- phenixbb - phenix-online.org

B factor over 300
by Daqi Tu 04 May '10

04 May '10

Hi, I refined my structure (of which the data is very anisotropic) using phenix.refine and with individual_sites, individual_adp, and tls options turned on. From the refined coordinates, the highest B-factor in the ANISO record (ie B_tls + B_individual) is 305. This number looks rather high. Is it something I should worry about? and is there an easy way to compute the individual B-factor component? Thanks. Daqi Tu Eck lab Dana-Farber Cancer Institute

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Re: [phenixbb] Rigid body refinement question
by Ralf W. Grosse-Kunstleve 03 May '10

03 May '10

> Is it possible to specify individual residues of a chain to undergo rigid > refinement while the rest of the chain does regular refinement? No, sorry. Ralf

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nucleic acid nomencalture
by riya doreen 30 Apr '10

30 Apr '10

Hi Everyone, I am interested in refining a DNA structure with phenix. However, as soon as I read my PDB, I get a warning for missing restraints: PHENIX could not find geometry restraints in the standard monomer library for one or more residues in the PDB file" what is the correct nomenclature for DNA and RNA for use in PHENIX? Can I access phenix.elbow from the GUI ? Thanks

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NCS problems using phenix GUI on a Mac
by John Pascal 29 Apr '10

29 Apr '10

Hello, I am having difficulties defining NCS parameters using the GUI interface (Mac 10.4.11; phenix 1.6-289). Phenix will automatically select NCS restraint groups and use them during refinement. But if I edit the automated selections to my liking then click on Update and Save, the refinement runs with the original parameters unedited. I have tried reading in a ncs.param file, but it does not get read during the refinement run. Also, an intermittent problem with this GUI is that I am not allowed to "Add" a new restraint group. When I click this button, it just clears out the selections on the last group, and does not add a new group. Any ideas? Thanks. Best, John -- John Pascal, PhD ph 215.503.4596 Assistant Professor fx 215.923.2117 Thomas Jefferson University Biochemistry & Molecular Biology 233 South 10th Street, BLSB 804 Philadelphia, Pennsylvania 19107 ---------------------------------------------------------------- This message was sent using IMP, the Internet Messaging Program.

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How do I make trisaccharide, tetrasaccharides
by Hansman, Grant (NIH/VRC) [F] 29 Apr '10

29 Apr '10

How do I make trisaccharide, tetrasaccharides, etc from single monosaccharides? I.e., how do I join the monosaccharides. Do I use ideal coordinates? Can I join them in coot? I want to make HBGA Trisaccharide B. That is, I want to join FUC-GAL-GLA, it would be FUC (C1)-GAL (O2)-GAL (C2) then GAL (C3)-GAL(O3)-GLA(C1) ATOM 1 C1 FUC A 1 1.410 0.468 -0.410 1.00 10.00 C ATOM 2 C2 FUC A 1 0.120 0.513 -1.233 1.00 10.00 C ATOM 3 C3 FUC A 1 -0.831 -0.576 -0.728 1.00 10.00 C ATOM 4 C4 FUC A 1 -1.016 -0.402 0.783 1.00 10.00 C ATOM 5 C5 FUC A 1 0.359 -0.379 1.454 1.00 10.00 C ATOM 6 C6 FUC A 1 0.185 -0.241 2.967 1.00 10.00 C ATOM 7 O1 FUC A 1 2.007 -0.823 -0.535 1.00 10.00 O ATOM 8 O2 FUC A 1 0.424 0.284 -2.610 1.00 10.00 O ATOM 9 O3 FUC A 1 -2.094 -0.452 -1.385 1.00 10.00 O ATOM 10 O4 FUC A 1 -1.700 0.824 1.044 1.00 10.00 O ATOM 11 O5 FUC A 1 1.116 0.724 0.961 1.00 10.00 O ATOM 1 C1 GAL A 1 1.384 0.161 -0.445 1.00 10.00 C ATOM 2 C2 GAL A 1 0.328 -0.139 -1.512 1.00 10.00 C ATOM 3 C3 GAL A 1 -0.975 0.575 -1.139 1.00 10.00 C ATOM 4 C4 GAL A 1 -1.360 0.176 0.289 1.00 10.00 C ATOM 5 C5 GAL A 1 -0.177 0.454 1.220 1.00 10.00 C ATOM 6 C6 GAL A 1 -0.563 0.093 2.655 1.00 10.00 C ATOM 7 O1 GAL A 1 2.612 -0.476 -0.802 1.00 10.00 O ATOM 8 O2 GAL A 1 0.785 0.328 -2.782 1.00 10.00 O ATOM 9 O3 GAL A 1 -2.011 0.186 -2.044 1.00 10.00 O ATOM 10 O4 GAL A 1 -1.686 -1.213 0.327 1.00 10.00 O ATOM 11 O5 GAL A 1 0.945 -0.328 0.819 1.00 10.00 O ATOM 12 O6 GAL A 1 0.539 0.355 3.526 1.00 10.00 O ATOM 1 C1 GLA A 1 1.424 -0.489 -0.382 1.00 10.00 C ATOM 2 C2 GLA A 1 0.392 -0.498 -1.512 1.00 10.00 C ATOM 3 C3 GLA A 1 -0.650 0.592 -1.244 1.00 10.00 C ATOM 4 C4 GLA A 1 -1.222 0.387 0.163 1.00 10.00 C ATOM 5 C5 GLA A 1 -0.068 0.330 1.166 1.00 10.00 C ATOM 6 C6 GLA A 1 -0.630 0.161 2.579 1.00 10.00 C ATOM 7 O1 GLA A 1 2.043 0.797 -0.316 1.00 10.00 O ATOM 8 O2 GLA A 1 1.044 -0.242 -2.757 1.00 10.00 O ATOM 9 O3 GLA A 1 -1.700 0.498 -2.209 1.00 10.00 O ATOM 10 O4 GLA A 1 -1.958 -0.836 0.206 1.00 10.00 O ATOM 11 O5 GLA A 1 0.783 -0.771 0.859 1.00 10.00 O ATOM 12 O6 GLA A 1 0.446 0.112 3.517 1.00 10.00 O

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AutoBuild error message prime and switch
by Rebecca Oot 29 Apr '10

29 Apr '10

Hi, I'm trying to use the AutoBuild wizard to calculate a prime and switch map. When I hit run I get the following error message: The key ignore_blanks is not in var_type_dict....this means the command-line Wizard needs a conversion in the autobuild.py script under 'Translating inputs' or else in excluded_inputs. Any insight would be appreciated. Thanks Rebecca

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ReadySet for special position metal
by TC Hu 27 Apr '10

27 Apr '10

Dear all, I am refining a structure with a metal ion on a 2-fold axis, coordinated by four histidines, two from the ASU and two from symmetry. I used phenix.ready_set to generate the metal coordination file and input it into phenix.refine. However, phenix.refine complains that the customized angle restraints contain a special position atom and cannot continue. I am using Phenix 1.5.2. Could anyone suggest me how to solve this problem? Thank you! Best, Tiancen

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how to generate sharpened map for input into Pymol
by Daqi Tu 25 Apr '10

25 Apr '10

Hi, I am generating a electron density map figure in pymol for my structure. Since the data is very anisotropic, map sharpening has proven to be quite useful. The structure was solved using Phenix. How do I generate an Xplor style map in Phenix that incorporates sharpening? Thanks. Daqi Tu Postdoc Eck lab Dana-Farber Cancer Institute The information in this e-mail is intended only for the person to whom it is addressed. If you believe this e-mail was sent to you in error and the e-mail contains patient information, please contact the Partners Compliance HelpLine at http://www.partners.org/complianceline . If the e-mail was sent to you in error but does not contain patient information, please contact the sender and properly dispose of the e-mail.

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apply_cif_link
by Hansman, Grant (NIH/VRC) [F] 24 Apr '10

24 Apr '10

I am trying to link my sugar molecule (FUC-GAL-NGA-FUC), Lewis y, for phenix.refine, but I keep on getting an error message. I am a beginner at this so I just don't know how to make the links. For , example, I am using this: refinement.pdb_interpretation { apply_cif_link { data_link = BETA1-2 residue_selection_1 = chain C and resname GAL and resid 224 residue_selection_2 = chain C and resname FUC and resid 223 } apply_cif_link { data_link = BETA1-3 residue_selection_1 = chain C and resname GAL and resid 224 residue_selection_2 = chain C and resname NGA and resid 225 } apply_cif_link { data_link = BETA1-3 residue_selection_1 = chain C and resname NGA and resid 225 residue_selection_2 = chain C and resname FUC and resid 226 Number of atoms: 46 Number of conformers: 1 Conformer: "" Number of residues, atoms: 4, 46 Unusual residues: {'GAL%DEL-HO2%DEL-HO3': 1, 'NGA%DEL-O1%DEL-HO3': 1, 'FUC%DEL-O1': 2} Unexpected atoms: {'NGA%DEL-O1%DEL-HO3,O1L': 1, 'NGA%DEL-O1%DEL-HO3,O': 1} Classifications: {'undetermined': 4} Modifications used: {'DEL-HO2': 1, 'DEL-HO3': 2, 'DEL-O1': 3} Link IDs: {None: 3} Unresolved non-hydrogen bonds: 3 Unresolved non-hydrogen angles: 6 Unresolved non-hydrogen dihedrals: 4 Unresolved non-hydrogen chiralities: 2 Unresolved apply_cif_link angles: 1 Unresolved apply_cif_link chiralities: 1 Number of atoms with unknown nonbonded energy type symbols: 2 "HETATM 5649 O NGA C 225 .*. O " "HETATM 5655 O1L NGA C 225 .*. O " Time building chain proxies: 2.31, per 1000 atoms: 0.41 Sorry: Fatal problems interpreting PDB file: Number of atoms with unknown nonbonded energy type symbols: 2 Please edit the PDB file to resolve the problems and/or supply a CIF file with matching restraint definitions, along with apply_cif_modification and apply_cif_link parameter definitions if necessary (see phenix.refine documentation). Also note that phenix.elbow is available to create restraint definitions for unknown ligands. Any help and direction would be appreciated. Grant

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Conflicting scattering type symbols: refine with TaBr
by Francis E Reyes 24 Apr '10

24 Apr '10

Hi All I'm getting an error refining with TaBr. Got tbr_exp.pdb from Hic-Up and prepared the cif with phenix.elbow. Try to do a refine with the pdb and cif and I get this error. Sorry: Conflicting scattering type symbols: initial symbol: "TA" (from pdb element column) new symbol: "T" (with residue name TBR) atom: "HETATM 1917 TA1 TBR B7131 .*. TA " What are people calling their TaBr records and/or how are they generating their cifs? Thanks F --------------------------------------------- Francis Reyes M.Sc. 215 UCB University of Colorado at Boulder gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D 8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D

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