| ASS | acute serum sickness; acute spinal stenosis; anterior superior spine; argininosuccinate synthetase |
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| ASSP | argininosuccinate synthetase pseudogene |
| ASSX | argininosuccinate synthetase pseudogene |
| CARS | Childhood Autism Rating Scale; Children's Affective Rating Scale; cysteinyl-transfer ribonucleic aci... |
| CPS | carbamoylphosphate synthetase; cardioplegic perfusion solution; centipoise; cervical pain syndrome; ... |
| alpha-aminoadipyl-cysteinyl-valine synthetase | <enzyme> As of 9/27/95 this has been separated from isopenicillin n synthetase Registry number: EC 6.3.2.- Synonym: acv synthetase, aa-cysteine synthetase, delta-(alpha-aminoadipyl)-cys-val synthetase, delta-(l-alpha-aminoadipyl)-l-cyteinyl-d-valine synthetase, pcbab gene product, acva gene product (26 Jun 1999) |
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| androsta-5,16-dien-3 beta-ol synthetase | <enzyme> Nadph- and o(2)-dependent; converts progesterone to 4,16-androstadien-3-one and converts pregnenolone to androstadienol Registry number: EC 1.- Synonym: pregnenolone side-chain cleavage enzyme, 5,16-androstadien-3 beta-ol synthetase, 5,16-androstadien-3-ol synthase, 4,16-androstadien-3-one synthesizing enzyme, 4,16-adien-3-one synthase, 4,16-ado synthase, delta(16)-c(19)-steroid synthetase, andien-beta-synthetase, 16-ene-synthetase (26 Jun 1999) |
| apiin synthetase | <enzyme> Transfers d-apiose from udpapiose to 4',5-dihydroxyflavon-7-yl beta-d-glucopyranoside Registry number: EC 2.4.2.- (26 Jun 1999) |
| arylamine synthetase | <chemical> Chorismic acid to p-aminophenylalanine Chemical name: synthetase, arylamine (26 Jun 1999) |
| asparagine synthetase | asparagine ligase |
| bacilysin synthetase | <enzyme> Catalyses the synthesis of bacilysin from alanine and anticapsin Registry number: EC 6.3.2.- (26 Jun 1999) |
| bacitracin synthetase | <enzyme> Amino acids are activated through formation of aminoacyladenylates and then transferred to thioester sites before polymerization on the enzyme Registry number: EC 6.3.2.- (26 Jun 1999) |
| beauvericin synthetase | <enzyme> Multifunctional enzyme catalyzing dipeptide formation in beauveria bassiana Registry number: EC 6.3.2.- (26 Jun 1999) |
| biotin synthetase | <enzyme> Converts dethiobiotin to biotin Registry number: EC 2.8.1.- Synonym: biotin synthase, bio2 protein, bio2 gene product (26 Jun 1999) |
| bis(monoacylglycero)phosphate synthetase | <enzyme> Converts phosphatidylglycerol, 1-acyl- or 2-acyllysophosphatidylglycerol to bis(monoacylglycero)phosphate Registry number: EC 2.3.1.- (26 Jun 1999) |
| branched-chain fatty acid synthetase | <enzyme> Analogous to fatty acid synthetase complex but starting with a branched chain keto acid; from bacillis subtilis Registry number: EC 2.3.1.- Synonym: bcfa synthetase (26 Jun 1999) |
| butyryl-CoA synthetase | Fatty acid thiokinase (medium chain), a ligase forming acyl-CoA's from medium-chain fatty acids and CoA with the conversion of ATP to AMP and PPi. A key step in activation of fatty acids. Synonym: acyl-activating enzyme, butyryl-CoA synthetase, octanoyl-CoA synthetase. (05 Mar 2000) |
| canavaninosuccinate synthetase | <enzyme> Aspartate + ureido homoserine + ATP yields canavaninosuccinate + AMP + ppi Registry number: EC 6.3.4.- (26 Jun 1999) |
| carbamoyl phosphate synthetase | A phosphotransferase catalyzing the formation of carbamoyl phosphate. There are two significant isozymes. Carbomoyl phosphate synthetase I is a mitochondrial enzyme that catalyses the reaction of 2ATP, NH3, CO2, and H2O to carbamoyl phosphate, 2ADP, and Pi. It is activated by N-acetylglutamate and participates in urea biosynthesis. A deficiency of carbamoyl phosphate synthetase I can result in hyperammonaemia. Carbamoyl phosphate synthetase II is a cytosolic enzyme that, under physiological conditions, uses l-glutamine as the nitrogen source (producing l-glutamate) instead of NH3, is not activated by N-acetylglutamate, and is found in pyrimidine biosynthesis. (05 Mar 2000) |
| carbamoylphosphate synthetase deficiency | <biochemistry> Carbamoylphosphate synthetase is the initial enzyme of the urea cycle, catalysing the synthesis of carbamoylphosphate from ammonia, bicarbonate and ATP as the first step of ammonia detoxification. The enzyme is an intramitochondrial form called CPS I. A different isozyme found in the cytoplasm, called CPS II, is much less active and apparently not involved in the urea cycle. The deficiency state is autosomal recessive and presents in infancy with massive hyperammonaemia and neurologic deficits in survivors. Diagnosis is suggested by the blood biochemistry and confirmed by specific enzyme assay on liver or rectal biopsy. Prenatal diagnosis by molecular methods has been used successfully in informative families. Inheritance: autosomal recessive. (07 Apr 1998) |