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Cytochrome c oxidase subunit 2

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Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J (September 2001). "Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II
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Ostergaard E, Weraarpachai W, Ravn K, Born AP, Jønson L, Duno M, Wibrand F, Shoubridge EA, Vissing J (March 2015). "Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature".
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Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG (April 1981). "Sequence and organization of the human mitochondrial genome".
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Chomyn A, Mariottini P, Cleeter MW, Ragan CI, Matsuno-Yagi A, Hatefi Y, Doolittle RF, Attardi G (1985). "Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase".
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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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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 (October 2013).
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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".
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Polyak K, Li Y, Zhu H, Lengauer C, Willson JK, Markowitz SD, Trush MA, Kinzler KW, Vogelstein B (November 1998). "Somatic mutations of the mitochondrial genome in human colorectal tumours".
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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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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".
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Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM (May 1999).
1491:(mammals). The N-terminal domain of cytochrome C oxidase contains two transmembrane alpha-helices. The structure of MT-CO2 is known to contain one redox center and a 1319: 1198: 2431:"An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy" 1154: 1142: 4079: 3774: 764: 745: 150: 3769: 3860: 3442: 3528: 1901: 1110: 3337: 1883: 3286: 3066:
Kato MV (March 1999). "The mechanisms of death of an erythroleukemic cell line by p53: involvement of the microtubule and mitochondria".
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Montoya J, Ojala D, Attardi G (April 1981). "Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs".
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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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Torroni A, Achilli A, Macaulay V, Richards M, Bandelt HJ (June 2006). "Harvesting the fruit of the human mtDNA tree".
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Rossmanith W, Freilinger M, Roka J, Raffelsberger T, Moser-Thier K, Prayer D, Bernert G, Bittner RE (February 2008).
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Hill BC (April 1993). "The sequence of electron carriers in the reaction of cytochrome c oxidase with oxygen".
1647: 1435: 1399: 809: 138: 1327: 1206: 3670: 3457: 1543:. MT-CO2 is one of the three subunits which are responsible for the formation of the functional core of the 790: 1017: 3665: 3322: 1761: 4039: 3779: 3655: 3491: 3469: 1532: 1323: 1202: 2943:"Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs" 1511:
at 204. Several bacterial MT-CO2 have a C-terminal extension that contains a covalently bound haem c.
121:, mitochondrially encoded cytochrome c oxidase II, COII, MTCO2, Cytochrome c oxidase subunit II, CO II 3880: 3786: 3643: 3592: 3538: 3147: 2954: 2905: 2860: 2814: 2776: 2521: 1753: 1701: 1681: 1643: 1592: 1544: 1524: 1431: 1383: 1123: 1048: 2512:
Barrell BG, Bankier AT, Drouin J (November 1979). "A different genetic code in human mitochondria".
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of a single nucleotide (7630delT) in the gene has been found to cause symptoms of reversible
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Capaldi RA, Malatesta F, Darley-Usmar VM (July 1983). "Structure of cytochrome c oxidase".
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Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N (October 1999).
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and the major part of the protein is exposed to the periplasmic or to the mitochondrial
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A wide range of symptoms have been found in patients with pathogenic mutations in the
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is one of the three cytochrome c oxidase subunit mitochondrial genes (orange boxes).
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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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Proceedings of the National Academy of Sciences of the United States of America
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gene in patients have shown clinical manifestations such as progressive gait
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García-Horsman JA, Barquera B, Rumbley J, Ma J, Gennis RB (September 1994).
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affecting several tissues and organs. Other Clinical Manifestations include
1567:, respectively. MT-CO2 provides the substrate-binding site and contains the 1508: 1450: 1359: 709: 497: 375: 320: 307: 242: 229: 154: 3263: 3244: 3218: 3167: 3122: 3087: 2504: 2464: 2407: 2371: 2296: 2260: 1986: 3050: 3021: 2986: 2967: 2925: 2880: 2834: 2796: 2759: 2730: 2687: 2669: 2636: 2606: 2584: 2242: 2168: 2133: 2098: 2044: 1119: 1005: 1000: 3764: 3638: 3271: 2697:"Nucleotide sequence of human mitochondrial cytochrome c oxidase II cDNA" 2541: 2208: 2190: 1813: 1781: 1737: 1615: 1500: 1263: 1086: 989: 854: 835: 3924: 3919: 3839: 3228:"Major genomic mitochondrial lineages delineate early human expansions" 2994:
Ruvolo M, Zehr S, von Dornum M, Pan D, Chang B, Lin J (November 1993).
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Capaldi RA (1990). "Structure and function of cytochrome c oxidase".
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in MT-CO2, including glutamate 129, aspartate 132, and glutamate 19.
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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).
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Bodenteich A, Mitchell LG, Polymeropoulos MH, Merril CR (May 1992).
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This article incorporates text from this source, which is in the
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mutation (7587T>C) which altered the initiation codon of the
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Enzyme of the respiratory chain encoded by a mitochondrial gene
2338:"Isolated cytochrome c oxidase deficiency as a cause of MELAS" 2025:
Biochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics
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positive regulation of hydrogen peroxide biosynthetic process
30:"COX2" redirects here. For the cyclooxygenase isoenzyme, see 1666:, which may be caused by an abnormality or deficiency of 1571:, probably the primary acceptor in cytochrome c oxidase. 1716:(7896G>A) of the gene resulted in phenotypes such as 1559:. It contains two adjacent transmembrane regions in its 660:
mitochondrial electron transport, cytochrome c to oxygen
344: 2996:"Mitochondrial COII sequences and modern human origins" 2559:"Dinucleotide repeat in the human mitochondrial D-loop" 2005:
Cardiac Organellar Protein Atlas Knowledgebase (COPaKB)
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Power MD, Kiefer MC, Barr PJ, Reeves R (August 1989).
2065:"The superfamily of heme-copper respiratory oxidases" 1595:
deficiency, a deficiency in an enzyme complex of the
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Cytochrome c oxidase subunit II, transmembrane domain
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Cold Spring Harbor Symposia on Quantitative Biology
1927:"Entrez Gene: COX2 cytochrome c oxidase subunit II" 1333: 1313: 1295: 1290: 1274: 1262: 1250: 1242: 1237: 1233:
Cytochrome C oxidase subunit II, periplasmic domain
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dentate gyrus of hippocampal formation granule cell
1862: 1860: 1858: 1841: 1839: 1837: 1426:gene produces a 25.6 kDa protein composed of 227 291: 213: 1796:have also been associated with mutations in the 1422:at position 12 and it spans 683 base pairs. The 3183:Finnilä S, Lehtonen MS, Majamaa K (June 2001). 1812:by the utilization of a lysine ring around the 1483:. The enzyme complex consists of 3-4 subunits ( 1366:. Cytochrome c oxidase subunit II, abbreviated 680:positive regulation of ATP biosynthetic process 2227:"UniProt: the universal protein knowledgebase" 1867:GRCm38: Ensembl release 89: ENSMUSG00000064354 3287: 2058: 2056: 2054: 2018: 2016: 2014: 8: 1846:GRCh38: Ensembl release 89: ENSG00000198712 4080:United States National Library of Medicine 3805: 3775:Mitochondrial permeability transition pore 3757: 3597: 3426: 3316: 3294: 3280: 3272: 1287: 1166: 1041: 705: 675:positive regulation of necrotic cell death 619:mitochondrial respiratory chain complex IV 535: 332: 254: 174: 76: 3253: 3243: 3208: 3185:"Phylogenetic network for European mtDNA" 3112: 3011: 2976: 2966: 2720: 2677: 2574: 2454: 2361: 2250: 2149:Journal of Bioenergetics and Biomembranes 2088: 1976: 4078:This article incorporates text from the 3770:Mitochondrial membrane transport protein 1921: 1919: 1917: 1915: 1441:) (Complex IV), an oligomeric enzymatic 1025:gene in the human mitochondrial genome. 1016: 665:ATP synthesis coupled electron transport 1833: 1523:gene encodes for the second subunit of 3529:Cholesterol side-chain cleavage enzyme 1229: 1032: 36: 3013:10.1093/oxfordjournals.molbev.a040068 2319:"Mitochondrial complex IV deficiency" 1607:. The deficiency is characterized by 296: 280: 275: 218: 200: 195: 7: 1430:. MT-CO2 is a subunit of the enzyme 3443:Coenzyme Q – cytochrome c reductase 2126:10.1146/annurev.bi.59.070190.003033 1580:Mitochondrial complex IV deficiency 3629:Oxoglutarate dehydrogenase complex 3564:Glycerol-3-phosphate dehydrogenase 3189:American Journal of Human Genetics 2435:American Journal of Human Genetics 931: 912: 888: 869: 845: 826: 800: 781: 755: 736: 514: 432: 370: 349: 25: 3574:Carnitine palmitoyltransferase II 1808:MT-CO2 is known to interact with 1527:(complex IV), a component of the 3698:Carbamoyl phosphate synthetase I 3338:Long-chain-fatty-acid—CoA ligase 3333:Carnitine palmitoyltransferase I 2207: This article incorporates 2202: 2081:10.1128/jb.176.18.5587-5600.1994 2001:"Cytochrome c oxidase subunit 2" 1931: 1712:. Furthermore, a patient with a 1599:that catalyzes the oxidation of 1551:to the bimetallic center of the 267: 187: 3559:Glutamate aspartate transporter 3000:Molecular Biology and Evolution 2237:(D1): D158–D169. January 2017. 1597:mitochondrial respiratory chain 1529:mitochondrial respiratory chain 1493:binuclear copper A center (CuA) 1447:mitochondrial respiratory chain 3676:Pyruvate dehydrogenase complex 3634:Succinyl coenzyme A synthetase 2658:Molecular and Cellular Biology 1588:have been associated with the 1386:. It is also one of the three 1362:that is encoded by the MT-CO2 655:proton transmembrane transport 599:integral component of membrane 498:More reference expression data 406:right hemisphere of cerebellum 1: 2289:10.1136/jmedgenet-2014-102914 2114:Annual Review of Biochemistry 1969:10.1161/CIRCRESAHA.113.301151 1291:Available protein structures: 1170:Available protein structures: 573:cytochrome-c oxidase activity 418:muscle layer of sigmoid colon 3480:Dihydroorotate dehydrogenase 2037:10.1016/0304-4173(83)90003-4 1470:mitochondrial inner membrane 1449:involved in the transfer of 624:mitochondrial inner membrane 589:respiratory chain complex IV 3534:Steroid 11-beta-hydroxylase 2752:10.1101/sqb.1986.051.01.013 2342:Journal of Medical Genetics 2277:Journal of Medical Genetics 1624:hypertrophic cardiomyopathy 1382:, is the second subunit of 4131: 3708:N-Acetylglutamate synthase 3703:Ornithine transcarbamylase 3507:Glycerol phosphate shuttle 3373:monoamine neurotransmitter 1499:is located in a conserved 1390:(mtDNA) encoded subunits ( 386:mucosa of transverse colon 29: 4100:Human mitochondrial genes 4062: 3760: 3736: 3433:oxidative phosphorylation 3080:10.3109/10428199909093740 2497:10.1016/j.tig.2006.04.001 1902:"Mouse PubMed Reference:" 1884:"Human PubMed Reference:" 1569:binuclear copper A center 1557:binuclear copper A center 1286: 1165: 1040: 1004: 999: 995: 988: 972: 953: 938: 919: 908: 895: 876: 865: 852: 848: 833: 829: 820: 807: 803: 788: 784: 775: 762: 758: 743: 739: 730: 715: 708: 704: 688: 538: 534: 522: 517: 508: 495: 444: 435: 382: 373: 343: 335: 331: 314: 301: 287: 282:Mitochondrial DNA (mouse) 266: 257: 253: 236: 223: 209: 203:Mitochondrial DNA (human) 186: 177: 173: 128: 125: 115: 108: 103: 84: 79: 62: 57: 52: 48: 44: 39: 3624:Isocitrate dehydrogenase 3502:Malate-aspartate shuttle 2563:Human Molecular Genetics 1648:developmental disability 1507:positions and conserved 640:electron transport chain 3671:Glutamate dehydrogenase 3458:Succinate dehydrogenase 3068:Leukemia & Lymphoma 2789:10.1126/science.3764430 2354:10.1136/jmg.2007.052076 2069:Journal of Bacteriology 1662:is also known to cause 1414:gene is located on the 1352:Cytochrome c oxidase II 568:oxidoreductase activity 4115:Transmembrane proteins 4067:mitochondrial diseases 3666:Aspartate transaminase 3323:fatty acid degradation 3245:10.1186/1471-2156-2-13 2713:10.1093/nar/17.16.6734 2701:Nucleic Acids Research 2231:Nucleic Acids Research 1762:pigmentary retinopathy 1614:ranging from isolated 1400:respiratory complex IV 1030: 3780:Mitochondrial carrier 3656:anaplerotic reactions 3492:mitochondrial shuttle 3470:pyrimidine metabolism 2968:10.1073/pnas.92.2.532 2670:10.1128/MCB.11.3.1631 2576:10.1093/hmg/1.2.140-a 1575:Clinical significance 1461:. In eukaryotes this 1020: 966:Chr M: 0.01 – 0.01 Mb 959:Chr M: 0.01 – 0.01 Mb 614:extracellular exosome 3787:Translocator protein 3644:Malate dehydrogenase 3539:Aldosterone synthase 2211:available under the 1957:Circulation Research 1754:cognitive impairment 1702:exercise intolerance 1644:exercise intolerance 1545:cytochrome c oxidase 1525:cytochrome c oxidase 1503:loop at 196 and 200 1432:Cytochrome c oxidase 1384:cytochrome c oxidase 1049:cytochrome c oxidase 80:List of PDB id codes 53:Available structures 3399:Intermembrane space 3152:2000Natur.408..708I 2959:1995PNAS...92..532H 2910:1981Natur.290..465M 2865:1981Natur.290..457A 2819:1985Natur.314..592C 2781:1986Sci...234..614C 2526:1979Natur.282..189B 2388:Annals of Neurology 2243:10.1093/nar/gkw1099 1620:multisystem disease 1565:intermembrane space 1553:catalytic subunit 1 1531:that catalyzes the 1479:it is found in the 4082:, which is in the 3754:Other/to be sorted 3719:alcohol metabolism 3579:Uncoupling protein 3453:NADH dehydrogenase 2629:10.1007/bf00206061 2485:Trends in Genetics 2161:10.1007/bf00762853 1768:, and mild distal- 1730:skin abnormalities 1668:cytochrome oxidase 1656:mental retardation 1468:is located in the 1055:indicated by blue. 1031: 810:ENSMUSG00000064354 633:Biological process 582:Cellular component 563:copper ion binding 546:Molecular function 410:hippocampus proper 398:right frontal lobe 4074: 4073: 4058: 4057: 3801:Mitochondrial DNA 3795: 3794: 3749: 3748: 3604:citric acid cycle 3587: 3586: 3393: 3392: 3385:Monoamine oxidase 1714:nonsense mutation 1706:mental impairment 1686:deletion mutation 1652:motor development 1632:liver dysfunction 1555:by utilizing its 1420:mitochondrial DNA 1388:mitochondrial DNA 1349: 1348: 1345: 1344: 1340:structure summary 1228: 1227: 1224: 1223: 1219:structure summary 1015: 1014: 1011: 1010: 984: 983: 949: 948: 928: 927: 904: 903: 885: 884: 861: 860: 842: 841: 816: 815: 797: 796: 771: 770: 752: 751: 700: 699: 558:metal ion binding 530: 529: 526: 525: 504: 503: 491: 490: 429: 428: 402:nucleus accumbens 327: 326: 249: 248: 99: 98: 95: 94: 63:Ortholog search: 16:(Redirected from 4122: 4110:Protein families 3938: 3913: 3883: 3863: 3813: 3806: 3758: 3721: 3691: 3659: 3614:Citrate synthase 3607: 3598: 3552: 3522: 3495: 3473: 3436: 3427: 3407:Adenylate kinase 3378: 3354: 3326: 3317: 3296: 3289: 3282: 3273: 3267: 3257: 3247: 3222: 3212: 3179: 3160:10.1038/35047064 3146:(6813): 708–13. 3134: 3116: 3091: 3062: 3025: 3015: 2990: 2980: 2970: 2937: 2918:10.1038/290465a0 2904:(5806): 465–70. 2892: 2873:10.1038/290457a0 2859:(5806): 457–65. 2846: 2827:10.1038/314592a0 2800: 2763: 2734: 2724: 2691: 2681: 2648: 2610: 2588: 2578: 2553: 2534:10.1038/282189a0 2520:(5735): 189–94. 2508: 2469: 2468: 2458: 2426: 2420: 2419: 2400:10.1002/ana.1141 2382: 2376: 2375: 2365: 2333: 2327: 2326: 2315: 2309: 2308: 2271: 2265: 2264: 2254: 2223: 2217: 2206: 2200: 2198: 2197: 2187: 2181: 2180: 2144: 2138: 2137: 2109: 2103: 2102: 2092: 2075:(18): 5587–600. 2060: 2049: 2048: 2020: 2009: 2008: 1997: 1991: 1990: 1980: 1947: 1941: 1935: 1934: 1930: 1923: 1910: 1909: 1898: 1892: 1891: 1880: 1874: 1864: 1853: 1843: 1764:, a decrease in 1605:molecular oxygen 1288: 1230: 1167: 1045: 1033: 1021:Location of the 997: 996: 968: 961: 944: 932: 923: 913: 909:RefSeq (protein) 899: 889: 880: 870: 846: 827: 801: 782: 756: 737: 706: 645:response to cold 536: 515: 500: 448:ventricular zone 440: 438:Top expressed in 433: 414:substantia nigra 378: 376:Top expressed in 371: 350: 333: 323: 310: 299: 283: 271: 255: 245: 232: 221: 205: 191: 175: 169: 167:COX2 - orthologs 120: 113: 90: 77: 71: 50: 49: 37: 32:Cyclooxygenase-2 21: 4130: 4129: 4125: 4124: 4123: 4121: 4120: 4119: 4105:Protein domains 4090: 4089: 4075: 4070: 4054: 3934: 3929: 3909: 3904: 3879: 3874: 3859: 3854: 3809: 3791: 3745: 3732: 3717: 3712: 3685: 3680: 3653: 3648: 3601: 3583: 3548: 3543: 3519:steroidogenesis 3516: 3511: 3489: 3484: 3467: 3462: 3430: 3416: 3412:Creatine kinase 3389: 3375: 3370: 3365: 3347: 3342: 3320: 3306: 3300: 3270: 3225: 3182: 3137: 3101:Nature Genetics 3094: 3065: 3031:Nature Genetics 3028: 2993: 2940: 2895: 2849: 2813:(6012): 592–7. 2803: 2775:(4776): 614–8. 2766: 2737: 2694: 2651: 2613: 2601:(13): 3718–25. 2595:Cancer Research 2591: 2556: 2511: 2482: 2478: 2476:Further reading 2473: 2472: 2428: 2427: 2423: 2384: 2383: 2379: 2335: 2334: 2330: 2323:www.uniprot.org 2317: 2316: 2312: 2273: 2272: 2268: 2225: 2224: 2220: 2195: 2193: 2189: 2188: 2184: 2146: 2145: 2141: 2111: 2110: 2106: 2062: 2061: 2052: 2022: 2021: 2012: 1999: 1998: 1994: 1949: 1948: 1944: 1932: 1925: 1924: 1913: 1900: 1899: 1895: 1882: 1881: 1877: 1865: 1856: 1844: 1835: 1830: 1806: 1790:lactic acidosis 1778: 1664:Leigh's disease 1658:. Mutations of 1640:muscle weakness 1582: 1577: 1517: 1481:plasma membrane 1410:In humans, the 1408: 1143:OPM superfamily 1056: 1006:View/Edit Mouse 1001:View/Edit Human 964: 957: 954:Location (UCSC) 940: 921: 897: 878: 791:ENSG00000198712 684: 628: 577: 553:protein binding 496: 487: 482: 480:proximal tubule 478: 474: 470: 466: 462: 458: 454: 450: 436: 425: 420: 416: 412: 408: 404: 400: 396: 394:caudate nucleus 392: 388: 374: 318: 305: 297: 281: 258:Gene location ( 240: 227: 219: 201: 178:Gene location ( 129: 116: 109: 86: 64: 35: 28: 23: 22: 15: 12: 11: 5: 4128: 4126: 4118: 4117: 4112: 4107: 4102: 4092: 4091: 4072: 4071: 4063: 4060: 4059: 4056: 4055: 4053: 4052: 4047: 4042: 4037: 4032: 4027: 4022: 4017: 4012: 4007: 4002: 3997: 3992: 3987: 3982: 3977: 3972: 3967: 3962: 3957: 3952: 3947: 3941: 3939: 3931: 3930: 3928: 3927: 3922: 3916: 3914: 3906: 3905: 3903: 3902: 3897: 3892: 3886: 3884: 3876: 3875: 3873: 3872: 3866: 3864: 3856: 3855: 3853: 3852: 3847: 3842: 3837: 3832: 3827: 3822: 3816: 3814: 3803: 3797: 3796: 3793: 3792: 3790: 3789: 3784: 3783: 3782: 3777: 3767: 3761: 3755: 3751: 3750: 3747: 3746: 3744: 3743: 3737: 3734: 3733: 3731: 3730: 3724: 3722: 3714: 3713: 3711: 3710: 3705: 3700: 3694: 3692: 3682: 3681: 3679: 3678: 3673: 3668: 3662: 3660: 3650: 3649: 3647: 3646: 3641: 3636: 3631: 3626: 3621: 3616: 3610: 3608: 3595: 3589: 3588: 3585: 3584: 3582: 3581: 3576: 3571: 3566: 3561: 3555: 3553: 3545: 3544: 3542: 3541: 3536: 3531: 3525: 3523: 3513: 3512: 3510: 3509: 3504: 3498: 3496: 3486: 3485: 3483: 3482: 3476: 3474: 3464: 3463: 3461: 3460: 3455: 3450: 3445: 3439: 3437: 3424: 3422:Inner membrane 3418: 3417: 3415: 3414: 3409: 3403: 3401: 3395: 3394: 3391: 3390: 3388: 3387: 3381: 3379: 3367: 3366: 3364: 3363: 3357: 3355: 3344: 3343: 3341: 3340: 3335: 3329: 3327: 3314: 3312:Outer membrane 3308: 3307: 3301: 3299: 3298: 3291: 3284: 3276: 3269: 3268: 3223: 3201:10.1086/320591 3195:(6): 1475–84. 3180: 3135: 3092: 3074:(1–2): 181–6. 3063: 3026: 3006:(6): 1115–35. 2991: 2938: 2893: 2847: 2801: 2764: 2735: 2692: 2649: 2617:Human Genetics 2611: 2589: 2554: 2509: 2479: 2477: 2474: 2471: 2470: 2447:10.1086/302361 2421: 2377: 2328: 2310: 2266: 2218: 2182: 2139: 2104: 2050: 2010: 1992: 1963:(9): 1043–53. 1942: 1911: 1893: 1875: 1854: 1832: 1831: 1829: 1826: 1805: 1802: 1786:encephalopathy 1777: 1774: 1770:muscle wasting 1704:, progressive 1684:deficiency. A 1677:gene with the 1581: 1578: 1576: 1573: 1516: 1513: 1487:) to up to 13 1407: 1404: 1347: 1346: 1343: 1342: 1337: 1331: 1330: 1317: 1311: 1310: 1300: 1293: 1292: 1284: 1283: 1278: 1272: 1271: 1266: 1260: 1259: 1254: 1248: 1247: 1244: 1240: 1239: 1235: 1234: 1226: 1225: 1222: 1221: 1216: 1210: 1209: 1196: 1190: 1189: 1179: 1172: 1171: 1163: 1162: 1157: 1151: 1150: 1145: 1139: 1138: 1133: 1127: 1126: 1113: 1107: 1106: 1101: 1095: 1094: 1089: 1083: 1082: 1077: 1071: 1070: 1067: 1063: 1062: 1058: 1057: 1046: 1038: 1037: 1013: 1012: 1009: 1008: 1003: 993: 992: 986: 985: 982: 981: 979: 977: 970: 969: 962: 955: 951: 950: 947: 946: 936: 935: 929: 926: 925: 917: 916: 910: 906: 905: 902: 901: 893: 892: 886: 883: 882: 874: 873: 867: 863: 862: 859: 858: 850: 849: 843: 840: 839: 831: 830: 824: 818: 817: 814: 813: 805: 804: 798: 795: 794: 786: 785: 779: 773: 772: 769: 768: 760: 759: 753: 750: 749: 741: 740: 734: 728: 727: 722: 717: 713: 712: 702: 701: 698: 697: 686: 685: 683: 682: 677: 672: 667: 662: 657: 652: 647: 642: 636: 634: 630: 629: 627: 626: 621: 616: 611: 606: 601: 596: 591: 585: 583: 579: 578: 576: 575: 570: 565: 560: 555: 549: 547: 543: 542: 532: 531: 528: 527: 524: 523: 520: 519: 512: 506: 505: 502: 501: 493: 492: 489: 488: 486: 485: 481: 477: 473: 469: 465: 461: 457: 453: 449: 445: 442: 441: 430: 427: 426: 424: 423: 419: 415: 411: 407: 403: 399: 395: 391: 387: 383: 380: 379: 367: 366: 358: 347: 341: 340: 337:RNA expression 329: 328: 325: 324: 316: 312: 311: 303: 300: 295: 289: 288: 285: 284: 279: 273: 272: 264: 263: 251: 250: 247: 246: 238: 234: 233: 225: 222: 217: 211: 210: 207: 206: 199: 193: 192: 184: 183: 171: 170: 127: 123: 122: 114: 106: 105: 101: 100: 97: 96: 93: 92: 82: 81: 73: 72: 61: 55: 54: 46: 45: 42: 41: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 4127: 4116: 4113: 4111: 4108: 4106: 4103: 4101: 4098: 4097: 4095: 4088: 4087: 4085: 4084:public domain 4081: 4069: 4068: 4061: 4051: 4048: 4046: 4043: 4041: 4038: 4036: 4033: 4031: 4028: 4026: 4023: 4021: 4018: 4016: 4013: 4011: 4008: 4006: 4003: 4001: 3998: 3996: 3993: 3991: 3988: 3986: 3983: 3981: 3978: 3976: 3973: 3971: 3968: 3966: 3963: 3961: 3958: 3956: 3953: 3951: 3948: 3946: 3943: 3942: 3940: 3937: 3932: 3926: 3923: 3921: 3918: 3917: 3915: 3912: 3907: 3901: 3898: 3896: 3893: 3891: 3888: 3887: 3885: 3882: 3877: 3871: 3868: 3867: 3865: 3862: 3857: 3851: 3848: 3846: 3843: 3841: 3838: 3836: 3833: 3831: 3828: 3826: 3823: 3821: 3818: 3817: 3815: 3812: 3807: 3804: 3802: 3798: 3788: 3785: 3781: 3778: 3776: 3773: 3772: 3771: 3768: 3766: 3763: 3762: 3759: 3756: 3752: 3742: 3739: 3738: 3735: 3729: 3726: 3725: 3723: 3720: 3715: 3709: 3706: 3704: 3701: 3699: 3696: 3695: 3693: 3690: 3689: 3683: 3677: 3674: 3672: 3669: 3667: 3664: 3663: 3661: 3658: 3657: 3651: 3645: 3642: 3640: 3637: 3635: 3632: 3630: 3627: 3625: 3622: 3620: 3617: 3615: 3612: 3611: 3609: 3606: 3605: 3599: 3596: 3594: 3590: 3580: 3577: 3575: 3572: 3570: 3567: 3565: 3562: 3560: 3557: 3556: 3554: 3551: 3546: 3540: 3537: 3535: 3532: 3530: 3527: 3526: 3524: 3521: 3520: 3514: 3508: 3505: 3503: 3500: 3499: 3497: 3494: 3493: 3487: 3481: 3478: 3477: 3475: 3472: 3471: 3465: 3459: 3456: 3454: 3451: 3449: 3446: 3444: 3441: 3440: 3438: 3435: 3434: 3428: 3425: 3423: 3419: 3413: 3410: 3408: 3405: 3404: 3402: 3400: 3396: 3386: 3383: 3382: 3380: 3377: 3374: 3368: 3362: 3359: 3358: 3356: 3353: 3351: 3345: 3339: 3336: 3334: 3331: 3330: 3328: 3325: 3324: 3318: 3315: 3313: 3309: 3304: 3303:Mitochondrial 3297: 3292: 3290: 3285: 3283: 3278: 3277: 3274: 3265: 3261: 3256: 3251: 3246: 3241: 3237: 3233: 3229: 3224: 3220: 3216: 3211: 3206: 3202: 3198: 3194: 3190: 3186: 3181: 3177: 3173: 3169: 3165: 3161: 3157: 3153: 3149: 3145: 3141: 3136: 3132: 3128: 3124: 3120: 3115: 3114:10.1038/13779 3110: 3106: 3102: 3098: 3093: 3089: 3085: 3081: 3077: 3073: 3069: 3064: 3060: 3056: 3052: 3048: 3044: 3040: 3036: 3032: 3027: 3023: 3019: 3014: 3009: 3005: 3001: 2997: 2992: 2988: 2984: 2979: 2974: 2969: 2964: 2960: 2956: 2952: 2948: 2944: 2939: 2935: 2931: 2927: 2923: 2919: 2915: 2911: 2907: 2903: 2899: 2894: 2890: 2886: 2882: 2878: 2874: 2870: 2866: 2862: 2858: 2854: 2848: 2844: 2840: 2836: 2832: 2828: 2824: 2820: 2816: 2812: 2808: 2802: 2798: 2794: 2790: 2786: 2782: 2778: 2774: 2770: 2765: 2761: 2757: 2753: 2749: 2746:(1): 103–14. 2745: 2741: 2736: 2732: 2728: 2723: 2718: 2714: 2710: 2706: 2702: 2698: 2693: 2689: 2685: 2680: 2675: 2671: 2667: 2664:(3): 1631–7. 2663: 2659: 2655: 2650: 2646: 2642: 2638: 2634: 2630: 2626: 2623:(2): 139–45. 2622: 2618: 2612: 2608: 2604: 2600: 2596: 2590: 2586: 2582: 2577: 2572: 2568: 2564: 2560: 2555: 2551: 2547: 2543: 2539: 2535: 2531: 2527: 2523: 2519: 2515: 2510: 2506: 2502: 2498: 2494: 2491:(6): 339–45. 2490: 2486: 2481: 2480: 2475: 2466: 2462: 2457: 2452: 2448: 2444: 2441:(5): 1330–9. 2440: 2436: 2432: 2425: 2422: 2417: 2413: 2409: 2405: 2401: 2397: 2394:(3): 409–13. 2393: 2389: 2381: 2378: 2373: 2369: 2364: 2359: 2355: 2351: 2348:(2): 117–21. 2347: 2343: 2339: 2332: 2329: 2324: 2320: 2314: 2311: 2306: 2302: 2298: 2294: 2290: 2286: 2282: 2278: 2270: 2267: 2262: 2258: 2253: 2248: 2244: 2240: 2236: 2232: 2228: 2222: 2219: 2216: 2214: 2210: 2205: 2192: 2186: 2183: 2178: 2174: 2170: 2166: 2162: 2158: 2155:(2): 115–20. 2154: 2150: 2143: 2140: 2135: 2131: 2127: 2123: 2119: 2115: 2108: 2105: 2100: 2096: 2091: 2086: 2082: 2078: 2074: 2070: 2066: 2059: 2057: 2055: 2051: 2046: 2042: 2038: 2034: 2031:(2): 135–48. 2030: 2026: 2019: 2017: 2015: 2011: 2006: 2002: 1996: 1993: 1988: 1984: 1979: 1974: 1970: 1966: 1962: 1958: 1954: 1946: 1943: 1939: 1938:public domain 1928: 1922: 1920: 1918: 1916: 1912: 1907: 1903: 1897: 1894: 1889: 1885: 1879: 1876: 1872: 1868: 1863: 1861: 1859: 1855: 1851: 1847: 1842: 1840: 1838: 1834: 1827: 1825: 1823: 1819: 1815: 1811: 1803: 1801: 1799: 1795: 1791: 1787: 1783: 1775: 1773: 1771: 1767: 1763: 1759: 1758:optic atrophy 1755: 1751: 1747: 1743: 1742:heteroplasmic 1739: 1736:, and normal 1735: 1731: 1727: 1723: 1719: 1718:short stature 1715: 1711: 1707: 1703: 1699: 1695: 1691: 1687: 1683: 1680: 1679:mitochondrial 1676: 1671: 1669: 1665: 1661: 1657: 1653: 1649: 1645: 1641: 1637: 1633: 1629: 1625: 1621: 1617: 1613: 1610: 1609:heterogeneous 1606: 1602: 1598: 1594: 1591: 1590:mitochondrial 1587: 1579: 1574: 1572: 1570: 1566: 1562: 1558: 1554: 1550: 1546: 1542: 1538: 1534: 1530: 1526: 1522: 1514: 1512: 1510: 1506: 1502: 1498: 1494: 1490: 1486: 1482: 1478: 1475: 1471: 1467: 1464: 1460: 1456: 1452: 1448: 1444: 1440: 1437: 1433: 1429: 1425: 1421: 1417: 1413: 1405: 1403: 1401: 1397: 1393: 1389: 1385: 1381: 1377: 1373: 1369: 1365: 1361: 1357: 1353: 1341: 1338: 1336: 1332: 1329: 1325: 1321: 1318: 1316: 1312: 1308: 1304: 1301: 1298: 1294: 1289: 1285: 1282: 1279: 1277: 1273: 1270: 1267: 1265: 1261: 1258: 1255: 1253: 1249: 1245: 1241: 1236: 1231: 1220: 1217: 1215: 1211: 1208: 1204: 1200: 1197: 1195: 1191: 1187: 1183: 1180: 1177: 1173: 1168: 1164: 1161: 1158: 1156: 1152: 1149: 1146: 1144: 1140: 1137: 1134: 1132: 1128: 1125: 1121: 1117: 1114: 1112: 1108: 1105: 1102: 1100: 1096: 1093: 1090: 1088: 1084: 1081: 1078: 1076: 1072: 1068: 1064: 1059: 1054: 1050: 1044: 1039: 1034: 1028: 1024: 1019: 1007: 1002: 998: 994: 991: 987: 980: 978: 975: 971: 967: 963: 960: 956: 952: 945: 943: 937: 933: 930: 924: 918: 914: 911: 907: 900: 894: 890: 887: 881: 875: 871: 868: 866:RefSeq (mRNA) 864: 857: 856: 851: 847: 844: 838: 837: 832: 828: 825: 823: 819: 812: 811: 806: 802: 799: 793: 792: 787: 783: 780: 778: 774: 767: 766: 761: 757: 754: 748: 747: 742: 738: 735: 733: 729: 726: 723: 721: 718: 714: 711: 707: 703: 696: 692: 687: 681: 678: 676: 673: 671: 668: 666: 663: 661: 658: 656: 653: 651: 648: 646: 643: 641: 638: 637: 635: 632: 631: 625: 622: 620: 617: 615: 612: 610: 607: 605: 604:mitochondrion 602: 600: 597: 595: 592: 590: 587: 586: 584: 581: 580: 574: 571: 569: 566: 564: 561: 559: 556: 554: 551: 550: 548: 545: 544: 541: 540:Gene ontology 537: 533: 521: 516: 513: 511: 507: 499: 494: 483: 479: 475: 471: 467: 463: 459: 455: 451: 447: 446: 443: 439: 434: 431: 421: 417: 413: 409: 405: 401: 397: 393: 389: 385: 384: 381: 377: 372: 369: 368: 365: 363: 359: 357: 356: 352: 351: 348: 346: 342: 338: 334: 330: 322: 317: 313: 309: 304: 294: 290: 286: 278: 274: 270: 265: 261: 256: 252: 244: 239: 235: 231: 226: 216: 212: 208: 204: 198: 194: 190: 185: 181: 176: 172: 168: 164: 160: 156: 152: 148: 144: 140: 136: 132: 124: 119: 112: 107: 102: 91: 89: 83: 78: 75: 74: 70: 67: 60: 56: 51: 47: 43: 38: 33: 19: 4077: 4076: 4064: 3911:ATP synthase 3718: 3686: 3654: 3602: 3569:ATP synthase 3549: 3517: 3490: 3468: 3448:Cytochrome c 3431: 3371: 3361:Kynureninase 3348: 3321: 3235: 3232:BMC Genetics 3231: 3192: 3188: 3143: 3139: 3104: 3100: 3071: 3067: 3043:10.1038/3108 3037:(3): 291–3. 3034: 3030: 3003: 2999: 2953:(2): 532–6. 2950: 2946: 2901: 2897: 2856: 2852: 2810: 2806: 2772: 2768: 2743: 2739: 2707:(16): 6734. 2704: 2700: 2661: 2657: 2620: 2616: 2598: 2594: 2566: 2562: 2517: 2513: 2488: 2484: 2438: 2434: 2424: 2391: 2387: 2380: 2345: 2341: 2331: 2322: 2313: 2283:(3): 203–7. 2280: 2276: 2269: 2234: 2230: 2221: 2201: 2194:. Retrieved 2185: 2152: 2148: 2142: 2117: 2113: 2107: 2072: 2068: 2028: 2024: 2004: 1995: 1960: 1956: 1945: 1905: 1896: 1887: 1878: 1822:cytochrome c 1810:cytochrome c 1807: 1804:Interactions 1797: 1779: 1766:color vision 1756:, bilateral 1745: 1726:microcephaly 1708:, and short 1674: 1672: 1659: 1628:hepatomegaly 1601:cytochrome c 1585: 1584:Variants of 1583: 1549:cytochrome c 1520: 1518: 1489:polypeptides 1455:cytochrome c 1423: 1411: 1409: 1379: 1375: 1371: 1367: 1351: 1350: 1052: 1026: 1022: 939: 920: 896: 877: 853: 834: 808: 789: 763: 744: 724: 719: 476:right kidney 460:zone of skin 422:hypothalamus 360: 353: 126:External IDs 85: 3861:Complex III 1816:containing 1698:hemianopsia 1694:hemiparesis 1485:prokaryotes 1477:prokaryotes 1428:amino acids 1238:Identifiers 1155:OPM protein 1061:Identifiers 594:respirasome 104:Identifiers 4094:Categories 3881:Complex IV 3688:urea cycle 3376:metabolism 3352:metabolism 3350:tryptophan 3107:(2): 147. 2569:(2): 140. 2196:2018-08-07 2120:: 569–96. 1873:, May 2017 1852:, May 2017 1828:References 1740:. A novel 1682:Complex IV 1650:, delayed 1618:to severe 1612:phenotypes 1603:utilizing 1593:Complex IV 1561:N-terminus 1505:amino acid 1394:, MT-CO2, 1360:eukaryotes 1303:structures 1182:structures 1053:Subunit II 1047:Bacterial 364:(ortholog) 147:HomoloGene 4065:see also 3811:Complex I 3619:Aconitase 2213:CC BY 4.0 1818:heme edge 1780:Juvenile 1734:hypotonia 1732:, severe 1636:hypotonia 1533:reduction 1509:histidine 1451:electrons 1406:Structure 1269:IPR002429 1104:PDOC00075 1092:IPR011759 1051:complex. 942:NP_904331 710:Orthologs 650:lactation 456:esophagus 155:GeneCards 3765:Frataxin 3639:Fumarase 3305:proteins 3264:11553319 3219:11349229 3176:52850476 3168:11130070 3131:32212178 3123:10508508 3088:10194136 3059:19786796 2843:32964006 2645:28048453 2505:16678300 2465:10205264 2416:23891106 2408:11558799 2372:18245391 2305:43018915 2297:25604084 2261:27899622 2215:license. 2177:45975377 1987:23965338 1869:– 1848:– 1814:carboxyl 1782:myopathy 1738:reflexes 1692:, right 1616:myopathy 1515:Function 1501:cysteine 1320:RCSB PDB 1264:InterPro 1199:RCSB PDB 1087:InterPro 990:Wikidata 689:Sources: 609:membrane 484:duodenum 468:epiblast 3925:MT-ATP8 3920:MT-ATP6 3840:MT-ND4L 3210:1226134 3148:Bibcode 3051:9806551 3022:8277847 2987:7530363 2955:Bibcode 2934:4358928 2926:7219535 2906:Bibcode 2889:4355527 2881:7219534 2861:Bibcode 2835:3921850 2815:Bibcode 2797:3764430 2777:Bibcode 2769:Science 2760:3472707 2731:2550900 2688:1996112 2637:1757091 2607:1377597 2585:1301157 2550:4335828 2522:Bibcode 2456:1377869 2386:gene". 2363:3027970 2252:5210571 2169:8389744 2134:2165384 2099:8083153 2045:6307356 1978:4076475 1871:Ensembl 1850:Ensembl 1710:stature 1690:aphasia 1474:aerobic 1466:complex 1445:of the 1443:complex 1439:1.9.3.1 1356:protein 1281:cd13912 1257:PF00116 1099:PROSITE 1080:PF02790 1069:COX2_TM 822:UniProt 777:Ensembl 716:Species 695:QuickGO 472:jejunum 390:putamen 339:pattern 111:Aliases 4030:MT-TS2 4025:MT-TS1 3995:MT-TL2 3990:MT-TL1 3900:MT-CO3 3895:MT-CO2 3890:MT-CO1 3870:MT-CYB 3850:MT-ND6 3845:MT-ND5 3835:MT-ND4 3830:MT-ND3 3825:MT-ND2 3820:MT-ND1 3593:Matrix 3262:  3252:  3238:: 13. 3217:  3207:  3174:  3166:  3140:Nature 3129:  3121:  3086:  3057:  3049:  3020:  2985:  2975:  2932:  2924:  2898:Nature 2887:  2879:  2853:Nature 2841:  2833:  2807:Nature 2795:  2758:  2729:  2722:318375 2719:  2686:  2679:369459 2676:  2643:  2635:  2605:  2583:  2548:  2542:226894 2540:  2514:Nature 2503:  2463:  2453:  2414:  2406:  2370:  2360:  2303:  2295:  2259:  2249:  2175:  2167:  2132:  2097:  2090:196760 2087:  2043:  1985:  1975:  1800:gene. 1798:MT-CO2 1794:stroke 1792:, and 1776:Others 1750:ataxia 1746:MT-CO2 1722:weight 1720:, low 1675:MT-CO2 1660:MT-CO2 1586:MT-CO2 1537:oxygen 1521:MT-CO2 1495:. The 1463:enzyme 1459:oxygen 1424:MT-CO2 1412:MT-CO2 1396:MT-CO3 1392:MT-CO1 1380:MT-CO2 1335:PDBsum 1309:  1299:  1243:Symbol 1214:PDBsum 1188:  1178:  1124:SUPFAM 1066:Symbol 1027:MT-CO2 1023:MT-CO2 976:search 974:PubMed 855:P00405 836:P00403 732:Entrez 510:BioGPS 319:7,696 306:7,013 241:8,269 228:7,586 143:102503 135:516040 18:MT-CO2 4050:MT-TY 4045:MT-TW 4040:MT-TV 4035:MT-TT 4020:MT-TR 4015:MT-TQ 4010:MT-TP 4005:MT-TN 4000:MT-TM 3985:MT-TK 3980:MT-TI 3975:MT-TH 3970:MT-TG 3965:MT-TF 3960:MT-TE 3955:MT-TD 3950:MT-TC 3945:MT-TA 3741:PMPCB 3728:ALDH2 3550:other 3255:55343 3172:S2CID 3127:S2CID 3055:S2CID 2978:42775 2930:S2CID 2885:S2CID 2839:S2CID 2641:S2CID 2546:S2CID 2412:S2CID 2301:S2CID 2173:S2CID 1541:water 1472:; in 1453:from 1416:p arm 1398:) of 1378:, or 1368:COXII 1354:is a 1136:3.D.4 1120:SCOPe 1111:SCOP2 765:17709 725:Mouse 720:Human 691:Amigo 464:ovary 362:Mouse 355:Human 302:Start 260:Mouse 224:Start 180:Human 3936:tRNA 3260:PMID 3215:PMID 3164:PMID 3119:PMID 3084:PMID 3047:PMID 3018:PMID 2983:PMID 2922:PMID 2877:PMID 2831:PMID 2793:PMID 2756:PMID 2727:PMID 2684:PMID 2633:PMID 2603:PMID 2581:PMID 2538:PMID 2501:PMID 2461:PMID 2404:PMID 2368:PMID 2293:PMID 2257:PMID 2209:text 2165:PMID 2130:PMID 2095:PMID 2041:PMID 1983:PMID 1654:and 1630:and 1519:The 1376:COII 1372:COX2 1364:gene 1328:PDBj 1324:PDBe 1307:ECOD 1297:Pfam 1252:Pfam 1246:COX2 1207:PDBj 1203:PDBe 1186:ECOD 1176:Pfam 1160:1v55 1131:TCDB 1116:1occ 1075:Pfam 746:4513 345:Bgee 293:Band 277:Chr. 215:Band 197:Chr. 159:COX2 151:5017 131:OMIM 118:COX2 88:3VRJ 69:RCSB 66:PDBe 40:COX2 3250:PMC 3240:doi 3205:PMC 3197:doi 3156:doi 3144:408 3109:doi 3076:doi 3039:doi 3008:doi 2973:PMC 2963:doi 2914:doi 2902:290 2869:doi 2857:290 2823:doi 2811:314 2785:doi 2773:234 2748:doi 2717:PMC 2709:doi 2674:PMC 2666:doi 2625:doi 2571:doi 2530:doi 2518:282 2493:doi 2451:PMC 2443:doi 2396:doi 2358:PMC 2350:doi 2285:doi 2247:PMC 2239:doi 2157:doi 2122:doi 2085:PMC 2077:doi 2073:176 2033:doi 2029:726 1973:PMC 1965:doi 1961:113 1820:of 1539:to 1535:of 1497:CuA 1457:to 1418:of 1358:in 1315:PDB 1276:CDD 1194:PDB 922:n/a 898:n/a 879:n/a 518:n/a 315:End 298:n/a 237:End 220:n/a 163:OMA 139:MGI 59:PDB 4096:: 3258:. 3248:. 3234:. 3230:. 3213:. 3203:. 3193:68 3191:. 3187:. 3170:. 3162:. 3154:. 3142:. 3125:. 3117:. 3105:23 3103:. 3099:. 3082:. 3072:33 3070:. 3053:. 3045:. 3035:20 3033:. 3016:. 3004:10 3002:. 2998:. 2981:. 2971:. 2961:. 2951:92 2949:. 2945:. 2928:. 2920:. 2912:. 2900:. 2883:. 2875:. 2867:. 2855:. 2837:. 2829:. 2821:. 2809:. 2791:. 2783:. 2771:. 2754:. 2744:51 2742:. 2725:. 2715:. 2705:17 2703:. 2699:. 2682:. 2672:. 2662:11 2660:. 2656:. 2639:. 2631:. 2621:88 2619:. 2599:52 2597:. 2579:. 2565:. 2561:. 2544:. 2536:. 2528:. 2516:. 2499:. 2489:22 2487:. 2459:. 2449:. 2439:64 2437:. 2433:. 2410:. 2402:. 2392:50 2390:. 2366:. 2356:. 2346:45 2344:. 2340:. 2321:. 2299:. 2291:. 2281:52 2279:. 2255:. 2245:. 2235:45 2233:. 2229:. 2171:. 2163:. 2153:25 2151:. 2128:. 2118:59 2116:. 2093:. 2083:. 2071:. 2067:. 2053:^ 2039:. 2027:. 2013:^ 2003:. 1981:. 1971:. 1959:. 1955:. 1914:^ 1904:. 1886:. 1857:^ 1836:^ 1788:, 1784:, 1772:. 1760:, 1752:, 1728:, 1724:, 1700:, 1696:, 1670:. 1646:, 1642:, 1638:, 1634:, 1626:, 1436:EC 1402:. 1374:, 1370:, 1326:; 1322:; 1305:/ 1205:; 1201:; 1184:/ 1122:/ 1118:/ 693:/ 321:bp 308:bp 243:bp 230:bp 161:; 157:: 153:; 149:: 145:; 141:: 137:; 133:: 4086:. 3295:e 3288:t 3281:v 3266:. 3242:: 3236:2 3221:. 3199:: 3178:. 3158:: 3150:: 3133:. 3111:: 3090:. 3078:: 3061:. 3041:: 3024:. 3010:: 2989:. 2965:: 2957:: 2936:. 2916:: 2908:: 2891:. 2871:: 2863:: 2845:. 2825:: 2817:: 2799:. 2787:: 2779:: 2762:. 2750:: 2733:. 2711:: 2690:. 2668:: 2647:. 2627:: 2609:. 2587:. 2573:: 2567:1 2552:. 2532:: 2524:: 2507:. 2495:: 2467:. 2445:: 2418:. 2398:: 2374:. 2352:: 2325:. 2307:. 2287:: 2263:. 2241:: 2199:. 2179:. 2159:: 2136:. 2124:: 2101:. 2079:: 2047:. 2035:: 2007:. 1989:. 1967:: 1940:. 1929:. 1908:. 1890:. 1434:( 1148:4 262:) 182:) 165:: 34:. 20:)

Index

MT-CO2
Cyclooxygenase-2
PDB
PDBe
RCSB
3VRJ
Aliases
COX2
OMIM
516040
MGI
102503
HomoloGene
5017
GeneCards
COX2
OMA
COX2 - orthologs
Human
Mitochondrial DNA (human)
Chr.
Mitochondrial DNA (human)
Band
bp
bp
Mouse
Mitochondrial DNA (mouse)
Chr.
Band
bp

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