Frataxin interacts functionally with mitochondrial electron transport chain proteins (Q24305373)

GOA release 2020-03-11

Ferroxidase YDL120W

1 reference

Rafael P Vázquez-Manrique

GOA release 2020-03-11

1 reference

object named as

Rafael P Vázquez-Manrique

2

0 references

Pascual Sanz

object named as

Pascual Sanz

4

0 references

Francesc Palau

object named as

Francesc Palau

5

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author name string

Pilar González-Cabo

1

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M Adelaida García-Gimeno

Frataxin gene of Friedreich's ataxia is targeted to mitochondria

3

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language of work or name

English

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publication date

1 August 2005

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published in

Human Molecular Genetics

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volume

14

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page(s)

2091-8

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issue

15

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cites work

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Ubisemiquinone is the electron donor for superoxide formation by complex III of heart mitochondria

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[12] One-step gene disruption in yeast

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Functional and molecular characterization of the frataxin homolog from Arabidopsis thaliana.

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The Saccharomyces cerevisiae mitochondrial succinate:ubiquinone oxidoreductase

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Saccharomyces cerevisiae 14-3-3 proteins Bmh1 and Bmh2 participate in the process of catabolite inactivation of maltose permease

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Mitochondrial functional interactions between frataxin and Isu1p, the iron-sulfur cluster scaffold protein, in Saccharomyces cerevisiae

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Deletion of the yeast homologue of the human gene associated with Friedreich's ataxia elicits iron accumulation in mitochondria.

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Low iron concentration and aconitase deficiency in a yeast frataxin homologue deficient strain

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Control of mitochondrial beta-oxidation flux

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Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction

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dfh is a Drosophila homolog of the Friedreich's ataxia disease gene

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Towards a structural understanding of Friedreich's ataxia: the solution structure of frataxin

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Structure of frataxin iron cores: an X-ray absorption spectroscopic study

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Iron-sulfur cluster biosynthesis. Characterization of frataxin as an iron donor for assembly of [2Fe-2S] clusters in ISU-type proteins

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A novel genetic system to detect protein-protein interactions

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Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

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7 January 2021

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

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Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue

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Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

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An interaction between frataxin and Isu1/Nfs1 that is crucial for Fe/S cluster synthesis on Isu1.

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7 January 2021

Inhibition of Fe-S cluster biosynthesis decreases mitochondrial iron export: evidence that Yfh1p affects Fe-S cluster synthesis

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Frataxin activates mitochondrial energy conversion and oxidative phosphorylation

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Lambda YES: a multifunctional cDNA expression vector for the isolation of genes by complementation of yeast and Escherichia coli mutations

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Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia

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Function and expression of flavohemoglobin in Saccharomyces cerevisiae. Evidence for a role in the oxidative stress response

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Flavohemoglobin expression and function in Saccharomyces cerevisiae. No relationship with respiration and complex response to oxidative stress

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Crystal structure of human frataxin

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Frataxin-mediated iron delivery to ferrochelatase in the final step of heme biosynthesis

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A defect in the cytochrome b large subunit in complex II causes both superoxide anion overproduction and abnormal energy metabolism in Caenorhabditis elegans

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Yeast Frataxin Sequentially Chaperones and Stores Iron by Coupling Protein Assembly with Iron Oxidation

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Yeast flavohemoglobin, a nitric oxide oxidoreductase, is located in both the cytosol and the mitochondrial matrix: effects of respiration, anoxia, and the mitochondrial genome on its intracellular level and distribution

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Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia

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Srb/mediator proteins interact functionally and physically with transcriptional repressor Sfl1.

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The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins

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Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

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The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis

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Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae.

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Iron use for haeme synthesis is under control of the yeast frataxin homologue (Yfh1).

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Candida albicans lacking the frataxin homologue: a relevant yeast model for studying the role of frataxin.

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Frataxin acts as an iron chaperone protein to modulate mitochondrial aconitase activity

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A protein kinase substrate identified by the two-hybrid system

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

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Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

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Identification of a new family of tissue-specific basic helix-loop-helix proteins with a two-hybrid system

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Regulatory interactions between the Reg1-Glc7 protein phosphatase and the Snf1 protein kinase

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release_syfzsbudaveg5dn2kprg7amcei

Identifiers

DOI

10.1093/HMG/DDI214

0 references

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/syfzsbudaveg5dn2kprg7amcei

24 November 2022