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Publication year
2011Source
FEBS Letters, 585, 5, (2011), pp. 737-43ISSN
Publication type
Article / Letter to editor
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Organization
CMBI
Paediatrics - OUD tm 2017
Laboratory of Genetic, Endocrine and Metabolic Diseases
Journal title
FEBS Letters
Volume
vol. 585
Issue
iss. 5
Page start
p. 737
Page end
p. 43
Subject
IGMD 8: Mitochondrial medicine; IGMD 8: Mitochondrial medicine NCMLS 4: Energy and redox metabolism; IGMD 8: Mitochondrial medicine NCMLS 5: Membrane transport and intracellular motility; NCMLS 4: Energy and redox metabolism IGMD 8: Mitochondrial medicine; NCMLS 7: Chemical and physical biology; Laboratory Medicine Radboud University Medical CenterAbstract
Complex I (NADH:ubiquinone oxidoreductase) is the first and largest protein complex of the oxidative phosphorylation. Crystal structures have elucidated the positions of most subunits of bacterial evolutionary origin in the complex, but the positions of the eukaryotic subunits are unknown. Based on the analysis of sequence conservation we propose intra-molecular disulfide bridges and the inter-membrane space localization of three Cx(9)C-containing subunits in human: NDUFS5, NDUFB7 and NDUFA8. We experimentally confirm the localization of the latter two, while our data are consistent with disulfide bridges in NDUFA8. We propose these subunits stabilize the membrane domain of complex I.
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- Electronic publications [134102]
- Faculty of Medical Sciences [93308]
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