Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core. - Wikidata - thesis-toulmin - TriplyDB

Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

http://www.wikidata.org/entity/Q34220248

about

Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2 Power(2): the power of yeast genetics applied to the powerhouse of the cell Mam33 promotes cytochrome c oxidase subunit I translation in Saccharomyces cerevisiae mitochondria.The INA complex facilitates assembly of the peripheral stalk of the mitochondrial F1Fo-ATP synthase Mitochondrial Cytochrome c Oxidase Biogenesis Is Regulated by the Redox State of a Heme-Binding Translational Activator Comparative transcriptome analyses of seven anurans reveal functions and adaptations of amphibian skin Next generation sequencing and comparative analyses of Xenopus mitogenomes Protein-protein interfaces from cytochrome c oxidase I evolve faster than nonbinding surfaces, yet negative selection is the driving force.LYRM7/MZM1L is a UQCRFS1 chaperone involved in the last steps of mitochondrial Complex III assembly in human cells.Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase.Like iron in the blood of the people: the requirement for heme trafficking in iron metabolism.Structure, function, and assembly of heme centers in mitochondrial respiratory complexes.Mitochondrial protein synthesis, import, and assembly.NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease.A mitochondrial CO2-adenylyl cyclase-cAMP signalosome controls yeast normoxic cytochrome c oxidase activity.The heme a synthase Cox15 associates with cytochrome c oxidase assembly intermediates during Cox1 maturation Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy.Mitochondrial genomes and exceptional longevity in a Chinese population: the Rugao longevity study Unraveling the molecular signatures of oxidative phosphorylation to cope with the nutritionally changing metabolic capabilities of liver and muscle tissues in farmed fish.Cardiac deficiency of single cytochrome oxidase assembly factor scox induces p53-dependent apoptosis in a Drosophila cardiomyopathy model Loop recognition and copper-mediated disulfide reduction underpin metal site assembly of CuA in human cytochrome oxidase The roles of Rhodobacter sphaeroides copper chaperones PCu(A)C and Sco (PrrC) in the assembly of the copper centers of the aa(3)-type and the cbb(3)-type cytochrome c oxidases Cytochrome c Oxidase Biogenesis and Metallochaperone Interactions: Steps in the Assembly Pathway of a Bacterial Complex.Mitochondrial disease genes COA6, COX6B and SCO2 have overlapping roles in COX2 biogenesis Modular assembly of yeast cytochrome oxidase hCOA3 stabilizes cytochrome c oxidase 1 (COX1) and promotes cytochrome c oxidase assembly in human mitochondria.Multiplexed, Proteome-Wide Protein Expression Profiling: Yeast Deubiquitylating Enzyme Knockout Strains.A Novel Function of Pet54 in Regulation of Cox1 Synthesis in Saccharomyces cerevisiae Mitochondria.Redox and reactive oxygen species regulation of mitochondrial cytochrome C oxidase biogenesis.Mechanisms of mitochondrial translational regulation.Nuclear gene mutations as the cause of mitochondrial complex III deficiency A CMC1-knockout reveals translation-independent control of human mitochondrial complex IV biogenesis.Cytochrome c Oxidase Activity Is a Metabolic Checkpoint that Regulates Cell Fate Decisions During T Cell Activation and Differentiation.Mitochondrial Protein Synthesis Adapts to Influx of Nuclear-Encoded Protein.Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.Overlapping Role of Respiratory Supercomplex Factor Rcf2 and Its N-terminal Homolog Rcf3 in Saccharomyces cerevisiae.The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity.Oms1 associates with cytochrome c oxidase assembly intermediates to stabilize newly synthesized Cox1.The ribosome-associated Mba1 escorts Cox2 from insertion machinery to maturing assembly intermediates.

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Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

http://www.wikidata.org/entity/Q34220248

description

2011 nî lūn-bûn

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2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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type

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Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

@en

Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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prefLabel

Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

@en

Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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J.BBABIO.2011.09.005

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Biochimica et Biophysica Acta

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Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core.

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P2093

Antoni Barrientos

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Flavia Fontanesi

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Ileana C Soto

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Jingjing Liu

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P2860

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

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

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

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

Energy transduction: proton transfer through the respiratory complexes

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

The conserved mitochondrial twin Cx9C protein Cmc2 Is a Cmc1 homologue essential for cytochrome c oxidase biogenesis

Mitochondrial matrix copper complex used in metallation of cytochrome oxidase and superoxide dismutase

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

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

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10.1016/J.BBABIO.2011.09.005

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6

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