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A novel GTP-binding protein hGBP3 interacts with NIK/HGK
Zhidong Luan1, Yan Zhang, Aihua Liu
1Max-Planck Guest Laboratory, Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, 320, Yye-Yang Road, Shanghai 200031, PR China.
Abstract:
A novel human guanylate-binding protein (GBP) hGBP3 was identified and characterized. Similar as the two human guanylate-binding proteins hGBP1 and hGBP2, hGBP3 has the first two motifs of the three classical guanylate-binding motifs, GXXXXGKS (T) and DXXG, but lacks the N (T) KXD motif. Escherichia coli-expressed hGBP3 protein specifically binds to guanosine triphosphate (GTP). Using a yeast two-hybrid system, it was revealed that the N-terminal region of hGBP3 binds to the C-terminal regulatory domain of NIK/HGK, a member of the group I GCK (germinal center kinase) family. This interaction was confirmed by in vitro glutathione-S-transferase (GST) pull-down and co-immunoprecipitation assays.