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8OG4

Exostosin-like 3 UDP complex

Summary for 8OG4
Entry DOI10.2210/pdb8og4/pdb
Related8OG1
DescriptorExostosin-like 3, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (6 entities in total)
Functional Keywordsglycosyltransferase, heparan sulfate, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight206814.65
Authors
Sammon, D.,Hohenester, E. (deposition date: 2023-03-18, release date: 2023-07-12, Last modification date: 2024-11-20)
Primary citationSammon, D.,Krueger, A.,Busse-Wicher, M.,Morgan, R.M.,Haslam, S.M.,Schumann, B.,Briggs, D.C.,Hohenester, E.
Molecular mechanism of decision-making in glycosaminoglycan biosynthesis.
Nat Commun, 14:6425-6425, 2023
Cited by
PubMed Abstract: Two major glycosaminoglycan types, heparan sulfate (HS) and chondroitin sulfate (CS), control many aspects of development and physiology in a type-specific manner. HS and CS are attached to core proteins via a common linker tetrasaccharide, but differ in their polymer backbones. How core proteins are specifically modified with HS or CS has been an enduring mystery. By reconstituting glycosaminoglycan biosynthesis in vitro, we establish that the CS-initiating N-acetylgalactosaminyltransferase CSGALNACT2 modifies all glycopeptide substrates equally, whereas the HS-initiating N-acetylglucosaminyltransferase EXTL3 is selective. Structure-function analysis reveals that acidic residues in the glycopeptide substrate and a basic exosite in EXTL3 are critical for specifying HS biosynthesis. Linker phosphorylation by the xylose kinase FAM20B accelerates linker synthesis and initiation of both HS and CS, but has no effect on the subsequent polymerisation of the backbone. Our results demonstrate that modification with CS occurs by default and must be overridden by EXTL3 to produce HS.
PubMed: 37828045
DOI: 10.1038/s41467-023-42236-z
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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PDB entries from 2024-12-18

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