Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.7.11.12 (
PKG
)
2,515
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Cyclic GMP (cGMP)-dependent protein kinase (
PKG
) has a limited substrate specificity, and only cerebellar G-substrate has been demonstrated in brain. In view of the physiological importance of cGMP and
PKG
in the nervous system, it is important to identify endogenous
PKG
substrates in rat brain. We devised a combination of ion-exchange and hydrophobic chromatographies to identify potential
PKG
substrates. Extracts from cytosol, peripheral membrane proteins, or a fraction enriched in Ca(2+)-sensitive lipid-binding proteins were partly purified and phosphorylated with purified
PKG
. Using whole extracts only a single specific
PKG
substrate-P34-was found. However, after chromatography we detected > 40 distinct proteins that were phosphorylated by
PKG
to a much greater extent than by cyclic AMP-dependent protein kinase or protein kinase C. Four
PKG
substrates--P140, P65, P32, and P18--were detected in the cytosol. Six
PKG
substrates--P130, P85 (doublet), P58,
P54
, and P38--were enriched from the Ca(2+)-sensitive lipid-binding protein fraction. In peripheral membrane fractions > 30 relatively specific
PKG
substrates were enriched after chromatography, especially P130, P94, P58, P52, P45, P40, P36, P34, P28, P26, P24, and P20. These results indicate that brain is not lacking in
PKG
substrates and show that many are apparently quite specific substrates for this enzyme. The identification of some of these novel
PKG
substrates will facilitate understanding the role of cGMP signaling in the brain.
...
PMID:Cyclic GMP-dependent protein kinase substrates in rat brain. 761 14