MAP3K8

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

Mitogen-activated protein kinase kinase kinase 8 is an enzyme that in humans is encoded by the MAP3K8 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesMAP3K8, COT, EST, ESTF, MEKK8, TPL2, Tpl-2, c-COT, AURA2, mitogen-activated protein kinase kinase kinase 8, Tpl2
Quick facts Available structures, PDB ...
MAP3K8
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMAP3K8, COT, EST, ESTF, MEKK8, TPL2, Tpl-2, c-COT, AURA2, mitogen-activated protein kinase kinase kinase 8, Tpl2
External IDsOMIM: 191195; MGI: 1346878; HomoloGene: 3812; GeneCards: MAP3K8; OMA:MAP3K8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001244134
NM_005204
NM_001320961

NM_007746

RefSeq (protein)

NP_001231063
NP_001307890
NP_005195

NP_031772

Location (UCSC)Chr 10: 30.43 – 30.46 MbChr 18: 4.33 – 4.35 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

Function

The gene was identified by its oncogenic transforming activity in cells. The encoded protein is a member of the serine/threonine-specific protein kinase family. This kinase can activate ERK1, ERK2 and p38 MAP kinases.[8][9] This kinase was shown to activate IkappaB kinases, and thus induce the nuclear production of NF-kappaB. This kinase was also found to promote the production of TNF-alpha and IL-2 during T lymphocyte activation. Studies of a similar gene in rat suggested the direct involvement of this kinase in the proteolysis of NF-kappaB1, p105 (NFKB1). This gene may also start transcription at a downstream in-frame translation start codon, and thus produce an isoform containing a shorter N-terminus. The shorter isoform has been shown to display weaker transforming activity.[7] In mice, the gene is known as TPL2 and is a tumor-suppressor gene whose absence contributes to the development and progression of cancer.[10] However, it functions in other organs as a oncogene, promoting cancer.[11]

Interactions

MAP3K8 has been shown to interact with AKT1,[12] CHUK,[13] NFKB2,[14] NFKB1,[14][15] C22orf25[16] and TNIP2.[17]

References

Further reading

Related Articles

Wikiwand AI