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Phorbol-12-myristate-13-acetate-induced protein 1

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

Phorbol-12-myristate-13-acetate-induced protein 1 is a protein that in humans is encoded by the PMAIP1 gene, and is also known as Noxa.[3][4][5]

AliasesPMAIP1, APR, NOXA, phorbol-12-myristate-13-acetate-induced protein 1
External IDsOMIM: 604959; GeneCards: PMAIP1
PDBHuman UniProt search: PDBe RCSB
Quick facts PMAIP1, Identifiers ...
PMAIP1
Identifiers
AliasesPMAIP1, APR, NOXA, phorbol-12-myristate-13-acetate-induced protein 1
External IDsOMIM: 604959; GeneCards: PMAIP1
Available structures
PDBHuman UniProt search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_021127

n/a

RefSeq (protein)

n/a

Location (UCSC)Chr 18: 59.9 – 59.9 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human
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Noxa (Latin for damage) is a pro-apoptotic member of the Bcl-2 protein family.[6] Bcl-2 family members can form hetero- or homodimers, and they act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The expression of Noxa is regulated by the tumor suppressor p53, and Noxa has been shown to be involved in p53-mediated apoptosis.

Interactions

Noxa has been shown to interact with:

See also

References

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