Search Results

Overview

Uniprot IDP17612
Protein NamecAMP-dependent protein kinase catalytic subunit alpha
Gene NamePRKACA
OrganismHomo sapiens

Kla Sites from experimental identification

Position Flanking peptide
280 LLQVDLTKRFGNLKN
310 WIAIYQRKVEAPFIP
48 LDQFERIKTLGTGSF
84 KQKVVKLKQIEHTLN
9 GNAAAAKKGSEQESV
93 IEHTLNEKRILQAVN

Function

Phosphorylates a large number of substrates in the cytoplasm and the nucleus (PubMed:15642694, PubMed:15905176, PubMed:16387847, PubMed:17333334, PubMed:17565987, PubMed:17693412, PubMed:18836454, PubMed:19949837, PubMed:20356841, PubMed:21085490, PubMed:21514275, PubMed:21812984, PubMed:21852232, PubMed:31112131, PubMed:41652173). Phosphorylates CDC25B, ABL1, NFKB1, CLDN3, histone H1.4 (H1-4), PSMC5/RPT6, PJA2, RYR2, RORA, SLC6A6, SOX9, UHRF1 and VASP (PubMed:15178447, PubMed:15642694, PubMed:15905176, PubMed:16387847, PubMed:17333334, PubMed:17565987, PubMed:17693412, PubMed:18836454, PubMed:19949837, PubMed:20356841, PubMed:21085490, PubMed:21514275, PubMed:21812984, PubMed:41652173). Regulates the abundance of compartmentalized pools of its regulatory subunits through phosphorylation of PJA2 which binds and ubiquitinates these subunits, leading to their subsequent proteolysis (PubMed:21423175). RORA is activated by phosphorylation (PubMed:21514275). Required for glucose-mediated adipogenic differentiation increase and osteogenic differentiation inhibition from osteoblasts (PubMed:19949837). Involved in chondrogenesis by mediating phosphorylation of SOX9 (By similarity). Involved in the regulation of platelets in response to thrombin and collagen; maintains circulating platelets in a resting state by phosphorylating proteins in numerous platelet inhibitory pathways when in complex with NF-kappa-B (NFKB1 and NFKB2) and I-kappa-B-alpha (NFKBIA), but thrombin and collagen disrupt these complexes and free active PRKACA stimulates platelets and leads to platelet aggregation by phosphorylating VASP (PubMed:15642694, PubMed:20356841). Prevents the antiproliferative and anti-invasive effects of alpha-difluoromethylornithine in breast cancer cells when activated (PubMed:17333334). RYR2 channel activity is potentiated by phosphorylation in presence of luminal Ca(2+), leading to reduced amplitude and increased frequency of store overload-induced Ca(2+) release (SOICR) characterized by an increased rate of Ca(2+) release and propagation velocity of spontaneous Ca(2+) waves, despite reduced wave amplitude and resting cytosolic Ca(2+) (PubMed:17693412). PSMC5/RPT6 activation by phosphorylation stimulates proteasome (PubMed:17565987). Negatively regulates tight junctions (TJs) in ovarian cancer cells via CLDN3 phosphorylation (PubMed:15905176). NFKB1 phosphorylation promotes NF-kappa-B p50-p50 DNA binding (PubMed:15642694). Acts as a key inhibitor of smoothened signaling pathway by mediating phosphorylation of GLI (GLI1, GLI2 and GLI3) transcription factors in absence of hedgehog (DHH, IHH or SHH) morphogens: GLI phosphorylation promotes their processing and prevents transcriptional activation of smoothened target genes (PubMed:16705181). GLI transcription factor phosphorylation is inhibited by interaction of PRKACA with SMO which sequesters PRKACA at the cell membrane (PubMed:36202993, PubMed:39138140). Also inhibits the smoothened signaling pathway in embryonic development by catalyzing phosphorylation of OFD1 in ciliogenesis (PubMed:33934390). Prevents meiosis resumption in prophase-arrested oocytes via CDC25B inactivation by phosphorylation (By similarity). May also regulate rapid eye movement (REM) sleep in the pedunculopontine tegmental (PPT) (By similarity). Phosphorylates APOBEC3G and AICDA (PubMed:16387847, PubMed:18836454). Phosphorylates HSF1; this phosphorylation promotes HSF1 nuclear localization and transcriptional activity upon heat shock (PubMed:21085490). Acts as a negative regulator of mTORC1 by mediating phosphorylation of RPTOR (PubMed:31112131). Phosphorylates AKAP19 (PubMed:27028580)

Protein Sequence

10 MGNAAAAKKG 20 SEQESVKEFL 30 AKAKEDFLKK 40 WESPAQNTAH 50 LDQFERIKTL 60 GTGSFGRVML 70 VKHKETGNHY 80 AMKILDKQKV 90 VKLKQIEHTL 100 NEKRILQAVN 110 FPFLVKLEFS 120 FKDNSNLYMV 130 MEYVPGGEMF 140 SHLRRIGRFS 150 EPHARFYAAQ 160 IVLTFEYLHS 170 LDLIYRDLKP 180 ENLLIDQQGY 190 IQVTDFGFAK 200 RVKGRTWTLC 210 GTPEYLAPEI 220 ILSKGYNKAV 230 DWWALGVLIY 240 EMAAGYPPFF 250 ADQPIQIYEK 260 IVSGKVRFPS 270 HFSSDLKDLL 280 RNLLQVDLTK 290 RFGNLKNGVN 300 DIKNHKWFAT 310 TDWIAIYQRK 320 VEAPFIPKFK 330 GPGDTSNFDD 340 YEEEEIRVSI 350 NEKCGKEFSE F

Gene Ontology

Classification GO ID Description
Cellular Component GO:0001669 acrosomal vesicle
Cellular Component GO:0034704 calcium channel complex
Cellular Component GO:0005952 cAMP-dependent protein kinase complex
Cellular Component GO:0005813 centrosome
Cellular Component GO:0097546 ciliary base
Cellular Component GO:0005737 cytoplasm
Cellular Component GO:0005829 cytosol
Cellular Component GO:0070062 extracellular exosome
Cellular Component GO:0098978 glutamatergic synapse
Cellular Component GO:0005811 lipid droplet
Cellular Component GO:0005759 mitochondrial matrix
Cellular Component GO:0031594 neuromuscular junction
Cellular Component GO:0016607 nuclear speck
Cellular Component GO:0005654 nucleoplasm
Cellular Component GO:0031588 nucleotide-activated protein kinase complex
Cellular Component GO:0005634 nucleus
Cellular Component GO:0048471 perinuclear region of cytoplasm
Cellular Component GO:0005886 plasma membrane
Cellular Component GO:0044853 plasma membrane raft
Cellular Component GO:0098794 postsynapse
Cellular Component GO:0036126 sperm flagellum
Cellular Component GO:0097225 sperm midpiece
Molecular Function GO:0005524 ATP binding
Molecular Function GO:0004691 cAMP-dependent protein kinase activity
Molecular Function GO:0099103 channel activator activity
Molecular Function GO:0140198 histone H1-4S35 kinase activity
Molecular Function GO:0000287 magnesium ion binding
Molecular Function GO:0030145 manganese ion binding
Molecular Function GO:0019870 potassium channel inhibitor activity
Molecular Function GO:0019904 protein domain specific binding
Molecular Function GO:0034237 protein kinase A regulatory subunit binding
Molecular Function GO:0019901 protein kinase binding
Molecular Function GO:0106310 protein serine kinase activity
Molecular Function GO:0004674 protein serine/threonine kinase activity
Molecular Function GO:0004712 protein serine/threonine/tyrosine kinase activity
Biological Process GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway
Biological Process GO:0007193 adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
Biological Process GO:0141156 cAMP/PKA signal transduction
Biological Process GO:0086064 cell communication by electrical coupling involved in cardiac conduction
Biological Process GO:0071872 cellular response to epinephrine stimulus
Biological Process GO:0071377 cellular response to glucagon stimulus
Biological Process GO:0071333 cellular response to glucose stimulus
Biological Process GO:0034605 cellular response to heat
Biological Process GO:0019221 cytokine-mediated signaling pathway
Biological Process GO:0034380 high-density lipoprotein particle assembly
Biological Process GO:0030007 intracellular potassium ion homeostasis
Biological Process GO:0035694 mitochondrial protein catabolic process
Biological Process GO:0006397 mRNA processing
Biological Process GO:1904539 negative regulation of glycolytic process through fructose-6-phosphate
Biological Process GO:0032703 negative regulation of interleukin-2 production
Biological Process GO:0120186 negative regulation of protein localization to chromatin
Biological Process GO:1904262 negative regulation of TORC1 signaling
Biological Process GO:0050850 positive regulation of calcium-mediated signaling
Biological Process GO:0045542 positive regulation of cholesterol biosynthetic process
Biological Process GO:0045722 positive regulation of gluconeogenesis
Biological Process GO:0032024 positive regulation of insulin secretion
Biological Process GO:0050766 positive regulation of phagocytosis
Biological Process GO:0010898 positive regulation of triglyceride catabolic process
Biological Process GO:0099170 postsynaptic modulation of chemical synaptic transmission
Biological Process GO:2000810 regulation of bicellular tight junction assembly
Biological Process GO:1903779 regulation of cardiac conduction
Biological Process GO:0055117 regulation of cardiac muscle contraction
Biological Process GO:0010881 regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion
Biological Process GO:0051726 regulation of cell cycle
Biological Process GO:0002027 regulation of heart rate
Biological Process GO:0016241 regulation of macroautophagy
Biological Process GO:0070507 regulation of microtubule cytoskeleton organization
Biological Process GO:0045667 regulation of osteoblast differentiation
Biological Process GO:0061136 regulation of proteasomal protein catabolic process
Biological Process GO:0003091 renal water homeostasis
Biological Process GO:0048240 sperm capacitation
Biological Process GO:0097700 vascular endothelial cell response to laminar fluid shear stress

Reference

[1] Yang Z, Yan C, Ma J, Peng P, Ren X et al.. Lactylome analysis suggests lactylation-dependent mechanisms of metabolic adaptation in hepatocellular carcinoma.. Nat Metab 5(1):61-79. 2023 Jan. PMID: 36593272.

[2] Hong H, Chen X, Wang H, Gu X, Yuan Y et al.. Global profiling of protein lysine lactylation and potential target modified protein analysis in hepatocellular carcinoma.. Proteomics 23(9):e2200432. 2023 May. PMID: 36625413.

[3] Shi CM, Wang QC, Li XL, Yang YH, Tang XY et al.. Global Profiling of Protein Lactylation in Human Hippocampi.. Proteomics Clin Appl 19(2):e202400061. 2025 Mar. PMID: 39610256.