Glycine transaminase
In enzymology, a glycine transaminase (EC 2.6.1.4) is an enzyme that catalyzes the chemical reaction glycine + 2-oxoglutarate ... Other names in common use include glutamic-glyoxylic transaminase, glycine aminotransferase, glyoxylate-glutamic transaminase, ... Nakada HI (1964). "Glutamic-glycine transaminase from rat liver". J. Biol. Chem. 239: 468-471. PMID 14169146. Thompson JS, ... Richardson KE (1966). "Isolation and characterization of a glutamate-glycine transaminase from human liver". Arch. Biochem. ...
Glycine-oxaloacetate transaminase
In enzymology, a glycine-oxaloacetate transaminase (EC 2.6.1.35) is an enzyme that catalyzes the chemical reaction glycine + ... The systematic name of this enzyme class is glycine:oxaloacetate aminotransferase. This enzyme is also called glycine- ... Gibbs RG, Morris JG (1966). "Formation of glycine from glyoxylate in Micrococcus denitrificans". Biochem. J. 99: 27. Portal: ... This enzyme belongs to the family of transferases, specifically the transaminases, which transfer nitrogenous groups. ...
Alanine-glyoxylate transaminase
... and L-alanine-glycine transaminase. This enzyme participates in alanine and aspartate metabolism and glycine, serine and ... glycine Thus, the two substrates of this enzyme are L-alanine and glyoxylate, whereas its two products are pyruvate and glycine ... In enzymology, an alanine-glyoxylate transaminase (EC 2.6.1.44) is an enzyme that catalyzes the chemical reaction L-alanine + ... This enzyme belongs to the family of transferases, specifically the transaminases, which transfer nitrogenous groups. The ...
List of EC numbers (EC 2)
... aspartate transaminase EC 2.6.1.2: alanine transaminase EC 2.6.1.3: cysteine transaminase EC 2.6.1.4: glycine transaminase EC ... UDP-N-acetylbacillosamine transaminase EC 2.6.1.35: glycine-oxaloacetate transaminase EC 2.6.1.36: L-lysine 6-transaminase EC ... D-amino-acid transaminase EC 2.6.1.11: acetylornithine transaminase EC 2.6.1.12: alanine-oxo-acid transaminase EC 2.6.1.13: ... neamine transaminase EC 2.6.1.94: 2′-deamino-2′-hydroxyneamine transaminase EC 2.6.1.95: neomycin C transaminase EC 2.6.1.96: 4 ...
Serine-pyruvate transaminase
Other names in common use include SPT, and hydroxypyruvate:L-alanine transaminase. This enzyme participates in glycine, serine ... In enzymology, a serine-pyruvate transaminase (EC 2.6.1.51) is an enzyme that catalyzes the chemical reaction L-serine + ... This enzyme belongs to the family of transferases, specifically the transaminases, which transfer nitrogenous groups. The ...
Serine-glyoxylate transaminase
This enzyme participates in glycine, serine and threonine metabolism. It employs one cofactor, pyridoxal phosphate. Ireland RJ ... In enzymology, a serine-glyoxylate transaminase (EC 2.6.1.45) is an enzyme that catalyzes the chemical reaction L-serine + ... This enzyme belongs to the family of transferases, specifically the transaminases, which transfer nitrogenous groups. The ... glyoxylate ⇌ {\displaystyle \rightleftharpoons } 3-hydroxypyruvate + glycine Thus, the two substrates of this enzyme are L- ...
Diaminobutyrate-2-oxoglutarate transaminase
This enzyme participates in glycine, serine and threonine metabolism. Ikai H, Yamamoto S (1997). "Identification and analysis ... In enzymology, a diaminobutyrate-2-oxoglutarate transaminase (EC 2.6.1.76) is an enzyme that catalyzes the chemical reaction L- ... This enzyme belongs to the family of transferases, specifically the transaminases, which transfer nitrogenous groups. The ...
International Working Group on Neurotransmitter Related Disorders
... the deficiency is called glycine encephalopathy or non-ketotic hyperglycinaemia), GABA-transaminase, and succinate-semialdehyde ...
4-aminobutyrate transaminase
... glycine The primary role of GABA-T is to break down GABA as part of the GABA-Shunt. In the next step of the shunt, the ... Wikimedia Commons has media related to 4-aminobutyrate transaminase. 4-Aminobutyrate+Transaminase at the U.S. National Library ... In enzymology, 4-aminobutyrate transaminase (EC 2.6.1.19), also called GABA transaminase or 4-aminobutyrate aminotransferase, ... As a transaminase, GABA-T's role is to move functional groups from an amino acid and a α-keto acid, and vice versa. In the case ...
Methionine-glyoxylate transaminase
... glycine Thus, the two substrates of this enzyme are L-methionine and glyoxylate, whereas its two products are 4-methylthio-2- ... oxobutanoate and glycine. This enzyme belongs to the family of transferases, specifically the transaminases, which transfer ... In enzymology, a methionine-glyoxylate transaminase (EC 2.6.1.73) is an enzyme that catalyzes the chemical reaction L- ...
Kynurenine-glyoxylate transaminase
4-dioxobutanoate and glycine. This enzyme belongs to the family of transferases, specifically the transaminases, which transfer ... In enzymology, a kynurenine-glyoxylate transaminase (EC 2.6.1.63) is an enzyme that catalyzes the chemical reaction: L- ... kynurenine + glyoxylate ⇌ {\displaystyle \rightleftharpoons } 4-(2-aminophenyl)-2,4-dioxobutanoate + glycine Thus, the two ...
4-aminobutyrate-pyruvate transaminase
... glycine This enzyme requires pyridoxal 5'-phosphate. Phenylethylidenehydrazine, the active metabolite of phenelzine, inhibits ... gamma-aminobutyric acid pyruvate transaminase, gamma-aminobutyric acid transaminase, gamma-aminobutyric transaminase, 4- ... 4-aminobutyrate---pyruvate+transaminase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: ... This enzyme is a type of GABA transaminase, which degrades the neurotransmitter GABA. The enzyme catalyses the following ...
Aromatic-amino-acid-glyoxylate transaminase
... glycine Thus, the two substrates of this enzyme are aromatic amino acid and glyoxylate, whereas its two products are aromatic ... oxo acid and glycine. This enzyme belongs to the family of transferases, specifically the transaminases, which transfer ... In enzymology, an aromatic-amino-acid-glyoxylate transaminase (EC 2.6.1.60) is an enzyme that catalyzes the chemical reaction ...
List of MeSH codes (D08)
... glycine transaminase MeSH D08.811.913.477.700.535 - leucine transaminase MeSH D08.811.913.477.700.550 - l-lysine 6-transaminase ... transaminases MeSH D08.811.913.477.700.100 - alanine transaminase MeSH D08.811.913.477.700.120 - 2-aminoadipate transaminase ... beta-alanine-pyruvate transaminase MeSH D08.811.913.477.700.347 - d-alanine transaminase MeSH D08.811.913.477.700.470 - ... glycine decarboxylase complex h-protein MeSH D08.811.600.391.200 - glycine dehydrogenase (decarboxylating) MeSH D08.811.600.465 ...
Kynurenic acid
As a noncompetitive antagonist at the glycine site of the NMDA receptor. As an antagonist of the α7 nicotinic acetylcholine ... It is formed from L-kynurenine in a reaction catalyzed by the enzyme kynurenine-oxoglutarate transaminase. KYNA has been ... Kynurenic acid acts in the brain as a glycine-site NMDAr antagonist, key in glutamatergic neurotransmission system, which is ...
Staphylococcus aureus
Two of these genes include rocD and gudB, which encode for the enzyme's ornithine-oxo-acid transaminase and glutamate ... Protein A Protein A is anchored to staphylococcal peptidoglycan pentaglycine bridges (chains of five glycine residues) by the ...
Serine
Glycine can also be formed from CO2, NH+ 4, and mTHF in a reaction catalyzed by glycine synthase. Industrially, L-serine is ... of this ketone by phosphoserine transaminase (EC 2.6.1.52) yields 3-phosphoserine (O-phosphoserine) which is hydrolyzed to ... D-serine is a more potent agonist at the glycine site on the NMDAR than glycine itself. D-serine was thought to exist only in ... Liu Y, Hill RH, Arhem P, von Euler G (2001). "NMDA and glycine regulate the affinity of the Mg2+-block site in NR1-1a/NR2A NMDA ...
Amino acid
Proline forms a cycle to the polypeptide backbone, and glycine is more flexible than other amino acids. Glycine and proline are ... This process involves transaminases, often the same as those used in amination during synthesis. In many vertebrates, the amino ... Glycine and leucine were discovered in 1820. The last of the 20 common amino acids to be discovered was threonine in 1935 by ... Glycine (Gly, G) could be considered a polar amino acid since its small size means that its solubility is largely determined by ...
Biochemistry
Enzymes called transaminases can easily transfer the amino group from one amino acid (making it an α-keto acid) to another α- ... "alanine-glycine-tryptophan-serine-glutamate-asparagine-glycine-lysine-...". Secondary structure is concerned with local ... Mammals do possess the enzymes to synthesize alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, ...
Succinic semialdehyde dehydrogenase deficiency
Under normal conditions, SSADH works with the enzyme GABA transaminase to convert GABA to succinic acid. Succinic acid can then ... This agent can eventually compromise the pathways of fatty acid, glycine, and pyruvate metabolism, and then become detectable ... Vigabatrin is an irreversible inhibitor of GABA transaminases which leads to decreased levels of GHB and elevation of GABA. ... Parviz, M.; Vogel, K.; Gibson, K.M.; Pearl, P.L. (2014). "Disorders of GABA Metabolism: SSADH and GABA-transaminase ...
Γ-Aminobutyric acid
3-Aminoisobutyric acid 4-aminobutyrate transaminase (GABA-transaminase) deficiency GABA analogue GABA receptor GABA tea Giant ... Olsen RW, Betz H (2006). "GABA and glycine". In Siegel GJ, Albers RW, Brady S, Price DD (eds.). Basic Neurochemistry: Molecular ... GABA transaminase enzymes catalyze the conversion of 4-aminobutanoic acid (GABA) and 2-oxoglutarate (α-ketoglutarate) into ... Parviz M, Vogel K, Gibson KM, Pearl PL (2014-11-25). "Disorders of GABA metabolism: SSADH and GABA-transaminase deficiencies". ...
Chromosome 12
Cysteine and glycine-rich protein 2 DDX23: DEAD-box helicase 23 DDX47: DEAD-box helicase 47 DHH: Desert hedgehog protein DPPA3 ... encoding protein Branched chain amino acid transaminase 1 C12orf24: encoding protein FAM216A C12orf42: encoding protein ...
Affinity chromatography
Elution of the antibodies of interest is most often achieved using a low pH buffer such as glycine pH 2.8. The eluate is ... and transaminases. Nucleic acids function to trap mRNA, DNA, rRNA, and other nucleic acids/oligonucleotides. Protein A/G method ...
Biosynthesis
For all standard amino acids, except glycine, the α-carbon is a chiral center. In the case of glycine, the α-carbon has two ... "MetaCyc: L-lysine biosynthesis I". PETERKOFSKY, B; GILVARG, C (May 1961). "N-Succinyl-L-diaminopimelic-glutamic transaminase". ... There are two known pathways for the biosynthesis of glycine. Organisms that use ethanol and acetate as the major carbon source ... The following step requires the activation of glycine by the addition of a phosphate group from ATP. GAR synthetase performs ...
Acetolactate synthase
The specific residue that is responsible for this is a glycine at position 511 in the protein. This is the one that requires a ... The ilvGMEDA operon encodes the ilvGM (ALS II) pair as well as a branched-chain-amino-acid transaminase (ilvE), dihydroxy-acid ...
Pyridoxal phosphate
In addition, PLP is used by aminotransferases (or transaminases) that act upon unusual sugars such as perosamine and desosamine ... Glycaldehyde was condensed with glycine and the phosphorylated product was 4-phosphohydroxythreonine (4PHT), the canonical ... liver cysteine desulfhydrase activity disappears and serine and threonine dehydrase and alanine glutamate transaminase ...
Amino acid synthesis
Serine is the first amino acid in this family to be produced; it is then modified to produce both glycine and cysteine (and ... The genes that encode both the dihydroxy acid dehydrase used in the creation of α-ketoisovalerate and Transaminase E, as well ... PurR binds directly to the control region of glyA and effectively turns the gene off so that glycine will not be produced by ... Since serine is the first amino acid produced in this family both glycine and cysteine will be regulated by the available ...
List of OMIM disorder codes
GK Glycine encephalopathy; 605899; AMT Glycine encephalopathy; 605899; GCSH Glycine encephalopathy; 605899; GLDC Glycine N- ... ABCA4 GABA-transaminase deficiency; 613163; ABAT Galactokinase deficiency with cataracts; 230200; GALK1 Galactose epimerase ...
List of diseases (G)
Galloway Mowat syndrome Gamborg-Nielsen syndrome Game-Friedman-Paradice syndrome Gamma aminobutyric acid transaminase ... dehydrogenase deficiency Glutathione synthetase deficiency Glyceraldehyde-3-phosphate dehydrogenase deficiency Glycine synthase ...
Vitamin B6
Transaminases break down amino acids with PLP as a cofactor. The proper activity of these enzymes is crucial for the process of ... a PLP-dependent enzyme that uses succinyl-CoA and glycine to generate aminolevulinic acid, a chlorophyll precursor. In addition ... To function as a transaminase coenzyme, PLP bound to a lysine of the enzyme then binds to a free amino acid via formation of a ... The PLP-dependent transaminases and glycogen phosphorylase provide the vitamin with its role in gluconeogenesis, so deprivation ...