Literature DB >> 17311134

Inhibition of pyruvate decarboxylase from Z. mobilis by novel analogues of thiamine pyrophosphate: investigating pyrophosphate mimics.

Karl M Erixon1, Chester L Dabalos, Finian J Leeper.   

Abstract

Replacement of the thiazolium ring of thiamine pyrophosphate with a triazole gives extremely potent inhibitors of pyruvate decarboxylase from Z. mobilis, with K(I) values down to 20 pM; this system was used to explore pyrophosphate mimics and several effective analogues were discovered.

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Year:  2006        PMID: 17311134     DOI: 10.1039/b615861g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

1.  A protecting group-free synthesis of deazathiamine: a step toward inhibitor design.

Authors:  Hong Zhao; Luiz Pedro S de Carvalho; Carl Nathan; Ouathek Ouerfelli
Journal:  Bioorg Med Chem Lett       Date:  2010-09-16       Impact factor: 2.823

2.  Novel TPP-riboswitch activators bypass metabolic enzyme dependency.

Authors:  Christina E Lünse; Fraser J Scott; Colin J Suckling; Günter Mayer
Journal:  Front Chem       Date:  2014-07-28       Impact factor: 5.221

3.  Gold(I)-catalysed synthesis of a furan analogue of thiamine pyrophosphate.

Authors:  Amjid Iqbal; El-Habib Sahraoui; Finian J Leeper
Journal:  Beilstein J Org Chem       Date:  2014-11-05       Impact factor: 2.883

4.  Structural insights into the prereaction state of pyruvate decarboxylase from Zymomonas mobilis .

Authors:  Xue-Yuan Pei; Karl M Erixon; Ben F Luisi; Finian J Leeper
Journal:  Biochemistry       Date:  2010-03-02       Impact factor: 3.162

  4 in total

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