- Chimera-users - RBVI Mailing Lists

opening image stack
by chinmaya joshi 17 Jun '11

17 Jun '11

Can you help me how I can open a stack of .png images using a command line in chimera. I will have a set of images and I want to open the stack in chimera using the command line. Is there any python script for this? Waiting for replies

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Sequence aligment
by Simon Sham 17 Jun '11

17 Jun '11

Hi, Is it possible that to do a sequence alignment in Chimera given only a text file with 2 protein amino acid sequences? I have the pdb files but there are some missing amino acids in them. Thanks for your help. Simon

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Chimera-1.5.3 on RHEL 5 Linux workstation does not display surface
by Starr Hazard 15 Jun '11

15 Jun '11

Folks, I recently upgraded my LINUX to RHEL 5 (its an old machine and RHEL 6 did not recognize my old graphics card so I settled for RHEL5). I have installed xterm (eg yum install xerm). I downloaded Chimera 1.5.3 build 33475 2011-5-24 17:23 When I read in a PDB file and then try to display a surface, the calculation finishes but the display of the surface is fragmented with only a few of the triangular surface components displayed. The issue is not confined to a particular PDB. A windows version 1.5.3 works nominally with respect to surface display. So I am wondering if I have my xterm properly installed. Can you suggest some things for me to examine? Thanks Starr

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Chimera API question
by Jonathan Rodgers 15 Jun '11

15 Jun '11

Hello, After looking through the Chimera documentation and examples, I couldn't find any mention of working with volumes. Is that data currently accessible through the API? Thanks, Jonathan Rodgers

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help
by chinmaya joshi 14 Jun '11

14 Jun '11

Hello, I want to write a script in python to open a set of images in chimera set a viewpoint(rotate, translate,etc). and make a movie out of them all through command line for my project. Can someone please let me know how it can be done. I am new to python. Can anyone tell me any good links for these? The documentation on chimera ucsf is a bit confusing. Thanks. Chinmaya

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Biological dimer shows up as a monomer
by James Ferrell 13 Jun '11

13 Jun '11

I'm new to Chimera and trying to create a figure panel for a paper. I'm running Chimera on a Mac from the graphical interface. The protein is a a yeast topoisomerase II. Its PDB ID is 2RGR. If I view the protein with Cn3D I can see the whole biological unit, in which the protein is present as a symmetrical dimer (with some DNA strands too). If I view it with Chimera I see a protein monomer. The problem is I want to illustrate a particular intermolecular salt bridge, which is present in the dimer but isn't present in the monomer. Is there some preference to toggle to allow Chimera to display the whole biological unit? Or would I have to artificially build a dimer out of two monomer models? Thanks, Jim -=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=- James E. Ferrell, Jr., M.D., Ph.D. Professor and Chair of Chemical and Systems Biology Stanford University School of Medicine

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Protein Design
by Jared Adolf-Bryfogle 13 Jun '11

13 Jun '11

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Re: [Chimera-users] [chimera-dev] Protofibril model
by Elaine Meng 09 Jun '11

09 Jun '11

Dear Lihong and others, The Multiscale Models tool in Chimera is meant for this purpose --- it shows low-resolution surfaces, which are often preferred for large complexes. In Chimera I tried opening 1ei3, then started Multiscale Models (in menu under Tools... Higher-Order Structure), then clicked the "Make models" button at the bottom of the multiscale dialog. This shows the structure with low-resolution surfaces and automatically uses different colors for the different chains. You can adjust the colors, surface resolution, etc. in the dialog. Click the dialog's Help button to see its manual page. There is also a copy here: <http://www.cgl.ucsf.edu/chimera/docs/ContributedSoftware/multiscale/framemu…> I also tried it with 1m1j, which also worked fine on my computer. I hope this helps, Elaine ---------- Elaine C. Meng, Ph.D. UCSF Computer Graphics Lab (Chimera team) and Babbitt Lab Department of Pharmaceutical Chemistry University of California, San Francisco On Jun 9, 2011, at 12:13 PM, Russell M. Taylor II wrote: > Dear Lihong, > I am glad to hear that Chimera let you start down this path. > I'm CCing the Chimera developer mailing list in case they know of a better solution. > You can also join the chimera users list at http://plato.cgl.ucsf.edu/mailman/listinfo/chimera-users/index.html and then post a query there. > > The following is a somewhat convoluted path to get where you want to go. Hopefully someone on one of the above mailing lists will know a better one. If you need to go down this path, we should probably set a time for us to sit down together and go through this. > > Download MGLTools from http://mgltools.scripps.edu/downloads. I ran the Windows installer. > This launched the Python Molecule Viewer. > Select Compute/Coarse Molecular Surface. Kept the default parameters. This produced a surface that was near the outside of the molecule. > Clicked to turn off the red dot under the CPK label so that we only see the surface. > Selected File/Save/VRML 2.0 (.wrl) file. Also saved STL file. > > I was able to load the resulting .wrl file back into Chimera. This should provide you with a simplified model. You should be able to adjust the parameters for the coarse saving to get different model quality. > > I attach the resulting coarse model (inside a Zip file) to this email. > Russ > > [Things below I tried that didn't work] > > (Fine surface) > Select File/Read Molecule. Opened 1EI3.pdb (when I used 1M1J.pdb, it crashed trying to make the surface). > Compute/Molecular Surface/Compute Molecular Surface. Used the default parameters (other parameters caused it to crash). This produced a fine molecular surface. This could be used directly or simplified. > > VMD uses a program called MSMS, but can't run it. When I go to the MSMS home page, it eventually redirects me to MGLTools from Scripps. > > NOPE: > > You can load the PDB file into the VMD program (File/New, select the file name and click Load on the Molecule File Browser). Then select Graphics/Representations from the VMD Main menu. Then pull down Drawing Method and select Surf. Turn off the "Apply Changes Automatically" control and then set the Probe Radius to 4.0 and click Apply. > To turn off the little axes display, select Display/Axes/Off > To save the resulting geometry, select File/Render from the main menu. Pull down "Render using" and select Wavefront. Change the .obj file name to one that is useful to you (I named id protofibril.obj). Click the "Start Rendering" button. > > Open Blender (available from blender.org) Press delete to get rid of the cube that is created by default. > Select File/Import/Wavefront to load the model. Pick the file name and then click "Import a Wavefront OBJ" > > At 10:18 AM 6/7/2011, lihong huang wrote: >> Dear Dr. Taylor, >> >> I am postdoc working in Dr. Susan Lord's lab. According to your suggestion, we set up the protofibril model using UCSF Chimera program which is very nice. Now we want to move on to make small fiber model, however, the program run very slowly when we add more fibrinogen molecules. We are thinking if we could make the fibrinogen molecule lose more details, maybe the program could run easily. Do you know which program could do this? We just want to show the basic shape of fibrinogen, no needs to show very detailed part, such as alpha, beta and gamma chains. Thanks a lot for your help. >> >> Lihong Huang, >> Postdco >> Pathology and lab medicine > > --- > Russell M. Taylor II, Ph.D. taylorr(a)cs.unc.edu > CB #3175, Sitterson Hall www.cs.unc.edu/~taylorr > University of North Carolina, Voice: (919) 962-1701 > Chapel Hill, NC 27599-3175 FAX: (919) 962-1799 <protofibril.zip>_______________________________________________ > Chimera-dev mailing list > Chimera-dev(a)cgl.ucsf.edu > http://plato.cgl.ucsf.edu/mailman/listinfo/chimera-dev

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Contacts
by George Tzotzos 07 Jun '11

07 Jun '11

Hi everybody, I'm trying to analyse AMBER trajectories of protein/ligand complexes. The objective of my exercise is to find out contacts/interactions between the ligand and the receptor in the course of the trajectory. Is there a way of doing this DIRECTLY in Chimera? Or one has to first perform clustering of structures and then work out clashes/contacts on the representative structures that are dumped from the trajectory. Best regards George

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mac default directory
by Dougherty, Matthew T 06 Jun '11

06 Jun '11

Hi- Where is the default directory for movie images on the mac? thanks, Matthew Dougherty National Center for Macromolecular Imaging Baylor College of Medicine

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