(Q34972244)

5 August 2017

title

Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1. (English)

1 reference

protein-disulfide reductase activity

5 August 2017

main subject

1 reference

GOA release 2020-03-11

author name string

Scot C Leary

1

1 reference

5 August 2017

Florin Sasarman

2

1 reference

5 August 2017

Tamiko Nishimura

3

1 reference

5 August 2017

Eric A Shoubridge

4

1 reference

5 August 2017

publication date

31 March 2009

1 reference

5 August 2017

published in

Human Molecular Genetics

1 reference

5 August 2017

volume

18

1 reference

5 August 2017

issue

12

1 reference

5 August 2017

page(s)

2230-2240

1 reference

Structure and assembly of cytochrome c oxidase

5 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Mitochondrial energy metabolism is regulated via nuclear-coded subunits of cytochrome c oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Assembly of cytochrome-c oxidase in cultured human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Cytochrome oxidase in health and disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Mitochondrial assembly in yeast.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Ethylmalonic encephalopathy is caused by mutations in ETHE1, a gene encoding a mitochondrial matrix protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Immunological identification of yeast SCO1 protein as a component of the inner mitochondrial membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Human SCO1 and SCO2 have independent, cooperative functions in copper delivery to cytochrome c oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Yeast Sco1, a protein essential for cytochrome c oxidase function is a Cu(I)-binding protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

The human cytochrome c oxidase assembly factors SCO1 and SCO2 have regulatory roles in the maintenance of cellular copper homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Ortholog search of proteins involved in copper delivery to cytochrome C oxidase and functional analysis of paralogs and gene neighbors by genomic context

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

The functions of Sco proteins from genome-based analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

A hint for the function of human Sco1 from different structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

A structural characterization of human SCO2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Human Sco1 and Sco2 function as copper-binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Spectroscopic studies of metal binding and metal selectivity in Bacillus subtilis BSco, a Homologue of the Yeast Mitochondrial Protein Sco1p

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Characterization of the redox and metal binding activity of BsSco, a protein implicated in the assembly of cytochrome c oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Mitochondrial copper(I) transfer from Cox17 to Sco1 is coupled to electron transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

The P174L mutation in human Sco1 severely compromises Cox17-dependent metallation but does not impair copper binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Human recombinant mutated forms of the mitochondrial COX assembly Sco2 protein differ from wild-type in physical state and copper binding capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Biogenesis of cytochrome oxidase-sophisticated assembly lines in the mitochondrial inner membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Cytochrome c oxidase assembly factors with a thioredoxin fold are conserved among prokaryotes and eukaryotes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Mechanism of CuA assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Crystal structure of human SCO1: implications for redox signaling by a mitochondrial cytochrome c oxidase "assembly" protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Human Sco1 functional studies and pathological implications of the P174L mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

Molecular characterization of Saccharomyces cerevisiae Sco2p reveals a high degree of redundancy with Sco1p

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP158

21 January 2018

Identifiers

DOI

10.1093/HMG/DDP158

1 reference

5 August 2017

1 reference