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1 izontal lineO species for the aromatic ortho-hydroxylation reaction.
2 h a Soret maximum at 420 nm during the L-Arg hydroxylation reaction.
3 otein product was sufficient to perform a 3'-hydroxylation reaction.
4 c carbons in addition to the normal aromatic hydroxylation reaction.
5 domain and catalyzes demethylation through a hydroxylation reaction.
6 tion reactions, rather than the more typical hydroxylation reaction.
7 cillary experimental data for this enzymatic hydroxylation reaction.
8 ate-limiting for all subsequent steps in the hydroxylation reaction.
9 d hydrogen radical abstraction followed by a hydroxylation reaction.
10 ecies participating in a multistep TauD self-hydroxylation reaction.
11 ept that Tyr289 is a critical residue in the hydroxylation reaction.
12 have formed and decayed in the course of the hydroxylation reaction.
13 es reversible transfer of protons during the hydroxylation reaction.
14 or 13-cis retinoic acid as substrate for the hydroxylation reaction.
15 sh that the UbiI protein functions in the C5-hydroxylation reaction.
16 e that is the active oxygen species in these hydroxylation reactions.
17 tems and are efficient oxidants of aliphatic hydroxylation reactions.
18 of mutants to catalyse synthetically useful hydroxylation reactions.
19 the same range as AKIE in previously studied hydroxylation reactions.
20 , and rosmarinic acid, that result from meta hydroxylation reactions.
21 Ser478 plays a role in the first and second hydroxylation reactions.
22 s is believed to be the oxygen donor in most hydroxylation reactions, an iron-peroxy species is appar
23 r the mycobacterial UDP-N-acetylmuramic acid hydroxylation reaction and demonstrated that Mycobacteri
24 of volicitin is plant derived whereas the 17-hydroxylation reaction and the conjugation with glutamin
25 the regioselectivity of P450 27A1-dependent hydroxylation reactions and conferred the P450 capacity
26 elative rate constants for the unmasking and hydroxylation reactions, and a qualitative correlation w
27 sition states for C-H bond cleavage in these hydroxylation reactions are either significantly nonline
29 which carry out a variety of highly specific hydroxylation reactions, are of great interest as potent
30 trate that these mutants catalyze the same 5-hydroxylation reaction as performed by human CYP2C19, th
31 mes, including peroxides as oxygen donors in hydroxylation reactions, as substrates for reductive bet
33 osfamide are activated in human liver by a 4-hydroxylation reaction catalyzed by multiple cytochrome
34 dical reduction during a single turnover Arg hydroxylation reaction catalyzed by neuronal NOS to docu
35 detailed modeling of the methane and ethane hydroxylation reactions catalyzed by the hydroxylase enz
36 are the kinetics of these transitions in Arg hydroxylation reactions catalyzed by the oxygenase domai
37 romatase (CYP19) catalyzes three consecutive hydroxylation reactions converting C19 androgens to arom
38 cytochrome P450, catalyzes three consecutive hydroxylation reactions converting C19 androgens to arom
39 cytochrome P450, catalyzes three consecutive hydroxylation reactions converting C19 androgens to arom
40 0% HF) was, therefore, used to calculate the hydroxylation reaction coordinate of P in [Cu(II)2(NO2-X
41 ance or inhibit O2-.-dependent oxidation and hydroxylation reactions depending upon their relative fl
42 revealed the activation barriers for the C-F hydroxylation reaction for the three complexes, consiste
43 (II)-alphaKG-dependent enzymes that catalyze hydroxylation reactions, halogenases catalyze a transfer
44 erestingly, NO inhibited this iron-catalyzed hydroxylation reaction in a concentration-dependent mann
46 l cytochromes P450 that mediate the last two hydroxylation reactions in the ecdysteroidogenic pathway
48 atalyzes an O(2)- and alphaKG-dependent self-hydroxylation reaction involving Tyr-73, yielding an Fe(
51 y of hemoproteins to catalyze epoxidation or hydroxylation reactions is usually associated with a cys
52 de, the proposed primary oxidant in the P450 hydroxylation reaction, is calculated to be 17.8 kcal/mo
53 es that favor chlorination by CytC3 over the hydroxylation reactions occurring in related enzymes.
55 ual oxidant in NOS enzymes that performs the hydroxylation reaction of arginine, which is in sharp co
56 noic acid (ODYA), were selected to probe the hydroxylation reaction of PCB3 in whole poplars in this
57 how that the SYR2 gene is required for the 4-hydroxylation reaction of sphingolipid long chain bases,
58 occurs by a mechanism involving consecutive hydroxylation reactions of the C-7 methyl group to form
59 t majority of flavin monooxygenases catalyze hydroxylation reactions on a single position of their su
61 nt substrate tolerance and performs multiple hydroxylation reactions on structurally variant macrolid
63 (mu-O)2 Co(III) ](2+) core through aromatic hydroxylation reactions represent a new domain for high-
65 es of individual steps of cholesterol 7alpha-hydroxylation reaction revealed several characteristics
67 on potential of neutral arginine, the actual hydroxylation reaction starts with an initial electron t
68 remove methyl groups from histones through a hydroxylation reaction that requires alpha-ketoglutarate
69 t isotope-sensitive processes in the overall hydroxylation reactions that are either competitive or s
70 ted molybdoflavoenzyme, catalyzes sequential hydroxylation reactions to convert hypoxanthine via xant
71 X) and 2B2 catalyzed both N-deethylation and hydroxylation reactions to generate MEGX and omega-dieth
72 rt here that all three enzymes will catalyze hydroxylation reactions using H(2)O(2) in place of tetra
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