PPM1A

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Proteinska fosFataza, Mg2+/Mn2+ zavisna, 1A

PDB prikaz baziran na 1a6q.
Dostupne strukture
1A6Q, 3FXJ, 3FXK, 3FXL, 3FXM, 3FXO
Identifikatori
SimboliPPM1A; PP2C-ALPHA; PP2CA; PP2Calpha
Vanjski IDOMIM: 606108 MGI: 99878 HomoloGene: 56428 GeneCards: PPM1A Gene
EC broj3.1.3.16
Ontologija gena
Molekularna funkcija vezivanje jona magnezijuma
aktivnost proteinske serin/treoninske fosfataze
aktivnost prenosnika signala
proteinsko vezivanje
vezivanje proteinskog C-terminusa
hidrolazna aktivnost
vezivanje jona mangana
aktivnost kalmodulin-zavisne proteinske fosfataze
R-SMAD vezivanje
Celularna komponenta membranska frakcija
nukleus
citozol
naponom kontrolisani kompleks kalcijumskog kanala
kompleks proteinske serin/treoninske fosfataze
neuronska projekcija
Biološki proces blokada ćelijskog ciklusa
prenos signala
signalni put insulinskog receptora
negativna regulacija formiranja kompleksa SMAD proteina
signalni put Wnt receptora
defosforilacija
pozitivna regulacija signalnog puta Wnt receptora
Pregled RNK izražavanja
podaci
Ortolozi
VrstaČovekMiš
Entrez549419042
EnsemblENSG00000100614ENSMUSG00000021096
UniProtP35813P49443
RefSeq (mRNA)NM_021003.4NM_008910.3
RefSeq (protein)NP_066283.1NP_032936.1
Lokacija (UCSC)Chr 14:
60.71 - 60.77 Mb
Chr 12:
73.86 - 73.9 Mb
PubMed pretraga[1][2]

PPM1A (Proteinska fosfataza 1A) je enzim koji je kod ljudi kodiran PPM1A genom.[1][2]

Protein kodiran ovim genom je član PP2C familije Ser/Thr proteinskih fosfataza. Članovi PP2C familije su poznati kao negativni regulatori ćelijskog puta kojim se odgovara na stres. Ova fosfataza defosforiliše, i negativno reguliše aktivnosti MAP kinaza i MAP kinaza kinaza. Pokazano je da inhibira aktivaciju p38 i JNK kaskade kinaza indukovanu stresovima životne sredine. Ova fosfataza može takođe da defosforiliše ciklin-zavisne kinaze, i stoga može da učestvuje u kontroli ćelijskog ciklusa. Prekomerno izražavanje ove fosfataze može da aktivira izražavanje tumor supresornih gena TP53/p53, što dovodi do G2/M blokade ćelijkog ciklusa i apoptoze. Poznate su tri alternativno splajsovane transkriptne varijante koje kodiraju dve distinktne izoforme.[2]

Interakcije

PPM1A formira interakcije sa metabotropnim glutamatnim receptor 3.[3] PPM1A može da prekine TGF-beta signalizaciju putem inaktivacije Smad3 defosforilacijom. Smad3 je esencijalna komponenta TGF-beta signalnog puta.

Reference

  1. Mann DJ, Campbell DG, McGowan CH, Cohen PT (Apr 1992). „Mammalian protein serine/threonine phosphatase 2C: cDNA cloning and comparative analysis of amino acid sequences”. Biochim Biophys Acta 1130 (1): 100–4. PMID 1311954. 
  2. 2,0 2,1 „Entrez Gene: PPM1A protein phosphatase 1A (formerly 2C), magnesium-dependent, alpha isoform”. 
  3. Flajolet, Marc; Rakhilin Sergey, Wang Hong, Starkova Natalia, Nuangchamnong Nina, Nairn Angus C, Greengard Paul (December 2003). „Protein phosphatase 2C binds selectively to and dephosphorylates metabotropic glutamate receptor 3”. Proc. Natl. Acad. Sci. U.S.A. (United States) 100 (26): 16006–11. DOI:10.1073/pnas.2136600100. ISSN 0027-8424. PMC 307683. PMID 14663150. 

Literatura

  • Redpath NT, Price NT, Severinov KV, Proud CG (1993). „Regulation of elongation factor-2 by multisite phosphorylation.”. Eur. J. Biochem. 213 (2): 689–99. DOI:10.1111/j.1432-1033.1993.tb17809.x. PMID 8386634. 
  • Das AK, Helps NR, Cohen PT, Barford D (1997). „Crystal structure of the protein serine/threonine phosphatase 2C at 2.0 A resolution.”. EMBO J. 15 (24): 6798–809. PMC 452505. PMID 9003755. 
  • Takekawa M, Maeda T, Saito H (1998). „Protein phosphatase 2Calpha inhibits the human stress-responsive p38 and JNK MAPK pathways.”. EMBO J. 17 (16): 4744–52. DOI:10.1093/emboj/17.16.4744. PMC 1170803. PMID 9707433. 
  • Fjeld CC, Denu JM (1999). „Kinetic analysis of human serine/threonine protein phosphatase 2Calpha.”. J. Biol. Chem. 274 (29): 20336–43. DOI:10.1074/jbc.274.29.20336. PMID 10400656. 
  • Hishiya A, Ohnishi M, Tamura S, Nakamura F (1999). „Protein phosphatase 2C inactivates F-actin binding of human platelet moesin.”. J. Biol. Chem. 274 (38): 26705–12. DOI:10.1074/jbc.274.38.26705. PMID 10480873. 
  • Cheng A, Ross KE, Kaldis P, Solomon MJ (2000). „Dephosphorylation of cyclin-dependent kinases by type 2C protein phosphatases.”. Genes Dev. 13 (22): 2946–57. DOI:10.1101/gad.13.22.2946. PMC 317162. PMID 10580002. 
  • Strovel ET, Wu D, Sussman DJ (2000). „Protein phosphatase 2Calpha dephosphorylates axin and activates LEF-1-dependent transcription.”. J. Biol. Chem. 275 (4): 2399–403. DOI:10.1074/jbc.275.4.2399. PMID 10644691. 
  • Lifschitz-Mercer B, Sheinin Y, Ben-Meir D, et al. (2001). „Protein phosphatase 2Calpha expression in normal human tissues: an immunohistochemical study.”. Histochem. Cell Biol. 116 (1): 31–9. PMID 11479720. 
  • Srivastava J, Goris J, Dilworth SM, Parker PJ (2002). „Dephosphorylation of PKCdelta by protein phosphatase 2Ac and its inhibition by nucleotides.”. FEBS Lett. 516 (1-3): 265–9. DOI:10.1016/S0014-5793(02)02500-0. PMID 11959144. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). „Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. DOI:10.1073/pnas.242603899. PMC 139241. PMID 12477932. 
  • Ofek P, Ben-Meir D, Kariv-Inbal Z, et al. (2003). „Cell cycle regulation and p53 activation by protein phosphatase 2C alpha.”. J. Biol. Chem. 278 (16): 14299–305. DOI:10.1074/jbc.M211699200. PMID 12514180. 
  • Matsuda A, Suzuki Y, Honda G, et al. (2003). „Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways.”. Oncogene 22 (21): 3307–18. DOI:10.1038/sj.onc.1206406. PMID 12761501. 
  • Flajolet M, Rakhilin S, Wang H, et al. (2004). „Protein phosphatase 2C binds selectively to and dephosphorylates metabotropic glutamate receptor 3.”. Proc. Natl. Acad. Sci. U.S.A. 100 (26): 16006–11. DOI:10.1073/pnas.2136600100. PMC 307683. PMID 14663150. 
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). „Complete sequencing and characterization of 21,243 full-length human cDNAs.”. Nat. Genet. 36 (1): 40–5. DOI:10.1038/ng1285. PMID 14702039. 
  • Yoshizaki T, Maegawa H, Egawa K, et al. (2004). „Protein phosphatase-2C alpha as a positive regulator of insulin sensitivity through direct activation of phosphatidylinositol 3-kinase in 3T3-L1 adipocytes.”. J. Biol. Chem. 279 (21): 22715–26. DOI:10.1074/jbc.M313745200. PMID 15016818. 
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). „The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).”. Genome Res. 14 (10B): 2121–7. DOI:10.1101/gr.2596504. PMC 528928. PMID 15489334. 
  • Li D, Wang F, Lai M, et al. (2005). „A protein phosphatase 2calpha-Ca2+ channel complex for dephosphorylation of neuronal Ca2+ channels phosphorylated by protein kinase C.”. J. Neurosci. 25 (8): 1914–23. DOI:10.1523/JNEUROSCI.4790-04.2005. PMID 15728831. 
  • Rual JF, Venkatesan K, Hao T, et al. (2005). „Towards a proteome-scale map of the human protein-protein interaction network.”. Nature 437 (7062): 1173–8. DOI:10.1038/nature04209. PMID 16189514. 
  • Kitajima TS, Sakuno T, Ishiguro K, et al. (2006). „Shugoshin collaborates with protein phosphatase 2A to protect cohesin.”. Nature 441 (7089): 46–52. DOI:10.1038/nature04663. PMID 16541025. 
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PDB Galerija
1a6q: Kristalna struktura proteinske serin-treoninske fosfataze 2C na 2 A rezoluciji
1a6q: Kristalna struktura proteinske serin-treoninske fosfataze 2C na 2 A rezoluciji