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Phosphoenolpyruvate carboxykinase deficiency
Also Known As:
Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic; Phosphoenolpyruvate carboxykinase-1 (PCK1) deficiency; Phosphoenolpyruvate carboxylase deficiency; Phosphopyruvate carboxylase deficiency
Networked:
4
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Inborn Genetic Diseases: 11939
Inborn Errors Metabolism: 1162
Inborn Errors Carbohydrate Metabolism
Phosphoenolpyruvate carboxykinase deficiency: 4
Nutritional and Metabolic Diseases: 15
Metabolic Diseases: 10142
Inborn Errors Metabolism: 1162
Inborn Errors Carbohydrate Metabolism
Phosphoenolpyruvate carboxykinase deficiency: 4
Digestive System Diseases: 1042
Liver Diseases: 41660
Phosphoenolpyruvate carboxykinase deficiency: 4
Enzymes and Coenzymes: 1
Enzymes: 152586
Lyases: 637
Carbon-Carbon Lyases
Carboxy-Lyases: 620
Phosphoenolpyruvate Carboxykinase (GTP): 14
Phosphoenolpyruvate carboxykinase deficiency: 4
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Phosphoenolpyruvate carboxykinase deficiency:
1.
Glutamic Acid (Glutamate)
FDA Link
04/01/1995 - "
A glutamate racemase gene of Lactobacillus brevis ATCC 8287 was cloned into Escherichia coli TM93 by the phenotypic complementation of a phosphoenolpyruvate carboxylase deficiency on minimum agar medium containing D-glutamate.
"
2.
Pyruvate Carboxylase
IBA
01/01/1989 - "
Hepatic phosphoenolpyruvate carboxykinase deficiency: a neonatal case with reduced activity of pyruvate carboxylase.
"
3.
Phenylalanine (L-Phenylalanine)
FDA Link
06/22/2023 - "
The resultant strain, harboring a phosphoenolpyruvate carboxylase deficiency, synthesized 50.7 mM phenylalanine from 444 mM glucose.
"
4.
Glucose (Dextrose)
FDA Link
Generic
06/22/2023 - "
The resultant strain, harboring a phosphoenolpyruvate carboxylase deficiency, synthesized 50.7 mM phenylalanine from 444 mM glucose.
"
5.
Enzymes
IBA
08/01/1980 - "
Phosphoenolpyruvate carboxykinase deficiency was evident in one case where the whole cells showed 17% of normal activity whereas the mitochondrial activity of this enzyme was 6% of normal.
"
6.
Agar
IBA
04/01/1995 - "
A glutamate racemase gene of Lactobacillus brevis ATCC 8287 was cloned into Escherichia coli TM93 by the phenotypic complementation of a phosphoenolpyruvate carboxylase deficiency on minimum agar medium containing D-glutamate.
"
7.
glutamate racemase
IBA
04/01/1995 - "
A glutamate racemase gene of Lactobacillus brevis ATCC 8287 was cloned into Escherichia coli TM93 by the phenotypic complementation of a phosphoenolpyruvate carboxylase deficiency on minimum agar medium containing D-glutamate.
"