(Q24337811)

GOA release 2020-03-11

6

Isabelle Bourget

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Sabrina Sacconi

Sabrina Sacconi

1

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Giuseppe Basso

Giuseppe Basso

9

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Salvatore DiMauro

10

Salvatore DiMauro

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Francesca Pistollato

3

Francesca Pistollato

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author name string

Eva Trevisson

2

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Maria Cristina Baldoin

4

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Roger Rezzonico

5

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Claude Desnuelle

7

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Romano Tenconi

8

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Leonardo Salviati

Biochemical and Biophysical Research Communications

11

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language of work or name

English

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publication date

25 November 2005

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published in

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volume

337

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issue

3

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page(s)

832-9

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cites work

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Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.

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Predotar: A tool for rapidly screening proteomes for N-terminal targeting sequences.

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Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain

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The role of charged amino acids in the localization of secreted and membrane proteins

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The Alb3/Oxa1/YidC protein family: membrane-localized chaperones facilitating membrane protein insertion?

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PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization

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Control of topology and mode of assembly of a polytopic membrane protein by positively charged residues

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

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Assembly of cytochrome-c oxidase in cultured human cells

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OPA1 requires mitofusin 1 to promote mitochondrial fusion

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

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Direct contact between T lymphocytes and human dermal fibroblasts or synoviocytes down-regulates types I and III collagen production via cell-associated cytokines.

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Membrane topology of the 60-kDa Oxa1p homologue from Escherichia coli.

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

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The mitochondrial permeability transition, release of cytochrome c and cell death. Correlation with the duration of pore openings in situ

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Characterization of COX19, a widely distributed gene required for expression of mitochondrial cytochrome oxidase

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Initiation of transcription of the MUC3A human intestinal mucin from a TATA-less promoter and comparison with the MUC3B amino terminus.

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

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

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Evolution of mitochondrial oxa proteins from bacterial YidC. Inherited and acquired functions of a conserved protein insertion machinery.

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Membrane topology mapping of vitamin K epoxide reductase by in vitro translation/cotranslocation.

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

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Cox18p is required for export of the mitochondrially encoded Saccharomyces cerevisiae Cox2p C-tail and interacts with Pnt1p and Mss2p in the inner membrane.

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GeneBuilder: interactive in silico prediction of gene structure.

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MaskerAid: a performance enhancement to RepeatMasker

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7 January 2021

Insertion into the mitochondrial inner membrane of a polytopic protein, the nuclear-encoded Oxa1p

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https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.09.127

7 January 2021

Ribosome binding to the Oxa1 complex facilitates co-translational protein insertion in mitochondria

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7 January 2021

Yeast Oxa1 interacts with mitochondrial ribosomes: the importance of the C-terminal region of Oxa1.

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Multiple sequence alignment with hierarchical clustering

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7 January 2021

UTRdb and UTRsite: a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs

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7 January 2021

Computational method to predict mitochondrially imported proteins and their targeting sequences

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7 January 2021

A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy

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https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.09.127

7 January 2021

Cytochrome c oxidase: structure and spectroscopy.

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https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.09.127

7 January 2021

Mutation screening in patients with isolated cytochrome c oxidase deficiency

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7 January 2021