Primary-structure requirements for inhibition by the heat-stable inhibitor of the cAMP-dependent protein kinase
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The substrate specificity and structure of mitogen-activated protein (MAP) kinase-activated protein kinase-2Cloning and mapping of human PKIB and PKIG, and comparison of tissue expression patterns of three members of the protein kinase inhibitor family, including PKIACyclin B targets p34cdc2 for tyrosine phosphorylationBioinformatic design of A-kinase anchoring protein-in silico: a potent and selective peptide antagonist of type II protein kinase A anchoringPhosphotransferase and substrate binding mechanism of the cAMP-dependent protein kinase catalytic subunit from porcine heart as deduced from the 2.0 A structure of the complex with Mn2+ adenylyl imidodiphosphate and inhibitor peptide PKI(5-24)Characterization of PKIgamma, a novel isoform of the protein kinase inhibitor of cAMP-dependent protein kinaseVascular endothelial cells express isoforms of protein kinase A inhibitorThe major catalytic subunit isoforms of cAMP-dependent protein kinase have distinct biochemical properties in vitro and in vivoDeciphering the Arginine-binding preferences at the substrate-binding groove of Ser/Thr kinases by computational surface mappingAn entirely specific type I A-kinase anchoring protein that can sequester two molecules of protein kinase A at mitochondriaAKAP79-mediated targeting of the cyclic AMP-dependent protein kinase to the beta1-adrenergic receptor promotes recycling and functional resensitization of the receptorcAMP-dependent protein kinase (PKA) complexes probed by complementary differential scanning fluorimetry and ion mobility-mass spectrometryMAP kinase activator from insulin-stimulated skeletal muscle is a protein threonine/tyrosine kinaseCharacterization of an A-kinase anchoring protein in human ciliary axonemesPhosphorylation of the RAS2 gene product by protein kinase A inhibits the activation of yeast adenylyl cyclase.Cyclin is a component of the sea urchin egg M-phase specific histone H1 kinaseAnalysis of serine-threonine kinase specificity using arrayed positional scanning peptide librariesActive site-directed inhibition of Ca2+/calmodulin-dependent protein kinase type II by a bifunctional calmodulin-binding peptide.Cell division in higher plants: a cdc2 gene, its 34-kDa product, and histone H1 kinase activity in pea.Inhibition of beta-adrenergic receptor kinase prevents rapid homologous desensitization of beta 2-adrenergic receptors.Adeno-associated virus type 2 Rep78 inhibition of PKA and PRKX: fine mapping and analysis of mechanism.Protein kinase A catalytic subunit isoform PRKACA; History, function and physiologyA requirement of hydrophobic and basic amino acid residues for substrate recognition by Ca2+/calmodulin-dependent protein kinase Ia.Selective disruption of the AKAP signaling complexesAscl1-induced neuronal differentiation of P19 cells requires expression of a specific inhibitor protein of cyclic AMP-dependent protein kinase.Zeta Inhibitory Peptide Disrupts Electrostatic Interactions That Maintain Atypical Protein Kinase C in Its Active Conformation on the Scaffold p62.Conformationally constrained analogs of protein kinase inhibitor (6-22)amide: effect of turn structures in the center of the peptide on inhibition of cAMP-dependent protein kinaseAnti-immunoglobulin M activates nuclear calcium/calmodulin-dependent protein kinase II in human B lymphocytes.Divalent Metal Ions Mg²⁺ and Ca²⁺ Have Distinct Effects on Protein Kinase A Activity and RegulationWAVE1 mediates suppression of phagocytosis by phospholipid-derived DAMPs.Fibroblast growth factor treatment of Swiss 3T3 cells activates a subunit S6 kinase that phosphorylates a synthetic peptide substrate.Enhanced cAMP-stimulated protein kinase A activity in human fibrolamellar hepatocellular carcinoma.Comparative rates of desensitization of beta-adrenergic receptors by the beta-adrenergic receptor kinase and the cyclic AMP-dependent protein kinaseProtein kinase C pharmacology: refining the toolbox.Isoform-specific differences in the potencies of murine protein kinase inhibitors are due to nonconserved amino-terminal residues.Delineation of type I protein kinase A-selective signaling events using an RI anchoring disruptor.The adenylate cyclase-coupled vasopressin V2-receptor is highly laterally mobile in membranes of LLC-PK1 renal epithelial cells at physiological temperature.GRK3 mediates desensitization of CRF1 receptors: a potential mechanism regulating stress adaptation.CRF facilitates calcium release from intracellular stores in midbrain dopamine neurons.MAPKAP kinase-2; a novel protein kinase activated by mitogen-activated protein kinase.
P2860
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P2860
Primary-structure requirements for inhibition by the heat-stable inhibitor of the cAMP-dependent protein kinase
description
1986 nî lūn-bûn
@nan
1986 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի մարտին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Primary-structure requirements ...... cAMP-dependent protein kinase
@ast
Primary-structure requirements ...... cAMP-dependent protein kinase
@en
Primary-structure requirements ...... cAMP-dependent protein kinase
@nl
type
label
Primary-structure requirements ...... cAMP-dependent protein kinase
@ast
Primary-structure requirements ...... cAMP-dependent protein kinase
@en
Primary-structure requirements ...... cAMP-dependent protein kinase
@nl
prefLabel
Primary-structure requirements ...... cAMP-dependent protein kinase
@ast
Primary-structure requirements ...... cAMP-dependent protein kinase
@en
Primary-structure requirements ...... cAMP-dependent protein kinase
@nl
P2093
P2860
P3181
P356
P1476
Primary-structure requirements ...... cAMP-dependent protein kinase
@en
P2093
E H Fischer
M B Glaccum
P2860
P304
P3181
P356
10.1073/PNAS.83.6.1613
P407
P577
1986-03-01T00:00:00Z