Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 102


Defects in the biosynthesis of mitochondrial heme c and heme a in yeast and mammals.

Moraes CT, Diaz F, Barrientos A.

Biochim Biophys Acta. 2004 Dec 6;1659(2-3):153-9. Review.


Regulation of the heme A biosynthetic pathway in Saccharomyces cerevisiae.

Barros MH, Tzagoloff A.

FEBS Lett. 2002 Apr 10;516(1-3):119-23.


Regulation of the heme A biosynthetic pathway: differential regulation of heme A synthase and heme O synthase in Saccharomyces cerevisiae.

Wang Z, Wang Y, Hegg EL.

J Biol Chem. 2009 Jan 9;284(2):839-47. doi: 10.1074/jbc.M804167200. Epub 2008 Oct 24.


Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.

Antonicka H, Leary SC, Guercin GH, Agar JN, Horvath R, Kennaway NG, Harding CO, Jaksch M, Shoubridge EA.

Hum Mol Genet. 2003 Oct 15;12(20):2693-702. Epub 2003 Aug 19.


The role of Coa2 in hemylation of yeast Cox1 revealed by its genetic interaction with Cox10.

Bestwick M, Khalimonchuk O, Pierrel F, Winge DR.

Mol Cell Biol. 2010 Jan;30(1):172-85. doi: 10.1128/MCB.00869-09.


On the functions of the yeast COX10 and COX11 gene products.

Tzagoloff A, Nobrega M, Gorman N, Sinclair P.

Biochem Mol Biol Int. 1993 Nov;31(3):593-8.


Analysis of Oligomerization Properties of Heme a Synthase Provides Insights into Its Function in Eukaryotes.

Swenson S, Cannon A, Harris NJ, Taylor NG, Fox JL, Khalimonchuk O.

J Biol Chem. 2016 May 6;291(19):10411-25. doi: 10.1074/jbc.M115.707539. Epub 2016 Mar 3.


A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency.

Valnot I, von Kleist-Retzow JC, Barrientos A, Gorbatyuk M, Taanman JW, Mehaye B, Rustin P, Tzagoloff A, Munnich A, Rötig A.

Hum Mol Genet. 2000 May 1;9(8):1245-9.


Oligomerization of heme o synthase in cytochrome oxidase biogenesis is mediated by cytochrome oxidase assembly factor Coa2.

Khalimonchuk O, Kim H, Watts T, Perez-Martinez X, Winge DR.

J Biol Chem. 2012 Aug 3;287(32):26715-26. doi: 10.1074/jbc.M112.377200. Epub 2012 Jun 5.


Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy.

Antonicka H, Mattman A, Carlson CG, Glerum DM, Hoffbuhr KC, Leary SC, Kennaway NG, Shoubridge EA.

Am J Hum Genet. 2003 Jan;72(1):101-14. Epub 2002 Dec 9.


The heme a synthase Cox15 associates with cytochrome c oxidase assembly intermediates during Cox1 maturation.

Bareth B, Dennerlein S, Mick DU, Nikolov M, Urlaub H, Rehling P.

Mol Cell Biol. 2013 Oct;33(20):4128-37. doi: 10.1128/MCB.00747-13. Epub 2013 Aug 26.


Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1.

Williams SL, Valnot I, Rustin P, Taanman JW.

J Biol Chem. 2004 Feb 27;279(9):7462-9. Epub 2003 Nov 7.


The Assembly Factor Pet117 Couples Heme a Synthase Activity to Cytochrome Oxidase Assembly.

Taylor NG, Swenson S, Harris NJ, Germany EM, Fox JL, Khalimonchuk O.

J Biol Chem. 2017 Feb 3;292(5):1815-1825. doi: 10.1074/jbc.M116.766980. Epub 2016 Dec 20.


Mitochondrial ferredoxin is required for heme A synthesis in Saccharomyces cerevisiae.

Barros MH, Nobrega FG, Tzagoloff A.

J Biol Chem. 2002 Mar 22;277(12):9997-10002. Epub 2002 Jan 11.


Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O.

Barros MH, Carlson CG, Glerum DM, Tzagoloff A.

FEBS Lett. 2001 Mar 9;492(1-2):133-8.


CCDC90A (MCUR1) is a cytochrome c oxidase assembly factor and not a regulator of the mitochondrial calcium uniporter.

Paupe V, Prudent J, Dassa EP, Rendon OZ, Shoubridge EA.

Cell Metab. 2015 Jan 6;21(1):109-16. doi: 10.1016/j.cmet.2014.12.004.


Cytochrome c oxidase is required for the assembly/stability of respiratory complex I in mouse fibroblasts.

Diaz F, Fukui H, Garcia S, Moraes CT.

Mol Cell Biol. 2006 Jul;26(13):4872-81.


Mitochondrial cytochrome c synthase: CP motifs are not necessary for heme attachment to apocytochrome c.

Moore RL, Stevens JM, Ferguson SJ.

FEBS Lett. 2011 Nov 4;585(21):3415-9. doi: 10.1016/j.febslet.2011.08.042. Epub 2011 Sep 6.


COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthood.

Pitceathly RD, Taanman JW, Rahman S, Meunier B, Sadowski M, Cirak S, Hargreaves I, Land JM, Nanji T, Polke JM, Woodward CE, Sweeney MG, Solanki S, Foley AR, Hurles ME, Stalker J, Blake J, Holton JL, Phadke R, Muntoni F, Reilly MM, Hanna MG; UK10K Consortium.

JAMA Neurol. 2013 Dec;70(12):1556-61. doi: 10.1001/jamaneurol.2013.3242.


Supplemental Content

Support Center