(Q34500004)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Fabien Pierrel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Yih-Chern Horng

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

author name string

Scot C Leary

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Florin Sasarman

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Eric A Shoubridge

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Dennis R Winge

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

language of work or name

English

0 references

publication date

6 March 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

Journal of Biological Chemistry

17 January 2020

number of pages

7

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

volume

281

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

issue

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

page(s)

12270-12276

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16520371%20AND%20SRC:MED&resulttype=core&format=json

Structures of metal sites of oxidized bovine heart cytochrome c oxidase at 2.8 A.

17 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

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/10.1074%2FJBC.M600496200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

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/10.1074%2FJBC.M600496200

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/10.1074%2FJBC.M600496200

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/10.1074%2FJBC.M600496200

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/10.1074%2FJBC.M600496200

Human Sco1 and Sco2 function as copper-binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

Human members of the SCO1 gene family: complementation analysis in yeast and intracellular localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

Cox17 Is Functional When Tethered to the Mitochondrial Inner Membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

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/10.1074%2FJBC.M600496200

Specific copper transfer from the Cox17 metallochaperone to both Sco1 and Cox11 in the assembly of yeast cytochrome C oxidase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

Purification, characterization, and localization of yeast Cox17p, a mitochondrial copper shuttle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

COX23, a homologue of COX17, is required for cytochrome oxidase assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200

Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M600496200