Cytochrome oxidase in health and disease. (Q34594190)

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9 December 2019

review article

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title

Cytochrome oxidase in health and disease (English)

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9 December 2019

2

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9 December 2019

author name string

Antoni Barrientos

1

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9 December 2019

Isabelle Valnot

3

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9 December 2019

Agnes Rötig

4

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9 December 2019

Pierre Rustin

5

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9 December 2019

Alexander Tzagoloff

6

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9 December 2019

language of work or name

English

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publication date

1 March 2002

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9 December 2019

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9 December 2019

volume

286

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9 December 2019

issue

1

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9 December 2019

page(s)

53-63

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Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment

9 December 2019

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Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O.

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OXA1, a Saccharomyces cerevisiae nuclear gene whose sequence is conserved from prokaryotes to eukaryotes controls cytochrome oxidase biogenesis

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Cloning of a human gene involved in cytochrome oxidase assembly by functional complementation of an oxa1- mutation in Saccharomyces cerevisiae

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An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy

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The MSS51 gene product is required for the translation of the COX1 mRNA in yeast mitochondria.

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Characterization of COX17, a yeast gene involved in copper metabolism and assembly of cytochrome oxidase

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SCO1 and SCO2 act as high copy suppressors of a mitochondrial copper recruitment defect in Saccharomyces cerevisiae

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Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

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Oxa1p mediates the export of the N- and C-termini of pCoxII from the mitochondrial matrix to the intermembrane space

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Oxa1p, an essential component of the N-tail protein export machinery in mitochondria

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7 January 2021

Identification of Cox20p, a novel protein involved in the maturation and assembly of cytochrome oxidase subunit 2.

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7 January 2021

Oxa1p acts as a general membrane insertion machinery for proteins encoded by mitochondrial DNA.

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7 January 2021

Cox11p is required for stable formation of the Cu(B) and magnesium centers of cytochrome c oxidase

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7 January 2021

Som1, a third component of the yeast mitochondrial inner membrane peptidase complex that contains Imp1 and Imp2.

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7 January 2021

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

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7 January 2021

A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria

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A mitochondrial ferredoxin is essential for biogenesis of cellular iron-sulfur proteins

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Sequence of introns and flanking exons in wild-type and box3 mutants of cytochrome b reveals an interlaced splicing protein coded by an intron

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Subacute necrotizing encephalomyelopathy in an infant

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7 January 2021

Mitochondrial introns aI1 and/or aI2 are needed for the in vivo deletion of intervening sequences

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Mitochondrial copper metabolism in yeast: interaction between Sco1p and Cox2p

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A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene

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SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration

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Proton pumping by cytochrome c oxidase

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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

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The P(174)L mutation in the human hSCO1 gene affects the assembly of cytochrome c oxidase

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7 January 2021

Structural features of cytochrome oxidase

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7 January 2021

SCO1, a yeast nuclear gene essential for accumulation of mitochondrial cytochrome c oxidase subunit II.

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7 January 2021

Mitochondrial splicing requires a protein from a novel helicase family

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7 January 2021

The complete sequence of a 33 kb fragment on the right arm of chromosome II from Saccharomyces cerevisiae reveals 16 open reading frames, including ten new open reading frames, five previously identified genes and a homologue of the SCO1 gene

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7 January 2021

Cloning and characterization of COX18, a Saccharomyces cerevisiae PET gene required for the assembly of cytochrome oxidase

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7 January 2021

Bacillus subtilis CtaA is a heme-containing membrane protein involved in heme A biosynthesis

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Bacillus subtilis CtaA and CtaB function in haem A biosynthesis.

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Low-spin heme A in the heme A biosynthetic protein CtaA from Bacillus subtilis

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Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

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A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome

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The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A

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A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

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Crystal structure of bovine heart cytochrome c oxidase at 2.8 A resolution

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X-ray structure and the reaction mechanism of bovine heart cytochrome c oxidase

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7 January 2021

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

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7 January 2021

10.1016/S0378-1119(01)00803-4

Identifiers

DOI

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9 December 2019

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