ライフサイエンスコーパス: oxidation-reduction

1 wo-electron, two-proton hydroquinone-quinone oxidation-reduction.

2 ion to a Paterno-Buchi-like product, without oxidation/reduction.

3 ons in terms of anion adsorption and surface oxidation/reduction.

4 ns which undergo charge change upon cofactor oxidation/reduction.

5 ly reproduce natural proton coupling to heme oxidation/reduction.

6 nal dithiols competent to undergo reversible oxidation/reduction.

7 e from each EC classification, including (i) oxidation-reduction activity of DHFR (EC 1.5.1.3); (ii)

8 ally interesting compound due to its unusual oxidation-reduction activity.

9 ith 4R or 4S stereochemistry, via Mitsunobu, oxidation, reduction, acylation, and substitution reacti

10 mical transformations, including alkylation, oxidation, reduction, acylation, and the use of a variet

11 ce of nitrosative stress without appropriate oxidation-reduction adaptation, whereas 3-NT modificatio

12 38, while stereotetrad 13 is accessed by an oxidation/reduction alcohol inversion sequence from ster

13 re induced by stressors, such as spontaneous oxidation/reduction, alkylation, and hyperthermia.

14 ls have layer structures and readily undergo oxidation reduction and cation-exchange reactions and pl

15 tein disulfide isomerase (PDI) catalyzes the oxidation reduction and isomerization of disulfide bonds

16 These include a wide range of oxidation reduction and metabolic genes, as well as gene

17 or 538 genes involved in primary metabolism, oxidation reduction and response to stimulus was changed

18 crucial for cycling sulfur compounds through oxidation, reduction and disproportionation reactions, f

19 a wide range of chemical reactions including oxidation, reduction and epimerisation.

20 in the expression of genes with key roles in oxidation-reduction and an associated accumulation of re

21 tenoids in the human eye involve a series of oxidation-reduction and double-bond isomerization reacti

22 Redox tumours are enriched for oxidation-reduction and glutathione pathways and harbor

23 arate, and succinate) influenced by cellular oxidation-reduction and involved in HIF1alpha hydroxylat

24 atrix are up-regulated by TGF-beta1, whereas oxidation-reduction and steroid metabolic process are do

25 henotype of FLC resistance, the processes of oxidation-reduction and transmembrane transport were det

26 By ruling out oxidation/reduction and compositional unmixing, we infer

27 that eliminates electrolysis-caused protein oxidation/reduction and constrains proteins in the desir

28 trons between the site of succinate-fumarate oxidation/reduction and the membrane domain harboring th

29 brane," "cytochrome P450," "microsome," and "oxidation reduction") and moderate CP ("regulation of ge

30 on control applications (selective catalytic oxidation/reduction) and during some industrial processe

31 These metabolites demonstrated that oxidation, reduction, and conjugation reactions were the

32 isulfide isomerase (PDI), catalyze disulfide oxidation, reduction, and isomerization, thereby playing

33 ze numerous mechanistic strategies involving oxidation, reduction, and substitution.

34 5,6-double bond of pyrimidines is subject to oxidation, reduction, and/or hydration in the DNA of org

35 al transmembrane potential, altered cellular oxidation-reduction, and participation of pro- and antia

36 ovides details of the biochemical, spectral, oxidation-reduction, and steady-state kinetic properties

37 solvents exhibits five stages of reversible oxidation/reduction, and hence fullerene can work either

38 re converted into 1,2-cis glycosides through oxidation-reduction as the key functional group transfor

39 in vitro antioxidative capacity by LC-MS and oxidation/reduction assay based methods.

40 the QTL affects multiple photosynthesis and oxidation-reduction associated genes in the immature gre

41 NosX and RnfF, which have been implicated in oxidation-reduction associated with nitrous oxide and ni

42 ometre-thick layers of dry glass and undergo oxidation/reduction at the buried platinum surface.

43 eaks were observed corresponding to the DNPs oxidation/reduction at the underlying gold electrode, wh

44 idant synergy and disruption of the reaction oxidation-reduction balance.

45 chieved by the coordinate control of various oxidation-reduction balancing mechanisms during phototro

46 on the photophysical and thermal properties, oxidation-reduction behavior, and dyeing performance was

47 ndicate that young animals have an effective oxidation-reduction buffering system in the liver that p

48 Rather, pH, oxygen, and oxidation reduction changes were restricted to the corne

49 ng CeO(2-x) electrodes undergo Ce(3+)/Ce(4+) oxidation-reduction changes with applied bias.

50 PLC exhibits reversible oxidation-reduction chemistry involving the thiol groups

51 The synthesis, electronic structure, and oxidation-reduction chemistry of a homologous series of

52 idazo-7,9-dimethoxycarbonyl analogues of the oxidation-reduction cofactor pyrroloquinoline quinone [4

53 These catalytic "oxidation-reduction condensation" reactions are carried

54 generation of S-acylthiosalicylamides under oxidation-reduction-condensation conditions from a varie

55 e previously described a new organocatalytic oxidation-reduction-condensation for amide/peptide const

56 highly effective and robust organocatalytic oxidation-reduction-condensation reactions that are base

57 that viral protease activity is sensitive to oxidation-reduction conditions, and that the viral prote

58 switch from fast to slow inactivation under oxidation/reduction conditions.

59 The reversible oxidation-reduction cycle of methionine involving MSRs h

60 amines when used as part of a chemoenzymatic oxidation-reduction cycle.

61 state and thereby minimizes potential futile oxidation-reduction cycles and may also enhance ERAD, wh

62 ings since Fe-rich clays commonly go through oxidation-reduction cycles in response to changing redox

63 Here we show that oxidation-reduction cycles of peroxiredoxin proteins con

64 micity, supported by the recent discovery of oxidation-reduction cycles of peroxiredoxin proteins, wh

65 The electrical charge involved in oxidation-reduction cycles of the osmium sites, the elli

66 nce dynamically shifting through competitive oxidation-reduction cycles.

67 p to 86 % of their charge capacity over 1000 oxidation/reduction cycles, despite the typical lability

68 >95% of its electrochromic response over 100 oxidation/reduction cycles.

69 ar expansion that persists across subsequent oxidation/reduction cycles.

70 crystallinity and porosity even after three oxidation/reduction cycles.

71 the capacity of the antioxidants to undergo oxidation-reduction cycling, implicating oxidative signa

72 n the natural products and (2) an integrated oxidation/reduction/cyclization (iORC) sequence for skel

73 ments for total synthesis, and unprecedented oxidation/reduction/cyclization processes were developed

74 ned genes to transform As, Hg and Cr through oxidation, reduction, efflux and demethylation, suggesti

75 This multicenter oxidation-reduction enzyme utilizes either NADH or NADPH

76 was a specific substrate of the multidomain oxidation-reduction enzyme, Mical, a poorly understood a

77 , along with studies of the pH dependence of oxidation/reduction equilibria, to identify and characte

78 electron-transport chain and regulated by an oxidation-reduction equilibrium of reactive oxygen inter

79 own agent 17-AAG in vitro and in vivo via an oxidation-reduction equilibrium, and we demonstrate that

80 y are about 2 orders of magnitude higher (in oxidation/reduction equivalents) than in previously expl

81 of substrate availability and obstruction of oxidation-reduction events.

82 II) surface sites at goethite in response to oxidation/reduction events.

83 ulant heparins produced by N-acetylation and oxidation/reduction (glycol-split) that lost antithrombi

84 Antioxidant systems maintain cellular redox (oxidation-reduction) homeostasis.

85 , atomic layer deposition, electrochemistry, oxidation, reduction, hydrolysis, the use of radicals an

86 Proteins involved in oxidation-reduction (i.e., LOX1/5), carbohydrate metabol

87 e cellular responses to oxidative stress and oxidation-reduction imbalance and the role of NF-kappaB

88 g of Pt(111) electrodes upon electrochemical oxidation/reduction in 0.1 M HClO4 was studied by in sit

89 the elucidation of the mechanism of quinone oxidation/reduction in the E. coli enzyme.

90 containing pH indicators, Lewis acids and an oxidation-reduction indicator.

91 Tyrosine oxidation-reduction involves proton-coupled electron tra

92 exchange with aqueous media coupled to heme oxidation/reduction is commonly seen but not understood

93 ns triggered by one-electron electrochemical oxidation/reduction is investigated by using pyridylbenz

94 which have different midpoint potentials and oxidation/reduction kinetics.

95 ely target of NO and other oxidants and that oxidation/reduction may serve as a mechanism for control

96 Thus, in vivo pH, oxygen, and oxidation reduction measurements were performed in the a

97 e at the level of the nucleotide sugar by an oxidation/reduction mechanism in the active site of the

98 of differentially expressed genes related to oxidation-reduction, metabolic process and protein catab

99 The oxidation--reduction midpoint potential of the donor is

100 The oxidation-reduction midpoint potential (E(m)) value beco

101 Two distinct oxidation-reduction midpoint potential (E(m)) values of

102 Oxidation-reduction midpoint potential (E(m)) values, at

103 Oxidation-reduction midpoint potential (E(m)) versus pH

104 complex formation significantly lowered the oxidation-reduction midpoint potential (Em) value of ami

105 It was also shown that the oxidation-reduction midpoint potential for AADH is 20 mV

106 One factor in this ability is a high oxidation-reduction midpoint potential for the dimer, al

107 related to functional properties such as the oxidation-reduction midpoint potential.

108 Oxidation-reduction midpoint potentials (E(m)) have been

109 Oxidation-reduction midpoint potentials were determined,

110 efers to the specific and usually reversible oxidation/reduction modification of molecules involved i

111 In the voltammetry measurements, W32 oxidation-reduction occurs on a time scale of about 4 ms

112 Oxidation-reduction of both hemes displays an unusually

113 Ilicicolin blocks oxidation-reduction of cytochrome b through center N of

114 oxidation-reduction, the data indicate that oxidation-reduction of the dehydrogenase flavin is not e

115 ns among these conformers that are linked to oxidation-reduction of the flavin can modulate the redox

116 Recently, oxidation/reduction of active-site cysteines of PTPs, in

117 lyte ion activity detection triggered by the oxidation/reduction of an underlying poly(3-octylthiophe

118 This feature allows exhaustive oxidation/reduction of certain analytes within typical e

119 c archaea use a [NiFe]-hydrogenase, Frh, for oxidation/reduction of F420, an important hydride carrie

120 r spectroelectrochemical response during the oxidation/reduction of ferrocenemethanol.

121 tics of malate dehydrogenase (MDH) catalyzed oxidation/reduction of L-malate/oxaloacetate is pH-depen

122 chanism for cytoplasmic MDH (cMDH) catalyzed oxidation/reduction of MAL/OAA.

123 ce oxides and dynamically tune the degree of oxidation/reduction of metals at/near the catalyst surfa

124 Dehydrogenases catalyzing the reversible oxidation/reduction of retinol and retinal are members o

125 mical activation of the nitroxyl fragment by oxidation/reduction of selected functions.

126 orts the chemical and kinetic competence for oxidation/reduction of the active-site cysteines of Cdc2

127 nt types of external intervention, i.e., via oxidation/reduction of the metal template and/or change

128 redox active amino acid side chain and that oxidation/reduction of the proximal Trp is important in

129 Oxidation/reduction of thiol residues in proteins is an

130 the imidazole ring facilitates the efficient oxidation/reduction of tyrosine D.

131 associated electrochemically induced polymer oxidation/reduction on multiple electrodes.

132 -guest charge transfer, resulting in partial oxidation, reduction or covalent modification of the gra

133 ication of the pyrimidine 5,6-double bond by oxidation, reduction or hydration.

134 their ability to modify sulfhydryl groups by oxidation, reduction, or alkylation.

135 e, Ta(CNDipp)6 undergoes facile one-electron oxidation, reduction, or disproportionation reactions.

136 biquitous thioredoxin fold proteins catalyze oxidation, reduction, or disulfide exchange reactions de

137 tiple substrates; and it can catalyze either oxidation, reduction, or isomerization of substrates.

138 This step is thought to proceed by an oxidation-reduction-oxidation sequence, in which the NAD

139 apably to a more subtle reaction sequence of oxidation-reduction-oxidation.

140 ogical manipulations to demonstrate that the oxidation-reduction pathway causally underpins the detri

141 e, cysteine sulfinic acid decarboxylase, and oxidation-reduction pathway genes.

142 rotein disulfide intermediate of the overall oxidation-reduction pathway.

143 ere significantly enriched in members of the oxidation-reduction pathway.

144 there is an absolute requirement for the C1 oxidation/reduction pathway for hydrogenotrophic and met

145 enes encoding the enzymes involved in the C1 oxidation/reduction pathway were constructed.

146 Taking the oxidation/reduction peak ratios from CV as analytical si

147 d pH dependence of the current amplitude and oxidation/reduction peaks, the catalytic mechanism is an

148 he tuning of the particle size of CN(x), the oxidation-reduction photochemistry of carbon nitride may

149 Measuring the oxidation-reduction potential (Eh) requires an interface

150 Midpoint oxidation-reduction potential (Em) values at pH 7.0 of -

151 to the formal potential of the two standard oxidation-reduction potential (ORP) calibrants, ZoBell's

152 ons, total organic carbon (TOC) amounts, and oxidation-reduction potential (ORP) displayed significan

153 ngs (N2Mix); and air injections triggered by oxidation-reduction potential (ORP) of <=-40 mV (RedoxCo

154 onductivity (EC), chlorophyll-a (Chl-a), pH, oxidation-reduction potential (ORP), and dissolved oxyge

155 , conductivity, d(2)H, and d(18)O, but lower oxidation-reduction potential and d(11)B, relative to th

156 Apart from these parameters, also local oxidation-reduction potential and electric field potenti

157 The overall two-electron oxidation-reduction potential of 4'-deoxy-FAD in solutio

158 l technique was used to measure the midpoint oxidation-reduction potential of PdR that had been caref

159 This is in accord with the high oxidation-reduction potential of the flavin, which therm

160 The oxidation-reduction potential of the new flavin was dete

161 Photoreduction and oxidation-reduction potential studies reveal that the S.

162 sulatus to maintain a balanced intracellular oxidation-reduction potential was considered; in additio

163 s pH, oxygen concentration, temperature, and oxidation-reduction potential were found to be significa

164 chain reaction analyses of CB1190 abundance, oxidation-reduction potential, and dissolved oxygen meas

165 snow shows increased levels of pollen, lower oxidation-reduction potential, decreased algal and incre

166 nm, which was used to determine the midpoint oxidation-reduction potential, which is +359 +/- 7 mV at

167 ecrease the pH of the water and increase the oxidation-reduction potential, which promotes the oxidat

168 ith biosolid pH, organic carbon content, and oxidation-reduction potential.

169 ess the interplay of vitamin levels with the oxidation/reduction potential in human feces and saliva.

170 We also discuss how changes in the oxidation/reduction potential may affect the function of

171 ota balance by rapid noninvasive on-the-spot oxidation/reduction potential monitoring for frequent an

172 Oxidation-reduction potentials (E degrees ', n = 2) for

173 which is evidenced by the parallel trends in oxidation-reduction potentials (ORP) and Tc dissolution

174 flavodoxins, with 169-176 residues, display oxidation-reduction potentials at pH 7 that vary from -5

175 lding and similar flavin environments, while oxidation-reduction potentials for the FAD/FADH2 couple

176 nd engineering systems based on the reported oxidation-reduction potentials of quinones/semiquinones

177 ought to contribute to the modulation of the oxidation-reduction potentials of the cofactor.

178 MMOR alters the oxidation-reduction potentials of the dinuclear iron clu

179 he neutral semiquinone and in modulating the oxidation-reduction potentials of the flavin cofactor in

180 gher) with those analogues exhibiting higher oxidation-reduction potentials than normal flavin and de

181 eptors, electron donors, carbon sources, and oxidation-reduction potentials, (ii) analyses of PFAS bi

182 lity to temperature and chemical denaturant, oxidation-reduction potentials, and electron-transfer ki

183 cid sequence alignments, molecular modeling, oxidation-reduction potentials, and spectral properties

184 The oxidation-reduction potentials, Eox/EH2 (two-electron re

185 ccurring at pH 4-6, 50-70 degrees C, and low oxidation-reduction potentials.

186 on Transport (GO:0006811; FDR 2.08E-02), and Oxidation-Reduction Process (GO:0055114; FDR 1.58E-07).

187 , conserving the free energy released by the oxidation-reduction process in the form of an electroche

188 cytochrome c oxidase undergo a two-electron oxidation-reduction process with added peroxynitrite, le

189 iological processes included photosynthesis, oxidation-reduction process, chlorophyll biosynthetic pr

190 4 significantly enriched GO terms, including oxidation-reduction process, metabolic process, and cata

191 gnal transduction, translation, and obsolete oxidation-reduction process.

192 These changes primarily affect oxidation-reduction processes and have a major effect on

193 tions in GO, which are indicative of surface oxidation-reduction processes or substituent doping (bor

194 rocatalysis have been widely used to conduct oxidation-reduction processes ranging from fuel generati

195 posures and are believed to be the result of oxidation-reduction processes that fill or create oxygen

196 design of bioinspired molecules that employ oxidation-reduction processes to move reversibly two, th

197 eral were categorized in gene ontology terms oxidation-reduction processes, ATP binding and ATPase ac

198 as critical monitors and modulators of vital oxidation-reduction processes, including mitochondrial b

199 l-tryptophan's role in protein catalysis of oxidation-reduction processes.

200 ession of Pc genes, mainly those involved in oxidation-reduction processes.

201 romodulatory G-protein coupled receptors and oxidation-reduction processes.

202 tion metal L-edges to gain insights into the oxidation/reduction processes of positive and negative a

203 site trends suggest potential photo- or dark oxidation/reduction processes within the ice and an even

204 ical and biochemical transformations involve oxidation/reduction processes, developing practical bioc

205 tional glutamates before pH-independent heme oxidation/reduction profiles are achieved.

206 thylotrophus (sp. W(3)A(1)) exhibits unusual oxidation-reduction properties and can only be reduced t

207 The results indicate that the oxidation-reduction properties of ETF are perturbed upon

208 er complex, which modulates the spectral and oxidation-reduction properties of ETF such that full red

209 plays an important role in establishing the oxidation-reduction properties of the bound cofactor as

210 We first examined redox (oxidation/reduction) properties and stability of 3-NT in

211 as the source of the reactive oxygen driving oxidation-reduction protein signaling in the epithelium.

212 An oxidation/reduction protocol was employed to set the C37

213 r could be recycled to the desired one by an oxidation/reduction protocol.

214 fide is electrochemically active, undergoing oxidation/reduction rather than chromium.

215 Our approach utilizes an oxidation-reduction reaction between ascorbic acid and m

216 counting method is conducted on the basis of oxidation-reduction reaction between hydrogen peroxide a

217 m the 4' position of the substrate after the oxidation-reduction reaction in the enzyme.

218 By this means, the endothermic oxidation-reduction reaction is pulled such that the ove

219 metallic complexes exhibit a special type of oxidation-reduction reaction that could directly split c

220 dinucleotide (NAD), a metabolite involved in oxidation-reduction reactions and in ATP synthesis.

221 This class of proteins largely functions in oxidation-reduction reactions and is critically involved

222 ontaining compound glutathione can influence oxidation-reduction reactions and perhaps disulfide bond

223 decomposition of the explosive and specific oxidation-reduction reactions between the energetic mole

224 least 2,500 km, thus demonstrating that self-oxidation-reduction reactions can preserve carbonates in

225 CET) is a fundamental process at the core of oxidation-reduction reactions for energy conversion.

226 ound such structural ambiguity is to examine oxidation-reduction reactions in protein crystals.

227 ly bound structure (ultrafast dynamics), and oxidation-reduction reactions in the latter prefer the f

228 inoid dehydrogenases/reductases catalyze key oxidation-reduction reactions in the visual cycle that c

229 Moreover, AA participates in many cellular oxidation-reduction reactions including hydroxylation of

230 lates glutaconyl-CoA to crotonyl-CoA without oxidation-reduction reactions of the dehydrogenase flavi

231 est that methane activation proceeds through oxidation-reduction reactions on the surface of catalyst

232 This picture also applies to other oxidation-reduction reactions over high work function me

233 FAD) interacts with flavoproteins to mediate oxidation-reduction reactions required for cellular ener

234 om aqueous waste streams via sorption and/or oxidation-reduction reactions show promise as eco-friend

235 na may be interconverted through a series of oxidation-reduction reactions similar to our earlier pro

236 be indispensable in a multitude of cellular oxidation-reduction reactions through its conversion to

237 Oxidation-reduction reactions underlie energy generation

238 of enzymes responsible for the catalysis of oxidation-reduction reactions, crucial in most bioenerge

239 These modular clusters undergo oxidation-reduction reactions, may be inserted or remove

240 Oxidation-reduction reactions, spectroelectrochemical st

241 e processes underlying PAE9 activity involve oxidation-reduction reactions.

242 ectron transport and helps to avoid unwanted oxidation-reduction reactions.

243 ability to participate in a diverse array of oxidation-reduction reactions.

244 een microbial communities and biogeochemical oxidation-reduction reactions.

245 orting the activity of enzymes that catalyze oxidation-reduction reactions.

246 and mobility is affected by microbes through oxidation/reduction reactions as part of resistance and

247 mplex, Ru(bpy)(3), that undergoes reversible oxidation/reduction reactions at both positive and negat

248 Oxidation/reduction reactions at metal oxide surfaces ar

249 on to mineral surfaces, and microbe-mediated oxidation/reduction reactions at the bacterial exterior

250 ate that Asp26 serves as an acid/base in the oxidation/reduction reactions catalyzed by Trx.

251 ion, diphenyleneiodonium was used to inhibit oxidation/reduction reactions in the cell.

252 We examined 1956 oxidation/reduction reactions in the KEGG database.

253 ity, in turn, is highly regulated in vivo by oxidation/reduction reactions involving the cysteine thi

254 to be regulated by changes in intracellular oxidation/reduction reactions involving the redox factor

255 Oxidation/reduction reactions of protein thiol groups (P

256 etal-redox strategy that employs spontaneous oxidation/reduction reactions to grow nanocrystalline al

257 gen and enzymes that catalyze glycolysis and oxidation/reduction reactions.

258 ge class of enzymes that catalyze biological oxidation/reduction reactions.

259 1979 led to the discovery of four additional oxidation-reduction (redox) cofactors, all of which resu

260 Here, we quantified how oxidation-reduction (redox) conditions impact the fate o

261 But the roles of the cellular oxidation-reduction (redox) environment in SOD1 folding

262 iently form disulfide bonds while catalyzing oxidation-reduction (redox) processes.

263 The optical oxidation-reduction (redox) ratio is a measure of cellul

264 Oxidation-reduction (redox) reactions are central to the

265 energy for cellular functions by catalyzing oxidation-reduction (redox) reactions that are out of eq

266 n functionally characterized are involved in oxidation-reduction (redox) reactions, with the Sec resi

267 To evaluate oxidation-reduction (redox) regulation of NRF-1 in Tfam

268 ch as ATP production, anabolism and cellular oxidation-reduction (redox) regulation.

269 In recent years, the intracellular oxidation-reduction (redox) state has gained increasing

270 Trace metal levels, including oxidation-reduction (redox)-active metal ions credited w

271 The hypothesis that intracellular oxidation/reduction (redox) reactions regulate the G(0)-

272 proteins and their functions have effect on oxidation-reduction regulation and antibiotic resistance

273 relevant gene expression, such as cytokines, oxidation-reduction-related enzymes, and adhesion molecu

274 regulating co-expression modules involved in oxidation reduction, response to water deprivation, plas

275 th the mitochondrial and cytosolic forms are oxidation-reduction sensitive, as indicated by a change

276 ereoselective epoxidation, fluorination, and oxidation-reduction sequence of the Vince lactam in 14 s

277 compounds from allylic alcohols involving an oxidation-reduction sequence, this protocol provides fun

278 of the secondary alcohol was effected via an oxidation-reduction sequence.

279 the central disaccharide from lactal via an oxidation-reduction sequence.

280 e unwanted aldol product was subjected to an oxidation/reduction sequence to rectify the C35 stereoce

281 y, electrochemical lignin degradation via an oxidation/reduction sequence under mild conditions has g

282 y neutrophils and gain new insight into this oxidation-reduction signaling, epithelial cells were tre

283 Oxidation-reduction spectroscopy and flow cytometry indi

284 s like diamide, which are known to alter the oxidation reduction state of the glutathione pool.

285 ma(R) (SigR), is increased by changes in the oxidation-reduction state of cytoplasmic disulphide bond

286 (P)H/NAD(P)H + FAD], was used to measure the oxidation-reduction state of PDCOs.

287 ing that the channel may be regulated by the oxidation-reduction state of the cell.

288 e respiratory pathway, thereby affecting the oxidation/reduction state of the ubiquinone pool, leadin

289 response to oxidants or changes in cellular oxidation-reduction status.

290 These results demonstrate that the oxidation/reduction status of the NTPase, the only paras

291 When combined with other kinetic and oxidation/reduction studies of this enzyme, these result

292 ical potential (E( plus sign in circle)) for oxidation/reduction that allows cysteine-containing prot

293 In the absence of detectable oxidation-reduction, the data indicate that oxidation-re

294 Oxidation-reduction titrations for the active-site disul

295 Oxidation-reduction titrations reveal the presence of tw

296 es and to retain the strong coupling of heme oxidation-reduction to glutamate acid-base transitions a

297 no acids in proteins that undergo reversible oxidation/reduction under biologic conditions and, as su

298 haved and exhibited characteristic porphyrin oxidation/reduction waves.

299 versible switch in the DNA-bound signal with oxidation/reduction, which is inhibited by mutation of t

300 ed by hydrogen peroxide and the cycle of the oxidation/reduction would continue until all hydrogen pe