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Literature summary for 5.4.99.9 extracted from

  • Dykhuizen, E.C.; Kiessling, L.L.
    Potent ligands for prokaryotic UDP-galactopyranose mutase that exploit an enzyme subsite (2009), Org. Lett., 11, 193-196.
    View publication on PubMedView publication on EuropePMC

Inhibitors

Inhibitors Comment Organism Structure
N-(4-[4-[8-([[3-carboxy-4-(6-hydroxy-3-oxo-3H-xanthen-9-yl)phenyl]carbamothioyl]amino)octyl]phenyl]-2,3-dihydro-1,3-thiazol-2-yl)-4-chlorophenylalanine
-
Mycobacterium tuberculosis

Organism

Organism UniProt Comment Textmining
Klebsiella pneumoniae
-
-
-
Mycobacterium tuberculosis
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
UDP-galactopyranose
-
Klebsiella pneumoniae UDP-galactofuranose
-
?
UDP-galactopyranose
-
Mycobacterium tuberculosis UDP-galactofuranose
-
?

Synonyms

Synonyms Comment Organism
Glf
-
Klebsiella pneumoniae
Glf
-
Mycobacterium tuberculosis
UGM
-
Klebsiella pneumoniae
UGM
-
Mycobacterium tuberculosis

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.0035
-
-
Mycobacterium tuberculosis N-(4-[4-[8-([[3-carboxy-4-(6-hydroxy-3-oxo-3H-xanthen-9-yl)phenyl]carbamothioyl]amino)octyl]phenyl]-2,3-dihydro-1,3-thiazol-2-yl)-4-chlorophenylalanine