| P2093 | author name string | Elah Pick | |
| | Tali S Berman | |
| P2860 | cites work | Regulation of retrotranslocation by p97-associated deubiquitinating enzyme ataxin-3 | Q24304415 |
| | UBXD7 binds multiple ubiquitin ligases and implicates p97 in HIF1alpha turnover | Q24310742 |
| | Mechanism of gate opening in the 20S proteasome by the proteasomal ATPases | Q24564109 |
| | Docking of the proteasomal ATPases' carboxyl termini in the 20S proteasome's alpha ring opens the gate for substrate entry | Q24674433 |
| | Interactions of PAN's C-termini with archaeal 20S proteasome and implications for the eukaryotic proteasome–ATPase interactions | Q27646619 |
| | The molecular basis of CRL4DDB2/CSA ubiquitin ligase architecture, targeting, and activation | Q27675805 |
| | The proteasomal subunit Rpn6 is a molecular clamp holding the core and regulatory subcomplexes together | Q27676340 |
| | RING domain E3 ubiquitin ligases | Q27860546 |
| | Cdc48 and Ufd3, new partners of the ubiquitin protease Ubp3, are required for ribophagy | Q27932851 |
| | A subcomplex of the proteasome regulatory particle required for ubiquitin-conjugate degradation and related to the COP9-signalosome and eIF3. | Q27936509 |
| | Functional division of substrate processing cofactors of the ubiquitin-selective Cdc48 chaperone | Q27937776 |
| | Cdc48/p97 mediates UV-dependent turnover of RNA Pol II. | Q27938488 |
| | Ecm29 fulfils quality control functions in proteasome assembly | Q27939879 |
| | Localization of the proteasomal ubiquitin receptors Rpn10 and Rpn13 by electron cryomicroscopy | Q28256624 |
| | Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system | Q28258706 |
| | Molecular architecture of the 26S proteasome holocomplex determined by an integrative approach | Q28259014 |
| | Expanding into new markets--VCP/p97 in endocytosis and autophagy | Q28262822 |
| | Neurospora COP9 signalosome integrity plays major roles for hyphal growth, conidial development, and circadian function | Q28483644 |
| | Glycoprotein-specific ubiquitin ligases recognize N-glycans in unfolded substrates | Q28508835 |
| | Near-atomic resolution structural model of the yeast 26S proteasome. | Q30524942 |
| | An archaebacterial ATPase, homologous to ATPases in the eukaryotic 26 S proteasome, activates protein breakdown by 20 S proteasomes | Q33873082 |
| | ATP binding to PAN or the 26S ATPases causes association with the 20S proteasome, gate opening, and translocation of unfolded proteins. | Q33991996 |
| | The COP9 signalosome: more than a protease | Q34014197 |
| | Properties of the hybrid form of the 26S proteasome containing both 19S and PA28 complexes. | Q34088438 |
| | Loss of Rpt5 protein interactions with the core particle and Nas2 protein causes the formation of faulty proteasomes that are inhibited by Ecm29 protein. | Q35378632 |
| | The COP9 signalosome: an alternative lid for the 26S proteasome? | Q35542510 |
| | NEDD8 links cullin-RING ubiquitin ligase function to the p97 pathway | Q35947206 |
| | A viral deubiquitylating enzyme restores dislocation of substrates from the endoplasmic reticulum (ER) in semi-intact cells. | Q36078784 |
| | Proteasome plasticity. | Q36125173 |
| | The archaeal proteasome is regulated by a network of AAA ATPases | Q36386004 |
| | ATP-dependent proteases of bacteria: recognition logic and operating principles | Q36639201 |
| | Structural basis for a reciprocal regulation between SCF and CSN. | Q36988986 |
| | COP9 signalosome interacts ATP-dependently with p97/valosin-containing protein (VCP) and controls the ubiquitination status of proteins bound to p97/VCP. | Q37454309 |
| | Proteasome activators | Q37826501 |
| | The cullin protein family | Q37873586 |
| | Cdc48: a power machine in protein degradation | Q37899368 |
| | Proteasomal AAA-ATPases: structure and function. | Q37912396 |
| | Stalled proteasomes are directly relieved by P97 recruitment | Q38263851 |
| | A genome-wide screen identifies p97 as an essential regulator of DNA damage-dependent CDT1 destruction. | Q38666669 |
| | Exploring the role of p97 and its UBX-domain cofactors through identification of their interacting proteins | Q39393263 |
| | Molecular model of the human 26S proteasome | Q41613713 |
| | At sixes and sevens: characterization of the symmetry mismatch of the ClpAP chaperone-assisted protease | Q41633089 |
| | Identification of the Cdc48•20S proteasome as an ancient AAA+ proteolytic machine. | Q41953180 |
| | Cell biology. An ancient portal to proteolysis | Q42177180 |
| | Stability of the proteasome can be regulated allosterically through engagement of its proteolytic active sites. | Q46891027 |
| | CSN facilitates Cullin-RING ubiquitin ligase function by counteracting autocatalytic adapter instability | Q47845473 |
| | Caenorhabditis elegans p97 controls germline-specific sex determination by controlling the TRA-1 level in a CUL-2-dependent manner | Q48713186 |
| | The COP9 signalosome: its regulation of cullin-based E3 ubiquitin ligases and role in photomorphogenesis. | Q50800615 |
| | Consequences of COP9 signalosome and 26S proteasome interaction. | Q52937446 |
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 389-393 | |
| P577 | publication date | 2013-01-17 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | Formation of alternative proteasomes: same lady, different cap? | |
| P478 | volume | 587 | |