Search Results - "Coyle, Travis"

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  1. 1

    Structural dissection of a complex Bacteroides ovatus gene locus conferring xyloglucan metabolism in the human gut by Hemsworth, Glyn R., Thompson, Andrew J., Stepper, Judith, Sobala, Łukasz F., Coyle, Travis, Larsbrink, Johan, Spadiut, Oliver, Goddard-Borger, Ethan D., Stubbs, Keith A., Brumer, Harry, Davies, Gideon J.

    Published in Open biology (01-07-2016)
    “…The human gastrointestinal tract harbours myriad bacterial species, collectively termed the microbiota, that strongly influence human health. Symbiotic members…”
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    Journal Article
  2. 2

    An improved preparation of some aryl [alpha]-l-arabinofuranosides for use as chromogenic substrates for [alpha]-l-arabinofuranosidases by Coyle, Travis, Brumer, Harry, Stubbs, Keith A

    Published in Canadian journal of chemistry (01-11-2015)
    “…A short, robust, and expedient synthesis of various aryl ...-l-arabinofuranosides using a trichloroacetimidate precursor is described. The procedure is…”
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    Journal Article
  3. 3

    Synthetic and Crystallographic Insight into Exploiting sp2 Hybridization in the Development of α‐l‐Fucosidase Inhibitors by Coyle, Travis, Wu, Liang, Debowski, Aleksandra W., Davies, Gideon J., Stubbs, Keith A.

    “…The sugar fucose plays a myriad of roles in biological recognition. Enzymes hydrolyzing fucose from glycoconjugates, α‐l‐fucosidases, are important targets for…”
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    Journal Article
  4. 4

    Exploiting sp2-Hybridisation in the Development of Potent 1,5-[alpha]-l-Arabinanase Inhibitors by Coyle, Travis, Debowski, Aleksandra W, Varrot, Annabelle, Stubbs, Keith A

    “…The synthesis of potent inhibitors of GH93 arabinanases as well as a synthesis of a chromogenic substrate to measure GH93 arabinanase activity are described…”
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    Journal Article
  5. 5

    Exploiting sp 2 -Hybridisation in the Development of Potent 1,5-α-l-Arabinanase Inhibitors by Coyle, Travis, Debowski, Aleksandra W, Varrot, Annabelle, Stubbs, Keith A

    “…The synthesis of potent inhibitors of GH93 arabinanases as well as a synthesis of a chromogenic substrate to measure GH93 arabinanase activity are described…”
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    Journal Article
  6. 6

    Exploiting sp2‐Hybridisation in the Development of Potent 1,5‐α‐l‐Arabinanase Inhibitors by Coyle, Travis, Debowski, Aleksandra W., Varrot, Annabelle, Stubbs, Keith A.

    “…The synthesis of potent inhibitors of GH93 arabinanases as well as a synthesis of a chromogenic substrate to measure GH93 arabinanase activity are described…”
    Get full text
    Journal Article
  7. 7

    Synthetic and Crystallographic Insight into Exploiting sp 2 Hybridization in the Development of α-l-Fucosidase Inhibitors by Coyle, Travis, Wu, Liang, Debowski, Aleksandra W, Davies, Gideon J, Stubbs, Keith A

    “…The sugar fucose plays a myriad of roles in biological recognition. Enzymes hydrolyzing fucose from glycoconjugates, α-l-fucosidases, are important targets for…”
    Get full text
    Journal Article
  8. 8

    An improved preparation of some aryl α-l-arabinofuranosides for use as chromogenic substrates for α-l-arabinofuranosidases by Coyle, Travis, Brumer, Harry, Stubbs, Keith A

    Published in Canadian journal of chemistry (01-11-2015)
    “…A short, robust, and expedient synthesis of various aryl α- l -arabinofuranosides using a trichloroacetimidate precursor is described. The procedure is…”
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    Journal Article
  9. 9

    Structure of a Talaromyces pinophilus GH62 arabinofuranosidase in complex with AraDNJ at 1.25 Å resolution by Moroz, Olga V., Sobala, Lukasz F., Blagova, Elena, Coyle, Travis, Peng, Wei, Mørkeberg Krogh, Kristian B. R., Stubbs, Keith A., Wilson, Keith S., Davies, Gideon J.

    “…The enzymatic hydrolysis of complex plant biomass is a major societal goal of the 21st century in order to deliver renewable energy from nonpetroleum and…”
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  10. 10

    Crystallization and preliminary diffraction analysis of an engineered cephalosporin acylase by Anandan, Anandhi, Vallet, Corinne, Coyle, Travis, Moustafa, Ibrahim M., Vrielink, Alice

    “…Crystallization conditions are reported for an engineered cephalosporin acylase based on the sequence of glutaryl‐7‐aminocephalosporanic acid acylase from…”
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