236 related articles for article (PubMed ID: 21454569)
1. Hydrogen peroxide elimination from C4a-hydroperoxyflavin in a flavoprotein oxidase occurs through a single proton transfer from flavin N5 to a peroxide leaving group.
Sucharitakul J; Wongnate T; Chaiyen P
J Biol Chem; 2011 May; 286(19):16900-9. PubMed ID: 21454569
[TBL] [Abstract][Full Text] [Related]
2. Proton-coupled electron transfer and adduct configuration are important for C4a-hydroperoxyflavin formation and stabilization in a flavoenzyme.
Wongnate T; Surawatanawong P; Visitsatthawong S; Sucharitakul J; Scrutton NS; Chaiyen P
J Am Chem Soc; 2014 Jan; 136(1):241-53. PubMed ID: 24368083
[TBL] [Abstract][Full Text] [Related]
3. Detection of a C4a-hydroperoxyflavin intermediate in the reaction of a flavoprotein oxidase.
Sucharitakul J; Prongjit M; Haltrich D; Chaiyen P
Biochemistry; 2008 Aug; 47(33):8485-90. PubMed ID: 18652479
[TBL] [Abstract][Full Text] [Related]
4. Stabilization of C4a-hydroperoxyflavin in a two-component flavin-dependent monooxygenase is achieved through interactions at flavin N5 and C4a atoms.
Thotsaporn K; Chenprakhon P; Sucharitakul J; Mattevi A; Chaiyen P
J Biol Chem; 2011 Aug; 286(32):28170-80. PubMed ID: 21680741
[TBL] [Abstract][Full Text] [Related]
5. C4a-hydroperoxyflavin formation in N-hydroxylating flavin monooxygenases is mediated by the 2'-OH of the nicotinamide ribose of NADP⁺.
Robinson R; Badieyan S; Sobrado P
Biochemistry; 2013 Dec; 52(51):9089-91. PubMed ID: 24321106
[TBL] [Abstract][Full Text] [Related]
6. Mechanism of Oxygen Activation in a Flavin-Dependent Monooxygenase: A Nearly Barrierless Formation of C4a-Hydroperoxyflavin via Proton-Coupled Electron Transfer.
Visitsatthawong S; Chenprakhon P; Chaiyen P; Surawatanawong P
J Am Chem Soc; 2015 Jul; 137(29):9363-74. PubMed ID: 26144862
[TBL] [Abstract][Full Text] [Related]
7. Oxidation mode of pyranose 2-oxidase is controlled by pH.
Prongjit M; Sucharitakul J; Palfey BA; Chaiyen P
Biochemistry; 2013 Feb; 52(8):1437-45. PubMed ID: 23356577
[TBL] [Abstract][Full Text] [Related]
8. Kinetic mechanism of pyranose 2-oxidase from trametes multicolor.
Prongjit M; Sucharitakul J; Wongnate T; Haltrich D; Chaiyen P
Biochemistry; 2009 May; 48(19):4170-80. PubMed ID: 19317444
[TBL] [Abstract][Full Text] [Related]
9. Kinetic isotope effects on the noncovalent flavin mutant protein of pyranose 2-oxidase reveal insights into the flavin reduction mechanism.
Sucharitakul J; Wongnate T; Chaiyen P
Biochemistry; 2010 May; 49(17):3753-65. PubMed ID: 20359206
[TBL] [Abstract][Full Text] [Related]
10. Relative timing of hydrogen and proton transfers in the reaction of flavin oxidation catalyzed by choline oxidase.
Gannavaram S; Gadda G
Biochemistry; 2013 Feb; 52(7):1221-6. PubMed ID: 23339467
[TBL] [Abstract][Full Text] [Related]
11. A conserved active-site threonine is important for both sugar and flavin oxidations of pyranose 2-oxidase.
Pitsawong W; Sucharitakul J; Prongjit M; Tan TC; Spadiut O; Haltrich D; Divne C; Chaiyen P
J Biol Chem; 2010 Mar; 285(13):9697-9705. PubMed ID: 20089849
[TBL] [Abstract][Full Text] [Related]
12. Mechanistic studies of cyclohexanone monooxygenase: chemical properties of intermediates involved in catalysis.
Sheng D; Ballou DP; Massey V
Biochemistry; 2001 Sep; 40(37):11156-67. PubMed ID: 11551214
[TBL] [Abstract][Full Text] [Related]
13. Dynamics involved in catalysis by single-component and two-component flavin-dependent aromatic hydroxylases.
Ballou DP; Entsch B; Cole LJ
Biochem Biophys Res Commun; 2005 Dec; 338(1):590-8. PubMed ID: 16236251
[TBL] [Abstract][Full Text] [Related]
14. A Reversible, Charge-Induced Intramolecular C4a-S-Cysteinyl-Flavin in Choline Oxidase Variant S101C.
Su D; Yuan H; Gadda G
Biochemistry; 2017 Dec; 56(51):6677-6690. PubMed ID: 29190076
[TBL] [Abstract][Full Text] [Related]
15. Neutral versus charged species in enzyme catalysis. Classical and free energy barriers for oxygen atom transfer from C4a-hydroperoxyflavin to dimethyl sulfide.
Canepa C; Bach RD; Dmitrenko O
J Org Chem; 2002 Nov; 67(24):8653-61. PubMed ID: 12444653
[TBL] [Abstract][Full Text] [Related]
16. Protonation status and control mechanism of flavin-oxygen intermediates in the reaction of bacterial luciferase.
Tinikul R; Lawan N; Akeratchatapan N; Pimviriyakul P; Chinantuya W; Suadee C; Sucharitakul J; Chenprakhon P; Ballou DP; Entsch B; Chaiyen P
FEBS J; 2021 May; 288(10):3246-3260. PubMed ID: 33289305
[TBL] [Abstract][Full Text] [Related]
17. Insights into the enzymatic formation, chemical features, and biological role of the flavin-N5-oxide.
Saleem-Batcha R; Teufel R
Curr Opin Chem Biol; 2018 Dec; 47():47-53. PubMed ID: 30165331
[TBL] [Abstract][Full Text] [Related]
18. Control of C4a-hydroperoxyflavin protonation in the oxygenase component of p-hydroxyphenylacetate-3-hydroxylase.
Chenprakhon P; Trisrivirat D; Thotsaporn K; Sucharitakul J; Chaiyen P
Biochemistry; 2014 Jul; 53(25):4084-6. PubMed ID: 24878148
[TBL] [Abstract][Full Text] [Related]
19. Probing the mechanism of proton coupled electron transfer to dioxygen: the oxidative half-reaction of bovine serum amine oxidase.
Su Q; Klinman JP
Biochemistry; 1998 Sep; 37(36):12513-25. PubMed ID: 9730824
[TBL] [Abstract][Full Text] [Related]
20. Kinetic mechanism of ornithine hydroxylase (PvdA) from Pseudomonas aeruginosa: substrate triggering of O2 addition but not flavin reduction.
Meneely KM; Barr EW; Bollinger JM; Lamb AL
Biochemistry; 2009 May; 48(20):4371-6. PubMed ID: 19368334
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
