Citation

BibTex format

@article{freemont:2017:10.1042/BCJ20160783,
author = {freemont, P and Stach, L},
doi = {10.1042/BCJ20160783},
journal = {Biochemical Journal},
pages = {2953--2976},
title = {The AAA+ ATPase p97, a cellular multi-tool},
url = {http://dx.doi.org/10.1042/BCJ20160783},
volume = {474},
year = {2017}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The AAA+ (ATPases associated with diverse cellular activities) ATPase p97 is essential to a wide range of cellular functions, including endoplasmic reticulum-associated degradation, membrane fusion, NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells) activation and chromatin-associated processes, which are regulated by ubiquitination. p97 acts downstream from ubiquitin signaling events and utilizes the energy from ATP hydrolysis to extract its substrate proteins from cellular structures or multiprotein complexes. A multitude of p97 cofactors have evolved which are essential to p97 function. Ubiquitin-interacting domains and p97-binding domains combine to form bi-functional cofactors, whose complexes with p97 enable the enzyme to interact with a wide range of ubiquitinated substrates. A set of mutations in p97 have been shown to cause the multisystem proteinopathy inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia. In addition, p97 inhibition has been identified as a promising approach to provoke proteotoxic stress in tumors. In this review, we will describe the cellular processes governed by p97, how the cofactors interact with both p97 and its ubiquitinated substrates, p97 enzymology and the current status in developing p97 inhibitors for cancer therapy.
AU - freemont,P
AU - Stach,L
DO - 10.1042/BCJ20160783
EP - 2976
PY - 2017///
SN - 1470-8728
SP - 2953
TI - The AAA+ ATPase p97, a cellular multi-tool
T2 - Biochemical Journal
UR - http://dx.doi.org/10.1042/BCJ20160783
UR - http://hdl.handle.net/10044/1/50187
VL - 474
ER -

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