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The regular vitamin D metabolic profiles illustrated with either wild-type mouse VDR or VDR null mice transgenic for the wild-type human VDR, but not the ligand binding-defective form of the protein, this suggests the essential roles of VDR on VD metabolism 25
The structure highlights the distinctive triple-proline motif (Pro-Pro-Pro) at positions 3-5 that contributes to the peptide's remarkable stability
In a study by Yan et al
Regarding additional residues of ScGrx7 that could form an interaction site for GSH, we suggest Asp144 and Glu147 in helix 3 as well as the hydroxyl group of conserved Tyr110: First, helix 3 and Tyr110 are both replaced in enzymatically inactive glutaredoxins 11,12 (Fig
Cancer Cell , 34 (1), 2143
Opuwari CS, Henkel RR
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