Human Sco1 functional studies and pathological implications of the P174L mutant - Wikidata - awgldk - TriplyDB

Human Sco1 functional studies and pathological implications of the P174L mutant

Human Sco1 functional studies and pathological implications of the P174L mutant

http://www.wikidata.org/entity/Q27640878

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sameAs

COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2 Oxidative switches in functioning of mammalian copper chaperone Cox17 A structural-dynamical characterization of human Cox17 Mechanism of CuA assembly Sco proteins are involved in electron transfer processes Functional Role of Two Interhelical Disulfide Bonds in Human Cox17 Protein from a Structural Perspective Copper metallochaperones H135A controls the redox activity of the Sco copper center. Kinetic and spectroscopic studies of the His135Ala variant of Bacillus subtilis Sco.Mitochondrial copper metabolism and delivery to cytochrome c oxidase Redox regulation of protein folding in the mitochondrial intermembrane space.Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1.A targetable fluorescent sensor reveals that copper-deficient SCO1 and SCO2 patient cells prioritize mitochondrial copper homeostasis.Loop recognition and copper-mediated disulfide reduction underpin metal site assembly of CuA in human cytochrome oxidase Mitochondrial copper(I) transfer from Cox17 to Sco1 is coupled to electron transfer.COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux.Function and redox state of mitochondrial localized cysteine-rich proteins important in the assembly of cytochrome c oxidase.The coiled coil-helix-coiled coil-helix proteins may be redox proteins.Seeking the determinants of the elusive functions of Sco proteins.Mapping the functional interaction of Sco1 and Cox2 in cytochrome oxidase biogenesis.Selenocysteine containing analogues of Atx1-based peptides protect cells from copper ion toxicity.Thiol-based copper handling by the copper chaperone Atox1.Copper trafficking in biology: an NMR approach.Novel mutations in SCO1 as a cause of fatal infantile encephalopathy and lactic acidosis.COX16 promotes COX2 metallation and assembly during respiratory complex IV biogenesis.Building the CuA site of cytochrome c oxidase: a complicated, redox-dependent process driven by a surprisingly large complement of accessory proteins.The mitochondrion: a central architect of copper homeostasis.Mitochondrial cytochrome c oxidase biogenesis: Recent developments.Identification of binding sites of cisplatin to human copper chaperone protein Cox17 by high-resolution FT-ICR-MS.

P2860

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P2860

Human Sco1 functional studies and pathological implications of the P174L mutant

http://www.wikidata.org/entity/Q27640878

description

2007 nî lūn-bûn

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2007 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հունվարին հրատարակված գիտական հոդված

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

@zh-my

2007年学术文章

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2007年學術文章

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name

Human Sco1 functional studies and pathological implications of the P174L mutant

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Human Sco1 functional studies and pathological implications of the P174L mutant

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Human Sco1 functional studies and pathological implications of the P174L mutant

@nl

type

label

Human Sco1 functional studies and pathological implications of the P174L mutant

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Human Sco1 functional studies and pathological implications of the P174L mutant

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Human Sco1 functional studies and pathological implications of the P174L mutant

@nl

prefLabel

Human Sco1 functional studies and pathological implications of the P174L mutant

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Human Sco1 functional studies and pathological implications of the P174L mutant

@en

Human Sco1 functional studies and pathological implications of the P174L mutant

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PNAS.0606189103

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Proceedings of the National Academy of Sciences of the United States of America

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Human Sco1 functional studies and pathological implications of the P174L mutant

@en

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Iliana Leontari

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Peep Palumaa

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Rannar Sillard

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Shenlin Wang

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P2860

Identification and characterization of a novel thioredoxin-related transmembrane protein of the endoplasmic reticulum

Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy.

A hint for the function of human Sco1 from different structures

PROCHECK: a program to check the stereochemical quality of protein structures

Solution structure of Sco1: a thioredoxin-like protein Involved in cytochrome c oxidase assembly

WHAT IF: a molecular modeling and drug design program

AQUA and PROCHECK-NMR: programs for checking the quality of protein structures solved by NMR

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

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

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

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15-20

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10.1073/PNAS.0606189103

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1

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104

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Simone Ciofi-Baffoni

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6617178

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17182746

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