Mix-and-diffuse serial synchrotron crystallography

Beyerlein, K.R.; Dierksmeyer, D.; Mariani, V.; Kuhn, M.; Sarrou, I.; Ottaviano, A.; Awel, S.; Knoska, J.; Fuglerud, S.; Jönsson, O.; Stern, S.; Wiedorn, M.O.; Yefanov, O.; Adriano, L.; Bean, R.; Burkhardt, A.; Fischer, P.; Heymann, M.; Horke, D.A.; Jungnickel, K.E.J.; Kovaleva, E.; Lorbeer, O.; Metz, M.; Meyer, J.; Morgan, A.; Pande, K.; Panneerselvam, S.; Seuring, C.; Tolstikova, A.; Lieske, J.; Aplin, S.; Roessle, M.; White, T.A.; Chapman, H.N.; Meents, A.; Oberthuer, D.

doi:10.1107/S2052252517013124

Figure 3
CTO bound to lysozyme: short-mixing case (a, b, c) and long-mixing case (d, e, f). (a) and (d) show the 2F_o − F_c (blue, 1σ) and F_o − F_c (green and red, 2.5σ) maps of the lysozyme binding site after initial refinement with ligand-free phases. (b) and (e) show the maps at the same levels after automatic ligand-placement and refinement, and (c) and (f) show the respective final refined models and maps. Residues forming hydrogen bonds to CTO are shown.

IUCrJ

Volume 4| Part 6| November 2017| Pages 769-777

ISSN: 2052-2525

https://doi.org/10.1107/S2052252517013124

BIOLOGY | MEDICINE

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