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. Author manuscript; available in PMC: 2017 Apr 15.
Published in final edited form as: Mol Cell Endocrinol. 2015 Dec 28;425:48–60. doi: 10.1016/j.mce.2015.12.006

Table 1.

IGFBP-1 peptide sequence (45-180) and possible phosphorylation sites for CK2, PKC and PKA.

IGFBP-1
sequence
(45-180)
graphic file with name nihms-758762-t0001.jpg
Protein
Kinase
Consensus phosphorylation site
motif sequence (X=any amino
acid):
IGFBP-1 peptides
with potential
substrate sites
Validated by in
vitro kinase
assay
CK2 pS/T-X-X-D/E *pS101TEITEEE
pS119EED
pS169GEE
Validated
Validated
Validated
PKC pS/T-X-R/K pT50 AR
pS58 CR
--
PKA R/K-R/K-X-pS/T pT50AR
pS58CR
--

IGFBP-1 residues Ser101, Ser119 and Ser169 have been shown to be potential sites for phosphorylation by CK2 in HepG2 cells in response to leucine deprivation in vitro, in human FGR umbilical cord plasma from FGR pregnancies and in baboon FGR fetal liver from maternal nutrient restriction in vivo.

*

pSer101 is not a precise consensus sequence site for CK2. Conversely, PKC and PKA are not likely to directly phosphorylate IGFBP-1 at Ser 101, 119 and 169 sites.