Sequestosome: Difference between revisions

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[[2kkc]] – rSQS PB1 domain (mutant) - NMR<br />
[[2kkc]] – rSQS PB1 domain (mutant) - NMR<br />
[[3ade]] – mSQS + KEAP-1 – mouse<br />
[[3ade]] – mSQS + KEAP-1 – mouse<br />
[[4mjs]] – hSQS-1 PB1 domain + protein kinase C zeta type<br />
[[4uf8]], [[4uf9]] – hSQS-1 PB1-P62 domain – Cryo EM<br />





Revision as of 14:01, 14 June 2015


Function

Sequestosome (SQS) or p62, is required for the formation and autophagic degredation of polyubiquitin-containg bodies. SQS may regulate signaling cascades through ubiquitination.

SQS is a multi-domain protein. SQS domain structure includes:
PB1 domain which contains Phox and Berm1
ZZ-type zinc finger
SMIR – SOD interaction domain
TB – TRAF6 binding motif
LC3 – microtubule-associated protein 1 light chain 3B
LIR – interaction region
UBA – ubiquitin association domain.

Disease

Relevance

Structural highlights

3D structures of sequestosome

Updated on 17-May-2025

1q02, 2jy7, 2jy8, 2k0b, 2knv – SQS UBA domain – human - NMR

3b0f – mSQS UBA domain – mouse
2rru – mSQS UBA domain - NMR
2ktr – rSQS PB1 domain – rat - NMR
2kkc – rSQS PB1 domain (mutant) - NMR
3ade – mSQS + KEAP-1 – mouse
4mjs – hSQS-1 PB1 domain + protein kinase C zeta type
4uf8, 4uf9 – hSQS-1 PB1-P62 domain – Cryo EM


Structure of human sequestosome UBA domain (PDB code 2jy8)

Drag the structure with the mouse to rotate

ReferencesReferences

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Michal Harel