ライフサイエンスコーパス: oxidoreductase

1 group 4 enzymes and complex I (NADH quinone oxidoreductase).

2 respiratory complex II (succinate:ubiquinone oxidoreductase).

3 oreductase functioning as an ETF:menaquinone oxidoreductase.

4 that its primary function is as a disulfide oxidoreductase.

5 previously identified putative molybdopterin oxidoreductase.

6 ns as a light-driven plastocyanin-ferredoxin oxidoreductase.

7 tionary links to Complex I, the NADH:quinone oxidoreductase.

8 of the highly conserved eukaryotic MIA40 IMS oxidoreductase.

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

10 tivity in this important and varied group of oxidoreductases.

11 ongs to the family of flavoprotein disulfide oxidoreductases.

12 ed in the presence of organic matter encoded oxidoreductases.

13 berine bridge enzyme and other FAD-dependent oxidoreductases.

14 l, a competitive inhibitor of naphthoquinone oxidoreductases.

15 pyruvate and alpha-ketoglutarate ferredoxin oxidoreductases.

16 from their (moderate) activity as disulfide oxidoreductases.

17 y through sortase A-mediated crosslinking of oxidoreductases.

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

19 NADPH reductase NAD(P)H: quinone oxidoreductase 1 (NQO1) is needed to maintain a cellular

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

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

22 of Nrf2 and its target genes NAD(P)H:quinone oxidoreductase 1 (NQO1), Bach1, cystine/glutamate transp

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

24 lle formulations maintained NAD(P)H: quinone oxidoreductase 1 (NQO1)-dependent cytotoxicity.

25 hibited purified Hsp90 in a NAD(P)H: quinone oxidoreductase 1 (NQO1)-dependent manner, demonstrating

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

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

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

29 ant proteins heme oxygenase-1, NADPH quinone oxidoreductase 1, and glutamate-cysteine ligase catalyti

30 ive genes, heme oxygenase-1, NAD(P)H quinone oxidoreductase 1, and glutathione-S transferase, with in

31 nd proteins, heme oxygenase 1, NADPH-quinone oxidoreductase 1, and growth factors were found.

32 moters of heme oxygenase-1 and NADPH quinone oxidoreductase 1.

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

34 zyme in human cancer cells, NAD(P)H: quinone oxidoreductase-1 (NQO1, DT-diaphorase, EC 1.6.99.2).

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

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

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

38 member 6, ER protein 44, and disulfide bond oxidoreductase A-like protein.

39 enzyme is related to octaheme hydroxylamine oxidoreductase, a key protein in aerobic ammonium-oxidiz

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

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

42 fusion gene inhibits both intracellular NADH oxidoreductase activities and protein translation.

43 The oxidoreductase activities of TRP14 thereby complement th

44 Through their oxidoreductase activities, the members of the Trx/Prdx s

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

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

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

48 ed in a 50% reduction of the NADH:ubiquinone oxidoreductase activity of the complex, which was compen

49 ar polysaccharide biosynthetic processes and oxidoreductase activity respectively.

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

51 e stress related to antioxidant activity and oxidoreductase activity.

52 strongly suggests that Steap1 harbors latent oxidoreductase activity.

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

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

55 duced ferredoxins between ferredoxin-NADP(+) oxidoreductase and hydrogenases, rather than due to the

56 ics of the full-length NADPH-cytochrome P450 oxidoreductase and its interaction with other membrane p

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

58 es must be directly addressed when designing oxidoreductase and molecular transport functions in man-

59 ted NO production from erythrocytic xanthine oxidoreductase and nitric-oxide synthase.

60 esident endoplasmic reticulum oxidoreductin1 oxidoreductase and protein disulfide isomerases.

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

62 inding site to shuttle electrons between the oxidoreductase and transmembrane domains, and it showed

63 lysis in many natural enzymes, including the oxidoreductases and allied transport and signaling prote

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

65 es approximately 50% of all metal-containing oxidoreductases and potentially catalyzed redox reaction

66 s in the activity of complex I (NADH:quinone oxidoreductase) and IV (cytochrome c oxidase) of this pa

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

68 er system of NADPH, spinach NADPH-ferredoxin oxidoreductase, and ferredoxin could also reduce the FMN

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

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

71 ly obtained with various other bidirectional oxidoreductases, and, possibly, synthetic inorganic cata

72 yzed by the host-encoded aldehyde ferredoxin oxidoreductase (AOR) and heterologously expressed AdhA,

73 ine residues and that several membrane-bound oxidoreductases are encoded in the corynebacterial genom

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

75 : nicotinamide adenine dinucleotide (NAD(+)) oxidoreductase at high H(2)/formate levels during fermen

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

77 Ubiquinol:cytochrome c oxidoreductase, bc1 complex, is the enzyme in the respir

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

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

80 proven to be a four-electron hydrogen/oxygen oxidoreductase, catalyzing the reaction 2 H2 + O2 = 2 H2

81 e generally viewed as components of distinct oxidoreductase-chaperone protein complexes.

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

83 Such substrate-oxidoreductase combinations offer Tg the potential for s

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

85 in/electron-transfer flavoprotein:ubiquinone oxidoreductase complex and associated dehydrogenases.

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

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

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

89 NADH:ubiquinone oxidoreductase (complex I) is a complicated respiratory

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

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

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

93 Respiratory complex II (succinate:ubiquinone oxidoreductase) connects the tricarboxylic acid cycle to

94 hich is a recurring theme in the research on oxidoreductases containing multiple redox-active sites.

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

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

97 multisubunit metalloenzyme, chlorophyllide a oxidoreductase (COR).

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

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

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

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

102 NADPH-cytochrome P450 oxidoreductase (CYPOR) is an essential redox partner of

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

104 x1, a glutaredoxin-like, mycothiol-dependent oxidoreductase, directly reduces the oxidized form of Mt

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

106 Although the cytoplasmic N-terminal oxidoreductase domain of Steap3 and Steap4 are relativel

107 t also in Steap1, which lacks the N-terminal oxidoreductase domain.

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

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

110 The proteins identified are NADH : flavin oxidoreductase (Dred_2421) and a protein complex compose

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

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

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

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

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

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

117 The immobilization of oxidoreductase enzyme HRP on the electrodes modified wit

118 e peptide NF04 (structurally derived from an oxidoreductase enzyme), which was found to be the sole p

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

120 ovides a solution to ensure functionality of oxidoreductase enzymes in oxygen-free environments.

121 Generally, this process is catalyzed by oxidoreductase enzymes that facilitate oxidation and als

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

123 primarily engaging the endoplasmic reticulum oxidoreductases ERp57 and protein disulfide isomerase.

124 Mia40 and the sulfhydryl:cytochrome c oxidoreductase Erv1/ALR are essential for oxidative prot

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

126 degradation are performed by NADP-dependent oxidoreductases explaining their in vivo deficiency.

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

128 3-one reductase or Fragaria x ananassa Enone Oxidoreductase (FaEO) catalyses the last reductive step

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

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

131 Dred_2421) and a protein complex composed of oxidoreductase flavin adenine dinucleotide/NAD(P)-bindin

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

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

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

135 opsis thaliana) leaf-type FERREDOXIN-NADP(+) OXIDOREDUCTASE (FNR) isoforms, the key enzymes linking t

136 homology to CYB2, the l-lactate cytochrome c oxidoreductase from the yeast Saccharomyces cerevisiae.

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

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

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

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

141 ause of a reduction in NADPH-cytochrome P450 oxidoreductase gene expression, protein, and activity.

142 atic disruption of the cytochrome p450 (CYP) oxidoreductase gene, encoding the single electron donor

143 The pH dependent redox potential of the oxidoreductase glucose oxidase (GOx) from Aspergillus ni

144 h a putative nucleus-encoded DHBV:ferredoxin oxidoreductase (GtPEBA).

145 A PEB:ferredoxin oxidoreductase (GtPEBB) was found to convert DHBV to PEB

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

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

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

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

150 detoxifying genes encoding cytochrome P450, oxidoreductase, hydrolase and transferase in tomato plan

151 e sequencing and quantification of hydrazine oxidoreductase (hzo) gene transcripts.

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

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

154 al for determining the enzymatic activity of oxidoreductases (i.e., laccase) both in vivo and in vitr

155 putative ion-translocating ferredoxin : NADH oxidoreductase (IfoAB) that may interact with HdrABC and

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

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

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

159 Many selenoproteins are oxidoreductases in which the reactive Sec is connected t

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

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

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

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

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

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

166 heterocyclic compounds that target DprE1, an oxidoreductase involved in the epimerization of decapren

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

168 While accurate kinetic modeling of oxidoreductases is thus important, current models suffer

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

170 Complex I (NADH:ubiquinone oxidoreductase) is a multisubunit, membrane-bound enzyme

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

172 Complex I (NADH:ubiquinone oxidoreductase) is central to cellular NAD(+) recycling

173 Complex I (NADH:ubiquinone oxidoreductase) is essential for oxidative phosphorylati

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

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

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

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

178 the cancer-associated human NAD(P)H:quinone oxidoreductase isozyme 1 (hNQO1).

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

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

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

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

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

184 Oxidoreductases mediate electron transfer (i.e., redox)

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

186 The oxidoreductase Mia40 is a central component of the pathw

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

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

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

190 uline] that encodes both cytochrome P450 and oxidoreductase modules, the latter belonging to the aldo

191 roxide radicals through its helix-turn-helix oxidoreductase motif, the C-terminal domain (Sesn-C) mod

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

193 Na(+)-pumping NADH:ubiquinone oxidoreductase (Na(+)-NQR) is responsible for maintainin

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

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

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

197 em with yeast Ndi1, a type 2 NADH:ubiquinone oxidoreductase (NDH-2) regarded as alternative complex I

198 NADH-dependent reduced ferredoxin:NADP oxidoreductase (NfnAB) is found in the cytoplasm of vari

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

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

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

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

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

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

205 pressing shRNA against NADPH-cytochrome P450 oxidoreductase or mitochondrial adrenodoxin.

206 egulation, fprA (encoding ferredoxin:NADP(+) oxidoreductase), or by Escherichia coli cysJI (encoding

207 NADH:ubiquinone oxidoreductase oxidizes NADH and reduces ubiquinone, usi

208 heterotrimer, the Escherichia coli aldehyde oxidoreductase PaoABC, that is co-translocated by the Ta

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

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

211 eukaryotes (protists) is pyruvate:ferredoxin oxidoreductase (PFO), which decarboxylates pyruvate and

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

213 electrons via pyruvate:flavodoxin/ferredoxin oxidoreductase (PFOR)-flavodoxin/ferredoxin under fermen

214 rdtii also possesses the pyruvate:ferredoxin oxidoreductase PFR1, which, like pyruvate:formate lyase

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

216 dentified the flavoprotein P450 (cytochrome) oxidoreductase (POR) as the predominant determinant of s

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

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

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

220 ique light-driven enzyme protochlorophyllide oxidoreductase (POR) is an important model system for un

221 NADPH:cytochrome P450 oxidoreductase (POR) is considered one of the major enzy

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

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

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

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

226 employs pyruvate and 2-oxoglutarate:acceptor oxidoreductases (Por and Oor), which contain labile (4Fe

227 e hepatic deletion of either cytochrome P450 oxidoreductase [POR; HRN (hepatic reductase null) line]

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

229 accharomyces cerevisiae is an integral thiol oxidoreductase protein of the endoplasmic reticulum/Golg

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

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

232 uggest that the induction of specific Fe(II) oxidoreductase proteins is not required for NDFO.

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

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

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

240 e final goal of integrating them in man-made oxidoreductases, remains elusive.

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

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

243 llel, comparative analyses of multiple thiol oxidoreductases revealed differences in the functions of

244 ling site, a sodium-motive ferredoxin:NAD(+) oxidoreductase (Rnf) in the acetogenic bacterium Acetoba

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

246 Silencing of sulfide quinone oxidoreductase (SQR) also reduced basal and 3-MP-stimula

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

248 ate reducing conditions, the sulfide:quinone oxidoreductase (SQR) pathway and the Sox (sulfur oxidati

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

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

251 very first step catalyzed by sulfide quinone oxidoreductase (SQR).

252 mbrane protein (DoxX), and a predicted thiol-oxidoreductase (SseA).

253 nement and reassessment of the hydroxylamine oxidoreductase structure from Nitrosomonas europaea, bot

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

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

256 tentially catalyzed by cell surface-secreted oxidoreductases such as thioredoxin (Trx) and protein di

257 harvesting complex I (LHCI)-ferredoxin-NADPH oxidoreductase supercomplexes.

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

259 he electron transfer flavoprotein/ubiquinone oxidoreductase system.

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

261 topic expression of yeast NDI1, a ubiquinone oxidoreductase that allows bypass of complex I function.

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

263 m Escherichia coli is a structurally complex oxidoreductase that catalyzes the six-electron reduction

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

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

266 Mia40 is the oxidoreductase that inserts two disulfide bonds into the

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

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

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

270 with SRK, have been proposed to function as oxidoreductases that negatively regulate SRK catalytic a

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

272 or specificity of a class of NADPH-dependent oxidoreductases, the ketol-acid reductoisomerases (KARIs

273 TxNIP), an endogenous inhibitor of the thiol oxidoreductase thioredoxin, is augmented by high glucose

274 Here we show that in plant immunity the oxidoreductase Thioredoxin-h5 (TRXh5) reverses SNO modif

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

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

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

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

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

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

281 hock proteins, superoxide dismutase, quinone oxidoreductase, UDP-glucose pyrophosphorylase and phosph

282 evolution of metal-binding domains in extant oxidoreductases using a flexible network approach and pe

283 The vitamin K oxidoreductase (VKORC1) recycles vitamin K to support th

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

285 The PA1225 gene, encoding a quinone oxidoreductase, was the most highly upregulated gene in

286 d a high-representation library enriched for oxidoreductases, we identified the flavoprotein P450 (cy

287 g Tg adduct C primarily engages the CaBP1/P5 oxidoreductase, whereas the slower migrating Tg adduct A

288 )-containing homodimeric pyridine nucleotide oxidoreductase which catalyzes the reduction of oxidized

289 pumping ferredoxin (Fd): type-I cytochrome c oxidoreductase, which transitions to a proton-pumping Fd

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

291 The WW domain-containing oxidoreductase (WWOX) encodes a 46-kDa tumor suppressor

292 association between the WW domain-containing oxidoreductase (WWOX) gene and HDL cholesterol levels.

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

294 The WW domain-containing oxidoreductase (WWOX) is a tumor suppressor spanning the

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

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

297 Xanthine oxidoreductase (XOR) modulates milk lipid secretion and

298 Allopurinol, an inhibitor of xanthine oxidoreductase (XOR), blocks the oxidation of xanthine t

299 regulators GadE or YdeO, but was lost if the oxidoreductase YdeP was also absent.

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