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beta-ureidopropionase

Also Known As:

N-carbamoyl beta-alanine amidohydrolase; beta-alanine synthase; N-carbamoyl-beta-alanine amidohydrolase

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Enzymes and Coenzymes: 1
- Enzymes: 152586
  - Hydrolases: 2166
    - Amidohydrolases: 43
      - beta-ureidopropionase: 2

Experts

1.	Kuhara, Tomiko: 1 article (12/2002)

Related Diseases

1.	Hyperammonemia 12/05/2002 - "In this review, the differential diagnosis for hyperammonemia are described; deficiencies of ornithine carbamoyl transferase, argininosuccinate synthase (citrullinemia), argininosuccinate lyase and arginase, lysinuric protein intolerance, hyperammonemia-hyperornithinemia-homocitrullinemia syndrome, and citrullinemia type II. The diagnosis of IEM of purine and pyrimidine such as deficiencies of hypoxanthine-guanine phosphoribosyl transferase, adenine phosphoribosyl transferase, dihydropyrimidine dehydrogenase, dihydropyrimidinase and beta-ureidopropionase are described. "
2.	Citrullinemia 12/05/2002 - "In this review, the differential diagnosis for hyperammonemia are described; deficiencies of ornithine carbamoyl transferase, argininosuccinate synthase (citrullinemia), argininosuccinate lyase and arginase, lysinuric protein intolerance, hyperammonemia-hyperornithinemia-homocitrullinemia syndrome, and citrullinemia type II. The diagnosis of IEM of purine and pyrimidine such as deficiencies of hypoxanthine-guanine phosphoribosyl transferase, adenine phosphoribosyl transferase, dihydropyrimidine dehydrogenase, dihydropyrimidinase and beta-ureidopropionase are described. "
3.	Protein Deficiency 10/01/1991 - "Protein deficiency (5%) also decreased the activity of beta-ureidopropionase. "
4.	Lysinuric Protein Intolerance 12/05/2002 - "In this review, the differential diagnosis for hyperammonemia are described; deficiencies of ornithine carbamoyl transferase, argininosuccinate synthase (citrullinemia), argininosuccinate lyase and arginase, lysinuric protein intolerance, hyperammonemia-hyperornithinemia-homocitrullinemia syndrome, and citrullinemia type II. The diagnosis of IEM of purine and pyrimidine such as deficiencies of hypoxanthine-guanine phosphoribosyl transferase, adenine phosphoribosyl transferase, dihydropyrimidine dehydrogenase, dihydropyrimidinase and beta-ureidopropionase are described. "

Related Drugs and Biologics

1.	Dihydrouracil Dehydrogenase (NADP) (Dihydropyrimidine Dehydrogenase)
2.	Carboxyl and Carbamoyl Transferases (Carbamoyltransferases)
3.	Hypoxanthine
4.	Transferases
5.	Ornithine
6.	Guanine
7.	Argininosuccinate Synthase (Argininosuccinate Synthetase)
8.	Argininosuccinate Lyase
9.	Arginase
10.	Adenine