Crystal structures of artocarpin, a Moraceae lectin with mannose specificity, and its complex with methyl-α-D-mannose: implications to the generation of carbohydrate specificity

Pratap, J. V. ; Arockia Jeyaprakash, A. ; Geetha Rani, P. ; Sekar, K. ; Surolia, A. ; Vijayan, M. (2002) Crystal structures of artocarpin, a Moraceae lectin with mannose specificity, and its complex with methyl-α-D-mannose: implications to the generation of carbohydrate specificity Journal of Molecular Biology, 317 (2). pp. 237-247. ISSN 0022-2836

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Official URL: http://www.sciencedirect.com/science/article/pii/s...

Related URL: http://dx.doi.org/10.1006/jmbi.2001.5432

Abstract

The seeds of jack fruit (Artocarpus integrifolia) contain two tetrameric lectins, jacalin and artocarpin. Jacalin was the first lectin found to exhibit the β-prism I fold, which is characteristic of the Moraceae plant lectin family. Jacalin contains two polypeptide chains produced by a post-translational proteolysis which has been shown to be crucial for generating its specificity for galactose. Artocarpin is a single chain protein with considerable sequence similarity with jacalin. It, however, exhibits many properties different from those of jacalin. In particular, it is specific to mannose. The structures of two crystal forms, form I and form II, of the native lectin have been determined at 2.4 and 2.5 Å resolution, respectively. The structure of the lectin complexed with methyl-α-mannose, has also been determined at 2.9 Å resolution. The structure is similar to jacalin, although differences exist in details. The crystal structures and detailed modelling studies indicate that the following differences between the carbohydrate binding sites of artocarpin and jacalin are responsible for the difference in the specificities of the two lectins. Firstly, artocarpin does not contain, unlike jacalin, an N terminus generated by post-translational proteolysis. Secondly, there is no aromatic residue in the binding site of artocarpin whereas there are four in that of jacalin. A comparison with similar lectins of known structures or sequences, suggests that, in general, stacking interactions with aromatic residues are important for the binding of galactose while such interactions are usually absent in the carbohydrate binding sites of mannose-specific lectins with the β-prism I fold.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:β-prism I Fold; Moraceae Lectin; Carbohydrate Specificity; Post-translational Modification; Stacking Interactions
ID Code:55211
Deposited On:18 Aug 2011 12:04
Last Modified:15 Jul 2012 18:11

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