Literature DB >> 10673108

Synthesis of dolichyl phosphate derivatives with fluorescent label at the omega-end of the chain, new tools to study protein glycosylation.

V N Shibaev1, V V Veselovsky, A V Lozanova, S D Maltsev, L L Danilov, W T Forsee, J Xing, H C Cheung, M J Jedrzejas.   

Abstract

Derivatives of dolichyl phosphate (Dol-P) with 2-aminopyridine or 1-aminonaphtalene fluorophore groups at the omega-end of the chain were synthesized. These products serve as substrates for recombinant yeast Dol-P-mannose synthase. Fluorescence resonance energy transfer between a Trp residue of the enzyme and the 1-aminonaphtalene group of the Dol-P analogue was demonstrated.

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Year:  2000        PMID: 10673108     DOI: 10.1016/s0960-894x(99)00662-9

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Novel prenyl-linked benzophenone substrate analogues of mycobacterial mannosyltransferases.

Authors:  Mark R Guy; Petr A Illarionov; Sudagar S Gurcha; Lynn G Dover; Kevin J C Gibson; Paul W Smith; David E Minnikin; Gurdyal S Besra
Journal:  Biochem J       Date:  2004-09-15       Impact factor: 3.857

  1 in total

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