Literature DB >> 12202255

Novel tools for the study of class I alpha-mannosidases: a chromogenic substrate and a substrate-analog inhibitor.

T Desmet1, W Nerinckx, I Stals, N Callewaert, R Contreras, M Claeyssens.   

Abstract

The use of chromogenic substrates for evaluation of class I alpha-mannosidase is described. 2('),4(')-Dinitrophenyl-alpha-D-mannopyranoside allows rapid and sensitive assays of enzymatic activities, e.g., of heterologously expressed alpha-1,2-mannosidase from Trichoderma reesei. Interaction constants of several ligands with alpha-mannosidases from class I and II could also be determined. Furthermore, novel types of inhibitors derived from D-lyxose are presented. Methyl-alpha-D-lyxopyranosyl-(1(')-->2)-alpha-D-mannopyranoside is a potent inhibitor of the alpha-1,2-mannosidase from T. reesei (K(i)=600 microM) and since it probably spans subsites -1/+1, this disaccharide could be valuable in crystallographic studies of class I alpha-mannosidases.

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Year:  2002        PMID: 12202255     DOI: 10.1016/s0003-2697(02)00039-8

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  3 in total

1.  Synthesis of the Mixed Acetal Segment of S-Glyceroplasmalopsychosine.

Authors:  Ajit K Parhi; David R Mootoo; Richard W Franck
Journal:  Tetrahedron       Date:  2008-10-13       Impact factor: 2.457

2.  Modulation of activity by Arg407: structure of a fungal alpha-1,2-mannosidase in complex with a substrate analogue.

Authors:  Yuri D Lobsanov; Takashi Yoshida; Tom Desmet; Wim Nerinckx; Patrick Yip; Marc Claeyssens; Annette Herscovics; P Lynne Howell
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2008-02-20

3.  Tandem Allylboration-Prins Reaction for the Rapid Construction of Substituted Tetrahydropyrans: Application to the Total Synthesis of (-)-Clavosolide A.

Authors:  Alba Millán; James R Smith; Jack L-Y Chen; Varinder K Aggarwal
Journal:  Angew Chem Int Ed Engl       Date:  2016-01-14       Impact factor: 15.336

  3 in total

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