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2. 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]
3. Analysis of the active site of the flavoprotein p-hydroxybenzoate hydroxylase and some ideas with respect to its reaction mechanism. Schreuder HA; Hol WG; Drenth J Biochemistry; 1990 Mar; 29(12):3101-8. PubMed ID: 2337581 [TBL] [Abstract][Full Text] [Related]
4. 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; 6(5):605-17. PubMed ID: 9634698 [TBL] [Abstract][Full Text] [Related]
6. Frontier orbital study on the 4-hydroxybenzoate-3-hydroxylase-dependent activity with benzoate derivatives. Vervoort J; Rietjens IM; van Berkel WJ; Veeger C Eur J Biochem; 1992 Jun; 206(2):479-84. PubMed ID: 1597186 [TBL] [Abstract][Full Text] [Related]
7. 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; 40(30):8705-16. PubMed ID: 11467930 [TBL] [Abstract][Full Text] [Related]
8. Flavin-oxygen derivatives involved in hydroxylation by p-hydroxybenzoate hydroxylase. Entsch B; Ballou DP; Massey V J Biol Chem; 1976 May; 251(9):2550-63. PubMed ID: 816794 [TBL] [Abstract][Full Text] [Related]
9. Tuning of p Pitsawong W; Chenprakhon P; Dhammaraj T; Medhanavyn D; Sucharitakul J; Tongsook C; van Berkel WJH; Chaiyen P; Miller AF J Biol Chem; 2020 Mar; 295(12):3965-3981. PubMed ID: 32014994 [TBL] [Abstract][Full Text] [Related]
10. Molecular modeling reveals the possible importance of a carbonyl oxygen binding pocket for the catalytic mechanism of p-hydroxybenzoate hydroxylase. Schreuder HA; Hol WG; Drenth J J Biol Chem; 1988 Mar; 263(7):3131-6. PubMed ID: 3343242 [TBL] [Abstract][Full Text] [Related]
11. Reaction mechanism of flavin-dependent hydroxylation. Evolution of a non-imitable enzyme. Visser CM Eur J Biochem; 1983 Oct; 135(3):543-8. PubMed ID: 6617648 [TBL] [Abstract][Full Text] [Related]
12. Flavin motion in p-hydroxybenzoate hydroxylase. Substrate and effector specificity of the Tyr22-->Ala mutant. van der Bolt FJ; Vervoort J; van Berkel WJ Eur J Biochem; 1996 May; 237(3):592-600. PubMed ID: 8647102 [TBL] [Abstract][Full Text] [Related]
13. Model studies on p-hydroxybenzoate hydroxylase. The catalytic role of Arg-214 and Tyr-201 in the hydroxylation step. Bach RD; Dmitrenko O J Am Chem Soc; 2004 Jan; 126(1):127-42. PubMed ID: 14709077 [TBL] [Abstract][Full Text] [Related]
14. Kinetics of proton-linked flavin conformational changes in p-hydroxybenzoate hydroxylase. Frederick KK; Palfey BA Biochemistry; 2005 Oct; 44(40):13304-14. PubMed ID: 16201756 [TBL] [Abstract][Full Text] [Related]
15. Evidence for flavin movement in the function of p-hydroxybenzoate hydroxylase from studies of the mutant Arg220Lys. Moran GR; Entsch B; Palfey BA; Ballou DP Biochemistry; 1996 Jul; 35(28):9278-85. PubMed ID: 8703933 [TBL] [Abstract][Full Text] [Related]
16. 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; 38(25):8124-37. PubMed ID: 10387058 [TBL] [Abstract][Full Text] [Related]
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20. Conversion of phenol derivatives to hydroxylated products by phenol hydroxylase from Trichosporon cutaneum. A comparison of regioselectivity and rate of conversion with calculated molecular orbital substrate characteristics. Peelen S; Rietjens IM; Boersma MG; Vervoort J Eur J Biochem; 1995 Jan; 227(1-2):284-91. PubMed ID: 7851397 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]