PT  - JOURNAL ARTICLE
AU  - Sarah A. Nordeen
AU  - Daniel L. Turman
AU  - Thomas U. Schwartz
TI  - Structure of the yeast Nup84-Nup133 complex details flexibility and reveals universal conservation of the membrane anchoring ALPS motif
AID  - 10.1101/2020.06.19.161133
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.06.19.161133
4099  - http://biorxiv.org/content/early/2020/06/20/2020.06.19.161133.short
4100  - http://biorxiv.org/content/early/2020/06/20/2020.06.19.161133.full
AB  - The hallmark of the eukaryotic cell is the complex endomembrane system that compartmentalizes cellular functions. Transport into and out of the nucleus, occurs through the Nuclear Pore Complex (NPC). The heptameric Nup84 or Y complex is an essential scaffolding component of the NPC. Here we report two nanobody-bound structures: the full-length Nup84-Nup133 C-terminal domain complex and the Nup133 N-terminal domain, both from S. cerevisiae. Together with previously published structures, this work enables the structural description of the entire 575 kDa Y complex, from one species. The structure of Nup84-Nup1 33CTD details the high flexibility of this dimeric unit of the Y complex. Further, the Nup133NTD contains a structurally conserved amphipathic lipid packing sensor (ALPS) motif, confirmed by liposome interaction studies. The new structures reveal important details about the function of the Y complex that affect our understanding of NPC structure and assembly.Competing Interest StatementThe authors have declared no competing interest.