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. 2009 Feb 11;106(9):3178–3183. doi: 10.1073/pnas.0900294106

Fig. 1.

Fig. 1.

Identification of a putative novel motif in GIV (amino acid 1623–1870) responsible for the preferential binding to GDP·Gαi3. (A) The indicated in vitro translated 35S-Met labeled GIV constructs were incubated with approximately 15 μg GST–Gαi3 or GST preloaded with GDP or GDP·AlF4 immobilized on glutathione beads. Bound proteins were analyzed by autoradiography, and equal loading of GST proteins was confirmed by protein staining (data not shown). (B) A phylogenetically conserved sequence in the C terminus of GIV (amino acid 1678–1694, “GEF motif”) shows similarity to the synthetic peptide KB-752. Sequences obtained from the accession numbers (Fig. S1) were aligned using Clustal W. Conserved residues are shaded in black, similar residues in gray.