On Aug 13, 2009, at 12:00 AM, Janet G Yang wrote:
Hi Elaine,
I'm a grad student in Geeta Narlikar's lab, and I've been to a few of your Chimera tutorials at UCSF and found them very helpful. I have a less analytical and more aesthetic structural task, and I'm wondering if you might have any insight. I would like to make a figure showing the structure of the nucleosome with some extra DNA docked in at the edges. The crystal structure of the nucleosome contains 147 bp wrapped around the histone octamer, and I would like to extend out the DNA on one side. I think I could just take the structure of the nucleosome, and that of some B form DNA, and somehow align them together. Is there a good way to do this?
Thanks a bunch janet
Hi Janet, My guess is that lots of people run across similar aesthetic issues -- making a figure is partly art, after all! Everything you say sounds reasonable. First you would need to get the extra B-form DNA, then position it relative to the nucleosome structure. (1) Getting the extra DNA. This could be from another PDB structure, or built using standard B-form parameters. The NDB atlas <http://ndbserver.rutgers.edu/atlas/xray/index.html
lists nucleic acid structures in categories such as B-DNA; you can use "File...Fetch by ID" in Chimera to fetch using NDB identifiers. Those structures might be shorter or less regular than what you need. Here is a server that will build canonical structures to order: <http://structure.usc.edu/make-na/server.html (I admit I haven't actually tried using it, but it looks promising)
(2) Positioning the extra DNA relative to the nucleosome structure. You could position it by hand and/or by matching overlapping sets of atoms. Positioning by hand requires activating/deactivating models for motion so that they can be moved relative to one another -- you would do that with the checkboxes below the Command Line, or with the "A(ctive)" checkboxes in the Model Panel. Matching would be done with the "match" command. It may be tedious to figure out the atom naming in the two structures and then figure out which sets of atoms to match to get the best result, but I don't really see any way around that trial and error process, unless you are really skilled at just positioning the structures by hand. I would probably do some matching and then maybe make slight manual adjustments depending on how it looked. <http://www.cgl.ucsf.edu/chimera/docs/UsersGuide/mouse.html#activedef> <http://www.cgl.ucsf.edu/chimera/docs/UsersGuide/midas/match.html> My answer was based on the understanding that you just want the DNA to trail away in a somewhat straight path, rather than continuing on curling as in the nucleosome. If you wanted that continued curling, there might be some fancy ways to do it with several copies of a curved segment and symmetry operators, but that is beyond my skill set! 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 http://www.cgl.ucsf.edu/home/meng/index.html