Mutations in POGLUT1 in Galli–Galli/Dowling–Degos disease von Wilson, N.J., Cole, C., Kroboth, K., Hunter, W.N., Mann, J.A., McLean, W.H.I., Kernland Lang, K., Beltraminelli, H., Sabroe, R.A., Tiffin, N., Sobey, G.J., Borradori, L., Simpson, E., Smith, F.J.D.

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The power of three von Weiss, M. S., Hunter, W. N.

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Structure of the macrocycle thiostrepton solved using the anomalous dispersion contribution of sulfur von Bond, Charles S., Shaw, Matthew P., Alphey, Magnus S., Hunter, William N.

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Macromolecular crystallography and what it can contribute to antiparasite drug discovery von Hunter, W. N., Weiss, Manfred S.

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The state-of-the art in macromolecular crystallization: the IYCr series concludes von Weiss, M. S., Hunter, W. N., Einspahr, H. M.

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The times they are a-changin' - news from Acta Crystallographica Section F von Hunter, W. N., Weiss, Manfred S.

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Crystals on the cover 2015 von Einspahr, Howard, Weiss, Manfred S., Hunter, W. N.

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Structures of Leishmania major Pteridine Reductase Complexes Reveal the Active Site Features Important for Ligand Binding and to Guide Inhibitor Design von Schüttelkopf, Alexander W., Hardy, Larry W., Beverley, Stephen M., Hunter, William N.

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The structure of guanosine-thymidine mismatches in B-DNA at 2.5-A resolution von Hunter, W.N., Brown, T., Kneale, G., Anand, N.N., Rabinovich, D., Kennard, O.

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Two interacting binding sites for quinacrine derivatives in the active site of trypanothione reductase: a template for drug design von Saravanamuthu, Ahilan, Vickers, Tim J, Bond, Charles S, Peterson, Mark R, Hunter, William N, Fairlamb, Alan H

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Crystals on the cover 2014 von Einspahr, Howard, Weiss, Manfred S., Hunter, W. N.

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Recombinant Human PPAR-β/δ Ligand-binding Domain is Locked in an Activated Conformation by Endogenous Fatty Acids von Fyffe, Stewart A., Alphey, Magnus S., Buetow, Lori, Smith, Terry K., Ferguson, Michael A.J., Sørensen, Morten D., Björkling, Fredrik, Hunter, William N.

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A structure-based approach to drug discovery; crystallography and implications for the development of antiparasite drugs von HUNTER, W. N.

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DNA conformation is determined by economics in the hydration of phosphate groups von Saenger, Wolfram, Hunter, William N, Kennard, Olga

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Biochemical characterization of the initial steps of the Kennedy pathway in Trypanosoma brucei : the ethanolamine and choline kinases von Gibellini, F., Hunter, W.N., Smith, T.K.

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Biosynthesis of Isoprenoids: Crystal Structure of 4-Diphosphocytidyl-2C-Methyl-D-Erythritol Kinase von Miallau, Linda, Alphey, Magnus S., Kemp, Lauris E., Leonard, Gordon A., McSweeney, Sean M., Hecht, Stefan, Bacher, Adelbert, Eisenreich, Wolfgang, Rohdich, Felix, Hunter, William N.

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Pteridine reductase mechanism correlates pterin metabolism with drug resistance in trypanosomatid parasites von Hunter, William N, Gourley, David G, Schüttelkopf, Alexander W, Leonard, Gordon A, Luba, James, Hardy, Larry W, Beverley, Stephen M

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Structure of 2C-Methyl-D-Erythritol 2,4-Cyclodiphosphate Synthase: An Essential Enzyme for Isoprenoid Biosynthesis and Target for Antimicrobial Drug Development von Kemp, Lauris E., Bond, Charles S., Hunter, William N.

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Crystal structure of Trypanosoma cruzi trypanothione reductase in complex with trypanothione, and the structure-based discovery of new natural product inhibitors von Bond, Charles S, Zhang, Yihong, Berriman, Matthew, Cunningham, Mark L, Fairlamb, Alan H, Hunter, William N

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Crystallization and preliminary X-ray diffraction studies of recombinant Escherichia coli 4-­diphosphocytidyl-2-C-methyl-d-erythritol synthetase von Kemp, Lauris E., Bond, Charles S., Hunter, William N.

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