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Postdoctoral position at the Drug Discovery Institute at Purdue University
by John M Hausman 17 Dec '18

17 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 15 Dec '18

15 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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speeding up effective resolution calculation
by Eric Williams 07 Dec '18

07 Dec '18

Greetings, all. I have what may be a naive question. :) I'm using phenix.resolution to calculate effective resolution, and I'm looking for ways to speed it up. I've tried a few different machine configurations, and it always takes around 20 minutes per structure. This is problematic for me, because I'm trying to collect data from the entire PDB. Does anyone here have experience using NumPy to optimize scripts and helpful suggestions for this case? Alternatively, how much speedup am I likely to get by rewriting the script in C and using it as a module? Thanks. :) Eric

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New PDB archive reference paper now in NAR 2019 Database issue
by John Berrisford 05 Dec '18

05 Dec '18

An important <https://doi.org/10.1093/nar/gky949> new publication describing the activities and development of the Protein Data Bank (PDB), and authored by the whole wwPDB consortium, has been recently released in the 2019 Database issue of Nucleic Acids Research. Please see the following news release from the <https://www.wwpdb.org/news/news?year=2018#5c05780d3675962a10fcf7a9> wwPDB website: " <https://doi.org/10.1093/nar/gky949> Protein Data Bank: the single global archive for 3D macromolecular structure data has been published in the 2019 Database issue of Nucleic Acids Research. The paper was authored by "wwPDB Consortium" to underscore the importance of the global wwPDB partnership in managing the PDB archive. This article describes the development of the PDB under the stewardship of wwPDB, such as new archival content, master format and dictionary and major remediation efforts. The publication also emphasizes the importance of continued community interactions, the scientific and technical challenges the PDB faces, and charts the road ahead." -- John Berrisford PDBe European Bioinformatics Institute (EMBL-EBI) European Molecular Biology Laboratory Wellcome Trust Genome Campus Hinxton Cambridge CB10 1SD UK Tel: +44 1223 492529 <http://www.pdbe.org/> http://www.pdbe.org <http://www.facebook.com/proteindatabank> http://www.facebook.com/proteindatabank <http://twitter.com/PDBeurope> http://twitter.com/PDBeurope

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Re: [phenixbb] Molprobity values on output pdb
by Christopher Williams 30 Nov '18

30 Nov '18

Hi Boaz, Is it possible for you to send me (and just me, not the bulletin board) your file for testing? Thank you, if so. Alternatively, you can try using our alternate site at http:// altmolprobity .biochem.duke.edu, where a bugfix that probably addresses this issue is currently under testing. Thanks and good luck, -Christopher Williams ---Richardson Lab, Duke University On Fri, Nov 30, 2018 at 11:57 AM Boaz Shaanan <bshaanan(a)bgu.ac.il> wrote: > Hi, > > > I noticed small differences between the molprobity > all-atoms clashscore reported in the output pdb file and the results > reported by the molprobity run (build 3318). > > > Cheers, > > > Boaz > > > > > > > > > > > > > *Boaz Shaanan, Ph.D. Dept. of Life > Sciences Ben-Gurion University of the > Negev Beer-Sheva > 84105 > Israel > E-mail: > bshaanan(a)bgu.ac.il <bshaanan(a)bgu.ac.il> Phone: 972-8-647-2220 > Fax: 972-8-647-2992 or 972-8-646-1710 * > > > > > > _______________________________________________ > phenixbb mailing list > phenixbb(a)phenix-online.org > http://phenix-online.org/mailman/listinfo/phenixbb > Unsubscribe: phenixbb-leave(a)phenix-online.org

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Validation Completeness Issue
by Antoine Koehl 29 Nov '18

29 Nov '18

Hi, I’m in the process of uploading data to the PDB. While AIMLESS had estimated my completeness at 94% (similar to the XTriage value of 93.2%), the internal PDB validation through EDS estimates my completeness to be closer to 83.5%. This is a rather large difference. Both are using the exact same resolution range (49.57-4.00). Is there something that EDS does differently for estimating completeness? Please advise, Antoine

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Test message
by Billy Poon 27 Nov '18

27 Nov '18

This is just a test. -- Billy K. Poon Research Scientist, Molecular Biophysics and Integrated Bioimaging Lawrence Berkeley National Laboratory 1 Cyclotron Road, M/S 33R0345 Berkeley, CA 94720 Tel: (510) 486-5709 Fax: (510) 486-5909 Web: https://phenix-online.org

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Alternate conformer clash problem in phenix.refine
by Aaron Oakley 19 Nov '18

19 Nov '18

Salve! I am refining a protein/ligand complex where the ligand is bound with two conformers. Conformer A is covalently bound to a cysteine residue. Conformer B is free. I have prepared an appropriate cif dictionary for the ligand including info on handling the link. The problem is that during refinement, non-bonded interactions between the two conformers appear to not be switched off and their geometry becomes distorted. Is this diagnosis correct? If so, is there a way to manually switch off interactions? With thanks, a++ Aaron Oakley Associate Professor School of Chemistry and Molecular Bioscience | Molecular Horizons | Faculty of Science, Medicine and Health University of Wollongong NSW 2522 Australia T +61 2 4221 4347 | F +61 2 4221 4287 [cid:[email protected]]

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exclude clashes for non-symmetry contacts
by Edwin Pozharski 16 Nov '18

16 Nov '18

Is there some way to make phenix.refine to ignore clashes for specific pair(s) of chains? I am dealing with a rare case of twinning where same protein molecule exists in two orientations in the same unit cell. I tried just to duplicate the molecule and set initial occupancy to 0.5, but refinement fails (as I expected) saying that there are too many close contacts. Ideally, I would like to proceed with ignoring close contacts between, say, chains A/B. I am aware that one can exclude groups of residues from symmetry clashes, but these two copies are in the same cell. I guess I could try shifting one into the next unit cell and then excluding symmetry clashes, but even assuming that will work it is a rather ugly hack. The alternative is probably to define the second orientation as an alternative conformation. Aside from aesthetic objections, I don't want to lose the ability to restrain NCS - I need two orientations to be identical structures, and I am not sure yet whether I can use NCS groups defined via alternative conformers. Cheers, Ed.

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Normalized B-factor
by Mehmet Sen 16 Nov '18

16 Nov '18

Hello, I used the Structural Comparison tool to obtain normalized B- factor values for a couple of models, each with multiple chains. Is there an efficient way to visualize the normalized B-factor values (by writing over the old B-factor values) for the models, preferably in PyMOL? Thanks, Joyce V.

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Protonation of a symmetry-related His in Zn coordination sphere
by Priit Eek 16 Nov '18

16 Nov '18

Hi, I have a structure in which one of the His-residues of a Zn coordination sphere is from a symmetry-related protein chain. I specified the symmetry in an edits file so the coordination sphere is nice and plays well in refinement. I now added hydrogens to the model, but the His from the other chain does not get protonated correctly. I assume reduce doesn’t detect the presence of the symmetry-related Zn. It protonates NE, while that is the atom that interacts with Zn, but ND should be protonated instead. What would be the best way to fix this? And another question on the same matter: is it possible to specify a LINK in PDB between these atoms? Best regards, Priit ——— Priit Eek, PhD Researcher Department of Chemistry and Biotechnology Tallinn University of Technology Tel. +372 620 4387 priit.eek(a)taltech.ee

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Postdoc Position - Berkeley
by Paul Adams 14 Nov '18

14 Nov '18

Lawrence Berkeley Laboratory Postdoctoral Researcher Job ID: 85784 Division: Molecular Biophysics & Integrated Bioimaging (Joint BioEnergy Institute) Date Opened: 11/1/2018 Summary: A postdoctoral position is immediately available to study the structure and function of macromolecular complexes and enzymes using biochemical, X-ray crystallographic and electron cryo-microscopy (cryo-EM) methods. The biological systems to be studied are: - Glycosyl transferases responsible for the synthesis of hemicelluloses in plants - Novel glycosyl hydrolases that are able to breakdown cellulosic material for biofuels production - Enzymes involved in lignin biosynthesis, degradation and valorization - Secondary metabolite and natural product enzymes This position will be part of the Structural Biology group of the Technology Division at the Joint BioEnergy Institute (JBEI) in Emeryville, California. To learn more about JBEI visit: http://www.jbei.org/ Duties: The successful candidate will have experience characterizing enzymes using biochemical techniques, and using crystallographic methods. Familiarity with cryo-EM methods would be helpful, but not essential. Robotic hardware for performing crystallization trials and imaging results are available. Crystals will be characterized and data collected using the beamline resources of the Berkeley Center for Structural Biology at the Advanced Light Source. For appropriate systems cryo-EM data will be obtained using in-house microscopes, the Bay Area Center for Cryo-EM, and other national user facilities. Qualifications: a Ph.D. in biochemistry, molecular biology, structural biology, chemistry or a related field. Demonstrated experience of scientific research using biochemistry techniques including enzymatic assays, and crystallographic methods. Experience with macromolecular crystallization techniques. Experience with cloning methods and protein purification methods would be helpful. Strong problem solving skills. Solid interpersonal skills and the ability to work in a team environment are critical. This is a full time, 2 years, postdoctoral appointment with the possibility of renewal based upon satisfactory job performance, continuing availability of funds and ongoing operational needs. You must have less than 3 years paid postdoctoral experience. Salary for Postdoctoral positions depends on years of experience post-degree. Berkeley Lab (LBNL) addresses the world’s most urgent scientific challenges by advancing sustainable energy, protecting human health, creating new materials, and revealing the origin and fate of the universe. Founded in 1931, Berkeley Lab’s scientific expertise has been recognized with 13 Nobel prizes. The University of California manages Berkeley Lab for the U.S. Department of Energy’s Office of Science. Berkeley Lab is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status. To apply visit https://lbl.taleo.net/careersection/2/jobsearch.ftl?lang=en and search for the job number 85784 or visit: https://lbl.referrals.selectminds.com/jobs/crystallography-postdoctoral-sch… -- Paul Adams Division Director, Molecular Biophysics & Integrated Bioimaging, Lawrence Berkeley Lab Division Deputy for Biosciences, Advanced Light Source, Lawrence Berkeley Lab Adjunct Professor, Department of Bioengineering, U.C. Berkeley Vice President for Technology, the Joint BioEnergy Institute Laboratory Research Manager, ENIGMA Science Focus Area Building 33, Room 347 Building 978, Room 4126 Tel: 1-510-486-4225, Fax: 1-510-486-5909 http://cci.lbl.gov/paul Lawrence Berkeley Laboratory 1 Cyclotron Road BLDG 33R0345 Berkeley, CA 94720, USA. Executive Assistant: Louise Benvenue [ LBenvenue(a)lbl.gov ][ 1-510-495-2506 ] --

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R-free was improved, however, “Temp. fact. variance analysis” in “Validation” tool of COOT was worsened.
by Manami Torimoto 08 Nov '18

08 Nov '18

Dear all, By phenix.refine, I attempted to refine one molecule of protein. R-free was improved in certain wxc by setting the weight wxu manually, however, the results of “Temp. fact. variance analysis” in “Validation” tool of COOT was worsened. Why did such a thing happen? Thank you. Manami

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Low resolution refinement
by Ashu Sharma 06 Nov '18

06 Nov '18

Dear All, I am refining a ~7A single particle cryo-em structure of a protein. The protein has two domains and high-resolution crystal structures of individual domains are already known. I could fit these two crystal structures in the low resolution cryoem map of the full-length protein. I have two questions: 1) Is it acceptable to refine with side chains in this case? In most of the cases, with the guidane from crystal structures, side chains could be placed with reasonable confidence, particularly smaller ones. Should I restrict to poly-ala model or take the advantage of crystal structures and include side chains also? 2) When I tried to refine with side chains, longer side chains like K, R, Q, E which have weaker density tend to bend towards the backbone density. Is there a way to prevent this happening? Suggestions/comments from the community would be highly appreciated. Thanks ! Ashu

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Real-space correlation list for nucleotides?
by Boaz Shaanan 05 Nov '18

05 Nov '18

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(no subject)
by Matthew Bick 05 Nov '18

05 Nov '18

Dear Phenix BB administrator. Could you please post the following job opening to the mailing list? Thank you. Sincerely, Matthew Bick Senior Fellow Baker Laboratory for Computational Protein Design University of Washington The Institute for Protein Design, in the Department of Biochemistry at the University of Washington, currently has an outstanding opportunity for a full time X-ray Crystallographer Staff Scientist. The Institute for Protein Design is designing a new world of synthetic proteins for 21st-century challenges. PRIMARY RESPONSIBILITIES Collaborate with the Investigator and numerous researchers at the Institute for Protein Design on the X-ray crystal structure determination of de novo designed proteins. Manage the activities of research scientists and undergraduate research support with oversight of all protein-to-structure activities at the Institute for Protein Design. Design of new concepts, approaches and programs for structure determination of computationally designed proteins, of a diverse nature. Perform various specialized scientific investigative procedures in X-ray structure determination in collaborative support of numerous research projects with minimal input from Investigator. Use bio-informatics tools and pertinent laboratory and public databases, including the Protein Data Bank (PDB), and information resources to support gene-to-structure research, including deposition of atomic coordinates in the PDB for archival, sharing, and publication. Direct the activities of technical support staff in the Baker lab and at the Institute for Protein Design in collaboration with other research staff. Collaborate with other research staff, postdoctoral fellows and graduate students to select and maintain relevant protein research equipment to insure the lab meets required current and future needs. Direct the development of new protein crystallization and X-ray structure determination strategies, and ascertain if they effectively addresses needs. Manage complex multi-task projects directed at the design, production and structural characterization of numerous de novo designed proteins with higher order function. Train laboratory research staff, postdoctoral fellows and graduate students in protein X-ray crystallography, as well as wet lab equipment for protein production, structural elucidation, and biochemical characterization. Direct projects with undefined time lines and uncertain outcomes requiring analysis from multiple perspectives. Use expert knowledge and judgment to develop new methods and techniques for obtaining solutions. MINIMUM QUALIFICATIONS: Ph.D in Biochemistry, or related field, and X-ray Crystallography +5 or more years of related experience Technical proficiency, scientific creativity, collaborative ability, as well as independent thought. Advanced expertise in X-ray crystal structure determination, both computational and wet lab areas, with a full understanding of the underlying principles and concepts. May be recognized as a leader in their area of expertise. Recognized as a resource for others to use in dealing with complex protein structure determination, computational and wet lab methods, equipment, processes, or procedures. Anticipate future needs in technology support. In-depth understanding of organizational structure both within and outside the work unit, including the role of each position in the group and in other groups. Ability to develop innovative processes to achieve goals. Direct others to develop essential tasks. Review work activities to determine where new information could improve processes or move projects forward. DESIRED QUALIFICATIONS: Ph.D. degree in an appropriate field of science or technology or equivalent in education and experience AND total of six year’s research experience in protein biophysics, X-ray crystallography, computational biology and bioinformatics specifically in the X-ray crystal structure determination. Interested candidates should send a cover letter and CV to Matthew Bick at bickm(a)uw.edu.

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Speeding direct summation ?
by Clement Degut 02 Nov '18

02 Nov '18

Hi, I have (very) high resolution data, for which direct summation method seems to give significantly better map than FFT (i.e. visible hydrogen vs not). My main problem is that refinement got from quite slow, to barely not really possible to handle slow. I have 2 question from that : Am I looking at an artifact ? Meaning should at this resolution (0.84A for CC1/2 at 30% and good overall statistics) see extreme difference between map quality with direct summation vs FFT ? And if yes, can I speed the process compiling phenix with openMP on our cluster ? Or shoul I just become patient ? Many thanks Clément

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Postdoctoral position in Indiana University School of Medicine
by Takagi, Yuichiro 02 Nov '18

02 Nov '18

Postdoctoral Fellow, Takagi Laboratory (https://medicine.iu.edu/research/faculty-labs/takagi/), Department of Biochemistry and Molecular Biology Indiana University School of Medicine We are looking for a highly motivated postdoctoral follow with a background in structural biology (X-ray crystallography, cryo-EM), to work on NIH-funded projects studying multi-protein complexes involved in eukaryotic transcription regulation. Who We Are: My laboratory is interested in understanding the mechanisms of assembly, structure and function of large multi-protein complexes -“molecular machines” - involved in eukaryotic gene regulation, utilizing both cryo-EM and X-ray crystallography. We are particularly interested in the Mediator complex in both yeast and humans. We believe that development and implementation of novel technologies is the key to unlocking the mysteries of how highly complex molecular machines (e.g. Mediator) function. Therefore, our overall research objective is two-fold: (i) development of novel technologies for studying multi-protein complexes, and (ii) application of these technologies to elucidate the structure and function of the Mediator complex. In addition, we have developed a novel technology for producing pure preparations of difficult-to-express proteins and protein complexes, which has enabled several exciting ongoing projects with outstanding collaborators, including work on: plant RNA polymerases, DNA helicases, DNA repair complexes, RNA editing complex, and insulator complex. What We Offer: State-of-the art protein and protein complex expression technologies (patent pending) enabling expression of difficult-to-express, problematic proteins and protein complexes Accessibility to crystallization drop-setting robots, home X-ray sources, Synchrotron data collection at the Advanced Photon Source (APS) at Argonne National Laboratory (within a 3 hour drive from our lab), as well as electron-microscopy (EM) facility: Titan Krios, Talos Artica, and JOEL-FS3200 A one-on-one mentoring opportunity by which a postdoctoral fellow can learn the craft of designing research strategy, preparing compelling grant proposals, and paper-writing and presentation skills The opportunity to work with multiple outstanding collaborators Who Should Apply: This position could be a great fit for you if: you have the expertise and experience in X-ray crystallography, and want to apply such skills toward structure determination of highly complex multi-protein complexes you are interested in learning and developing for the cutting-edge protein complex engineering and expression technologies you would like to extend your skill sets to cryo-EM you are self-confident and can communicate with the PI, other lab members, and collaborators with ease, and enjoy discussing research results and how to overcome technical challenges the specific research focus of our laboratory inspires you you love to gather information from the literatures and helps generate creative ideas and technical solutions you relish working on technically challenging problems, which often require an extended persistent effort to crack Job Description, Qualification, and Expectations: Primary activities in this position include, but are not limited to: Expression and purification of the protein complexes for biochemical and structural studies (cyo-EM, crystallization Structure determination of the protein complexes by cryo-EM or/and X-ray crystallography Biochemical assays to characterize the recombinant protein complexes Providing intellectual contributions to the projects including writing manuscripts, fellowship application and helping PI for grant applications Ph.D. in structural biology (X-ray crystallography, cryo-EM) is strongly preferred. If interested, please email a cover letter, CV, and two reference letters to ytakagi(a)iu.edu Applications will be screened until a suitable candidate is found. Indiana University is an equal opportunity/affirmative action employer.

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Submitting SLURM jobs through PHENIX GUI
by Thomas Cleveland 01 Nov '18

01 Nov '18

Hi all, Has anyone gotten SLURM job submission to work through the PHENIX GUI? Under Preferences/Processes, I set Queueing system to SLURM with queue submit comand "sbatch." The job does indeed submit to the queue, and I can see it in the listing using the "squeue" command. However, there is quickly an error, "OSError : [Errno 2] No such file or directory: '/home/clevelandt/data/MX/181016_P1_merge/phenix/.phenix/tmp/10.libtbx_info.LOCK'". I've attached the full error log. Basically the program is looking for a lock file that isn't there. I'm not sure why it's not there. All compute nodes should have access to this directory, and there is no caching of any kind, so any files placed there should immediately be accessible. I can manually submit e.g. phenix.refine jobs to the queue using the command line and everything works fine. It would be really nice to have it through the GUI though. Thanks for any help, Tom

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Protein Crystallography Facility Manager, MRC Laboratory of Molecular Biology, Cambridge, UK
by David Barford 31 Oct '18

31 Oct '18

Protein Crystallography Facility Manager, MRC Laboratory of Molecular Biology, Cambridge, UK The MRC Laboratory of Molecular Biology (LMB) seeks to appoint a Protein Crystallography Facility Manager. The LMB is one of the birthplaces of structural biology and remains at the forefront of methods development as protein crystallography is a critical technique for understanding the mechanisms of macromolecular complexes, one of the major goals of the LMB. The post-holder will provide support to researchers from all Divisions of the LMB in the collection of X-ray diffraction data using both synchrotrons and in-house X-ray facilities, will maintain and develop the in-house facilities, will provide expert advice and support during subsequent structure determinations, and will act as the coordinator for LMB's synchrotron access. It is expected that there will be the opportunity for collaboration on structural projects with research groups at the LMB. The successful applicant will have several years of post-doctoral experience in the field of protein crystallography including data collection at synchrotrons and all aspects of structure determination. Excellent communication and inter-personal skills are required because the post will involve interacting with a diverse range of scientists with different levels of expertise. Closing date for applications: 28th November 2018 For further details and information on how to apply please visit: Jobs.ac: https://www.jobs.ac.uk/job/BNU298/protein-crystallography-facility-manager-… <https://www.jobs.ac.uk/job/BNU298/protein-crystallography-facility-manager-…> Nature: https://www.nature.com/naturecareers/job?id=661643 <https://www.nature.com/naturecareers/job?id=661643> Informal enquires should be addressed to Dr. David Barford. E.mail: dbarford(a)mrc-lmb.cam.ac.uk <mailto:[email protected]>

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Protein Crystallography Facility Manager, MRC Laboratory of Molecular Biology, Cambridge, UK
by David Barford 31 Oct '18

31 Oct '18

Protein Crystallography Facility Manager, MRC Laboratory of Molecular Biology, Cambridge, UK The MRC Laboratory of Molecular Biology (LMB) seeks to appoint a Protein Crystallography Facility Manager. The LMB is one of the birthplaces of structural biology and remains at the forefront of methods development as protein crystallography is a critical technique for understanding the mechanisms of macromolecular complexes, one of the major goals of the LMB. The post-holder will provide support to researchers from all Divisions of the LMB in the collection of X-ray diffraction data using both synchrotrons and in-house X-ray facilities, will maintain and develop the in-house facilities, will provide expert advice and support during subsequent structure determinations, and will act as the coordinator for LMB's synchrotron access. It is expected that there will be the opportunity for collaboration on structural projects with research groups at the LMB. The successful applicant will have several years of post-doctoral experience in the field of protein crystallography including data collection at synchrotrons and all aspects of structure determination. Excellent communication and inter-personal skills are required because the post will involve interacting with a diverse range of scientists with different levels of expertise. Closing date for applications: 28th November 2018 For further details and information on how to apply please visit: Jobs.ac: https://www.jobs.ac.uk/job/BNU298/protein-crystallography-facility-manager-… <https://www.jobs.ac.uk/job/BNU298/protein-crystallography-facility-manager-…> Nature: https://www.nature.com/naturecareers/job?id=661643 <https://www.nature.com/naturecareers/job?id=661643> Informal enquires should be addressed to Dr. David Barford. E.mail: dbarford(a)mrc-lmb.cam.ac.uk <mailto:[email protected]>

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RNA starting with triphosphate
by Phoebe A. Rice 25 Oct '18

25 Oct '18

A question from my collaborators: what is the best way to get phenix to handle a GTP as nt #1 of an RNA chain? That is, what is the best way to specify a covalent bond with the proper geometry between the 3’ O of GTP1 and the 5’ P of nt #2? Thanks in advance, Phoebe ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Phoebe A. Rice Dept. of Biochem & Mol. Biol. and Committee on Microbiology https://voices.uchicago.edu/phoebericelab/

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RapiData 2019 applications open!
by Smith, Clyde 24 Oct '18

24 Oct '18

Dear all, Applications are now open for the 2019 edition of RapiData at SSRL. RapiData is a practical course in macromolecular X-ray diffraction data collection, data processing and structure solution. The aim of the RapiData course is to educate and train young scientists in data collection and processing methods at synchrotron beamlines, using state-of-the-art software and instrumentation. The course will be held at the Stanford Synchrotron Radiation Lightsource (SSRL) located on the SLAC National Accelerator Laboratory campus in Menlo Park, CA, from May 5-10 2019. Course organizers for 2019 are Silvia Russi, Clyde Smith and Jeney Wierman. 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. The application deadline is December 31 2018. Successful applicants will be notified early in January 2019 and invited to register and book accommodation at the SLAC Guesthouse at that time. A limited amount of travel support funding may be available. Please direct questions to Silvia Russi (srussi(a)slac.stanford.edu), Jeney Wierman (jwierman(a)slac.stanford.edu) or Clyde Smith (csmith(a)slac.stanford.edu).

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Computational cryo-EM faculty position at the Morgridge Institute for Research and UW-Madison
by Eric Montemayor 19 Oct '18

19 Oct '18

Dear Colleagues, A great faculty-level opportunity between the Morgridge Institute for Research and the University of Wisconsin-Madison. We seek to hire a tenure-track assistant/associate/full professor in the broad area of cryo-EM centered quantitative image processing and analysis. This position is part of a major campus cryo-EM expansion, comprising new faculty hires in experimental and computational cryo-EM, and a facility to house four new cryo-microscopes including Thermo Fisher’s 300 kV Titan Krios, 200 kV Talos Arctica, 120 kV Talos L120C, and Aquilos cryo-FIB-SEM. For more information about this post and the application process, please click the link below. Deadline for applications is December 15, 2018. Morgridge (computational cryo-EM) - https://morgridge.org/job-posting/investigator-cryo-em/ For more information about the other cryo-EM related faculty positions, please click the links below. Each search has its own deadline for receipt of applications. The positions will remain open until filled. Biochemistry - http://jobs.hr.wisc.edu/cw/en-us/job/499479/biochemistry-faculty Virology - http://jobs.hr.wisc.edu/cw/en-us/job/499366/virus-proteinnucleic-acid-ultra… Bacteriology - http://jobs.hr.wisc.edu/cw/en-us/job/499304/assistant-professor For additional information, please contact Liz Wright (erwright2(a)wisc.edu). -- Eric J. Montemayor Associate Scientist Department of Biochemistry University of Wisconsin Madison 433 Babcock Dr. Room 145 Madison, WI 53706

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Submit Phenixbb
by 张晓帅 19 Oct '18

19 Oct '18

i want to post to list.Thank you.

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