Molecular modeling of the Trypanosoma brucei aminopurine transporter P2/TbAT1, implicated in resistance to both diamidine and melaminophenyl arsenical classes of drugs, predicts that residues F19 (left), D140 (top) and F316 (right) interact with substrates. The binding site of adenosine (green carbon atoms) and diminazene (yellow carbon atoms) is shown with hydrogen bonds between Asp140 and bound adenosine in dashed blue lines. For details, see the article by Munday et al. on pp. 887–900 of this issue.

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John Wiley & Sons Inc

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