2A7F
On the Routine Use of Soft X-Rays in Macromolecular Crystallography, Part III- The Optimal Data Collection Wavelength
Summary for 2A7F
Entry DOI | 10.2210/pdb2a7f/pdb |
Descriptor | Lysozyme C, CHLORIDE ION, SODIUM ION, ... (4 entities in total) |
Functional Keywords | hydrolase |
Biological source | Gallus gallus (chicken) |
Cellular location | Secreted: P00698 |
Total number of polymer chains | 1 |
Total formula weight | 14602.32 |
Authors | Mueller-Dieckmann, C.,Panjikar, S.,Tucker, P.A.,Weiss, M.S. (deposition date: 2005-07-05, release date: 2005-07-19, Last modification date: 2024-10-30) |
Primary citation | Mueller-Dieckmann, C.,Panjikar, S.,Tucker, P.A.,Weiss, M.S. On the routine use of soft X-rays in macromolecular crystallography. Part III. The optimal data-collection wavelength. Acta Crystallogr.,Sect.D, 61:1263-1272, 2005 Cited by PubMed Abstract: Complete and highly redundant data sets were collected at different wavelengths between 0.80 and 2.65 A for a total of ten different protein and DNA model systems. The magnitude of the anomalous signal-to-noise ratio as assessed by the quotient R(anom)/R(r.i.m.) was found to be influenced by the data-collection wavelength and the nature of the anomalously scattering substructure. By utilizing simple empirical correlations, for instance between the estimated deltaF/F and the expected R(anom) or the data-collection wavelength and the expected R(r.i.m.), the wavelength at which the highest anomalous signal-to-noise ratio can be expected could be estimated even before the experiment. Almost independent of the nature of the anomalously scattering substructure and provided that no elemental X-ray absorption edge is nearby, this optimal wavelength is 2.1 A. PubMed: 16131760DOI: 10.1107/S0907444905021475 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.85 Å) |
Structure validation
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