Sequestosome 1

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Sequestosome-1 is a protein that in humans is encoded by the SQSTM1 gene.[5][6][7] Also known as the ubiquitin-binding protein p62,[8] it is an autophagosome cargo protein that targets other proteins that bind to it for selective autophagy. By interacting with GATA4 and targeting it for degradation, it can inhibit GATA-4 associated senescence and senescence-associated secretory phenotype.[9]

PDBOrtholog search: PDBe RCSB
AliasesSQSTM1, A170, OSIL, PDB3, ZIP3, p60, p62, p62B, FTDALS3, Sequestosome 1, NADGP, DMRV
Quick facts SQSTM1, Available structures ...
SQSTM1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSQSTM1, A170, OSIL, PDB3, ZIP3, p60, p62, p62B, FTDALS3, Sequestosome 1, NADGP, DMRV
External IDsOMIM: 601530; MGI: 107931; HomoloGene: 31202; GeneCards: SQSTM1; OMA:SQSTM1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001142298
NM_001142299
NM_003900

NM_001290769
NM_011018

RefSeq (protein)

NP_001135770
NP_001135771
NP_003891

NP_001277698
NP_035148

Location (UCSC)Chr 5: 179.81 – 179.84 MbChr 11: 50.09 – 50.1 Mb
PubMed search[3][4]
Wikidata
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Mutations in SQSTM1 are a common cause of Paget's disease of bone.[10]

Interactions

Sequestosome 1 has been shown to interact with:

Role in cancer

The SQSTM1 gene, which is actively transcribed as part of normal cellular function, is sometimes identified in fusion proteins, which can cause cancer when SQSTM1 is abnormally fused to a tyrosine kinase or other pro-proliferation gene. These genes are normally tightly regulated, but when bound to a minimally regulated gene like SQSTM1, they cause abnormal over-expression.[21]

References

Further reading

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