Pub. Date : 1993
PMID : 20301460
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Primary Hyperoxaluria Type 1 CLINICAL CHARACTERISTICS: Primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver peroxisomal enzyme alanine:glyoxylate-aminotransferase (AGT), which catalyzes the conversion of glyoxylate to glycine. | Glycine | alanine--glyoxylate and serine--pyruvate aminotransferase | Homo sapiens |
| 2 | Primary Hyperoxaluria Type 1 CLINICAL CHARACTERISTICS: Primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver peroxisomal enzyme alanine:glyoxylate-aminotransferase (AGT), which catalyzes the conversion of glyoxylate to glycine. | Glycine | alanine--glyoxylate and serine--pyruvate aminotransferase | Homo sapiens |