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  • carboxylase
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  • pyruvate
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  • pyruvate kinase
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  • pyruvate
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  • carboxylase
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  • pyruvate kinase
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  • pyruvate
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  • GPT => glutamic pyruvate transaminase
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  • glutamate pyruvate transaminase
    ±Û·çŽÇÇ·çºó»êÆ®¶õ½º¾Æ¹Ì³ªÁ¦
  • pyruvate
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  • pyruvate kinase
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  • pyruvate pathway
    ÇÇ·çºê»ê¿°´ë»ç°æ·Î(¡­ß«ç¤ÓÛÞóÌèÖØ).
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  • carboxylase
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  • glutamate pyruvate transaminase
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  • pyruvate
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  • pyruvate kinase
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  • pyruvate pathway
    ÇÇ·çºê»ê¿°´ë»ç°æ·Î(¡­ß«ç¤ÓÛÞóÌèÖØ).
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  • pyruvate carboxylase
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  • active pyruvate
    Ȱ¼º(üÀàõ)ÆÄÀÌ·çºê»ê¿° (ß«ç¤)
  • citrate-pyruvate cycle
    ½ÃÆ®¸£»ê(ß«)-ÇǸ£ºê»êȸ·Î(ß«üÞÖØ)
  • pyruvate dehydrogenase complex
    ÆÄÀÌ·çºê»ê(ß«) µðÇÏÀ̵å·ÎÀú³×À̽º º¹ÇÕü(ÜÜùêô÷)
  • pyruvate kinase
    ÆÄÀÌ·çºê»ê(ß«) Ä«À̳×À̽º
  • pyruvate oxidation factor
    ÆÄÀÌ·çºê»ê(ß«) »êÈ­ÀÎÀÚ(ß«ûùì×í­)
  • acetyl coenzyme A carboxylase
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  • biotin carboxylase
    ¹ÙÀÌ¿Àƾ Ä«¸£º¹½Ç·¹À̽º
  • diphosphoribulose carboxylase
    "ÀÌÀλê(ì£×òß«)¶óÀ̺ҷνº Ä«¸£º¹½Ç·¹À̽º, (ÔÒ) ribulose-I, 5-bisphosphate carboxylase"
  • pentose phosphate carboxylase
    Àλê(×òß«)ÆæÅ佺 Ä«¸£º¹½Ç·¹À̽º
  • phosphoenolpyruvate carboxylase
    Æ÷½ºÆ÷¿¡³îÆÄÀÌ·çºê»ê(ß«) Ä«¸£º¹½Ç·¹À̽º
  • "ribulose-1,5-bisphosphate carboxylase"
    "¶óÀ̺ҷνº 1,5 ¾çÀλê(å»×òß«)Ä«¸£º¹½Ç·¹À̽º"
  • RuBP carboxylase
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KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
PC   1) Phosphatidyl Choline
  2) Pyruvate Carboxylase
PC avoirdupois weight [Lat. pondus civile]; packed cells; paper chromatography; paracortex; parent cell...
DDC L-Dopa De-Carboxylase
ACC accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst...
BMCC beta-methylcrotonyl coenzyme A carboxylase
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
PEPC phosphoeno/pyruvate carboxylase
PC Pyruvate carboxylase
PYC Pyruvate carboxylase
ACC Acetyl coenzyme A carboxylase
ACC Acetyl-CoA carboxylase
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
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  • carboxylase
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    ¾ËÆÄ ŰÅä»êÀÇ Ä«¸£º¹½Ç±â¿¡¼­ ÀÌ»êÈ­ ź¼Ò¸¦ Á¦°ÅÇÏ´Â È¿¼Ò. ÆÄÀÌ·çºó»êÀÇ Å»Åº»êÀº ¾ËÄÝ ¹ßÈ¿¿¡¼­ Áß¿äÇÑ ´Ü°è·Î¼­, ÆÄÀÌ·çºó»êÀÌ ¾Æ¼¼Æ®¾Ëµ¥ÇÏÀ̵å¿Í ÀÌ»êÈ­ ź¼Ò·Î ÀüȯÇÑ´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
pyruvate carboxylase <enzyme> An enzyme that catalyses the formation of oxaloacetate from pyruvate, carbon dioxide and ATP in gluconeogenesis.
(18 Nov 1997)
pyruvate carboxylase deficiency An autosomal recessive pyruvate metabolism disorder resulting from absent or deficient expression of pyruvate carboxylase activity. Decreased production of oxaloacetate leads to decreased gluconeogenesis, thereby causing fasting hypoglycaemia, lactic acid acidosis, and decreased synthesis of amino acid neurotransmitters. Clinical presentations include acidosis, ataxia, mental retardation; sometimes co-occurs with leigh disease.
(12 Dec 1998)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
acetone carboxylase <enzyme> An ATP-dependent carboxylase
Registry number: EC 4.1.1.-
(26 Jun 1999)
acetyl-CoA carboxylase <enzyme> A carboxylating enzyme that catalyses the conversion of ATP, acetyl-CoA, and hco3- to ADP, orthophosphate, and malonyl-CoA. It is a biotinyl-protein that also catalyses transcarboxylation. The plant enzyme also carboxylates propanoyl-CoA and butanoyl-CoA
Chemical name: Acetyl-CoA:carbon-dioxide ligase (ADP-forming)
Registry number: EC 6.4.1.2
(12 Dec 1998)
acetyl CoA carboxylase phosphatase <enzyme> Phosphatase occurs in complex with the carboxylase
Registry number: EC 3.1.3.-
Synonym: acc-phosphatase, acetyl coenzyme a carboxylase phosphatase
(26 Jun 1999)
acyl-CoA carboxylase <enzyme> Catalyses carboxylation (ATP, mg ++, mco(3)-dependent) of acetyl-CoA, propionyl CoA, and butyryl CoA; from nematode turbatrix aceti
Registry number: EC 6.4.1.-
Synonym: acyl-coenzyme a carboxylase
(26 Jun 1999)
biotin carboxylase <enzyme> A subunit of acetyl-CoA carboxylase
Registry number: EC 6.3.4.14
(26 Jun 1999)
carboxylase 1. One of several carboxy-lyases, trivially named carboxylases or decarboxylases (EC subclass 4.1.1), catalyzing the addition of CO2 to all or part of another molecule to create an additional -COOH group (e.g., ribulose-1,5-bisphosphate carboxylase).
2. Obsolete name for pyruvate decarboxylase.
(05 Mar 2000)
gamma-glutamyl carboxylase <enzyme> An enzyme that catalyses the formation of gamma-carboxyglutamyl residues in many proteins, several appearing in the blood clotting cascade.
(05 Mar 2000)
glutamyl carboxylase <enzyme> Carboxylates glutamyl residues in a microsomal protein precursor of plasma prothrombin to form gamma-carboxyglutamic acid residues
Registry number: EC 6.4.-
Synonym: vitamin k-dependent carboxylase, glutamate carboxylase, vitamin k dependent carboxylase, vitamin k-dependent gamma-glutamyl carboxylase, k-dependent carboxylase, gamma-glutamyl carboxylase
(26 Jun 1999)
PEP carboxylase <enzyme> Enzyme responsible for the primary fixation of carbon dioxide in C4 plants. Carboxylates PEP phosphoenolpyruvate to give oxaloacetate. Also important in crassulacean acid metabolism, since it is responsible for carbon dioxide fixation in the dark.
(18 Nov 1997)
ribulose-1,5-bisphosphate carboxylase A dimerizing carboxy-lyase; an enzyme that catalyses the addition of carbon dioxide to d-ribulose 1,5-bisphosphate and the hydrolysis of the addition product to two molecules of 3-d-phosphoglyceric acid, a key reaction in the fixation of CO2 in photosynthesis.
Synonym: carboxydismutase.
(05 Mar 2000)
ribulose-1,5-bisphosphate carboxylase-oxygenase large subunit epsilonN-methyltransferase <enzyme> An aspect of EC 2.1.1.43; trimethylates lys-14 of rubisco
Registry number: EC 2.1.1.-
Synonym: rubisco lsmt, rubisco large subunit lysine n-methyltransferase
(26 Jun 1999)
ribulose bisphosphate carboxylase <enzyme> A copper protein that catalyses the formation of 2 moles of 3-phosphoglycerate from ribulose 1,5-biphosphate in the presence of carbon dioxide and is responsible for carbon dioxide fixation in photosynthesis.
Carbon dioxide is combined with ribulose diphosphate to give two molecules of 3 phosphoglycerate, as part of the Calvin Benson cycle. It is the sole carbon dioxide fixing enzyme in C3 plants and collaborates with PEP carboxylase in carbon dioxide fixation in C4 plants.
In the presence of oxygen the products of the reaction are one molecule of phosphoglyceric acid and one molecule of phosphoglycolic acid. The latter is the initial substrate for photorespiration and this oxygenase function occurs in C3 plants where the enzyme is not protected from ambient oxygen, in C4 plants the enzyme acts exclusively as a carboxylase since it is protected from oxygen.
Also called Fraction 1 protein, the major protein of leaves.
Chemical name: 3-Phospho-D-glycerate carboxy-lyase (dimerizing)
Registry number: EC 4.1.1.39
(12 Dec 1998)
ribulosebisphosphate carboxylase-oxygenase activase <chemical> Requires ATP; amino acid sequence given in first source
Synonym: rubisco activase, rca protein
(26 Jun 1999)
ribulose diphosphate carboxylase <enzyme> A copper protein that catalyses the formation of 2 moles of 3-phosphoglycerate from ribulose 1,5-biphosphate in the presence of carbon dioxide and is responsible for carbon dioxide fixation in photosynthesis.
Carbon dioxide is combined with ribulose diphosphate to give two molecules of 3 phosphoglycerate, as part of the Calvin Benson cycle. It is the sole carbon dioxide fixing enzyme in C3 plants and collaborates with PEP carboxylase in carbon dioxide fixation in C4 plants.
In the presence of oxygen the products of the reaction are one molecule of phosphoglyceric acid and one molecule of phosphoglycolic acid. The latter is the initial substrate for photorespiration and this oxygenase function occurs in C3 plants where the enzyme is not protected from ambient oxygen, in C4 plants the enzyme acts exclusively as a carboxylase since it is protected from oxygen.
Also called Fraction 1 protein, the major protein of leaves.
Chemical name: 3-Phospho-D-glycerate carboxy-lyase (dimerizing)
Registry number: EC 4.1.1.39
(12 Dec 1998)
RuDP carboxylase <enzyme> A copper protein that catalyses the formation of 2 moles of 3-phosphoglycerate from ribulose 1,5-biphosphate in the presence of carbon dioxide and is responsible for carbon dioxide fixation in photosynthesis.
Carbon dioxide is combined with ribulose diphosphate to give two molecules of 3 phosphoglycerate, as part of the Calvin Benson cycle. It is the sole carbon dioxide fixing enzyme in C3 plants and collaborates with PEP carboxylase in carbon dioxide fixation in C4 plants.
In the presence of oxygen the products of the reaction are one molecule of phosphoglyceric acid and one molecule of phosphoglycolic acid. The latter is the initial substrate for photorespiration and this oxygenase function occurs in C3 plants where the enzyme is not protected from ambient oxygen, in C4 plants the enzyme acts exclusively as a carboxylase since it is protected from oxygen.
Also called Fraction 1 protein, the major protein of leaves.
Chemical name: 3-Phospho-D-glycerate carboxy-lyase (dimerizing)
Registry number: EC 4.1.1.39
(12 Dec 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 2 ÆäÀÌÁö: 1
  • Pyruvate Carboxylase - »õâ 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.
    Synonyms : Carboxylase, Pyruvate
  • Pyruvate Carboxylase Deficiency Disease - »õâ An autosomal recessive metabolic disorder caused by absent or decreased PYRUVATE CARBOXYLASE activity, the enzyme that regulates gluconeogenesis, lipogenesis, and neurotransmitter synthesis. Clinical manifestations include lactic acidosis, seizures, respiratory distress, marked psychomotor delay, periodic HYPOGLYCEMIA, and hypotonia. The clinical course may be similar to LEIGH DISEASE. (From Am J Hum Genet 1998 Jun;62(6):1312-9)
    Synonyms : Deficiency Disease, Pyruvate Carboxylase, Type II Ataxia with Lactic Acidosis
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pyruvate carboxylase [EC 6.4.1.1] an enzyme of the ligase class that catalyzes the irreversible carboxylation of pyruvate to form oxaloacetate. The enzyme is a mitochondrial protein containing a biotin prosthetic group, requiring Mg2+ or Mn2+ and acetyl CoA, and occurs in liver but not in muscle. The reaction is necessary for gluconeogenesis from lactate or amino acids forming pyruvate and also provides four-carbon compounds for the tricarboxylic acid cycle. Deficiency of the enzyme, an autosomal recessive trait, causes severe psychomotor retardation and lactic acidosis in infants; there is a particularly severe, rapidly fatal form, in which hyperammonemia, citrullinemia, and hyperlysinemia are also present.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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