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AB125663

Recombinant ヒト p38 beta/MAPK11 protein (GST tag N-Terminus)

Recombinant human p38 beta/MAPK11 protein (GST tag N-Terminus)

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Recombinant human p38 beta/MAPK11 protein (GST tag N-Terminus) is a Human Full Length protein, in the 1 to 364 aa range, expressed in Baculovirus infected Sf9 cells, with >95%, suitable for SDS-PAGE, WB, FuncS.

別名を表示する

PRKM11, SAPK2, SAPK2B, MAPK11, Mitogen-activated protein kinase 11, MAP kinase 11, MAPK 11, Mitogen-activated protein kinase p38 beta, Stress-activated protein kinase 2b, p38-2, MAP kinase p38 beta, p38b, SAPK2b

2 Images
Functional Studies - Recombinant human p38 beta/MAPK11 protein (GST tag N-Terminus) (AB125663)
  • FuncS

Unknown

Functional Studies - Recombinant human p38 beta/MAPK11 protein (GST tag N-Terminus) (AB125663)

The specific activity of ab125663 was determined to be 780 nmol/min/mg by Kinase Assay.

SDS-PAGE - Recombinant human p38 beta/MAPK11 protein (GST tag N-Terminus) (AB125663)
  • SDS-PAGE

Unknown

SDS-PAGE - Recombinant human p38 beta/MAPK11 protein (GST tag N-Terminus) (AB125663)

SDS-PAGE analysis of ab125663.

Key facts

精製度

>95% Densitometry

Purity was determined to be >95% by densitometry. Affinity purified.

発現系

Baculovirus infected Sf9 cells

タグ

GST tag N-Terminus

アプリケーション

SDS-PAGE, WB, FuncS

applications

生物活性

Yes

生物学的活性

The specific activity of ab125663 was determined to be 780 nmol/min/mg.

アクセッション番号

Q15759

アニマルフリー

No

キャリアフリー

No

Human

バッファー組成

pH: 7.5 Constituents: 25% Glycerol (glycerin, glycerine), 0.88% Sodium chloride, 0.79% Tris HCl, 0.31% Glutathione, 0.004% (R*,R*)-1,4-Dimercaptobutan-2,3-diol, 0.003% EDTA, 0.002% PMSF

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "SDS-PAGE": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "WB": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "FuncS": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

配列情報

[{"linker":null,"sequence":"","proteinLength":"Full Length","predictedMolecularWeight":"71 kDa","actualMolecularWeight":null,"aminoAcidEnd":364,"aminoAcidStart":1,"nature":"Recombinant","expressionSystem":null,"accessionNumber":"Q15759","tags":[{"tag":"GST","terminus":"N-Terminus"}]}]

出荷温度及び保存条件

製品の状態
Liquid
精製方法
Affinity purification
出荷温度
Dry Ice
短期保存温度
-80°C
長期保存温度
-80°C
分注に関する情報
Upon delivery aliquot
保管に関する情報
Avoid freeze / thaw cycle
True

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

The target p38 beta also known as MAPK11 is a member of the mitogen-activated protein kinase (MAPK) family specifically the p38 MAPK subfamily. It weighs approximately 41 kDa and can be expressed in various tissues but shows higher levels in skeletal muscle and heart tissue. This protein operates as a serine/threonine kinase playing an important role in delivering signals from the cell surface to the DNA in the cell nucleus. p38 beta influences transcription factors leading to the regulation of gene expression in response to external stimuli.
Biological function summary

The p38 beta/MAPK11 protein serves an essential role in cellular processes such as inflammation cell differentiation and apoptosis. It can form part of a larger signaling complex that is activated by various stress signals including cytokines and environmental stress suggesting its involvement in stress response pathways. The activation of this kinase results in the phosphorylation of downstream targets leading to various biological responses.

Pathways

P38 beta/MAPK11 is important in the MAPK signaling pathway and is closely linked to the stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK) pathway. In these pathways it interacts with other proteins such as MKK3 and MKK6 which are upstream activators. This pathway mediates responses to stress and inflammatory cytokines and regulates the production of inflammatory proteins and apoptosis-related factors.

P38 beta/MAPK11 plays an important role in conditions like cancer and chronic inflammatory diseases. Its modulation can affect cancer cell proliferation where it interacts with other MAPK family members. Alterations in the p38 MAPK signaling have been associated with rheumatoid arthritis where p38 beta works alongside p38 alpha to mediate pro-inflammatory cytokine production. Understanding these connections helps develop targeted therapies for these diseases.

一般的な情報

機能

Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). MAPK11 is one of the four p38 MAPKs which play an important role in the cascades of cellular responses evoked by extracellular stimuli such as pro-inflammatory cytokines or physical stress leading to direct activation of transcription factors (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). Accordingly, p38 MAPKs phosphorylate a broad range of proteins and it has been estimated that they may have approximately 200 to 300 substrates each (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). MAPK11 functions are mostly redundant with those of MAPK14 (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). Some of the targets are downstream kinases which are activated through phosphorylation and further phosphorylate additional targets (PubMed : 12452429, PubMed : 20626350). RPS6KA5/MSK1 and RPS6KA4/MSK2 can directly phosphorylate and activate transcription factors such as CREB1, ATF1, the NF-kappa-B isoform RELA/NFKB3, STAT1 and STAT3, but can also phosphorylate histone H3 and the nucleosomal protein HMGN1 (PubMed : 9687510). RPS6KA5/MSK1 and RPS6KA4/MSK2 play important roles in the rapid induction of immediate-early genes in response to stress or mitogenic stimuli, either by inducing chromatin remodeling or by recruiting the transcription machinery. On the other hand, two other kinase targets, MAPKAPK2/MK2 and MAPKAPK3/MK3, participate in the control of gene expression mostly at the post-transcriptional level, by phosphorylating ZFP36 (tristetraprolin) and ELAVL1, and by regulating EEF2K, which is important for the elongation of mRNA during translation. MKNK1/MNK1 and MKNK2/MNK2, two other kinases activated by p38 MAPKs, regulate protein synthesis by phosphorylating the initiation factor EIF4E2 (PubMed : 11154262). In the cytoplasm, the p38 MAPK pathway is an important regulator of protein turnover. For example, CFLAR is an inhibitor of TNF-induced apoptosis whose proteasome-mediated degradation is regulated by p38 MAPK phosphorylation. Ectodomain shedding of transmembrane proteins is regulated by p38 MAPKs as well. In response to inflammatory stimuli, p38 MAPKs phosphorylate the membrane-associated metalloprotease ADAM17. Such phosphorylation is required for ADAM17-mediated ectodomain shedding of TGF-alpha family ligands, which results in the activation of EGFR signaling and cell proliferation. Additional examples of p38 MAPK substrates are the FGFR1. FGFR1 can be translocated from the extracellular space into the cytosol and nucleus of target cells, and regulates processes such as rRNA synthesis and cell growth. FGFR1 translocation requires p38 MAPK activation. In the nucleus, many transcription factors are phosphorylated and activated by p38 MAPKs in response to different stimuli. Classical examples include ATF1, ATF2, ATF6, ELK1, PTPRH, DDIT3, TP53/p53 and MEF2C and MEF2A (PubMed : 10330143, PubMed : 15356147, PubMed : 9430721). The p38 MAPKs are emerging as important modulators of gene expression by regulating chromatin modifiers and remodelers (PubMed : 10330143, PubMed : 15356147, PubMed : 9430721). The promoters of several genes involved in the inflammatory response, such as IL6, IL8 and IL12B, display a p38 MAPK-dependent enrichment of histone H3 phosphorylation on 'Ser-10' (H3S10ph) in LPS-stimulated myeloid cells. This phosphorylation enhances the accessibility of the cryptic NF-kappa-B-binding sites marking promoters for increased NF-kappa-B recruitment. Phosphorylates NLRP1 downstream of MAP3K20/ZAK in response to UV-B irradiation and ribosome collisions, promoting activation of the NLRP1 inflammasome and pyroptosis (PubMed : 35857590). Phosphorylates methyltransferase DOT1L on 'Ser-834', 'Thr-900', 'Ser-902', 'Thr-984', 'Ser-1001', 'Ser-1009' and 'Ser-1104' (PubMed : 38270553).

配列の類似性

Belongs to the protein kinase superfamily. CMGC Ser/Thr protein kinase family. MAP kinase subfamily.

翻訳後修飾

Dually phosphorylated on Thr-180 and Tyr-182 by MAP2K3/MKK3, MAP2K4/MKK4 and MAP2K6/MKK6, which activates the enzyme.

細胞内局在性

Nucleus

製品プロトコール

ターゲットの情報

Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). MAPK11 is one of the four p38 MAPKs which play an important role in the cascades of cellular responses evoked by extracellular stimuli such as pro-inflammatory cytokines or physical stress leading to direct activation of transcription factors (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). Accordingly, p38 MAPKs phosphorylate a broad range of proteins and it has been estimated that they may have approximately 200 to 300 substrates each (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). MAPK11 functions are mostly redundant with those of MAPK14 (PubMed : 12452429, PubMed : 20626350, PubMed : 35857590). Some of the targets are downstream kinases which are activated through phosphorylation and further phosphorylate additional targets (PubMed : 12452429, PubMed : 20626350). RPS6KA5/MSK1 and RPS6KA4/MSK2 can directly phosphorylate and activate transcription factors such as CREB1, ATF1, the NF-kappa-B isoform RELA/NFKB3, STAT1 and STAT3, but can also phosphorylate histone H3 and the nucleosomal protein HMGN1 (PubMed : 9687510). RPS6KA5/MSK1 and RPS6KA4/MSK2 play important roles in the rapid induction of immediate-early genes in response to stress or mitogenic stimuli, either by inducing chromatin remodeling or by recruiting the transcription machinery. On the other hand, two other kinase targets, MAPKAPK2/MK2 and MAPKAPK3/MK3, participate in the control of gene expression mostly at the post-transcriptional level, by phosphorylating ZFP36 (tristetraprolin) and ELAVL1, and by regulating EEF2K, which is important for the elongation of mRNA during translation. MKNK1/MNK1 and MKNK2/MNK2, two other kinases activated by p38 MAPKs, regulate protein synthesis by phosphorylating the initiation factor EIF4E2 (PubMed : 11154262). In the cytoplasm, the p38 MAPK pathway is an important regulator of protein turnover. For example, CFLAR is an inhibitor of TNF-induced apoptosis whose proteasome-mediated degradation is regulated by p38 MAPK phosphorylation. Ectodomain shedding of transmembrane proteins is regulated by p38 MAPKs as well. In response to inflammatory stimuli, p38 MAPKs phosphorylate the membrane-associated metalloprotease ADAM17. Such phosphorylation is required for ADAM17-mediated ectodomain shedding of TGF-alpha family ligands, which results in the activation of EGFR signaling and cell proliferation. Additional examples of p38 MAPK substrates are the FGFR1. FGFR1 can be translocated from the extracellular space into the cytosol and nucleus of target cells, and regulates processes such as rRNA synthesis and cell growth. FGFR1 translocation requires p38 MAPK activation. In the nucleus, many transcription factors are phosphorylated and activated by p38 MAPKs in response to different stimuli. Classical examples include ATF1, ATF2, ATF6, ELK1, PTPRH, DDIT3, TP53/p53 and MEF2C and MEF2A (PubMed : 10330143, PubMed : 15356147, PubMed : 9430721). The p38 MAPKs are emerging as important modulators of gene expression by regulating chromatin modifiers and remodelers (PubMed : 10330143, PubMed : 15356147, PubMed : 9430721). The promoters of several genes involved in the inflammatory response, such as IL6, IL8 and IL12B, display a p38 MAPK-dependent enrichment of histone H3 phosphorylation on 'Ser-10' (H3S10ph) in LPS-stimulated myeloid cells. This phosphorylation enhances the accessibility of the cryptic NF-kappa-B-binding sites marking promoters for increased NF-kappa-B recruitment. Phosphorylates NLRP1 downstream of MAP3K20/ZAK in response to UV-B irradiation and ribosome collisions, promoting activation of the NLRP1 inflammasome and pyroptosis (PubMed : 35857590). Phosphorylates methyltransferase DOT1L on 'Ser-834', 'Thr-900', 'Ser-902', 'Thr-984', 'Ser-1001', 'Ser-1009' and 'Ser-1104' (PubMed : 38270553).
See full target information MAPK11

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