Any feedback?
Please rate this page
(all_enzymes.php)
(0/150)

BRENDA support

4.2.1.115: UDP-N-acetylglucosamine 4,6-dehydratase (configuration-inverting)

This is an abbreviated version!
For detailed information about UDP-N-acetylglucosamine 4,6-dehydratase (configuration-inverting), go to the full flat file.

Word Map on EC 4.2.1.115

Reaction

UDP-N-acetyl-alpha-D-glucosamine
=
UDP-2-acetamido-2,6-dideoxy-beta-L-arabino-hex-4-ulose
+
H2O

Synonyms

4,6-dehydratase/5-epimerase, CapE, Cj1293, FlaA1, HP0840, inverting 4,6-dehydratase, Mg534, More, NAD(P)+-dependent dehydratase/epimerase, PseB, UDP-alpha-D-GlcNAc modifying dehydratase, UDP-GlcNAc 5-inverting 4,6-dehydratase, UDP-GlcNAc C6 dehydratase, UDP-GlcNAc C6 dehydratase/C4 reductase, UDP-N-acetylglucosamine 5-inverting 4,6-dehydratase, WbpM

ECTree

     4 Lyases
         4.2 Carbon-oxygen lyases
             4.2.1 Hydro-lyases
                4.2.1.115 UDP-N-acetylglucosamine 4,6-dehydratase (configuration-inverting)

Purification

Purification on EC 4.2.1.115 - UDP-N-acetylglucosamine 4,6-dehydratase (configuration-inverting)

Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
recombinant GST-tagged enzyme from Escherichia coli strain BL-21 GOLD by glutathione affinity chromatography, proteolytic removal of the GST-tag, and ultrafiltration, recombinant His6-tagged enzyme from Escherichia coli strain Rosetta(DE3) by nickel affinity chromatography, proteolytic removal of the His-tag, another step of nickel affinity chromatography, and desalting gel filtration, thereby the recombinant protein corresponds to the native enzyme in which the initial methionine is replaced by GPGS sequence resulting from the cleavage site
recombinant His-tagged FlaA1 9.9fold from Escherichia coli strain BL21(DE3) to homogeneity by nickel chelation and cation exchange chromatography
-
recombinant His-tagged wild-type and mutant enzymes from Escherichia coli strain BL21(DE3)
-
recombinant N-terminally His-tagged and C-terminally His-tagged WbpMs from Escherichia coli by selective solubilization from the inner membrane by lauryl sarcosine and nickel chelation chromatography