PPP1CA

PPP1CA
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 3E7A, 3E7B, 3EGG, 3EGH, 3HVQ, 3N5U, 3V4Y, 4G9J, 4MOV, 4MOY, 4MP0, 4XPN, 1FJM
Identifiers
Aliases	PPP1CA , PP-1A, PP1A, PP1alpha, PPP1A, protein phosphatase 1 catalytic subunit alpha
External IDs	OMIM: 176875; MGI: 103016; HomoloGene: 105262; GeneCards: PPP1CA; OMA:PPP1CA - orthologs
Gene location (Human) Chr. Chromosome 11 (human) [1] Band 11q13.2 Start 67,398,181 bp [1] End 67,421,183 bp [1]
Gene location (Mouse) Chr. Chromosome 19 (mouse) [2] Band 19|19 A Start 4,242,064 bp [2] End 4,245,419 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in granulocyte mucosa of transverse colon monocyte spleen thymus apex of heart blood lymph node mucosa of pharynx human penis Top expressed in striatum of neuraxis tail of embryo granulocyte yolk sac neural tube thymus mesencephalon white adipose tissue epiblast olfactory bulb More reference expression data BioGPS More reference expression data
Gene ontology Molecular function phosphoprotein phosphatase activity metal ion binding protein binding hydrolase activity cadherin binding involved in cell-cell adhesion protein serine/threonine phosphatase activity phosphatase activity protein phosphatase 1 binding ribonucleoprotein complex binding protein-containing complex binding Cellular component cytoplasm plasma membrane nucleoplasm PTW/PP1 phosphatase complex nucleolus extracellular exosome nucleus cytosol protein phosphatase type 1 complex glycogen granule neuron projection neuronal cell body dendritic spine perikaryon presynapse postsynapse glutamatergic synapse Biological process regulation of canonical Wnt signaling pathway negative regulation of protein binding cell division glycogen metabolic process cell cycle regulation of translational initiation by eIF2 alpha dephosphorylation beta-catenin destruction complex disassembly dephosphorylation cell-cell adhesion protein dephosphorylation circadian regulation of gene expression regulation of circadian rhythm entrainment of circadian clock by photoperiod carbohydrate metabolic process regulation of glycogen biosynthetic process regulation of glycogen catabolic process response to lead ion lung development peptidyl-threonine dephosphorylation branching morphogenesis of an epithelial tube peptidyl-serine dephosphorylation positive regulation of extrinsic apoptotic signaling pathway in absence of ligand viral process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 5499 19045 Ensembl ENSG00000172531 ENSMUSG00000040385 UniProt P62136 P62137 RefSeq (mRNA) NM_206873 NM_001008709 NM_002708 NM_031868 RefSeq (protein) NP_001008709 NP_002699 NP_996756 NP_114074 Location (UCSC) Chr 11: 67.4 – 67.42 Mb Chr 19: 4.24 – 4.25 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Serine/threonine-protein phosphatase PP1-alpha catalytic subunit is an enzyme that in humans is encoded by the PPP1CA gene.

Function

The protein encoded by this gene is one of the three catalytic subunits of protein phosphatase 1 (PP1). PP1 is a serine/threonine specific protein phosphatase known to be involved in the regulation of a variety of cellular processes, such as cell division, glycogen metabolism, muscle contractility, protein synthesis, and HIV-1 viral transcription. Increased PP1 activity has been observed in the end stage of heart failure. Studies in both human and mice suggest that PP1 is an important regulator of cardiac function. Three alternatively spliced transcript variants encoding different isoforms have been found for this gene. ^[5]

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles. ^{[§ 1]}

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|alt=Nicotine Activity on Dopaminergic Neurons edit]]

Nicotine Activity on Dopaminergic Neurons edit

1. The interactive pathway map can be edited at WikiPathways: "NicotineDopaminergic_WP1602".

Interactions

PPP1CA has been shown to interact with:

• AKAP11, ^{[6] [7]}
• BCL2-like 1, ^[8]
• BCL2L2, ^[8]
• BRCA1, ^[9]
• CDC5L, ^[10]
• Host cell factor C1, ^[11]
• KvLQT1, ^[12]
• LMTK2, ^[13]
• PHACTR3, ^[14]
• PPP1R15A, ^{[15] [16] [17]}
• PPP1R8, ^{[11] [18]}
• PPP1R9B, ^[19]
• Protein kinase R, ^[20] and
• SMARCB1. ^[16]

References

1. GRCh38: Ensembl release 89: ENSG00000172531 – Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000040385 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. "Entrez Gene: PPP1CA protein phosphatase 1, catalytic subunit, alpha isoform".
6. Tanji C, Yamamoto H, Yorioka N, Kohno N, Kikuchi K, Kikuchi A (October 2002). "A-kinase anchoring protein AKAP220 binds to glycogen synthase kinase-3beta (GSK-3beta ) and mediates protein kinase A-dependent inhibition of GSK-3beta". J. Biol. Chem. 277 (40): 36955–61. doi: 10.1074/jbc.M206210200 . PMID   12147701.
7. Schillace RV, Scott JD (March 1999). "Association of the type 1 protein phosphatase PP1 with the A-kinase anchoring protein AKAP220". Curr. Biol. 9 (6): 321–4. Bibcode:1999CBio....9..321S. doi: 10.1016/s0960-9822(99)80141-9 . PMID   10209101. S2CID   9188320.
8. Ayllón V, Cayla X, García A, Fleischer A, Rebollo A (July 2002). "The anti-apoptotic molecules Bcl-xL and Bcl-w target protein phosphatase 1alpha to Bad". Eur. J. Immunol. 32 (7): 1847–55. doi: 10.1002/1521-4141(200207)32:7<1847::AID-IMMU1847>3.0.CO;2-7 . PMID   12115603.
9. Liu Y, Virshup DM, White RL, Hsu LC (November 2002). "Regulation of BRCA1 phosphorylation by interaction with protein phosphatase 1alpha". Cancer Res. 62 (22): 6357–61. PMID   12438214.
10. Ajuh P, Kuster B, Panov K, Zomerdijk JC, Mann M, Lamond AI (December 2000). "Functional analysis of the human CDC5L complex and identification of its components by mass spectrometry". EMBO J. 19 (23): 6569–81. doi:10.1093/emboj/19.23.6569. PMC   305846 . PMID   11101529.
11. Ajuh PM, Browne GJ, Hawkes NA, Cohen PT, Roberts SG, Lamond AI (February 2000). "Association of a protein phosphatase 1 activity with the human factor C1 (HCF) complex". Nucleic Acids Res. 28 (3): 678–86. doi:10.1093/nar/28.3.678. PMC   102561 . PMID   10637318.
12. Marx SO, Kurokawa J, Reiken S, Motoike H, D'Armiento J, Marks AR, Kass RS (January 2002). "Requirement of a macromolecular signaling complex for beta adrenergic receptor modulation of the KCNQ1-KCNE1 potassium channel". Science. 295 (5554): 496–9. Bibcode:2002Sci...295..496M. doi:10.1126/science.1066843. PMID   11799244. S2CID   6153394.
13. Wang H, Brautigan DL (December 2002). "A novel transmembrane Ser/Thr kinase complexes with protein phosphatase-1 and inhibitor-2". J. Biol. Chem. 277 (51): 49605–12. doi: 10.1074/jbc.M209335200 . PMID   12393858.
14. Sagara J, Higuchi T, Hattori Y, Moriya M, Sarvotham H, Shima H, Shirato H, Kikuchi K, Taniguchi S (November 2003). "Scapinin, a putative protein phosphatase-1 regulatory subunit associated with the nuclear nonchromatin structure". J. Biol. Chem. 278 (46): 45611–9. doi: 10.1074/jbc.M305227200 . PMID   12925532.
15. Hung WJ, Roberson RS, Taft J, Wu DY (May 2003). "Human BAG-1 proteins bind to the cellular stress response protein GADD34 and interfere with GADD34 functions". Mol. Cell. Biol. 23 (10): 3477–86. doi:10.1128/mcb.23.10.3477-3486.2003. PMC   164759 . PMID   12724406.
16. Wu DY, Tkachuck DC, Roberson RS, Schubach WH (August 2002). "The human SNF5/INI1 protein facilitates the function of the growth arrest and DNA damage-inducible protein (GADD34) and modulates GADD34-bound protein phosphatase-1 activity". J. Biol. Chem. 277 (31): 27706–15. doi: 10.1074/jbc.M200955200 . PMID   12016208.
17. Connor JH, Weiser DC, Li S, Hallenbeck JM, Shenolikar S (October 2001). "Growth arrest and DNA damage-inducible protein GADD34 assembles a novel signaling complex containing protein phosphatase 1 and inhibitor 1". Mol. Cell. Biol. 21 (20): 6841–50. doi:10.1128/MCB.21.20.6841-6850.2001. PMC   99861 . PMID   11564868.
18. Jin Q, van Eynde A, Beullens M, Roy N, Thiel G, Stalmans W, Bollen M (August 2003). "The protein phosphatase-1 (PP1) regulator, nuclear inhibitor of PP1 (NIPP1), interacts with the polycomb group protein, embryonic ectoderm development (EED), and functions as a transcriptional repressor". J. Biol. Chem. 278 (33): 30677–85. doi: 10.1074/jbc.M302273200 . PMID   12788942.
19. Hsieh-Wilson LC, Allen PB, Watanabe T, Nairn AC, Greengard P (April 1999). "Characterization of the neuronal targeting protein spinophilin and its interactions with protein phosphatase-1". Biochemistry. 38 (14): 4365–73. doi:10.1021/bi982900m. PMID   10194355.
20. Tan SL, Tareen SU, Melville MW, Blakely CM, Katze MG (September 2002). "The direct binding of the catalytic subunit of protein phosphatase 1 to the PKR protein kinase is necessary but not sufficient for inactivation and disruption of enzyme dimer formation". J. Biol. Chem. 277 (39): 36109–17. doi: 10.1074/jbc.M205109200 . PMID   12138106.

Further reading

• Cohen PT (2002). "Protein phosphatase 1--targeted in many directions". J. Cell Sci. 115 (Pt 2): 241–56. doi:10.1242/jcs.115.2.241. PMID   11839776.
• Barker HM, Jones TA, da Cruz e Silva EF, Spurr NK, Sheer D, Cohen PT (1990). "Localization of the gene encoding a type I protein phosphatase catalytic subunit to human chromosome band 11q13". Genomics. 7 (2): 159–66. doi:10.1016/0888-7543(90)90536-4. PMID   2161401.
• Carrey EA, Campbell DG, Hardie DG (1986). "Phosphorylation and activation of hamster carbamyl phosphate synthetase II by cAMP-dependent protein kinase. A novel mechanism for regulation of pyrimidine nucleotide biosynthesis". EMBO J. 4 (13B): 3735–42. doi:10.1002/j.1460-2075.1985.tb04142.x. PMC   554725 . PMID   4092695.
• Saadat M, Mizuno Y, Kikuchi K, Yoshida MC (1995). "Comparative mapping of the gene encoding the catalytic subunit of protein phosphatase type 1 alpha (PPP1CA) to human, rat, and mouse chromosomes". Cytogenet. Cell Genet. 70 (1–2): 55–7. doi:10.1159/000133991. PMID   7736790.
• Durfee T, Becherer K, Chen PL, Yeh SH, Yang Y, Kilburn AE, Lee WH, Elledge SJ (1993). "The retinoblastoma protein associates with the protein phosphatase type 1 catalytic subunit". Genes Dev. 7 (4): 555–69. doi: 10.1101/gad.7.4.555 . PMID   8384581.
• Song Q, Khanna KK, Lu H, Lavin MF (1993). "Cloning and characterization of a human protein phosphatase 1-encoding cDNA". Gene. 129 (2): 291–5. doi:10.1016/0378-1119(93)90282-8. PMID   8392016.
• Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi: 10.1101/gr.6.9.791 . PMID   8889548.
• Kwon YG, Huang HB, Desdouits F, Girault JA, Greengard P, Nairn AC (1997). "Characterization of the interaction between DARPP-32 and protein phosphatase 1 (PP-1): DARPP-32 peptides antagonize the interaction of PP-1 with binding proteins". Proc. Natl. Acad. Sci. U.S.A. 94 (8): 3536–41. Bibcode:1997PNAS...94.3536K. doi: 10.1073/pnas.94.8.3536 . PMC   20474 . PMID   9108011.
• Colbran RJ, Bass MA, McNeill RB, Bollen M, Zhao S, Wadzinski BE, Strack S (1997). "Association of brain protein phosphatase 1 with cytoskeletal targeting/regulatory subunits". J. Neurochem. 69 (3): 920–9. doi: 10.1046/j.1471-4159.1997.69030920.x . PMID   9282913. S2CID   34789662.
• Allen PB, Kwon YG, Nairn AC, Greengard P (1998). "Isolation and characterization of PNUTS, a putative protein phosphatase 1 nuclear targeting subunit". J. Biol. Chem. 273 (7): 4089–95. doi: 10.1074/jbc.273.7.4089 . PMID   9461602.
• Zhang J, Zhang L, Zhao S, Lee EY (1998). "Identification and characterization of the human HCG V gene product as a novel inhibitor of protein phosphatase-1". Biochemistry. 37 (47): 16728–34. doi:10.1021/bi981169g. PMID   9843442.
• Neumann J, Maas R, Bokník P, Jones LR, Zimmermann N, Scholz H (1999). "Pharmacological characterization of protein phosphatase activities in preparations from failing human hearts". J. Pharmacol. Exp. Ther. 289 (1): 188–93. PMID   10087003.
• Schillace RV, Scott JD (1999). "Association of the type 1 protein phosphatase PP1 with the A-kinase anchoring protein AKAP220". Curr. Biol. 9 (6): 321–4. Bibcode:1999CBio....9..321S. doi: 10.1016/S0960-9822(99)80141-9 . PMID   10209101. S2CID   9188320.
• Takahashi M, Shibata H, Shimakawa M, Miyamoto M, Mukai H, Ono Y (1999). "Characterization of a novel giant scaffolding protein, CG-NAP, that anchors multiple signaling enzymes to centrosome and the golgi apparatus". J. Biol. Chem. 274 (24): 17267–74. doi: 10.1074/jbc.274.24.17267 . PMID   10358086.
• McAvoy T, Allen PB, Obaishi H, Nakanishi H, Takai Y, Greengard P, Nairn AC, Hemmings HC (1999). "Regulation of neurabin I interaction with protein phosphatase 1 by phosphorylation". Biochemistry. 38 (39): 12943–9. doi:10.1021/bi991227d. PMID   10504266.
• Yoshida K, Watanabe M, Kato H, Dutta A, Sugano S (1999). "BH-protocadherin-c, a member of the cadherin superfamily, interacts with protein phosphatase 1 alpha through its intracellular domain". FEBS Lett. 460 (1): 93–8. Bibcode:1999FEBSL.460...93Y. doi:10.1016/S0014-5793(99)01309-5. PMID   10571067. S2CID   24377126.
• Yang J, Hurley TD, DePaoli-Roach AA (2000). "Interaction of inhibitor-2 with the catalytic subunit of type 1 protein phosphatase. Identification of a sequence analogous to the consensus type 1 protein phosphatase-binding motif". J. Biol. Chem. 275 (30): 22635–44. doi: 10.1074/jbc.M003082200 . PMID   10807923.
• Ayllón V, Martínez-A C, García A, Cayla X, Rebollo A (2000). "Protein phosphatase 1alpha is a Ras-activated Bad phosphatase that regulates interleukin-2 deprivation-induced apoptosis". EMBO J. 19 (10): 2237–46. doi:10.1093/emboj/19.10.2237. PMC   384373 . PMID   10811615.
• Boudrez A, Beullens M, Groenen P, Van Eynde A, Vulsteke V, Jagiello I, Murray M, Krainer AR, Stalmans W, Bollen M (2000). "NIPP1-mediated interaction of protein phosphatase-1 with CDC5L, a regulator of pre-mRNA splicing and mitotic entry". J. Biol. Chem. 275 (33): 25411–7. doi: 10.1074/jbc.M001676200 . PMID   10827081.
• Helps NR, Luo X, Barker HM, Cohen PT (2001). "NIMA-related kinase 2 (Nek2), a cell-cycle-regulated protein kinase localized to centrosomes, is complexed to protein phosphatase 1". Biochem. J. 349 (Pt 2): 509–18. doi:10.1042/0264-6021:3490509. PMC   1221174 . PMID   10880350.