- 101. pyruvate
- [ ] (UMLS (CSP) C0034354) =Organic Chemical =Fatty Acids, Volatile;
=PEP | - 105. Pyruvate Metabolism
- [The chemical reactions and pathways involving pyruvate, 2-oxopropanoate. [GOC:go_curators] ( GO )] (UMLS (NCI) C1158861) Pyruvate Metabolism Pathway =Molecular Function
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- 102. pyruvate carboxylase
- [A biotin-dependent enzyme belonging to the ligase family that catalyzes the addition of CARBON DIOXIDE to pyruvate. It is occurs in both plants and animals. Deficiency of this enzyme causes severe psychomotor retardation and ACIDOSIS, LACTIC in infants. EC 6.4.1.1. ( MSH )] (UMLS (CSP) C0034340) =Amino Acid, Peptide, or Protein; Enzyme ;
=carbon carbon ligase;
| - 106. pyruvate oxidase
- [ ] (UMLS (CSP) C0034351) =Amino Acid, Peptide, or Protein; Enzyme ;
=aldehyde/ketone oxidoreductase;
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- 103. pyruvate dehydrogenase
- [a component of the multi-enzyme pyruvate dehydrogenase complex also another name for EC 4.1.1.1, PYRUVATE DECARBOXYLASE, do not confuse. ( CSP )] (UMLS (CSP) C0034343) =Amino Acid, Peptide, or Protein; Enzyme ;
=aldehyde/ketone oxidoreductase;
respiratory enzyme | - 107. Pyrvinium Pamoate
- (UMLS (NCI) C0139597) =Organic Chemical; Pharmacologic Substance
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- 104. pyruvate kinase deficiency
- [autosomal recessive deficiency of the erythrocytic isozyme of pyruvate kinase, the most common glycolytic enzyme defect in the Embden-Meyerhof pathway; deficient product (ATP) causes chronic hemolytic anemia of widely variable severity. ( CSP )] (UMLS (CSP) C0340968) =Disease or Syndrome =ANEMIA HEMOLITIKOA;
Congenital Metabolic Disorder;
enzyme deficiency;
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