December 2014 - Chimera-users - RBVI Mailing Lists

How to change colour of H-bond between atoms
by Mahendra B Thapa 18 Dec '14

18 Dec '14

Dear Chimera Users, There is a hydrogen bond between, say, H20 of a ligand (LIG,res no: 240; this H-atom is attached with N atom of LIG) and O atom of GLU 120 residue. There are other hydrogen bonds too, but I am interested to change the color of that H-bond only to, say, red. I tried some like bondcolor red :240@H20 But, it is not working. Any suggestion might help me. Also, is there any way to change width of the H-bond? Thank you, Mahendra Thapa University of Cincinnati,OH

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constrain measurement of rotation to a particular axis?
by Oliver Clarke 17 Dec '14

17 Dec '14

Hi all, When using the “measure rotation” command, is there any way to constrain the rotation to be measured about a particular axis? I am thinking specifically of a case where I have multiple structures of a protein with different inter domain hinge angles - I can use chimera to measure the hinge angle, but for each pair of structures it chooses a slightly different rotation axis, whereas I would like to keep the same axis so I can directly compare the rotation observed between pairs of structures. Or perhaps there is there another way to do this that would make more sense? Suggestions are welcome... Best, Oliver.

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Re: [Chimera-users] Request for Source code
by Elaine Meng 16 Dec '14

16 Dec '14

Dear Jayaraman T, You can turn off helical correction and mass weighting using command options, for example with this command: define axis perHelix true helicalCorrection false massWeighting false See: <http://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/define.html> I’m just trying to convince you this is the easy way! However, you already also have the source code in your download, as Eric described in his reply: <http://plato.cgl.ucsf.edu/pipermail/chimera-users/2014-December/010574.html> Best, Elaine On Dec 15, 2014, at 6:57 PM, Jayaraman T <jaai.nasa(a)gmail.com> wrote: > Yes Elaine, > > We can use Chimera but there are helical correction and mass weighting options exist. And am trying to get it done for all these helices without these options. > > Anyway let me follow up and write you back if there is a need of further assistance. > > I think it would help us more and thanks again for your kindness. > > Good day. > > On Tue, Dec 16, 2014 at 6:51 AM, Elaine Meng <meng(a)cgl.ucsf.edu> wrote: > Dear Jayaraman T, > Chimera download already includes the Python code, but why not just use Chimera? It seems like that would be much, much easier than trying to find and understand all the parts of the code to do it. You can script it with Chimera commands “define” to create helix axes cylinders and “angle” to measure the angle between any pair of those. > > See: > <http://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/define.html> > <http://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/angle.html> > > …and information on looping through structures: > <http://www.rbvi.ucsf.edu/chimera/docs/ProgrammersGuide/basicPrimer.html> > > 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 Dec 14, 2014, at 6:25 PM, Jayaraman T <jaai.nasa(a)gmail.com> wrote: > > > Dear, > > I'm Jayaraman T pursuing PhD here in Pusan National University. Since we are interested to calculate the interhelical angle and axes for a set of proteins, we found Chimera is really helpful for getting us the results. And i would like to do certain analysis on the basis of these interhelical angles, so i kindly request you to provide me the source code and other requirements for calculating the angle between helices. It would be grateful to you and please help me out at your earliest convenience. > > Thanks > > > > -- > Regards > > > Jram | 201493155 > PhD Student > Bio molecular Engineering Lab > School of Chemical Engineering > Pusan National University. > 30 Jangjeon-dong, Geumjeong-gu, > Busan, South Korea - 609-735. > +8210 9906 3680 > jram(a)pusan.ac.kr >

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Request for Source code
by Jayaraman T 15 Dec '14

15 Dec '14

Dear, I'm Jayaraman T pursuing PhD here in Pusan National University. Since we are interested to calculate the interhelical angle and axes for a set of proteins, we found Chimera is really helpful for getting us the results. And i would like to do certain analysis on the basis of these interhelical angles, so i kindly request you to provide me the source code and other requirements for calculating the angle between helices. It would be grateful to you and please help me out at your earliest convenience. Thanks -- Regards Jram | 201493155 PhD Student Bio molecular Engineering Lab School of Chemical Engineering Pusan National University. 30 Jangjeon-dong, Geumjeong-gu, Busan, South Korea - 609-735. +8210 9906 3680 jram(a)pusan.ac.kr

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different behavior of the Win and OS-X version seen in case of surface calculations
by Marek Maly 15 Dec '14

15 Dec '14

Hello, I found already several times the differences between OS-X and Win version of Chimera (1.10.). Problem is regarding the ability to calculate molecular surface. There are some cases when Win version of Chimera 1.10 is not able to calculate molecular surface of some more complicated molecular structure (e.g. protein) but on the other hand the OS-X version of Chimera (again 1.10) is able to do it (although writes warning that there was some partial problems). Moreover when I create PY session of such molecule with surface calculated/visualized under OS-X and then I want to open this session under Win version it is opened but without the surface and writes many errors into the log - see below. In both versions I am using default settings (no special changes in parameters important for the surface calc.). How is this different behavior of the same program under Win and OS-X possible ? Do you have any recommendation how to eliminate this problem ? Thank you in advance, Best wishes, Marek Here is the err list after the attempt to load into Win Chimera 1.10 session containing "problematic" molecule with surface calculated under OS-X version of the Chimera 1.10 ***** C:\Program Files\Chimera 1.10\bin\mscalc.exe 1.400000 2.000000 0 MSMSLIB 1.3 started on Local PC Copyright M.F. Sanner (March 2000) Compilation flags Surface calculation failed, mscalc returned code 5. Surface calculation frequently fails for large, multi-chain structures. The calculation may be successful if the chains are treated individually, by using the "split" command before generating a surface. If splitting is not desired or the structure is already a single chain, changing molecular surface parameters in the Selection Inspector or (before surface creation) the New Surfaces category of Preferences may allow the calculation to succeed. More details are given at http://www.cgl.ucsf.edu/chimera/docs/UsersGuide/surfprobs.html Traceback (most recent call last): File "gB_2G_S16_A.py", line 2669, in <module> restoreCoreModels() File "gB_2G_S16_A.py", line 2654, in restoreCoreModels restoreSurfaces(surfInfo) File "C:\Program Files\Chimera 1.10\share\SimpleSession\versions\v40.py", line 55, in restoreSurfaces elif len(customColors) != len(s.triangleData()[0]): TypeError: 'NoneType' object has no attribute '__getitem__' Error restoring core models: TypeError: 'NoneType' object has no attribute '__getitem__' File "C:\Program Files\Chimera 1.10\share\SimpleSession\versions\v40.py", line 55, in restoreSurfaces elif len(customColors) != len(s.triangleData()[0]): See reply log for Python traceback. Traceback (most recent call last): File "gB_2G_S16_A.py", line 3025, in <module> restoreRemainder() File "gB_2G_S16_A.py", line 3020, in restoreRemainder restoreSilhouettes(silhouettes) File "C:\Program Files\Chimera 1.10\share\SimpleSession\versions\v62.py", line 265, in restoreSilhouettes model = idLookup(modelID) File "C:\Program Files\Chimera 1.10\share\SimpleSession\versions\v23.py", line 162, in idLookup return globals.sessionMap[sesID] KeyError: 27136 Error restoring post-model state: KeyError: 27136 File "C:\Program Files\Chimera 1.10\share\SimpleSession\versions\v23.py", line 162, in idLookup return globals.sessionMap[sesID] See reply log for Python traceback. Warning: Could not restore surface color on surface model with id 0.0 because that surface was not restored. C:\Program Files\Chimera 1.10\bin\lib\site-packages\matplotlib\axes.py:2369: UserWarning: Attempting to set identical left==right results in singular transformations; automatically expanding. left=1, right=1 + 'left=%s, right=%s') % (left, right)) -- Tato zpráva byla vytvořena převratným poštovním klientem Opery: http://www.opera.com/mail/

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Chimera Published Paper
by Kurt Degabriele 08 Dec '14

08 Dec '14

Dear sir/madame, I am a pharmacy student currently undergoing my 4th year pharmacy project at the University of Malta as part of my 5 year study course; I am currently doing research within the Med. Chem. field and would like to ask if you can send me a copy of the following paper so I can include it in my study: UCSF Chimera—A visualization system for exploratory research and analysisEric F. Pettersen, Thomas D. Goddard,Conrad C. Huang, Gregory S. Couch,Daniel M. Greenblatt, Elaine C. Meng andThomas E. Ferrin* Article first published online: 1 JUL 2004DOI: 10.1002/jcc.20084 Regards Kurt

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Re: [Chimera-users] How to use a colour-valued attribute?
by Elaine Meng 04 Dec '14

04 Dec '14

On Dec 3, 2014, at 1:30 AM, Mungo Carstairs (Staff) <g.m.carstairs(a)dundee.ac.uk> wrote: > Thanks all. > Tom, your suggestion of comma- instead or or-delimiter improves speed several times! > Elaine, your point about specifying the chain is noted. > > Conrad, I didn't explain too clearly: my 'real' command is the 'non-contiguous' example (think Zappo colouring with some custom features colours on top). The 'contiguous' example was just what I was using to explore behaviour of setattr / defattr / rangecolor. > (Also by the way the REST API is working fine for me.) > > Instead of 'color' I am now using 'setattr' followed by 'rangecolor'. > I tried both 'setattr' and 'defattr' (passing a temporary file) and didn't see any significant performance difference between them, at the scales I am testing so far (up to 3 models of 1600 residues). > > So I have what I need for now. But I'm still curious to know if / how you get Chimera to 'act on' (display) a colour-valued attribute. > > Best regards, > Mungo Hi Mungo, Setting the color attribute with setattr or defattr does change the color immediately. The problem in what you sent earlier: setattr r color green #0:1-84.B … is that there is no residue attribute named “color". There are atom and molecule-model attributes by that name (setattr a color …) but the only per-residue color setting is ribbon color, name “ribbonColor” … thus you would want something like: setattr r ribbonColor green #0:54.a,76.a … and that would only color the ribbon, not the atoms/bonds. <http://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/atom_spec.html#respr…> Actually I am mystified as to why this would be any faster than using the color command with the same atomspec (#0:54.a,76.a in the example above), but maybe the others who know more about the “guts” of Chimera can comment. Best, Elaine ----- Elaine C. Meng, Ph.D. UCSF Computer Graphics Lab (Chimera team) and Babbitt Lab Department of Pharmaceutical Chemistry University of California, San Francisco

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Commands for multiscale models?
by Hurt, Darrell (NIH/NIAID) [E] 03 Dec '14

03 Dec '14

Hi Chimera friends, I was reading this post from 2009 that indicates that there are no Chimera commands for multiscale models: http://www.cgl.ucsf.edu/pipermail/chimera-users/2009-June/004009.html Is it still the case that there are no Chimera commands for manipulating the multiscale models? I saw the blue-tongue virus example script for doing something similar using Python itself: https://www.cgl.ucsf.edu/chimera/docs/ContributedSoftware/multiscale/blueto… I want to script the loading of an arbitrary VIPERdb model and then create multiscale model surfaces for every chain (not just the copies). Can it be done with Chimera commands? Or do I need to work up my Python-fu? Thanks, Darrell -- Darrell Hurt, Ph.D. Section Head, Computational Biology Bioinformatics and Computational Biosciences Branch (BCBB) OCICB/OSMO/OD/NIAID/NIH 31 Center Drive, Room 3B62B, MSC 2135 Bethesda, MD 20892-2135 Bethesda office: 301-402-0095 Rockville office: 240-669-2741 Mobile: 301-758-3559 Web: BCBB Home Page<http://www.niaid.nih.gov/about/organization/odoffices/omo/ocicb/Pages/bcbb.…> Twitter: @niaidbioit<https://twitter.com/niaidbioit> , @NIH3Dprint<https://twitter.com/nih3dprint> Disclaimer: The information in this e-mail and any of its attachments is confidential and may contain sensitive information. It should not be used by anyone who is not the original intended recipient. If you have received this e-mail in error please inform the sender and delete it from your mailbox or any other storage devices. National Institute of Allergy and Infectious Diseases shall not accept liability for any statements made that are sender's own and not expressly made on behalf of the NIAID by one of its representatives.

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volume viewer step value
by Ludovic Renault 03 Dec '14

03 Dec '14

Hi, When I load different EM volumes into Chimera, depending on the size of the box the display step value changes from 1 to 4. Is it possible to force chimera to always load the 3d map with a step value of 1? Or at least change some parameters in preferences to have step 1 loaded with my routine volumes (up to 300 pixel boxes for example). Thanks, Ludo

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show surface fails
by Hartzell Jr., Criss 03 Dec '14

03 Dec '14

I am struggling to show an electrostatic surface on the solvent accessible surface for several related proteins. It works fine in Pymol with APBS but with Chimera I continue to get "surface calculation failed, mscalc returned code 5". I have read posts going back at least 5 years about this problem and I have tried all of the various work-arounds (vdwdef, split, probe radius and vertex density). Has this problem been solved? I am using version 1.8.1 on a PC. Is there a way to identify which part of the protein is causing the problem? Criss Hartzell Professor Department of Cell Biology Emory University School of Medicine Atlanta, GA 30322 ________________________________ This e-mail message (including any attachments) is for the sole use of the intended recipient(s) and may contain confidential and privileged information. If the reader of this message is not the intended recipient, you are hereby notified that any dissemination, distribution or copying of this message (including any attachments) is strictly prohibited. If you have received this message in error, please contact the sender by reply e-mail message and destroy all copies of the original message (including attachments).

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