Sandbox Reserved 431

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- Asymmetric dimer <br>
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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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- Consists of α-helices, β-sheets (mostly on one side of the molecule) with a heme buried inside the protein <br>
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- Two molecules of 2-hydroxypropyl-β-cyclodextrin are found near the dimer interface <br>
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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

caption for Molecular Playground (PDB entry 3c6g)

Drag the structure with the mouse to rotate
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