BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 23794404)

  • 1. Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated C=C-bonds using flavin-dependent ene-reductases.
    Winkler CK; Clay D; van Heerden E; Faber K
    Biotechnol Bioeng; 2013 Dec; 110(12):3085-92. PubMed ID: 23794404
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biocatalytic reduction of activated CC-bonds and beyond: emerging trends.
    Winkler CK; Faber K; Hall M
    Curr Opin Chem Biol; 2018 Apr; 43():97-105. PubMed ID: 29275291
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Design and application of a bi-functional redox biocatalyst through covalent co-immobilization of ene-reductase and glucose dehydrogenase.
    Nagy F; Gyujto I; Tasnádi G; Barna B; Balogh-Weiser D; Faber K; Poppe L; Hall M
    J Biotechnol; 2020 Nov; 323():246-253. PubMed ID: 32891641
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Thermal, electrochemical and photochemical reactions involving catalytically versatile ene reductase enzymes.
    Toogood HS; Scrutton NS
    Enzymes; 2020; 47():491-515. PubMed ID: 32951833
    [TBL] [Abstract][Full Text] [Related]  

  • 5. NAD(P)H-independent asymmetric C=C bond reduction catalyzed by ene reductases by using artificial co-substrates as the hydrogen donor.
    Winkler CK; Clay D; Entner M; Plank M; Faber K
    Chemistry; 2014 Jan; 20(5):1403-9. PubMed ID: 24382795
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Bioreduction and disproportionation of cyclohex-2-enone catalyzed by ene-reductase OYE-1 in 'micro-aqueous' organic solvents.
    Clay D; Winkler CK; Tasnádi G; Faber K
    Biotechnol Lett; 2014 Jun; 36(6):1329-33. PubMed ID: 24563324
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An enoate reductase Achr-OYE4 from Achromobacter sp. JA81: characterization and application in asymmetric bioreduction of C=C bonds.
    Wang HB; Pei XQ; Wu ZL
    Appl Microbiol Biotechnol; 2014 Jan; 98(2):705-15. PubMed ID: 23644746
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Asymmetric Reduction of (R)-Carvone through a Thermostable and Organic-Solvent-Tolerant Ene-Reductase.
    Tischler D; Gädke E; Eggerichs D; Gomez Baraibar A; Mügge C; Scholtissek A; Paul CE
    Chembiochem; 2020 Apr; 21(8):1217-1225. PubMed ID: 31692216
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Asymmetric Ene-Reduction of α,β-Unsaturated Compounds by F
    Kang SW; Antoney J; Frkic RL; Lupton DW; Speight R; Scott C; Jackson CJ
    Biochemistry; 2023 Feb; 62(3):873-891. PubMed ID: 36637210
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family.
    Stuermer R; Hauer B; Hall M; Faber K
    Curr Opin Chem Biol; 2007 Apr; 11(2):203-13. PubMed ID: 17353140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An Enzymatic Cofactor Regeneration System for the in-Vitro Reduction of Isolated C=C Bonds by Geranylgeranyl Reductases.
    Niese R; Deshpande K; Müller M
    Chembiochem; 2024 Jan; 25(1):e202300409. PubMed ID: 37948327
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Asymmetric bioreduction of alkenes using ene-reductases YersER and KYE1 and effects of organic solvents.
    Yanto Y; Winkler CK; Lohr S; Hall M; Faber K; Bommarius AS
    Org Lett; 2011 May; 13(10):2540-3. PubMed ID: 21510626
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mechanisms of reduced flavin transfer in the two-component flavin-dependent monooxygenases.
    Sucharitakul J; Tinikul R; Chaiyen P
    Arch Biochem Biophys; 2014 Aug; 555-556():33-46. PubMed ID: 24857824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Flavin and 5-deazaflavin: a chemical evaluation of 'modified' flavoproteins with respect to the mechanisms of redox biocatalysis.
    Hemmerich P; Massey V
    FEBS Lett; 1977 Dec; 84(1):5-21. PubMed ID: 145377
    [No Abstract]   [Full Text] [Related]  

  • 15. Determinants of substrate binding and protonation in the flavoenzyme xenobiotic reductase A.
    Spiegelhauer O; Werther T; Mende S; Knauer SH; Dobbek H
    J Mol Biol; 2010 Oct; 403(2):286-98. PubMed ID: 20826164
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nicotinamide-independent asymmetric bioreduction of C=C-bonds via disproportionation of enones catalyzed by enoate reductases.
    Stueckler C; Reiter TC; Baudendistel N; Faber K
    Tetrahedron; 2010 Jan; 66(3-2):663-667. PubMed ID: 21270958
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Selectivity through discriminatory induced fit enables switching of NAD(P)H coenzyme specificity in Old Yellow Enzyme ene-reductases.
    Iorgu AI; Hedison TM; Hay S; Scrutton NS
    FEBS J; 2019 Aug; 286(16):3117-3128. PubMed ID: 31033202
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An ene reductase from Clavispora lusitaniae for asymmetric reduction of activated alkenes.
    Ni Y; Yu HL; Lin GQ; Xu JH
    Enzyme Microb Technol; 2014 Mar; 56():40-5. PubMed ID: 24564901
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A highly efficient ADH-coupled NADH-recycling system for the asymmetric bioreduction of carbon-carbon double bonds using enoate reductases.
    Tauber K; Hall M; Kroutil W; Fabian WM; Faber K; Glueck SM
    Biotechnol Bioeng; 2011 Jun; 108(6):1462-7. PubMed ID: 21328323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Asymmetric Ene-Reduction by F
    Kang SW; Antoney J; Lupton DW; Speight R; Scott C; Jackson CJ
    Chembiochem; 2023 Apr; 24(8):e202200797. PubMed ID: 36716144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.