The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase (Q24310363)

Copper chaperone for superoxide dismutase

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

chaperone binding

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Journal of Biological Chemistry

GOA release 2020-03-11

copper

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author name string

R L Casareno

series ordinal

1

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D Waggoner

series ordinal

2

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J D Gitlin

series ordinal

3

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language of work or name

English

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publication date

11 September 1998

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published in

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volume

273

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page(s)

23625-8

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issue

37

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cites work

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

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

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

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Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

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An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

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

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Reduced fertility in female mice lacking copper-zinc superoxide dismutase

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Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

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A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide

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Delivering copper inside yeast and human cells

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The copper chaperone for superoxide dismutase

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Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase

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TRADD-TRAF2 and TRADD-FADD interactions define two distinct TNF receptor 1 signal transduction pathways

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Biochemical characterization and intracellular localization of the Menkes disease protein

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

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Structure and mechanism of copper, zinc superoxide dismutase

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Organization of P-type ATPases: significance of structural diversity

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CPx-type ATPases: a class of P-type ATPases that pump heavy metals

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The ATX1 gene of Saccharomyces cerevisiae encodes a small metal homeostasis factor that protects cells against reactive oxygen toxicity

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Metal ion chaperone function of the soluble Cu(I) receptor Atx1.

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Identification and functional expression of HAH1, a novel human gene involved in copper homeostasis

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HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defense

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Copper,zinc superoxide dismutase is primarily a cytosolic protein in human cells

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Regional and ultrastructural immunolocalization of copper-zinc superoxide dismutase in rat central nervous system.

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The copper chelator d-penicillamine delays onset of disease and extends survival in a transgenic mouse model of familial amyotrophic lateral sclerosis

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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

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A quantitative test for copper using bicinchoninic acid

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

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Cell anchorage permits efficient signal transduction between ras and its downstream kinases

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Characterization of a novel, membrane-bound, 80-kDa matrix-degrading protease from human breast cancer cells. Monoclonal antibody production, isolation, and localization

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release_lpouthfw4ze7zcacxjuwoxhbjq

Identifiers

DOI

10.1074/JBC.273.37.23625

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Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lpouthfw4ze7zcacxjuwoxhbjq

24 November 2022