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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                                    Selective oxidative deamination has long been considered to be an
8 e observed to undergo spontaneous N-terminal oxidative deamination in aqueous solution in the presenc
9 lank the cisplatin ICLs undergo preferential oxidative deamination in vitro, and AP endonuclease 1 (A
10 also impacts mutation rates, via spontaneous oxidative deamination of 5-methylcytosine (5mC) to thymi
11  can arise from oxidation of thymine or from oxidative deamination of 5-methylcytosine, and is then p
12              Monoamine oxidase catalyzes the oxidative deamination of a number of neurotransmitters.
13 ive, the small subunit of AADH catalyzes the oxidative deamination of a variety of amine substrates.
14 including hypoxanthine that is formed by the oxidative deamination of adenine.
15 rine base that most commonly arises from the oxidative deamination of adenine.
16 sine (I), which results from the spontaneous oxidative deamination of adenosine, and catalyzes the hy
17 Here, we demonstrate that MftD catalyzes the oxidative deamination of AHDP, forming an alpha-keto moi
18 inopimelate dehydrogenase catalyzes the only oxidative deamination of an amino acid of D configuratio
19 employs levulinic acid as nucleophile in the oxidative deamination of an N-acetylneuraminic acid thio
20 decarboxylation or decarboxylation-dependent oxidative deamination of aromatic l-amino acids to produ
21         We show that 4 catalyzes the aerobic oxidative deamination of benzylamine, though turnover ev
22    Monoamine oxidase B (MAO B) catalyzes the oxidative deamination of biogenic and xenobiotic amines.
23 hosphorylation in these organelles can cause oxidative deamination of cytosine and lead to uracil in
24          DADH catalyzes the flavin-dependent oxidative deamination of d-amino acids to the correspond
25 genase (DADH) catalyzes the flavin-dependent oxidative deamination of D-arginine and other D-amino ac
26 ents of the purified enzymes: DauA catalyzes oxidative deamination of D-arginine into 2-ketoarginine
27                                              Oxidative deamination of dopamine produces the highly to
28  (DOPAL) is a toxic metabolite formed by the oxidative deamination of dopamine.
29                          LOXL2 catalyzes the oxidative deamination of epsilon-amines of lysine and hy
30                  Leucine activates GDH1, and oxidative deamination of glutamate is increased further
31        Glutamate dehydrogenase catalyses the oxidative deamination of glutamate to 2-oxoglutarate wit
32  is found in all organisms and catalyzes the oxidative deamination of glutamate to 2-oxoglutarate.
33 tochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarat
34 cine activation is associated with increased oxidative deamination of glutamate via GDH.
35  336-kDa metabolic enzyme that catalyzes the oxidative deamination of glutamate.
36 NAD+-binding pocket of GDH, thereby blocking oxidative deamination of glutamate.
37 ated from Nocardioides simplex catalyzes the oxidative deamination of histamine to imidazole acetalde
38                                              Oxidative deamination of intestinal d-aa by DAO, which y
39 hydrogenase (EC 1.4.1.1) (Ald) catalyzes the oxidative deamination of L-alanine and the reductive ami
40  Glutamate dehydrogenase (GDH) catalyzes the oxidative deamination of L-glutamate and, in animals, is
41  kinetic approach has been used to study the oxidative deamination of L-glutamate catalyzed by beef l
42 xameric enzyme that catalyzes the reversible oxidative deamination of l-glutamate to 2-oxoglutarate u
43 n all organisms and catalyzes the reversible oxidative deamination of L-glutamate to 2-oxoglutarate.
44  is found in all organisms and catalyses the oxidative deamination of l-glutamate to 2-oxoglutarate.
45 es for the glutamate dehydrogenase catalyzed oxidative deamination of L-glutamate to identify the occ
46  the same sequence of chemical events in the oxidative deamination of L-glutamate.
47 he reversible, pyridine nucleotide-dependent oxidative deamination of L-phenylalanine to form phenylp
48       The carbonylation pathway involves the oxidative deamination of lysine residues to yield a carb
49 atrix that crosslinks collagens by mediating oxidative deamination of lysine residues.
50 onoamine oxidases (MAO) A and B catalyze the oxidative deamination of many biogenic and dietary amine
51 thylamine dehydrogenase (MADH) catalyzes the oxidative deamination of methylamine to formaldehyde and
52                                          The oxidative deamination of methylated putrescine by a diam
53 , encoded by the X chromosome, catalyzes the oxidative deamination of monoamine neurotransmitters, su
54 Monoamine oxidase (MAO) A and B catalyze the oxidative deamination of neuroactive and dietary monoami
55 AOA is a mitochondrial enzyme that catalyzes oxidative deamination of neurotransmitters and dietary a
56                      Lysyl oxidase catalyzes oxidative deamination of peptidyl-lysine and hydroxylysi
57 a lyase (PAL) isoforms that catalyze the non-oxidative deamination of Phe to trans-cinnamic acid, the
58   Copper amine oxidases (CuAOs) catalyze the oxidative deamination of primary amines operating throug
59 mine oxidases (CAOs) are responsible for the oxidative deamination of primary amines to their corresp
60 rihydroxyphenylalanine quinone (TPQ) and the oxidative deamination of primary amines using TPQ.
61 hese, the copper amine oxidases catalyze the oxidative deamination of primary amines utilizing a type
62 ine serum amine oxidase (BSAO) catalyzes the oxidative deamination of primary amines, concomitant wit
63  (MAO-N) is a flavoenzyme that catalyses the oxidative deamination of primary amines.
64 is of a self-derived coenzyme and subsequent oxidative deamination of primary amines.
65 ne (CTQ) prosthetic group that catalyzes the oxidative deamination of primary amines.
66 lquinone-dependent enzyme that catalyzes the oxidative deamination of primary amines.
67 ne (TTQ) dependent enzyme that catalyzes the oxidative deamination of primary amines.
68 ide-sensitive amine oxidase (SSAO) catalyses oxidative deamination of primary amines.
69 the reversible pyridine nucleotide-dependent oxidative deamination of saccharopine to generate alpha-
70 ne dehydrogenase catalyzes the NAD-dependent oxidative deamination of saccharopine to give l-lysine a
71 AOA) and B (MAOB), which are involved in the oxidative deamination of several neurotransmitters, incl
72 enylalanine quinone, TPQ) and the subsequent oxidative deamination of substrate amines.
73  reversible, pyridine dinucleotide-dependent oxidative deamination of the D-amino acid stereocenter o
74              A study of the mechanism of the oxidative deamination of the N-nitroso-N-acetyl sialyl g
75 t affect the rates of mitochondria-catalyzed oxidative deamination of these monoamines, raised the po
76 ine oxidases (CAOs) have evolved to catalyze oxidative deamination of unbranchedprimary amines to ald
77 ange of useful nucleophiles employed in this oxidative deamination process to include phenols and thi
78 erves as external nucleophile in the general oxidative deamination process.
79 hermore, NEIL1 binds to 5-hydroxyuracil, the oxidative deamination product of C, in replication prote
80 wed by the addition of acetic acid, gives an oxidative deamination product, in which the AcN(NO)-C5 b
81 length, transient-state kinetic study of the oxidative deamination reaction catalyzed by Clostridium
82  (thio-NAD), can serve as a substrate in the oxidative deamination reaction, as can a number of alpha
83                   Comparisons are drawn with oxidative deamination reactions of 4-amino-4-deoxy and 2
84                                          The oxidative deamination results in the formation of a free
85 fluoromethanesulfonate as nucleophile in the oxidative deamination step when the 5-O-triflyl KDN deri
86 osed to alkaline conditions, 16 underwent an oxidative deamination to produce 3,5'- cyclo-2'-deoxyxan
87 s amino sugar then undergoes a NAD dependent oxidative deamination to produce 3,7-dideoxy-d-threo-hep
88 intact spinosyn A by a novel F-TEDA-promoted oxidative deamination to the 4' '-ketone 5, stereoselect
89  we present a green and efficient method for oxidative deamination, using water as the oxidant, catal
90                                         This oxidative deamination was confirmed by 13C NMR, 1H NMR,