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

udgivet i: Human Molecular Genetics

dato for udgivelse: 2009-03-31

main subject: protein-disulfide reductase activity

Cites articles 40

Date

Titel

Forfattere

2009-02

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

Ivano Di Meo, Alessandro Prelle, Valeria Tiranti, Massimo Zeviani, Gigliola Fagiolari
2008-09-04

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

Valeria Tiranti, Erika Fernandez-Vizarra, Daniele Ghezzi, Ann Saada, Massimo Zeviani
2008-05-05

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

Lucia Banci, Ivano Bertini, Simone Ciofi-Baffoni
2008-10

Mechanism of CuA assembly

Lucia Banci, Simone Ciofi-Baffoni, Ivano Bertini, Shenlin Wang, Georgios A Spyroulias
2007-01

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

Pierre Rustin, Paul Cobine, Rita Horvath
2007-02-15

The functions of Sco proteins from genome-based analysis.

Antonio Rosato, Lucia Banci, Ivano Bertini, Gabriele Cavallaro
2007-09

A structural characterization of human SCO2

Lucia Banci, Simone Ciofi-Baffoni, Manuele Martinelli, Ivano Bertini, Shenlin Wang, Iliana Leontari
2007-01-02

Human Sco1 functional studies and pathological implications of the P174L mutant

Lucia Banci, Simone Ciofi-Baffoni, Manuele Martinelli, Ivano Bertini, Shenlin Wang, Iliana Leontari
2006-06-09

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

Timothy Wai, Lorne Clarke, Hilary Vallance
2006-06-06

A hint for the function of human Sco1 from different structures

Lucia Banci, Simone Ciofi-Baffoni, Manuele Martinelli, Ivano Bertini, Vito Calderone, Stefano Mangani, Shenlin Wang
2006-03-06

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

Paul Cobine, Fabien Pierrel, Yih-Chern Horng
2005-01-01

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

Manuele Martinelli, Fabio Arnesano, Lucia Banci, Ivano Bertini
2005-08-09

Human Sco1 and Sco2 function as copper-binding proteins

Yih-Chern Horng, Paul Cobine, Fiona B Young, Graham N. George
2005-11-01

Spectroscopic studies of metal binding and metal selectivity in Bacillus subtilis BSco, a Homologue of the Yeast Mitochondrial Protein Sco1p
2005-12-01

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

Brahm Yachnin
2005-12-15

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

Petr Pecina, Markéta Tesařová, Jiri Zeman, Hana Hansíková
2005-07-01

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

Soledad Funes
2005-04-15

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

Carolyn Sue
2004-01-19

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

Valeria Tiranti, Adamo Pio d'Adamo, Eleonora Lamantea, Brigitte Vollmer, Carlo Dionisi-Vici, Barbara Garavaglia, Massimo Zeviani, Paolo Gasparini, Shamima Rahman
2004-09-01

Human SCO1 and SCO2 have independent, cooperative functions in copper delivery to cytochrome c oxidase
2004-03-01

Human recombinant mutated forms of the mitochondrial COX assembly Sco2 protein differ from wild-type in physical state and copper binding capacity
2003-01-14

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

Eric Lander, Jakob Bunkenborg, Robert Sladek, John D. Rioux, Terrye A. Delmonte, Thomas J. Hudson
2003-01

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

Hana Antonicka
2002-03-01

Cytochrome oxidase in health and disease

Mario H. Barros
2002-08-01

Molecular characterization of Saccharomyces cerevisiae Sco2p reveals a high degree of redundancy with Sco1p
2001-09-06

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

Graham N. George
2001-10-01

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

Rita Horvath, Dorothee P. Auer
2001-12-15

Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts
2000-08-01

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

Maik Hüttemann
2000-05-01

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

Arnold Munnich
2000-03-22

Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency
2000-01-01

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

Yurii Chinenov

Artikel - wd:Q34972244

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