EC Number |
Title |
Organism |
---|
4.1.3.16 | Cellular degradation of 4-hydroxy-2-oxoglutarate aldolase leads to absolute deficiency in primary hyperoxaluria type 3 |
Homo sapiens |
4.1.3.16 | Extended substrate range of thiamine diphosphate-dependent MenD enzyme by coupling of two C-C-bonding reactions |
Escherichia coli |
4.1.3.16 | HOGA1 gene mutations of primary hyperoxaluria type 3 in tunisian patients |
Homo sapiens |
4.1.3.16 | Use of a novel microtitration protocol to obtain diffraction-quality crystals of 4-hydroxy-2-oxoglutarate aldolase from Bos taurus |
Bos taurus |
4.1.3.16 | 2-keto-4-Hydroxybutyrate aldolase. Identification as 2-keto-4-hydroxyglutarate aldolase, catalytic properties, and role in mammalian metabolism of L-homoserine |
Bos taurus |
4.1.3.16 | 2-keto-4-Hydroxybutyrate aldolase. Identification as 2-keto-4-hydroxyglutarate aldolase, catalytic properties, and role in mammalian metabolism of L-homoserine |
Mammalia |
4.1.3.16 | 2-keto-4-Hydroxyglutarate aldolase from bovine liver |
Bos taurus |
4.1.3.16 | 2-keto-4-Hydroxyglutarate aldolase: purification of the homogeneous enzyme from bovine kidney |
Bos taurus |
4.1.3.16 | 4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition |
Homo sapiens |
4.1.3.16 | Enzymes and intermediates of hydroxyproline degradation |
Rattus norvegicus |