ライフサイエンスコーパス: oxidoreductase

1 respiratory complex II (succinate:ubiquinone oxidoreductase).

2 de (NO) via its reduction by tissue xanthine oxidoreductase.

3 some Tpx and, another, as yet unidentified, oxidoreductase.

4 of the highly conserved eukaryotic MIA40 IMS oxidoreductase.

5 ine, signature features of a thiol-disulfide oxidoreductase.

6 , along with the well-characterized xanthine oxidoreductase.

7 activated the oxidative half reaction of the oxidoreductase.

8 oreductase functioning as an ETF:menaquinone oxidoreductase.

9 that its primary function is as a disulfide oxidoreductase.

10 support the assignment of this protein as an oxidoreductase.

11 des through electron-transfer flavoprotein:Q-oxidoreductase.

12 carboxylic group by TcCHH, a cytochrome P450 oxidoreductase.

13 alyzed by dark-operative protochlorophyllide oxidoreductase.

14 pyruvate and alpha-ketoglutarate ferredoxin oxidoreductases.

15 from their (moderate) activity as disulfide oxidoreductases.

16 y through sortase A-mediated crosslinking of oxidoreductases.

17 tivity in this important and varied group of oxidoreductases.

18 ongs to the family of flavoprotein disulfide oxidoreductases.

19 gase, a fatty acid desaturase and associated oxidoreductases.

20 ansfer electrons to cyanobacterially encoded oxidoreductases.

21 NAD(P)H:quinone oxidoreductase 1 (NQO1) and mitochondrial complex III we

22 NAD(P)H:quinone oxidoreductase 1 (NQO1) appears to be the main intracell

23 -mediated repression of the NAD(P)H: quinone oxidoreductase 1 (NQO1) gene antioxidant response elemen

24 Nrf2 target antioxidant gene NAD(P)H-quinone oxidoreductase 1 (NQO1) in both glycolytic and oxidative

25 Elevated expression of NAD(P)H:quinone oxidoreductase 1 (NQO1) is frequent in pancreatic cancer

26 NAD(P)H:quinone oxidoreductase 1 (NQO1) is highly enriched in multiple t

27 NAD(P)H: quinone oxidoreductase 1 (NQO1) was the top oxidoreductase "hit"

28 .R139W and p.P187S) in human NAD(P)H quinone oxidoreductase 1 (NQO1), a FAD-dependent enzyme which ac

29 ated by high levels of Nrf2, NAD(P)H quinone oxidoreductase 1 (NQO1), heme oxygenase-1 (HO-1) and a h

30 ing agents, we synthesized a NAD(P)H quinone oxidoreductase 1 (NQO1)-activatable NIR fluorescent prob

31 Lapachone is bioactivated by NAD(P)H:quinone oxidoreductase 1 (NQO1).

32 ity and stability in vivo of NAD(P)H:quinone oxidoreductase 1 (NQO1).

33 trast to its next of a kind, NAD(P)H:quinone oxidoreductase 1 (NQO1).

34 igase catalytic subunit, and NAD(P)H quinone oxidoreductase 1 in macrophages.

35 those for heme oxygenase 1, NAD(P)H quinone oxidoreductase 1, and CD36.

36 side increased activities of NAD(P)H:Quinone Oxidoreductase 1, Carnitine Palmitoyl-CoA Transferase an

37 OS level in cancer cells via NAD(P)H:quinone oxidoreductase-1 (NQO1) catalysis, which induces the cas

38 Herein, a NAD(P)H:quinone oxidoreductase-1 (NQO1)-specific chemiluminescent probe

39 -mediated heme oxygenase-1 and NADPH quinone oxidoreductase-1 induction.

40 The protein expression of NAD(P)H quinone oxidoreductase-1, a major cellular antioxidant and detox

41 N-ribosyldihydronicotinamide:quinone oxidoreductase 2 (NQO2/QR2, Enzyme Commission number 1.1

42 tion of N-ribosyldihydronicotinamide:quinone oxidoreductase 2 while catalyzing the reduction of ortho

43 otein X), and nuoN (encoding NADH:ubiquinone oxidoreductase); 2) by investigating co-regulation of en

44 at MDM2 negatively regulates NADH:ubiquinone oxidoreductase 75 kDa Fe-S protein 1 (NDUFS1), leading t

45 Complex I (mitochondrial NADH:ubiquinone oxidoreductase), a membrane-bound redox-driven proton pu

46 and other eye components, and also xanthine oxidoreductase, a nitrate and nitrite reductase, in corn

47 ich encodes a membrane-bound thiol-disulfide oxidoreductase, abrogates pilus assembly and alters cell

48 tathione reductase family 2 of FAD-dependent oxidoreductases according to the structurally conserved

49 , i.e., with constant KIEs for each involved oxidoreductase across all species.

50 mechanistic repertoire of flavoenzymes with oxidoreductase activity and pave the way to explore new

51 to be integrally involved in regulating Trx oxidoreductase activity and that the regulation of Txnip

52 Dynamic control of thioredoxin (Trx) oxidoreductase activity is essential for balancing the n

53 on the binding to the IMS protein Mia40, the oxidoreductase activity of Mia40 is surprisingly dispens

54 a reassessment of PKCbeta regulation of the oxidoreductase activity of p66.

55 ar polysaccharide biosynthetic processes and oxidoreductase activity respectively.

56 HPP) treatments on the polyphenolic profile, oxidoreductase activity, colour, and browning index of c

57 anti-apoptotic Bcl-2 protein, impaired NADPH oxidoreductase activity, increased mitochondrial protein

58 zed by a metabolic shift, with impairment of oxidoreductase activity, pyruvate metabolism and the tri

59 ion of genes enriched in GO terms related to oxidoreductase activity, respiratory chain and other mit

60 e stress related to antioxidant activity and oxidoreductase activity.

61 has been difficult to prove because multiple oxidoreductases affect the NADPH pool simultaneously.

62 ation sequence, in which the NADPH-dependent oxidoreductase AflM catalyzes the enclosed reduction ste

63 A reduction in NADPH-protochlorophyllide oxidoreductase, along with photodegradation, has been su

64 binding region for the CYP46A1 redox partner oxidoreductase and found that the allosteric and redox p

65 M. girerdii encodes pyruvate-ferredoxin oxidoreductase and may be sensitive to metronidazole.

66 ifurcating NADH-dependent ferredoxin-NADP(+) oxidoreductase and the non-bifurcating flavoproteins nit

67 GPT1 contacted two oxidoreductases and also peroxins that mediate import of

68 , they appear with greatest frequency in the oxidoreductases and hydrolases.

69 as well as downregulation of genes encoding oxidoreductases and nutrient transporters, occurs in the

70 avoprotein "DDOR" (diflavin-linked disulfide oxidoreductase) and propose that its activity is linked

71 enriched protein targets in the thioredoxin, oxidoreductase, and protein disulfide isomerase (PDI) fa

72 n by the redox partner NADPH-cytochrome P450 oxidoreductase, and the amount of P450 reduced.

73 es secrete mixtures of glycoside hydrolases, oxidoreductases, and accessory enzymes to deconstruct po

74 udies, TaoR activates expression of aldehyde oxidoreductase aor and represses tungsten-specific ABC-t

75 Most modern oxidoreductases are complex in their structure and chemi

76 in mitochondrial complex I (NADH:ubiquinone oxidoreductase) are both genetically and clinically high

77 In order to address these two obstacles to oxidoreductase-based asymmetric synthesis, a biphasic bi

78 Two obstacles limit the application of oxidoreductase-based asymmetric synthesis.

79 Ubiquinol cytochrome c oxidoreductase (bc1 complex) serves as an important elec

80 isting of dark-operative protochlorophyllide oxidoreductase, BchF, and BchC.

81 Extensive studies with a range of oxidoreductases belonging to the "ene" reductase family

82 rhizospheres were the most diverse biomes in oxidoreductases but not in taxonomy.

83 Respiratory complex I (NADH:ubiquinone oxidoreductase) captures the free energy from oxidising

84 2-ketopropyl-coenzyme M oxidoreductase/carboxylase (2-KPCC) is a bacterial disul

85 s in primary adipocytes through the xanthine oxidoreductase-catalyzed reduction of nitrate to NO and

86 ly categorized into solute-binding proteins, oxidoreductases, cell envelope biosynthesis enzymes, and

87 ts as a substrate of the intermembrane space oxidoreductase CHCHD4 (also known as Mia40).

88 A, DoxX, and SseA form a membrane-associated oxidoreductase complex (MRC) that physically links radic

89 NDUFAF6 encodes NADH:ubiquinone oxidoreductase complex assembly factor 6, also known as

90 A homologous NADH:quinone oxidoreductase complex IA likely operates in the opposit

91 nesis was used to show that the NADH:quinone oxidoreductase complex IE was essential for phototrophic

92 NADH-ubiquinone oxidoreductase (complex I) is the largest ( approximatel

93 The activity of NADH:ubiquinone oxidoreductase (complex I) was inhibited by metformin.

94 iron-sulfur protein subunit of cytochrome c oxidoreductase (complex III of the electron transport ch

95 The FAD-dependent oxidoreductase-containing domain 1 (FOXRED1) protein is

96 Dark-operative protochlorophyllide oxidoreductase contains two [4Fe-4S]-containing componen

97 ial complex I (also known as NADH:ubiquinone oxidoreductase) contributes to cellular energy productio

98 ochrome oxidase 2 (COX2) and NADH:ubiquinone oxidoreductase core subunit 4 (MT-ND4)) are encoded by m

99 sclosed that ferredoxin (flavodoxin):NADP(+) oxidoreductase could use NADH to reduce Fd and thus faci

100 sized that thioredoxin-1 (Trx1), a cytosolic oxidoreductase, could be involved in restoring GC1 basal

101 old in the presence of cytochrome P450 NADPH:oxidoreductase (CPR) from the liver and bone marrow.

102 transfer catalyzed by shared cytochrome P450 oxidoreductases (CPRs), making these auxiliary proteins

103 r (AIF), an FAD-containing and NADH-specific oxidoreductase critically important for energy metabolis

104 pectrometry, we show that neonates with P450 oxidoreductase deficiency produce androgens through the

105 Congenital adrenal hyperplasia due to P450 oxidoreductase deficiency results in disrupted dehydroep

106 y congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.

107 t represents the most diverse gene family of oxidoreductases described in a single genus to date.

108 Based on oxidoreductases' description of microbial communities, t

109 iations with Cadherin13 and glucose-fructose oxidoreductase domain 1 genes.

110 Here, we identify Aifm2, a NADH oxidoreductase domain containing flavoprotein, as a lipi

111 tide phosphate (NADPH) cofactor bound to the oxidoreductase domain(8,9) of Shaker's K(V)beta subunit,

112 Dark-operative protochlorophyllide oxidoreductase (DPOR) is a key enzyme to produce chlorop

113 related dark-operative protochlorophyllide a oxidoreductase (DPOR).

114 alyzed by dark-operative protochlorophyllide oxidoreductase (DPOR).

115 eby the secretion of a glutathione-dependent oxidoreductase drives angiogenesis and cancer progressio

116 his process, the periplasmic thiol-disulfide oxidoreductase DsbA is thought to catalyze the formation

117 es a single homodimeric disulfide bond (DSB) oxidoreductase DsbA2 to catalyze extracytoplasmic protei

118 f the N-terminal domain of the key bacterial oxidoreductase DsbD (nDsbD), introduces frustration ulti

119 arboxylase (2-KPCC) is a bacterial disulfide oxidoreductase (DSOR) that, uniquely in this family, cat

120 dent monooxygenase that requires an NADH:FMN oxidoreductase (EmoB) to provide FMNH2 as a cosubstrate.

121 cterium tuberculosis rv2466c gene encodes an oxidoreductase enzyme annotated as DsbA.

122 al anaerobic-aerobic), and the extracellular oxidoreductase enzyme horseradish peroxidase (HRP) were

123 ombinant Xenopus laevis H3-H4 tetramer is an oxidoreductase enzyme that binds Cu(2+) and catalyzes it

124 of enzymes that comprise the superfamily of oxidoreductases (Enzyme Classification EC1).

125 chanistic study that can be applied to other oxidoreductase enzymes and to biomimetic complexes.

126 first to report direct electron transfer of oxidoreductase enzymes enabled by single walled carbon n

127 case, but the method is generalizable across oxidoreductase enzymes that rely on electron transfer me

128 cells are bioelectronic devices that utilize oxidoreductase enzymes to catalyze the conversion of che

129 eact with redox proteins including disulfide oxidoreductase enzymes, accounting for their stronger Nr

130 re counteracted by the activities of various oxidoreductase enzymes, such as thioredoxin (Trx), which

131 Here, we show that ER-resident oxidoreductase ERp18 associates with ATF6alpha following

132 Protein disulfide isomerase (PDI) is an oxidoreductase essential for folding proteins in the end

133 e hydroxylase 3 (PHD3), one of the important oxidoreductases expressed under hypoxic conditions.

134 3-one reductase or Fragaria x ananassa Enone Oxidoreductase (FaEO) catalyses the last reductive step

135 that the broader flavin-containing disulfide oxidoreductase family is more diverse than previously co

136 d this new member of the aldehyde ferredoxin oxidoreductase family of tungstoenzymes.

137 gs to the CYP71 clade of the cytochrome P450 oxidoreductase family.

138 rfamily of flavin- and deazaflavin-dependent oxidoreductases (FDORs) and is widely distributed in myc

139 hese plants with ndufs4 (for NADH:ubiquinone oxidoreductase Fe-S protein4) mutants possessing trace a

140 X-ray diffraction structures of oxidoreductase flavoenzymes have revealed recurrent feat

141 atalytic subunit NDUFV1 (for NADH:ubiquinone oxidoreductase flavoprotein1) and compared these plants

142 ew family of NADH dehydrogenases, the flavin oxidoreductase (FlxABCD, previously called FloxABCD), wa

143 S NRs) transfer to 2-oxoglutarate:ferredoxin oxidoreductase from Magnetococcus marinus MC-1 (MmOGOR),

144 creased supply of NADH for respiratory chain oxidoreductases from central carbon catabolism (glycolys

145 Ancient oxidoreductases from the Archean Eon between ca. 3.5 and

146 A number of oxidoreductases from the VAO/para-cresol methylhydroxyla

147 Twenty-one of these "hits" belonged to the oxidoreductase functional category.

148 eoxidation of ETFred to a membrane-bound FeS oxidoreductase functioning as an ETF:menaquinone oxidore

149 We show that profiles of oxidoreductase genes support the highest biome different

150 glyceraldehyde-3-phosphate (GAP) ferredoxin oxidoreductase (GOR) present not only in all known Caldi

151 is model, the multiheme enzyme hydroxylamine oxidoreductase (HAO) catalyzes the four-electron oxidati

152 gs related to octaheme hydroxylamine (NH2OH) oxidoreductase (HAO).

153 Oxidoreductases have evolved to minimise energy wastage

154 le, approximately half of the dioxygen-using oxidoreductases have Tyr/Trp chain lengths >/=3 residues

155 quinone oxidoreductase 1 (NQO1) was the top oxidoreductase "hit".

156 sed enzyme NADH-dependent ferredoxin NADP(+) oxidoreductase I (NfnI) from the hyperthermophillic arch

157 ifurcating NADH-dependent ferredoxin-NADP(+) oxidoreductase I and can be an indication of capacity fo

158 S) where it interacts with the mitochondrial oxidoreductase import and assembly protein 40 (AtMIA40),

159 sialin, a nitrate transporter, and xanthine oxidoreductase in human skeletal muscle, indicating that

160 the Saccharomyces cerevisiae NADH:ubiquinone oxidoreductase in L6 cells.

161 tion obviates the need for a thiol/disulfide oxidoreductase in that compartment.

162 icant reduction in NADPH-protochlorophyllide oxidoreductase in the yellow sectors of Var1 and Var33.

163 teria carry genes coding for thiol-disulfide oxidoreductases in their genomes.

164 nce of endoplasmic reticulum (ER)-associated oxidoreductases in these processes is largely unexplored

165 Complex I (NADH ubiquinone oxidoreductase) in mammalian mitochondria is an L-shaped

166 confirmed the role of HER2, which encodes an oxidoreductase, in the responsiveness to E-2-hexenal.

167 de chain, conserved in other flavin mediated oxidoreductases, in a second shell away from the FAD cof

168 Many oxidoreductases, including components of membrane-bound

169 d aid the design of new strategies for thiol oxidoreductase inhibition.

170 that transfer electrons from photosystems to oxidoreductases involved in nutrient assimilation.

171 at the catalytic activity of cytochrome P450 oxidoreductase is a function of the length, sequence, an

172 bioreductive enzymes such as cytochrome P450 oxidoreductase is likely to be futile.

173 of soluble guanylyl cyclase, where xanthine oxidoreductase is proposed to mediate the reduction of n

174 Complex I (NADH ubiquinone oxidoreductase) is a large multisubunit enzyme that cata

175 al complex I (proton-pumping NADH:ubiquinone oxidoreductase) is an essential respiratory enzyme.

176 ucing respiratory complex I (NADH:ubiquinone oxidoreductase) is one of the largest and most complicat

177 We found that TSV, a putative plastidic oxidoreductase, is a new type of virescent protein.

178 Renalase, a recently identified oxidoreductase, is emerging as a novel regulator of card

179 aled that YjbH, a predicted thioredoxin-like oxidoreductase, is predominantly responsible for the obs

180 s that influence protein structure via their oxidoreductase, isomerase, and chaperone activities.

181 ed supernumerary subunits of NADH:ubiquinone oxidoreductase, known as complex I (cI), the first and l

182 e liver-specific deletion of cytochrome P450 oxidoreductase (KO mice).

183 ensitive and identified two highly conserved oxidoreductase-like C-X-X-C motifs that are essential fo

184 he expression levels of the disulfide-bond A oxidoreductase-like protein (DsbA-L) are significantly r

185 ported that upregulation of disulfide-bond A oxidoreductase-like protein (DsbA-L) prevented lipid-ind

186 ctions as a light-driven cyt c(6)-ferredoxin/oxidoreductase located in the thylakoid membrane.

187 We then identified a thiol-disulfide oxidoreductase (MdbA), whose structure exhibits a conser

188 at many methanotrophs encode a hydroxylamine oxidoreductase (mHAO) in their genome to remove hydroxyl

189 rane space has an analogous pathway with the oxidoreductase Mia40 and sulfhydryl oxidase Erv1, termed

190 he sulfhydryl oxidase Erv1 partners with the oxidoreductase Mia40 to import cysteine-rich proteins in

191 The main component of this pathway is the oxidoreductase Mia40, which introduces disulfides into i

192 culine to 1,2-dehydroreticuline, whereas the oxidoreductase module converts 1,2-dehydroreticuline to

193 ococcal malate-quinone and l-lactate-quinone oxidoreductases (Mqo and Lqo), both of which are critica

194 ents and assembly factors of NADH:ubiquinone oxidoreductase, Mtln does not alter its enzymatic activi

195 n vitro evidence that the corresponding P450 oxidoreductase mutations predominantly support alternati

196 t RimO can utilize the flavodoxin/flavodoxin oxidoreductase/NADPH reducing system from Escherichia co

197 in dehydrogenase component, NADH:menaquinone oxidoreductase (Ndh) of Mycobacterium tuberculosis (Mtb)

198 Type II NADH:quinone oxidoreductase (NDH-2) is central to the respiratory cha

199 Type II NADH:quinone oxidoreductase (NDH-2) plays a crucial role in the respi

200 ifurcating NADH-dependent ferredoxin NADP(+) oxidoreductase (NfnI).

201 Imiquimod and CL097 inhibited the quinone oxidoreductases NQO2 and mitochondrial Complex I.

202 tress in plant cells, the pathogen-inducible oxidoreductase Nucleoredoxin 1 (NRX1) targets enzymes of

203 ng taxa (ammonia monooxygenase-amoA, nitrite oxidoreductase-nxrB, respectively) was conducted from lo

204 merase A1 (PDIA1/P4HB), the most abundant ER oxidoreductase of over 17 members, can interact with pro

205 metabolism, involving a tungsten-containing oxidoreductase of unknown function.

206 Respiratory complex I (NADH:ubiquinone oxidoreductase), one of the largest membrane-bound enzym

207 Complex I (NADH:ubiquinone oxidoreductase), one of the largest membrane-bound enzym

208 iamine pyrophosphate (TPP)-dependent oxalate oxidoreductase (OOR) metabolizes oxalate, generating two

209 alterations, such as knocking down the MIA40 oxidoreductase or knocking out NDUFA11 protein.

210 g the yeast lectin-like protein Htm1 and the oxidoreductase Pdi1 converts Man8GlcNAc2 on glycoprotein

211 gh 15,16-dihydrobiliverdin (DHBV):ferredoxin oxidoreductase (PebA) catalyzes the two-electron reducti

212 verdin IXalpha to 15,16-DHBV, PEB:ferredoxin oxidoreductase (PebB) reduces this intermediate further

213 ion pathway, which comprises sulfide quinone oxidoreductase, persulfide dioxygenase (PDO), rhodanese,

214 amixicile, that targets pyruvate:ferredoxin oxidoreductase (PFOR), a major metabolic enzyme involved

215 :formate lyase (PFL) and pyruvate:ferredoxin oxidoreductase (PFOR), that lose activity upon aeration.

216 Ndufc2, a subunit of the NADH: ubiquinone oxidoreductase, plays a key role in the assembly and act

217 The enzyme protochlorophyllide oxidoreductase (POR) catalyses a light-dependent step in

218 ed a conditional knock-out of the NADPH-P450 oxidoreductase (Por) gene combined with Il2rg (- /-) /Ra

219 Human NADPH-cytochrome P450 oxidoreductase (POR) gene mutations are associated with

220 onal activity of the two protochlorophyllide oxidoreductase (POR) genes involved in chlorophyll biosy

221 NADPH:protochlorophyllide oxidoreductase (POR) is a key enzyme for the light-induc

222 ar body (PLB) and normal PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR) levels, was used to demonstrate a r

223 lant P450s receive electrons from NADPH P450 oxidoreductase (POR) to orchestrate the bio-synthesis of

224 oral THC administration for cytochrome P450 oxidoreductase (Por), involved in toxin processing and d

225 anscriptionally regulate PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR), PHYTOCHROME INTERACTING FACTOR3 (P

226 IL3 for the stability of protochlorophyllide oxidoreductase (POR).

227 and driven by the NADPH:protochlorophyllide oxidoreductase (POR).

228 The enzyme protochlorophyllide oxidoreductase (POR, EC 1.3.1.33) has a key role in plan

229 ce through the action of protochlorophyllide oxidoreductases (PORs) that convert protochlorophyllide

230 gulated in V. parvula, including 39 genes in oxidoreductase processes.

231 Because GC1 interacts with the oxidoreductase protein-disulfide isomerase, we hypothesi

232 The mitochondrial SQRD-1 (sulfide quinone oxidoreductase) protein is a highly conserved enzyme inv

233 Here we report that the putative periplasmic oxidoreductase PvdO of Pseudomonas fluorescens A506 is r

234 We characterize variants in the oxidoreductase PYROXD1 as a cause of early-onset myopath

235 hl and complete reversed pyruvate ferredoxin oxidoreductase / pyruvate-formate-lyase-dependent (rPFOR

236 (Wood-Ljungdahl pathway, pyruvate:ferredoxin oxidoreductase reaction and anaplerotic pathways) and Re

237 f using an engineered yeast strain harboring oxidoreductase reactions to overcome the thermodynamic l

238 McFarland et al. now show that the mouse oxidoreductase RECON acts as a sensor for some bacterial

239 rs for bacterial cdNs, and we identified the oxidoreductase RECON.

240 nprecedented interplay between Trx and GSNOR oxidoreductases regulates the biosynthesis of styrylpyro

241 named TaoR (for tungsten-containing aldehyde oxidoreductase regulator).

242 Mitochondrial proton-pumping NADH:ubiquinone oxidoreductase (respiratory complex I) comprises more th

243 Here we show that the oxidoreductase retinol saturase (RetSat) is involved in

244 ted the multistep enzymatic mechanism of the oxidoreductase (RgNanOx) that leads to the reversible co

245 enzymes, the ferredoxin:[Formula: see text] oxidoreductase (Rnf complex) and the energy-converting h

246 reactions: the reversed pyruvate:ferredoxin oxidoreductase (rPFOR), which incorporates CO2 using ace

247 Diheme-containing succinate:menaquinone oxidoreductases (Sdh) are widespread in Gram-positive ba

248 ncoding a putative short-chain dehydrogenase/oxidoreductase (SDR) in Burkholderia pseudomallei, was i

249 Sulfide quinone oxidoreductase (SQOR) catalyzes the first step in sulfid

250 its function as cofactor for sulfide:quinone oxidoreductase (SQOR), the first enzyme in the sulfide o

251 terotrophic bacteria contain sulfide:quinone oxidoreductase (SQR) and persulfide dioxygenase (PDO) ge

252 (0) ) and high expression of sulfide quinone oxidoreductase (SQR) genes indicates that sulfide oxidat

253 tion pathway is catalyzed by sulfide quinone oxidoreductase (SQR), which belongs to the family of fla

254 catalyzed by a flavoprotein, sulfide quinone oxidoreductase (SQR), which converts H2S to a persulfide

255 containing the mutant human NADH ubiquinone oxidoreductase subunit 4 (ND4) gene followed by mitochon

256 mitochondrial gene encoding NADH:ubiquinone oxidoreductase subunit 4 (ND4).

257 chondrial disease that lacks NADH:ubiquinone oxidoreductase subunit S4 (NDUFS4), a subunit of mitocho

258 (missing the catalytic subunit STT3B or the oxidoreductase subunits magnesium transporter 1/tumor su

259 An NADPH/flavoprotein oxidoreductase system restores polysulfide-carrying hemo

260 he electron transfer flavoprotein/ubiquinone oxidoreductase system.

261 aracterization of a thermostable F420: NADPH oxidoreductase (Tfu-FNO) from T. fusca, the first F420-d

262 thioredoxin (Trx), a ubiquitous, cytoplasmic oxidoreductase that can denitrosylate proteins in vivo a

263 e 2,3-dioxygenase 1 (IDO1) is a single chain oxidoreductase that catalyzes tryptophan degradation to

264 r 2,7-anhydro-Neu5Ac and by the action of an oxidoreductase that converts 2,7-anhydro-Neu5Ac into Neu

265 UGDH encodes an oxidoreductase that converts UDP-glucose to UDP-glucuron

266 es light, Chl f synthase is probably a photo-oxidoreductase that employs catalytically useful Chl a m

267 g protein disulfide isomerase A6 (PDIA6), an oxidoreductase that functions in nascent protein folding

268 Rv2466c is a key oxidoreductase that mediates the reductive activation of

269 rase (PDI) is a ubiquitous dithiol-disulfide oxidoreductase that performs an array of cellular functi

270 the plasma membrane where it functions as an oxidoreductase that reduces coenzyme Q(10) (CoQ) (also k

271 st relative expression levels of STEAP3, the oxidoreductase that reduces ferric iron to the ferrous o

272 CLIC3 acts as a glutathione-dependent oxidoreductase that reduces TGM2 and regulates TGM2 bind

273 energy harvested from light to phage-encoded oxidoreductases that enhance viral fitness, but it is un

274 ery encompasses multiple Dsb thiol-disulfide oxidoreductases that mediate oxidative protein folding a

275 mitochondrial complex I (CI; NADH:ubiquinone oxidoreductase), the first enzyme of the respiratory cha

276 ysteines is mediated by a small 12-kDa thiol oxidoreductase, thioredoxin (Trx).

277 cal processes and nutrient recycling through oxidoreductases, this functional diversity should be rel

278 One candidate is the redox-sensitive oxidoreductase TMX1 that is enriched on the mitochondria

279 a CGFS-type loop switched its function from oxidoreductase to FeS transferase.

280 ally stimulating the production of microbial oxidoreductases to counter oxidative stress caused by ox

281 y chain and diversion of electrons from NADH oxidoreductases to oxygen.

282 SOR and membrane-bound thiosulphate-quinone oxidoreductase (TQO) from Sulfolobus tokodaii 'restored'

283 obacterial ammonia monooxygenase and nitrite oxidoreductase transcript abundances revealed that mRNA

284 s abundant proteins associated with binding, oxidoreductase/transferase activities, cytoskeletal and

285 ficant number of proteins that classified as oxidoreductases, transferases, hydrolases, lyases, and l

286 NADPH-cytochrome P450 oxidoreductase transfers electrons from NADPH to cytochr

287 it exhibits non-bifurcating ferredoxin NADP oxidoreductase-type activity.

288 ing a subunit of the menaquinol cytochrome c oxidoreductase, was resistant to compounds in this serie

289 e decolorization via the enzymatic action of oxidoreductases, which have already a strong presence in

290 S-type (class I) glutaredoxins (Grxs) act as oxidoreductases, while CGFS-type (class II) Grxs act as

291 s (Grxs) are small proteins that function as oxidoreductases with roles in deglutathionylation of pro

292 mouse tumor suppressor WW Domain Containing Oxidoreductase (WWOX) gene.

293 imetastatic function of WW domain-containing oxidoreductase (WWOX) in TNBC and identifies the Myc/miR

294 WW domain-containing oxidoreductase (WWOX), originally marked as a likely tum

295 s milk lipid by this mechanism, and xanthine oxidoreductase (XOR) has long been thought to be functio

296 re alllograft outcomes according to xanthine oxidoreductase (XOR) inhibitor treatment status at trans

297 d to compare alllograft outcomes by xanthine oxidoreductase (XOR) inhibitor treatment status at trans

298 Xanthine oxidoreductase (XOR) modulates milk lipid secretion and

299 facilitated by elevated activity of xanthine oxidoreductase (XOR), which is the sole source of uric a

300 es are commonly found in the active sites of oxidoreductases, yet the overwhelming majority of studie