ライフサイエンスコーパス: aminobutyrate

1 g opening with the production of 2-hydroxy-4-aminobutyrate.

2 additional capability to excrete lactate and aminobutyrate.

3 ural specificity for the native substrate, 4-aminobutyrate.

4 eta-alanine transamination enzymes, namely 4-aminobutyrate-2-oxoglutarate transaminase (GABA-T) and a

5 e for the mammalian transaminating enzymes 4-aminobutyrate-2-oxoglutarate transaminase and alanine-gl

6 Gamma-aminobutyrate acid, L-glutamate, and N-methyl-D-aspartat

7 function of DABA DC is, together with l-2,4-aminobutyrate aminotransferase (DABA AT), to synthesize

8 The E. coli isozyme of gamma-aminobutyrate aminotransferase (GABA-AT) is a tetrameric

9 ve site structure comparisons with pig gamma-aminobutyrate aminotransferase and dialkylglycine decarb

10 he L4 dorsal root or intrathecal infusion of aminobutyrate aminotransferase inhibitor attenuated the

11 The ability of gamma-aminobutyrate aminotransferase to act on primary amine s

12 crystal structures of Escherichia coli gamma-aminobutyrate aminotransferase unbound and bound to the

13 slr1022, was shown to also function as gamma-aminobutyrate aminotransferase, catalysing gamma-aminobu

14 mRNAs than unedited miR-376b-3p, including 4-aminobutyrate aminotransferase, encoding the enzyme resp

15 uble mutation PD cases involved ornithine, 2-aminobutyrate and 2-hydroxybutyrate as well as for mitoc

16 P]-PP(i)-ATP exchange assay to show that S-2-aminobutyrate and beta-chloro-L-alanine were alternate s

17 tes in PBC), methionine (lower methionine, 2-aminobutyrate, and 2-hydroxybutyrate levels in PBC), ala

18 o acids (leucine, isoleucine, valine), gamma-aminobutyrate, and as yet unknown ligands.

19 d accumulation, in particular alanine, gamma-aminobutyrate, and aspartate in both roots and leaves.

20 Kd values for the binding of L-Glu, L-alpha-aminobutyrate, and ATP to free enzyme are 2.6, 5.1, and

21 anslocation of misactivated threonine, alpha-aminobutyrate, and cysteine.

22 NA synthetase, misactivates threonine, alpha-aminobutyrate, and cysteine.

23 Ps were linked to 2-acetylpyrrolidine, gamma-aminobutyrate, anthocyanin, tannins, flavonoids and rela

24 A and gadB) and the gene for glutamate-gamma-aminobutyrate antiporter (gadC) induced by the polyamine

25 Unlike the mammalian enzyme, L-alpha-aminobutyrate (apparent Km = 10 mM) is a poor substitute

26 iosensors showed different patterns: a gamma-aminobutyrate biosensor was active only inside nodules,

27 obutyrate aminotransferase, catalysing gamma-aminobutyrate conversion to succinic semialdehyde.

28 old, whereas the binding of L-Glu or L-alpha-aminobutyrate decreases the binding affinity of the othe

29 own to contain d-alanine and unprecedented D-aminobutyrate derived from serine and threonine, respect

30 abolites in the metabolite-only model were 2-aminobutyrate, fumarate, hypoxanthine, acetone, leucine,

31 ycnH (gabD) genes were shown to encode gamma-aminobutyrate (GABA) aminotransferase and succinic semi-

32 rmine), which was proposed to convert into 4-aminobutyrate (GABA) and succinate before entering the t

33 The action of gamma-aminobutyrate (GABA) as an intercellular signaling molec

34 ut to vestibular nucleus neurons, with gamma-aminobutyrate (GABA) as neurotransmitter.

35 concentrations during ripening, while gamma-aminobutyrate (GABA) shows an approximately stoichiometr

36 Ethanol enhances gamma-aminobutyrate (GABA) signaling in the brain, but its act

37 rmease (GabP) is the exclusive mediator of 4-aminobutyrate (GABA) transport across the Escherichia co

38 Current produced by a gamma-aminobutyrate (GABA) transporter stably transfected into

39 line, alpha-aminoisobutyrate (AIB) and gamma-aminobutyrate (GABA), as evidenced from direct transport

40 The targets include gamma-aminobutyrate (GABA)-positive amacrine cells (gammaACs),

41 : putrescine, arginine, ornithine, and gamma-aminobutyrate (GABA).

42 nched-chain amino acids, creatine, lysine, 2-aminobutyrate, glutamine, glycine, trimethylamine, and 1

43 nd a possible beneficial intracellular gamma-aminobutyrate/glutathione-mediated antioxidant mechanism

44 Presynaptic gamma-aminobutyrate-immunoreactive (GABA+) profiles were mappe

45 se to act on primary amine substrates (gamma-aminobutyrate) in the first half-reaction and alpha-amin

46 Transport of 4-aminobutyrate into Escherichia coli is catalyzed by gab

47 Similarly, 2-aminobutyrate is also observed under electrolysis condit

48 GABA (gamma-aminobutyrate) is the most prevalent inhibitory transmit

49 d in its ability to utilize allantoin, gamma-aminobutyrate, isoleucine, nitrate, urea, and valine as

50 PCP2 not only the natural L-Cys but also S-2-aminobutyrate, L-beta-chloroalanine, and L-Ser, enabling

51 from Wallerian degeneration; reversed gamma-aminobutyrate-mediated depolarization occurring in traum

52 yde dehydrogenase (Slr0370), and/or in gamma-aminobutyrate metabolism (Slr1022) were constructed.

53 The Krebs cycle, neoribogenesis, gamma-aminobutyrate metabolism, and salvage synthesis of purin

54 neated the effects on the Krebs cycle, gamma-aminobutyrate metabolism, gluconeogenesis, and purine sa

55 metal chelator nicotianamine (NA) from the 2-aminobutyrate moieties of three SAM molecules.

56 e presence of excess concentrations of alpha-aminobutyrate, one of the amino acids that is misactivat

57 a model compound, 2-phenyloxazol-5-one-gamma-aminobutyrate (Ox), as a drug proxy.

58 The levels of isoleucine, glucose, gamma-aminobutyrate, phenylalanine, and fructose remained simi

59 ipeptides derived from beta-alanine or gamma-aminobutyrate, PM20D2 also acted at lower rates on some

60 The rho1 gamma-aminobutyrate receptor (GABArho1) is expressed predomina

61 trast to previous work suggesting that gamma aminobutyrate's (GABA) role in regulating growth cone ca

62 samination half-reactions of L-alanine and L-aminobutyrate show long-wavelength absorption characteri

63 le isotope analysis indicated that the gamma-aminobutyrate shunt catalysed conversion of glutamate to

64 that in wild type, suggesting that the gamma-aminobutyrate shunt has a larger impact on metabolite fl

65 oxoglutarate decarboxylase bypass, the gamma-aminobutyrate shunt is a major contributor to flux from

66 c semialdehyde to succinate, an intact gamma-aminobutyrate shunt is present in Synechocystis.

67 ed [U-(14)C]glutamate very slowly, the gamma-aminobutyrate shunt is unlikely to be the pathway respon

68 ia coli functions in the conversion of gamma-aminobutyrate to succinate.

69 sitive and able to export its product, gamma-aminobutyrate, to the extracellular medium.

70 de dehydrogenase (PatD/YdcW and PuuC), gamma-aminobutyrate transaminase (GabT and PuuE), and succinic

71 cytochromes P450 while the fourth is a gamma-aminobutyrate transaminase; together they produce verazi

72 e to positive allosteric modulators of gamma aminobutyrate type A (GABA(A)) receptors.

73 the actions of ethanol are mediated by gamma-aminobutyrate type A (GABA(A)) receptors.

74 gamma-Aminobutyrate type C (GABA(C)) receptors are ligand-gate

75 A novel subunit of the gamma-aminobutyrate, type A (GABAA) receptor family has been i

76 milation pathway, or the metabolism of gamma-aminobutyrate, which in turn affect plant development.