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Title: NDUFB7 and NDUFA8 are located at the intermembrane surface of complex I
Author(s): Szklarczyk, R.J. (308248481)
Wanschers, B.F.J. (310279143)
Nabuurs, S.B. (291535941)
Nouws, J. (321595998)
Nijtmans, L.G.J. (298975106)
Huynen, M.A. (298200597)
Publication year: 2011
Document type: Article / Letter to editor
Journal: Febs Letters
ISSN: 0014-5793
Volume: vol. 585
Issue: iss. 5
Start page: p. 737
End page: p. 743
Annotation: Szklarczyk, Radek Wanschers, Bas F J Nabuurs, Sander B Nouws, Jessica Nijtmans, Leo G Huynen, Martijn A Research Support, Non-U.S. Gov't Netherlands FEBS Lett. 2011 Mar 9;585(5):737-43. Epub 2011 Feb 22.
Abstract: 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.
Subject: IGMD 8: Mitochondrial medicine
IGMD 8: Mitochondrial medicine NCMLS 2A: Energy and redox metabolism
IGMD 8: Mitochondrial medicine NCMLS 2B: Membrane transport and intracellular motility
NCMLS 2A: Energy and redox metabolism IGMD 8: Mitochondrial medicine
NCMLS 3B: Chemical and physical biology
Subject: IGMD 8: Mitochondrial medicine NCMLS 2A: Energy and redox metabolism
Organization: CMBI
Paediatrics
Laboratory of Genetic, Endocrine and Metabolic Diseases
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/98132

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