User menu

Metabolite Proofreading in Carnosine and Homocarnosine Synthesis

Bibliographic reference Veiga da Cunha, Maria ; Chevalier, Nathalie ; Stroobant, Vincent ; Vertommen, Didier ; Van Schaftingen, Emile. Metabolite Proofreading in Carnosine and Homocarnosine Synthesis. In: Journal of Biological Chemistry, Vol. 289, no.28, p. 19726-19736 (2014)
Permanent URL http://hdl.handle.net/2078.1/156211
  1. Linster Carole L, Van Schaftingen Emile, Hanson Andrew D, Metabolite damage and its repair or pre-emption, 10.1038/nchembio.1141
  2. Linster Carole L., Noël Gaëtane, Stroobant Vincent, Vertommen Didier, Vincent Marie-Françoise, Bommer Guido T., Veiga-da-Cunha Maria, Van Schaftingen Emile, Ethylmalonyl-CoA Decarboxylase, a New Enzyme Involved in Metabolite Proofreading, 10.1074/jbc.m111.281527
  3. Kalyankar, J. Biol. Chem, 234, 3210 (1959)
  4. Horinishi Hiroo, Grillo Mary, Margolis Frank L., PURIFICATION AND CHARACTERIZATION OF CARNOSINE SYNTHETASE FROM MOUSE OLFACTORY BULBS, 10.1111/j.1471-4159.1978.tb00127.x
  5. Matsuoka M., Nakajima T., Sano I., Identification of α-(β-alanyl)-lysine in rabbit muscle, 10.1016/0304-4165(69)90083-x
  6. Nakajima T., Kakimoto Y., Kumon A., Matsuoka M., Sano I., ?-(?-AMINOBUTYRYL)-LYSINE IN MAMMALIAN BRAIN: ITS IDENTIFICATION AND DISTRIBUTION, 10.1111/j.1471-4159.1969.tb10382.x
  7. Drozak Jakub, Veiga-da-Cunha Maria, Vertommen Didier, Stroobant Vincent, Van Schaftingen Emile, Molecular Identification of Carnosine Synthase as ATP-grasp Domain-containing Protein 1 (ATPGD1), 10.1074/jbc.m109.095505
  8. Boldyrev A. A., Aldini G., Derave W., Physiology and Pathophysiology of Carnosine, 10.1152/physrev.00039.2012
  9. Kohen R., Yamamoto Y., Cundy K. C., Ames B. N., Antioxidant activity of carnosine, homocarnosine, and anserine present in muscle and brain., 10.1073/pnas.85.9.3175
  10. Bauer Karl, Carnosine and Homocarnosine, the Forgotten, Enigmatic Peptides of the Brain, 10.1007/s11064-005-8806-z
  11. Arts I. S., Ball G., Leverrier P., Garvis S., Nicolaes V., Vertommen D., Ize B., Tamu Dufe V., Messens J., Voulhoux R., Collet J.-F., Dissecting the Machinery That Introduces Disulfide Bonds in Pseudomonas aeruginosa, 10.1128/mbio.00912-13
  12. Veiga-da-Cunha Maria, Hadi Farah, Balligand Thomas, Stroobant Vincent, Van Schaftingen Emile, Molecular Identification of Hydroxylysine Kinase and of Ammoniophospholyases Acting on 5-Phosphohydroxy-l-lysine and Phosphoethanolamine, 10.1074/jbc.m111.323485
  13. Van Schaftingen Emile, Rzem Rim, Marbaix Alexandre, Collard François, Veiga-da-Cunha Maria, Linster Carole L., Metabolite proofreading, a neglected aspect of intermediary metabolism, 10.1007/s10545-012-9571-1
  14. Veiga-da-Cunha Maria, Tyteca Donatienne, Stroobant Vincent, Courtoy Pierre J., Opperdoes Fred R., Van Schaftingen Emile, Molecular Identification of NAT8 as the Enzyme That Acetylates CysteineS-Conjugates to Mercapturic Acids, 10.1074/jbc.m110.110924
  15. Teufel Michael, Saudek Vladimir, Ledig Jean-Pierre, Bernhardt Annie, Boularand Sylviane, Carreau Alexandra, Cairns Nigel J., Carter Christopher, Cowley David J., Duverger Danielle, Ganzhorn Axel J., Guenet Chantal, Heintzelmann Blanche, Laucher Veronique, Sauvage Claude, Smirnova Tatiana, Sequence Identification and Characterization of Human Carnosinase and a Closely Related Non-specific Dipeptidase, 10.1074/jbc.m209764200
  16. Kumon Akira, Matsuoka Yukio, Kakimoto Yasuo, Nakajima Teruo, Sano Isamu, A peptidase that hydrolyzes Na-(γ-aminobutyryl)lysine, 10.1016/0005-2795(70)90103-0
  17. KUNZE Norbert, KLEINKAUF Horst, BAUER Karl, Characterization of two carnosine-degrading enzymes from rat brain. Partial purification and characterization of a carnosinase and a beta-alanyl-arginine hydrolase, 10.1111/j.1432-1033.1986.tb10081.x
  18. Sass Jörn Oliver, Mohr Verena, Olbrich Heike, Engelke Udo, Horvath Judit, Fliegauf Manfred, Loges Niki Tomas, Schweitzer-Krantz Susanne, Moebus Ralf, Weiler Polly, Kispert Andreas, Superti-Furga Andrea, Wevers Ron A., Omran Heymut, Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of Metabolism, 10.1086/500563
  19. Kaur Hardeep, Kumar Chitranshu, Junot Christophe, Toledano Michel B., Bachhawat Anand K., Dug1p Is a Cys-Gly Peptidase of the γ-Glutamyl Cycle ofSaccharomyces cerevisiaeand Represents a Novel Family of Cys-Gly Peptidases, 10.1074/jbc.m808952200
  20. Botelho Tiago O., Guevara Tibisay, Marrero Aniebrys, Arêde Pedro, Fluxà Viviana S., Reymond Jean-Louis, Oliveira Duarte C., Gomis-Rüth F. Xavier, Structural and Functional Analyses Reveal ThatStaphylococcus aureusAntibiotic Resistance Factor HmrA Is a Zinc-dependent Endopeptidase, 10.1074/jbc.m111.247437
  21. Green J. M., Hollandsworth R., Pitstick L., Carter E. L., Purification and Characterization of the Folate Catabolic Enzyme p-Aminobenzoyl-Glutamate Hydrolase from Escherichia coli, 10.1128/jb.01362-09
  22. Bitto Eduard, Bingman Craig A., Bittova Lenka, Houston Norma L., Boston Rebecca S., Fox Brian G., Phillips George N., X-ray structure of ILL2, an auxin-conjugate amidohydrolase fromArabidopsis thaliana, 10.1002/prot.22124
  23. Stellingwerff Trent, Anwander Helen, Egger Andrea, Buehler Tania, Kreis Roland, Decombaz Jacques, Boesch Chris, Effect of two β-alanine dosing protocols on muscle carnosine synthesis and washout, 10.1007/s00726-011-1054-4
  24. Rzem R., Veiga-da-Cunha M., Noel G., Goffette S., Nassogne M.-C., Tabarki B., Scholler C., Marquardt T., Vikkula M., Van Schaftingen E., A gene encoding a putative FAD-dependent L-2-hydroxyglutarate dehydrogenase is mutated in L-2-hydroxyglutaric aciduria, 10.1073/pnas.0404840101
  25. Jackson Mel C., Kucera Christine M., Lenney James F., Purification and properties of human serum carnosinase, 10.1016/0009-8981(91)90073-l
  26. Lenney James F., Peppers Steven C., Kucera Christine M., Sjaastad Ottar, Homocamosinosis: lack of serum carnosinase is the defect probably responsible for elevated brain and CSF homocarnosine, 10.1016/0009-8981(83)90243-7
  27. Gjessing, J. Neural. Transm. Suppl, 29, 91 (1990)
  28. Rzem R., Van Schaftingen E., Veiga-da-Cunha M., The gene mutated in l-2-hydroxyglutaric aciduria encodes l-2-hydroxyglutarate dehydrogenase, 10.1016/j.biochi.2005.06.005
  29. Rzem R., Vincent M.-F., Van Schaftingen E., Veiga-da-Cunha M., l-2-Hydroxyglutaric aciduria, a defect of metabolite repair, 10.1007/s10545-007-0487-0
  30. Van Schaftingen E., Rzem R., Veiga-da-Cunha M., l-2-Hydroxyglutaric aciduria, a disorder of metabolite repair, 10.1007/s10545-008-1042-3
  31. Haliloglu G., Jobard F., Oguz K., Anlar B., Akalan N., Coskun T., Sass J., Fischer J., Topcu M., L-2-Hydroxyglutaric Aciduria and Brain Tumors in Children with Mutations in theL2HGDHGene: Neuroimaging Findings, 10.1055/s-2008-1081217
  32. Kranendijk Martijn, Struys Eduard A., Salomons Gajja S., Van der Knaap Marjo S., Jakobs Cornelis, Progress in understanding 2-hydroxyglutaric acidurias, 10.1007/s10545-012-9462-5
  33. Marbaix Alexandre Y., Noël Gaëtane, Detroux Aline M., Vertommen Didier, Van Schaftingen Emile, Linster Carole L., Extremely Conserved ATP- or ADP-dependent Enzymatic System for Nicotinamide Nucleotide Repair, 10.1074/jbc.c111.310847