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dc.contributor.authorBrohawn, Stephen G.
dc.contributor.authorSchwartz, Thomas
dc.date.accessioned2012-11-01T20:20:39Z
dc.date.available2012-11-01T20:20:39Z
dc.date.issued2009-10
dc.date.submitted2009-07
dc.identifier.issn1545-9993
dc.identifier.issn1545-9985
dc.identifier.urihttp://hdl.handle.net/1721.1/74558
dc.description.abstractNuclear pore complexes (NPCs) facilitate all nucleocytoplasmic transport. These massive protein assemblies are modular, with a stable structural scaffold supporting more dynamically attached components. The scaffold is made from multiple copies of the heptameric Y complex and the heteromeric Nic96 complex. We previously showed that members of these core subcomplexes specifically share an ACE1 fold with Sec31 of the COPII vesicle coat, and we proposed a lattice model for the NPC based on this commonality. Here we present the crystal structure of the heterotrimeric 134-kDa complex of Nup84–Nup145C–Sec13 of the Y complex. The heterotypic ACE1 interaction of Nup84 and Nup145C is analogous to the homotypic ACE1 interaction of Sec31 that forms COPII lattice edge elements and is inconsistent with the alternative 'fence-like' NPC model. We construct a molecular model of the Y complex and compare the architectural principles of COPII and NPC lattices.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM77537)en_US
dc.description.sponsorshipPew Charitable Trusts (Scholar Award)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nsmb.1713en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleMolecular architecture of the Nup84–Nup145C–Sec13 edge element in the nuclear pore complex latticeen_US
dc.typeArticleen_US
dc.identifier.citationBrohawn, Stephen G, and Thomas U Schwartz. “Molecular Architecture of the Nup84–Nup145C–Sec13 Edge Element in the Nuclear Pore Complex Lattice.” Nature Structural & Molecular Biology 16.11 (2009): 1173–1177.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorBrohawn, Stephen G.
dc.contributor.mitauthorSchwartz, Thomas
dc.relation.journalNature Structural & Molecular Biologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsBrohawn, Stephen G; Schwartz, Thomas Uen
dc.identifier.orcidhttps://orcid.org/0000-0001-8012-1512
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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