Jmol/Visualizing membrane position

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Viewing the model in [[FirstGlance in Jmol]], you can use ''Hydrophobic/Polar'' (Views tab) to visualize the domain with a hydrophobic surface. Touching or clicking on atoms at the domain boundaries will identify those amino acids. If you wish, you can center a particular residue, then zoom in, and see atomic detail with ''Vines/Sticks'' (Views tab).
Viewing the model in [[FirstGlance in Jmol]], you can use ''Hydrophobic/Polar'' (Views tab) to visualize the domain with a hydrophobic surface. Touching or clicking on atoms at the domain boundaries will identify those amino acids. If you wish, you can center a particular residue, then zoom in, and see atomic detail with ''Vines/Sticks'' (Views tab).
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For 5LiL, I chose thr607.og1 and leu250.cd1. "OG1" means "oxygen, gamma one", namely a sidechain oxygen that is 2 bonds away from the alpha carbon. CD1: carbon, delta one. It would have worked equally well to use the entire residues, simply thr607 and leu250.
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For 5LiL, I chose thr607 and leu250. These will be used in the example commands below, but you must substitute appropriate amino acids for your model.
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5LiL is a homo-dimer of chains A and B. Since I did not specify a chain in the commands below, the position of, for example, thr607 will be the average position of all the atoms in thr607 in both chains. That average position will be at the axis of the rod-shaped molecule. Your molecule may require a different strategy.
===Generate the Cylinder===
===Generate the Cylinder===
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After displaying the cylinder with your new green link, if you then click a different green link, the cylinder may persist, unwanted. To fix this:
After displaying the cylinder with your new green link, if you then click a different green link, the cylinder may persist, unwanted. To fix this:
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# In the SAT, load the other scene.
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# In the SAT, load the other scene. It doesn't matter if the cylinder is not visible in the SAT.
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**It doesn't matter if the cylinder is not visible in the SAT.
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# Open the command console.
# Open the command console.
# Enter the above ''delete'' command.
# Enter the above ''delete'' command.
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# Update the green link to use the newly saved version of the scene.
# Update the green link to use the newly saved version of the scene.
# Test.
# Test.
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===Color The Cylinder Ends===
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Here are the commands to generate a translucent cylinder with a red top and a blue bottom:
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<pre>draw cyl1 cylinder diameter 100.0 color gray (thr607) (leu250) nofill mesh
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draw cyl1 color translucent -1
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draw ctop circle diameter 100.0 color red (thr607) (leu250)
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draw ctop color translucent -1
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draw cbot circle diameter 100.0 color blue (leu250) (thr607)
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draw cbot color translucent -1</pre>
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*Adding '''nofill mesh''' to the end of the first ''draw'' command removes the ends of the gray cylinder.
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*Notice the reversed order of the amino acids in the two ''circle'' commands. The first position is the center of the circle. The second position makes the circle perpindicular to the axis between the two specified positions.
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Revision as of 19:54, 30 March 2018

Caption for this structure

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References

  1. 1.0 1.1 Lomize MA, Pogozheva ID, Joo H, Mosberg HI, Lomize AL. OPM database and PPM web server: resources for positioning of proteins in membranes. Nucleic Acids Res. 2012 Jan;40(Database issue):D370-6. doi: 10.1093/nar/gkr703., Epub 2011 Sep 2. PMID:21890895 doi:http://dx.doi.org/10.1093/nar/gkr703

Proteopedia Page Contributors and Editors (what is this?)

Eric Martz, Kristen Procko

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