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Journal Abstract Search

127 related items for PubMed ID: 240687

  • 1. Spectroscopic evidence for the formation of a 4-keto intermediate in the UDP-apiose/UDP-xylose synthase reaction.
    Gebb C, Baron D, Grisebach H.
    Eur J Biochem; 1975 Jun; 54(2):493-8. PubMed ID: 240687
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  • 4. Real-time NMR monitoring of intermediates and labile products of the bifunctional enzyme UDP-apiose/UDP-xylose synthase.
    Guyett P, Glushka J, Gu X, Bar-Peled M.
    Carbohydr Res; 2009 Jun 12; 344(9):1072-8. PubMed ID: 19375693
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  • 5. Synthesis, characterization and properties of uridine 5'-( -D-apio-D-furanosyl pyrophosphate).
    Kindel PK, Watson RR.
    Biochem J; 1973 Jun 12; 133(2):227-41. PubMed ID: 4723773
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  • 6. Purification and properties of an enzyme from cell suspension cultures of parsley catalyzing the synthesis of UDP-apiose and UDP-D-xylose from UDP-D-glucuronic acid.
    Baron D, Wellmann E, Grisebach H.
    Biochim Biophys Acta; 1972 Jan 20; 258(1):310-8. PubMed ID: 4333589
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  • 7. Biosynthesis of type 3 capsular polysaccharide in Streptococcus pneumoniae. Enzymatic chain release by an abortive translocation process.
    Forsee WT, Cartee RT, Yother J.
    J Biol Chem; 2000 Aug 25; 275(34):25972-8. PubMed ID: 10854426
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  • 8. Transcriptome-guided gene isolation and functional characterization of UDP-xylose synthase and UDP-D-apiose/UDP-D-xylose synthase families from Ornithogalum caudatum Ait.
    Yin S, Kong JQ.
    Plant Cell Rep; 2016 Nov 25; 35(11):2403-2421. PubMed ID: 27591771
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  • 9. A fluoro analogue of UDP-α-D-glucuronic acid is an inhibitor of UDP-α-D-apiose/UDP-α-D-xylose synthase.
    Choi SH, Ruszczycky MW, Zhang H, Liu HW.
    Chem Commun (Camb); 2011 Sep 28; 47(36):10130-2. PubMed ID: 21826368
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  • 10. Analysis of UDP-D-apiose/UDP-D-xylose synthase-catalyzed conversion of UDP-D-apiose phosphonate to UDP-D-xylose phosphonate: implications for a retroaldol-aldol mechanism.
    Choi SH, Mansoorabadi SO, Liu YN, Chien TC, Liu HW.
    J Am Chem Soc; 2012 Aug 29; 134(34):13946-9. PubMed ID: 22830643
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  • 11. Reconstruction of de novo pathway for synthesis of UDP-glucuronic acid and UDP-xylose from intrinsic UDP-glucose in Saccharomyces cerevisiae.
    Oka T, Jigami Y.
    FEBS J; 2006 Jun 29; 273(12):2645-57. PubMed ID: 16817893
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  • 12. Interaction of periodate-oxidized UDP-glucuronic acid with recombinant human liver UDP-glucuronosyltransferase 1A6.
    Battaglia E, Terrier N, Mizeracka M, Senay C, Magdalou J, Fournel-Gigleux S, Radominska-Pandya A.
    Drug Metab Dispos; 1998 Aug 29; 26(8):812-7. PubMed ID: 9698297
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  • 13. Structure and mechanism of human UDP-xylose synthase: evidence for a promoting role of sugar ring distortion in a three-step catalytic conversion of UDP-glucuronic acid.
    Eixelsberger T, Sykora S, Egger S, Brunsteiner M, Kavanagh KL, Oppermann U, Brecker L, Nidetzky B.
    J Biol Chem; 2012 Sep 07; 287(37):31349-58. PubMed ID: 22810237
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  • 14. Probing of the reaction pathway of human UDP-xylose synthase with site-directed mutagenesis.
    Eixelsberger T, Weber H, Nidetzky B.
    Carbohydr Res; 2015 Oct 30; 416():1-6. PubMed ID: 26342152
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  • 15. Conversion of UDP-D-glucuronic acid to UDP-D-apiose and UDP-D-xylose by an enzyme isolated from Lemna minor.
    Mendicino J, Abou-Issa H.
    Biochim Biophys Acta; 1974 Sep 11; 364(1):159-72. PubMed ID: 4373069
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  • 16. UDP-glucuronate carboxy-lyase in cultured chondrocytes.
    John KV, Schwartz NB, Ankel H.
    J Biol Chem; 1977 Oct 10; 252(19):6707-10. PubMed ID: 197101
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  • 17. Purification and kinetic properties of UDP-glucose dehydrogenase from sugarcane.
    Turner W, Botha FC.
    Arch Biochem Biophys; 2002 Nov 15; 407(2):209-16. PubMed ID: 12413493
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  • 18. Mechanism of Sugar Ring Contraction and Closure Catalyzed by UDP-d-apiose/UDP-d-xylose Synthase (UAXS).
    Wang Y, Li X, Wei J, Zhang X, Liu Y.
    J Chem Inf Model; 2022 Feb 14; 62(3):632-646. PubMed ID: 35043627
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  • 19. Separation and allosteric properties of two forms of UDP-glucuronate carboxy-lyase.
    John KV, Schutzbach JS, Ankel H.
    J Biol Chem; 1977 Nov 25; 252(22):8013-7. PubMed ID: 914860
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