ライフサイエンスコーパス: oxidative deamination

1 strated that the nickel-dependent N-terminal oxidative deamination also occurred in His-2 peptides us

2 Both the oxidative deamination and cross-linking are exclusive to

3 ein product of the MJ1249 gene catalyzes the oxidative deamination and the cyclization reactions.

4 quired for redox active Ni(II) complexation, oxidative deamination, and cross-linking.

5 occur, but also a surprisingly high level of oxidative deamination at the terminal primary nitrogens

6 of L-arginine via transamination instead of oxidative deamination by dehydrogenase or oxidase as ori

7 e observed to undergo spontaneous N-terminal oxidative deamination in aqueous solution in the presenc

8 lank the cisplatin ICLs undergo preferential oxidative deamination in vitro, and AP endonuclease 1 (A

9 can arise from oxidation of thymine or from oxidative deamination of 5-methylcytosine, and is then p

10 Monoamine oxidase catalyzes the oxidative deamination of a number of neurotransmitters.

11 ive, the small subunit of AADH catalyzes the oxidative deamination of a variety of amine substrates.

12 including hypoxanthine that is formed by the oxidative deamination of adenine.

13 rine base that most commonly arises from the oxidative deamination of adenine.

14 sine (I), which results from the spontaneous oxidative deamination of adenosine, and catalyzes the hy

15 inopimelate dehydrogenase catalyzes the only oxidative deamination of an amino acid of D configuratio

16 employs levulinic acid as nucleophile in the oxidative deamination of an N-acetylneuraminic acid thio

17 We show that 4 catalyzes the aerobic oxidative deamination of benzylamine, though turnover ev

18 Monoamine oxidase B (MAO B) catalyzes the oxidative deamination of biogenic and xenobiotic amines.

19 hosphorylation in these organelles can cause oxidative deamination of cytosine and lead to uracil in

20 DADH catalyzes the flavin-dependent oxidative deamination of d-amino acids to the correspond

21 genase (DADH) catalyzes the flavin-dependent oxidative deamination of D-arginine and other D-amino ac

22 ents of the purified enzymes: DauA catalyzes oxidative deamination of D-arginine into 2-ketoarginine

23 Oxidative deamination of dopamine produces the highly to

24 (DOPAL) is a toxic metabolite formed by the oxidative deamination of dopamine.

25 LOXL2 catalyzes the oxidative deamination of epsilon-amines of lysine and hy

26 Leucine activates GDH1, and oxidative deamination of glutamate is increased further

27 Glutamate dehydrogenase catalyses the oxidative deamination of glutamate to 2-oxoglutarate wit

28 is found in all organisms and catalyzes the oxidative deamination of glutamate to 2-oxoglutarate.

29 tochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarat

30 cine activation is associated with increased oxidative deamination of glutamate via GDH.

31 336-kDa metabolic enzyme that catalyzes the oxidative deamination of glutamate.

32 ated from Nocardioides simplex catalyzes the oxidative deamination of histamine to imidazole acetalde

33 Oxidative deamination of intestinal d-aa by DAO, which y

34 hydrogenase (EC 1.4.1.1) (Ald) catalyzes the oxidative deamination of L-alanine and the reductive ami

35 Glutamate dehydrogenase (GDH) catalyzes the oxidative deamination of L-glutamate and, in animals, is

36 kinetic approach has been used to study the oxidative deamination of L-glutamate catalyzed by beef l

37 xameric enzyme that catalyzes the reversible oxidative deamination of l-glutamate to 2-oxoglutarate u

38 n all organisms and catalyzes the reversible oxidative deamination of L-glutamate to 2-oxoglutarate.

39 is found in all organisms and catalyses the oxidative deamination of l-glutamate to 2-oxoglutarate.

40 es for the glutamate dehydrogenase catalyzed oxidative deamination of L-glutamate to identify the occ

41 the same sequence of chemical events in the oxidative deamination of L-glutamate.

42 he reversible, pyridine nucleotide-dependent oxidative deamination of L-phenylalanine to form phenylp

43 The carbonylation pathway involves the oxidative deamination of lysine residues to yield a carb

44 atrix that crosslinks collagens by mediating oxidative deamination of lysine residues.

45 onoamine oxidases (MAO) A and B catalyze the oxidative deamination of many biogenic and dietary amine

46 thylamine dehydrogenase (MADH) catalyzes the oxidative deamination of methylamine to formaldehyde and

47 The oxidative deamination of methylated putrescine by a diam

48 , encoded by the X chromosome, catalyzes the oxidative deamination of monoamine neurotransmitters, su

49 Monoamine oxidase (MAO) A and B catalyze the oxidative deamination of neuroactive and dietary monoami

50 Lysyl oxidase catalyzes oxidative deamination of peptidyl-lysine and hydroxylysi

51 a lyase (PAL) isoforms that catalyze the non-oxidative deamination of Phe to trans-cinnamic acid, the

52 Copper amine oxidases (CuAOs) catalyze the oxidative deamination of primary amines operating throug

53 mine oxidases (CAOs) are responsible for the oxidative deamination of primary amines to their corresp

54 rihydroxyphenylalanine quinone (TPQ) and the oxidative deamination of primary amines using TPQ.

55 hese, the copper amine oxidases catalyze the oxidative deamination of primary amines utilizing a type

56 ine serum amine oxidase (BSAO) catalyzes the oxidative deamination of primary amines, concomitant wit

57 ide-sensitive amine oxidase (SSAO) catalyses oxidative deamination of primary amines.

58 (MAO-N) is a flavoenzyme that catalyses the oxidative deamination of primary amines.

59 is of a self-derived coenzyme and subsequent oxidative deamination of primary amines.

60 ne (CTQ) prosthetic group that catalyzes the oxidative deamination of primary amines.

61 lquinone-dependent enzyme that catalyzes the oxidative deamination of primary amines.

62 ne (TTQ) dependent enzyme that catalyzes the oxidative deamination of primary amines.

63 the reversible pyridine nucleotide-dependent oxidative deamination of saccharopine to generate alpha-

64 ne dehydrogenase catalyzes the NAD-dependent oxidative deamination of saccharopine to give l-lysine a

65 AOA) and B (MAOB), which are involved in the oxidative deamination of several neurotransmitters, incl

66 enylalanine quinone, TPQ) and the subsequent oxidative deamination of substrate amines.

67 reversible, pyridine dinucleotide-dependent oxidative deamination of the D-amino acid stereocenter o

68 A study of the mechanism of the oxidative deamination of the N-nitroso-N-acetyl sialyl g

69 t affect the rates of mitochondria-catalyzed oxidative deamination of these monoamines, raised the po

70 ine oxidases (CAOs) have evolved to catalyze oxidative deamination of unbranchedprimary amines to ald

71 erves as external nucleophile in the general oxidative deamination process.

72 hermore, NEIL1 binds to 5-hydroxyuracil, the oxidative deamination product of C, in replication prote

73 length, transient-state kinetic study of the oxidative deamination reaction catalyzed by Clostridium

74 (thio-NAD), can serve as a substrate in the oxidative deamination reaction, as can a number of alpha

75 Comparisons are drawn with oxidative deamination reactions of 4-amino-4-deoxy and 2

76 The oxidative deamination results in the formation of a free

77 fluoromethanesulfonate as nucleophile in the oxidative deamination step when the 5-O-triflyl KDN deri

78 osed to alkaline conditions, 16 underwent an oxidative deamination to produce 3,5'- cyclo-2'-deoxyxan

79 s amino sugar then undergoes a NAD dependent oxidative deamination to produce 3,7-dideoxy-d-threo-hep

80 intact spinosyn A by a novel F-TEDA-promoted oxidative deamination to the 4' '-ketone 5, stereoselect

81 This oxidative deamination was confirmed by 13C NMR, 1H NMR,