Details for: PRKAR1A

Gene ID: 5573

Symbol: PRKAR1A

Ensembl ID: ENSG00000108946

Description: protein kinase cAMP-dependent type I regulatory subunit alpha

Associated with

Other Information

Genular Protein ID: 110432363

Symbol: KAP0_HUMAN

Name: cAMP-dependent protein kinase type I-alpha regulatory subunit

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 3426618

Title: Molecular cloning, cDNA structure and deduced amino acid sequence for a type I regulatory subunit of cAMP-dependent protein kinase from human testis.

PubMed ID: 3426618

DOI: 10.1016/0006-291x(87)90499-2

PubMed ID: 2310396

Title: The two mRNA forms for the type I alpha regulatory subunit of cAMP-dependent protein kinase from human testis are due to the use of different polyadenylation site signals.

PubMed ID: 2310396

DOI: 10.1016/0006-291x(90)91768-n

PubMed ID: 1889088

Title: Subtractive hybridization cloning of a tissue-specific extinguisher: TSE1 encodes a regulatory subunit of protein kinase A.

PubMed ID: 1889088

DOI: 10.1016/0092-8674(91)90433-y

PubMed ID: 8977401

Title: The human gene for the regulatory subunit RI alpha of cyclic adenosine 3', 5'-monophosphate-dependent protein kinase: two distinct promoters provide differential regulation of alternately spliced messenger ribonucleic acids.

PubMed ID: 8977401

DOI: 10.1210/endo.138.1.4864

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 12665801

Title: Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides.

PubMed ID: 12665801

DOI: 10.1038/nbt810

PubMed ID: 12213893

Title: Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease.

PubMed ID: 12213893

DOI: 10.1210/jc.2002-020592

PubMed ID: 14654843

Title: Proteomic characterization of the human centrosome by protein correlation profiling.

PubMed ID: 14654843

DOI: 10.1038/nature02166

PubMed ID: 15655353

Title: The second subunit of the replication factor C complex (RFC40) and the regulatory subunit (RIalpha) of protein kinase A form a protein complex promoting cell survival.

PubMed ID: 15655353

PubMed ID: 17081983

Title: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.

PubMed ID: 17081983

DOI: 10.1016/j.cell.2006.09.026

PubMed ID: 16491121

Title: Smad6 is a protein kinase X phosphorylation substrate and is required for HL-60 cell differentiation.

PubMed ID: 16491121

DOI: 10.1038/sj.onc.1209436

PubMed ID: 16387847

Title: PKA-mediated phosphorylation regulates the function of activation-induced deaminase (AID) in B cells.

PubMed ID: 16387847

DOI: 10.1073/pnas.0509969103

PubMed ID: 19367720

Title: Phosphorylation analysis of primary human T lymphocytes using sequential IMAC and titanium oxide enrichment.

PubMed ID: 19367720

DOI: 10.1021/pr800500r

PubMed ID: 18088087

Title: Phosphoproteome of resting human platelets.

PubMed ID: 18088087

DOI: 10.1021/pr0704130

PubMed ID: 18691976

Title: Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.

PubMed ID: 18691976

DOI: 10.1016/j.molcel.2008.07.007

PubMed ID: 18669648

Title: A quantitative atlas of mitotic phosphorylation.

PubMed ID: 18669648

DOI: 10.1073/pnas.0805139105

PubMed ID: 18318008

Title: Large-scale phosphoproteome analysis of human liver tissue by enrichment and fractionation of phosphopeptides with strong anion exchange chromatography.

PubMed ID: 18318008

DOI: 10.1002/pmic.200700884

PubMed ID: 19413330

Title: Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.

PubMed ID: 19413330

DOI: 10.1021/ac9004309

PubMed ID: 19369195

Title: Large-scale proteomics analysis of the human kinome.

PubMed ID: 19369195

DOI: 10.1074/mcp.m800588-mcp200

PubMed ID: 19690332

Title: Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.

PubMed ID: 19690332

DOI: 10.1126/scisignal.2000007

PubMed ID: 20215566

Title: Activity of retinoic acid receptor-alpha is directly regulated at its protein kinase A sites in response to follicle-stimulating hormone signaling.

PubMed ID: 20215566

DOI: 10.1210/en.2009-1338

PubMed ID: 20068231

Title: Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.

PubMed ID: 20068231

DOI: 10.1126/scisignal.2000475

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 21651393

Title: Recurrent PRKAR1A mutation in acrodysostosis with hormone resistance.

PubMed ID: 21651393

DOI: 10.1056/nejmoa1012717

PubMed ID: 21423175

Title: Control of PKA stability and signalling by the RING ligase praja2.

PubMed ID: 21423175

DOI: 10.1038/ncb2209

PubMed ID: 21406692

Title: System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.

PubMed ID: 21406692

DOI: 10.1126/scisignal.2001570

PubMed ID: 22785148

Title: An unusual presentation of Carney complex with diffuse primary pigmented nodular adrenocortical disease on one adrenal gland and a nonpigmented adrenocortical adenoma and focal primary pigmented nodular adrenocortical disease on the other.

PubMed ID: 22785148

DOI: 10.1507/endocrj.ej12-0040

PubMed ID: 23115245

Title: A small novel A-kinase anchoring protein (AKAP) that localizes specifically protein kinase A-regulatory subunit I (PKA-RI) to the plasma membrane.

PubMed ID: 23115245

DOI: 10.1074/jbc.m112.395970

PubMed ID: 23323113

Title: Novel Mutation in PRKAR1A in Carney Complex.

PubMed ID: 23323113

DOI: 10.4132/koreanjpathol.2012.46.6.595

PubMed ID: 22223895

Title: Comparative large-scale characterisation of plant vs. mammal proteins reveals similar and idiosyncratic N-alpha acetylation features.

PubMed ID: 22223895

DOI: 10.1074/mcp.m111.015131

PubMed ID: 22814378

Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.

PubMed ID: 22814378

DOI: 10.1073/pnas.1210303109

PubMed ID: 23186163

Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

PubMed ID: 33058759

Title: Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome.

PubMed ID: 33058759

DOI: 10.1016/j.ajhg.2020.09.005

PubMed ID: 15371594

Title: Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice.

PubMed ID: 15371594

DOI: 10.1073/pnas.0405535101

PubMed ID: 18241045

Title: In vitro functional studies of naturally occurring pathogenic PRKAR1A mutations that are not subject to nonsense mRNA decay.

PubMed ID: 18241045

DOI: 10.1002/humu.20688

PubMed ID: 22464250

Title: Exome sequencing identifies PDE4D mutations as another cause of acrodysostosis.

PubMed ID: 22464250

DOI: 10.1016/j.ajhg.2012.03.003

PubMed ID: 22464252

Title: Exome sequencing identifies PDE4D mutations in acrodysostosis.

PubMed ID: 22464252

DOI: 10.1016/j.ajhg.2012.03.004

PubMed ID: 23043190

Title: PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance.

PubMed ID: 23043190

DOI: 10.1210/jc.2012-2326

PubMed ID: 22723333

Title: PRKAR1A mutation affecting cAMP-mediated G protein-coupled receptor signaling in a patient with acrodysostosis and hormone resistance.

PubMed ID: 22723333

DOI: 10.1210/jc.2012-1369

PubMed ID: 23425300

Title: Novel mutations of the PRKAR1A gene in patients with acrodysostosis.

PubMed ID: 23425300

DOI: 10.1111/cge.12106

PubMed ID: 26405036

Title: Functional characterization of PRKAR1A mutations reveals a unique molecular mechanism causing acrodysostosis but multiple mechanisms causing carney complex.

PubMed ID: 26405036

DOI: 10.1074/jbc.m115.656553

Sequence Information:

  • Length: 381
  • Mass: 42982
  • Checksum: 2D04F08CE8857A6D
  • Sequence:
  • MESGSTAASE EARSLRECEL YVQKHNIQAL LKDSIVQLCT ARPERPMAFL REYFERLEKE 
    EAKQIQNLQK AGTRTDSRED EISPPPPNPV VKGRRRRGAI SAEVYTEEDA ASYVRKVIPK 
    DYKTMAALAK AIEKNVLFSH LDDNERSDIF DAMFSVSFIA GETVIQQGDE GDNFYVIDQG 
    ETDVYVNNEW ATSVGEGGSF GELALIYGTP RAATVKAKTN VKLWGIDRDS YRRILMGSTL 
    RKRKMYEEFL SKVSILESLD KWERLTVADA LEPVQFEDGQ KIVVQGEPGD EFFIILEGSA 
    AVLQRRSENE EFVEVGRLGP SDYFGEIALL MNRPRAATVV ARGPLKCVKL DRPRFERVLG 
    PCSDILKRNI QQYNSFVSLS V

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.