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Journal Abstract Search

272 related items for PubMed ID: 15049701

  • 1.
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  • 2. Flavoenzymes catalyzing oxidative aromatic ring-cleavage reactions.
    Chaiyen P.
    Arch Biochem Biophys; 2010 Jan 01; 493(1):62-70. PubMed ID: 19728986
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  • 7. A study of the spectral and redox properties and covalent flavinylation of the flavoprotein component of p-cresol methylhydroxylase reconstituted with FAD analogues.
    Efimov I, McIntire WS.
    Biochemistry; 2004 Aug 17; 43(32):10532-46. PubMed ID: 15301551
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  • 8. Role of the Tyr270 residue in 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase from Mesorhizobium loti.
    Kobayashi J, Yoshida H, Yagi T, Kamitori S, Hayashi H, Mizutani K, Takahashi N, Mikami B.
    J Biosci Bioeng; 2017 Feb 17; 123(2):154-162. PubMed ID: 27568368
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  • 9. Synergistic interactions of multiple mutations on catalysis during the hydroxylation reaction of p-hydroxybenzoate hydroxylase: studies of the Lys297Met, Asn300Asp, and Tyr385Phe mutants reconstituted with 8-Cl-flavin.
    Ortiz-Maldonado M, Aeschliman SM, Ballou DP, Massey V.
    Biochemistry; 2001 Jul 31; 40(30):8705-16. PubMed ID: 11467930
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  • 10. Catalytic roles of active-site residues in 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase: an ONIOM/DFT study.
    Tian B, Strid Å, Eriksson LA.
    J Phys Chem B; 2011 Mar 03; 115(8):1918-26. PubMed ID: 21291225
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  • 11. The crystal structure of phenol hydroxylase in complex with FAD and phenol provides evidence for a concerted conformational change in the enzyme and its cofactor during catalysis.
    Enroth C, Neujahr H, Schneider G, Lindqvist Y.
    Structure; 1998 May 15; 6(5):605-17. PubMed ID: 9634698
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  • 12. Structure of the PLP degradative enzyme 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase from Mesorhizobium loti MAFF303099 and its mechanistic implications.
    McCulloch KM, Mukherjee T, Begley TP, Ealick SE.
    Biochemistry; 2009 May 19; 48(19):4139-49. PubMed ID: 19317437
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  • 13. Reaction of 2-methyl-3-hydroxypyridine-5-carboxylic acid (MHPC) oxygenase with N-methyl-5-hydroxynicotinic acid: studies on the mode of binding, and protonation status of the substrate.
    Chaiyen P, Brissette P, Ballou DP, Massey V.
    Biochemistry; 1997 Nov 11; 36(45):13856-64. PubMed ID: 9374863
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  • 14. Relationship between charge-transfer interactions, redox potentials, and catalysis for different forms of the flavoprotein component of p-cresol methylhydroxylase.
    Efimov I, McIntire WS.
    J Am Chem Soc; 2005 Jan 19; 127(2):732-41. PubMed ID: 15643899
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  • 15. Use of free energy relationships to probe the individual steps of hydroxylation of p-hydroxybenzoate hydroxylase: studies with a series of 8-substituted flavins.
    Ortiz-Maldonado M, Ballou DP, Massey V.
    Biochemistry; 1999 Jun 22; 38(25):8124-37. PubMed ID: 10387058
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  • 16. Tyr217 and His213 are important for substrate binding and hydroxylation of 3-hydroxybenzoate 6-hydroxylase from Rhodococcus jostii RHA1.
    Sucharitakul J, Medhanavyn D, Pakotiprapha D, van Berkel WJ, Chaiyen P.
    FEBS J; 2016 Mar 22; 283(5):860-81. PubMed ID: 26709612
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  • 17. A rate-limiting conformational change of the flavin in p-hydroxybenzoate hydroxylase is necessary for ligand exchange and catalysis: studies with 8-mercapto- and 8-hydroxy-flavins.
    Ortiz-Maldonado M, Ballou DP, Massey V.
    Biochemistry; 2001 Jan 30; 40(4):1091-101. PubMed ID: 11170433
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  • 18. The intraflavin hydrogen bond in human electron transfer flavoprotein modulates redox potentials and may participate in electron transfer.
    Dwyer TM, Mortl S, Kemter K, Bacher A, Fauq A, Frerman FE.
    Biochemistry; 1999 Jul 27; 38(30):9735-45. PubMed ID: 10423253
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  • 19. Crystallization and preliminary X-ray crystallographic analysis of 2-methyl-3-hydroxypyridine-5-carboxylic acid (MHPC) oxygenase from Pseudomonas sp. MA-1.
    Oonanant W, Sucharitakul J, Yuvaniyama J, Chaiyen P.
    Acta Crystallogr Sect F Struct Biol Cryst Commun; 2005 Mar 01; 61(Pt 3):312-4. PubMed ID: 16511028
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  • 20. Effects of noncovalent and covalent FAD binding on the redox and catalytic properties of p-cresol methylhydroxylase.
    Efimov I, Cronin CN, McIntire WS.
    Biochemistry; 2001 Feb 20; 40(7):2155-66. PubMed ID: 11329284
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