- phenixbb - phenix-online.org

Jumping Rfree upon bulk solvent modeling
by Weinert Tobias (PSI) 09 Jan '19

09 Jan '19

Dear PHENIXBB community, i have come across a strange behavior in Phenix: * I copied Rfree-flags from a dataset with very slightly different unit cell * Refined the previously refined model against the new data * Rfactors in first round were good * Second round in refinement Rfree was up by 10 % just from the start during bulk solvent modeling and scaling * In another round Rfree was high in the beginning, and then dropped by those 10 % during bulk solvent modelling and scaling. * In yet another round Rfree started 10% lower than the previous round during bulk solvent modeling in the first cycle and then it jumps up again in the second cycle. What could be wrong? Many thanks and kind regards, Tobias Weinert

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mmCIF in Phenix 1.14-3260
by Dominik Oberthuer 31 Dec '18

31 Dec '18

Dear all, I recently found that phenix.refine in version 1.14-3260 generates coordinate mmCIFs that the PDB deposition system can't handle. After struggling with this for some time I used an installation of Phenix 1.13-2998 I still have on my MacBook and used the mmCIF/PDB-conversion tool from this version and had no more trouble with uploading the mmCIF to the PDB. Maybe it is worthwhile to check which changes from 1.13 to 1.14 might have caused these issues. Thanks! Dominik -- Dr. Dominik Oberthür CFEL - Center for Free-Electron Laser Science - DESY Coherent Imaging Division Notkestrasse 85 22607 Hamburg Germany phone: +49 (0)40 8998 6394 dominik.oberthuer(a)cfel.de

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smaller the cell parameter of EM map
by dancingdream＠163.com 30 Dec '18

30 Dec '18

Dear all, The cell parameter of the EM map is always too large, which will make the model building program running very slow. But in factor, the structure is a smal part of cell. So can I smaller the cell parameter when I use phenix.map_to_structure_factors to convert the EM map to mtz file. Thank a lot! Wei

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RapiData at SSRL 2019 - application closing data extended
by Smith, Clyde 27 Dec '18

27 Dec '18

Hi everyone, It has come to our attention that due to scheduled computer and power outages at SLAC over the Christmas/New Year period, the connection to the server supporting the RapiData 2019 page is down. Please use the following link to apply for the workshop: https://app.certain.com/profile/2831400 Because of this issue, we will be extending the closing date for applications to January 6 2019. If you have any problems don't hesitate to contact one of us. Cheers, Clyde Smith, Silvia Russi and Jeney Wierman (Organizers) csmith(a)slac.stanford.edu srussi(a)slac.stanford.edu jwierman(a)slac.stanford.edu

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RapiData at SSRL 2019 reminder - just a week left to apply!
by Smith, Clyde 22 Dec '18

22 Dec '18

Hi all, A reminder that there is only a week left to apply for a place at the RapiData 2019 @ SSRL workshop. Applications close at the end of this month, December 31 2018. The workshop will be held from May 5-10 2019 on the SLAC campus in Menlo Park, California. The course will comprise hands-on experiments at the SSRL beamlines, software tutorials, and lectures on the following topics: Specimen preparation, Data collection strategies, X-ray light sources, X-ray detectors, Data reduction, Structure solution by MAD, SAD and Molecular Replacement, Complementary methods (spectroscopy and small angle scattering). Please visit http://smb.slac.stanford.edu/news/rapidata/rapidata-2019/ and use the links on the "registration" page to apply for the course. Successful applicants will be notified early in January 2019 and invited to register at that time. A limited amount of travel support funding may be available. We look forward to seeing you all out in sunny California in May 2019! Silvia Russi, Clyde Smith and Jeney Wierman (Organizers) srussi(a)slac.stanford.edu jwierman(a)slac.stanford.edu csmith(a)slac.stanford.edu

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Computational Crystallography Newsletter (CCN) submissions
by Nigel Moriarty 21 Dec '18

21 Dec '18

Folks Calling for articles and short communications of interest to structural biologists. The deadline for submission for the January 2019 issue is 20 January 2019. The Computational Crystallography Newsletter (CCN) is an electronic newsletter for structural biologists, and is published online every 6 months. Feature articles, meeting announcements and reports can be submitted to me at any time for consideration. Submission of text by email or word-processing files using the CCN templates is requested. Past newsletters and a Microsoft Word template are available at www.phenix-online.org/newsletter. Cheers Nigel --- Nigel W. Moriarty Building 33R0349, Molecular Biophysics and Integrated Bioimaging Lawrence Berkeley National Laboratory Berkeley, CA 94720-8235 Phone : 510-486-5709 Email : NWMoriarty(a)LBL.gov Fax : 510-486-5909 Web : CCI.LBL.gov

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phenix.refine does not work with afitt
by Guenter Fritz 21 Dec '18

21 Dec '18

Dear phenix developers, I am trying to run phenix.refine with afitt (phenix 1.14 3260, afitt 2.4.1.2). However, I receive the an error: "Sorry: Unknown command line parameter definition: use_afitt = True" This I get on my mac or on my linux box . Is support for afitt discontinued? Any help is appreciated! Thanks and best regards, guenter

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JRH Report on International Data Week 2018
by John R Helliwell 21 Dec '18

21 Dec '18

Dear Colleagues, I mention that my report on International Data Week 2018 can be found here:- http://forums.iucr.org/viewtopic.php?f=39&t=409 and which I imagine will be of general interest. All best wishes, John Emeritus Professor John R Helliwell DSc IUCr Representative to CODATA and Chairman of the IUCr Committee on Data

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Postdoctoral position at the Drug Discovery Institute at Purdue University
by John M Hausman 18 Dec '18

18 Dec '18

Dear All: A position is available for a highly qualified and motivated postdoc with a strong background in Molecular/Cell Biology or Immunology. The successful applicant will be responsible for conducting research aimed at identifying and characterizing new drug targets for treatment of important human diseases. Activities may involve i) expressing and characterizing proteins that are upregulated in various disease states, ii) cloning, mutating, expressing and developing assays for studying functional aspects of the target proteins, iii) immunofluorescent staining of tissue sections from diseased tissues, iv) shRNA knockdown of desired proteins in cultured cells, and v) immunoblotting and other common biochemical assays. Management of day-to-day research goals and priorities, supervision of graduate students assigned to the same project, and mentoring of other research personnel regarding the design and execution of specific research methods/approaches may also be required. The lab is directed by Professor Philip S. Low in the new Drug Discovery Institute on the West Lafayette Campus of Purdue University. Other members of the lab are involved in designing new therapies for cancer, fibrotic diseases, infectious diseases, sickle cell disease, bone fractures and related pathologies, and autoimmune diseases, etc. Participation in some of these existing projects may also be required. Please send CV and list of three names of potential referees to: Philip S. Low Presidential Scholar for Drug Discovery Ralph C. Corley Distinguished Professor Department of Chemistry Purdue University 720 Clinic Dr. West Lafayette, IN 47907 Email: plow(a)purdue.edu<mailto:[email protected]> ________________________________

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Help with AutoBuild
by Parthasarathy Sampathkumar 16 Dec '18

16 Dec '18

Dear All, These days my research often involves structure determination of the Antigen:Fab complexes, wherein the antigen structure is already known. Given this: (1). I would like to run AutoBuild in such a way that the program does not to touch antigen model, but only Re-builds only the Fab molecule; and (2). in some cases, due to structural-symmetry within the variable and constant domains of heavy- and light- chains, AutoBuild is searching and applying NCS operator while it is not present, and would like to avoid the same. How could these be done either in GUI or in command-line?!! Many Thanks in advance, Best Wishes Partha PS: Of course, when the data is at "high-enough resolution", I build Fab model manually after MR and Refinement. But, in the above case, resolution is only 3-ish angstrom.

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