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| - | + | Cytochrome P450 exists as an asymmetric dimer. Two molecules of 2-hydroxypropyl-β-cyclodextrin, which is used to dissolve vitamin D3, are found near the dimer interface. The dimeric interface of cytochrome 450 is additionally stabilized by electrostatic interactions between the <font color='red'>C terminus</font> of the G helix of one molecule (Arg259 and Asp255) with the <font color='blue'>N terminus</font> residues of the F helix of the second molecule (Asp206 and His209) and vice versa. | |
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==Binding Interactions== | ==Binding Interactions== | ||
Revision as of 20:36, 8 April 2016
| This Sandbox is Reserved from January 19, 2016, through August 31, 2016 for use for Proteopedia Team Projects by the class Chemistry 423 Biochemistry for Chemists taught by Lynmarie K Thompson at University of Massachusetts Amherst, USA. This reservation includes Sandbox Reserved 425 through Sandbox Reserved 439. |
Vitamin D activation by cytochrome P450, Rickets (3c6g)[1]
by Isabel Hand, Elizabeth Humble, Kati Johnson, Samantha Kriksceonaitis, and Matthew Tiller
Student Projects for UMass Chemistry 423 Spring 2016
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