Literature DB >> 18438607

UBX domain proteins: major regulators of the AAA ATPase Cdc48/p97.

C Schuberth1, A Buchberger.   

Abstract

The highly conserved AAA ATPase Cdc48/p97 acts on ubiquitylated substrate proteins in cellular processes as diverse as the fusion of homotypic membranes and the degradation of misfolded proteins. The 'Ubiquitin regulatory X' (UBX) domain-containing proteins constitute the so far largest family of Cdc48/p97 cofactors. UBX proteins are involved in substrate recruitment to Cdc48/p97 and in the temporal and spatial regulation of its activity. In combination with UBX-like proteins and other cofactors, they can assemble into a large variety of Cdc48/p97-cofactor complexes possessing distinct cellular functions. This review gives an overview of the different subfamilies of UBX proteins and their functions, and discusses general principles of Cdc48/p97 regulation by these cofactors.

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Year:  2008        PMID: 18438607     DOI: 10.1007/s00018-008-8072-8

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  132 in total

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5.  Cdc48/VCP and Endocytosis Regulate TDP-43 and FUS Toxicity and Turnover.

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Journal:  Mol Cell Biol       Date:  2020-01-30       Impact factor: 4.272

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7.  Ubx4 modulates cdc48 activity and influences degradation of misfolded proteins of the endoplasmic reticulum.

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Journal:  J Biol Chem       Date:  2009-04-09       Impact factor: 5.157

8.  Phosphorylation regulates VCIP135 function in Golgi membrane fusion during the cell cycle.

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Journal:  J Cell Sci       Date:  2013-10-25       Impact factor: 5.285

9.  Ubiquitin- and ATP-dependent unfoldase activity of P97/VCP•NPLOC4•UFD1L is enhanced by a mutation that causes multisystem proteinopathy.

Authors:  Emily E Blythe; Kristine C Olson; Vincent Chau; Raymond J Deshaies
Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-16       Impact factor: 11.205

10.  Isolation of mammalian 26S proteasomes and p97/VCP complexes using the ubiquitin-like domain from HHR23B reveals novel proteasome-associated proteins.

Authors:  Henrike C Besche; Wilhelm Haas; Steven P Gygi; Alfred L Goldberg
Journal:  Biochemistry       Date:  2009-03-24       Impact factor: 3.162

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