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150 related items for PubMed ID: 16403573

  • 21. Potentiometric and further kinetic characterization of the flavin-binding domain of Saccharomyces cerevisiae flavocytochrome b2. Inhibition by anions binding in the active site.
    Cénas N, Lê KH, Terrier M, Lederer F.
    Biochemistry; 2007 Apr 17; 46(15):4661-70. PubMed ID: 17373777
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  • 22. Propene activation by the oxo-iron active species of taurine/alpha-ketoglutarate dioxygenase (TauD) enzyme. How does the catalysis compare to heme-enzymes?
    de Visser SP.
    J Am Chem Soc; 2006 Aug 02; 128(30):9813-24. PubMed ID: 16866538
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  • 23. Ipso-substitution by cytochrome P450 with conversion of p-hydroxybenzene derivatives to hydroquinone: evidence for hydroperoxo-iron as the active oxygen species.
    Vatsis KP, Coon MJ.
    Arch Biochem Biophys; 2002 Jan 01; 397(1):119-29. PubMed ID: 11747318
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  • 27. Laser photoexcitation of NAD(P)H induces reduction of P450 BM3 heme domain on the microsecond time scale.
    Girvan HM, Heyes DJ, Scrutton NS, Munro AW.
    J Am Chem Soc; 2007 May 23; 129(20):6647-53. PubMed ID: 17465554
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  • 30. Effect of the Insertion of a Glycine Residue into the Loop Spanning Residues 536-541 on the Semiquinone State and Redox Properties of the Flavin Mononucleotide-Binding Domain of Flavocytochrome P450BM-3 from Bacillus megaterium.
    Chen HC, Swenson RP.
    Biochemistry; 2008 Dec 30; 47(52):13788-99. PubMed ID: 19055322
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  • 35. The unusual redox properties of flavocytochrome P450 BM3 flavodoxin domain.
    Hanley SC, Ost TW, Daff S.
    Biochem Biophys Res Commun; 2004 Dec 24; 325(4):1418-23. PubMed ID: 15555585
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  • 36. The dimeric form of flavocytochrome P450 BM3 is catalytically functional as a fatty acid hydroxylase.
    Neeli R, Girvan HM, Lawrence A, Warren MJ, Leys D, Scrutton NS, Munro AW.
    FEBS Lett; 2005 Oct 24; 579(25):5582-8. PubMed ID: 16214136
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