(Q34693562)

4 August 2017

1 reference

title

AAA+ ATPases: achieving diversity of function with conserved machinery (English)

1 reference

4 August 2017

Susan Roehl White

1

1 reference

PubMed ID

17897320

4 August 2017

Brett Lauring

series ordinal

2

1 reference

4 August 2017

26 September 2007

1 reference

4 August 2017

1 reference

4 August 2017

8

1 reference

4 August 2017

1657-1667

1 reference

4 August 2017

12

1 reference

A link between sequence conservation and domain motion within the AAA+ family.

4 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Crystal structures of the HslVU peptidase-ATPase complex reveal an ATP-dependent proteolysis mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Conserved Pore Residues in the AAA Protease FtsH Are Important for Proteolysis and Its Coupling to ATP Hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Role of the processing pore of the ClpX AAA+ ATPase in the recognition and engagement of specific protein substrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Evidence for an unfolding/threading mechanism for protein disaggregation by Saccharomyces cerevisiae Hsp104.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Substrate recognition by the AAA+ chaperone ClpB.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

AAA+ proteins: have engine, will work

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The Escherichia coli FtsH protein is a prokaryotic member of a protein family of putative ATPases involved in membrane functions, cell cycle control, and gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Evolutionary history and higher order classification of AAA+ ATPases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Cooperative kinetics of both Hsp104 ATPase domains and interdomain communication revealed by AAA sensor-1 mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Central pore residues mediate the p97/VCP activity required for ERAD

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Purification of an N-ethylmaleimide-sensitive protein catalyzing vesicular transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

A vacuolar v-t-SNARE complex, the predominant form in vivo and on isolated vacuoles, is disassembled and activated for docking and fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Functional role of the AAA peroxins in dislocation of the cycling PTS1 receptor back to the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Sequential mechanism of solubilization and refolding of stable protein aggregates by a bichaperone network

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The role of the ClpA chaperone in proteolysis by ClpAP

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Dynamics of substrate denaturation and translocation by the ClpXP degradation machine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

A subcomplex of the proteasome regulatory particle required for ubiquitin-conjugate degradation and related to the COP9-signalosome and eIF3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Identification and characterization of AFG3L2, a novel paraplegin-related gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Regulation of mitochondrial morphology through proteolytic cleavage of OPA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Identification and characterization of YME1L1, a novel paraplegin-related gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

A new function in translocation for the mitochondrial i-AAA protease Yme1: import of polynucleotide phosphorylase into the intermembrane space

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Membrane fusion and the cell cycle: Cdc48p participates in the fusion of ER membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

An NSF-like ATPase, p97, and NSF mediate cisternal regrowth from mitotic Golgi fragments

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear assembly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Diverse functions with a common regulator: ubiquitin takes command of an AAA ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Cytoplasmic dynein participates in the centrosomal localization of the Golgi complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Disruption of mitotic spindle orientation in a yeast dynein mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Structural comparison of purified dynein proteins with in situ dynein arms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Functional elements within the dynein microtubule-binding domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Recent progress in dynein structure and mechanism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Identification of katanin, an ATPase that severs and disassembles stable microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The Drosophila homologue of the hereditary spastic paraplegia protein, spastin, severs and disassembles microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Katanin controls mitotic and meiotic spindle length

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Katanin, a microtubule-severing protein, is a novel AAA ATPase that targets to the centrosome using a WD40-containing subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Three microtubule severing enzymes contribute to the "Pacman-flux" machinery that moves chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

An essential role for katanin in severing microtubules in the neuron

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Mutational studies on HslU and its docking mode with HslV

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Loops in the central channel of ClpA chaperone mediate protein binding, unfolding, and translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Atomic snapshots of an RNA packaging motor reveal conformational changes linking ATP hydrolysis to RNA translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Structural and mechanistic studies of VPS4 proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Substrate specific consequences of central pore mutations in the i-AAA protease Yme1 on substrate engagement

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Asymmetric interactions of ATP with the AAA+ ClpX6 unfoldase: allosteric control of a protein machine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Rebuilt AAA + motors reveal operating principles for ATP-fuelled machines

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Asymmetric deceleration of ClpB or Hsp104 ATPase activity unleashes protein-remodeling activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Did2 coordinates Vps4-mediated dissociation of ESCRT-III from endosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Homology of a 150K cytoplasmic dynein-associated polypeptide with the Drosophila gene Glued

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Brain dynein (MAP1C) localizes on both anterogradely and retrogradely transported membranous organelles in vivo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Recycling of ESCRTs by the AAA-ATPase Vps4 is regulated by a conserved VSL region in Vta1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Vta1p and Vps46p regulate the membrane association and ATPase activity of Vps4p at the yeast multivesicular body

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Functional division of substrate processing cofactors of the ubiquitin-selective Cdc48 chaperone

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

M domains couple the ClpB threading motor with the DnaK chaperone activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Visualizing the ATPase cycle in a protein disaggregating machine: structural basis for substrate binding by ClpB

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Missense mutations in the BCS1L gene as a cause of the Björnstad syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Characterization of human torsinA and its dystonia-associated mutant form

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

TorsinA in the nuclear envelope

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Gamma-tubulin distribution in the neuron: implications for the origins of neuritic microtubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

An extended microtubule-binding structure within the dynein motor domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2007.00642.X

10.1111/J.1600-0854.2007.00642.X

21 January 2018

Identifiers

DOI

1 reference

4 August 2017

1 reference

PubMed ID

17897320