A novel GTP-binding protein hGBP3 interacts with NIK/HGK

FEBS Lett. 2002 Oct 23;530(1-3):233-8. doi: 10.1016/s0014-5793(02)03467-1.

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.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Binding Sites
  • Blotting, Northern
  • Brain / metabolism
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cloning, Molecular
  • DNA, Complementary
  • GTP-Binding Proteins
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Molecular Sequence Data
  • Protein Serine-Threonine Kinases / metabolism*

Substances

  • Carrier Proteins
  • DNA, Complementary
  • GBP3 protein, human
  • Intracellular Signaling Peptides and Proteins
  • MAP4K4 protein, human
  • Protein Serine-Threonine Kinases
  • GTP-Binding Proteins