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Hyperglycemia and prematurity: a narrative review

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DOI: 10.1007/s11884-019-00571-2 full text here: McKernan, L.C., Johnson, B.N., Crofford, L., Lumley, M.A., Bruehl, S., & Cheavens, J.C

7i, we similarly performed molecular docking simulations and found that the active site, selenocysteine (U46), was the most favorable site for the covalent binding of GPX4 by ACE (Protein Data Bank ID 6NH3)