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Cytochrome c oxidase subunit I

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1766:. Panels A, B were cut across the long axes of the crypts and panels C, D were cut parallel to the long axes of the crypts. In panel A the bar shows 100 μm and allows an estimate of the frequency of crypts in the colonic epithelium. Panel B includes three crypts in cross-section, each with one segment deficient for MT-COI expression and at least one crypt, on the right side, undergoing fission into two crypts. Panel C shows, on the left side, a crypt fissioning into two crypts. Panel D shows typical small clusters of two and three MT-COI deficient crypts (the bar shows 50 μm). The images were made from original photomicrographs, but panels A, B and D were also included in an article and illustrations were published with Creative Commons Attribution-Noncommercial License allowing re-use. 1743: 203: 1153: 123: 1336:
well as a low-spin heme, both ligated to six conserved histidine residues near the outer side of four transmembrane spans within COI is common to all family members. In contrast to eukaryotes the respiratory chain of prokaryotes is branched to multiple terminal oxidases. The enzyme complexes vary in heme and copper composition, substrate type and substrate affinity. The different respiratory oxidases allow the cells to customize their respiratory systems according to a variety of environmental growth conditions.
4653: 4638: 4683: 4668: 1832:). There are about 100 to 700 mitochondria per cell, depending on cell type. Furthermore, there is fairly rapid turnover of mitochondria, so that a mitochondrion with MT-COI-mutated chromosomes and a positive selection bias could shortly become the major type of mitochondrion in a cell. The average half-life of mitochondria in rats, depending on cell type, is between 9 and 24 days, and in mice is about 2 days. In humans it is likely that the half life of mitochondria is also a matter of days to weeks. 1844:
the same cell to generate homoplasmy for MT-COI-deficiency. Another suggestion was that cells with a deficiency in cytochrome c oxidase are apoptosis resistant, and thus more likely to survive. The linkage of MT-COI to apoptosis arises because active cytochrome c oxidase oxidizes cytochrome c, which then activates pro-caspase 9, leading to apoptosis. These two factors may contribute to the frequent occurrence of MT-COI-deficient colonic crypts with age or during carcinogenesis in the human colon.
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Greaves et al. showed that deficiencies of MT-COI in colonic crypts are due to mutations in the MT-COI gene. As seen in panel B, a portion of the stem cells of three crypts appear to have a mutation in MT-COI, so that 40% to 50% of the cells arising from those stem cells form a white segment in the cross-cut area.
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It is not clear why a deficiency of MT-COI should have a positive selective bias. One suggestion is that deficiency of MT-COI in a mitochondrion leads to lower reactive oxygen production (and less oxidative damage) and this provides a selective advantage in competition with other mitochondria within
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A stem cell at the base of a colonic crypt that was largely MT-COI-deficient may compete with the other 4 or 5 stem cells to take over the stem cell niche. If this occurs, then the colonic crypt would be deficient in MT-COI in all 1700 to 5,000 cells, as is indicated for some crypts in panels A, B
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Crypts of the colon can reproduce by fission, as seen in panel C, where a crypt is fissioning to form two crypts, and in panel B where at least one crypt appears to be fissioning. Most crypts deficient in MT-COI are in clusters of crypts (clones of crypts) with two or more MT-COI-deficient crypts
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The occurrence of frequent crypts with almost complete loss of MT-COI in their 1700 to 5,000 cells suggests a process of natural selection. However, it has also been shown that a deficiency throughout a particular crypt due to an initial mitochondrial DNA mutation may occasionally occur through a
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The enzyme complex consists of 3-4 subunits (prokaryotes) up to 13 polypeptides (mammals) of which only the catalytic subunit (equivalent to mammalian subunit I (COI)) is found in all heme-copper respiratory oxidases. The presence of a bimetallic centre (formed by a high-spin heme and copper B) as
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Most of the human colonic crypts in the images have high expression of the brown-orange stained MT-COI. However, in some of the colonic crypts all of the cells lack MT-COI and appear mostly white, with their main color being the blue-gray staining of the nuclei at the outer walls of the crypts.
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In humans, the percent of colonic crypts deficient for MT-COI is less than 1% before age 40, but then increases linearly with age. On average, the percent of colonic crypts deficient for MT-COI reaches 18% in women and 23% in men by 80–84 years of age. Colonic tumors often arise in a field of
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As seen in panels C and D, crypts are about 75 to about 110 cells long. The average crypt circumference is 23 cells. Based on these measurements, crypts have between 1725 and 2530 cells. Another report gave a range of 1500 to 4900 cells per colonic crypt.
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sequence differences are too small to be detected between closely related species, more than 2% sequence divergence is typically detected between closely related animal species, suggesting that the barcode is effective for most animals. In most if not all
1332:), is directly involved in the coupling between dioxygen reduction and proton pumping. Some terminal oxidases generate a transmembrane proton gradient across the plasma membrane (prokaryotes) or the mitochondrial inner membrane (eukaryotes). 1817:. There are multiple copies of the chromosome in most mitochondria, usually between 2 and 6 per mitochondrion. If a mutation occurs in MT-COI in one chromosome of a mitochondrion, there may be random segregation of the chromosomes during 3946:
Lu X, Walker T, MacManus JP, Seligy VL (July 1992). "Differentiation of HT-29 human colonic adenocarcinoma cells correlates with increased expression of mitochondrial RNA: effects of trehalose on cell growth and maturation".
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adjacent to each other (see panel D). This illustrates that clones of deficient crypts often arise, and thus that there is likely a positive selective bias that has allowed them to spread in the human colonic epithelium.
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Chomyn A, Mariottini P, Cleeter MW, Ragan CI, Matsuno-Yagi A, Hatefi Y, et al. (1985). "Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase".
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Lucioli S, Hoffmeier K, Carrozzo R, Tessa A, Ludwig B, Santorelli FM (March 2006). "Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patient".
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inner surface of the colon is punctuated by invaginations, the colonic crypts. The colon crypts are shaped like microscopic thick walled test tubes with a central hole down the length of the tube (the crypt
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Marzuki S, Noer AS, Lertrit P, Thyagarajan D, Kapsa R, Utthanaphol P, Byrne E (December 1991). "Normal variants of human mitochondrial DNA and translation products: the building of a reference data base".
1642: 1628: 1656: 1782:(colon). However, MT-COI is frequently lost in colonic crypts with age in humans and is also often absent in field defects that give rise to colon cancers as well as in portions of colon cancers. 1485:
Mutations in this gene can cause mitochondrial Complex IV deficiency, a disease of the mitochondrial respiratory chain displaying a wide variety of clinical manifestations ranging from isolated
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stochastic process. Nevertheless, the frequent occurrence of MT-COI deficiency in many crypts within a colon epithelium indicates that absence of MT-COI likely provides a selective advantage.
1595:(necrosis or disintegration of skeletal muscle) associated with muscle pain and weakness, exercise intolerance, low muscle capacity for oxidative phosphorylation, and followed by excretion of 4049:
Attardi G, Chomyn A, Doolittle RF, Mariottini P, Ragan CI (1987). "Seven unidentified reading frames of human mitochondrial DNA encode subunits of the respiratory chain NADH dehydrogenase".
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Karadimas CL, Greenstein P, Sue CM, Joseph JT, Tanji K, Haller RG, et al. (September 2000). "Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA".
1365:) exists in denitrifying species of archaea and eubacteria and is a heterodimer of cytochromes b and c. Phenazine methosulphate can act as acceptor. It has been suggested that cytochrome 1979:
Tsukihara T, Aoyama H, Yamashita E, Tomizaki T, Yamaguchi H, Shinzawa-Itoh K, et al. (May 1996). "The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A".
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Bröker S, Meunier B, Rich P, Gattermann N, Hofhaus G (November 1998). "MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase".
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Chomyn A, Cleeter MW, Ragan CI, Riley M, Doolittle RF, Attardi G (October 1986). "URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit".
1619:. Affected individuals manifest progressive, postlingual, sensorineural hearing loss involving high frequencies. The mutation, A1555G, has been associated with this disease. 4652: 4637: 4682: 4667: 1120: 2048: 1454:
may be involved in the development of acquired idiopathic sideroblastic anemia. Mutations in mitochondrial DNA can cause respiratory chain dysfunction, preventing
3913:"A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I" 2618:"A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I" 2659:"Heteroplasmic point mutations of mitochondrial DNA affecting subunit I of cytochrome c oxidase in two patients with acquired idiopathic sideroblastic anemia" 1802:
crypts containing a large cluster (as many as 410) of MT-COI-deficient crypts. In colonic cancers, up to 80% of tumor cells can be deficient in MT-COI.
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oxidase in Gram-positive bacteria and that archaebacterial quinol oxidase has an independent origin. A considerable amount of evidence suggests that
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Coller HA, Bodyak ND, Khrapko K (April 2002). "Frequent intracellular clonal expansions of somatic mtDNA mutations: significance and mechanisms".
1794:). Four tissue sections are shown in the image in this section, two cut across the long axes of the crypts and two cut parallel to the long axes. 4157:
Sanger F, Coulson AR, Barrell BG, Smith AJ, Roe BA (October 1980). "Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing".
2049:"COI barcoding of Nebelid testate amoebae (Amoebozoa: Arcellinida): extensive cryptic diversity and redefinition of the Hyalospheniidae Schultze" 1064: 1052: 4517: 3333:"Age-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic crypts" 3022:"Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia" 1961: 1943: 4697: 4592: 4562: 4622: 4577: 4532: 2981:"Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I" 55:, mitochondrially encoded cytochrome c oxidase I, COI, MTCO1, Main subunit of cytochrome c oxidase, CO I, cytochrome c oxidase subunit I 5538: 5219: 1877: 1869: 4547: 5214: 4186:
Montoya J, Ojala D, Attardi G (April 1981). "Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs".
3660:"Mitochondrial turnover in liver is fast in vivo and is accelerated by dietary restriction: application of a simple dynamic model" 5305: 4887: 3536:
Robin ED, Wong R (September 1988). "Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells".
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Ingman M, Kaessmann H, Pääbo S, Gyllensten U (December 2000). "Mitochondrial genome variation and the origin of modern humans".
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Bodenteich A, Mitchell LG, Polymeropoulos MH, Merril CR (May 1992). "Dinucleotide repeat in the human mitochondrial D-loop".
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Satoh M, Kuroiwa T (September 1991). "Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell".
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to generate new mitochondria. This can give rise to a mitochondrion with primarily or solely MT-COI-mutated chromosomes.
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and also because its sequence is conserved among conspecifics. Contrary to the primary objection raised by skeptics that
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Torroni A, Achilli A, Macaulay V, Richards M, Bandelt HJ (June 2006). "Harvesting the fruit of the human mtDNA tree".
5018: 4843: 3225:"Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission" 2820:"Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission" 3490:
Legros F, Malka F, Frachon P, Lombès A, Rojo M (June 2004). "Organization and dynamics of human mitochondrial DNA".
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oxidase catalytic subunits evolved from ancient nitric oxide reductases that could reduce both nitrogen and oxygen.
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of the cells (located at the outer edges of the cells lining the walls of the crypts) are stained blue-gray with
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in the urine. It has been associated with mitochondrial myopathy. A G5920A mutation, and a heteroplasmic G6708A
5120: 5078: 1347:(also known as proteobacteria or purple bacteria) acquired quinol oxidase through a lateral gene transfer from 743: 1292: 1128: 1313:
Proton pumping heme-copper oxidases represent the terminal, energy-transfer enzymes of respiratory chains in
724: 4924: 4866: 4756: 1857: 64: 1321:. The CuB-heme a3 (or heme o) binuclear centre, associated with the largest subunit I of cytochrome c and 4978: 3750:"MITRAC7 Acts as a COX1-Specific Chaperone and Reveals a Checkpoint during Cytochrome c Oxidase Assembly" 1731: 1522: 3431:
Nekhaeva E, Bodyak ND, Kraytsberg Y, McGrath SB, Van Orsouw NJ, Pluzhnikov A, et al. (April 2002).
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Nooteboom M, Johnson R, Taylor RW, Wright NA, Lightowlers RN, Kirkwood TB, et al. (February 2010).
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Within the MITRAC (mitochondrial translation regulation assembly intermediate of cytochrome c oxidase)
1518: 1124: 4233:"Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs" 3282:
Baker AM, Cereser B, Melton S, Fletcher AG, Rodriguez-Justo M, Tadrous PJ, et al. (August 2014).
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Bernstein C, Facista A, Nguyen H, Zaitlin B, Hassounah N, Loustaunau C, et al. (December 2010).
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Pandya A, Xia XJ, Erdenetungalag R, Amendola M, Landa B, Radnaabazar J, et al. (December 1999).
2879:"A mitochondrial DNA mutation linked to colon cancer results in proton leaks in cytochrome c oxidase" 1828:
in order to frequently become the main type of mitochondrion in a cell (a cell with MT-COI-deficient
1307: 1076: 1033: 136: 1081: 51: 5563: 5068: 4946: 1359: 1326: 1303: 1296: 72: 1872:. This interaction with SMIM20 stabilizes the newly synthesized MT-CO1 and prevents its premature 5115: 4902: 3748:
Dennerlein S, Oeljeklaus S, Jans D, Hellwig C, Bareth B, Jakobs S, et al. (September 2015).
3071:"Barcoding animal life: cytochrome c oxidase subunit 1 divergences among closely related species" 1514: 1440: 4661:: Cadmium ion binding structure of bovine heart cytochrome C oxidase in the fully oxidized state 3223:
Greaves LC, Preston SL, Tadrous PJ, Taylor RW, Barron MJ, Oukrif D, et al. (January 2006).
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Greaves LC, Preston SL, Tadrous PJ, Taylor RW, Barron MJ, Oukrif D, et al. (January 2006).
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Papa S, Capitanio N, Glaser P, Villani G (May 1994). "The proton pump of heme-copper oxidases".
875: 5110: 4767: 4646:: Cadmium ion binding structure of bovine heart cytochrome C oxidase in the fully reduced state 2733:
Varlamov DA, Kudin AP, Vielhaber S, Schröder R, Sassen R, Becker A, et al. (August 2002).
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Lorenzi I, Oeljeklaus S, Aich A, Ronsör C, Callegari S, Dudek J, et al. (February 2018).
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Gattermann N, Retzlaff S, Wang YL, Hofhaus G, Heinisch J, Aul C, Schneider W (December 1997).
5484: 5224: 5100: 4936: 4914: 4691:: Zinc ion binding structure of bovine heart cytochrome C oxidase in the fully oxidized state 1818: 1742: 1612: 1455: 1428: 4676:: Zinc ion binding structure of bovine heart cytochrome C oxidase in the fully reduced state 2577:"Denitrification and aerobic respiration, hybrid electron transport chains and co-evolution" 2125:"MT-CO1 - Cytochrome c oxidase subunit 1 - Homo sapiens (Human) - MT-CO1 gene & protein" 1489:
to a severe multisystem disease affecting multiple organs and tissues. Symptoms may include
5325: 5231: 5088: 5037: 4983: 4468: 4336: 4244: 4195: 4121: 4083: 3444: 3433:"Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues" 3389: 3236: 2890: 2831: 1988: 1751: 1616: 1506: 1392: 1388: 1288: 1232: 1228: 1217: 1107: 4284:
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N (October 1999).
3776: 3284:"Quantification of crypt and stem cell evolution in the normal and neoplastic human colon" 2146: 2141: 92: 8: 4286:"Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA" 2439: 4340: 4248: 4199: 4125: 4087: 4008:"Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region" 3448: 3393: 3240: 2894: 2835: 1992: 1477:. The result is a ferric accumulation in mitochondria and insufficient heme production. 1152: 5255: 5023: 4897: 4398: 4373: 4360: 4315: 4219: 4145: 3994: 3929: 3912: 3825: 3800: 3684: 3659: 3561: 3515: 3413: 3401: 3357: 3332: 3308: 3283: 3259: 3224: 3200: 3173: 3095: 3070: 3046: 3021: 2961: 2913: 2878: 2854: 2819: 2800: 2711: 2634: 2617: 2557: 2494: 2406: 2371: 2251: 2226: 2202: 2177: 2012: 1572: 1435:
defects. Because this disease is a result of mitochondrial DNA mutations affecting the
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A mitochondrion with largely MT-COI-mutated chromosomes would need to have a positive
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The MT-COI protein, also known as CCOI, is usually expressed at a high level in the
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is one of the three cytochrome c oxidase subunit mitochondrial genes (orange boxes).
989: 5058: 4851: 4438: 4428: 4393: 4385: 4344: 4297: 4262: 4252: 4223: 4203: 4166: 4129: 4091: 4054: 4027: 4019: 3978: 3924: 3891: 3862: 3820: 3812: 3771: 3761: 3720: 3679: 3671: 3630: 3619:"The turnover of mitochondria in a variety of tissues of young adult and aged rats" 3591: 3565: 3545: 3499: 3462: 3452: 3397: 3352: 3344: 3303: 3295: 3254: 3244: 3195: 3185: 3131: 3090: 3082: 3041: 3033: 2992: 2945: 2908: 2898: 2849: 2839: 2784: 2746: 2707: 2670: 2629: 2588: 2561: 2539: 2498: 2490: 2451: 2410: 2402: 2355: 2318: 2310: 2246: 2238: 2197: 2189: 2063: 1996: 1873: 1775: 1576: 1420: 1103: 295: 226: 193: 148: 76: 20: 2242: 2000: 1069: 5531: 4963: 4856: 3816: 3766: 3749: 3725: 3708: 3299: 2593: 2576: 2067: 1853: 1791: 1779: 1678: 1664: 1650: 1636: 1552: 1502: 1302:) is a key enzyme in aerobic metabolism. It is the third and final enzyme of the 1045: 1001: 270: 100: 19:"Cox1" redirects here. Particularly in a medical context, this can also refer to 4058: 4006:
Moraes CT, Andreetta F, Bonilla E, Shanske S, DiMauro S, Schon EA (March 1991).
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National Center for Biotechnology Information, U.S. National Library of Medicine
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National Center for Biotechnology Information, U.S. National Library of Medicine
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In humans, the MT-CO1 gene is located from nucleotide pairs 5904 to 7444 on the
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
1825: 1592: 1568: 1559:. Numerous such genetic alterations are often involved with the progression of 1530: 1470: 1344: 371: 3866: 2788: 2675: 2658: 1544:
mutations play a role in colorectal cancer, a very complex disease displaying
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It has been shown that eubacterial quinol oxidase was derived from cytochrome
5552: 5542: 4747: 3174:"Cancer and age related colonic crypt deficiencies in cytochrome c oxidase I" 2751: 2734: 2225:
Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013).
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Kosakyan A, Heger TJ, Leander BS, Todorov M, Mitchell EA, Lara E (May 2012).
1755: 1694: 1490: 1404: 1244: 473: 4511:: STRUCTURE OF BOVINE HEART CYTOCHROME C OXIDASE AT THE FULLY OXIDIZED STATE 4095: 3911:
Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC (August 1992).
3895: 3249: 3190: 2997: 2980: 2903: 2844: 2735:"Metabolic consequences of a novel missense mutation of the mtDNA CO I gene" 2616:
Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC (August 1992).
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García-Horsman JA, Barquera B, Rumbley J, Ma J, Gennis RB (September 1994).
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protein cytochrome c oxidase subunit I (CCOI, synonym for MT-COI), and the
1494: 288: 113: 4276: 4257: 4215: 4178: 4141: 4103: 4066: 4041: 4023: 3990: 3960: 3938: 3903: 3644: 3603: 3557: 2719: 2684: 2643: 2553: 2512: 2463: 2424: 2391:"Evolution of cytochrome oxidase, an enzyme older than atmospheric oxygen" 2367: 2332: 2193: 2008: 1029: 939: 934: 4716: 3120:"Potentiality of the cox1 gene in the taxonomic resolution of soil fungi" 3118:
Molitor C, Inthavong B, Sage L, Geremia RA, Mouhamadou B (January 2010).
2949: 2124: 2033: 1580: 1526: 1432: 1329: 1264: 788: 769: 3801:"The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis" 2979:
Kollberg G, Moslemi AR, Lindberg C, Holme E, Oldfors A (February 2005).
1362: 5132: 4794: 4417:"Major genomic mitochondrial lineages delineate early human expansions" 3982: 1829: 1786: 1715: 1560: 1545: 1314: 1299: 1013: 210: 130: 80: 3881: 3503: 2528:"Cytochrome oxidase evolved by tinkering with denitrification enzymes" 5063: 4348: 4207: 4133: 1771: 1596: 1498: 1318: 1195: 643: 254: 241: 176: 163: 88: 4415:
Maca-Meyer N, González AM, Larruga JM, Flores C, Cabrera VM (2003).
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Horai S, Hayasaka K, Kondo R, Tsugane K, Takahata N (January 1995).
1525:. In some patients, the hypertrophic cardiomyopathy is fatal at the 5527: 5209: 5083: 4389: 3037: 1702: 1673: 1659: 1645: 1631: 1486: 1377: 996: 923: 16:
Enzyme of the respiratory chain encoded by the mitochondrial genome
4526:: BOVINE HEART CYTOCHROME C OXIDASE IN CARBON MONOXIDE-BOUND STATE 4302: 4285: 1220:
complex. In humans, mutations in MT-CO1 have been associated with
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RM-MT is a disease that is characterized by recurrent attacks of
1466: 1256: 1184: 1008: 755: 710: 628: 624: 4048: 2095: 1978: 1606: 1586: 68: 5474: 5469: 5439: 5434: 5314: 5294: 5289: 5279: 5274: 5269: 5264: 4706:: BOVINE HEART CYTOCHROME C OXIDASE AT THE FULLY OXIDIZED STATE 4601:: Bovine heart cytochrome C oxidase at the fully oxidized state 4571:: Bovine heart cytochrome c oxidase at the fully oxidized state 4414: 3747: 3430: 3019: 2296: 1865: 1750:) within four tissue sections. The cells have been stained by 1556: 1548: 1480: 1459: 1284: 1280: 1275:
Cytochrome c oxidase subunit I (CO1 or MT-CO1) is one of three
1135: 960: 907: 665: 4631:: Bovine heart cytochrome C oxidase in the fully reduced state 4586:: Bovine heart cytochrome c oxidase at the fully reduced state 4541:: BOVINE HEART CYTOCHROME C OXIDASE IN THE FULLY REDUCED STATE 4460: 4326: 3852: 2732: 2479:"Structural models of the redox centres in cytochrome oxidase" 2444:
Biochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics
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Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
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rate is generally fast enough to distinguish closely related
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iron, which is required for the final step in mitochondrial
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Castresana J, Lübben M, Saraste M, Higgins DG (June 1994).
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Structure of the 13-subunit oxidized cytochrome c oxidase.
4230: 4156: 3068: 2145: This article incorporates text available under the 1734:(the gene most commonly used for mycological barcoding). 4556:: BOVINE HEART CYTOCHROME C OXIDASE IN AZIDE-BOUND STATE 3657: 3489: 604:
mitochondrial electron transport, cytochrome c to oxygen
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Cardiac Organellar Protein Atlas Knowledgebase (COPaKB)
1263:. The gene product is a 57 kDa protein composed of 513 5522:
This article incorporates text from the public domain
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to show a brown-orange color if the cells produce the
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Hebert PD, Ratnasingham S, deWaard JR (August 2003).
2299:"The superfamily of heme-copper respiratory oxidases" 443: 4616:: Bovine heart cytochrome C oxidase modified by DCCD 3658:
Miwa S, Lawless C, von Zglinicki T (December 2008).
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Journal of Neuropathology and Experimental Neurology
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gene sequence is suitable for this role because its
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have been associated with COX deficiency and RM-MT.
1216:. Cytochrome c oxidase I is the main subunit of the 4185: 4051:
Cold Spring Harbor Symposia on Quantitative Biology
3713:
Biochimica et Biophysica Acta (BBA) - Bioenergetics
3379: 2876: 2581:
Biochimica et Biophysica Acta (BBA) - Bioenergetics
2476: 382:
dentate gyrus of hippocampal formation granule cell
2442:(July 1983). "Structure of cytochrome c oxidase". 1922: 1920: 1918: 1901: 1899: 1897: 2525: 225: 147: 5550: 2477:Holm L, Saraste M, Wikström M (September 1987). 4372:Finnilä S, Lehtonen MS, Majamaa K (June 2001). 1915: 1894: 1529:stage. Other affected individuals may manifest 3706: 2292: 2290: 2288: 2178:"UniProt: the universal protein knowledgebase" 1927:GRCm38: Ensembl release 89: ENSMUSG00000064351 1722:is very slow. It has also been suggested that 1671:Cytochrome c oxidase, subunit I bacterial type 1177:mitochondrially encoded cytochrome c oxidase I 4732: 4476: 2034:"Entrez Gene: Cytochrome c oxidase subunit I" 1607:Deafness, sensorineural, mitochondrial (DFNM) 1587:Recurrent myoglobinuria mitochondrial (RM-MT) 3700: 3651: 3581: 3483: 3424: 3373: 3324: 3216: 3167: 3165: 3163: 3161: 3159: 3157: 3155: 3062: 2568: 1481:Mitochondrial Complex IV deficiency (MT-C4D) 3616: 3610: 3111: 2519: 2470: 2431: 2382: 2339: 2285: 2224: 2040: 1906:GRCh38: Ensembl release 89: ENSG00000198804 1380:in this gene in humans are associated with 614:electron transport coupled proton transport 553:mitochondrial respiratory chain complex III 5539:United States National Library of Medicine 5220:Mitochondrial permeability transition pore 4746: 4739: 4725: 4483: 4469: 3382:Annals of the New York Academy of Sciences 3178:World Journal of Gastrointestinal Oncology 2574: 2267: 1972: 1726:may be a better gene for DNA barcoding of 1536: 1411:Leber's hereditary optic neuropathy (LHON) 959: 558:mitochondrial respiratory chain complex IV 4442: 4432: 4397: 4374:"Phylogenetic network for European mtDNA" 4301: 4266: 4256: 4031: 3928: 3824: 3775: 3765: 3724: 3683: 3634: 3535: 3466: 3456: 3356: 3307: 3258: 3248: 3199: 3189: 3152: 3135: 3094: 3045: 2996: 2912: 2902: 2853: 2843: 2750: 2674: 2633: 2592: 2543: 2502: 2414: 2322: 2275:"MT-CO1 - Cytochrome c oxidase subunit 1" 2250: 2201: 1643:Cytochrome o ubiquinol oxidase, subunit I 1629:Cytochrome c oxidase cbb3-type, subunit I 5537:This article incorporates text from the 5215:Mitochondrial membrane transport protein 3577: 3575: 3531: 3529: 2877:Namslauer I, Brzezinski P (March 2009). 2028: 2026: 1741: 1657:Cytochrome aa3 quinol oxidase, subunit I 1447:Acquired Idiopathic Sideroblastic Anemia 1372: 1160:gene in the human mitochondrial genome. 1151: 1685: 5551: 4974:Cholesterol side-chain cleavage enzyme 2526:Saraste M, Castresana J (March 1994). 2218: 4720: 4464: 3572: 3526: 3275: 2172: 2170: 2168: 2166: 2164: 2162: 2160: 2158: 2156: 2023: 230: 214: 209: 152: 134: 129: 2119: 2117: 2115: 2113: 2111: 2109: 2107: 2105: 2103: 2087: 2085: 1718:, however, the rate of evolution of 1423:, causing subacute or acute central 4888:Coenzyme Q – cytochrome c reductase 3623:The Journal of Biological Chemistry 2092:Online Mendelian Inheritance in Man 1415:LHON, correlated with mutations in 1382:Leber's hereditary optic neuropathy 1222:Leber's hereditary optic neuropathy 13: 5074:Oxoglutarate dehydrogenase complex 5009:Glycerol-3-phosphate dehydrogenase 4378:American Journal of Human Genetics 3917:American Journal of Human Genetics 3845: 3617:Menzies RA, Gold PH (April 1971). 3402:10.1111/j.1749-6632.2002.tb02113.x 3026:American Journal of Human Genetics 2712:10.1046/j.1432-1327.1998.2580132.x 2622:American Journal of Human Genetics 2575:Chen J, Strous M (February 2013). 2495:10.1002/j.1460-2075.1987.tb02578.x 2407:10.1002/j.1460-2075.1994.tb06541.x 2153: 1876:. Additionally, it interacts with 1693:is a gene that is often used as a 1279:(mtDNA) encoded subunits (MT-CO1, 14: 5585: 5019:Carnitine palmitoyltransferase II 2100: 2082: 1738:MT-COI (= CCOI) in colonic crypts 5143:Carbamoyl phosphate synthetase I 4783:Long-chain-fatty-acid—CoA ligase 4778:Carnitine palmitoyltransferase I 4696: 4681: 4666: 4651: 4636: 4621: 4606: 4591: 4576: 4561: 4546: 4531: 4516: 4501: 3676:10.1111/j.1474-9726.2008.00426.x 3349:10.1111/j.1474-9726.2009.00531.x 3137:10.1111/j.1574-6968.2009.01839.x 3075:Proceedings. Biological Sciences 2700:European Journal of Biochemistry 2315:10.1128/jb.176.18.5587-5600.1994 2140: 1697:to identify animal species. The 201: 121: 5004:Glutamate aspartate transporter 4490: 3792: 3741: 3013: 2972: 2929: 2870: 2811: 2767: 2726: 2691: 2650: 2609: 2188:(D1): D158–D169. January 2017. 1847: 584:response to electrical stimulus 5121:Pyruvate dehydrogenase complex 5079:Succinyl coenzyme A synthetase 4012:Molecular and Cellular Biology 3777:11858/00-001M-0000-0028-466E-C 3707:Brown GC, Borutaite V (2008). 3538:Journal of Cellular Physiology 1954: 1936: 1622: 954:Cytochrome c oxidase subunit I 523:integral component of membrane 432:More reference expression data 1: 3636:10.1016/S0021-9258(18)62305-1 2243:10.1161/CIRCRESAHA.113.301151 2001:10.1126/science.272.5265.1136 1887: 1092:Available protein structures: 487:cytochrome-c oxidase activity 4925:Dihydroorotate dehydrogenase 4171:10.1016/0022-2836(80)90196-5 4159:Journal of Molecular Biology 3817:10.1016/j.bbamcr.2017.11.010 3767:10.1016/j.celrep.2015.08.009 3726:10.1016/j.bbabio.2008.03.024 3596:10.1016/0014-4827(91)90467-9 3300:10.1016/j.celrep.2014.07.019 2594:10.1016/j.bbabio.2012.10.002 2545:10.1016/0014-5793(94)80228-9 2456:10.1016/0304-4173(83)90003-4 2068:10.1016/j.protis.2011.10.003 1427:. Some patients may display 1250: 589:response to oxidative stress 548:respiratory chain complex IV 538:mitochondrial inner membrane 7: 4979:Steroid 11-beta-hydroxylase 4059:10.1101/sqb.1986.051.01.013 1813:MT-COI is coded for by the 1523:hypertrophic cardiomyopathy 1437:respiratory chain complexes 1270: 1259:-rich heavy (H) section of 332:stromal cell of endometrium 10: 5590: 5521: 5153:N-Acetylglutamate synthase 5148:Ornithine transcarbamylase 4952:Glycerol phosphate shuttle 4818:monoamine neurotransmitter 3584:Experimental Cell Research 2348:Cell Biology International 1551:in the inner walls of the 1198:. The gene is also called 18: 5559:Human mitochondrial genes 5507: 5378: 5353: 5323: 5303: 5253: 5244: 5205: 5198: 5181: 5161: 5129: 5097: 5045: 5036: 4992: 4960: 4933: 4911: 4878:oxidative phosphorylation 4874: 4865: 4842: 4814: 4791: 4764: 4755: 4496: 3867:10.1016/j.tig.2006.04.001 3124:FEMS Microbiology Letters 2789:10.1007/s10048-005-0015-z 2676:10.1182/blood.V90.12.4961 2438:Capaldi RA, Malatesta F, 1962:"Mouse PubMed Reference:" 1944:"Human PubMed Reference:" 1579:, and family history are 1308:oxidative phosphorylation 1134: 1114: 1096: 1091: 1087: 1075: 1063: 1051: 1039: 1019: 1007: 995: 983: 975: 970: 958: 953: 938: 933: 929: 922: 906: 887: 872: 868: 853: 849: 842: 829: 825: 810: 806: 799: 786: 782: 767: 763: 754: 741: 737: 722: 718: 709: 696: 692: 677: 673: 664: 649: 642: 638: 622: 599:oxidative phosphorylation 472: 468: 456: 451: 442: 429: 378: 369: 316: 307: 277: 269: 265: 248: 235: 221: 216:Mitochondrial DNA (mouse) 200: 191: 187: 170: 157: 143: 137:Mitochondrial DNA (human) 120: 111: 107: 62: 59: 49: 42: 37: 33: 28: 5069:Isocitrate dehydrogenase 4947:Malate-aspartate shuttle 4053:. 51 Pt 1 (1): 103–114. 3884:Human Molecular Genetics 2739:Human Molecular Genetics 1815:mitochondrial chromosome 1304:electron transport chain 1295:. Cytochrome c oxidase ( 5116:Glutamate dehydrogenase 4903:Succinate dehydrogenase 4096:10.1126/science.3764430 3492:Journal of Cell Science 3250:10.1073/pnas.0505903103 3191:10.4251/wjgo.v2.i12.429 2904:10.1073/pnas.0811450106 2845:10.1073/pnas.0505903103 2303:Journal of Bacteriology 1583:for colorectal cancer. 1537:Colorectal cancer (CRC) 1421:optic nerve dysfunction 1187:that is encoded by the 507:oxidoreductase activity 5574:Transmembrane proteins 5512:mitochondrial diseases 5111:Aspartate transaminase 4768:fatty acid degradation 4434:10.1186/1471-2156-2-13 3550:10.1002/jcp.1041360316 3458:10.1073/pnas.072670199 3087:10.1098/rsbl.2003.0025 2752:10.1093/hmg/11.16.1797 2360:10.1006/cbir.1994.1084 2182:Nucleic Acids Research 1856:, the encoded protein 1767: 1613:non-syndromic deafness 1419:, is characterized by 1401:sensorineural deafness 1356:nitric-oxide reductase 1349:Gram-positive bacteria 1241:sensorineural deafness 1169:Cytochrome c oxidase I 1165: 594:cerebellum development 574:response to copper ion 402:superior frontal gyrus 398:Cortex of frontal lobe 5225:Mitochondrial carrier 5101:anaplerotic reactions 4937:mitochondrial shuttle 4915:pyrimidine metabolism 4258:10.1073/pnas.92.2.532 4024:10.1128/MCB.11.3.1631 3896:10.1093/hmg/1.2.140-a 2998:10.1093/jnen/64.2.123 1819:mitochondrial fission 1745: 1567:lesions, to invasive 1373:Clinical significance 1155: 900:Chr M: 0.01 – 0.01 Mb 893:Chr M: 0.01 – 0.01 Mb 394:primary visual cortex 336:right coronary artery 5232:Translocator protein 5089:Malate dehydrogenase 4984:Aldosterone synthase 3498:(Pt 13): 2653–2662. 3081:(Suppl 1): S96–S99. 2950:10.1212/wnl.55.5.644 2231:Circulation Research 1836:and D of the image. 1752:immunohistochemistry 1686:Use in DNA barcoding 1617:maternal inheritance 1507:exercise intolerance 1441:inherited maternally 1389:sideroblastic anemia 1289:cytochrome c oxidase 1229:sideroblastic anemia 1218:cytochrome c oxidase 348:smooth muscle tissue 4844:Intermembrane space 4341:2000Natur.408..708I 4249:1995PNAS...92..532H 4200:1981Natur.290..465M 4126:1985Natur.314..592C 4088:1986Sci...234..614C 3449:2002PNAS...99.5521N 3394:2002NYASA.959..434C 3241:2006PNAS..103..714G 2895:2009PNAS..106.3402N 2836:2006PNAS..103..714G 2194:10.1093/nar/gkw1099 1993:1996Sci...272.1136T 1987:(5265): 1136–1144. 1884:-dependent manner. 1519:developmental delay 609:aerobic respiration 418:ganglionic eminence 5541:, which is in the 5199:Other/to be sorted 5164:alcohol metabolism 5024:Uncoupling protein 4898:NADH dehydrogenase 3983:10.1007/bf00206061 3855:Trends in Genetics 1768: 1611:DFNM is a form of 1573:ulcerative colitis 1515:mental retardation 1433:cardiac conduction 1323:ubiquinol oxidases 1166: 744:ENSMUSG00000064351 567:Biological process 516:Cellular component 480:Molecular function 406:hippocampus proper 320:right uterine tube 5519: 5518: 5503: 5502: 5246:Mitochondrial DNA 5240: 5239: 5194: 5193: 5049:citric acid cycle 5032: 5031: 4838: 4837: 4830:Monoamine oxidase 4714: 4713: 4335:(6813): 708–713. 4194:(5806): 465–470. 4120:(6012): 592–597. 4082:(4776): 614–618. 3955:(13): 3718–3725. 3760:(10): 1644–1655. 3504:10.1242/jcs.01134 2745:(16): 1797–1805. 2669:(12): 4961–4972. 2401:(11): 2516–2525. 2309:(18): 5587–5600. 1748:intestinal glands 1601:nonsense mutation 1511:motor development 1491:liver dysfunction 1397:colorectal cancer 1384:(LHON), acquired 1306:of mitochondrial 1277:mitochondrial DNA 1237:colorectal cancer 1224:(LHON), acquired 1150: 1149: 1146: 1145: 1141:structure summary 949: 948: 945: 944: 918: 917: 883: 882: 862: 861: 838: 837: 819: 818: 795: 794: 776: 775: 750: 749: 731: 730: 705: 704: 686: 685: 634: 633: 492:metal ion binding 464: 463: 460: 459: 438: 437: 425: 424: 386:cerebellar cortex 363: 362: 261: 260: 183: 182: 5581: 5569:Protein families 5383: 5358: 5328: 5308: 5258: 5251: 5250: 5203: 5202: 5166: 5136: 5104: 5059:Citrate synthase 5052: 5043: 5042: 4997: 4967: 4940: 4918: 4881: 4872: 4871: 4852:Adenylate kinase 4823: 4799: 4771: 4762: 4761: 4741: 4734: 4727: 4718: 4717: 4700: 4685: 4670: 4655: 4640: 4625: 4610: 4595: 4580: 4565: 4550: 4535: 4520: 4505: 4485: 4478: 4471: 4462: 4461: 4456: 4446: 4436: 4411: 4401: 4384:(6): 1475–1484. 4368: 4349:10.1038/35047064 4323: 4305: 4280: 4270: 4260: 4227: 4208:10.1038/290465a0 4182: 4153: 4134:10.1038/314592a0 4107: 4070: 4045: 4035: 4018:(3): 1631–1637. 4002: 3964: 3942: 3932: 3907: 3878: 3839: 3838: 3828: 3796: 3790: 3789: 3779: 3769: 3745: 3739: 3738: 3728: 3719:(7–8): 877–881. 3704: 3698: 3697: 3687: 3655: 3649: 3648: 3638: 3629:(8): 2425–2429. 3614: 3608: 3607: 3579: 3570: 3569: 3533: 3524: 3523: 3487: 3481: 3480: 3470: 3460: 3443:(8): 5521–5526. 3428: 3422: 3421: 3377: 3371: 3370: 3360: 3328: 3322: 3321: 3311: 3279: 3273: 3272: 3262: 3252: 3220: 3214: 3213: 3203: 3193: 3169: 3150: 3149: 3139: 3115: 3109: 3108: 3098: 3066: 3060: 3059: 3049: 3032:(6): 1803–1806. 3017: 3011: 3010: 3000: 2976: 2970: 2969: 2933: 2927: 2926: 2916: 2906: 2889:(9): 3402–3407. 2874: 2868: 2867: 2857: 2847: 2815: 2809: 2808: 2771: 2765: 2764: 2754: 2730: 2724: 2723: 2695: 2689: 2688: 2678: 2654: 2648: 2647: 2637: 2613: 2607: 2606: 2596: 2572: 2566: 2565: 2547: 2523: 2517: 2516: 2506: 2489:(9): 2819–2823. 2483:The EMBO Journal 2474: 2468: 2467: 2435: 2429: 2428: 2418: 2395:The EMBO Journal 2386: 2380: 2379: 2343: 2337: 2336: 2326: 2294: 2283: 2282: 2271: 2265: 2264: 2254: 2237:(9): 1043–1053. 2222: 2216: 2215: 2205: 2174: 2151: 2144: 2138: 2136: 2135: 2121: 2098: 2089: 2080: 2079: 2053: 2044: 2038: 2037: 2030: 2021: 2020: 1976: 1970: 1969: 1958: 1952: 1951: 1940: 1934: 1924: 1913: 1903: 1746:Colonic crypts ( 1571:. Long-standing 1403:, and recurrent 1291:, also known as 1243:, and recurrent 1175:) also known as 1156:Location of the 1089: 1088: 963: 951: 950: 931: 930: 902: 895: 878: 866: 865: 857: 847: 846: 843:RefSeq (protein) 833: 823: 822: 814: 804: 803: 780: 779: 761: 760: 735: 734: 716: 715: 690: 689: 671: 670: 640: 639: 470: 469: 449: 448: 434: 374: 372:Top expressed in 367: 366: 312: 310:Top expressed in 305: 304: 284: 283: 267: 266: 257: 244: 233: 217: 205: 189: 188: 179: 166: 155: 139: 125: 109: 108: 103: 101:COX1 - orthologs 54: 47: 26: 25: 21:cyclooxygenase-1 5589: 5588: 5584: 5583: 5582: 5580: 5579: 5578: 5564:Protein domains 5549: 5548: 5534: 5520: 5515: 5499: 5379: 5374: 5354: 5349: 5324: 5319: 5304: 5299: 5254: 5236: 5190: 5177: 5162: 5157: 5130: 5125: 5098: 5093: 5046: 5028: 4993: 4988: 4964:steroidogenesis 4961: 4956: 4934: 4929: 4912: 4907: 4875: 4861: 4857:Creatine kinase 4834: 4820: 4815: 4810: 4792: 4787: 4765: 4751: 4745: 4715: 4710: 4707: 4701: 4692: 4686: 4677: 4671: 4662: 4656: 4647: 4641: 4632: 4626: 4617: 4611: 4602: 4596: 4587: 4581: 4572: 4566: 4557: 4551: 4542: 4536: 4527: 4521: 4512: 4506: 4492: 4489: 4459: 4290:Nature Genetics 3949:Cancer Research 3848: 3846:Further reading 3843: 3842: 3797: 3793: 3746: 3742: 3705: 3701: 3656: 3652: 3615: 3611: 3580: 3573: 3534: 3527: 3488: 3484: 3429: 3425: 3378: 3374: 3329: 3325: 3280: 3276: 3221: 3217: 3184:(12): 429–442. 3170: 3153: 3116: 3112: 3067: 3063: 3018: 3014: 2977: 2973: 2934: 2930: 2875: 2871: 2816: 2812: 2772: 2768: 2731: 2727: 2696: 2692: 2655: 2651: 2614: 2610: 2573: 2569: 2524: 2520: 2475: 2471: 2440:Darley-Usmar VM 2436: 2432: 2387: 2383: 2344: 2340: 2295: 2286: 2273: 2272: 2268: 2223: 2219: 2176: 2175: 2154: 2133: 2131: 2129:www.uniprot.org 2123: 2122: 2101: 2090: 2083: 2051: 2045: 2041: 2032: 2031: 2024: 1977: 1973: 1960: 1959: 1955: 1942: 1941: 1937: 1925: 1916: 1904: 1895: 1890: 1850: 1780:large intestine 1740: 1688: 1625: 1609: 1589: 1539: 1503:muscle weakness 1483: 1449: 1413: 1375: 1273: 1253: 1053:OPM superfamily 966: 940:View/Edit Mouse 935:View/Edit Human 898: 891: 888:Location (UCSC) 874: 855: 831: 812: 725:ENSG00000198804 618: 562: 511: 497:protein binding 430: 421: 416: 412: 410:muscle of thigh 408: 404: 400: 396: 392: 388: 384: 370: 359: 354: 350: 346: 344:Brodmann area 9 342: 338: 334: 330: 326: 322: 308: 252: 239: 231: 215: 192:Gene location ( 174: 161: 153: 135: 112:Gene location ( 63: 50: 43: 24: 17: 12: 11: 5: 5587: 5577: 5576: 5571: 5566: 5561: 5517: 5516: 5508: 5505: 5504: 5501: 5500: 5498: 5497: 5492: 5487: 5482: 5477: 5472: 5467: 5462: 5457: 5452: 5447: 5442: 5437: 5432: 5427: 5422: 5417: 5412: 5407: 5402: 5397: 5392: 5386: 5384: 5376: 5375: 5373: 5372: 5367: 5361: 5359: 5351: 5350: 5348: 5347: 5342: 5337: 5331: 5329: 5321: 5320: 5318: 5317: 5311: 5309: 5301: 5300: 5298: 5297: 5292: 5287: 5282: 5277: 5272: 5267: 5261: 5259: 5248: 5242: 5241: 5238: 5237: 5235: 5234: 5229: 5228: 5227: 5222: 5212: 5206: 5200: 5196: 5195: 5192: 5191: 5189: 5188: 5182: 5179: 5178: 5176: 5175: 5169: 5167: 5159: 5158: 5156: 5155: 5150: 5145: 5139: 5137: 5127: 5126: 5124: 5123: 5118: 5113: 5107: 5105: 5095: 5094: 5092: 5091: 5086: 5081: 5076: 5071: 5066: 5061: 5055: 5053: 5040: 5034: 5033: 5030: 5029: 5027: 5026: 5021: 5016: 5011: 5006: 5000: 4998: 4990: 4989: 4987: 4986: 4981: 4976: 4970: 4968: 4958: 4957: 4955: 4954: 4949: 4943: 4941: 4931: 4930: 4928: 4927: 4921: 4919: 4909: 4908: 4906: 4905: 4900: 4895: 4890: 4884: 4882: 4869: 4867:Inner membrane 4863: 4862: 4860: 4859: 4854: 4848: 4846: 4840: 4839: 4836: 4835: 4833: 4832: 4826: 4824: 4812: 4811: 4809: 4808: 4802: 4800: 4789: 4788: 4786: 4785: 4780: 4774: 4772: 4759: 4757:Outer membrane 4753: 4752: 4744: 4743: 4736: 4729: 4721: 4712: 4711: 4709: 4708: 4702: 4695: 4693: 4687: 4680: 4678: 4672: 4665: 4663: 4657: 4650: 4648: 4642: 4635: 4633: 4627: 4620: 4618: 4612: 4605: 4603: 4597: 4590: 4588: 4582: 4575: 4573: 4567: 4560: 4558: 4552: 4545: 4543: 4537: 4530: 4528: 4522: 4515: 4513: 4507: 4500: 4497: 4494: 4493: 4488: 4487: 4480: 4473: 4465: 4458: 4457: 4412: 4390:10.1086/320591 4369: 4324: 4281: 4243:(2): 532–536. 4228: 4183: 4165:(2): 161–178. 4154: 4108: 4071: 4046: 4003: 3977:(2): 139–145. 3971:Human Genetics 3965: 3943: 3923:(2): 378–385. 3908: 3879: 3861:(6): 339–345. 3849: 3847: 3844: 3841: 3840: 3811:(2): 323–333. 3791: 3740: 3699: 3670:(6): 920–923. 3650: 3609: 3590:(1): 137–140. 3571: 3544:(3): 507–513. 3525: 3482: 3423: 3388:(1): 434–447. 3372: 3323: 3294:(4): 940–947. 3274: 3235:(3): 714–719. 3215: 3151: 3110: 3061: 3038:10.1086/302658 3012: 2991:(2): 123–128. 2971: 2944:(5): 644–649. 2928: 2869: 2830:(3): 714–719. 2810: 2766: 2725: 2706:(1): 132–138. 2690: 2649: 2628:(2): 378–385. 2608: 2587:(2): 136–144. 2567: 2518: 2469: 2450:(2): 135–148. 2430: 2381: 2354:(5): 345–355. 2338: 2284: 2266: 2217: 2152: 2099: 2081: 2062:(3): 415–434. 2039: 2022: 1971: 1953: 1935: 1914: 1892: 1891: 1889: 1886: 1849: 1846: 1826:selection bias 1776:colonic crypts 1739: 1736: 1687: 1684: 1683: 1682: 1668: 1654: 1640: 1624: 1621: 1608: 1605: 1593:rhabdomyolysis 1588: 1585: 1569:adenocarcinoma 1538: 1535: 1482: 1479: 1448: 1445: 1412: 1409: 1374: 1371: 1345:Pseudomonadota 1272: 1269: 1252: 1249: 1148: 1147: 1144: 1143: 1138: 1132: 1131: 1118: 1112: 1111: 1101: 1094: 1093: 1085: 1084: 1079: 1073: 1072: 1067: 1061: 1060: 1055: 1049: 1048: 1043: 1037: 1036: 1023: 1017: 1016: 1011: 1005: 1004: 999: 993: 992: 987: 981: 980: 977: 973: 972: 968: 967: 964: 956: 955: 947: 946: 943: 942: 937: 927: 926: 920: 919: 916: 915: 913: 911: 904: 903: 896: 889: 885: 884: 881: 880: 870: 869: 863: 860: 859: 851: 850: 844: 840: 839: 836: 835: 827: 826: 820: 817: 816: 808: 807: 801: 797: 796: 793: 792: 784: 783: 777: 774: 773: 765: 764: 758: 752: 751: 748: 747: 739: 738: 732: 729: 728: 720: 719: 713: 707: 706: 703: 702: 694: 693: 687: 684: 683: 675: 674: 668: 662: 661: 656: 651: 647: 646: 636: 635: 632: 631: 620: 619: 617: 616: 611: 606: 601: 596: 591: 586: 581: 576: 570: 568: 564: 563: 561: 560: 555: 550: 545: 540: 535: 530: 525: 519: 517: 513: 512: 510: 509: 504: 499: 494: 489: 483: 481: 477: 476: 466: 465: 462: 461: 458: 457: 454: 453: 446: 440: 439: 436: 435: 427: 426: 423: 422: 420: 419: 415: 411: 407: 403: 399: 395: 391: 387: 383: 379: 376: 375: 364: 361: 360: 358: 357: 353: 349: 345: 341: 337: 333: 329: 325: 321: 317: 314: 313: 301: 300: 292: 281: 275: 274: 271:RNA expression 263: 262: 259: 258: 250: 246: 245: 237: 234: 229: 223: 222: 219: 218: 213: 207: 206: 198: 197: 185: 184: 181: 180: 172: 168: 167: 159: 156: 151: 145: 144: 141: 140: 133: 127: 126: 118: 117: 105: 104: 61: 57: 56: 48: 40: 39: 35: 34: 31: 30: 15: 9: 6: 4: 3: 2: 5586: 5575: 5572: 5570: 5567: 5565: 5562: 5560: 5557: 5556: 5554: 5547: 5546: 5544: 5543:public domain 5540: 5533: 5529: 5525: 5514: 5513: 5506: 5496: 5493: 5491: 5488: 5486: 5483: 5481: 5478: 5476: 5473: 5471: 5468: 5466: 5463: 5461: 5458: 5456: 5453: 5451: 5448: 5446: 5443: 5441: 5438: 5436: 5433: 5431: 5428: 5426: 5423: 5421: 5418: 5416: 5413: 5411: 5408: 5406: 5403: 5401: 5398: 5396: 5393: 5391: 5388: 5387: 5385: 5382: 5377: 5371: 5368: 5366: 5363: 5362: 5360: 5357: 5352: 5346: 5343: 5341: 5338: 5336: 5333: 5332: 5330: 5327: 5322: 5316: 5313: 5312: 5310: 5307: 5302: 5296: 5293: 5291: 5288: 5286: 5283: 5281: 5278: 5276: 5273: 5271: 5268: 5266: 5263: 5262: 5260: 5257: 5252: 5249: 5247: 5243: 5233: 5230: 5226: 5223: 5221: 5218: 5217: 5216: 5213: 5211: 5208: 5207: 5204: 5201: 5197: 5187: 5184: 5183: 5180: 5174: 5171: 5170: 5168: 5165: 5160: 5154: 5151: 5149: 5146: 5144: 5141: 5140: 5138: 5135: 5134: 5128: 5122: 5119: 5117: 5114: 5112: 5109: 5108: 5106: 5103: 5102: 5096: 5090: 5087: 5085: 5082: 5080: 5077: 5075: 5072: 5070: 5067: 5065: 5062: 5060: 5057: 5056: 5054: 5051: 5050: 5044: 5041: 5039: 5035: 5025: 5022: 5020: 5017: 5015: 5012: 5010: 5007: 5005: 5002: 5001: 4999: 4996: 4991: 4985: 4982: 4980: 4977: 4975: 4972: 4971: 4969: 4966: 4965: 4959: 4953: 4950: 4948: 4945: 4944: 4942: 4939: 4938: 4932: 4926: 4923: 4922: 4920: 4917: 4916: 4910: 4904: 4901: 4899: 4896: 4894: 4891: 4889: 4886: 4885: 4883: 4880: 4879: 4873: 4870: 4868: 4864: 4858: 4855: 4853: 4850: 4849: 4847: 4845: 4841: 4831: 4828: 4827: 4825: 4822: 4819: 4813: 4807: 4804: 4803: 4801: 4798: 4796: 4790: 4784: 4781: 4779: 4776: 4775: 4773: 4770: 4769: 4763: 4760: 4758: 4754: 4749: 4748:Mitochondrial 4742: 4737: 4735: 4730: 4728: 4723: 4722: 4719: 4705: 4699: 4694: 4690: 4684: 4679: 4675: 4669: 4664: 4660: 4654: 4649: 4645: 4639: 4634: 4630: 4624: 4619: 4615: 4609: 4604: 4600: 4594: 4589: 4585: 4579: 4574: 4570: 4564: 4559: 4555: 4549: 4544: 4540: 4534: 4529: 4525: 4519: 4514: 4510: 4504: 4499: 4498: 4495: 4486: 4481: 4479: 4474: 4472: 4467: 4466: 4463: 4454: 4450: 4445: 4440: 4435: 4430: 4426: 4422: 4418: 4413: 4409: 4405: 4400: 4395: 4391: 4387: 4383: 4379: 4375: 4370: 4366: 4362: 4358: 4354: 4350: 4346: 4342: 4338: 4334: 4330: 4325: 4321: 4317: 4313: 4309: 4304: 4303:10.1038/13779 4299: 4295: 4291: 4287: 4282: 4278: 4274: 4269: 4264: 4259: 4254: 4250: 4246: 4242: 4238: 4234: 4229: 4225: 4221: 4217: 4213: 4209: 4205: 4201: 4197: 4193: 4189: 4184: 4180: 4176: 4172: 4168: 4164: 4160: 4155: 4151: 4147: 4143: 4139: 4135: 4131: 4127: 4123: 4119: 4115: 4109: 4105: 4101: 4097: 4093: 4089: 4085: 4081: 4077: 4072: 4068: 4064: 4060: 4056: 4052: 4047: 4043: 4039: 4034: 4029: 4025: 4021: 4017: 4013: 4009: 4004: 4000: 3996: 3992: 3988: 3984: 3980: 3976: 3972: 3966: 3962: 3958: 3954: 3950: 3944: 3940: 3936: 3931: 3926: 3922: 3918: 3914: 3909: 3905: 3901: 3897: 3893: 3889: 3885: 3880: 3876: 3872: 3868: 3864: 3860: 3856: 3851: 3850: 3836: 3832: 3827: 3822: 3818: 3814: 3810: 3806: 3802: 3795: 3787: 3783: 3778: 3773: 3768: 3763: 3759: 3755: 3751: 3744: 3736: 3732: 3727: 3722: 3718: 3714: 3710: 3703: 3695: 3691: 3686: 3681: 3677: 3673: 3669: 3665: 3661: 3654: 3646: 3642: 3637: 3632: 3628: 3624: 3620: 3613: 3605: 3601: 3597: 3593: 3589: 3585: 3578: 3576: 3567: 3563: 3559: 3555: 3551: 3547: 3543: 3539: 3532: 3530: 3521: 3517: 3513: 3509: 3505: 3501: 3497: 3493: 3486: 3478: 3474: 3469: 3464: 3459: 3454: 3450: 3446: 3442: 3438: 3434: 3427: 3419: 3415: 3411: 3407: 3403: 3399: 3395: 3391: 3387: 3383: 3376: 3368: 3364: 3359: 3354: 3350: 3346: 3342: 3338: 3334: 3327: 3319: 3315: 3310: 3305: 3301: 3297: 3293: 3289: 3285: 3278: 3270: 3266: 3261: 3256: 3251: 3246: 3242: 3238: 3234: 3230: 3226: 3219: 3211: 3207: 3202: 3197: 3192: 3187: 3183: 3179: 3175: 3168: 3166: 3164: 3162: 3160: 3158: 3156: 3147: 3143: 3138: 3133: 3129: 3125: 3121: 3114: 3106: 3102: 3097: 3092: 3088: 3084: 3080: 3076: 3072: 3065: 3057: 3053: 3048: 3043: 3039: 3035: 3031: 3027: 3023: 3016: 3008: 3004: 2999: 2994: 2990: 2986: 2982: 2975: 2967: 2963: 2959: 2955: 2951: 2947: 2943: 2939: 2932: 2924: 2920: 2915: 2910: 2905: 2900: 2896: 2892: 2888: 2884: 2880: 2873: 2865: 2861: 2856: 2851: 2846: 2841: 2837: 2833: 2829: 2825: 2821: 2814: 2806: 2802: 2798: 2794: 2790: 2786: 2782: 2778: 2777:Neurogenetics 2770: 2762: 2758: 2753: 2748: 2744: 2740: 2736: 2729: 2721: 2717: 2713: 2709: 2705: 2701: 2694: 2686: 2682: 2677: 2672: 2668: 2664: 2660: 2653: 2645: 2641: 2636: 2631: 2627: 2623: 2619: 2612: 2604: 2600: 2595: 2590: 2586: 2582: 2578: 2571: 2563: 2559: 2555: 2551: 2546: 2541: 2537: 2533: 2529: 2522: 2514: 2510: 2505: 2500: 2496: 2492: 2488: 2484: 2480: 2473: 2465: 2461: 2457: 2453: 2449: 2445: 2441: 2434: 2426: 2422: 2417: 2412: 2408: 2404: 2400: 2396: 2392: 2385: 2377: 2373: 2369: 2365: 2361: 2357: 2353: 2349: 2342: 2334: 2330: 2325: 2320: 2316: 2312: 2308: 2304: 2300: 2293: 2291: 2289: 2280: 2276: 2270: 2262: 2258: 2253: 2248: 2244: 2240: 2236: 2232: 2228: 2221: 2213: 2209: 2204: 2199: 2195: 2191: 2187: 2183: 2179: 2173: 2171: 2169: 2167: 2165: 2163: 2161: 2159: 2157: 2150: 2148: 2143: 2130: 2126: 2120: 2118: 2116: 2114: 2112: 2110: 2108: 2106: 2104: 2097: 2093: 2088: 2086: 2077: 2073: 2069: 2065: 2061: 2057: 2050: 2043: 2035: 2029: 2027: 2018: 2014: 2010: 2006: 2002: 1998: 1994: 1990: 1986: 1982: 1975: 1967: 1963: 1957: 1949: 1945: 1939: 1932: 1928: 1923: 1921: 1919: 1911: 1907: 1902: 1900: 1898: 1893: 1885: 1883: 1879: 1875: 1871: 1867: 1863: 1859: 1855: 1845: 1841: 1837: 1833: 1831: 1827: 1822: 1820: 1816: 1811: 1807: 1803: 1799: 1795: 1793: 1788: 1783: 1781: 1778:of the human 1777: 1773: 1765: 1761: 1757: 1756:mitochondrial 1753: 1749: 1744: 1735: 1733: 1729: 1725: 1721: 1717: 1712: 1708: 1704: 1700: 1696: 1692: 1681: 1680: 1675: 1672: 1669: 1667: 1666: 1661: 1658: 1655: 1653: 1652: 1647: 1644: 1641: 1639: 1638: 1633: 1630: 1627: 1626: 1620: 1618: 1614: 1604: 1602: 1598: 1594: 1584: 1582: 1578: 1574: 1570: 1566: 1562: 1558: 1554: 1550: 1547: 1543: 1534: 1532: 1531:Leigh disease 1528: 1524: 1520: 1516: 1512: 1508: 1504: 1500: 1496: 1492: 1488: 1478: 1476: 1472: 1468: 1464: 1461: 1457: 1453: 1444: 1442: 1438: 1434: 1430: 1426: 1422: 1418: 1408: 1406: 1405:myoglobinuria 1402: 1398: 1394: 1390: 1387: 1383: 1379: 1370: 1368: 1364: 1361: 1357: 1352: 1350: 1346: 1342: 1337: 1333: 1331: 1328: 1324: 1320: 1316: 1311: 1309: 1305: 1301: 1298: 1294: 1290: 1286: 1282: 1278: 1268: 1266: 1262: 1258: 1248: 1246: 1245:myoglobinuria 1242: 1238: 1234: 1230: 1227: 1223: 1219: 1215: 1214: 1209: 1208: 1203: 1202: 1197: 1193: 1190: 1186: 1182: 1178: 1174: 1170: 1163: 1159: 1154: 1142: 1139: 1137: 1133: 1130: 1126: 1122: 1119: 1117: 1113: 1109: 1105: 1102: 1099: 1095: 1090: 1086: 1083: 1080: 1078: 1074: 1071: 1068: 1066: 1062: 1059: 1056: 1054: 1050: 1047: 1044: 1042: 1038: 1035: 1031: 1027: 1024: 1022: 1018: 1015: 1012: 1010: 1006: 1003: 1000: 998: 994: 991: 988: 986: 982: 978: 974: 969: 962: 957: 952: 941: 936: 932: 928: 925: 921: 914: 912: 909: 905: 901: 897: 894: 890: 886: 879: 877: 871: 867: 864: 858: 852: 848: 845: 841: 834: 828: 824: 821: 815: 809: 805: 802: 800:RefSeq (mRNA) 798: 791: 790: 785: 781: 778: 772: 771: 766: 762: 759: 757: 753: 746: 745: 740: 736: 733: 727: 726: 721: 717: 714: 712: 708: 701: 700: 695: 691: 688: 682: 681: 676: 672: 669: 667: 663: 660: 657: 655: 652: 648: 645: 641: 637: 630: 626: 621: 615: 612: 610: 607: 605: 602: 600: 597: 595: 592: 590: 587: 585: 582: 580: 577: 575: 572: 571: 569: 566: 565: 559: 556: 554: 551: 549: 546: 544: 541: 539: 536: 534: 533:mitochondrion 531: 529: 526: 524: 521: 520: 518: 515: 514: 508: 505: 503: 500: 498: 495: 493: 490: 488: 485: 484: 482: 479: 478: 475: 474:Gene ontology 471: 467: 455: 450: 447: 445: 441: 433: 428: 417: 413: 409: 405: 401: 397: 393: 389: 385: 381: 380: 377: 373: 368: 365: 355: 351: 347: 343: 339: 335: 331: 327: 324:apex of heart 323: 319: 318: 315: 311: 306: 303: 302: 299: 297: 293: 291: 290: 286: 285: 282: 280: 276: 272: 268: 264: 256: 251: 247: 243: 238: 228: 224: 220: 212: 208: 204: 199: 195: 190: 186: 178: 173: 169: 165: 160: 150: 146: 142: 138: 132: 128: 124: 119: 115: 110: 106: 102: 98: 94: 90: 86: 82: 78: 74: 70: 66: 58: 53: 46: 41: 36: 32: 27: 22: 5536: 5535: 5509: 5356:ATP synthase 5334: 5163: 5131: 5099: 5047: 5014:ATP synthase 4994: 4962: 4935: 4913: 4893:Cytochrome c 4876: 4816: 4806:Kynureninase 4793: 4766: 4703: 4688: 4673: 4658: 4643: 4628: 4613: 4598: 4583: 4568: 4553: 4538: 4523: 4508: 4424: 4421:BMC Genetics 4420: 4381: 4377: 4332: 4328: 4293: 4289: 4240: 4236: 4191: 4187: 4162: 4158: 4117: 4113: 4079: 4075: 4050: 4015: 4011: 3974: 3970: 3952: 3948: 3920: 3916: 3887: 3883: 3858: 3854: 3808: 3804: 3794: 3757: 3754:Cell Reports 3753: 3743: 3716: 3712: 3702: 3667: 3663: 3653: 3626: 3622: 3612: 3587: 3583: 3541: 3537: 3495: 3491: 3485: 3440: 3436: 3426: 3385: 3381: 3375: 3343:(1): 96–99. 3340: 3336: 3326: 3291: 3288:Cell Reports 3287: 3277: 3232: 3228: 3218: 3181: 3177: 3130:(1): 76–84. 3127: 3123: 3113: 3078: 3074: 3064: 3029: 3025: 3015: 2988: 2984: 2974: 2941: 2937: 2931: 2886: 2882: 2872: 2827: 2823: 2813: 2783:(1): 51–57. 2780: 2776: 2769: 2742: 2738: 2728: 2703: 2699: 2693: 2666: 2662: 2652: 2625: 2621: 2611: 2584: 2580: 2570: 2535: 2532:FEBS Letters 2531: 2521: 2486: 2482: 2472: 2447: 2443: 2433: 2398: 2394: 2384: 2351: 2347: 2341: 2306: 2302: 2278: 2269: 2234: 2230: 2220: 2185: 2181: 2139: 2132:. Retrieved 2128: 2059: 2055: 2042: 1984: 1980: 1974: 1965: 1956: 1947: 1938: 1851: 1848:Interactions 1842: 1838: 1834: 1823: 1812: 1808: 1804: 1800: 1796: 1784: 1769: 1764:haematoxylin 1723: 1719: 1710: 1698: 1690: 1689: 1677: 1663: 1649: 1635: 1610: 1590: 1581:risk factors 1577:colon polyps 1565:premalignant 1541: 1540: 1495:hepatomegaly 1484: 1471:biosynthesis 1451: 1450: 1429:neurological 1416: 1414: 1395:deficiency, 1376: 1366: 1353: 1340: 1338: 1334: 1312: 1274: 1254: 1235:deficiency, 1212: 1211: 1206: 1205: 1200: 1199: 1188: 1180: 1176: 1172: 1168: 1167: 1161: 1157: 873: 854: 830: 811: 787: 768: 742: 723: 697: 678: 658: 653: 579:human ageing 502:heme binding 294: 287: 60:External IDs 5306:Complex III 4491:PDB gallery 1716:seed plants 1695:DNA barcode 1623:Subfamilies 1425:vision loss 1315:prokaryotes 1265:amino acids 1065:OPM protein 979:COX1 or COI 971:Identifiers 543:respirasome 352:gallbladder 38:Identifiers 5553:Categories 5326:Complex IV 5133:urea cycle 4821:metabolism 4797:metabolism 4795:tryptophan 4296:(2): 147. 3890:(2): 140. 3664:Aging Cell 3337:Aging Cell 2538:(1): 1–4. 2134:2018-08-13 1933:, May 2017 1912:, May 2017 1888:References 1830:homoplasmy 1787:epithelial 1728:soil fungi 1509:, delayed 1393:Complex IV 1386:idiopathic 1354:A related 1319:eukaryotes 1293:complex IV 1233:Complex IV 1226:idiopathic 1196:eukaryotes 1104:structures 298:(ortholog) 81:HomoloGene 5532:IPR000883 5510:see also 5256:Complex I 5064:Aconitase 2938:Neurology 2147:CC BY 4.0 1858:interacts 1772:cytoplasm 1679:IPR014241 1665:IPR014233 1651:IPR014207 1637:IPR004677 1597:myoglobin 1546:malignant 1499:hypotonia 1456:reduction 1378:Mutations 1330:1.10.3.10 1251:Structure 1014:PDOC00074 1002:IPR000883 876:NP_904330 644:Orthologs 390:esophagus 89:GeneCards 5528:InterPro 5210:Frataxin 5084:Fumarase 4750:proteins 4453:11553319 4408:11349229 4365:52850476 4357:11130070 4320:32212178 4312:10508508 4150:32964006 3999:28048453 3875:16678300 3835:29154948 3786:26321642 3735:18439415 3694:18691181 3520:14335558 3512:15138283 3477:11943860 3418:40639679 3410:11976216 3367:19878146 3318:25127143 3269:16407113 3210:21191537 3146:19909345 3105:12952648 3056:10577941 3007:15751226 2966:26776388 2958:10980727 2923:19218458 2864:16407113 2805:21304246 2797:16284789 2761:12140182 2603:23044391 2376:36428993 2261:23965338 2212:27899622 2149:license. 2094:(OMIM): 2076:22130576 2017:20860573 1929:– 1908:– 1874:turnover 1703:mutation 1674:InterPro 1660:InterPro 1646:InterPro 1632:InterPro 1527:neonatal 1487:myopathy 1439:, it is 1363:1.7.99.7 1271:Function 1121:RCSB PDB 997:InterPro 924:Wikidata 623:Sources: 528:membrane 356:appendix 328:duodenum 5370:MT-ATP8 5365:MT-ATP6 5285:MT-ND4L 4399:1226134 4337:Bibcode 4277:7530363 4245:Bibcode 4224:4358928 4216:7219535 4196:Bibcode 4179:6260957 4142:3921850 4122:Bibcode 4104:3764430 4084:Bibcode 4076:Science 4067:3472707 4042:1996112 3991:1757091 3961:1377597 3939:1322638 3930:1682694 3904:1301157 3826:5764226 3685:2659384 3645:5553400 3604:1715276 3566:2841036 3558:3170646 3445:Bibcode 3390:Bibcode 3358:2816353 3309:4471679 3260:1325106 3237:Bibcode 3201:3011097 3096:1698023 3047:1288397 2914:2651238 2891:Bibcode 2855:1325106 2832:Bibcode 2720:9851701 2685:9389715 2644:1322638 2635:1682694 2562:1248917 2554:8137905 2513:2824194 2464:6307356 2425:8013452 2368:8049679 2333:8083153 2252:4076475 2203:5210571 2056:Protist 2009:8638158 1989:Bibcode 1981:Science 1931:Ensembl 1910:Ensembl 1878:TMEM177 1870:MITRAC7 1854:complex 1707:species 1676::  1662::  1648::  1634::  1561:adenoma 1549:lesions 1467:ferrous 1300:1.9.3.1 1257:guanine 1185:protein 1183:) is a 1082:cd01663 1009:PROSITE 990:PF00115 756:UniProt 711:Ensembl 650:Species 629:QuickGO 414:jejunum 273:pattern 45:Aliases 5475:MT-TS2 5470:MT-TS1 5440:MT-TL2 5435:MT-TL1 5345:MT-CO3 5340:MT-CO2 5335:MT-CO1 5315:MT-CYB 5295:MT-ND6 5290:MT-ND5 5280:MT-ND4 5275:MT-ND3 5270:MT-ND2 5265:MT-ND1 5038:Matrix 4451:  4441:  4427:: 13. 4406:  4396:  4363:  4355:  4329:Nature 4318:  4310:  4275:  4265:  4222:  4214:  4188:Nature 4177:  4148:  4140:  4114:Nature 4102:  4065:  4040:  4033:369459 4030:  3997:  3989:  3959:  3937:  3927:  3902:  3873:  3833:  3823:  3784:  3733:  3692:  3682:  3643:  3602:  3564:  3556:  3518:  3510:  3475:  3468:122802 3465:  3416:  3408:  3365:  3355:  3316:  3306:  3267:  3257:  3208:  3198:  3144:  3103:  3093:  3054:  3044:  3005:  2964:  2956:  2921:  2911:  2862:  2852:  2803:  2795:  2759:  2718:  2683:  2642:  2632:  2601:  2560:  2552:  2511:  2504:553708 2501:  2462:  2423:  2416:395125 2413:  2374:  2366:  2331:  2324:196760 2321:  2259:  2249:  2210:  2200:  2096:516030 2074:  2015:  2007:  1866:SMIM20 1760:nuclei 1724:MT-CO1 1720:MT-CO1 1711:MT-CO1 1699:MT-CO1 1691:MT-CO1 1557:rectum 1542:MT-CO1 1521:, and 1460:ferric 1452:MT-CO1 1417:MT-CO1 1285:MT-CO3 1281:MT-CO2 1189:MT-CO1 1181:MT-CO1 1162:MT-CO1 1158:MT-CO1 1136:PDBsum 1110:  1100:  1034:SUPFAM 976:Symbol 910:search 908:PubMed 789:P00397 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Index

cyclooxygenase-1
Aliases
COX1
OMIM
516030
MGI
102504
HomoloGene
5016
GeneCards
COX1
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COX1 - orthologs
Human
Mitochondrial DNA (human)
Chr.
Mitochondrial DNA (human)
Band
bp
bp
Mouse
Mitochondrial DNA (mouse)
Chr.
Band
bp
bp
RNA expression
Bgee
Human
Mouse

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