2.4.1.218: hydroquinone glucosyltransferase
This is an abbreviated version!
For detailed information about hydroquinone glucosyltransferase, go to the full flat file.
Reaction
Synonyms
arbutin synthase, arbutin synthetase, AS, glucosyltransferase, uridine diphosphoglucose-hydroquinone, hydroquinone glucosyl transferase, hydroquinone O-glucosyltransferase, hydroquinone:O-glucosyltransferase, More, uridine diphosphate-glucose:hydroquinone glucosyltransferase
ECTree
2.4.1.218 hydroquinone glucosyltransferaseAdvanced search results
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results (Inhibitors
Inhibitors on EC 2.4.1.218 - hydroquinone glucosyltransferase
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INHIBITOR 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
IMAGE
Hg2+
10 mM, complete inhibition, reversed by addition of 20 mM 2-mercaptoethanol
hydroquinone
Glu274 is acting as an acidic backbone acceptor residue. Lys262, a basic amino acid from the active site of wheat Hydroquinone glucosyltransferase interacts with the hydroxyl group of hydroquinone and behaves as a side chain donor molecule. Asp264 is also observed as an interacting residue from the active site of hydroquinone glucosyltransferase. It binds to the hydroxyl group of hydroquinone inhibitor and donates hydrogen ion from its side chain group
N-(n-butyl) phosphorothiocic triamide
Glu274 is acting as an acidic backbone donor residue and interacts with the amino group of the inhibitor
phenyl phosphorodiamate
Glu395 is directly interacting with amino group of the inhibitor
additional information
enzyme molecular docking of urease inhibitors hydroquinone, phenyl phosphorodiamate, and N-(n-butyl) phosphorothiocic triamide, three-dimensional structure analysis using homology modeling, and interactions analysis, overview
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additional information
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enzyme molecular docking of urease inhibitors hydroquinone, phenyl phosphorodiamate, and N-(n-butyl) phosphorothiocic triamide, three-dimensional structure analysis using homology modeling, and interactions analysis, overview
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