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PDBsum entry 4ee3
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References listed in PDB file
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Key reference
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Title
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Binding of n-Acetylglucosamine (glcnac) β1-6-Branched oligosaccharide acceptors to β4-Galactosyltransferase i reveals a new ligand binding mode.
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Authors
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B.Ramakrishnan,
E.Boeggeman,
P.K.Qasba.
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Ref.
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J Biol Chem, 2012,
287,
28666-28674.
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PubMed id
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Abstract
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N-acetyllactosamine is the most prevalent disaccharide moiety in the glycans on
the surface of mammalian cells and often found as repeat units in the linear and
branched polylactosamines, known as i- and I-antigen, respectively. The
β1-4-galactosyltransferase-I (β4Gal-T1) enzyme is responsible for the
synthesis of the N-acetyllactosamine moiety. To understand its oligosaccharide
acceptor specificity, we have previously investigated the binding of tri- and
pentasaccharides of N-glycan with a GlcNAc at their nonreducing end and found
that the extended sugar moiety in these acceptor substrates binds to the crevice
present at the acceptor substrate binding site of the β4Gal-T1 molecule. Here
we report seven crystal structures of β4Gal-T1 in complex with an
oligosaccharide acceptor with a nonreducing end GlcNAc that has a
β1-6-glycosidic link and that are analogous to either N-glycan or i/I-antigen.
In the crystal structure of the complex of β4Gal-T1 with I-antigen analog
pentasaccharide, the β1-6-branched GlcNAc moiety is bound to the sugar acceptor
binding site of the β4Gal-T1 molecule in a way similar to the crystal
structures described previously; however, the extended linear tetrasaccharide
moiety does not interact with the previously found extended sugar binding site
on the β4Gal-T1 molecule. Instead, it interacts with the different hydrophobic
surface of the protein molecule formed by the residues Tyr-276, Trp-310, and
Phe-356. Results from the present and previous studies suggest that β4Gal-T1
molecule has two different oligosaccharide binding regions for the binding of
the extended oligosaccharide moiety of the acceptor substrate.
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