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  • synthase
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  • Glycogen synthase
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  • glycogen synthase
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  • cystathionine beta-synthase
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  • glycogen synthase
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  • amylose synthetase(synthase)
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  • ATP synthase
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  • synthase-phosphorylase kinase
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CPS carbamoylphosphate synthetase; cardioplegic perfusion solution; centipoise; cervical pain syndrome; ...
ALAS delta-aminolevulinate synthase
ALASH delta-aminolevulinate synthase, housekeeping type
bNOS brain nitric oxide synthase
CBS cervicobrachial syndrome; chronic brain syndrome; clinical behavioral science; conjugated bile salts...
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NO Synthase nitric oxide synthase
iNOS 1.Inducible NO synthase
HPS 3-Hexulosephosphate synthase
ALAS 5'-aminolevulinate synthase
EPSPS 5-enol-pyruvyl shikimate-3-phosphate synthase
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
carbamoyl-phosphate synthase (ammonia) <enzyme> An enzyme that catalyses the formation of carbamoyl phosphate from ATP, carbon dioxide, and ammonia. This enzyme is specific for arginine biosynthesis or the urea cycle.
Chemical name: Carbon dioxide:ammonia ligase (ADP-forming, carbamate-phosphorylating)
Registry number: EC 6.3.4.16
(12 Dec 1998)
carbamoyl-phosphate synthase (glutamine-hydrolyzing) <enzyme> An enzyme that catalyses the formation of carbamoyl phosphate from ATP, carbon dioxide, and glutamine. This enzyme is important in the de novo biosynthesis of pyrimidines.
Chemical name: Carbon dioxide:L-glutamine amido-ligase (ADP-forming, carbamate-phosphorylating)
Registry number: EC 6.3.5.5
(12 Dec 1998)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
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)
abequose synthase <enzyme> Converts cdp-4-keto-3,6-dideoxy-d-glucose to cdp-3,6-dideoxy-d-galactose (cdp-abequose); requires NADPH, analogous to udp-glucose-4-epimerase
Registry number: EC 5.1.3.-
Synonym: rfbj gene product
(26 Jun 1999)
acetoacetyl-acyl carrier protein synthase <enzyme> E coli enzyme, that catalyses condensation of malonyl-acyl carrier protein plus acetyl-acyl carrier protein; not inhibited by cerulenin
Registry number: EC 2.3.1.-
Synonym: acetoacetyl-acp synthase
(26 Jun 1999)
acetolactate synthase <enzyme> A flavoprotein that catalyses the formation of acetolactate from 2 moles of pyruvate in the biosynthesis of valine and the formation of acetohydroxybutyrate from pyruvate and alpha-ketobutyrate in the biosynthesis of isoleucine.
Chemical name: Acetolactate pyruvate-lyase (carboxylating)
Registry number: EC 4.1.3.18
(12 Dec 1998)
acridone synthase <enzyme> Catalyses the condensation of n-methylanthraniloyl-CoA and 3 malonyl-CoA to produce 1,3-dihydroxy-n-methylacridone
Registry number: EC 2.3.1.-
(26 Jun 1999)
acyl-malonyl-ACP synthase <enzyme> An enzyme condensing malonyl-ACP and acyl-cys-protein to 3-oxoacyl-ACP + cys-protein + CO2, and similar reactions, as steps in fatty acid synthesis; cys-protein is also a part of the fatty acid synthase complex.
Synonym: acyl-malonyl-ACP synthase, beta-ketoacyl-ACP synthase.
(05 Mar 2000)
adenylosuccinate synthase <enzyme> A carbon-nitrogen ligase. During purine ribonucleotide biosynthesis, this enzyme catalyses the synthesis of adenylosuccinate from GTP, imp, and aspartate with the formation of orthophosphate and GDP.
Chemical name: IMP:L-aspartate ligase (GDP-forming)
Registry number: EC 6.3.4.4
(12 Dec 1998)
adenylylosuccinate synthase <enzyme> A carbon-nitrogen ligase. During purine ribonucleotide biosynthesis, this enzyme catalyses the synthesis of adenylosuccinate from GTP, imp, and aspartate with the formation of orthophosphate and GDP.
Chemical name: IMP:L-aspartate ligase (GDP-forming)
Registry number: EC 6.3.4.4
(12 Dec 1998)
agropine synthase <enzyme> Final enzyme in the three enzyme pathway for agropine synthesis; cyclises deoxymannityl-glutamine to the lactone, agropine
Registry number: EC 4.2.1.-
Synonym: ags gene product
(26 Jun 1999)
alkylglycerone-phosphate synthase <enzyme> Replaces the acyl moiety of acyldhap with a long chain fatty alcohol; intact alcohol including the oxygen atom is incorporated into alkyl-dhap
Registry number: EC 2.5.1.26
Synonym: adhps, alkyl-dihydroxyacetone phosphate synthase, alkyl-dhap synthase, alkyldihydroxyacetone phosphate synthetase, acylglycerone-3-phosphate-long chain-alcohol o-3-phospho-2-oxopropanyl transferase, alkyldihydroxyacetonephosphate synthase
(26 Jun 1999)
aminoadipic d-saemialdehyde synthase <enzyme> A bifunctional enzyme used in lysine degradation; it has a lysine:alpha-ketoglutarate reductase activity as well as a saccharopine dehydrogenase activity. A deficiency of this enzyme results in familial hyperlysinaemia.
(05 Mar 2000)
aminoadipic saemialdehyde synthase <enzyme> Bifunctional enzyme with both lysine-ketoglutarate reductase (EC 1.5.1.8) and saccharopine dehydrogenase (EC 1.5.1.9) activities
Registry number: EC 1.5.1.-
Synonym: aasa synthase
(26 Jun 1999)
aminodeoxychorismate synthase <enzyme> From E coli; probably catalyses the conversion of chorismate to 4-amino-4-deoxychorismate; see also paba protein
Registry number: EC 2.6.1.-
Synonym: pabb gene product, adc synthase
(26 Jun 1999)
amylopectin synthase <enzyme> From eimeria tenella; catalyses udpglucose alpha 1,4-glucan alpha-4-glucosyltransferase forming amylopectin, similar to glycogen synthase in eukaryotes
Registry number: EC 2.4.1.-
(26 Jun 1999)
anthranilate synthase <enzyme> An enzyme that catalyses the formation of anthranilate (o-aminobenzoate) and pyruvic acid from chorismate and glutamine. Anthranilate is the biosynthetic precurser of tryptophan and numerous secondary metabolites, including inducible plant defense compounds.
Chemical name: Chorismate pyruvate-lyase (amino-accepting)
Registry number: EC 4.1.3.27
(12 Dec 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 3 ÆäÀÌÁö: 1
  • Carbamoyl-Phosphate Synthase (Ammonia) - »õâ An enzyme that catalyzes the formation of carbamoyl phosphate from ATP, carbon dioxide, and ammonia. This enzyme is specific for arginine biosynthesis or the urea cycle. Absence or lack of this enzyme may cause CARBAMOYL-PHOSPHATE SYNTHASE I DEFICIENCY DISEASE. EC 6.3.4.16.
    Synonyms : CP Synthase I, Carbamoyl-Phosphate Synthetase (Ammonia), Carbamoyl-Phosphate Synthetase I, Carbamoylphosphate Synthetase I, Carbamyl Phosphate Synthase (Ammonia), Carbamyl-Phosphate Synthase (Ammonia), I, Carbamoyl-Phosphate Synthetase, Synthase I, CP
  • Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) - »õâ An enzyme that catalyzes the formation of carbamoyl phosphate from ATP, carbon dioxide, and glutamine. This enzyme is important in the de novo biosynthesis of pyrimidines. EC 6.3.5.5.
    Synonyms : Carbamoyl-Phosphate Synthase (Glutamine), Carbamoylphosphate Synthetase II, Carbamyl Phosphate Synthase II, Carbamyl-Phosphate Synthase (Glutamine), Synthetase II, Carbamoylphosphate
  • Carbamoyl-Phosphate Synthase I Deficiency Disease - »õâ A urea cycle disorder manifesting in infancy as lethargy, emesis, seizures, alterations of muscle tone, abnormal eye movements, and an elevation of serum ammonia. The disorder is caused by a reduction in the activity of hepatic mitochondrial CARBAMOYL-PHOSPHATE SYNTHASE (AMMONIA). (Menkes, Textbook of Child Neurology, 5th ed, pp50-1)
    Synonyms : Carbamoyl Phosphate Synthase (Ammonia) Deficiency Disease, Carbamoyl-Phosphate Synthetase I Deficiency Disease, Carbamoylphosphate Synthetase I Deficiency Disease, Carbamyl Phosphate Synthetase Deficiency Disease
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
carbamoyl-phosphate synthase (ammonia) [EC 6.3.4.16] an enzyme of the ligase class that catalyzes the synthesis of carbamoyl phosphate from ammonia and carbon dioxide, the first committed step in the urea cycle (see illustration at urea cycle, under cycle). The reaction occurs predominantly in liver mitochondria, requires N-acetylglutamate as a cofactor, and hydrolyzes two molecules of ATP. Decreased enzyme activity, an autosomal recessive trait, causes carbamoyl phosphate synthetase deficiency.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
carbamoyl-phosphate synthase (glutamine-hydrolyzing) [EC 6.3.5.5] an enzyme activity of the trifunctional CAD protein (q.v.); it is a ligase that catalyzes the formation of carbamoyl phosphate as the first step in the biosynthesis of pyrimidine nucleotides. Glutamine is the nitrogen donor in the reaction, which is cytosolic and is inhibited by UTP.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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