Accepted Name |
cAMP-dependent protein kinase
|
Alternative Name(s) |
PKA |
PKA C |
protein kinase A |
Reaction catalysed |
- L-seryl-[protein] + ATP = O-phospho-L-seryl-[protein] + ADP + H(+)
- L-threonyl-[protein] + ATP = O-phospho-L-threonyl-[protein] + ADP + H(+)
|
Comment(s) |
- This eukaryotic enzyme recognizes the sequence -Arg-Arg-X-
Ser*/Thr*-Hpo, where * indicates the phosphorylated residue and Hpo
indicates a hydrophobic residue.
- The inactive holoenzyme is a heterotetramer composed of two
regulatory (R) subunits and two catalytic (C) subunits.
- Each R subunit occludes the active site of a C subunit and contains
two binding sites for 3',5'-cyclic-AMP (cAMP).
- Binding of cAMP activates the enzyme by causing conformational
changes that release two free monomeric C subunits from a dimer of
the R subunits, i.e. R2C2 + 4 cAMP = R2(cAMP)4 + 2 C.
- Activity requires phosphorylation of a conserved Thr in the
activation loop (T-loop) sequence (Thr(198) in human Calpha; Thr(224)
in budding yeast Tpk2), installed by auto-phosphorylation or by the
3-phosphoinositide-dependent protein kinase-1 (PDPK1).
- Certain R2C2 combinations can be localized to particular subcellular
regions by their association with diverse species of 'A Kinase-
Anchoring Proteins' (AKAPs).
- The enzyme has been characterized from many organisms. Humans have
three C units (Calpha, Cbeta, and Cgamma) encoded by the paralogous
genes PRKACA, PRKACB and PRKACG, respectively, and four R subunits
(R1alpha, RIbeta, RIIalpha and RIIbeta), encoded by PKRAR1A, PKRAR1B,
PKRAR2A and PKRAR2B, respectively. Yeast (Saccharomyces cerevisiae)
has three C subunits (Tpk1, Tpk2, and Tpk3) encoded by the paralogous
genes TPK1, TPK2 and TPK3, respectively, and a single R subunit
(Bcy1) encoded by the BCY1 gene.
- Some validated substrates of the enzyme include cAMP-response
element-binding protein (CREB), phosphorylase kinase alpha subunit
(PHKA), and tyrosine 3-monooxygenase (TH) in mammals; Adr1, Whi3,
Nej1, and Pyk1 in yeast.
- Formerly EC 2.7.1.37.
|
Cross-references |
BRENDA | 2.7.11.11 |
EC2PDB | 2.7.11.11 |
ExplorEnz | 2.7.11.11 |
PRIAM enzyme-specific profiles | 2.7.11.11 |
KEGG Ligand Database for Enzyme Nomenclature | 2.7.11.11 |
IUBMB Enzyme Nomenclature | 2.7.11.11 |
IntEnz | 2.7.11.11 |
MEDLINE | Find literature relating to 2.7.11.11 |
MetaCyc | 2.7.11.11 |
Rhea expert-curated reactions | 2.7.11.11 |
UniProtKB/Swiss-Prot |
P06244, KAPA_YEAST | P40376, KAPB_SCHPO | P06245, KAPB_YEAST |
A8XW88, KAPC1_CAEBR | P21137, KAPC1_CAEEL | P12370, KAPC1_DROME |
A8XJQ6, KAPC2_CAEBR | Q7JP68, KAPC2_CAEEL | P00517, KAPCA_BOVIN |
Q8MJ44, KAPCA_CANLF | P25321, KAPCA_CRIGR | P17612, KAPCA_HUMAN |
P05132, KAPCA_MOUSE | P36887, KAPCA_PIG | P27791, KAPCA_RAT |
Q9MZD9, KAPCA_SHEEP | P05131, KAPCB_BOVIN | P68180, KAPCB_CRIGR |
P22694, KAPCB_HUMAN | P68181, KAPCB_MOUSE | P05383, KAPCB_PIG |
P68182, KAPCB_RAT | P22612, KAPCG_HUMAN | O62846, KAPCG_MACMU |
P49673, KAPC_ASCSU | P34099, KAPC_DICDI | Q8SRK8, KAPC_ENCCU |
P05986, KAPC_YEAST |
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