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1 P-dependent reactions in solution, including transamination.
2 turnover, suggesting a lower rate of leucine transamination.
3     Hyperglucagonemia did not affect leucine transamination.
4 ces to be highly reactive toward RS-mediated transamination.
5 of E1 toward dehydration, epimerization, and transamination.
6 etone body production, glucose synthesis and transamination.
7        Neither enantiomer is a substrate for transamination.
8  HF elimination than GABA is a substrate for transamination.
9 ced functional enzymes that catalyze alanine transamination.
10 me could not efficiently catalyze kynurenine transamination.
11 d rate of inactivation by substrate-mediated transamination.
12 e protein synthesis (PS) and reduced leucine transamination.
13 nhancing AA-induced PS, and reducing leucine transamination.
14 for allosteric activation and glutamate from transaminations.
15  also presented that this substrate-mediated transamination accelerates normal degradation of S-adeno
16 residues critical for the dehydration versus transamination activity.
17 ne carbon flux, indicating increased leucine transamination (an important biochemical process for nit
18 ized to monitor stereoselective biocatalytic transamination and assign the absolute configuration of
19 complish this by introducing three exogenous transamination and deamination cycles, which provide an
20 lglycine decarboxylase, which catalyzes both transamination and decarboxylation half-reactions in its
21 r many important enzymatic reactions such as transamination and decarboxylation.
22  from the BCATc(-/-) mouse exhibit lower Leu transamination and higher intracellular Leu concentratio
23 imates of the in vivo rates of phenylalanine transamination and protein degradation.
24 es may also be common to pyridoxal-catalyzed transamination and related reactions in biological syste
25 ys performed with these mutants show that RS transamination and subsequent modification with alkoxyam
26                                              Transamination and the two decarboxylase systems (NADP-m
27 compartment model and assuming insignificant transamination and transmethylation in this tissue.
28 reactions typically proceed by electrophilic transamination and/or addition-elimination reaction mech
29 ecific activity with the serine : glyoxylate transamination, and apparent Km measurements indicate th
30  involves a carboligation step, a subsequent transamination, and finally a Pictet-Spengler reaction w
31 thway intermediates revealed that methionine transamination, and not the transmethylation or transsul
32 into the hepatic vein, leucine oxidation and transamination, and synthesis and degradation of hepatic
33 d to undergo beta-elimination in addition to transamination, and the transamination product of N-term
34 nd introducing the nitrogen by oxidation and transamination at C-3.
35 tetrahydrohydroxyphenylpyruvate (H(4)HPP), a transamination away (via BacF) from 2S-H(4)Tyr.
36 to 3,5-dihydroxyphenylglyoxylate, which is a transamination away from Dpg.
37 boxylase-catalyzed decarboxylation-dependent transamination between 2-aminoisobutyrate (AIB) and pyru
38 notransferase (ALT) catalyzes the reversible transamination between alanine and 2-oxoglutarate to for
39 used radiochemical procedure, which measures transamination between alpha-ketoiso[1-14C]valerate and
40                                              Transamination between glutamine and alpha-keto-gamma-me
41                                              Transamination between L-glutamate (or L-phenylalanine)
42                  The products resulting from transamination between L-phenylalanine and the alpha-ket
43 al phosphate-dependent enzyme that catalyzes transamination between primary amines and alpha-keto aci
44 notransferases were identified that catalyze transamination between several L-amino acids (e.g., phen
45 y to act as a substrate for GABA-AT, not for transamination, but for HF elimination.
46 ital to the 1,3-prototropic shift central to transamination, but not to reactions catalyzed by alanin
47 lases were inactivated by substrate-mediated transamination, but this reaction occurred much more fre
48                         The hBCATm-catalyzed transamination can be described in molecular terms toget
49  including hydrazone formation and Katritzky transamination, can be monitored simultaneously without
50 al recombinant enzyme that catalyzes alanine transamination, confirming that the enzyme is an ALT.
51 d (DP), whose formation involves consecutive transamination, cyclization, and isomerization steps.
52                                 The combined transamination-deoxygenation activity places ColD in a c
53 he putative contribution of two beta-alanine transamination enzymes, namely 4-aminobutyrate-2-oxoglut
54 4-amino-4,6-dideoxy-d-glucose that couples a transamination equilibrium to the thermodynamically favo
55 ism of inactivation most probably involves a transamination followed by aromatization to form an arom
56                The rate-determining step for transamination follows the formation of the quinonoid in
57 m of DGD-PLP is 25 s(-1), while that for the transamination half-reaction between DGD-PMP and pyruvat
58    The primary [2-(2)H]-L-alanine KIE on the transamination half-reaction is unity.
59            The maximal rate constant for the transamination half-reaction of the potassium form of DG
60  the ketimine intermediate for the L-alanine transamination half-reaction.
61 ad-time of the stopped-flow in the L-alanine transamination half-reaction.
62 and breaking in both the decarboxylation and transamination half-reactions occurs at the "A" subsite,
63     The spectra for the first species in the transamination half-reactions of L-alanine and L-aminobu
64 osphate (PLP) catalyzed decarboxylations and transaminations have been revisited experimentally.
65                    AAs also enhanced leucine transamination in both splanchnic and muscle beds.
66 zyme that catalyzes both decarboxylation and transamination in its normal catalytic cycle.
67 had no effect on protein dynamics or leucine transamination in splanchnic bed.
68 yzes two reaction types, decarboxylation and transamination, in the same active site.
69                              The fact that a transamination initiates this pathway could help explain
70 oves the alpha-amino group of L-arginine via transamination instead of oxidative deamination by dehyd
71 city for beta-elimination/replacement versus transamination is dictated in part by the protonation st
72                                   Ethylamine transamination is inhibited 4-fold by Al(3+) metalation,
73 d 4-fold by Al(3+) metalation, while alanine transamination is inhibited only 1.3-fold.
74 ucing bacteria, its catalysis of periplasmic transaminations is most likely a general tool for specif
75 tory T (iTreg) cells, we show that increased transamination, mainly catalysed by GOT1, leads to incre
76 that the enzyme metabolizes 1 according to a transamination mechanism.
77  the transmethylation, transsulfuration, and transamination metabolic pathways.
78  transaminase responsible for catalyzing the transamination of 3-hydroxykynurenine (3-HK) to xanthure
79  is primarily responsible for catalyzing the transamination of 3-hydroxykynurenine (3-HK) to xanthure
80 the pyridoxal phosphate-dependent equatorial transamination of 3-oxo-alpha-D-glucose 6-phosphate to f
81 ate from [alpha,delta-(15)N(2)]ornithine and transamination of [(15)N]glutamate to [(15)N]aspartate.
82                             It catalyzes the transamination of a number of amino acids and uses many
83 eading to accelerated leucine catabolism and transamination of alpha-ketoglutarate to glutamate, with
84 , catalyzing the N-acetylornithine-dependent transamination of alpha-ketoglutarate.
85 cids were the preferred amino donors for the transamination of alpha-ketomethiobutyrate to methionine
86                    This enzyme catalyzed the transamination of aspartate, glutamate, phosphoserine, a
87                          BCAT1 catalyzes the transamination of branched-chain amino acids while conve
88 ation was achieved via a bisulfite-catalyzed transamination of cytosine after endonuclease cleavage o
89 ary amides of iron(II), were obtained by the transamination of Fe{N(SiMe(3))(2)}(2), with HN(SiMe(3))
90         The (R)-enantiomer also inhibits the transamination of GABA 10 times more effectively than th
91        The best enzyme mimic accelerated the transamination of indole-3-pyruvic acid by a factor of 4
92 thionine decarboxylase by substrate-mediated transamination of its pyruvoyl cofactor.
93     These data indicate that KICSIS requires transamination of KIC and glutamate to leucine and alpha
94 erase II (hKAT-II) efficiently catalyzes the transamination of knunrenine to kynurenic acid (KYNA).
95 mKAT III is able to efficiently catalyze the transamination of kynurenine to KYNA and has optimum act
96 ased by d-amphetamine may interfere with the transamination of L-kynurenine to KYNA specifically in t
97                                              Transamination of L-leucine with alpha-ketoglutarate res
98 , including those formed by TATase-catalyzed transamination of l-phenylalanine, l-tyrosine, l-tryptop
99 chain aminotransferase) catalyzes reversible transamination of leucine and alpha-ketoglutarate to KIC
100    The kinetic parameters determined for the transamination of phenylalanine by TATase (kcat = 180 s-
101 rst step in phenyllactic acid synthesis, the transamination of phenylalanine to phenylpyruvate.
102 sms, an aminotransferase is required for the transamination of prephenate into arogenate, but the ide
103 of UDP-glucuronic acid, followed by the C-4" transamination of the product to generate the novel suga
104 nvolve oxidation of the 5'-alcohol by Pac11, transamination of the resulting aldehyde by Pac5, and de
105             One plausible explanation is the transamination of the three acids to produce glutamic ac
106                                              Transamination of {(PEt(3))(2)RhN(SiMePh(2))(2)} (1a) or
107 or a range of protein substrates, N-terminal transamination offers a convenient way to install a reac
108        Neither compound can be oxidized by a transamination or addition/elimination mechanism, but bo
109 ionine and derived-sulfur metabolites in the transamination pathway activate the GCN5 acetyltransfera
110 SP, probably using the same methionine (Met) transamination pathway as macroalgae and phytoplankton(1
111 to dopamine and suggest this may occur via a transamination pathway in which DHPPA is an intermediary
112                                          The transamination product of leucine, alpha-ketoisocaproic
113 ation in addition to transamination, and the transamination product of N-terminal Gln was resistant t
114 matic ketoacids, including indolepyruvate, a transamination product of tryptophan.
115 ularly leucine, and can be reproduced by its transamination product, ketoisocaproic acid.
116 ed Delta(1)-piperideine-2-carboxylate as its transamination product.
117  were employed to detect the presence of the transamination products 2-ketoarginine and L-alanine, th
118 imulates PHAS-I phosphorylation although the transamination products of isoleucine and valine are ine
119 dapD and dapE mutants and to catalyze LL-DAP transamination, providing functional evidence for a role
120  treatment reduced leucine nitrogen flux and transamination rates in subjects with type 2 diabetes.
121 iabetic subjects, but leucine nitrogen flux, transamination rates, and plasma ketoisocaproate level w
122 capable of facilitating further steps of the transamination reaction after the formation of the exter
123 rcaptopyruvic acid (VI, formed by a Cys-APAP transamination reaction in kidney), 3,3'-biacetaminophen
124   This was followed by a bisulfite-catalyzed transamination reaction in order to biotinylate the dsDN
125                                          The transamination reaction of ethylamine is 75-fold slower
126 specific protein modification method using a transamination reaction that chemoselectively oxidizes t
127 usively catalyze a decarboxylation-dependent transamination reaction to form pyridoxamine 5-phosphate
128 no group of TM to a carbonyl group through a transamination reaction with glyoxylate produced a prote
129                                          The transamination reaction with l-alanine was coupled in th
130 (CH(3))(2)N)(4)Ti, TDMAT), which undergoes a transamination reaction with sufficiently nucleophilic a
131 ate at which the enzyme catalyses its normal transamination reaction.
132 the block of its conversion to lactate, with transamination reactions converting pyruvate to form the
133 We previously showed that in decarboxylative transamination reactions under credible prebiotic condit
134 xpressed in Escherichia coli catalyzed three transamination reactions using the following amino donor
135 somal photorespiratory enzyme that catalyzes transamination reactions with multiple substrates.
136 ozymes, the channeling of metabolic flow via transamination reactions, and active transport mechanism
137             This finding establishes RS as a transamination reagent that is particularly well suited
138 lt, RS) was identified as a highly effective transamination reagent when paired with glutamate-termin
139  benzenesulfonate (Rapoport's salt, RS) as a transamination reagent, which oxidizes the N-terminal am
140 creening platform as a method to explore new transamination reagents while simultaneously identifying
141               From methionine, the steps are transamination, reduction and S-methylation to give the
142             This pathway involves an initial transamination step followed by tautomerization to form
143 ependent and its catalysis is initiated by a transamination step in which pyridoxal 5'-phosphate (PLP
144  organic synthesis, including the following: transamination substitution reactions with virtually any
145 uence of the need for increased reactions of transamination to cope with the liver metabolic derangem
146 pha-ketobutyrate and ammonia) and L-alanine (transamination to form pyruvate), which have uncharged s
147 tein was proposed to catalyze the subsequent transamination to form UDP 2-acetamido-3-amino-2,3-dideo
148 alpha-(32)P]UDP-glucuronic acid, followed by transamination to generate [alpha-(32)P]UDP-l-Ara4N, whe
149 ual aspartate was liberated enzymatically by transamination to oxaloacetate with aspartate aminotrans
150 c acid is derived from phenylalanine via its transamination to phenylpyruvate, and mining of the tran
151 suppressed by hepatic and renal beta-alanine transamination upon oral beta-alanine intake.
152           Although leucine oxidation and KIC transamination were blocked in BCATm(-/-) islets, KIC ox
153 ction of BCATc correlates with increased Leu transamination, whereas T cells from the BCATc(-/-) mous
154 nates the pyridine nitrogen for catalysis of transamination, while both alanine racemase and O-acetyl
155 l-4-chloro-piperidine, were accomplished via transamination with a quaternary ammonium piperidone or
156 ine in the reaction mixture is followed by a transamination with oleylamine, the solvent of the react
157 acid is a substrate for YwfG, which promotes transamination (with L-Phe as amino donor), to form tetr

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