Literature DB >> 19072094

Synthesis and biological evaluation of a chitobiose-based peptide N-glycanase inhibitor library.

Martin D Witte1, Danielle Horst, Emmanuel J H J Wiertz, Gijsbert A van der Marel, Herman S Overkleeft.   

Abstract

Peptide N-glycanase (PNGase), the enzyme responsible for the deglycosylation of N-linked glycoproteins, has an active site related to that of cysteine proteases. Chitiobiose was equipped with electrophilic traps often used in cysteine protease inhibitors, and the resulting compounds were evaluated as PNGase inhibitors. We found that the electrophilic trap of the inhibitor has a great influence on the potency of the compounds with the chloromethyl ketone inhibitor being the first potent C-glycoside-based PNGase inhibitor.

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Year:  2009        PMID: 19072094     DOI: 10.1021/jo801906s

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  4 in total

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2.  'Naked' and hydrated conformers of the conserved core pentasaccharide of N-linked glycoproteins and its building blocks.

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3.  Inhibition of NGLY1 Inactivates the Transcription Factor Nrf1 and Potentiates Proteasome Inhibitor Cytotoxicity.

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Journal:  ACS Cent Sci       Date:  2017-10-25       Impact factor: 14.553

4.  Transcription factor Nrf1 is topologically repartitioned across membranes to enable target gene transactivation through its acidic glucose-responsive domains.

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  4 in total

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