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Peculiarity in crystal packing of anti-HIV lectin actinohivin in complex with α(1–2)mannobiose

Author Affiliations
Iwaki Meisei University, University of Rajshahi, Tokyo Institute of Technology
Published InActa Crystallographica Section D Biological Crystallography
Year2013
Citations3

Abstract

Previously, the anti-HIV lectin actinohivin (AH) was cocrystallized with the target α(1-2)mannobiose (MB) in the apparent space group P213. However, three MB-bound AH rotamers generated by ±120° rotations around the molecular pseudo-threefold rotation axis are packed randomly in the unit cell according to P212121 symmetry [Hoque et al. (2012). Acta Cryst. D68, 1671-1679]. It was found that the AH used for crystallization contains short peptides attached to the N-terminus [Suzuki et al. (2012). Acta Cryst. F68, 1060-1063], which cause packing disorder. In the present study, the fully mature homogeneous AH has been cocrystallized with MB into two new crystal forms at different pH. X-ray analyses of the two forms reveal that they have peculiar character in that the space groups…
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