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Unlocking the Hydrolytic Mechanism of GH92 α-1,2-Mannosidases: Computation Inspires the use of C-Glycosides as Michaelis Complex Mimics

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F22%3A00553763" target="_blank" >RIV/61388963:_____/22:00553763 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/chem.202200148" target="_blank" >https://doi.org/10.1002/chem.202200148</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/chem.202200148" target="_blank" >10.1002/chem.202200148</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Unlocking the Hydrolytic Mechanism of GH92 α-1,2-Mannosidases: Computation Inspires the use of C-Glycosides as Michaelis Complex Mimics

  • Original language description

    The conformational changes in a sugar moiety along the hydrolytic pathway are key to understand the mechanism of glycoside hydrolases (GHs) and to design new inhibitors. The two predominant itineraries for mannosidases go via S-O(2)-> B-2,B-5> S-1(5) and S-3(1)-> H-3(4)-> C-1(4). For the CAZy family 92, the conformational itinerary was unknown. Published complexes of Bacteroides thetaiotaomicron GH92 catalyst with a S-glycoside and mannoimidazole indicate a C-4(1)-> H-4(5)/S-1(5)-> S-1(5) mechanism. However, as observed with the GH125 family, S-glycosides may not act always as good mimics of GH's natural substrate. Here we present a cooperative study between computations and experiments where our results predict the E-5> B-2,B-5/S-1(5)-> S-1(5) pathway for GH92 enzymes. Furthermore, we demonstrate the Michaelis complex mimicry of a new kind of C-disaccharides, whose biochemical applicability was still a chimera.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

    <a href="/en/project/LTAUSA18085" target="_blank" >LTAUSA18085: Poly-β-malic acid and its role as a possible primitive predecessor of nucleic acids</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Chemistry - A European Journal

  • ISSN

    0947-6539

  • e-ISSN

    1521-3765

  • Volume of the periodical

    28

  • Issue of the periodical within the volume

    14

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    6

  • Pages from-to

    e202200148

  • UT code for WoS article

    000750616400001

  • EID of the result in the Scopus database

    2-s2.0-85124159903