spacer
spacer

Jump to: InterProScan Databases Documentation FTP site Help Advanced search

InterPro: IPR001694 NADH:ubiquinone oxidoreductase, subunit 1

Protein matchesHelp
UniProtKB
Matches:
13213 proteins
AccessionHelp IPR001694 NADH_UbQ_OxRdtase_su1
TypeHelp Family
SignaturesHelp
InterPro RelationshipsHelp
Contains IPR018086 NADH:ubiquinone oxidoreductase, subunit 1, conserved site
GO Term annotationHelp
Process GO:0055114 oxidation reduction
Component GO:0016020 membrane
InterPro annotation
BioMart Logo Entry Details in BioMart
AbstractHelp

NADH:ubiquinone oxidoreductase (complex I) (EC:1.6.5.3) is a respiratory-chain enzyme that catalyses the transfer of two electrons from NADH to ubiquinone in a reaction that is associated with proton translocation across the membrane (NADH + ubiquinone = NAD+ + ubiquinol) [1]. Complex I is a major source of reactive oxygen species (ROS) that are predominantly formed by electron transfer from FMNH(2). Complex I is found in bacteria, cyanobacteria (as a NADH-plastoquinone oxidoreductase), archaea [2], mitochondira, and in the hydrogenosome, a mitochondria-derived organelle. In general, the bacterial complex consists of 14 different subunits, while the mitochondrial complex contains homologues to these subunits in addition to approximately 31 additional proteins [3]. Mitochondrial complex I, which is located in the inner mitochondrial membrane, is the largest multimeric respiratory enzyme in the mitochondria, consisting of more than 40 subunits, one FMN co-factor and eight FeS clusters [4]. The assembly of mitochondrial complex I is an intricate process that requires the cooperation of the nuclear and mitochondrial genomes [4, 5]. Mitochondrial complex I can cycle between active and deactive forms that can be distinguished by the reactivity towards divalent cations and thiol-reactive agents. All redox prosthetic groups reside in the peripheral arm of the L-shaped structure. The NADH oxidation domain harbouring the FMN cofactor is connected via a chain of iron-sulphur clusters to the ubiquinone reduction site that is located in a large pocket formed by the PSST and 49kDa subunits of complex I [6].

This entry represents subunit 1 NADH:ubiquinone oxidoreductase [7, 8]. Among the many polypeptide subunits that make up complex I, there are fifteen which are located in the membrane part, seven of which are encoded by the mitochondrial and chloroplast genomes of most species. The most conserved of these organelle-encoded subunits is known as subunit 1 (gene ND1 in mitochondrion, and NDH1 in chloroplast) and seems to contain the ubiquinone binding site.

The ND1 subunit is highly similar to subunit 4 of Escherichia coli formate hydrogenlyase (gene hycD), subunit C of hydrogenase-4 (gene hyfC). Paracoccus denitrificans NQO8 and Escherichia coli nuoH NADH-ubiquinone oxidoreductase subunits also belong to this family [9].

Database linksHelp
PDBe-motif: PS00667 , PS00668
Enzyme: EC:1.6
PROSITE doc: PDOC00570
PANDIT: PF00146
Blocks: IPB001694

Taxonomic coverageHelp

Overlapping InterPro entriesHelp
IPR001694 Numbers of overlapping proteins Average numbers of overlapping amino acids

Example proteinsHelp
P03886 NADH-ubiquinone oxidoreductase chain 1

P03888 NADH-ubiquinone oxidoreductase chain 1

P18929 NADH-ubiquinone oxidoreductase chain 1

P24887 NADH-ubiquinone oxidoreductase chain 1

P92558 NADH-ubiquinone oxidoreductase chain 1

More proteins


Example Proteins Key


InterPro entry accession number/name and structure databases Colour code
IPR001694 NADH:ubiquinone oxidoreductase, subunit 1
IPR018086 NADH:ubiquinone oxidoreductase, subunit 1, conserved site
ModBase

PublicationsHelp
1. Walker JE.
The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains.
Q. Rev. Biophys. 25 253-324 1992 [PubMed: 1470679]
2. Friedrich T, Scheide D.
The respiratory complex I of bacteria, archaea and eukarya and its module common with membrane-bound multisubunit hydrogenases.
FEBS Lett. 479 1-5 2000 [PubMed: 10940377]
http://dx.doi.org/10.1016/S0014-5793(00)01867-6
3. Schneider D, Pohl T, Walter J, Dorner K, Kohlstadt M, Berger A, Spehr V, Friedrich T.
Assembly of the Escherichia coli NADH:ubiquinone oxidoreductase (complex I).
Biochim. Biophys. Acta 1777 735-9 2008 [PubMed: 18394423]
http://dx.doi.org/10.1016/j.bbabio.2008.03.003
4. Remacle C, Barbieri MR, Cardol P, Hamel PP.
Eukaryotic complex I: functional diversity and experimental systems to unravel the assembly process.
Mol. Genet. Genomics 280 93-110 2008 [PubMed: 18563446]
http://dx.doi.org/10.1007/s00438-008-0350-5
5. Vogel RO, Smeitink JA, Nijtmans LG.
Human mitochondrial complex I assembly: a dynamic and versatile process.
Biochim. Biophys. Acta 1767 1215-27 2007 [PubMed: 17854760]
http://dx.doi.org/10.1016/j.bbabio.2007.07.008
6. Zickermann V, Drose S, Tocilescu MA, Zwicker K, Kerscher S, Brandt U.
Challenges in elucidating structure and mechanism of proton pumping NADH:ubiquinone oxidoreductase (complex I).
J. Bioenerg. Biomembr. 40 475-83 2008 [PubMed: 18982432]
http://dx.doi.org/10.1007/s10863-008-9171-9
7. Ragan CI.
Structure of NADH-ubiquinone reductase (complex I).
Curr. Top. Bioenerg. 15 1-36 1987
8. Weiss H, Friedrich T, Hofhaus G, Preis D.
The respiratory-chain NADH dehydrogenase (complex I) of mitochondria.
Eur. J. Biochem. 197 563-76 1991 [PubMed: 2029890]
http://dx.doi.org/10.1111/j.1432-1033.1991.tb15945.x
9. Weidner U, Geier S, Ptock A, Friedrich T, Leif H, Weiss H.
The gene locus of the proton-translocating NADH: ubiquinone oxidoreductase in Escherichia coli. Organization of the 14 genes and relationship between the derived proteins and subunits of mitochondrial complex I.
J. Mol. Biol. 233 109-22 1993 [PubMed: 7690854]
http://dx.doi.org/10.1006/jmbi.1993.1488

spacer
spacer
InterPro 23.1