NDUFA2

NDUFA2
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1S3A
Identifiers
Aliases	NDUFA2, B8, CD14, CIB8, NADH:ubiquinone oxidoreductase subunit A2, MC1DN13
External IDs	OMIM: 602137; MGI: 1343103; HomoloGene: 37628; GeneCards: NDUFA2; OMA:NDUFA2 - orthologs
Gene location (Human) Chr. Chromosome 5 (human)[1] Band 5q31.3 Start 140,638,740 bp[1] End 140,647,771 bp[1]
Gene location (Mouse) Chr. Chromosome 18 (mouse)[2] Band 18|18 B2 Start 36,875,385 bp[2] End 36,877,610 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in biceps brachii right ventricle triceps brachii muscle vastus lateralis muscle thoracic diaphragm left ventricle body of tongue right adrenal gland gastrocnemius muscle trabecular bone Top expressed in aortic valve fossa facial motor nucleus ascending aorta medullary collecting duct condyle renal corpuscle intercostal muscle Paneth cell endocardial cushion More reference expression data BioGPS More reference expression data
Gene ontology Molecular function NADH dehydrogenase (ubiquinone) activity Cellular component mitochondrial inner membrane mitochondrial respiratory chain complex I respirasome membrane mitochondrion mitochondrial membranes Biological process mitochondrial respiratory chain complex I assembly mitochondrial electron transport, NADH to ubiquinone blastocyst hatching Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 4695 17991 Ensembl ENSG00000131495 ENSMUSG00000014294 UniProt O43678 Q9CQ75 RefSeq (mRNA) NM_001185012 NM_002488 NM_010885 RefSeq (protein) NP_001171941 NP_002479 NP_035015 Location (UCSC) Chr 5: 140.64 – 140.65 Mb Chr 18: 36.88 – 36.88 Mb PubMed search [3] [4]
Wikidata
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NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 is a protein that in humans is encoded by the NDUFA2 gene.^[5][6] The NDUFA2 protein is a subunit of NADH dehydrogenase (ubiquinone), which is located in the mitochondrial inner membrane and is the largest of the five complexes of the electron transport chain.^[7] Mutations in the NDUFA2 gene are associated with Leigh's syndrome.^[6]

Structure

The NDUFA2 gene is located on the long (q) arm of chromosome 5 at position 31.2 and it spans 2,422 base pairs.^[6] The NDUFA2 gene produces an 11 kDa protein composed of 99 amino acids.^[8][9] NDUFA2 is a subunit of the enzyme NADH dehydrogenase (ubiquinone), the largest of the respiratory complexes. The structure is L-shaped with a long, hydrophobic transmembrane domain and a hydrophilic domain for the peripheral arm that includes all the known redox centers and the NADH binding site.^[7] NDUFA2 is one of about 31 hydrophobic subunits that form the transmembrane region of Complex I. It has been noted that the N-terminal hydrophobic domain has the potential to be folded into an alpha helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular subunits of Complex I. The highly conserved two-domain structure suggests that this feature is critical for the protein function and that the hydrophobic domain acts as an anchor for the NADH:ubiquinone oxidoreductase complex at the inner mitochondrial membrane.^[6]

Function

The human NDUFA2 gene codes for a subunit of Complex I of the respiratory chain, which transfers electrons from NADH to ubiquinone. NDUFA2 is an accessory subunit of Complex I that is believed not to be involved in catalysis but may be involved in regulating Complex I activity or its assembly via assistance in redox processes.^[6][10] Initially, NADH binds to Complex I and transfers two electrons to the isoalloxazine ring of the flavin mononucleotide (FMN) prosthetic arm to form FMNH₂. The electrons are transferred through a series of iron-sulfur (Fe-S) clusters in the prosthetic arm and finally to coenzyme Q10 (CoQ), which is reduced to ubiquinol (CoQH₂). The flow of electrons changes the redox state of the protein, resulting in a conformational change and pK shift of the ionizable side chain, which pumps four hydrogen ions out of the mitochondrial matrix.^[7]

Clinical significance

Mutations in the NDUFA2 gene can result in Leigh's syndrome, a severe neurological disorder that typically arises in the first year of life.^[6] One such mutation interferes with normal splicing patterns and results in exon 2 being skipped. This causes a reduction in Complex I activity and disturbs its assembly. The NDUFA2 mutation is also associated with the depolarization of the mitochondria.^[11]

Interactions

NDUFA2 has many protein interactions, including interactions with other members of the NADH dehydrogenase [ubiquinone] 1 alpha subcomplex, other subunits of Complex I as well as with redox proteins. This may be due to its potential role in Complex I assembly and assistance in redox processes.^[6]

References

Further reading