Structural consequences of the familial amyotrophic lateral sclerosis SOD1 mutant His46Arg. (Q42252269)

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10 January 2020

title

Structural consequences of the familial amyotrophic lateral sclerosis SOD1 mutant His46Arg (English)

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amyotrophic lateral sclerosis

10 January 2020

main subject

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author

Svetlana Antonyuk

1

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10 January 2020

Michael Hough

3

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10 January 2020

author name string

Richard W Strange

4

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10 January 2020

Peter A Doucette

5

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10 January 2020

Jorge A Rodriguez

6

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10 January 2020

Lawrence J Hayward

7

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10 January 2020

Joan Selverstone Valentine

8

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10 January 2020

P John Hart

9

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10 January 2020

S Samar Hasnain

10

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10 January 2020

Jennifer Stine Elam

2

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10 January 2020

publication date

1 May 2005

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10 January 2020

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10 January 2020

volume

14

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10 January 2020

issue

5

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10 January 2020

page(s)

1201-1213

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Refinement of macromolecular structures by the maximum-likelihood method

10 January 2020

cites work

1 reference

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26 October 2017

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26 October 2017

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The structure of holo and metal-deficient wild-type human Cu, Zn superoxide dismutase and its relevance to familial amyotrophic lateral sclerosis

26 October 2017

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26 October 2017

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

26 October 2017

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Insights into Lou Gehrig's disease from the structure and instability of the A4V mutant of human Cu,Zn superoxide dismutase

26 October 2017

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26 October 2017

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Direct detection of hydrogen bonds in monomeric superoxide dismutase: biological implications

26 October 2017

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

26 October 2017

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26 October 2017

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Copper(2+) binding to the surface residue cysteine 111 of His46Arg human copper-zinc superoxide dismutase, a familial amyotrophic lateral sclerosis mutant

26 October 2017

1 reference

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Loss of in vitro metal ion binding specificity in mutant copper-zinc superoxide dismutases associated with familial amyotrophic lateral sclerosis

26 October 2017

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Aberrant copper chemistry as a major mediator of oxidative stress in a human cellular model of amyotrophic lateral sclerosis

26 October 2017

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Rapid automated molecular replacement by evolutionary search

26 October 2017

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Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

26 October 2017

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Mutations in copper-zinc superoxide dismutase that cause amyotrophic lateral sclerosis alter the zinc binding site and the redox behavior of the protein

26 October 2017

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Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury

26 October 2017

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

26 October 2017

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Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

26 October 2017

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Copper-dependent metabolism of Cu,Zn-superoxide dismutase in human K562 cells. Lack of specific transcriptional activation and accumulation of a partially inactivated enzyme

26 October 2017

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

26 October 2017

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Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells

26 October 2017

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26 October 2017

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26 October 2017

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26 October 2017

Superoxide dismutases

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26 October 2017

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Subunit asymmetry in the three-dimensional structure of a human CuZnSOD mutant found in familial amyotrophic lateral sclerosis

26 October 2017

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Increase of Cu,Zn-superoxide dismutase activity during differentiation of human K562 cells involves activation by copper of a constantly expressed copper-deficient protein

29 May 2018

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Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families

29 May 2018

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No correlation between aggregates of Cu/Zn superoxide dismutase and cell death in familial amyotrophic lateral sclerosis

17 August 2018

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17 August 2018

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

17 August 2018

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Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction.

17 August 2018

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Identification of an apo-superoxide dismutase (Cu,Zn) pool in human lymphoblasts

17 August 2018

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12 December 2020

Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase

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12 December 2020

Copper activation of superoxide dismutase 1 (SOD1) in vivo. Role for protein-protein interactions with the copper chaperone for SOD1

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12 December 2020

Decreased zinc affinity of amyotrophic lateral sclerosis-associated superoxide dismutase mutants leads to enhanced catalysis of tyrosine nitration by peroxynitrite

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12 December 2020

Mitochondrial localization of mutant superoxide dismutase 1 triggers caspase-dependent cell death in a cellular model of familial amyotrophic lateral sclerosis

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12 December 2020

Stability of mutant superoxide dismutase-1 associated with familial amyotrophic lateral sclerosis determines the manner of copper release and induction of thioredoxin in erythrocytes

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12 December 2020

Impaired copper binding by the H46R mutant of human Cu,Zn superoxide dismutase, involved in amyotrophic lateral sclerosis

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12 December 2020

The metal binding properties of the zinc site of yeast copper-zinc superoxide dismutase: implications for amyotrophic lateral sclerosis

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12 December 2020

Simple and defined method to detect the SOD-1 mutants from patients with familial amyotrophic lateral sclerosis by mass spectrometry

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12 December 2020

Transgenic animal models of familial amyotrophic lateral sclerosis

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12 December 2020

Molecular analyses of the Cu/Zn superoxide dismutase gene in patients with familial amyotrophic lateral sclerosis (ALS) in Japan

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12 December 2020

Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS

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12 December 2020

Accumulation of SOD1 mutants in postnatal motoneurons does not cause motoneuron pathology or motoneuron disease

1 reference

12 December 2020

Rats expressing human cytosolic copper-zinc superoxide dismutase transgenes with amyotrophic lateral sclerosis: associated mutations develop motor neuron disease

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12 December 2020

Identifiers

DOI

10.1110/PS.041256705

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15840828%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

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10 January 2020

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