Search Reference

4.1.3.16

Cellular degradation of 4-hydroxy-2-oxoglutarate aldolase leads to absolute deficiency in primary hyperoxaluria type 3

FEBS Lett.

590

1467-1476

2016

4.1.3.16

Extended substrate range of thiamine diphosphate-dependent MenD enzyme by coupling of two C-C-bonding reactions

Appl. Microbiol. Biotechnol.

102

8359-8372

2018

4.1.3.16

HOGA1 gene mutations of primary hyperoxaluria type 3 in tunisian patients

J. Clin. Lab. Anal.

31

e22053

2017

4.1.3.16

Use of a novel microtitration protocol to obtain diffraction-quality crystals of 4-hydroxy-2-oxoglutarate aldolase from Bos taurus

Acta Crystallogr. Sect. F

70

1546-1549

2014

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

Biochemistry

10

1353-1364

1971

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

Biochemistry

10

1353-1364

1971

4.1.3.16

2-keto-4-Hydroxyglutarate aldolase from bovine liver

Methods Enzymol.

42C

280-285

1975

4.1.3.16

2-keto-4-Hydroxyglutarate aldolase: purification of the homogeneous enzyme from bovine kidney

J. Biol. Chem.

267

10507-10514

1992

4.1.3.16

4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition

Biochim. Biophys. Acta

1822

1544-1552

2012

4.1.3.16

Enzymes and intermediates of hydroxyproline degradation

Methods Enzymol.

17B

266-306

1971

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