This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


Search results

From Proteopedia

You searched for P62/sqstm1

Jump to: navigation, search

There is no page with the exact title "P62/sqstm1". The search results for "P62/sqstm1" are displayed below. You can create a page titled P62/sqstm1 (by clicking on the red link).

For more information about searching Proteopedia, see Help.

To exclude pages titled with 4-character PDB codes, use the checkbox "only Human created pages" at the bottom of this page.

Showing below up to 20 results starting with #1.


View (previous 20) (next 20) (20 | 50 | 100 | 250 | 500)

Article title matches

  1. Category:P62/sqstm1 (41 bytes)
    1: List of pages with the keyword P62/sqstm1
  2. Sqstm1 (26 bytes)

Page text matches

  1. 1q02 (6,337 bytes)
    2: ==NMR structure of the UBA domain of p62 (SQSTM1)==
    10: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
    25: ...nt on a common loss of ubiquitin chain binding by p62.
    27: ...ucture of the ubiquitin-associated domain of p62 (SQSTM1) and implications for mutations that cause Paget'...
  2. 2jy7 (4,189 bytes)
    2: ... of the ubiquitin associated (UBA) domain of p62 (SQSTM1). RDC refined==
    10: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
  3. 2jy8 (4,215 bytes)
    2: ... of the ubiquitin associated (UBA) domain of p62 (SQSTM1) in complex with ubiquitin. RDC refined==
    10: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
  4. 2k0b (5,710 bytes)
    2: ==NMR structure of the UBA domain of p62 (SQSTM1)==
    10: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
    25: The ubiquitin associated domain of p62 is a small three-helix bundle of approximately 50...
    27: ... dynamics of the three-helix bundle UBA domain of p62 from experiment and simulation.,Evans CL, Long JE...
  5. 2knv (6,137 bytes)
    2: ==NMR dimer structure of the UBA domain of p62 (SQSTM1)==
    10: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
    25: ... with reduced NF-kappaB activity compared with wt-p62.
    27: Dimerisation of the UBA domain of p62 inhibits ubiquitin binding and regulates NF-kappa...
  6. Category:P62/sqstm1 (41 bytes)
    1: List of pages with the keyword P62/sqstm1
  7. 6khz (5,369 bytes)
    2: ==p62/SQSTM1 ZZ domain with Gly-peptide==
    11: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
  8. 4mjs (6,130 bytes)
    11: ...omoter through MEF2C. Through binding with SQSTM1/p62, functions in interleukin-1 signaling and activat...
    14: ...anisms of the homo-or hetero-interactions between p62 and PKCzeta and provide the basis for designing i...
    16: ...the homotypic PB1-PB1 complex between PKCzeta and p62.,Ren J, Wang J, Wang Z, Wu J Sci China Life Sci. ...
  9. 2mgw (3,817 bytes)
    13: ...lated autophagic substrates more efficiently than p62.
  10. 2mj5 (5,155 bytes)
    13: ...lated autophagic substrates more efficiently than p62.
  11. 8gu7 (4,205 bytes)
    13: ...sphate; RUBCN rubicon autophagy regulator; SQSTM1/p62 sequestosome 1; UVRAG UV radiation resistance ass...
  12. 4uf8 (5,116 bytes)
    2: ==Electron cryo-microscopy structure of PB1-p62 filaments==
    10: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
    15: ...hortening of filaments. These studies explain how p62 assemblies provide a large molecular scaffold for...
    17: The Selective Autophagy Receptor p62 Forms a Flexible Filamentous Helical Scaffold.,Ci...
  13. 4uf9 (5,123 bytes)
    2: ==Electron cryo-microscopy structure of PB1-p62 type T filaments==
    10: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
    15: ...hortening of filaments. These studies explain how p62 assemblies provide a large molecular scaffold for...
    17: The Selective Autophagy Receptor p62 Forms a Flexible Filamentous Helical Scaffold.,Ci...
  14. 4zy3 (4,489 bytes)
    14: ...tis C virus (HCV). An inhibitor of phosphorylated p62-dependent Nrf2 activation suppresses the prolifer...
    16: p62/Sqstm1 promotes malignancy of HCV-positive hepatocellula...
  15. 5xv3 (4,942 bytes)
    14: ...n of Atg13 from Schizosaccharomyces pombe; SQSTM1/p62: sequestosome 1; ULK1: unc51-like autophagy activ...
  16. 5xv4 (4,765 bytes)
    13: ...n of Atg13 from Schizosaccharomyces pombe; SQSTM1/p62: sequestosome 1; ULK1: unc51-like autophagy activ...
  17. 5xv6 (4,765 bytes)
    13: ...n of Atg13 from Schizosaccharomyces pombe; SQSTM1/p62: sequestosome 1; ULK1: unc51-like autophagy activ...
  18. 5yp7 (3,622 bytes)
    2: ==p62/SQSTM1 ZZ domain==
    11: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
  19. 5yp8 (5,382 bytes)
    2: ==p62/SQSTM1 ZZ domain with Arg-peptide==
    11: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...
  20. 5ypa (5,382 bytes)
    2: ==p62/SQSTM1 ZZ domain with Lys-peptide==
    11: ...t.org/uniprot/SQSTM_HUMAN SQSTM_HUMAN] Defects in SQSTM1 are a cause of Paget disease of bone (PDB) [MIM:[...

View (previous 20) (next 20) (20 | 50 | 100 | 250 | 500)



Search in namespaces:

Include only Seeded (Automatic) pages - only Human created pages
List redirects
Search for

You may also try
Views
Personal tools