MAPKAPK2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

MAP kinase-activated protein kinase 2 is an enzyme that in humans is encoded by the MAPKAPK2 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesMAPKAPK2, MAPKAP-K2, MK-2, MK2, mitogen-activated protein kinase-activated protein kinase 2, MAPK activated protein kinase 2
Quick facts Available structures, PDB ...
MAPKAPK2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMAPKAPK2, MAPKAP-K2, MK-2, MK2, mitogen-activated protein kinase-activated protein kinase 2, MAPK activated protein kinase 2
External IDsOMIM: 602006; MGI: 109298; HomoloGene: 56412; GeneCards: MAPKAPK2; OMA:MAPKAPK2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004759
NM_032960

NM_008551

RefSeq (protein)

NP_004750
NP_116584

NP_032577

Location (UCSC)Chr 1: 206.68 – 206.73 MbChr 1: 130.98 – 131.03 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of the Ser/Thr protein kinase family. This kinase is regulated through direct phosphorylation by p38 MAP kinase. In conjunction with p38 MAP kinase, this kinase is known to be involved in many cellular processes including stress and inflammatory responses, nuclear export, gene expression regulation and cell proliferation. Heat shock protein HSP27 was shown to be its major direct substrate in vivo. Two transcript variants encoding two different isoforms have been found for this gene.[8]

Vascular barrier

MK2 pathway has been demonstrated to have a key role in maintaining and repairing the integrity of endothelial barrier in the lung via actin[9] and vimentin remodeling. Activation of MK2 via its phosphorylation by p38 has been shown to restore the vascular barrier[7] and repair vascular leak,[10] associated with over 60 medical conditions, including Acute Respiratory Distress Syndrome (ARDS), a major cause of death around the world.[11]

SASP initiation

MAPKAPK2 mediates the initiation of the senescence-associated secretory phenotype (SASP) by mTOR (mechanistic target of rapamycin).[12][13] Interleukin 1 alpha (IL1A) is found on the surface of senescent cells, where it contributes to the production of SASP factors due to a positive feedback loop with NF-κB.[14][15] Translation of mRNA for IL1A is highly dependent upon mTOR activity.[16] mTOR activity increases levels of IL1A, mediated by MAPKAPK2.[14]

See also

  • SB 203580, suppresses the activation of MAPKAPK2
  • MK2-AP directly activates MAPKAPK2 independent of p38.[7]

Interactions

MAPKAPK2 has been shown to interact with:

References

Further reading

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