The 2-oxoacid dehydrogenase complexes in mitochondria can produce superoxide/hydrogen peroxide at much higher rates than complex I
about
Relationship between Oxidative Stress, Circadian Rhythms, and AMDThe Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age-Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in AdultsHyperglycemic Stress and Carbon Stress in Diabetic GlucotoxicityReactive oxygen species and mitochondria: A nexus of cellular homeostasisReactive oxygen species, nutrition, hypoxia and diseases: Problems solved?Mitochondrial ROS in cancer: initiators, amplifiers or an Achilles' heel?Glutathione and mitochondriaSexual Preferences in Nutrient Utilization Regulate Oxygen Consumption and Reactive Oxygen Species Generation in Schistosoma mansoni: Potential Implications for Parasite Redox BiologyThe novel component Kgd4 recruits the E3 subunit to the mitochondrial α-ketoglutarate dehydrogenase.Ischemic A/D transition of mitochondrial complex I and its role in ROS generationMultiple Forms of Glutamate Dehydrogenase in Animals: Structural Determinants and Physiological ImplicationsSources and implications of NADH/NAD(+) redox imbalance in diabetes and its complicationsKnown unknowns of cardiolipin signaling: the best is yet to comeStructural alterations induced by ten disease-causing mutations of human dihydrolipoamide dehydrogenase analyzed by hydrogen/deuterium-exchange mass spectrometry: Implications for the structural basis of E3 deficiency.Protein redox modification as a cellular defense mechanism against tissue ischemic injury.Dietary supplementation of heat-treated Gracilaria and Ulva seaweeds enhanced acute hypoxia tolerance in gilthead sea bream (Sparus aurata).Pathogenesis of chronic hyperglycemia: from reductive stress to oxidative stress.Mitochondrial oxidative stress in the retinal pigment epithelium leads to localized retinal degenerationSources of superoxide/H2O2 during mitochondrial proline oxidationHuman 2-oxoglutarate dehydrogenase complex E1 component forms a thiamin-derived radical by aerobic oxidation of the enamine intermediate.Aging: A mitochondrial DNA perspective, critical analysis and an update.Genetic activation of pyruvate dehydrogenase alters oxidative substrate selection to induce skeletal muscle insulin resistance.Sites of superoxide and hydrogen peroxide production by muscle mitochondria assessed ex vivo under conditions mimicking rest and exerciseEthanol-induced alcohol dehydrogenase E (AdhE) potentiates pneumolysin in Streptococcus pneumoniae.Teaching the fundamentals of electron transfer reactions in mitochondria and the production and detection of reactive oxygen species.Mitochondrial physiology in the major arbovirus vector Aedes aegypti: substrate preferences and sexual differences define respiratory capacity and superoxide productionIncreased reactive oxygen species production during reductive stress: The roles of mitochondrial glutathione and thioredoxin reductases.The RNA-binding protein HuR is essential for the B cell antibody response.Interactions between mitochondrial reactive oxygen species and cellular glucose metabolism.Mitochondrial ROS Metabolism: 10 Years Later.Molecular mechanisms of the non-coenzyme action of thiamin in brain: biochemical, structural and pathway analysis.The Redox Code.Reperfusion injury and reactive oxygen species: The evolution of a concept.Protein-mediated assembly of succinate dehydrogenase and its cofactorsMitochondrial metabolism mediates oxidative stress and inflammation in fatty liver.Catalytic Coupling of Oxidative Phosphorylation, ATP Demand, and Reactive Oxygen Species GenerationReactive oxygen species production in cardiac mitochondria after complex I inhibition: Modulation by substrate-dependent regulation of the NADH/NAD(+) ratio.Metformin inhibits Branched Chain Amino Acid (BCAA) derived ketoacidosis and promotes metabolic homeostasis in MSUD.Inhibition of mitochondrial 2-oxoglutarate dehydrogenase impairs viability of cancer cells in a cell-specific metabolism-dependent manner.Functional and evolutionary characterization of Ohr proteins in eukaryotes reveals many active homologs among pathogenic fungi.
P2860
Q26765278-C5600BF7-04FC-413E-8A95-896997A7F440Q26765813-0453BEB5-D9FD-415C-B8CD-95049B9E33B2Q26773988-DD39DAA4-078F-49D0-80B1-DC18F14FDA8DQ26782529-3170B221-D947-40DB-BF03-B02FF0CB0407Q26784413-88753797-7FF1-4A5F-BC3A-1E8E85BA47BAQ26852282-706A5E6E-FE3D-4974-8FB9-AD81D3907E28Q26865589-E56D98F8-0F31-4E60-9F91-CA2944292632Q27468987-AE263BB5-B87B-447C-9F9B-7D59481C6206Q27935604-9E72EE85-0B68-4781-8504-C5606828D526Q28074253-47421DE2-3E4F-4388-B494-737ADDF53E14Q28074448-52E9671C-C568-4CF1-BC3F-9EEBF8408E6DQ28076120-D162B2C6-F3F4-4305-9F81-C3EA8B5320D6Q28917160-ACDCBB3E-12D8-4C92-9763-CE364E718E69Q30392030-AD966A7D-97BD-4851-9C1C-63E0792F6783Q33634920-10FAB721-AEA8-4752-9D11-3F51B57CDE11Q33830573-CDB91CC7-F48A-4B4E-BE0B-8C5F52229194Q33849720-7B8FEBD1-AA91-4BFD-A103-F4C6F60A520CQ33957336-AAA4D660-21A6-4172-BD85-669F1D25F96CQ34085968-2976F205-37B5-421F-AC07-CBC423958398Q34396873-A1DE87F3-5BE2-4B35-9FC0-DD6C02824A10Q34543522-CEB01B30-539A-4B70-9C09-5ECF9E8ED02BQ34581335-D27278F0-3250-4A15-8EBB-A187B0E55BCDQ34801364-6713FFF6-C78D-4B8A-9520-DFE5EA34F60BQ34889616-725DE813-F01A-42CB-A6A0-E3009908C1E1Q35143664-13F9E6E8-410F-442A-9C59-9C5C7D2D9E9EQ35214409-DF598893-DBC3-4A27-A237-7503146372FCQ35588949-085A5E87-8BEA-4FA2-8B31-B33321FBB296Q35776191-4BEB0BAB-7A5C-4344-9BAF-79BE9E89BA33Q35868556-6D40A687-12C4-433C-947F-D71FC5D4023EQ35879792-15A49583-49B3-411E-9695-B8E588521647Q35891366-87A14F19-CA25-4AE2-8076-0C8EB2A63495Q36086638-CBFD8430-C8CF-41BF-9561-5E50F5D70C7EQ36221276-DBA76C4B-FD81-4292-A066-4F3731620E88Q36300096-68671824-AB8A-4A56-91E4-D0B303A165B8Q36335957-9BAF2C1C-472A-4155-B5BA-D9861966B708Q36644952-53418670-B67A-4745-BD41-71AB21CEC27DQ37017333-A2C67CE7-6C27-467A-8231-EC6E49B97183Q37061615-CB639FA9-16AE-47C1-8E48-2A37D3323C2FQ37295678-18A232CD-2C27-4DA9-891F-5ADFDE226AD4Q37741617-E2FA2A25-B647-4D09-B58D-02A528170A45
P2860
The 2-oxoacid dehydrogenase complexes in mitochondria can produce superoxide/hydrogen peroxide at much higher rates than complex I
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 10 February 2014
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The 2-oxoacid dehydrogenase co ...... ch higher rates than complex I
@en
The 2-oxoacid dehydrogenase co ...... h higher rates than complex I.
@nl
type
label
The 2-oxoacid dehydrogenase co ...... ch higher rates than complex I
@en
The 2-oxoacid dehydrogenase co ...... h higher rates than complex I.
@nl
prefLabel
The 2-oxoacid dehydrogenase co ...... ch higher rates than complex I
@en
The 2-oxoacid dehydrogenase co ...... h higher rates than complex I.
@nl
P2093
P2860
P356
P1476
The 2-oxoacid dehydrogenase co ...... ch higher rates than complex I
@en
P2093
Martin Hey-Mogensen
Nagendra Yadava
Renata L S Goncalves
Victoria I Bunik
P2860
P304
P356
10.1074/JBC.M113.545301
P407
P577
2014-02-10T00:00:00Z