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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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