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2GNA

Crystal structure of UDP-GlcNAc inverting 4,6-dehydratase in complex with NADP and UDP-Gal

Summary for 2GNA
Entry DOI10.2210/pdb2gna/pdb
Related2GN4 2GN6 2GN8 2GN9
DescriptorUDP-GlcNAc C6 dehydratase, GALACTOSE-URIDINE-5'-DIPHOSPHATE, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ... (5 entities in total)
Functional Keywordsrossmann fold, tyk triad, sdr, enzyme, dehydratase, udp-glcnac, nadp, lyase
Biological sourceHelicobacter pylori
Total number of polymer chains2
Total formula weight80264.07
Authors
Ishiyama, N.,Creuzenet, C.,Lam, J.S.,Berghuis, A.M. (deposition date: 2006-04-09, release date: 2006-05-09, Last modification date: 2023-08-30)
Primary citationIshiyama, N.,Creuzenet, C.,Miller, W.L.,Demendi, M.,Anderson, E.M.,Harauz, G.,Lam, J.S.,Berghuis, A.M.
Structural Studies of FlaA1 from Helicobacter pylori Reveal the Mechanism for Inverting 4,6-Dehydratase Activity.
J.Biol.Chem., 281:24489-24495, 2006
Cited by
PubMed Abstract: FlaA1 from the human pathogen Helicobacter pylori is an enzyme involved in saccharide biosynthesis that has been shown to be essential for pathogenicity. Here we present five crystal structures of FlaA1 in the presence of substrate, inhibitors, and bound cofactor, with resolutions ranging from 2.8 to 1.9 A. These structures reveal that the enzyme is a novel member of the short-chain dehydrogenase/reductase superfamily. Additional electron microscopy studies show the enzyme to possess a hexameric doughnut-shaped quaternary structure. NMR analyses of "real time" enzyme-substrate reactions indicate that FlaA1 is a UDP-GlcNAc-inverting 4,6-dehydratase, suggesting that the enzyme catalyzes the first step in the biosynthetic pathway of a pseudaminic acid derivative, which is implicated in protein glycosylation. Guided by evidence from site-directed mutagenesis and computational simulations, a three-step reaction mechanism is proposed that involves Lys-133 functioning as both a catalytic acid and base.
PubMed: 16651261
DOI: 10.1074/jbc.M602393200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

226707

數據於2024-10-30公開中

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