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1 ep, rather than the previously described two-step reaction.
2 t the second (rearrangement) step of the two-step reaction.
3 t plasminogen is converted to AS4.5 in a two-step reaction.
4 t this mode of chromatin remodeling is a two-step reaction.
5 analog was prepared similarly, but in a two step reaction.
6 reduced to 1-hexadecanol by LiAlH4 in a one-step reaction.
7 ase A2 and were synthesized in a one-pot two-step reaction.
8 to reversible self-cleavage but was a three-step reaction.
9 ing a one-pot hydrothermal method via single-step reaction.
10 in contrast to DB-JBP1, which binds in a one-step reaction.
11 sized in high yields on gram scales in a one-step reaction.
12 Binding of gHgL to integrins is a two-step reaction.
13 entrance and the heme group during the three-step reaction.
14 the transformation of AA to LTA(4) in a two-step reaction.
15 erted into the substrate via a consecutive 2-step reaction.
16 -Cryp) was successfully synthesized by a one-step reaction.
17 es the formation of NO via a consecutive two-step reaction.
18 activation of acetate to acetyl-CoA in a two-step reaction.
19 2).(diamine)] can be synthesized in a single-step reaction.
20 difficult, particularly in complicated multi-step reactions.
21 location as a sequence of coupled hydrolysis-stepping reactions.
24 peak, is easily synthesized via a simple one-step reaction and is formulated in water with high stabi
25 ycloisomerization becomes a complex multiple-step reaction and proceeds with a rate-determining barri
26 ins can be more complex than a simple single-step reaction, and that application of several methods c
27 hereas the discrimination in the overall two-step reaction arises from very weak binding of noncognat
28 were obtained in quantitative yield in a one-step reaction at ambient temperature from the commercial
29 DnaK-peptide complexes according to the two-step reaction, ATP + DnaK-P if ATP-DnaK-P if ATP-DnaK +
30 f the reaction course indicate a virtual one-step reaction between the NHC and the silanorbornadiene.
31 Protein splicing proceeds through a four-step reaction but the catalytic mechanism is not fully u
32 ediators formed from arachidonic acid in a 2-step reaction catalyzed by 5-lipoxygenase (5-LOX) requir
33 rom soluble Mn(II) to Mn(IV) oxides is a two-step reaction catalyzed by an MCO-containing complex.
34 reaction is a "simple" extension of the two-step reaction catalyzed by MR: base-catalyzed proton abs
35 , indicating that ester production was a two-step reaction consisting of hydrolysis and esterificatio
36 -chlorobenzoyl-coenzyme A formation in a two-step reaction consisting of the adenylation of 4-chlorob
37 red reaction pathway, compared to the single-step reaction, constitute the key advantages of this tan
39 the behavior of KIEobs for a reversible two-step reaction for all possible values of the rate consta
40 In this Communication, we describe a two-step reaction for preparing three-dimensional electrodes
41 strate availability, we also developed a two-step reaction for the enzymatic synthesis of UDP-l-rhamn
42 Under a new approach, we developed a one step reaction for the interconversion of artemisinin 1 i
43 g intermediate participates in normal second-step reactions, forming spliced exon and linear intron R
44 ing deterrent that can be formed in a single step reaction from 3-dehydroquinate catalyzed by quinate
47 gens to estrogens through a sequential three-step reaction, generating 19-hydroxy and 19-aldehyde int
51 of highly sulfated keratan sulfate by a two-step reaction in vitro with a mixture of beta3GnT7/beta4
52 ts in tyrosine nitration, catalyzed as a two-step reaction in which nitric-oxide synthase induction i
53 alysis of PCNA opening by RFC revealed a two-step reaction in which RFC binds PCNA before opening PCN
56 halose biosynthesis in plants involves a two-step reaction in which trehalose-6-phosphate (T6P) is sy
57 onine S-adenosyltransferase) catalyzes a two-step reaction in which tripolyphosphate (PPPi) is a tigh
58 ediate species in total, we map out relevant step reactions in a model size growth reaction from mole
60 h seven 1,3,5-triazines was studied in a one-step reaction (in situ formation of 3-aminopyrrole) and
61 BP1 binds to J-DNA or glu-5-hmC-DNA in a two-step reaction, in contrast to DB-JBP1, which binds in a
62 f class II synthetases and carries out a two-step reaction, in which lysine is activated by being att
63 xperiments and computations indicate a three-step reaction including isomerization of diazomethane, a
64 tic resonance spectroscopy, with temperature-step reaction initiation, starting from the enzyme-coenz
66 sor messenger RNA (pre-mRNA) splicing, a two-step reaction involved in a multitude of RNA structural
67 ab' fragments was also consistent with a two-step reaction involving fast high-affinity binding and a
68 s the addition of water to epoxides in a two-step reaction involving initial attack of an active site
69 slational modification is performed in a two-step reaction involving the addition of a beta-lysine mo
70 midation of bioactive peptides through a two-step reaction involving the monooxygenase and lyase doma
71 presence of both catalyst and solvent, a two-step reaction is predicted, corresponding to the stepwis
72 hase (NOS) generates NO via a sequential two-step reaction [l-arginine (l-Arg) --> N-hydroxy-l-argini
74 ld and made it possible to demonstrate a two-step reaction mechanism for des-PPW with K init = 10.4 +
78 inds single-headed myosin VI following a two-step reaction mechanism with formation of a low affinity
79 er the entire temperature range with a three-step reaction mechanism, originally proposed by Ashton e
80 However, kinetic modeling indicated a two-step reaction mechanism, with formation of peroxocarbona
81 sociation of a protein complex follows a two step reaction mechanism, with the first step being the f
86 spliceosomal and group II introns, the first-step reaction occurs by nucleophilic attack on the 5' sp
87 0 Da poly(propylene fumarate) (PPF) by a two-step reaction of diethyl fumarate and propylene glycol t
88 substituents are synthesized by using a one-step reaction of H(8)BINOL with amino methanols that wer
89 e DFT-level mechanism elucidation of the two-step reaction of non-heteroatom-stabilized carbenes with
95 athway comprising three nucleotidyl transfer steps: reaction of Rtc with ATP to form a covalent Rtc-(
96 d carbon dioxide can be produced in a single-step reaction over the catalyst, with no detectable CO (
97 s of ghrelin follows an unprecedented single-step reaction pathway and the single-step acylation proc
100 s the first time demonstrating that a single-step reaction pathway is possible for an ester hydrolysi
101 tions provide evidence for an unexpected two-step reaction pathway, which involves dehydrogenative in
104 oselectivity differences thus enabled single-step reaction pathways to an effective collection of dox
106 proteins at cysteine residues, but this two-step reaction requires lengthy incubations and produces
109 midating monooxygenase (PAM) catalyzes a two-step reaction resulting in the C-terminal amidation of p
113 e other as the emitter electrode, a multiple-step reaction scheme was achieved that included consecut
117 fold diversity has been achieved using a two-step reaction sequence involving allylic substitution an
118 -R species, where R = H or -CH3, using a two-step reaction sequence involving chlorination of H-Si(11
124 orts to design selective catalysts for multi-step reactions, such as hydrodeoxygenation (HDO), have e
125 -Hydroxybenzoate hydroxylase catalyzes a two-step reaction that demands precise control of solvent ac
126 on a large scale, in high yield using a one-step reaction that employs commercially available reagen
128 protein synthase III (FabH) catalyzes a two step reaction that initiates the pathway of fatty acid b
130 enzymes catalyze mechanistically similar two-step reactions that proceed through an enzyme-bound acyl
133 imetric analysis results, which show the two-step reaction to be exothermic by -215 kJ mol(-1), in ag
135 orming family of enzymes that catalyze a two-step reaction to first activate a carboxylate substrate
136 ch using LCA as a template, along with a two-step reaction to generate sodium 3-hydroxyolean-12-en-30
138 mines (-NH2), and this allowed for the multi-step reactions to be carried out in tandem within the MO
139 ated actin filaments in an apparently single step reaction upon binding, whereas the stabilization by
141 ocked by stoichiometric acetylation in a one-step reaction using sulfosuccinimidyl acetate (S-NHSAc)
142 situ formation of 3-aminopyrrole) and a two-step reaction (using the tetraphenylborate salt and an a
143 dic acid is typically synthesized in a three-step reaction utilizing three enzymes: glycerol 3-phosph
145 te kinetics applicable to realistic multiple step reactions, we present here the successful applicati
147 batteries, whose lithiation undergoes a two-step reaction, whereby intercalation and conversion occu
148 hibitor was shown to bind thrombin via a two-step reaction wherein the initially formed thrombin-inhi
150 0 kDa) proteins was accomplished in a single-step reaction with a commercially available bis(2,2'-bip
151 ry in optically pure form using a simple one-step reaction with commercially available reagents.
152 They can be additionally modified in a one-step reaction with functional groups for covalent labeli
154 ther spliceosomal components, performs a two-step reaction with two short RNA oligonucleotides as sub
156 es RNA 2',3' cyclic phosphate ends via three steps: reaction with ATP to form a covalent RtcA-(histid
157 oth DNA substrates occurs by a minimum three-step reaction, with the bimolecular step followed by two
158 coccus triterpene synthases, catalyzes a two-step reaction within a single enzyme unit without interm
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