Application of the use of high-throughput technologies to the determination of protein structures of bacterial and viral pathogens

Fogg, M.J.; Alzari, P.; Bahar, M.; Bertini, I.; Betton, J.-M.; Burmeister, W.P.; Cambillau, C.; Canard, B.; Carrondo, M.; Coll, M.; Daenke, S.; Dym, O.; Egloff, M.-P.; Enguita, F.J.; Geerlof, A.; Haouz, A.; Jones, T.A.; Ma, Q.; Manicka, S.N.; Migliardi, M.; Nordlund, P.; Owens, R.J.; Peleg, Y.; Schneider, G.; Schnell, R.; Stuart, D.I.; Tarbouriech, N.; Unge, T.; Wilkinson, A.J.; Wilmanns, M.; Wilson, K.S.; Zimhony, O.; Grimes, J.M.

doi:10.1107/S0907444906030915

Acta Crystallographica Section D
Acta Crystallographica
Section D BIOLOGICAL CRYSTALLOGRAPHY

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Figure 3
Structures of representative viral targets described in §

4. All cartoons are drawn with each monomer coloured from blue to red from the N- to the C-terminus. (a) The trimeric receptor-binding protein from lactococcal bacteriophage P2. The threefold axis is vertical and the separate architectural units of the molecule are labelled according to Spinelli et al. (2006

). (b) The dimeric molecule of SAR-CoV nsp9, viewed orthogonal to the molecular twofold axis. (c) Ribbon diagram of A41L of VACV (M. Bahar, unpublished work). (d) Ribbon representation of EBV dUTPase in complex with an atomic representation of dUMP (C, O, N and P atoms drawn in yellow, red, blue and orange, respectively).

BIOLOGICAL
CRYSTALLOGRAPHY

ISSN: 1399-0047

Volume 62| Part 10| September 2006| Pages 1196-1207

doi:10.1107/S0907444906030915

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