EC Number   |
Natural Substrates |
|---|
    2.7.1.60 | ATP + N-acetyl-D-mannosamine |
- |
| 2.7.1.60 | ATP + N-acetyl-D-mannosamine |
highly specific for ATP and N-acetyl-D-mannosamine |
| 2.7.1.60 | ATP + N-acetyl-D-mannosamine |
involved in N-acetylneuraminic acid metabolism, key enzyme in N-acetylneuraminic acid biosynthesis |
| 2.7.1.60 | ATP + N-acetyl-D-mannosamine |
metabolic pathway between hexoses and sialic acids |
| 2.7.1.60 | ATP + N-acetyl-D-mannosamine |
enzyme is involved in sialic acid metabolism |
| 2.7.1.60 | ATP + N-acyl-D-mannosamine |
- |
| 2.7.1.60 | ATP + N-acyl-D-mannosamine |
key and rate limiting enzyme in the synthesis of N-acetylneuraminic acid and therefore of nearly all other sialic acids, enzyme mutations can cause hereditary inclusion body myopathy |
| 2.7.1.60 | ATP + N-acyl-D-mannosamine |
key enzyme in the synthesis of N-acetylneuraminic acid and therefore of nearly all other sialic acids |
| 2.7.1.60 | ATP + N-acyl-D-mannosamine |
key enzyme in the synthesis of N-acetylneuraminic acid and therefore of nearly all other sialic acids, essential for early embryonic development |
| 2.7.1.60 | ATP + N-acyl-D-mannosamine |
key enzyme in the synthesis of N-acetylneuraminic acid and therefore of nearly all other sialic acids, essential for early embryonic development, enzyme involved in several genetic disorders such as sialuria, hereditary inclusion body myopathy, and Nonaka myopathy |
