(Q46728737)

24 December 2017

title

Proteasomal degradation of mutant superoxide dismutases linked to amyotrophic lateral sclerosis (English)

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24 December 2017

amyotrophic lateral sclerosis

main subject

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author name string

Luca Di Noto

1

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24 December 2017

Lisa J Whitson

2

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24 December 2017

Xiaohang Cao

3

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24 December 2017

P John Hart

4

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24 December 2017

Rodney L Levine

5

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24 December 2017

language of work or name

English

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publication date

29 September 2005

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24 December 2017

Journal of Biological Chemistry

published in

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24 December 2017

volume

280

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24 December 2017

issue

48

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24 December 2017

page(s)

39907-39913

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24 December 2017

Amyotrophic lateral sclerosis

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Unraveling the mechanisms involved in motor neuron degeneration in ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Superoxide dismutase 1 subunits with mutations linked to familial amyotrophic lateral sclerosis do not affect wild-type subunit function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Oxidative stress causes abnormal accumulation of familial amyotrophic lateral sclerosis-related mutant SOD1 in transgenic Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Structure of 20S proteasome from yeast at 2.4 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

NEDL1, a novel ubiquitin-protein isopeptide ligase for dishevelled-1, targets mutant superoxide dismutase-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Enhanced degradation of oxidized glutamine synthetase in vitro and after microinjection into hepatoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Macroxyproteinase (M.O.P.): a 670 kDa proteinase complex that degrades oxidatively denatured proteins in red blood cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Ubiquitin conjugation is not required for the degradation of oxidized proteins by proteasome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Dissociation of human copper-zinc superoxide dismutase dimers using chaotrope and reductant. Insights into the molecular basis for dimer stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Iron regulatory protein 2 as iron sensor. Iron-dependent oxidative modification of cysteine

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Oxidation of either methionine 351 or methionine 358 in alpha 1-antitrypsin causes loss of anti-neutrophil elastase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Susceptibility of glucose-6-phosphate dehydrogenase modified by 4-hydroxy-2-nonenal and metal-catalyzed oxidation to proteolysis by the multicatalytic protease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Substrate access and processing by the 20S proteasome core particle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Structural basis for the interaction of the fluorescence probe 8-anilino-1-naphthalene sulfonate (ANS) with the antibiotic target MurA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Evidence for the existence of an unfolding intermediate of thyroglobulin during denaturation by guanidine hydrochloride

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Subunit association and side-chain reactivities of bovine erythrocyte superoxide dismutase in denaturing solvents

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Common denominator of Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis: decreased stability of the apo state

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Familial amyotrophic lateral sclerosis mutants of copper/zinc superoxide dismutase are susceptible to disulfide reduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Exposure of hydrophobic moieties promotes the selective degradation of hydrogen peroxide-modified hemoglobin by the multicatalytic proteinase complex, proteasome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Methionine residues as endogenous antioxidants in proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

The pore of activated 20S proteasomes has an ordered 7-fold symmetric conformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

The axial channel of the 20S proteasome opens upon binding of the PA200 activator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Binding of hydrophobic peptides to several non-catalytic sites promotes peptide hydrolysis by all active sites of 20 S proteasomes. Evidence for peptide-induced channel opening in the alpha-rings

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Mechanisms of biosynthesis of mammalian copper/zinc superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Misfolded CuZnSOD and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Amyloid-like filaments and water-filled nanotubes formed by SOD1 mutant proteins linked to familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

An alternative mechanism of bicarbonate-mediated peroxidation by copper-zinc superoxide dismutase: rates enhanced via proposed enzyme-associated peroxycarbonate intermediate

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Protofibrils, pores, fibrils, and neurodegeneration: separating the responsible protein aggregates from the innocent bystanders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

High molecular weight complexes of mutant superoxide dismutase 1: age-dependent and tissue-specific accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Familial amyotrophic lateral sclerosis-associated mutations decrease the thermal stability of distinctly metallated species of human copper/zinc superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

Destabilization of apoprotein is insufficient to explain Cu,Zn-superoxide dismutase-linked ALS pathogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506247200

21 January 2018

Identifiers

DOI

10.1074/JBC.M506247200

1 reference

24 December 2017

PubMed ID

16195234

1 reference

24 December 2017