February 2022 - Chimera-users - RBVI Mailing Lists

calculating orientation parameters between two asymmetric units
by Sen, Anindito 04 Feb '22

04 Feb '22

Dear All, How can I compute the parameters (angle , shift) of orientation between 2 asymmetric units w.r.t the central axis in a density map (and the map is not helical). Stay safe & Regards Anindito Sen. Ph.D Microscopy and Imaging Center Texas A&M University 301 Old Main Dr College Station, TX 77843-2257 Office: ILSB Room 1133 <http://microscopy.tamu.edu/>Tel. 979-458-9881 fax: 979-847-8933 http://microscopy.tamu.edu<http://microscopy.tamu.edu/>

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Re: [Chimera-users] [chimerax-users] Automate calculation and saving of residues' structural attributes
by Elaine Meng 04 Feb '22

04 Feb '22

Hi Christian, I guess this is a Chimera question now, so I set the "reply to" to chimera-users in case this generates further messages. The following pertains to Chimera. I believe it uses the MSMS code without modification to do the actual calculation, so it might be needless work to run all this benchmarking. Nevertheless I can understand why you want to figure out the cause of any differences. (a) I would expect differences in VDW radii to be a major factor. The Chimera default radii are described/listed in the User Guide, see this and links therein: <https://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/vdwrad.html> You could try assigning the MSMS-provided radii within Chimera before performing the area calculation in Chimera. See the bottom section of the help page URL above for possible ways of assigning different VDW radius values. (b) secondarily, it depends how you use the command... if you just used Chimera command "surface" it would automatically just surface the macromolecules and try to omit waters, ligands, etc. However, you can use "surfcat" command to define whatever sets of atoms you like for subsequent "surface" calculations. Chimera surface command <https://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/surface.html> Chimera surfcat command <https://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/msms.html> (c) dealing with the code is beyond my skill set, so if you still need pointers to look therein, somebody else would have to advise. I hope this helps, Elaine ----- Elaine C. Meng, Ph.D. UCSF Chimera(X) team Department of Pharmaceutical Chemistry University of California, San Francisco > On Feb 3, 2022, at 12:33 AM, Christian Tüting via ChimeraX-users <chimerax-users(a)cgl.ucsf.edu> wrote: > > Hi All, > > Andre and I continued this conversation in private, as this was not > Chimera related anymore. > > Somehow, we have a question regarding the calculation of the of the SES > and SAS. > > In principle, I looked into the calcsurf.py file in the chimera folder, > and figured out, that this calculation is done by msms with a probe > radius of 1.4 and a density of 2 and noh. So I copied the code into my > workflow and tested this with a xyzr file, generated by the pdb_to_xyzr > shell script from msms, and got the same results, as if I am running > directly msms from command line. So far not suprisingly. > > But when we take the same pdb file, the msms code itself gives slightly > different values than chimera. Often, it's not siginificant, but Andre > benchmarked this, and sometimes the difference is more than 1.2 fold. > > > > So this let us come to the conclusion, that chimera somehow calculates a > different xyzr file, compared to what the shell script is doing. I was > not able to find the code for caluclating the xyzr file. Another > explanation is, that chimera treats the results a bit differently. msms > results ses and sas per atom, we "just" summed them per residue to get > the per residue value. But I don't think, that this is done differently > here. > > > So our questions are: > (a) is the radius definition different in chimera from what is given > with the msms software ( https://ccsb.scripps.edu/msms/downloads/; there > is a shellscript and, more importantly a text file, which defines the > radius of each atom, with a lot of special cases ). > (b) is the structure somehow "filtered" prior to surface calculation. > E.g. are waters, ions, ligands considered part of the structure, of are > they excluded, as this might introduce also some differences > (c) or can you help us find the actual code for this in chimera, than I > will be able to anwser the question myself > > Thanks in advance. > > Christian > > > >>>> André <andre.jfmdm(a)gmail.com> 01/21/22 7:06 PM >>> > Hi Elaine, > > Thank you so much for your very helpful answer! > > Yeah, Tom told me before that it wouldn't be possible to directly > calculate > SESA and relSESA with ChimeraX. So, I'll probably have to stick with > Chimera. I've just discovered the "list" command (functional in > Chimera), > and I think that with it I'll be able to easily get all the attributes > by > using the --nogui startup. > I'll work on it in the following days, then I'll come back with updates. > > Once again, thank you very much! > > Best, > André. > > Em sex., 21 de jan. de 2022 às 13:55, Elaine Meng <meng(a)cgl.ucsf.edu> > escreveu: > >> Hi André, >> Although it displays an SES, ChimeraX does not calculate SES areas, > only >> SAS areas (command "measure sasa" which also assigns a residue > attribute). >> <https://rbvi.ucsf.edu/chimerax/docs/user/commands/measure.html#sasa> >> >> For Chimera, another group had provided SES reference areas for the >> exposed state represented by G-X-G tripeptides, but I don't know of a >> similar SAS reference area set for ChimeraX that could be used to > calculate >> relative exposure, sorry. In case others are interested, the Chimera >> relative exposure calculation giving relSESA is described here: >> <https://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/surfnorm.html> >> >> So depending on the importance of SESA and relSESA, you may need to > use >> Chimera, or at least some method outside of ChimeraX. >> >> In both ChimeraX and Chimera, bfactor is read from the input PDB file, > and >> phi and psi are calculated automatically for peptide/protein > structures >> when they are read in. ChimeraX atom and residue attributes: >> <https://rbvi.ucsf.edu/chimerax/docs/user/attributes.html#atom> >> <https://rbvi.ucsf.edu/chimerax/docs/user/attributes.html#residue> >> >> kdHydrophobicity is not a calculation, but a simple lookup table by > amino >> acid type. You may not need either program to "calculate" it, but it > is >> automatically assigned in Chimera. It can be assigned in ChimeraX by >> running this comand script: >> < >> > https://rbvi.ucsf.edu/chimerax/docs/user/kyte-doolittle> values along with some alternative hydrophobicity scales (lookup > tables) >> are summarized here: >> > <https://www.rbvi.ucsf.edu/chimera/docs/UsersGuide/midas/hydrophob.html> >> >> I hope this helps, >> Elaine >> ----- >> Elaine C. Meng, Ph.D. >> UCSF Chimera(X) team >> Department of Pharmaceutical Chemistry >> University of California, San Francisco >> >>> On Jan 21, 2022, at 7:28 AM, André via ChimeraX-users < >> chimerax-users(a)cgl.ucsf.edu> wrote: >>> >>> Hi Christian, >>> >>> Thank you so much for your solution! That indeed helps a lot, since > it >> shows me how to execute ChimeraX scripts independently and directly > from >> Python! >>> >>> Now, do you know which commands I should use to calculate the > following >> structural attributes for all residues: areaSAS, areaSES, relSESA, > bfactor, >> kdhydro, phi, psi? >>> >>> I do it manually in Chimera (haven't figured out how to do the same > in >> ChimeraX yet), by following the route: Tools -> Structure Analysis -> >> Render by Attribute -> File -> Save Attributes -> Attribute to Save, > which >> allows each attribute of residues to be saved as txt files, which > contain >> the residue number and respective attribute, for all residues in the >> protein. For example, the file for areaSAS looks like this: >>> >>> attribute: areaSAS >>> recipient: residues >>> :1.B 116.71626508235931 >>> :2.B 118.39353680610657 >>> ... >>> >>> Thus, that's what I wanted to do: figure out which commands I should > use >> to get the same result as the manual route above (although it is not >> really necessary that the txt file is generated directly -- if the > needed >> information appear in the stdout_as_str string, just like in the > example >> you showed, I'd be able to parse it to a file, and the problem would > be >> solved!). >>> >>> Once again, thank you for your help! >>> >>> Best, >>> André. >>> >>> >>> >>> Em sex., 21 de jan. de 2022 às 09:56, Christian Tüting < >> christian.tueting(a)biochemtech.uni-halle.de> escreveu: >>> Hi André, >>> >>> i am pretty sure, that my solution is very crude and that there are >>> better ways of doing it (like importing chimerax in the python code >>> directly). I guess, you'll get more anwsers soon. >>> >>> I quickly wrote a script, which performs a chimerax task > independently, >>> by just running python code. >>> >>> First: a chimerax script file with the desired commands: >>> >>> script.cxc: >>> open 7ott >>> surface #1 >>> mearuse area #1 >>> exit >>> >>> Note: the exit command is needed, otherwise the subprocress will > idle in >>> the chimerax cmd line. >>> >>> >>> Second: a python script, which execute this script in chimerax and >>> fetches the output: >>> >>> test.py: >>> >>> import subprocess >>> import os >>> >>> cwd = os.getcwd() >>> >>> chimerax = > "/Applications/ChimeraX_Daily.app/Contents/MacOS/ChimeraX" >>> scriptfile = f"{cwd}/script.cxc" >>> >>> cmd = [chimerax, "--nogui",scriptfile] >>> p = subprocess.run(" ".join(cmd),shell = True,capture_output=True) >>> >>> stdout_as_str = p.stdout.decode("utf-8") >>> print(stdout_as_str) >>> >>> This just runs a subprocess and fetches the output to a string, > which >>> you can than further analyse. >>> >>> >>> Best >>> Christian >>> >>> >>> >>> Dr. rer. nat. Christian Tüting >>> >>> Kastritis Laboratory for Biomolecular Research >>> Cryo-Electron Microscopy & Computational Structural Biology >>> ________________________________________________ >>> Martin-Luther-Universität Halle-Wittenberg >>> Biozentrum, Room A.2.19 >>> IWE ZIK HALOmem NWG III >>> "Kryo-Elektronenmikroskopie an Membranproteinkomplexen" >>> Weinbergweg 22, 06120 Halle >>> tel: +49 345 5524985 >>> web (Lab): https://blogs.urz.uni-halle.de/kastritislab/ >>> web (HALOmem): https://www.halomem.de/en/ >>>>>> André via ChimeraX-users <chimerax-users(a)cgl.ucsf.edu> 01/21/22 > 1:29 >>> PM >>> >>> Hello! >>> >>> I'm working on an automated pipeline (in Python) for the structural >>> analysis of proteins. In particular, I'm using Chimera to> > areaSES, relSESA, bfactor, kdhydro, phi, psi). These files are the >>> inputs >>> of the pipeline. >>> However, currently the files are exported manually, and, for the > purpose >>> of >>> building a fully automated pipeline, it would be great to also > automate >>> this step of calculating the attributes and exporting their > respective >>> files. >>> >>> I searched a lot, and tried some ways to achieve such an automation >>> (using >>> Chimera), but nothing worked. >>> And I also considered using ChimeraX. In particular, I went through >>> ChimeraX Programming Manual ( >>> https://www.cgl.ucsf.edu/chimerax/docs/devel/index.html#) but, if I >>> understood correctly, I'd only be able to import chimerax and use > its >>> functions in the Python interpreter within ChimeraX (Tools >> > General >> >>> Shell). >>> At first, I'd like to import chimerax as a module in a Python >>> interpreter >>> outside of ChimeraX, so that manually opening ChimeraX wouldn't be >>> necessary in order to save the files with the residues' attributes. > But, >>> from some other threads in the mailing list, I found that it > wouldn't be >>> possible (right?) >>> >>> But I also found out that I could write a .py script which > calculates >>> and >>> exports the files with the residues' properties, and then run it > with >>> ChimeraX application from the command-line, something like: > *chimerax >>> --nogui myscript.py* >>> If that works, I think that my automation problem would be solved! > The >>> only >>> problem is that I really couldn't figure out the Python code to >>> calculate >>> and export the aforementioned residues' properties (I took a look in >>> ChimeraX Recipes (https://rbvi.github.io/chimerax-recipes/) but I >>> couldn't >>> find what I need, nor more detailed documentation). >>> >>> Given that, I'd like to know if anyone has done something like this, >>> and/or >>> have any guidance on how I could proceed. >>> >>> I really appreciate any help you can provide! >>> (And thanks to Tom Goddard for suggesting moving the discussion here > to >>> the >>> ChimeraX mailing list). >>> >>> Thank you so much, >>> André. >>> >>> _______________________________________________ >>> ChimeraX-users mailing list >>> ChimeraX-users(a)cgl.ucsf.edu >>> Manage subscription: >>> https://plato.cgl.ucsf.edu/mailman/listinfo/chimerax-users >> >> > > _______________________________________________ > ChimeraX-users mailing list > ChimeraX-users(a)cgl.ucsf.edu > Manage subscription: > https://plato.cgl.ucsf.edu/mailman/listinfo/chimerax-users >

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Fwd: choose the rotation center
by Eric Pettersen 01 Feb '22

01 Feb '22

> Begin forwarded message: > > From: Yanhe Zhao <yanhezhao1990(a)gmail.com> > Subject: choose the rotation center > Date: February 1, 2022 at 1:02:12 PM PST > To: chimera-users-owner(a)cgl.ucsf.edu > > Hello there, > > I want to fixed the center for my rotation but have two questions here: > 1, how I easily read out the xyz coordinate of the point I want to use as center? > 2, as attached, what the xyz sequence here, xyz from top to bottom? > > Thanks and appreciate for your help! > Yanhe

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Location of executable local docking path
by Shreeramesh 01 Feb '22

01 Feb '22

Dear Sir, I am performing molecular docking using Autodock vina in Chimera. Could you please guide me how to operate an executable location locally? Which is the file to be loaded in the local path? I will be thankful to you for your kind help *Thanks & Regards* *Dr. Ramesh M* *B. Pharma., M.Pharma., Ph.D. (MedChem)* *Post-Doctoral Fellow (PDF) in Pharmaceutical Sciences* *Researcher ID:* https://orcid.org/0000-0003-0119-206X <https://www.portfoliobox.net/pb4/admin/#/drrameshm> *Website: *https://scholar.google.com/citations?user=VHOE1dgAAAAJ&hl=en Hyderabad, INDIA Email: shreeramesh(a)gmail.com Mob.: +91-9542200332

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Calculating correlation value between PDB and volume
by Long Gui 01 Feb '22

01 Feb '22

Dear Chimera-user group, I am using Chimera version 1.14. After I have manually place the PDB model in the volume file, I would like to calculate the correlation value between the current position of PDB file and the volume. I have used "Fit dialog" and "use simulated map" but the correlation value only displayed the optimized value after shift and rotation. I have also disabled "rotation" and "shift" but the results were the same. Because my volume contains more proteins than the PDB files, the "Fit in map" always place the PDB files into the densities corresponding to other proteins. I just want to have the correlation value between the manually placed PDB and the volume. How could I do this in Chimera? Thanks, Long Gui, Ph.D. Postdoc Researcher, Nicastro Lab University of Texas Southwestern Medical Center Long.Gui(a)utsouthwestern.edu Tel: (214)-645-1561 ________________________________ UT Southwestern Medical Center The future of medicine, today.

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"Cartoon" command unrecognized
by Dmitry Lyumkis 01 Feb '22

01 Feb '22

Dear Chimera support, I am trying to display a protein as tubes, using the “cartoon” command. I am following some of the instructions here: https://www.cgl.ucsf.edu/chimerax/docs/user/commands/cartoon.html#style However, I get “unrecognized command” when I enter “cartoon” on the command line. Could this be a version issue? My Chimera version is 1.15 (build 42258) 2020-12-18. Best, Dmitry

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