{"code":"SASDB94","status":"Published","type_of_curve":"Single concentration","angular_unit":"1/nm","project":{"title":"A shape-shifting redox foldase contributes to Proteus mirabilis copper resistance.","publication":{"title":"A shape-shifting redox foldase contributes to Proteus mirabilis copper resistance.","author_list":"Furlong EJ, Lo AW, Kurth F, Premkumar L, Totsika M, Achard MES, Halili MA, Heras B, Whitten AE, Choudhury HG, Schembri MA, Martin JL","journal":"Nat Commun","doi":"10.1038/ncomms16065","pmid":"28722010","published_date":"2017 Jul 19"},"status":"released","submitted_date":"2016-10-04","released_date":"2017-06-16"},"pddf_data":"https://www.sasbdb.org/media/p_of_R_files/SASDB94.out","intensities_data":"https://www.sasbdb.org/media/intensities_files/SASDB94.dat","intensities_log_plot":"https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDB94_dat_img.png","intensities_kratky_plot":"https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDB94_kratky_img.png","pddf_plot":"https://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDB94_pofr_img.png","intensities_guinier_plot":"https://www.sasbdb.org/media/intensities_files/scattering_plots/SASDB94_guinier_img.png","sascif_data":"https://www.sasbdb.org/media/sascif/sascif_files/SASDB94.sascif","experiment":{"instrument":{"detector":{"type":"Dectris","name":"Pilatus 1M","resolution":172.0},"name":"Australian  Synchrotron","city":"Melbourne","country":"Australia","beamline_name":"SAXS/WAXS","beam_geometry":"Point","type_of_source":"X-ray 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GNOM","pddf_software_version":null,"i0_calibration_standard":null,"description":null,"experiment_description":"X-ray synchrotron radiation scattering data from solutions of Suppressor of Copper Sensitivity C protein (ScsC) from Proteus mirabilis in 25 mM HEPES 150mM NaCl, 1mM DTT, pH 7.5 were collected on the SAXS/WAXS beam line of the Australian Synchrotron (Melbourne, Australia) using a 2D Photon counting Pilatus 1M-W pixel detector (s = 4π sin θ/λ, where 2θ is the scattering angle). Fourteen successive 2 second frames were collected across solute concentrations of 2.15-8.85 mg/ml. The SAXS data displayed this entry was derived from a 2.15 mg/ml sample. The data were normalized to the intensity of the transmitted beam and radially averaged and the scattering of the solvent-blank was subtracted. The models and corresponding fits include those derived from rigid-body modelling using CORAL (top) and a representative ensemble of six trimeric ScsC structures determined using ensemble optimization method (EOM). The Rg and Dmax distributions derived from EOM are included in the full entry zip archive.","tags":[],"intensity_unit":null,"experimental_mw":69.9,"experimental_mw_error":null,"guinier_i0_mw":null,"guinier_i0_mw_error":null,"porod_mw":null,"porod_mw_error":null,"pddf_i0":0.1006,"pddf_i0_error":0.00016,"guinier_i0":0.101,"guinier_i0_error":null,"pddf_rg":3.6,"pddf_rg_error":0.01,"guinier_rg":3.65,"guinier_rg_error":null,"pddf_dmax":10.5,"pddf_dmax_error":null,"porod_volume":92.0,"porod_volume_error":null,"estimated_volume":null,"estimated_volume_error":null,"guinier_point_first":3,"guinier_point_last":21,"pddf_point_first":null,"pddf_point_last":null,"i0_calibration_standard_data":null,"intensities_log_log_plot":"SASDB94_datloglog_img.png","symmetry":null,"last_modified":"2020-08-28T15:27:57.490687+02:00","bragg_peak":[]}