Protein-mediated assembly of succinate dehydrogenase and its cofactors
暂无分享,去创建一个
[1] R. Lill,et al. Specialized function of yeast Isa1 and Isa2 proteins in the maturation of mitochondrial [4Fe-4S] proteins. , 2017, The Journal of Biological Chemistry.
[2] S. Uribe-Carvajal,et al. The Saccharomyces cerevisiae mitochondrial unselective channel behaves as a physiological uncoupling system regulated by Ca2+, Mg2+, phosphate and ATP , 2015, Journal of Bioenergetics and Biomembranes.
[3] S. Gygi,et al. SDHAF4 promotes mitochondrial succinate dehydrogenase activity and prevents neurodegeneration. , 2014, Cell metabolism.
[4] C. Thummel,et al. The LYR factors SDHAF1 and SDHAF3 mediate maturation of the iron-sulfur subunit of succinate dehydrogenase. , 2014, Cell metabolism.
[5] L. Banci,et al. [2Fe-2S] cluster transfer in iron–sulfur protein biogenesis , 2014, Proceedings of the National Academy of Sciences.
[6] Asako Kounosu. Analysis of covalent flavinylation using thermostable succinate dehydrogenase from Thermus thermophilus and Sulfolobus tokodaii lacking SdhE homologs , 2014, FEBS letters.
[7] Anamika Singh,et al. Cochaperone binding to LYR motifs confers specificity of iron sulfur cluster delivery. , 2014, Cell metabolism.
[8] V. Bunik,et al. The 2-Oxoacid Dehydrogenase Complexes in Mitochondria Can Produce Superoxide/Hydrogen Peroxide at Much Higher Rates Than Complex I* , 2014, The Journal of Biological Chemistry.
[9] Malene B. Rasmussen,et al. Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5. , 2014, Brain : a journal of neurology.
[10] R. Casadio,et al. Analysis of all subunits, SDHA, SDHB, SDHC, SDHD, of the succinate dehydrogenase complex in KIT/PDGFRA wild-type GIST , 2013, European Journal of Human Genetics.
[11] S. Gallati,et al. Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency , 2013, Journal of Medical Genetics.
[12] V. Mootha,et al. Mutations in LYRM4, encoding iron-sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes. , 2013, Human molecular genetics.
[13] T. Stemmler,et al. Frataxin Directly Stimulates Mitochondrial Cysteine Desulfurase by Exposing Substrate-binding Sites, and a Mutant Fe-S Cluster Scaffold Protein with Frataxin-bypassing Ability Acts Similarly*♦ , 2013, The Journal of Biological Chemistry.
[14] E. Craig,et al. Binding of the Chaperone Jac1 Protein and Cysteine Desulfurase Nfs1 to the Iron-Sulfur Cluster Scaffold Isu Protein Is Mutually Exclusive* , 2013, The Journal of Biological Chemistry.
[15] P. Govaert,et al. Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy. , 2013, Human molecular genetics.
[16] Marta A. Uzarska,et al. The mitochondrial Hsp70 chaperone Ssq1 facilitates Fe/S cluster transfer from Isu1 to Grx5 by complex formation , 2013, Molecular biology of the cell.
[17] D. Winge,et al. Emerging concepts in the flavinylation of succinate dehydrogenase. , 2013, Biochimica et biophysica acta.
[18] J. Bayley,et al. The role of complex II in disease. , 2013, Biochimica et biophysica acta.
[19] Amy C. Kelly,et al. Saccharomyces cerevisiae , 2013, Prion.
[20] S. Blaser,et al. Complex II deficiency—A case report and review of the literature , 2013, American journal of medical genetics. Part A.
[21] Jan Dudek,et al. Mitochondrial protein import: common principles and physiological networks. , 2013, Biochimica et biophysica acta.
[22] J. A. Arranz,et al. Protein expression profiles in patients carrying NFU1 mutations. Contribution to the pathophysiology of the disease , 2013, Journal of Inherited Metabolic Disease.
[23] D. Pain,et al. Persulfide formation on mitochondrial cysteine desulfurase: enzyme activation by a eukaryote-specific interacting protein and Fe-S cluster synthesis. , 2012, The Biochemical journal.
[24] G. Montelione,et al. Solution NMR structure of yeast succinate dehydrogenase flavinylation factor Sdh5 reveals a putative Sdh1 binding site. , 2012, Biochemistry.
[25] D. Winge,et al. Flavinylation and Assembly of Succinate Dehydrogenase Are Dependent on the C-terminal Tail of the Flavoprotein Subunit* , 2012, The Journal of Biological Chemistry.
[26] R. Haller,et al. Tissue Specificity of a Human Mitochondrial Disease , 2012, The Journal of Biological Chemistry.
[27] M. Fontecave,et al. Molecular organization, biochemical function, cellular role and evolution of NfuA, an atypical Fe‐S carrier , 2012, Molecular microbiology.
[28] Ann Saada,et al. Leukoencephalopathy with accumulated succinate is indicative of SDHAF1 related complex II deficiency , 2012, Orphanet Journal of Rare Diseases.
[29] Marta A. Uzarska,et al. The role of mitochondria in cellular iron-sulfur protein biogenesis and iron metabolism. , 2012, Biochimica et biophysica acta.
[30] Robert W. Taylor,et al. Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency , 2012, Journal of Medical Genetics.
[31] C. Outten,et al. Monothiol CGFS glutaredoxins and BolA-like proteins: [2Fe-2S] binding partners in iron homeostasis. , 2012, Biochemistry.
[32] H. Elsässer,et al. The human mitochondrial ISCA1, ISCA2, and IBA57 proteins are required for [4Fe-4S] protein maturation , 2012, Molecular biology of the cell.
[33] Szymon J. Ciesielski,et al. Interaction of J-protein co-chaperone Jac1 with Fe-S scaffold Isu is indispensable in vivo and conserved in evolution. , 2012, Journal of molecular biology.
[34] Marta A. Uzarska,et al. A fatal mitochondrial disease is associated with defective NFU1 function in the maturation of a subset of mitochondrial Fe-S proteins. , 2011, American journal of human genetics.
[35] R. Lill,et al. Specialized Function of Yeast Isa1 and Isa2 Proteins in the Maturation of Mitochondrial [4Fe-4S] Proteins* , 2011, The Journal of Biological Chemistry.
[36] E. Shoubridge,et al. Mutations in iron-sulfur cluster scaffold genes NFU1 and BOLA3 cause a fatal deficiency of multiple respiratory chain and 2-oxoacid dehydrogenase enzymes. , 2011, American journal of human genetics.
[37] V. Fellman,et al. Mitochondrial disorders caused by mutations in respiratory chain assembly factors. , 2011, Seminars in fetal & neonatal medicine.
[38] R. Casadio,et al. SDHA loss-of-function mutations in KIT-PDGFRA wild-type gastrointestinal stromal tumors identified by massively parallel sequencing. , 2011, Journal of the National Cancer Institute.
[39] S. Grimm,et al. Specific disintegration of complex II succinate:ubiquinone oxidoreductase links pH changes to oxidative stress for apoptosis induction , 2011, Cell Death and Differentiation.
[40] A. Martelli,et al. Mammalian Frataxin: An Essential Function for Cellular Viability through an Interaction with a Preformed ISCU/NFS1/ISD11 Iron-Sulfur Assembly Complex , 2011, PloS one.
[41] K. Kavanagh,et al. The crystal structure of human GLRX5: iron-sulfur cluster co-ordination, tetrameric assembly and monomer activity. , 2011, The Biochemical journal.
[42] C. Antonescu,et al. Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations , 2010, Proceedings of the National Academy of Sciences.
[43] Chi-Lin Tsai,et al. Human frataxin is an allosteric switch that activates the Fe-S cluster biosynthetic complex. , 2010, Biochemistry.
[44] P. Bénit,et al. SDHA is a tumor suppressor gene causing paraganglioma. , 2010, Human molecular genetics.
[45] H. Elsässer,et al. Humans possess two mitochondrial ferredoxins, Fdx1 and Fdx2, with distinct roles in steroidogenesis, heme, and Fe/S cluster biosynthesis , 2010, Proceedings of the National Academy of Sciences.
[46] D. Winge,et al. Succinate dehydrogenase - Assembly, regulation and role in human disease. , 2010, Mitochondrion.
[47] Oleh Khalimonchuk,et al. Mzm1 Influences a Labile Pool of Mitochondrial Zinc Important for Respiratory Function* , 2010, The Journal of Biological Chemistry.
[48] M. Roberti,et al. Mitochondrial localization of human FAD synthetase isoform 1. , 2010, Mitochondrion.
[49] Steven P. Gygi,et al. SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma , 2009, Science.
[50] T. Strom,et al. SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy , 2009, Nature Genetics.
[51] V. Tiranti,et al. Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects. , 2009, Biochimica et biophysica acta.
[52] D. Winge,et al. Coa2 Is an Assembly Factor for Yeast Cytochrome c Oxidase Biogenesis That Facilitates the Maturation of Cox1 , 2008, Molecular and Cellular Biology.
[53] C. Eng,et al. Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation , 2008, Nature Clinical Practice Endocrinology &Metabolism.
[54] R. Lill,et al. Mitochondrial Iba57p Is Required for Fe/S Cluster Formation on Aconitase and Activation of Radical SAM Enzymes , 2007, Molecular and Cellular Biology.
[55] C. S. Sit,et al. The Saccharomyces cerevisiae succinate dehydrogenase does not require heme for ubiquinone reduction. , 2007, Biochimica et biophysica acta.
[56] N. Chandel,et al. Loss of the SdhB, but Not the SdhA, Subunit of Complex II Triggers Reactive Oxygen Species-Dependent Hypoxia-Inducible Factor Activation and Tumorigenesis , 2007, Molecular and Cellular Biology.
[57] D. Winge,et al. Coa1 links the Mss51 post‐translational function to Cox1 cofactor insertion in cytochrome c oxidase assembly , 2007, The EMBO journal.
[58] B. Lemire,et al. The role of Sdh4p Tyr-89 in ubiquinone reduction by the Saccharomyces cerevisiae succinate dehydrogenase. , 2007, Biochimica et biophysica acta.
[59] J. Imlay. Iron‐sulphur clusters and the problem with oxygen , 2006, Molecular microbiology.
[60] H. Prokisch,et al. Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA) , 2005, Journal of Neurology, Neurosurgery & Psychiatry.
[61] Z. Rao,et al. Crystal Structure of Mitochondrial Respiratory Membrane Protein Complex II , 2005, Cell.
[62] Okio Hino,et al. A mutation in the SDHC gene of complex II increases oxidative stress, resulting in apoptosis and tumorigenesis. , 2005, Cancer research.
[63] E. Boles,et al. Riboflavin Uptake and FAD Synthesis in Saccharomyces cerevisiae Mitochondria , 2004, Journal of Biological Chemistry.
[64] L. Aaltonen,et al. Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. , 2004, American journal of human genetics.
[65] S. Iwata,et al. Architecture of Succinate Dehydrogenase and Reactive Oxygen Species Generation , 2003, Science.
[66] Kevin R. Messner,et al. Mechanism of Superoxide and Hydrogen Peroxide Formation by Fumarate Reductase, Succinate Dehydrogenase, and Aspartate Oxidase* , 2002, The Journal of Biological Chemistry.
[67] Enrique Herrero,et al. Grx5 is a mitochondrial glutaredoxin required for the activity of iron/sulfur enzymes. , 2002, Molecular biology of the cell.
[68] B. Lemire,et al. The Saccharomyces cerevisiae mitochondrial succinate:ubiquinone oxidoreductase. , 2002, Biochimica et biophysica acta.
[69] R. Gunsalus,et al. Succinate dehydrogenase and fumarate reductase from Escherichia coli. , 2002, Biochimica et biophysica acta.
[70] E S Husebye,et al. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. , 2001, American journal of human genetics.
[71] B. Lemire,et al. The Quinone-binding Sites of the Saccharomyces cerevisiae Succinate-ubiquinone Oxidoreductase* , 2001, The Journal of Biological Chemistry.
[72] H. Inokuchi,et al. Abortive assembly of succinate-ubiquinone reductase (Complex II) in a ferrochelatase-deficient mutant of Escherichia coli , 2001, Molecular Genetics and Genomics.
[73] J. Revuelta,et al. Molecular Characterization of FMN1, the Structural Gene for the Monofunctional Flavokinase of Saccharomyces cerevisiae* , 2000, The Journal of Biological Chemistry.
[74] L. T. Jensen,et al. Role of Saccharomyces cerevisiae ISA1and ISA2 in Iron Homeostasis , 2000, Molecular and Cellular Biology.
[75] B. Devlin,et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. , 2000, Science.
[76] C. Hägerhäll,et al. Succinate: quinone oxidoreductases. Variations on a conserved theme. , 1997, Biochimica et biophysica acta.
[77] D. Glerum,et al. SHY1, the Yeast Homolog of the MammalianSURF-1 Gene, Encodes a Mitochondrial Protein Required for Respiration* , 1997, The Journal of Biological Chemistry.
[78] D. Glerum,et al. FLX1 Codes for a Carrier Protein Involved in Maintaining a Proper Balance of Flavin Nucleotides in Yeast Mitochondria (*) , 1996, The Journal of Biological Chemistry.
[79] B. Lemire,et al. Covalent Attachment of FAD to the Yeast Succinate Dehydrogenase Flavoprotein Requires Import into Mitochondria, Presequence Removal, and Folding (*) , 1996, The Journal of Biological Chemistry.
[80] Thomas Bourgeron,et al. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency , 1995, Nature Genetics.
[81] D. Glerum,et al. Synthetase of Saccharomyces Cerevisiae. Structural Gene for Flavin Adenine Dinucleotide Cloning and Characterization of Fad1, The , 1994 .
[82] J. Weiner,et al. The covalent attachment of FAD to the flavoprotein of Saccharomyces cerevisiae succinate dehydrogenase is not necessary for import and assembly into mitochondria. , 1994, European journal of biochemistry.
[83] R. E. Hall,et al. Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins. , 1993, The Journal of clinical investigation.
[84] Dietmar Schomburg,et al. D-Aspartate oxidase , 1993 .
[85] R. Brandsch,et al. Covalent cofactor binding to flavoenzymes requires specific effectors. , 1989, European journal of biochemistry.
[86] H. Beinert,et al. The role of iron in the activation-inactivation of aconitase. , 1983, The Journal of biological chemistry.
[87] W. Kenney,et al. Succinate dehydrogenase. , 2020, Advances in enzymology and related areas of molecular biology.