[PDF][PDF] Molecular mechanisms for the RNA-dependent ATPase activity of Upf1 and its regulation by Upf2

…, U Jayachandran, F Bonneau, F Fiorini, C Basquin… - Molecular cell, 2011 - cell.com
… (C) RNase protection assays of Upf1 and Upf1DCH in presence of different nucleotides. …
(C) Crystal structure of yeast Upf1 in complex with eight ribonucleotides of a U15 RNA and ADP:…

The Na+/I symporter mediates active iodide uptake in the intestine

JP Nicola, C Basquin, C Portulano… - … of Physiology-Cell …, 2009 - journals.physiology.org
… Samples were heated to 95C for 5 min and then subjected to 36 cycles of … at 95C for 30 s,
annealing at 59C for 30 s, and extension at 72C for 30 s, followed by a 7-min extension at 72C

The Na+/I symporter (NIS) mediates electroneutral active transport of the environmental pollutant perchlorate

O Dohán, C Portulano, C Basquin… - Proceedings of the …, 2007 - National Acad Sciences
The Na + /I − symporter (NIS) is a key plasma membrane protein that mediates active I −
uptake in the thyroid, lactating breast, and other tissues with an electrogenic stoichiometry of 2 …

The mRNA export protein DBP5 binds RNA and the cytoplasmic nucleoporin NUP214 in a mutually exclusive manner

H Von Moeller, C Basquin, E Conti - Nature structural & molecular …, 2009 - nature.com
The DEAD-box protein DBP5 is essential for mRNA export in both yeast and humans. It binds
RNA and is concentrated and locally activated at the cytoplasmic side of the nuclear pore …

[PDF][PDF] Architecture of the nuclease module of the yeast Ccr4-not complex: the Not1-Caf1-Ccr4 interaction

J Basquin, VV Roudko, M Rode, C Basquin… - Molecular cell, 2012 - cell.com
… As a control, we generated a plasmid with a C-terminal truncation (Not11–1696) that eliminates
an essential portion of Not1 involved in the interaction with Not2/3/5 (of unknown function…

RNA degradation paths in a 12-subunit nuclear exosome complex

…, B Schuch, E Stegmann, M Baumgärtner, C Basquin… - Nature, 2015 - nature.com
… The C-terminal region (Rrp6 C ) wraps around the outer surface of Exo-9 contacting Mtr3,
Rrp43 and Csl4. Rrp6 C contributes the strongest interaction of Rrp6 to the exosome both in …

The exosome‐binding factors Rrp6 and Rrp47 form a composite surface for recruiting the Mtr4 helicase

…, M Feigenbutz, DL Makino, S Falk, C Basquin… - The EMBO …, 2014 - embopress.org
… Mutation of conserved residues within Rrp6 and Mtr4 at the structural interface disrupts their
interaction and inhibits growth of strains expressing a C‐terminal GFP fusion of Mtr4. These …

Insights into the recruitment of the NMD machinery from the crystal structure of a core EJC-UPF3b complex.

G Buchwald, J Ebert, C Basquin… - Proceedings of the …, 2010 - National Acad Sciences
… (RRM) domain that mediates the interaction with the C-terminal MIF4G (middle portion of
eIF4G) domain of UPF2 (18). At the C terminus, human UPF3 contains a region that has been …

[PDF][PDF] Structural basis for the recognition of phosphorylated histone h3 by the survivin subunit of the chromosomal passenger complex

AA Jeyaprakash, C Basquin, U Jayachandran, E Conti - Structure, 2011 - cell.com
… 4 C for 2 h followed by 20 C for 15 min. The excitation and emission wavelengths were 485
and 535 nm, respectively. Each titration point was measured three times using ten readings …

Crystal structure of the intraflagellar transport complex 25/27

…, M Taschner, M Morawetz, C Basquin… - The EMBO …, 2011 - embopress.org
… between IFT27, Rab8 and Rab11, the C-termini of the proteins are highly divergent. A typical
hallmark of Rab proteins is the presence of a C-terminal prenylation motif consisting of one …