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Structures of adenosine kinase from Trypanosoma brucei brucei

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JournalActa Crystallographica Section F: Structural Biology and Crystallization Communications
DatePublished - Jan 2014
Issue number1
Volume70
Number of pages6
Pages (from-to)34-39
Original languageEnglish

Abstract

Trypanosoma brucei is a single-cellular parasite of the genus Kinetoplastida and is the causative agent of African sleeping sickness in humans. Adenosine kinase is a key enzyme in the purine-salvage pathway, phosphorylating adenosine to AMP, and also activates cytotoxic analogues such as cordycepin and Ara-A by their phosphorylation. The structures of T. brucei brucei adenosine kinase (TbAK) in its unliganded open conformation and complexed with adenosine and ADP in the closed conformation are both reported to 2.6 Å resolution. The structures give insight into the binding mode of the substrates and the conformational change induced upon substrate binding. This information can be used to guide the improvement of cytotoxic substrate analogues as potential antitrypanosomal drugs.

    Research areas

  • adenosine kinase, ligand complex, Trypanosoma brucei brucei

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