Coenzyme Q supplementation or over-expression of the yeast Coq8 putative kinase stabilizes multi-subunit Coq polypeptide complexes in yeast coq null mutants.
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Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 to enable coenzyme Q biosynthesisMitochondrial ADCK3 employs an atypical protein kinase-like fold to enable coenzyme Q biosynthesisCerebellar Ataxia and Coenzyme Q Deficiency through Loss of Unorthodox Kinase ActivityIdentification of Coq11, a new coenzyme Q biosynthetic protein in the CoQ-synthome in Saccharomyces cerevisiaeCharacterization of a Plasmodium falciparum Orthologue of the Yeast Ubiquinone-Binding Protein, Coq10pMitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain FunctionThe COQ2 genotype predicts the severity of coenzyme Q10 deficiencyCoenzyme Q Biosynthesis: Evidence for a Substrate Access Channel in the FAD-Dependent Monooxygenase Coq6Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis.Human COQ9 Rescues a coq9 Yeast Mutant by Enhancing Coenzyme Q Biosynthesis from 4-Hydroxybenzoic Acid and Stabilizing the CoQ-SynthomeA Gly-zipper motif mediates homodimerization of the transmembrane domain of the mitochondrial kinase ADCK3.Resveratrol and para-coumarate serve as ring precursors for coenzyme Q biosynthesis.Yeast Coq9 controls deamination of coenzyme Q intermediates that derive from para-aminobenzoic acid.Cellular factories for coenzyme Q10 production.Biosynthesis of coenzyme Q in eukaryotes.Integrative proteomics and biochemical analyses define Ptc6p as the Saccharomyces cerevisiae pyruvate dehydrogenase phosphatase.Suppression of coenzyme Q₁₀ levels and the induction of multiple PDSS and COQ genes in human cells following oligomycin treatment.Impact of Chemical Analogs of 4-Hydroxybenzoic Acid on Coenzyme Q Biosynthesis: From Inhibition to Bypass of Coenzyme Q Deficiency.Coq6 is responsible for the C4-deamination reaction in coenzyme Q biosynthesis in Saccharomyces cerevisiae.Pathogenicity of two COQ7 mutations and responses to 2,4-dihydroxybenzoate bypass treatmentCerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3Balanced CoQ6 biosynthesis is required for lifespan and mitophagy in yeast.A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency.Multi-omics Reveal Specific Targets of the RNA-Binding Protein Puf3p and Its Orchestration of Mitochondrial Biogenesis.Biochemistry of Mitochondrial Coenzyme Q Biosynthesis.Mitochondrial CoQ deficiency is a common driver of mitochondrial oxidants and insulin resistance.Coenzyme Q10 Supplementation in Aging and Disease.Modeling of process parameters for enhanced production of coenzyme Q10 from Rhodotorula glutinis.RNA-binding proteins regulate cell respiration and coenzyme Q biosynthesis by post-transcriptional regulation of COQ7.
P2860
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P2860
Coenzyme Q supplementation or over-expression of the yeast Coq8 putative kinase stabilizes multi-subunit Coq polypeptide complexes in yeast coq null mutants.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 07 January 2014
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Coenzyme Q supplementation or ...... xes in yeast coq null mutants.
@en
Coenzyme Q supplementation or ...... xes in yeast coq null mutants.
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type
label
Coenzyme Q supplementation or ...... xes in yeast coq null mutants.
@en
Coenzyme Q supplementation or ...... xes in yeast coq null mutants.
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prefLabel
Coenzyme Q supplementation or ...... xes in yeast coq null mutants.
@en
Coenzyme Q supplementation or ...... xes in yeast coq null mutants.
@nl
P2093
P2860
P1476
Coenzyme Q supplementation or ...... xes in yeast coq null mutants.
@en
P2093
Catherine F Clarke
Christopher M Allan
Cuiwen H He
Letian X Xie
Uyenphuong C Tran
P2860
P304
P356
10.1016/J.BBALIP.2013.12.017
P407
P577
2014-01-07T00:00:00Z