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Journal Abstract Search

178 related items for PubMed ID: 25500577

  • 21.
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  • 22. The many functions of carbohydrate-active enzymes in family GH65: diversity and application.
    De Beul E, Franceus J, Desmet T.
    Appl Microbiol Biotechnol; 2024 Sep 30; 108(1):476. PubMed ID: 39348028
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  • 23.
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  • 24. Structural and mutational analysis of substrate recognition in kojibiose phosphorylase.
    Okada S, Yamamoto T, Watanabe H, Nishimoto T, Chaen H, Fukuda S, Wakagi T, Fushinobu S.
    FEBS J; 2014 Feb 30; 281(3):778-86. PubMed ID: 24255995
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  • 25. Discovery of solabiose phosphorylase and its application for enzymatic synthesis of solabiose from sucrose and lactose.
    Saburi W, Nihira T, Nakai H, Kitaoka M, Mori H.
    Sci Rep; 2022 Jan 07; 12(1):259. PubMed ID: 34997180
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  • 26. Exploration of GH94 Sequence Space for Enzyme Discovery Reveals a Novel Glucosylgalactose Phosphorylase Specificity.
    De Doncker M, De Graeve C, Franceus J, Beerens K, Křen V, Pelantová H, Vercauteren R, Desmet T.
    Chembiochem; 2021 Dec 02; 22(23):3319-3325. PubMed ID: 34541742
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  • 28. Exploring the sequence diversity in glycoside hydrolase family 13_18 reveals a novel glucosylglycerol phosphorylase.
    Franceus J, Decuyper L, D'hooghe M, Desmet T.
    Appl Microbiol Biotechnol; 2018 Apr 02; 102(7):3183-3191. PubMed ID: 29470619
    [Abstract] [Full Text] [Related]

  • 29. Crystallization and X-ray diffraction studies of inverting trehalose phosphorylase from Thermoanaerobacter sp.
    Van Hoorebeke A, Stout J, Van der Meeren R, Kyndt J, Van Beeumen J, Savvides SN.
    Acta Crystallogr Sect F Struct Biol Cryst Commun; 2010 Apr 01; 66(Pt 4):442-7. PubMed ID: 20383018
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  • 30.
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  • 31. Characterization of β-galactoside phosphorylases with diverging acceptor specificities.
    Chen C, Soetaert W, Desmet T.
    Enzyme Microb Technol; 2011 Jun 10; 49(1):59-65. PubMed ID: 22112272
    [Abstract] [Full Text] [Related]

  • 32. Biochemical characterization of engineered amylopullulanase from Thermoanaerobacter ethanolicus 39E-implicating the non-necessity of its 100 C-terminal amino acid residues.
    Lin HY, Chuang HH, Lin FP.
    Extremophiles; 2008 Sep 10; 12(5):641-50. PubMed ID: 18500431
    [Abstract] [Full Text] [Related]

  • 33. Functions, structures, and applications of cellobiose 2-epimerase and glycoside hydrolase family 130 mannoside phosphorylases.
    Saburi W.
    Biosci Biotechnol Biochem; 2016 Jul 10; 80(7):1294-305. PubMed ID: 27031293
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  • 34.
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  • 35. Rational engineering of Lactobacillus acidophilus NCFM maltose phosphorylase into either trehalose or kojibiose dual specificity phosphorylase.
    Nakai H, Petersen BO, Westphal Y, Dilokpimol A, Abou Hachem M, Duus JØ, Schols HA, Svensson B.
    Protein Eng Des Sel; 2010 Oct 10; 23(10):781-7. PubMed ID: 20713411
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  • 36.
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  • 37. Structural basis for reversible phosphorolysis and hydrolysis reactions of 2-O-α-glucosylglycerol phosphorylase.
    Touhara KK, Nihira T, Kitaoka M, Nakai H, Fushinobu S.
    J Biol Chem; 2014 Jun 27; 289(26):18067-75. PubMed ID: 24828502
    [Abstract] [Full Text] [Related]

  • 38. N-acetylglucosaminidases from CAZy family GH3 are really glycoside phosphorylases, thereby explaining their use of histidine as an acid/base catalyst in place of glutamic acid.
    Macdonald SS, Blaukopf M, Withers SG.
    J Biol Chem; 2015 Feb 20; 290(8):4887-4895. PubMed ID: 25533455
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  • 39.
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