1OAI: Complex between Tap UBA domain and FxFG nucleoporin peptide

The mRNA nuclear export function of Tap/NXF1 requires interactions with nuclear pore proteins (nucleoporins) that contain characteristic Phe-Gly repeats based on FG, GLFG or FxFG cores separated by hydrophilic linkers. FG-nucleoporins bind the two most C-terminal domains of Tap, which have NTF2 and UBA folds, respectively. We used a combination of NMR and X-ray crystallography to define the interaction interface between Tap UBA and FxFG nucleoporins and show that it involves primarily the two aromatic rings of the FxFG core that bind in a hydrophobic surface depression centred on Tap Cys588. NMR evidence indicates that the same depression mediates the binding of GLFG nucleoporins, which we confirmed by demonstrating competition between the two classes of repeat for binding to Tap UBA. Moreover, modification of Cys588 reduced the binding of Tap UBA to both GLFG and FxFG nucleoporins as well as to nuclear envelopes. These data underscore the central role of the conserved FG-nucleoporin repeat cores in binding to Tap UBA and indicate that functional differences between different classes of nucleoporins depend more on their spatial distribution in nuclear pores than on their binding to different sites on Tap UBA.
PDB ID: 1OAIDownload
MMDB ID: 22219
PDB Deposition Date: 2003/1/14
Updated in MMDB: 2007/10
Experimental Method:
x-ray diffraction
Resolution: 1  Å
Source Organism:
Similar Structures:
Biological Unit for 1OAI: dimeric; determined by author and by software (PQS)
Molecular Components in 1OAI
Label Count Molecule
Proteins (2 molecules)
Nuclear RNA Export Factor(Gene symbol: NXF1)
Molecule annotation
Fxfg Nucleoporin Peptide
Molecule annotation
* Click molecule labels to explore molecular sequence information.

Citing MMDB