5DWK
Diacylglycerol Kinase solved by multi crystal multi orientation native SAD
Summary for 5DWK
| Entry DOI | 10.2210/pdb5dwk/pdb |
| Descriptor | Diacylglycerol kinase, (2R)-2,3-DIHYDROXYPROPYL(7Z)-PENTADEC-7-ENOATE, (2S)-2,3-DIHYDROXYPROPYL(7Z)-PENTADEC-7-ENOATE, ... (8 entities in total) |
| Functional Keywords | native sad, dagk, multi crystal, multi orientation, transferase |
| Biological source | Escherichia coli |
| Cellular location | Cell inner membrane; Multi-pass membrane protein: P0ABN1 |
| Total number of polymer chains | 6 |
| Total formula weight | 89654.25 |
| Authors | Weinert, T.,Olieric, V.,Finke, A.D.,Li, D.,Caffrey, M.,Wang, M. (deposition date: 2015-09-22, release date: 2016-03-23, Last modification date: 2024-05-08) |
| Primary citation | Olieric, V.,Weinert, T.,Finke, A.D.,Anders, C.,Li, D.,Olieric, N.,Borca, C.N.,Steinmetz, M.O.,Caffrey, M.,Jinek, M.,Wang, M. Data-collection strategy for challenging native SAD phasing. Acta Crystallogr D Struct Biol, 72:421-429, 2016 Cited by PubMed Abstract: Recent improvements in data-collection strategies have pushed the limits of native SAD (single-wavelength anomalous diffraction) phasing, a method that uses the weak anomalous signal of light elements naturally present in macromolecules. These involve the merging of multiple data sets from either multiple crystals or from a single crystal collected in multiple orientations at a low X-ray dose. Both approaches yield data of high multiplicity while minimizing radiation damage and systematic error, thus ensuring accurate measurements of the anomalous differences. Here, the combined use of these two strategies is described to solve cases of native SAD phasing that were particular challenges: the integral membrane diacylglycerol kinase (DgkA) with a low Bijvoet ratio of 1% and the large 200 kDa complex of the CRISPR-associated endonuclease (Cas9) bound to guide RNA and target DNA crystallized in the low-symmetry space group C2. The optimal native SAD data-collection strategy based on systematic measurements performed on the 266 kDa multiprotein/multiligand tubulin complex is discussed. PubMed: 26960129DOI: 10.1107/S2059798315024110 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.601 Å) |
Structure validation
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