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EC Number	Application	Commentary	Reference
2.7.7.23	drug development	the identification of a selective inhibitory allosteric binding site in the parasite enzyme and the fact that the human and trypanosome enzymes both display a strictly ordered bi-bi mechanism, but with the order of substrate binding reversed, makes the enzyme a good target for drug development	737319

Results 11 - 11 of 11

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Release 2023.1 (January 2023)