1k7u

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[[Image:1k7u.gif|left|200px]]
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[[Image:1k7u.png|left|200px]]
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{{STRUCTURE_1k7u| PDB=1k7u | SCENE= }}
{{STRUCTURE_1k7u| PDB=1k7u | SCENE= }}
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'''Crystal Structure Analysis of crosslinked-WGA3/GlcNAcbeta1,4GlcNAc complex'''
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===Crystal Structure Analysis of crosslinked-WGA3/GlcNAcbeta1,4GlcNAc complex===
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==Overview==
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The interactions of wheat-germ agglutinin (WGA) with the GlcNAc beta 1,6Gal sequence, a characteristic component of branched poly-N-acetyllactosaminoglycans, were investigated using isothermal titration calorimetry and X-ray crystallography. GlcNAc beta 1,6Gal exhibited an affinity greater than GlcNAc beta 1,4GlcNAc to all WGA isolectins, whereas Gal beta 1,6GlcNAc showed much less affinity than GlcNAc beta 1,4GlcNAc. X-ray structural analyses of the glutaraldehyde-crosslinked WGA isolectin 3 crystals in complex with GlcNAc beta 1,6Gal, GlcNAc beta 1,4GlcNAc and GlcNAc beta 1,6Gal beta 1,4Glc were performed at 2.4, 2.2 and 2.2 A resolution, respectively. In spite of different glycosidic linkages, GlcNAc beta 1,6Gal and GlcNAc beta 1,4GlcNAc exhibited basically similar binding modes to each other, in contact with side chains of two aromatic residues, Tyr64 and His66. However, the conformations of the ligands in the two primary binding sites were not always identical. GlcNAc beta 1,6Gal showed more extensive variation in the parameters defining the glycosidic linkage structure compared to GlcNAc beta 1,4GlcNAc, demonstrating large conformational flexibility of the former ligand in the interaction with WGA. The difference in the ligand binding conformation was accompanied by alterations of the side chain conformation of the amino acid residues involved in the interactions. The hydrogen bond between Ser62 and the non-reducing end GlcNAc was always observed regardless of the ligand type, indicating the key role of this interaction. In addition to the hydrogen bonding and van der Waals interactions, CH--pi interactions involving Tyr64, His66 and Tyr73 are suggested to play an essential role in determining the ligand binding conformation in all complexes. One of the GlcNAc beta 1,6Gal ligands had no crystal packing contact with another WGA molecule, therefore the conformation might be more relevant to the interaction mode in solution.
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(as it appears on PubMed at http://www.pubmed.gov), where 11853952 is the PubMed ID number.
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{{ABSTRACT_PUBMED_11853952}}
==About this Structure==
==About this Structure==
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[[Category: Muraki, M.]]
[[Category: Muraki, M.]]
[[Category: Hevein-type fold]]
[[Category: Hevein-type fold]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 22:24:43 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 2 09:54:55 2008''

Revision as of 06:54, 2 July 2008

Image:1k7u.png

Template:STRUCTURE 1k7u

Crystal Structure Analysis of crosslinked-WGA3/GlcNAcbeta1,4GlcNAc complex

Template:ABSTRACT PUBMED 11853952

About this Structure

1K7U is a Single protein structure of sequence from Triticum aestivum. Full crystallographic information is available from OCA.

Reference

Interactions of wheat-germ agglutinin with GlcNAc beta 1,6Gal sequence., Muraki M, Ishimura M, Harata K, Biochim Biophys Acta. 2002 Jan 15;1569(1-3):10-20. PMID:11853952

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