ERT2

MAPK3
Estruturas disponíveis
PDB	Pesquisa Human UniProt: PDBe RCSB
Lista de códigos id do PDB
	2ZOQ, 4QTB
Identificadores
Nomes alternativos	MAPK3, p44MAPK, ERT2, ERK1
IDs externos	OMIM: 601795 HomoloGene: 55682 GeneCards: MAPK3
Targeted by Drug
	ravoxertinib, ulixertinib
Ontologia genética
Função molecular	• phosphatase binding; • ATP binding; • protein kinase activity; • MAP kinase activity; • transferase activity; • phosphotyrosine residue binding; • scaffold protein binding; • GO:0001948, GO:0016582 ligação a proteínas plasmáticas; • nucleotide binding; • kinase activity; • protein serine/threonine kinase activity; • MAP kinase kinase activity; • identical protein binding;
Componente celular	• citosol; • envelope nuclear; • focal adhesion; • mitocôndria; • citoesqueleto; • núcleo celular; • late endosome; • complexo de Golgi; • early endosome; • pseudópode; • cariolinfa; • citoplasma; • membrana plasmática; • caveola; • membrane; • GO:0009327 complexo macromolecular;
Processo biológico	• caveolin-mediated endocytosis; • positive regulation of protein phosphorylation; • positive regulation of telomere capping; • response to exogenous dsRNA; • cardiac neural crest cell development involved in heart development; • positive regulation of xenophagy; • positive regulation of translation; • cellular response to DNA damage stimulus; • platelet activation; • Fc-epsilon receptor signaling pathway; • protein phosphorylation; • cellular response to mechanical stimulus; • face development; • GO:0033129 positive regulation of histone modification; • regulation of DNA-binding transcription factor activity; • DNA damage induced protein phosphorylation; • positive regulation of ERK1 and ERK2 cascade; • animal organ morphogenesis; • ciclo celular; • GO:0097285 apoptose; • Fc-gamma receptor signaling pathway involved in phagocytosis; • thymus development; • ERK1 and ERK2 cascade; • negative regulation of apolipoprotein binding; • transcription, DNA-templated; • cartilage development; • GO:0022415 viral process; • response to toxic substance; • regulation of stress-activated MAPK cascade; • fosforilação; • outer ear morphogenesis; • BMP signaling pathway; • response to lipopolysaccharide; • thyroid gland development; • response to epidermal growth factor; • positive regulation of MAP kinase activity; • positive regulation of telomerase activity; • peptidyl-tyrosine autophosphorylation; • nocicepção; • positive regulation of cyclase activity; • trachea formation; • lipopolysaccharide-mediated signaling pathway; • GO:0007243 intracellular signal transduction; • lung morphogenesis; • neural crest cell development; • transcription initiation from RNA polymerase I promoter; • regulation of early endosome to late endosome transport; • positive regulation of telomere maintenance via telomerase; • MAPK cascade; • positive regulation of histone acetylation; • Guia do axônio; • interleukin-1-mediated signaling pathway; • fibroblast growth factor receptor signaling pathway; • GO:0035404 peptidyl-serine phosphorylation; • regulation of cellular response to heat; • Bergmann glial cell differentiation; • regulation of Golgi inheritance; • arachidonic acid metabolic process; • regulation of cytoskeleton organization; • GO:0003257, GO:0010735, GO:1901228, GO:1900622, GO:1904488 positive regulation of transcription by RNA polymerase II; • regulation of phosphatidylinositol 3-kinase signaling; • regulation of ossification; • GO:1901313 positive regulation of gene expression; • positive regulation of macrophage chemotaxis; • cellular response to amino acid starvation; • GO:0072353 cellular response to reactive oxygen species; • stress-activated MAPK cascade; • cellular response to cadmium ion; • cellular response to dopamine; • positive regulation of metallopeptidase activity; • regulation of cellular pH; • GO:0034622 protein-containing complex assembly; • cellular response to tumor necrosis factor; • regulação genética; • cellular response to organic substance; • GO:0010260 envelhecimento; • decidualization;
	Sources:Amigo / QuickGO
Padrão de expressão RNA
	Mais dados de referência de expressão
Ortólogos
	5595
	n/a
	ENSG00000102882
	n/a
	P27361
	n/a
	NM_001040056; NM_001109891; NM_002746
	n/a
	NP_001035145; NP_001103361; NP_002737
	n/a
	Wikidata
Ver/Editar Humano

ERT2, também conhecida como p44MAPK, MAPK3 e ERK1, é uma enzima que em humanos é codificada pelo gene MAPK3.^[3]

Ela é um membro da superfamília de proteína quinase, família de proteína cinase CMGC Ser/Thr, subfamília de MAP quinase. ERT2 é um apelido para o gene, proteína quinase 3 (ativada por mitógeno), em seres humanos.^[4]^[5] Os pesquisadores fundiram a enzima a ERT2, em seguida ativaram o complexo com um análogo de tamoxifeno, 4-hidroxitamoxifeno, no caso de Cas9, a fim de colocar os controles no sistema CRISPR/Cas9.^[6].

Interações

MAPK3 demonstrou interagir com:

Leitura adicional

Peruzzi F, Gordon J, Darbinian N, Amini S (2002). «Tat-induced deregulation of neuronal differentiation and survival by nerve growth factor pathway». J. Neurovirol. 8 Suppl 2 (2): 91–6. PMID 12491158. doi:10.1080/13550280290167885
Meloche S, Pouysségur J (2007). «The ERK1/2 mitogen-activated protein kinase pathway as a master regulator of the G1- to S-phase transition». Oncogene. 26 (22): 3227–39. PMID 17496918. doi:10.1038/sj.onc.1210414
Ruscica M, Dozio E, Motta M, Magni P (2007), «Modulatory Actions of Neuropeptide y on Prostate Cancer Growth: Role of MAP Kinase/ERK 1/2 Activatio», Modulatory actions of neuropeptide Y on prostate cancer growth: role of MAP kinase/ERK 1/2 activation, ISBN 978-0-387-69114-5, Advances In Experimental Medicine And Biology, 604, pp. 96–100, PMID 17695723, doi:10.1007/978-0-387-69116-9_7

Referências

↑ «Drogas que interagem fisicamente com mitogen-activated protein kinase 3 ver/editar referências no wikidata»
↑ «Human PubMed Reference:»
↑ Garcı́a, F.; Zalba, G.; Páez, G.; Encı́o, I.; de Miguel, C. (15 de maio de 1998). «Molecular Cloning and Characterization of the Human p44 Mitogen-Activated Protein Kinase Gene». Genomics (em inglês) (1): 69–78. ISSN 0888-7543. doi:10.1006/geno.1998.5315. Consultado em 30 de junho de 2021
↑ Anti-ERT2 Antibody Products from Bio-Rad Antibodies publicado por "Biocompare"
↑ From Gene Targeting to Genome Editing: Transgenic animals applications and beyond por Mauricio Rocha-Martins et al, publicado pela An. Acad. Bras. Ciênc. vol.87 no.2 supl.0 Rio de Janeiro Aug. 2015 ISSN 1678-2690
↑ Toggling CRISPR Activity with a Chemical Switch Researchers design a Cas9 enzyme that cuts DNA only in the presence of particular drug. por Kerry Grens (2016)
↑ Todd JL, Tanner KG, Denu JM (maio de 1999). «Extracellular regulated kinases (ERK) 1 and ERK2 are authentic substrates for the dual-specificity protein-tyrosine phosphatase VHR. A novel role in down-regulating the ERK pathway». J. Biol. Chem. 274 (19): 13271–80. PMID 10224087. doi:10.1074/jbc.274.19.13271
↑ Muda M, Theodosiou A, Gillieron C, Smith A, Chabert C, Camps M, Boschert U, Rodrigues N, Davies K, Ashworth A, Arkinstall S (abril de 1998). «The mitogen-activated protein kinase phosphatase-3 N-terminal noncatalytic region is responsible for tight substrate binding and enzymatic specificity». J. Biol. Chem. 273 (15): 9323–9. PMID 9535927. doi:10.1074/jbc.273.15.9323
↑ Kim DW, Cochran BH (fevereiro de 2000). «Extracellular signal-regulated kinase binds to TFII-I and regulates its activation of the c-fos promoter». Mol. Cell. Biol. 20 (4): 1140–8. PMC 85232. PMID 10648599. doi:10.1128/mcb.20.4.1140-1148.2000
↑ Zhou X, Richon VM, Wang AH, Yang XJ, Rifkind RA, Marks PA (dezembro de 2000). «Histone deacetylase 4 associates with extracellular signal-regulated kinases 1 and 2, and its cellular localization is regulated by oncogenic Ras». Proc. Natl. Acad. Sci. U.S.A. 97 (26): 14329–33. PMC 18918. PMID 11114188. doi:10.1073/pnas.250494697
↑ ^a ^b Marti A, Luo Z, Cunningham C, Ohta Y, Hartwig J, Stossel TP, Kyriakis JM, Avruch J (janeiro de 1997). «Actin-binding protein-280 binds the stress-activated protein kinase (SAPK) activator SEK-1 and is required for tumor necrosis factor-alpha activation of SAPK in melanoma cells». J. Biol. Chem. 272 (5): 2620–8. PMID 9006895. doi:10.1074/jbc.272.5.2620
↑ ^a ^b Butch ER, Guan KL (fevereiro de 1996). «Characterization of ERK1 activation site mutants and the effect on recognition by MEK1 and MEK2». J. Biol. Chem. 271 (8): 4230–5. PMID 8626767. doi:10.1074/jbc.271.8.4230
↑ Elion EA (setembro de 1998). «Routing MAP kinase cascades». Science. 281 (5383): 1625–6. PMID 9767029. doi:10.1126/science.281.5383.1625
↑ Yung Y, Yao Z, Hanoch T, Seger R (maio de 2000). «ERK1b, a 46-kDa ERK isoform that is differentially regulated by MEK». J. Biol. Chem. 275 (21): 15799–808. PMID 10748187. doi:10.1074/jbc.M910060199
↑ ^a ^b Zheng CF, Guan KL (novembro de 1993). «Properties of MEKs, the kinases that phosphorylate and activate the extracellular signal-regulated kinases». J. Biol. Chem. 268 (32): 23933–9. PMID 8226933
↑ Pettiford SM, Herbst R (fevereiro de 2000). «The MAP-kinase ERK2 is a specific substrate of the protein tyrosine phosphatase HePTP». Oncogene. 19 (7): 858–69. PMID 10702794. doi:10.1038/sj.onc.1203408
↑ Saxena M, Williams S, Taskén K, Mustelin T (setembro de 1999). «Crosstalk between cAMP-dependent kinase and MAP kinase through a protein tyrosine phosphatase». Nat. Cell Biol. 1 (5): 305–11. PMID 10559944. doi:10.1038/13024
↑ Saxena M, Williams S, Brockdorff J, Gilman J, Mustelin T (abril de 1999). «Inhibition of T cell signaling by mitogen-activated protein kinase-targeted hematopoietic tyrosine phosphatase (HePTP)». J. Biol. Chem. 274 (17): 11693–700. PMID 10206983. doi:10.1074/jbc.274.17.11693
↑ Roux PP, Richards SA, Blenis J (julho de 2003). «Phosphorylation of p90 ribosomal S6 kinase (RSK) regulates extracellular signal-regulated kinase docking and RSK activity». Mol. Cell. Biol. 23 (14): 4796–804. PMC 162206. PMID 12832467. doi:10.1128/mcb.23.14.4796-4804.2003
↑ Zhao Y, Bjorbaek C, Moller DE (novembro de 1996). «Regulation and interaction of pp90(rsk) isoforms with mitogen-activated protein kinases». J. Biol. Chem. 271 (47): 29773–9. PMID 8939914. doi:10.1074/jbc.271.47.29773
↑ Mao C, Ray-Gallet D, Tavitian A, Moreau-Gachelin F (fevereiro de 1996). «Differential phosphorylations of Spi-B and Spi-1 transcription factors». Oncogene. 12 (4): 863–73. PMID 8632909

Ligações externas

[1] «Drogas que interagem fisicamente com mitogen-activated protein kinase 3 ver/editar referências no wikidata»

[2] «Human PubMed Reference:»

[3] Garcı́a, F.; Zalba, G.; Páez, G.; Encı́o, I.; de Miguel, C. (15 de maio de 1998). «Molecular Cloning and Characterization of the Human p44 Mitogen-Activated Protein Kinase Gene». Genomics (em inglês) (1): 69–78. ISSN 0888-7543. doi:10.1006/geno.1998.5315. Consultado em 30 de junho de 2021

[4] Anti-ERT2 Antibody Products from Bio-Rad Antibodies publicado por "Biocompare"

[5] From Gene Targeting to Genome Editing: Transgenic animals applications and beyond por Mauricio Rocha-Martins et al, publicado pela An. Acad. Bras. Ciênc. vol.87 no.2 supl.0 Rio de Janeiro Aug. 2015 ISSN 1678-2690

[6] Toggling CRISPR Activity with a Chemical Switch Researchers design a Cas9 enzyme that cuts DNA only in the presence of particular drug. por Kerry Grens (2016)

[pmid10224087-7] Todd JL, Tanner KG, Denu JM (maio de 1999). «Extracellular regulated kinases (ERK) 1 and ERK2 are authentic substrates for the dual-specificity protein-tyrosine phosphatase VHR. A novel role in down-regulating the ERK pathway». J. Biol. Chem. 274 (19): 13271–80. PMID 10224087. doi:10.1074/jbc.274.19.13271

[pmid9535927-8] Muda M, Theodosiou A, Gillieron C, Smith A, Chabert C, Camps M, Boschert U, Rodrigues N, Davies K, Ashworth A, Arkinstall S (abril de 1998). «The mitogen-activated protein kinase phosphatase-3 N-terminal noncatalytic region is responsible for tight substrate binding and enzymatic specificity». J. Biol. Chem. 273 (15): 9323–9. PMID 9535927. doi:10.1074/jbc.273.15.9323

[pmid10648599-9] Kim DW, Cochran BH (fevereiro de 2000). «Extracellular signal-regulated kinase binds to TFII-I and regulates its activation of the c-fos promoter». Mol. Cell. Biol. 20 (4): 1140–8. PMC 85232. PMID 10648599. doi:10.1128/mcb.20.4.1140-1148.2000

[pmid11114188-10] Zhou X, Richon VM, Wang AH, Yang XJ, Rifkind RA, Marks PA (dezembro de 2000). «Histone deacetylase 4 associates with extracellular signal-regulated kinases 1 and 2, and its cellular localization is regulated by oncogenic Ras». Proc. Natl. Acad. Sci. U.S.A. 97 (26): 14329–33. PMC 18918. PMID 11114188. doi:10.1073/pnas.250494697

[pmid9006895-11] Marti A, Luo Z, Cunningham C, Ohta Y, Hartwig J, Stossel TP, Kyriakis JM, Avruch J (janeiro de 1997). «Actin-binding protein-280 binds the stress-activated protein kinase (SAPK) activator SEK-1 and is required for tumor necrosis factor-alpha activation of SAPK in melanoma cells». J. Biol. Chem. 272 (5): 2620–8. PMID 9006895. doi:10.1074/jbc.272.5.2620

[pmid8626767-12] Butch ER, Guan KL (fevereiro de 1996). «Characterization of ERK1 activation site mutants and the effect on recognition by MEK1 and MEK2». J. Biol. Chem. 271 (8): 4230–5. PMID 8626767. doi:10.1074/jbc.271.8.4230

[pmid9733512-13] Elion EA (setembro de 1998). «Routing MAP kinase cascades». Science. 281 (5383): 1625–6. PMID 9767029. doi:10.1126/science.281.5383.1625

[pmid10748187-14] Yung Y, Yao Z, Hanoch T, Seger R (maio de 2000). «ERK1b, a 46-kDa ERK isoform that is differentially regulated by MEK». J. Biol. Chem. 275 (21): 15799–808. PMID 10748187. doi:10.1074/jbc.M910060199

[pmid8226933-15] Zheng CF, Guan KL (novembro de 1993). «Properties of MEKs, the kinases that phosphorylate and activate the extracellular signal-regulated kinases». J. Biol. Chem. 268 (32): 23933–9. PMID 8226933

[pmid10702794-16] Pettiford SM, Herbst R (fevereiro de 2000). «The MAP-kinase ERK2 is a specific substrate of the protein tyrosine phosphatase HePTP». Oncogene. 19 (7): 858–69. PMID 10702794. doi:10.1038/sj.onc.1203408

[pmid10559944-17] Saxena M, Williams S, Taskén K, Mustelin T (setembro de 1999). «Crosstalk between cAMP-dependent kinase and MAP kinase through a protein tyrosine phosphatase». Nat. Cell Biol. 1 (5): 305–11. PMID 10559944. doi:10.1038/13024

[pmid10206983-18] Saxena M, Williams S, Brockdorff J, Gilman J, Mustelin T (abril de 1999). «Inhibition of T cell signaling by mitogen-activated protein kinase-targeted hematopoietic tyrosine phosphatase (HePTP)». J. Biol. Chem. 274 (17): 11693–700. PMID 10206983. doi:10.1074/jbc.274.17.11693

[pmid12832467-19] Roux PP, Richards SA, Blenis J (julho de 2003). «Phosphorylation of p90 ribosomal S6 kinase (RSK) regulates extracellular signal-regulated kinase docking and RSK activity». Mol. Cell. Biol. 23 (14): 4796–804. PMC 162206. PMID 12832467. doi:10.1128/mcb.23.14.4796-4804.2003

[pmid8939914-20] Zhao Y, Bjorbaek C, Moller DE (novembro de 1996). «Regulation and interaction of pp90(rsk) isoforms with mitogen-activated protein kinases». J. Biol. Chem. 271 (47): 29773–9. PMID 8939914. doi:10.1074/jbc.271.47.29773

[pmid8632909-21] Mao C, Ray-Gallet D, Tavitian A, Moreau-Gachelin F (fevereiro de 1996). «Differential phosphorylations of Spi-B and Spi-1 transcription factors». Oncogene. 12 (4): 863–73. PMID 8632909

[1]

[2]

[3]

[4]

[5]

[6]

[7]

[8]

[9]

[10]

[11]

[12]

[13]

[14]

[15]

[16]

[17]

[18]

[19]

[20]

[21]

v d e Proteínas
Processos	Síntese proteica Modificação pós-traducional Enovelamento de proteínas Proteoma
Estruturas	Estrutura da proteína Domínio proteico Proteassoma
Tipos	Proteína membranar Proteína globular Globulina Albumina Escleroproteína

v d e Genoma humano
Autossomas	1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · 11 · 12 · 13 · 14 · 15 · 16 · 17 · 18 · 19 · 20 · 21 · 22
Cromossomas sexuais	X · Y
Tópicos relacionados	Projeto Genoma Humano