EC: 5.1.3.8

N-acylglucosamine 2-epimerase (N-Acyl-D-glucosamine 2-epimerase)

enzyme lambda metabolic reaction experiment
uniprot:P51606 [ATP]

N_Acetyl_D_mannosamine -> N_Acetyl_D_glucosamine		 (( (Vmax * S) ) / (Km + S)) buffer: 0.1 M Tris-HCl, 10 mM MgCl2
PH: 7.5
Temperature: 37
uniprot:P51606 [ATP]

N_Acetyl_D_mannosamine -> N_Acetyl_D_glucosamine		 (( (Vmax * A) ) / (Ka + A)) buffer: 0.1 M Tris-HCl, 10 mM MgCl2
PH: 7.5
Temperature: 37
uniprot:P51606 [ATP]

N_Acetyl_D_glucosamine -> N_Acetyl_D_mannosamine		 (( (Vmax * S) ) / (Km + S)) buffer: 0.1 M Tris-HCl, 10 mM MgCl2
PH: 7.5
Temperature: 37

Pathways

pathway id name
Reactome:R-HSA-392499 Metabolism of proteins
Reactome:R-HSA-597592 Post-translational protein modification
Reactome:R-MMU-446219 Synthesis of substrates in N-glycan biosythesis
Reactome:R-RNO-597592 Post-translational protein modification
Reactome:R-HSA-446219 Synthesis of substrates in N-glycan biosythesis
Reactome:R-MMU-446193 Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
Reactome:R-RNO-392499 Metabolism of proteins
Reactome:R-RNO-446219 Synthesis of substrates in N-glycan biosythesis
Reactome:R-HSA-446203 Asparagine N-linked glycosylation
Reactome:R-HSA-446210 Synthesis of UDP-N-acetyl-glucosamine
Reactome:R-MMU-392499 Metabolism of proteins
Reactome:R-MMU-597592 Post-translational protein modification
Reactome:R-RNO-446203 Asparagine N-linked glycosylation
Reactome:R-RNO-446210 Synthesis of UDP-N-acetyl-glucosamine
Reactome:R-HSA-446193 Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
Reactome:R-MMU-446203 Asparagine N-linked glycosylation
Reactome:R-MMU-446210 Synthesis of UDP-N-acetyl-glucosamine
Reactome:R-RNO-446193 Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
PathBank:SMP0120818 G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease
PathBank:SMP0120524 Salla Disease/Infantile Sialic Acid Storage Disease
PathBank:SMP0000240 Salla Disease/Infantile Sialic Acid Storage Disease
PathBank:SMP0120737 Sialuria or French Type Sialuria
PathBank:SMP0120765 Tay-Sachs Disease
PathBank:SMP0000045 Amino Sugar Metabolism
PathBank:SMP0000216 Sialuria or French Type Sialuria
PathBank:SMP0087281 Amino Sugar Metabolism
PathBank:SMP0120744 Salla Disease/Infantile Sialic Acid Storage Disease
PathBank:SMP0120517 Sialuria or French Type Sialuria
PathBank:SMP0120545 Tay-Sachs Disease
PathBank:SMP0000390 Tay-Sachs Disease
PathBank:SMP0087175 Amino Sugar Metabolism
PathBank:SMP0120599 G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease
PathBank:SMP0000534 G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease
PathBank:SMP0063580 Amino Sugar Metabolism