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1 sh that the UbiI protein functions in the C5-hydroxylation reaction.
2 izontal lineO species for the aromatic ortho-hydroxylation reaction.
3 h a Soret maximum at 420 nm during the L-Arg hydroxylation reaction.
4 otein product was sufficient to perform a 3'-hydroxylation reaction.
5 c carbons in addition to the normal aromatic hydroxylation reaction.
6 domain and catalyzes demethylation through a hydroxylation reaction.
7 tion reactions, rather than the more typical hydroxylation reaction.
8 cillary experimental data for this enzymatic hydroxylation reaction.
9 ate-limiting for all subsequent steps in the hydroxylation reaction.
10 d hydrogen radical abstraction followed by a hydroxylation reaction.
11 ecies participating in a multistep TauD self-hydroxylation reaction.
12 ept that Tyr289 is a critical residue in the hydroxylation reaction.
13 have formed and decayed in the course of the hydroxylation reaction.
14 es reversible transfer of protons during the hydroxylation reaction.
15 or 13-cis retinoic acid as substrate for the hydroxylation reaction.
16 favorable cases, from the generally dominant hydroxylation reaction.
17 factor to mediate an O(2)-dependent C-H bond hydroxylation reaction.
18 of inhibitors of a cytochrome P450-catalyzed hydroxylation reaction.
19 e catalytic cycle of aerobic carbon-hydrogen hydroxylation reaction.
20 ependent and requires electron input for the hydroxylation reaction.
21  bonds, so only 3 engages in stereoretentive hydroxylation reactions.
22 e that is the active oxygen species in these hydroxylation reactions.
23 tems and are efficient oxidants of aliphatic hydroxylation reactions.
24  of mutants to catalyse synthetically useful hydroxylation reactions.
25 , and rosmarinic acid, that result from meta hydroxylation reactions.
26  Ser478 plays a role in the first and second hydroxylation reactions.
27 the same range as AKIE in previously studied hydroxylation reactions.
28 inine oxidases that catalyze desaturation or hydroxylation reactions.
29 g carboxylation, sulfonation and up to three hydroxylation reactions.
30 ate thus plays a key role in H4Bip-dependent hydroxylation reactions.
31 s is believed to be the oxygen donor in most hydroxylation reactions, an iron-peroxy species is appar
32 r the mycobacterial UDP-N-acetylmuramic acid hydroxylation reaction and demonstrated that Mycobacteri
33 of volicitin is plant derived whereas the 17-hydroxylation reaction and the conjugation with glutamin
34  the regioselectivity of P450 27A1-dependent hydroxylation reactions and conferred the P450 capacity
35 elative rate constants for the unmasking and hydroxylation reactions, and a qualitative correlation w
36                                    Catalytic hydroxylation reactions are conveniently performed in an
37 sition states for C-H bond cleavage in these hydroxylation reactions are either significantly nonline
38                                         Both hydroxylation reactions are linked to oxygen availabilit
39                               All biological hydroxylation reactions are thought to derive the oxygen
40 which carry out a variety of highly specific hydroxylation reactions, are of great interest as potent
41 trate that these mutants catalyze the same 5-hydroxylation reaction as performed by human CYP2C19, th
42 no acid metabolism and DNA, RNA, and protein hydroxylation reactions, as cellular membranes are thoug
43 mes, including peroxides as oxygen donors in hydroxylation reactions, as substrates for reductive bet
44 alloenzymes harness O(2) to mediate C-H bond hydroxylation reactions, but most commonly feature iron
45                              The rate of the hydroxylation reaction can be mildly stimulated by the f
46       Pathway prediction suggested that ring hydroxylation reactions catalysed by Rieske-type dioxyge
47 osfamide are activated in human liver by a 4-hydroxylation reaction catalyzed by multiple cytochrome
48 dical reduction during a single turnover Arg hydroxylation reaction catalyzed by neuronal NOS to docu
49 ultidomain enzyme that donates electrons for hydroxylation reactions catalyzed by class II cytochrome
50  detailed modeling of the methane and ethane hydroxylation reactions catalyzed by the hydroxylase enz
51 are the kinetics of these transitions in Arg hydroxylation reactions catalyzed by the oxygenase domai
52 romatase (CYP19) catalyzes three consecutive hydroxylation reactions converting C19 androgens to arom
53 cytochrome P450, catalyzes three consecutive hydroxylation reactions converting C19 androgens to arom
54 cytochrome P450, catalyzes three consecutive hydroxylation reactions converting C19 androgens to arom
55 0% HF) was, therefore, used to calculate the hydroxylation reaction coordinate of P in [Cu(II)2(NO2-X
56 ance or inhibit O2-.-dependent oxidation and hydroxylation reactions depending upon their relative fl
57 ate of tetrahydrobiopterin (H4Bip)-dependent hydroxylation reactions, essential in living organisms,
58 e (CPR) electron transfer chain for its para-hydroxylation reaction, ferulate 5-hydroxylase uses both
59 revealed the activation barriers for the C-F hydroxylation reaction for the three complexes, consiste
60                           After its namesake hydroxylation reaction, H6H then couples the newly insta
61 (II)-alphaKG-dependent enzymes that catalyze hydroxylation reactions, halogenases catalyze a transfer
62               However, the transiency of the hydroxylation reaction hinders the identification of hyd
63 erestingly, NO inhibited this iron-catalyzed hydroxylation reaction in a concentration-dependent mann
64  that an alternative enzyme catalyzes the C5-hydroxylation reaction in the absence of oxygen.
65 l cytochromes P450 that mediate the last two hydroxylation reactions in the ecdysteroidogenic pathway
66                              The rate of the hydroxylation reaction increases with pH in a manner con
67 te-dependent dioxygenases (2-OGDDs) catalyze hydroxylation reactions involved in cell metabolism, the
68 mong higher plants and features a critical 3-hydroxylation reaction involving phenolic esters.
69 atalyzes an O(2)- and alphaKG-dependent self-hydroxylation reaction involving Tyr-73, yielding an Fe(
70                       The data show that the hydroxylation reaction is initiated by homolytic cleavag
71 s that carry out intramolecular aromatic C-F hydroxylation reactions is reported.
72 y of hemoproteins to catalyze epoxidation or hydroxylation reactions is usually associated with a cys
73 de, the proposed primary oxidant in the P450 hydroxylation reaction, is calculated to be 17.8 kcal/mo
74 es that favor chlorination by CytC3 over the hydroxylation reactions occurring in related enzymes.
75 e(IV)(O) complex, an unprecedented arene C-F hydroxylation reaction occurs.
76 ual oxidant in NOS enzymes that performs the hydroxylation reaction of arginine, which is in sharp co
77 noic acid (ODYA), were selected to probe the hydroxylation reaction of PCB3 in whole poplars in this
78 how that the SYR2 gene is required for the 4-hydroxylation reaction of sphingolipid long chain bases,
79                                          The hydroxylation reactions of adducts were carried out with
80  occurs by a mechanism involving consecutive hydroxylation reactions of the C-7 methyl group to form
81 t majority of flavin monooxygenases catalyze hydroxylation reactions on a single position of their su
82            P450 17A1 was found to perform 16-hydroxylation reactions on its 17alpha-hydroxylated prod
83 nt substrate tolerance and performs multiple hydroxylation reactions on structurally variant macrolid
84 d scission generally accepted for the phenol hydroxylation reaction performed by tyrosinase.
85  (mu-O)2 Co(III) ](2+) core through aromatic hydroxylation reactions represent a new domain for high-
86                         Prephenate-dependent hydroxylation reactions represent a unique biochemical s
87 which selectively catalyze ring-expansion or hydroxylation reactions, respectively.
88 es of individual steps of cholesterol 7alpha-hydroxylation reaction revealed several characteristics
89          Analysis of a single turnover L-Arg hydroxylation reaction revealed that a new heme species
90 on potential of neutral arginine, the actual hydroxylation reaction starts with an initial electron t
91                           In addition to the hydroxylation reaction that is commonly observed, other
92 remove methyl groups from histones through a hydroxylation reaction that requires alpha-ketoglutarate
93 t isotope-sensitive processes in the overall hydroxylation reactions that are either competitive or s
94 ted molybdoflavoenzyme, catalyzes sequential hydroxylation reactions to convert hypoxanthine via xant
95 X) and 2B2 catalyzed both N-deethylation and hydroxylation reactions to generate MEGX and omega-dieth
96 rt here that all three enzymes will catalyze hydroxylation reactions using H(2)O(2) in place of tetra
97 ectories for a non-native, remote C(sp(3))-H hydroxylation reaction, we demonstrate that the stabiliz
98                               The 18- and 19-hydroxylation reactions were attributed to P450 3A4, and
99 rome P450s catalyze N-demethylation and ring-hydroxylation reactions within the early steps in the bi