Resolution|resolution]] 2.20Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[8bfh]] is a 1 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=8BFH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8BFH FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.2Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</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=8bfh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8bfh OCA], [https://pdbe.org/8bfh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8bfh RCSB], [https://www.ebi.ac.uk/pdbsum/8bfh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8bfh ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | The evolutionary conserved CCR4-NOT complex functions in the cytoplasm as the main mRNA deadenylase in both constitutive mRNA turnover and regulated mRNA decay pathways. The versatility of this complex is underpinned by its modular multi-subunit organization, with distinct structural modules actuating different functions. The structure and function of all modules are known, except for that of the N-terminal module. Using different structural approaches, we obtained high-resolution data revealing the architecture of the human N-terminal module composed of CNOT1, CNOT10, and CNOT11. The structure shows how two helical domains of CNOT1 sandwich CNOT10 and CNOT11, leaving the most conserved domain of CNOT11 protruding into solvent as an antenna. We discovered that GGNBP2, a protein identified as a tumor suppressor and spermatogenic factor, is a conserved interacting partner of the CNOT11 antenna domain. Structural and biochemical analyses thus pinpoint the N-terminal CNOT1-CNOT10-CNOT11 module as a conserved protein-protein interaction platform. | ||
| - | + | The human CNOT1-CNOT10-CNOT11 complex forms a structural platform for protein-protein interactions.,Mauxion F, Basquin J, Ozgur S, Rame M, Albrecht J, Schafer I, Seraphin B, Conti E Cell Rep. 2023 Jan 31;42(1):111902. doi: 10.1016/j.celrep.2022.111902. Epub 2022 , Dec 30. PMID:36586408<ref>PMID:36586408</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| - | [[Category: | + | <div class="pdbe-citations 8bfh" style="background-color:#fffaf0;"></div> |
| - | [[Category: | + | == References == |
| - | [[Category: | + | <references/> |
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Basquin J]] | ||
| + | [[Category: Conti E]] | ||
| + | [[Category: Ozgur S]] | ||
Current revision
CNOT11
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