NDUFA8

{{Short description|Protein-coding gene in the species Homo sapiens}} {{Infobox_gene}} '''NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8''' is an enzyme that in humans is encoded by the '''NDUFA8''' gene.<ref name="entrez">{{cite web | title = Entrez Gene: NDUFA8 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 8 | url = https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=4702 }}</ref> The NDUFA8 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.<ref name = Biochem>{{cite book|author=Donald Voet|author2=Judith G. Voet|author3=Charlotte W. Pratt|title=Fundamentals of biochemistry : life at the molecular level|date=2013|publisher=Wiley|location=Hoboken, NJ|isbn=9780470547847|chapter = 18 | pages=581–620|edition=4th}}</ref><ref name="pmid9763677">{{cite journal | vauthors = Emahazion T, Beskow A, Gyllensten U, Brookes AJ | title = Intron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain | journal = Cytogenet Cell Genet | volume = 82 | issue = 1–2 | pages = 115–9 |date=Nov 1998 | pmid = 9763677 | doi =10.1159/000015082 | s2cid = 46818955 }}</ref>

==Structure== The NDUFA8 gene is located on the q arm of chromosome 9 in position 33.2 and spans 27,354 base pairs.<ref name = "entrez"/> The gene produces a 20 kDa protein composed of 172 amino acids.<ref name=COPaKB>{{cite journal | vauthors = Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P | title = Integration of cardiac proteome biology and medicine by a specialized knowledgebase | journal = Circulation Research | volume = 113 | issue = 9 | pages = 1043–53 | date = Oct 2013 | pmid = 23965338 | pmc = 4076475 | doi = 10.1161/CIRCRESAHA.113.301151 }}</ref><ref name="url_COPaKB">{{cite web | url = https://amino.heartproteome.org/web/protein/P51970 | work = Cardiac Organellar Protein Atlas Knowledgebase (COPaKB) | title = NDUFA8 - NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8 }}{{Dead link|date=July 2025 |bot=InternetArchiveBot |fix-attempted=yes }}</ref> NDUFA8 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.<ref name = Biochem /> 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 dehydrogenase (ubiquinone) complex at the inner mitochondrial membrane. NDUFA8 is one of about 31 hydrophobic subunits that form the transmembrane region of Complex I. The predicted secondary structure is primarily alpha helix, but the carboxy-terminal half of the protein has high potential to adopt a coiled-coil form. The amino-terminal part contains a putative beta sheet rich in hydrophobic amino acids that may serve as mitochondrial import signal. Related pseudogenes have also been identified on four other chromosomes.<ref name="entrez"/><ref name="pmid9763677"/><ref name="pmid9763676">{{cite journal | vauthors = Emahazion T, Brookes AJ | title = Mapping of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping | journal = Cytogenet Cell Genet | volume = 82 | issue = 1–2 | pages = 114 |date=Nov 1998 | pmid = 9763676 | doi =10.1159/000015081 | s2cid = 46861680 }}</ref><ref name="pmid9425316">{{cite journal | vauthors = Ton C, Hwang DM, Dempsey AA, Liew CC | title = Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits | journal = Biochem Biophys Res Commun | volume = 241 | issue = 2 | pages = 589–94 |date=Jan 1998 | pmid = 9425316 | doi = 10.1006/bbrc.1997.7707 }}</ref>

==Function== The human NDUFA8 gene codes for a subunit of Complex I of the respiratory chain, which transfers electrons from NADH to ubiquinone.<ref name="entrez"/> 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 p''K'' shift of the ionizable side chain, which pumps four hydrogen ions out of the mitochondrial matrix.<ref name=Biochem />

==References== {{reflist}}

==Further reading== {{refbegin | 2}} * {{cite journal | vauthors=Smeitink J, van den Heuvel L |title=Human mitochondrial complex I in health and disease. |journal=Am. J. Hum. Genet. |volume=64 |issue= 6 |pages= 1505–10 |year= 1999 |pmid= 10330338 |doi=10.1086/302432 | pmc=1377894 }} * {{cite journal |vauthors=Sarto C, Marocchi A, Sanchez JC, etal |title=Renal cell carcinoma and normal kidney protein expression. |journal=Electrophoresis |volume=18 |issue= 3–4 |pages= 599–604 |year= 1997 |pmid= 9150947 |doi= 10.1002/elps.1150180343 |s2cid=26023225 }} * {{cite journal |vauthors=Smeitink J, Loeffen J, Smeets R, etal |title=Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I. |journal=Hum. Genet. |volume=103 |issue= 2 |pages= 245–50 |year= 1998 |pmid= 9760212 |doi=10.1007/s004390050813 |s2cid=25046670 }} * {{cite journal |vauthors=Triepels R, van den Heuvel L, Loeffen J, etal |title=The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients. |journal=Hum. Genet. |volume=103 |issue= 5 |pages= 557–63 |year= 1999 |pmid= 9860297 |doi=10.1007/s004390050869 |s2cid=2325305 }} * {{cite journal |vauthors=Loeffen JL, Triepels RH, van den Heuvel LP, etal |title=cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed. |journal=Biochem. Biophys. Res. Commun. |volume=253 |issue= 2 |pages= 415–22 |year= 1999 |pmid= 9878551 |doi= 10.1006/bbrc.1998.9786 }} * {{cite journal |vauthors=Bénit P, Chretien D, Kadhom N, etal |title=Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency. |journal=Am. J. Hum. Genet. |volume=68 |issue= 6 |pages= 1344–52 |year= 2001 |pmid= 11349233 |doi=10.1086/320603 | pmc=1226121 }} * {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |bibcode=2002PNAS...9916899M |doi-access=free }} * {{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }} {{refend}}

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Category:Human proteins