Figure 1
Figure 1. The crystal structure of GPIbβ ectodomain (GPIbβE). (A) Sequence alignment of GPIbβE (blue), GPIXE (purple), and GPIbβEabc (blue and purple) with respective residue numbers for GPIbβE and GPIX marked on the top and bottom. Elements of secondary structure in GPIbβE are shown on top and colored as in panel B. Residues affected by BSS missense mutations are in red. Three stretches of the GPIXE sequence that are included in GPIbβEabc are shown in purple. (B) Two orientations are shown of a ribbon diagram of the GPIbβE structure viewed from the concave face (left), with β-strands labeled in blue, α-helices in red, 310 helices in purple, and loop regions in gray. Asn residues 40, 41, and 64 are shown as stick, and a single residue from the N-linked oligosaccharide attached to Asn41 is also shown in green. The diagram on the right is rotated 180 degrees with side chains in the inter-LRR cap cation-π interaction shown as stick. (C) Refined 1.25-Å electron density, calculated with 2Fo-Fc coefficients and contoured at 1.5 rms.

The crystal structure of GPIbβ ectodomain (GPIbβE). (A) Sequence alignment of GPIbβE (blue), GPIXE (purple), and GPIbβEabc (blue and purple) with respective residue numbers for GPIbβE and GPIX marked on the top and bottom. Elements of secondary structure in GPIbβE are shown on top and colored as in panel B. Residues affected by BSS missense mutations are in red. Three stretches of the GPIXE sequence that are included in GPIbβEabc are shown in purple. (B) Two orientations are shown of a ribbon diagram of the GPIbβE structure viewed from the concave face (left), with β-strands labeled in blue, α-helices in red, 310 helices in purple, and loop regions in gray. Asn residues 40, 41, and 64 are shown as stick, and a single residue from the N-linked oligosaccharide attached to Asn41 is also shown in green. The diagram on the right is rotated 180 degrees with side chains in the inter-LRR cap cation-π interaction shown as stick. (C) Refined 1.25-Å electron density, calculated with 2Fo-Fc coefficients and contoured at 1.5 rms.

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