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5DWK

Diacylglycerol Kinase solved by multi crystal multi orientation native SAD

Summary for 5DWK
Entry DOI10.2210/pdb5dwk/pdb
DescriptorDiacylglycerol kinase, (2R)-2,3-DIHYDROXYPROPYL(7Z)-PENTADEC-7-ENOATE, (2S)-2,3-DIHYDROXYPROPYL(7Z)-PENTADEC-7-ENOATE, ... (8 entities in total)
Functional Keywordsnative sad, dagk, multi crystal, multi orientation, transferase
Biological sourceEscherichia coli
Cellular locationCell inner membrane; Multi-pass membrane protein: P0ABN1
Total number of polymer chains6
Total formula weight89654.25
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 citationOlieric, 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: 26960129
DOI: 10.1107/S2059798315024110
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.601 Å)
Structure validation

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