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549 related items for PubMed ID: 25639849

  • 1. Selectivity of substrate binding and ionization of 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase.
    Luanloet T, Sucharitakul J, Chaiyen P.
    FEBS J; 2015 Aug; 282(16):3107-25. PubMed ID: 25639849
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  • 2. 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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  • 3. 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 11; 123(2):154-162. PubMed ID: 27568368
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  • 6. 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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  • 7. Use of 8-substituted-FAD analogues to investigate the hydroxylation mechanism of the flavoprotein 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase.
    Chaiyen P, Sucharitakul J, Svasti J, Entsch B, Massey V, Ballou DP.
    Biochemistry; 2004 Apr 06; 43(13):3933-43. PubMed ID: 15049701
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  • 8. Thermodynamics and reduction kinetics properties of 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase.
    Chaiyen P, Brissette P, Ballou DP, Massey V.
    Biochemistry; 1997 Mar 04; 36(9):2612-21. PubMed ID: 9054568
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  • 9. 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 04; 283(5):860-81. PubMed ID: 26709612
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  • 12. Speeding up the product release: a second-sphere contribution from Tyr191 to the reactivity of L-lactate oxidase revealed in crystallographic and kinetic studies of site-directed variants.
    Stoisser T, Klimacek M, Wilson DK, Nidetzky B.
    FEBS J; 2015 Nov 04; 282(21):4130-40. PubMed ID: 26260739
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  • 15. Interactions with the substrate phenolic group are essential for hydroxylation by the oxygenase component of p-hydroxyphenylacetate 3-hydroxylase.
    Tongsook C, Sucharitakul J, Thotsaporn K, Chaiyen P.
    J Biol Chem; 2011 Dec 30; 286(52):44491-502. PubMed ID: 22052902
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  • 16. Mechanism of 6-Hydroxynicotinate 3-Monooxygenase, a Flavin-Dependent Decarboxylative Hydroxylase Involved in Bacterial Nicotinic Acid Degradation.
    Nakamoto KD, Perkins SW, Campbell RG, Bauerle MR, Gerwig TJ, Gerislioglu S, Wesdemiotis C, Anderson MA, Hicks KA, Snider MJ.
    Biochemistry; 2019 Apr 02; 58(13):1751-1763. PubMed ID: 30810301
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  • 18. Mechanistic and computational studies of the reductive half-reaction of tyrosine to phenylalanine active site variants of D-arginine dehydrogenase.
    Gannavaram S, Sirin S, Sherman W, Gadda G.
    Biochemistry; 2014 Oct 21; 53(41):6574-83. PubMed ID: 25243743
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  • 19. Engineering the substrate specificity of Bacillus megaterium cytochrome P-450 BM3: hydroxylation of alkyl trimethylammonium compounds.
    Oliver CF, Modi S, Primrose WU, Lian LY, Roberts GC.
    Biochem J; 1997 Oct 15; 327 ( Pt 2)(Pt 2):537-44. PubMed ID: 9359427
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  • 20. Hydroxylation and ring-opening mechanism of an unusual flavoprotein monooxygenase, 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase: a theoretical study.
    Tian B, Tu Y, Strid A, Eriksson LA.
    Chemistry; 2010 Feb 22; 16(8):2557-66. PubMed ID: 20066695
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