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A nitrate molecule was found in both the open and closed form of the catalytic site of PTP1B. This complex was modelled using quantum mechanics and compared to the crystal structure.

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The crystal structure of the heterodimeric ligand-binding domains of the B. ovis ecdysone receptor was solved in the presence of an ecdysteroid and a synthetic methylene lactam insecticide, respectively. Analysis of these structures reveals a new level of conformational flexibility for the ecdysone receptor upon binding of ligands.

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The structure of vanin 1, a human ectoenzyme involved in inflammation and metabolic disease, is shown to be regulated by an unusual allosteric mechanism.
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