Literature DB >> 6819005

The use of inhibitors in the study of glycosidases.

P Lalégerie, G Legler, J M Yon.   

Abstract

The use of non-covalent as well as covalent inhibitors can be a useful tool to approach the mechanism of activity of glycosidases. An efficient method to determine the essential amino-acid groups directly or indirectly involved in the catalytic process is the use of active site directed irreversible inhibitors. Epoxide derivatives from conduritol B and conduritol C are the most important inhibitors in this group. The use of active site reversible inhibitors: cationic and basic glycosyl derivatives, glycals, glyconolactones, thioglycosides, is effective to study the different charges at the active site or the transition state during catalysis and also to detect conformational adaptability of an enzyme. Furthermore, inhibitors can be valuable tools to investigate various aspects of the physiological role of glycosidases.

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Year:  1982        PMID: 6819005     DOI: 10.1016/s0300-9084(82)80379-9

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  12 in total

1.  Chorismate synthase. Pre-steady-state kinetics of phosphate release from 5-enolpyruvylshikimate 3-phosphate.

Authors:  T R Hawkes; T Lewis; J R Coggins; D M Mousdale; D J Lowe; R N Thorneley
Journal:  Biochem J       Date:  1990-02-01       Impact factor: 3.857

2.  Phospho-beta-glucosidase from Fusobacterium mortiferum: purification, cloning, and inactivation by 6-phosphoglucono-delta-lactone.

Authors:  J Thompson; S A Robrish; C L Bouma; D I Freedberg; J E Folk
Journal:  J Bacteriol       Date:  1997-03       Impact factor: 3.490

3.  Inhibition of the alpha-L-arabinofuranosidase III of Monilinia fructigena by 1,4-dideoxy-1,4-imino-L-threitol and 1,4-dideoxy-1,4-imino-L-arabinitol.

Authors:  M T Axamawaty; G W Fleet; K A Hannah; S K Namgoong; M L Sinnott
Journal:  Biochem J       Date:  1990-02-15       Impact factor: 3.857

4.  On the antiperiplanar lone pair hypothesis and its application to catalysis by glycosidases.

Authors:  M L Sinnott
Journal:  Biochem J       Date:  1984-12-15       Impact factor: 3.857

5.  Histidines, histamines and imidazoles as glycosidase inhibitors.

Authors:  R A Field; A H Haines; E J Chrystal; M C Luszniak
Journal:  Biochem J       Date:  1991-03-15       Impact factor: 3.857

6.  A new entry to glycosylamines.

Authors:  F L Merchán; P Merino; T Tejero
Journal:  Glycoconj J       Date:  1997-06       Impact factor: 2.916

7.  Inhibition of cell wall-associated enzymes in vitro and in vivo with sugar analogs.

Authors:  G Nagahashi; S I Tu; G Fleet; S K Namgoong
Journal:  Plant Physiol       Date:  1990-02       Impact factor: 8.340

8.  2,3-di-O-tetradecyl-1-O-(beta-D-glucopyranosyl)-sn-glycerol is a substrate for human glucocerebrosidase.

Authors:  R H Glew; V Gopalan; C A Hubbell; R V Devraj; R A Lawson; W F Diven; D A Mannock
Journal:  Biochem J       Date:  1991-03-01       Impact factor: 3.857

9.  Effects of deuterium substitution alpha and beta to the reaction centre, 18O substitution in the leaving group, and aglycone acidity on hydrolyses of aryl glucosides and glucosyl pyridinium ions by yeast alpha-glucosidase. A probable failure of the antiperiplanar-lone-pair hypothesis in glycosidase catalysis.

Authors:  L Hosie; M L Sinnott
Journal:  Biochem J       Date:  1985-03-01       Impact factor: 3.857

10.  Evidence for the involvement of glycanase activities in the dissociation of cortical cell walls during the emergence of callus from rice root tissues in the presence of 2,4-D.

Authors:  K Yoshida
Journal:  Plant Cell Rep       Date:  1995-01       Impact factor: 4.570

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