6h7w
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==Model of retromer-Vps5 complex assembled on membrane.== | |
+ | <StructureSection load='6h7w' size='340' side='right' caption='[[6h7w]], [[Resolution|resolution]] 11.40Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[6h7w]] is a 20 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6H7W OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6H7W FirstGlance]. <br> | ||
+ | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6h7w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6h7w OCA], [http://pdbe.org/6h7w PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6h7w RCSB], [http://www.ebi.ac.uk/pdbsum/6h7w PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6h7w ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
+ | [[http://www.uniprot.org/uniprot/G0S709_CHATD G0S709_CHATD]] Plays a role in vesicular protein sorting.[PIRNR:PIRNR009375] | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | Eukaryotic cells traffic proteins and lipids between different compartments using protein-coated vesicles and tubules. The retromer complex is required to generate cargo-selective tubulovesicular carriers from endosomal membranes(1-3). Conserved in eukaryotes, retromer controls the cellular localization and homeostasis of hundreds of transmembrane proteins, and its disruption is associated with major neurodegenerative disorders(4-7). How retromer is assembled and how it is recruited to form coated tubules is not known. Here we describe the structure of the retromer complex (Vps26-Vps29-Vps35) assembled on membrane tubules with the bin/amphiphysin/rvs-domain-containing sorting nexin protein Vps5, using cryo-electron tomography and subtomogram averaging. This reveals a membrane-associated Vps5 array, from which arches of retromer extend away from the membrane surface. Vps35 forms the 'legs' of these arches, and Vps29 resides at the apex where it is free to interact with regulatory factors. The bases of the arches connect to each other and to Vps5 through Vps26, and the presence of the same arches on coated tubules within cells confirms their functional importance. Vps5 binds to Vps26 at a position analogous to the previously described cargo- and Snx3-binding site, which suggests the existence of distinct retromer-sorting nexin assemblies. The structure provides insight into the architecture of the coat and its mechanism of assembly, and suggests that retromer promotes tubule formation by directing the distribution of sorting nexin proteins on the membrane surface while providing a scaffold for regulatory-protein interactions. | ||
- | + | Structure of the membrane-assembled retromer coat determined by cryo-electron tomography.,Kovtun O, Leneva N, Bykov YS, Ariotti N, Teasdale RD, Schaffer M, Engel BD, Owen DJ, Briggs JAG, Collins BM Nature. 2018 Sep 17. pii: 10.1038/s41586-018-0526-z. doi:, 10.1038/s41586-018-0526-z. PMID:30224749<ref>PMID:30224749</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | + | </div> | |
- | + | <div class="pdbe-citations 6h7w" style="background-color:#fffaf0;"></div> | |
- | + | == References == | |
- | + | <references/> | |
+ | __TOC__ | ||
+ | </StructureSection> | ||
[[Category: Ariotti, N]] | [[Category: Ariotti, N]] | ||
- | [[Category: | + | [[Category: Briggs, J A.G]] |
- | [[Category: | + | [[Category: Collins, B M]] |
+ | [[Category: Kovtun, O]] | ||
[[Category: Leneva, N]] | [[Category: Leneva, N]] | ||
+ | [[Category: Owen, D J]] | ||
+ | [[Category: Rohan, T S]] | ||
+ | [[Category: Bar]] | ||
+ | [[Category: Endosome]] | ||
+ | [[Category: Membrane trafficking]] | ||
+ | [[Category: Protein transport]] | ||
+ | [[Category: Retromer]] | ||
+ | [[Category: Sorting nexin]] |
Revision as of 08:17, 26 September 2018
Model of retromer-Vps5 complex assembled on membrane.
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Categories: Ariotti, N | Briggs, J A.G | Collins, B M | Kovtun, O | Leneva, N | Owen, D J | Rohan, T S | Bar | Endosome | Membrane trafficking | Protein transport | Retromer | Sorting nexin