ライフサイエンスコーパス: rate constant

1 substituent, respectively, impacts the PCET rate constant.

2 ionships between the aggregation and binding rate constants.

3 ome of the charge-transfer and corresponding rate constants.

4 s BCFs are slightly more accessible than the rate constants.

5 distribution of association and dissociation rate constants.

6 breastmilk-to-infant and infant elimination rate constants.

7 se without the need to introduce fluctuating rate constants.

8 primarily due to differences in dissociation rate constants.

9 tively) due mainly to decreases in radiative rate constants.

10 y of HAT energy for predicting NAC reduction rate constants.

11 dithiolanes were then predicted by using the rate constants.

12 association rate constants and dissociation rate constants.

13 of starvation and to determine translocation rate constants.

14 ies of directly measuring (3)CDOM* quenching rate constants.

15 determine photoreduction and photobleaching rate constants.

16 y and ratio of the dissolution and diffusion rate-constants.

17 n-rate constant 1.61-fold greater and an off-rate constant 0.563-fold smaller than that of albumin.

18 cm(-2)) and heterogeneous electron transfer rate constant (0.0032 s(-1)) which indicate enhanced sur

19 y), standard heterogeneous electron transfer rate constant (0.336 s(-1) and 0.590 s(-1) for AT and VC

20 xidized seven different electron donors with rate constants (0.089-3.06) x 10(10) M(-1) s(-1).

21 degraded much faster than MS2 (inactivation rate constant = 0.14 cm(2) mJ(-1)).

22 ) inactivation curve for HuNoV (inactivation rate constant = 0.27 cm(2) mJ(-1)).

23 or SWCNTs than albumin, with a fibrinogen on-rate constant 1.61-fold greater and an off-rate constant

24 ter cleaning and then decreased with removal rate constants 1.2-7.2 times larger than ACR, indicating

25 3 has the highest rate constant (1.5 M(-1) s(-1) at -60 degrees C) for oxi

26 between the heterogeneous electron-transfer rate constant (10(-3) cm s(-1)) and the diffusion coeffi

27 C(P)SOH to C(P)SO(2) (-) with a second-order rate constant 2 orders of magnitude higher than that of

28 process was run and the kinetic parameters (rate constant, activation energy, and temperature quotie

29 ications dramatically change binding kinetic rate constants, affording compounds with a clozapine-lik

30 e of an emissive transition with a radiative rate constant an order of magnitude higher than that of

31 We have measured the rate constant and activation parameters for the direct r

32 Based on the rate constant and steady-state concentrations of (1)O(2)

33 Both potential methylation rate constants and % MeHg were the highest in sediments

34 The rate constants and activation energies of HDX for peptid

35 portional relationships between the measured rate constants and associated gene transcripts for nitri

36 termined from correlations between radiative rate constants and average emission frequencies.

37 the kinetic binding affinities, association rate constants and dissociation rate constants.

38 chloride were used to extrapolate unfolding rate constants and half-lives of the crystallins in the

39 tic modeling yielded invariable second-order rate constants and increasing concentrations of reactive

40 the initial guess of model parameters (i.e., rate constants and initial counts of molecules in a cell

41 The observed rate constants and KIEs were examined as a function of h

42 he use of global kinetic modeling to extract rate constants and kinetic barriers.

43 sp(3) C-H bonds up to 87 kcal/mol to afford rate constants and kinetic isotope effects (KIEs) of 2-6

44 on between the logarithms of the Diels-Alder rate constants and measured K(1:1) values.

45 The linear free energy relationships between rate constants and pK(a) of the leaving group are curved

46 tamol clearance, determined from elimination rate constants and reported total larval volumes of 253,

47 s observed, leading to increased dissolution rate constants and solubility in some cases.

48 ing a Lewis base X, affording faster kinetic rate constants and the ability to cleave stronger C-H bo

49 QCM setup, the association and dissociation rate constants and the associated equilibrium constants

50 The resulting second-order rate constants and the previously published reactivity p

51 a and the TK parameters (sorption and uptake rate constants and the resulting BCF) were found, but no

52 a protein and a small molecule with defined rate constants and, thus, K(d) of their interaction-allo

53 hydrolysis of a model organophosphate, with rate constants approximately 10(5)-fold higher than the

54 cond molecular dynamics, and the ET and PCET rate constants are calculated with the corresponding non

55 ngle-nucleotide and multinucleotide addition rate constants are faster than those of Pol II.

56 Computational estimated rate constants are in fair agreement with experimental v

57 the intermolecular binding and dissociation rate constants are quantitatively and independently dete

58 ic tetrazines that react with isonitriles at rate constants as high as 57 L mol(-1) s(-1) were access

59 charged side chains bracket the experimental rate constants, as expected for the acidic bath used in

60 f the thiazoline product, and determined the rate constants associated with the stepwise condensation

61 the PCET driving force, which attenuates the rate constant at smaller distances.

62 a(2) can be calculated, one can compare the rate constants at different times with statistical rigor

63 dots") show similar singlet oxygen quenching rate constants, based on the molar concentration of the

64 )) and the influx (K (1)) and efflux (k (2)) rate constants between plasma and selected brain regions

65 in the most favorable cases accelerate SF to rate constants beyond (100 fs)(-1).

66 ceable differences in the (3)CDOM* quenching rate constants by HDA and unquenchable triplet fractions

67 ues, we developed a simple algorithm for the rate constant calculation based on a single labeled samp

68 The improved 2 time-point method enables the rate constant calculation with less than 10% relative er

69 t concentrations; (ii) different gill uptake rate constant calculations (k(1)); (iii) protein binding

70 y, we include multistructural effects in the rate constant calculations.

71 ameters such as the receptor desensitization rate constant can be estimated if the mechanism is known

72 ole, the DOM concentration dependence of the rate constant consisted of a sharp decrease up to ~1.0 m

73 ary displacements or slow the working stroke rate constant, consistent with the mutation disrupting a

74 In contrast, the dissolution rate constant correlated with pH for pH < 6.3 ( R(2) = 0

75 Cytometry of Reaction Rate Constant (CRRC) uses time-lapse fluorescence micros

76 The rate constant derived for the O(3)-NPM reaction is 1 x 1

77 However, second-order oxidation rate constants did not correlate strictly with the (1)O(

78 The extraction rate constant, energy of activation for diffusion, Biot

79 ndicate that this variant has a dissociation rate constant essentially equivalent to the wild type, i

80 ti-compartmental pharmacokinetic model (with rate constants estimated from in vitro experiments) pred

81 h of the spacer and correlated well with the rate constants estimated from the BP triplet lifetimes.

82 Rate constant estimation with heavy water requires a lon

83 use in AOPWIN, a common model for OH radical rate constant estimations.

84 and extend the rate constant evaluation down to 200 K.

85 our analysis suggests that the few-parameter rate constant expression of Marcus theory explains both

86 The first (1)O(2) bimolecular reaction rate constant for a RiPP, the thiazole-containing peptid

87 For the major isomer 5a, the computed SCT rate constant for bond shifting at 80 K is 0.16 s(-1), c

88 ever, even at the optimal driving force, the rate constant for charge transfer from the triplet state

89 esults show that m(6)A minimally impacts the rate constant for duplex dissociation, changing k(off) b

90 ard TC dissociation rather than by a smaller rate constant for GTP hydrolysis for near- and non-cogna

91 sterol depletion did not affect the observed rate constant for K(+) occlusion by phosphorylated Na(+)

92 and have uncovered a mechanism in which the rate constant for pyrophosphate release is slowed for ce

93 The results reveal that the rate constant for ring opening of radical cations derive

94 The pseudo-second-order rate constant for the BPA pollutant is 182.3 g mg(-1) mi

95 The bimolecular rate constant for the DA reaction with (1)O(2) determine

96 The third-order rate constant for the demetalation of chlorophyll-a to p

97 and led to an increased enzymatic hydrolysis rate constant for the first stage of hydrolysis and fina

98 tronic absorption spectrum and calculate the rate constant for the photolytic process HNO(3) + hnu ->

99 The yield rate constant for the ultrasound extraction was almost t

100 ignal in the hypoperfused myocardium, K (1) (rate constant for transfer from arterial plasma to tissu

101 the proton-coupled electron transfer (PCET) rate constants for a series of biomimetic oligoproline p

102 We experimentally parameterized conditional rate constants for aqueous U uptake, dietary U uptake, a

103 Rate constants for bimolecular electron transfer (ET) in

104 Second-order rate constants for Cl(2), Cl(2)O, and HOCl were computed

105 The rate constants for CO loss span 12 orders of magnitude a

106 rmodynamic equilibrium constants and kinetic rate constants for complex, multiple-step biological int

107 ted at unconfined type-(i) environments, the rate constants for cyclohexene epoxidation (323 K, 0.05

108 ping peptides that cover the whole sequence, rate constants for each amide hydrogen exchange (or equi

109 The rate constants for electron transfer through the dual hy

110 The rate constants for formation of the 1:1 and 1:2 complexe

111 e more than 100 ab initio computed (MP2:DFT) rate constants for H-SSZ-13 are used in a batch reactor

112 ted a three-step model and provided apparent rate constants for intermediate formation (i.e. a k'(2)

113 Rate constants for intramolecular tyrosine oxidation wer

114 o examine whether the experimentally derived rate constants for N. triangulifer could be generalized

115 In this work, we determined the rate constants for oxidation by OH radicals and Cl atoms

116 es of anthracene-phenol-pyridine triads give rate constants for PCET charge recombination that are sl

117 ed with gamma-terpinene concentration, while rate constants for radical-trapping were unchanged by ga

118 generate statistically unbiased estimates of rate constants for rare events such as folding; no biasi

119 ion, with observed decreases consistent with rate constants for reactions of the compounds with hydro

120 The rate constants for reactions with Cl atoms with the same

121 vibronically nonadiabatic PCET theory yield rate constants for simultaneous tunneling of the electro

122 The rate constants for the aqueous reaction, between pH 0 an

123 The derived reaction rate constants for the heterogeneous loss of EHDP and DP

124 drogen-bonding equilibrium constants and the rate constants for the PCET event from deconvolution of

125 The determined second-order rate constants for the quenching of DMABN(*+) by phenols

126 The apparent second order rate constants for the reaction of MGO with trans-resver

127 We estimate site-specific kinetic rate constants for the restoration of methyl marks on >1

128 elying on nuanced changes in the microscopic rate constants for the short-circuiting reactions.

129 The rate constants for the stochastic clock network are cons

130 The rate constants for tyrosine oxidation decreased by 125-f

131 ficient [Formula: see text] and with the ORR rate constant [Formula: see text] in nonaqueous Li-, Na-

132 8 in LUFA 2.2 soil decreased the dissolution rate constant from 0.56 mol(1/3).kg(1/3).s(-1) to 0.17 m

133 dictions and experimentally measured removal rate constants from the water column were strongly corre

134 The k(H) rate constants gave good linear Hammett correlation with

135 d in good agreement with the model peptide's rate constant, highlighting the potential of using model

136 omparison with the experimentally determined rate constant in aqueous solution yields a k(calculated)

137 scaffold, were noted, with the second-order rate constant in cycloadditions with diazoacetamides exc

138 By comparison, related intramolecular ET rate constants in very similar constructs were reported

139 Kinetic calculations predict a rate constant increase by ~4 orders of magnitude relativ

140 For DOM, quenching rate constants increased with the phenolic content of th

141 A reaction rate constant is determined for every cell, and a kineti

142 e air-water interface, a lower limit for the rate constant is k = 1.2 x 10(-9) cm(3).molecule(-1).s(-

143 inetic histogram "number of cells versus the rate constant" is used to determine quantitative paramet

144 can be explained by a wide variation of the rate constant k Additionally, by developing a mathematic

145 ism, the new 3-step mechanism being: A -> B (rate constant k(1)), A + B -> C (rate constant k(2)), an

146 ng: A -> B (rate constant k(1)), A + B -> C (rate constant k(2)), and A + C -> 1.5C (rate constant k(

147 > C (rate constant k(2)), and A + C -> 1.5C (rate constant k(3)), where A represents the monomeric na

148 ), propagation oxidizability R(n), composite rate constant k(c), and LOOH decomposition rate constant

149 e rate constant k(c), and LOOH decomposition rate constant k(d).

150 ne synthesis capacity (indexed as the influx rate constant K(i)(cer)) and structural 3T MRI.

151 d by induction period IP, overall initiation rate constant k(IP), initiation oxidizability O(i), and

152 The first-order rate constant k(obs) was not affected by the concentrati

153 fluorescence (TADF) emitter with a radiative rate constant k(r) of ca. 9 x 10(5) s(-1), exceeding tho

154 facial enhancement in the observed catalytic rate constant k(s) (~5 orders of magnitude) over the mon

155 odels was performed to calculate the kinetic rate constants K (1), k (2), k (3), and k (4) The analys

156 The resulting second-order rate constants k(2) followed the correlation log k(2)(20

157 mpd-II(LutH(+)) reacts with the second order rate constants k(2)(9,10-dihydroanthracene; DHA) = 0.485

158 -1.17), the apparent second-order hydroxide rate constant (k(1)('), rho = 0.87), the hydroxide-indep

159 wash-in and wash-out traces, the association rate constant (k(1)) is somewhat decreased for both AMT

160 MT and RMT in the S31N, but the dissociation rate constant (k(2)) is dramatically increased compared

161 veloped to quantify the SO(4)(*-) scavenging rate constant (k(=S)) for alumina, a naturally occurring

162 etry of inhibition of 3.8 and an association rate constant (k(ass)) of 3.3 x 10(5) M(-1)s(-1).

163 In PB, the values of the inactivation rate constant (k(d)) decreased with an increase in pH, w

164 sfer NMR experiments to measure the exchange rate constant (k(ex)) of the imino protons in the unboun

165 ingle cardiomyocyte in terms of the apparent rate constant (k(f)) of the regeneration rate of ferroce

166 ar acids, which causes the oxidation by HOCl rate constant (k(HOCl)) to nearly double and oxidation b

167 at 0.2 mg*mL(-1) and the highest hydrolysis rate constant (k(obt)).

168 ed k(d) and particle-associated inactivation rate constant (k(p)).

169 The surface area-normalized rate constant (k(SA)) showed a strong pH dependency betw

170 The total quenching rate constant (k(T)) of singlet oxygen of the alkene sur

171 Motor detachment rate constants (k (off)) can be measured via single-mole

172 molecule experiments, but motor reattachment rate constants (k (on)) are generally unknown, as they i

173 The E-I E-II exchange rate constants (k(ex)(185 K)) for different catalyst-sub

174 eased rapidly and irreversibly, with removal rate constants (k(H(2)O(2))) 17-73 times larger than air

175 ed and become lower than the radiative decay rate constants (k(r) = 10(5) s(-1)).

176 ate law for both Mg anode materials, and the rate constants (k) depended upon the struvite layer morp

177 Total PAH fomration rate constants (k) increased with the drying temperature

178 by IR spectroscopy, temperature-independent rate constants (k~1.4x10(-3) s(-1) ; half-life of ~8 min

179 ward volume transfer constant [K(trans)] and rate constant [K(ep)]) and apparent diffusion coefficien

180 Among the rate constants, k(d) better highlighted oxidizabilities

181 PFA, with determined ICT-based inactivation rate constants, k(d), of 1.024 +/- 0.038 L/(mg.min) and

182 K(eq), that span ~6 orders and dissociation rate constants, k(diss), that span ~7 orders of magnitud

183 epsilon decreases with increasing reduction rate constants normalized by cell density and initial U(

184 f ligand binding in the MFED and the kinetic rate constants observed agree with independent measureme

185 )O, and HOCl were computed from experimental rate constants obtained at various pH values, [Cl(-)], a

186 y chain-carrying HO(2)(*) occurs with a high rate constant of >=6 x 10(8) M(-1) s(-1) (toluene).

187 ion of sulfinate is also significant, with a rate constant of (4.1 +/- 0.6) x 10(6) M(-1) s(-1) in me

188 emely fast redox kinetics (electron-transfer rate constant of 0.32 cm s(-1) ), excellent stability in

189 ) undergoes cyclopropane ring opening with a rate constant of 1.7 x 10(8) s(-1), demonstrating that l

190 acts with internalized NO with a bimolecular rate constant of 10(10) M(-1) s(-1) forming nitrate, whi

191 with the cysteine of GSH, with a calculated rate constant of 2 x 10(5) m(-1) s(-1) (pH 8.0, 23 degre

192 boxyl moieties of Finland trityl with a high rate constant of 3.53 x 10(8) M(-1) s(-1), leading to a

193 This contrasts with the CVT rate constant of 8.0 x 10(-15) s(-1) at 80 K.

194 e-lapse fluorescence microscopy to measure a rate constant of a catalytic reaction in individual cell

195 nts is robust, with an intrinsic association rate constant of a magnitude similar to that mediating m

196 ared excitons and surface plasmons, with the rate constant of about 5.7 x 10(7) s(-1).

197 well-mixed ODE model is that the association rate constant of binding reactions is multiplied by a co

198 This indicates that the dissociation rate constant of DOX from lung tissue components is very

199 We found that the catalytic rate constant of DUBA is enhanced by phosphorylation.

200 In addition, the observed rate constant of EBS increased in the presence of sorbic

201 fficient (D), rate of nucleation (N(0)), and rate constant of electrolyte decomposition (k(SEI)), can

202 In apple and orange juices, the reaction rate constant of glucosone formation was found higher th

203 The photolysis rate constant of HNO(3(s)) varied with D(HNO3) and surfa

204 Photolysis rate constant of HNO(3) on the surface (HNO(3(s))) has b

205 terms of initial hydrolysis rate, r(0), and rate constant of hydrolysis, k(h), and enzyme inactivati

206 ent removal kinetics with a maximum apparent rate constant of k ~1 x 10(4) M(-1) s(-1) at pH >= 9.

207 With an apparent rate constant of k(O3) = (1.8 +/- 0.7) x 10(3) M(-1) s(-

208 n undergoes cyclopropane ring opening with a rate constant of only 4.1 x 10(4) s(-1), too slow to com

209 The deprotonation rate constant of radical-cations (k(H)) of 10(5) s(-1) a

210 the distal histidine (His211); (2) The decay rate constant of the ferryl intermediate is not strongly

211 The rate constant of the fluorescence decrease was determine

212 nsitivity across all species was the killing rate constant of the GUTS-RED-SD model (the reduced gene

213 tions (k(H)) of 10(5) s(-1) and the reaction rate constant of the phenoxy radicals (k(R)) in the orde

214 The second-order rate constant of the QMSH is ~0.631 L mg(-1) min(-1) , w

215 the QDs with isonicotinic acid increases the rate constant of this reaction by a factor of 2.4 by col

216 The rate constant of this reaction is determined by hyperpol

217 l indicated a relatively low estimate of the rate constant of tracer trapping, suggesting that the 1-

218 At pH > 8, the rate constant of Y(32)(*) formation (k(PCET)) increases

219 WT Cel7A had on/off-rate constants of 1 x 10(5) m(-1) s(-1) and 5 x 10(-3) s

220 in a sequence of second-order reactions with rate constants of 4.0 +/- 0.4, 2.7 +/- 0.3, and 0.28 +/-

221 erved for carbon-normalized photodegradation rate constants of atorvastatin, carbamazepine, and venla

222 tivariate models to predict the second order rate constants of bioorthogonal inverse-electron demand

223 The boron adsorption rate constants of both frameworks, determined via a pseu

224 f this work, including oxidation bimolecular rate constants of CPA and CPA analogs (~9 x 10(8) to 4 x

225 )O in data modeling could yield second-order rate constants of dubious validity.

226 r the first time that the pseudo-first-order rate constants of fast bimolecular processes in solution

227 dical clocks have been used to determine the rate constants of HAT reactions (k(H)), but no radical c

228 ange of conditions allowed estimation of the rate constants of PAA with (*)OH (k((*)OH/PAA) = 1.3 +/-

229 no radical clock is available to measure the rate constants of PRA reactions (k(add)).

230 constants between DNA and Ag(+), the kinetic rate constants of sequence-specific Ag(+) reduction path

231 Decay rate constants of short-tailed mRNAs vary broadly (1000-

232 molecule imaging in human cells to determine rate constants of the AGO2 cleavage cycle in vivo.

233 The rate constants of the CH(3) OH + OH reaction catalyzed b

234 rowth conditions as well as in the catalytic rate constants of the corresponding enzymes.

235 The computed rate constants of the HO(*) radical scavenging of SA wer

236 Removal rate constants of the majority of reactive TrOCs were hi

237 It was shown that the rate constants of the phthalimide-N-oxyl radicals' self-

238 We determined the rate constants of the reaction between [Formula: see tex

239 s utilized to determine kinetic profiles and rate constants of the reaction uncovering o-quinone meth

240 We obtained the rate constants of the steps by steady-state and pre-stea

241 egradation, and DNA damage repair) and using rate constants of these reactions to establish accurate

242 investigate the dependence of the effective rate constant on temperature.

243 The shallower dependence of the PCET rate constant on the ET donor-acceptor distance is expla

244 The dependence of the rate constants on the Gutmann donor numbers was shown.

245 xponential voltage-dependent gating variable rate constants, parameterized to fit experimental iPSC-C

246 The system was robust to reaction rate constant perturbations.

247 Fitted zero-order rate constants ranged from 50 to 510 mg L(-1) d(-1), and

248 om 50 to 510 mg L(-1) d(-1), and first-order rate constants ranged from 60 to 400 d(-1), which agree

249 alues characterizing the extraction process (rate constants ranging from 0.21 to 0.01 min(-1) for the

250 y present in the catalyst resting state, the rate constants reflect confining environments exclusivel

251 erature effect on the kinetic parameters and rate constants representing lipid hydroperoxides (LOOH)

252 methods by using many kinetic parameters and rate constants representing the two phases.

253 input data and the lack of uptake/depuration rate constants required for the TK model.

254 tion of the relevant equilibrium binding and rate constants requires the appropriate analysis of not

255 Theoretical analysis of these exchange rate constants revealed the involvement of an intermedia

256 molecular dynamics simulations predict that rate constants should be exquisitely sensitive to the ch

257 measured their (1)O(2) bimolecular reaction rate constants, showing slow photooxidation under enviro

258 pon hydroxylation, oxidation occurred with a rate constant similar to the k (cat) The structure of As

259 We find that post-replication remethylation rate constants span approximately two orders of magnitud

260 The energetics of binding and the rate constants suggest that the first step is copper com

261 encounter duration rather than a standard on-rate constant, suggesting that membrane fluidity and dyn

262 Yet, those with intermediate decay-rate constants switched from reaction limitation to tran

263 Gln intracellular transport, was the kinetic rate constant that was most correlated both with SUV at

264 The results provide estimates for rate constants that define a diffusion-reaction model fo

265 , glutamate binding with a diffusion-limited rate constant to iGlu(h) and Fl-GluBP is detected for th

266 e parent ferrocene, leading the dissociation rate constant to increase by several orders of magnitude

267 planation for the greater sensitivity of the rate constant to the carboxylate basicity than to the re

268 riability of predicted sunlight inactivation rate constants to different factors.

269 is provided well-constrained values for nine rate constants to establish a complete free-energy profi

270 s, enabling the large range in deadenylation rate constants to impart a similarly large range in stab

271 ial selection is achieved by larger backward rate constants toward TC dissociation rather than by a s

272 ecies have an enhanced catalytic impact with rate constants up to 1000 times larger than would be est

273 s utilized to predict the ratio of quenching rate constants upon changing the PC, enabling selection

274 ree descriptors with experimental activation rate constants using multivariate linear regression.

275 Second-order rate constants utilizing C-H and C-D substrates were obt

276 arison with a water-benzene mixture, and the rate constant values depend on the type of surfactant us

277 The measured ET rate constant values, from Laviron analysis, are also hi

278 r, the magnitude and accuracy of the binding rate constant-values was highly dependent on the used ra

279 critical for NO(2)(-) precursor ions, whose rate constant varied as a function of NO(2) concentratio

280 Potential methylation rate constants varied 52-fold across the experiment.

281 n of the fluorenyl-benzoate follows the same rate constant vs driving force trend determined for ther

282 The K1 rate constant was converted to MBF using previously dete

283 Especially the off-rate constant was many orders of magnitude lower than ty

284 d transducers - k(o) (standard heterogeneous rate constant) was 2.56 x 10(-3) cm(2)/s (nu = 100 mV/s

285 ddition to establishing a HuNoV inactivation rate constant, we developed an approach using a single q

286 Pseudo-first-order rate constants were determined for the Friedel-Crafts al

287 The second-order rate constants were determined in competition kinetic ex

288 and, binding (k'(on)) and unbinding (k(off)) rate constants were extracted from (1)H-(1)H exchange sp

289 Furthermore, the association rate constants were lower when algae were exposed to MeH

290 as well as actin-activated phosphate release rate constants were not significantly different from WT.

291 The corresponding fragmentation rate constants were translated into a vibrational effect

292 The rate constants were used to evaluate the possible compet

293 less shallow distance dependence of the PCET rate constant when imidazole rather than hydrogen phosph

294 ration efficiency, there was a wide range of rate constants when incorporating a correct nucleotide o

295 e maximum ATP hydrolysis and recovery-stroke rate constants, whereas the F750L mutation enhanced thes

296 e a broad (1000-fold) range of deadenylation rate constants, which correspond to cytoplasmic lifetime

297 for this metal, (ii) the first-order in-line rate constant with respect to divalent cations is >200 t

298 nopeptidase showed second-order inactivation rate constants with (1)O(2) comparable to those of free

299 Measured rate constants with OH radicals were (1.20 +/- 0.09) x 1

300 s useful to quantify the interaction kinetic rate constants without using the traditional single-mole