ライフサイエンスコーパス: alcohol dehydrogenase

1 models for C-H activation in the context of alcohol dehydrogenase.

2 d using tryptic digests of yeast enolase and alcohol dehydrogenase.

3 g of light by beta- and gamma-crystallin and alcohol dehydrogenase.

4 s the hydride ion, whose paradigm example is alcohol dehydrogenase.

5 er, namely dihydrofolate reductase and liver alcohol dehydrogenase.

6 e chaperone-like activity against denaturing alcohol dehydrogenase.

7 on the oxidation of benzyl alcohol by yeast alcohol dehydrogenase.

8 m as a consequence of ethanol metabolism via alcohol dehydrogenase.

9 t cytochrome P450, an alcohol oxidase and an alcohol dehydrogenase.

10 cess is catalyzed by an ene-reductase and an alcohol dehydrogenase.

11 thod (FRESCO) to guide the engineering of an alcohol dehydrogenase.

12 in vertebrates, in addition to a specialized alcohol dehydrogenase.

13 uit that comprises glucose dehydrogenase and alcohol dehydrogenase.

14 o-atRA formation is mediated by a microsomal alcohol dehydrogenase.

15 unctional acetaldehyde-CoA dehydrogenase and alcohol dehydrogenase.

16 idium thermocellum bifunctional acetaldehyde/alcohol dehydrogenase.

17 -keto reductases and three genes that encode alcohol dehydrogenases.

18 t controls C-H activation in the prokaryotic alcohol dehydrogenases.

19 hibitors selectively inhibit GSNOR among the alcohol dehydrogenases.

20 same pot by enzymatic reductions mediated by alcohol dehydrogenases.

21 itous or overlapping activities of redundant alcohol dehydrogenases.

22 itamin that serves as a cofactor in numerous alcohol dehydrogenases.

23 r characteristics to well known medium-chain alcohol dehydrogenases.

24 nzyme classes, lipoxygenases and prokaryotic alcohol dehydrogenases.

25 nzyme families, dihydrofolate reductases and alcohol dehydrogenases.

26 g the conversion of erythrose to erythritol: alcohol dehydrogenase 1 (ADH1) and sorbitol dehydrogenas

27 In Schizosaccharomyces pombe, alcohol dehydrogenase 1 (Adh1) is an abundant zinc-requi

28 to produce acetaldehyde, which is reduced by alcohol dehydrogenase 1 (Adh1) to ethanol, which accumul

29 downregulation of Sub1C and upregulation of Alcohol dehydrogenase 1 (Adh1), indicating that Sub1A-1

30 In yeast, Adh1 (alcohol dehydrogenase 1) is an abundant zinc-binding pro

31 els, of EtOH-metabolizing enzymes, including alcohol dehydrogenase 1, aldehyde dehydrogenase 1A1, and

32 clear (internal transcribed spacer, ITS; and alcohol dehydrogenase 1A, Adh) and plastid (trnT-trnL sp

33 notyped for the alcohol-metabolizing enzymes alcohol dehydrogenase 1B (ADH-1B; rs1229984) and alcohol

34 A coding variant in alcohol dehydrogenase 1B (ADH1B) (rs1229984) that leads

35 Alcohol dehydrogenase 1B (ADH1B) is involved in alcohol

36 hol dehydrogenase 1B (ADH-1B; rs1229984) and alcohol dehydrogenase 1c (ADH-1C; rs698).

37 Variants in the alcohol dehydrogenase 1C (ADH1C) gene may modify the ass

38 to investigate whether a polymorphism in the alcohol dehydrogenase 1c (ADH1C) gene modifies the assoc

39 Human alcohol dehydrogenase 4 (ADH4) is one of the key enzymes

40 oise responses and enables identification of alcohol dehydrogenase 5 (ADH5) as an enzyme that regulat

41 genous formaldehyde is removed by the enzyme alcohol dehydrogenase 5 (ADH5/GSNOR), and Adh5(-/-) mice

42 a specific SNO-CoA reductase encoded by the alcohol dehydrogenase 6 (ADH6) gene and show that deleti

43 we identified members of the plant cinnamyl alcohol dehydrogenase 7 (CAD7) subfamily as targets of m

44 Our ~2.7 angstrom structure of alcohol dehydrogenase (82 kDa) proves that bound ligands

45 BAC sequences surrounding the gene encoding alcohol dehydrogenase A (AdhA) from four cotton genomes:

46 act alpha-, beta-, and gamma-crystallins and alcohol dehydrogenase, a protein used in aggregation stu

47 mber of oxidoreductases, including XoxF-type alcohol dehydrogenases, a type II secretion system, and

48 ol oxidases (AAO) and the intracellular aryl-alcohol dehydrogenases (AAD) were also produced after ex

49 Here, we demonstrate that Abeta-binding alcohol dehydrogenase (ABAD) is a direct molecular link

50 Abeta binding alcohol dehydrogenase (ABAD) is an NAD-dependent mitocho

51 Amyloid-beta (Abeta) peptide-binding alcohol dehydrogenase (ABAD), an enzyme present in neuro

52 Amyloid-beta peptide (Abeta) binding alcohol dehydrogenase (ABAD), an enzyme present in neuro

53 , also known as amyloid beta-peptide-binding alcohol dehydrogenase (ABAD), has been implicated in the

54 ted with increased level of Abeta binding to alcohol dehydrogenase (ABAD).

55 nteraction between Abeta and amyloid-binding alcohol dehydrogenase (ABAD).

56 6 plants were shown to have limited cinnamyl alcohol dehydrogenase activity (CAD; EC 1.1.1.195), the

57 in, red-pigmented stems, low CAD and sinapyl alcohol dehydrogenase activity, low lignin contents, and

58 gloeosporioides) incidence, without inducing alcohol dehydrogenase activity, which suggests that coat

59 LDH the redox balance is maintained through alcohol dehydrogenase activity.

60 monoclonal antibody against the C. albicans alcohol dehydrogenase (Adh) 1.

61 s that the aldehyde dehydrogenase (ALDH) and alcohol dehydrogenase (ADH) active sites reside at the o

62 on alcohol metabolism because inhibition of alcohol dehydrogenase (ADH) activity blunted ChREBP EtOH

63 of plasticity in a classic functional trait, alcohol dehydrogenase (ADH) activity in D. melanogaster,

64 The relationships between some alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (

65 h two steps of oxidative catabolism in which alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (

66 nt HepG2 cells (VL-17A cells), which express alcohol dehydrogenase (ADH) and CYP2E1.

67 ge was associated with the activation of the alcohol dehydrogenase (ADH) and greater anaerobic metabo

68 ting partially unfolded betaL crystallin and alcohol dehydrogenase (ADH) and significantly less effec

69 ing proteins [superoxide dismutase (SOD) and alcohol dehydrogenase (ADH) as protein models] showed th

70 ctrochemical transistor (OECT) modified with alcohol dehydrogenase (ADH) as the sensor.

71 chemical tuning of alcohol oxidase (AOx) and alcohol dehydrogenase (ADH) biocatalysis towards butanol

72 r we designed and investigated bioanode with alcohol dehydrogenase (ADH) catalysing oxidation of glyc

73 asis of ecologically relevant differences in Alcohol dehydrogenase (Adh) enzyme activity between and

74 ty of the approach by genetically dissecting alcohol dehydrogenase (ADH) enzyme activity.

75 ously reported elevations in hepatic Class 1 alcohol dehydrogenase (ADH) expression in ethanol-fed ra

76 internal standard to absolutely quantify the alcohol dehydrogenase (ADH) expression level in a human

77 The alcohol dehydrogenase (ADH) family of enzymes catalyzes

78 FurX is a tetrameric Zn-dependent alcohol dehydrogenase (ADH) from Cupriavidus necator JMP

79 he structure of the recombinant medium chain alcohol dehydrogenase (ADH) from the hyperthermophilic a

80 aturally occurring tandem duplication of the Alcohol dehydrogenase (Adh) gene exhibits 2.6-fold great

81 al reduction of codon bias in the Drosophila alcohol dehydrogenase (Adh) gene led to a significant de

82 We aimed to test whether alcohol dehydrogenase (ADH) gene variants were associate

83 cated on chromosome 4q, in the region of the alcohol dehydrogenase (ADH) genes, affected risk for alc

84 ously reported associations of AD with seven alcohol dehydrogenase (ADH) genes.

85 study focuses on the population genetics of alcohol dehydrogenase (Adh) in cactophilic Drosophila.

86 l blood mononuclear cell (PBMC) responses to alcohol dehydrogenase (ADH) in patients with alcohol-rel

87 rthern blotting analyses to demonstrate that alcohol dehydrogenase (ADH) is downregulated in Candida

88 Histidine-51 in horse liver alcohol dehydrogenase (ADH) is part of a hydrogen-bonded

89 Inhibition of alcohol dehydrogenase (ADH) or deletion of transient rec

90 ed to Arabidopsis roots with the Arabidopsis alcohol dehydrogenase (Adh) promoter (Adh::TaPCS1/cad1-3

91 Polymorphism in the alcohol dehydrogenase (ADH) protein of Drosophila melano

92 tion removing acetaldehyde produced from the alcohol dehydrogenase (ADH) reaction was shown to improv

93 in derived from the still extant short-chain alcohol dehydrogenase (ADH) through retroposition, provi

94 anol biosensor through the immobilization of alcohol dehydrogenase (ADH) via Nafion entrapment, with

95 sequence data for orthologous regions of the Alcohol dehydrogenase (Adh), Alcohol dehydrogenase relat

96 ocused on oxidations in mammals catalyzed by alcohol dehydrogenase (ADH), aldehyde dehydrogenase (ALD

97 alcohol-metabolizing enzyme, hepatic Class I alcohol dehydrogenase (ADH), and this mechanism involves

98 er disease (ALD) have antibodies directed to alcohol dehydrogenase (ADH), anti-ADH titers being assoc

99 ing to the Old Yellow Enzyme family) with an alcohol dehydrogenase (ADH), applying the in situ substr

100 Sequences were analyzed from the Alcohol dehydrogenase (Adh), big brain (bib), and timele

101 N-Heptylformamide, a potent inhibitor of alcohol dehydrogenase (ADH), decreased the conversion of

102 e nicotinamide ring of the coenzyme bound to alcohol dehydrogenase (ADH), may facilitate hydride tran

103 y was to determine whether class I and/or IV alcohol dehydrogenase (ADH), medium chain ADHs that can

104 siren1 and siren2 are novel alcohol dehydrogenase (Adh)-derived chimeric genes in th

105 cytochromes P450 from the CYP71 clan and an alcohol dehydrogenase (ADH).

106 ession of keto-acid decarboxylases (KDC) and alcohol dehydrogenase (ADH).

107 We then analyzed the relation of maternal alcohol dehydrogenase (ADH)1B genotype (rs1229984) with

108 th monoenzymatic [utilizing a single enzyme, alcohol dehydrogenase (ADH)] and bienzymatic (anchoring

109 sed to probe gas-phase structural changes of alcohol dehydrogenase (ADH, 4mer) under varying degrees

110 tosan, glassy carbon, platinum) and enzymes (alcohol dehydrogenase, ADH; lactate dehydrogenase, LDH;

111 Previous genetic studies have revealed that alcohol dehydrogenase Adh1 is required for efficient cle

112 ify were associated with four genes encoding Alcohol Dehydrogenase - ADH1A, ADH1B, ADH1C and ADH4.

113 e dehydrogenase (ALDH2) and the super-active alcohol dehydrogenase (ADH2) alleles may promote hepatic

114 ith the oxidation of geraniol to geranial by alcohol dehydrogenase ADH3, followed by the enantioselec

115 Here, we resurrect digestive alcohol dehydrogenases (ADH4) from our primate ancestors

116 ucted by insertion of the gene for bacterial alcohol dehydrogenase (AdhA) into the archaeon Pyrococcu

117 tes of histidine phosphorylation on aldehyde-alcohol dehydrogenase (AdhE) and pyruvate kinase (PykF)

118 Acetaldehyde-alcohol dehydrogenase (AdhE) enzymes are a key metabolic

119 Aldehyde-alcohol dehydrogenase (AdhE) is a key enzyme in bacteria

120 d that substitution of bifunctional aldehyde/alcohol dehydrogenase (AdhE2) with separate butyraldehyd

121 A was reduced to yield 1-hexanol by aldehyde/alcohol dehydrogenase (AdhE2).

122 Aldehyde/alcohol dehydrogenases (ADHEs) are bifunctional enzymes

123 in coding and non-coding regions of class IB alcohol dehydrogenase (ADHIB) and evaluated for altered

124 1D1V2; tabersonine 3-oxygenase (T3O)] and an alcohol dehydrogenase [ADHL1; tabersonine 3-reductase (T

125 of chiral beta-hydroxy nitriles catalyzed by alcohol dehydrogenase (AdhS) and halohydrin dehalogenase

126 ose of bacterial and archaeal homotetrameric alcohol dehydrogenases (ADHs) and also to the mammalian

127 : oxidation of retinol into retinaldehyde by alcohol dehydrogenases (ADHs) or retinol dehydrogenases

128 hyde by a distinct family of metal-dependent alcohol dehydrogenases (ADHs).

129 acterization of two cDNAs encoding zebrafish alcohol dehydrogenases (ADHs).

130 ysis, identified and cloned a novel cinnamyl alcohol dehydrogenase allele (SbCAD2) that has an 8-bp d

131 Only slow ethanol metabolizers (alcohol dehydrogenase alleles [ADH1B*1] carriers) signif

132 ly involved in natural product metabolism-an alcohol dehydrogenase and a cytochrome P450-produces une

133 Hepatic alcohol dehydrogenase and aldehyde dehydrogenase activit

134 for enzymes that metabolise alcohol, such as alcohol dehydrogenase and aldehyde dehydrogenase; those

135 oiled-coil cross-links, and (2) it expresses alcohol dehydrogenase and aldo-keto reductase activity n

136 kB and AlmA, two CYP153 cytochrome P450s, an alcohol dehydrogenase and an aldehyde dehydrogenase.

137 Similarity also exists between liver alcohol dehydrogenase and cAMP-dependent protein kinase

138 lin, and in vitro chaperone target proteins, alcohol dehydrogenase and citrate synthase.

139 VL-17A cells (HepG2 cells overexpressing alcohol dehydrogenase and cytochrome P450-2E1) were expo

140 ere we report that in HepG2 cells expressing alcohol dehydrogenase and hepatocytes of ethanol-fed rat

141 Here, in both HepG2 cells overexpressing alcohol dehydrogenase and in rat hepatocytes, we found t

142 d crySI, were found to reduce aggregation of alcohol dehydrogenase and insulin, which demonstrates th

143 D(+) and N(tz)ADH to be substrates for yeast alcohol dehydrogenase and lactate dehydrogenase, respect

144 the alcohol-metabolizing enzymes, cytosolic alcohol dehydrogenase and mitochondrial aldehyde dehydro

145 ar starvation results in a weak induction of alcohol dehydrogenase and other anaerobic genes.

146 nded networks], the activation of C-H bonds [alcohol dehydrogenase and soybean lipoxygenase (SLO) as

147 biquitous nature of beta-oxidation, aldehyde/alcohol dehydrogenase and thioesterase enzymes has the p

148 tive analogues of the aldehyde substrates of alcohol dehydrogenases and are useful for structure-func

149 reactions that employ esterases, lipases or alcohol dehydrogenases and gold(I) or ruthenium(II) comp

150 iscent of the NAD(+)-dependent mechanisms of alcohol dehydrogenases and sirtuins and the RNA-mediated

151 e thermal aggregation of beta(H) crystallin, alcohol dehydrogenase, and citrate synthase in vitro.

152 her dehydrogenases (d-lactate dehydrogenase, alcohol dehydrogenase, and formate dehydrogenase, respec

153 de 3-phosphate dehydrogenase, transaldolase, alcohol dehydrogenase, and phosphoenolpyruvate carboxyki

154 te aminotransferase, citrate synthase, liver alcohol dehydrogenase, and the catalytic subunit of cAMP

155 hol dissolution into carboxylic acid through alcohol dehydrogenase, and voltage-regulated H(+) channe

156 KIEs in solution are compared to those with alcohol dehydrogenases, and sources of the observed "puz

157 that the EutD phosphotransacetylase and EutG alcohol dehydrogenase are important to maintain metaboli

158 e enzymes involved in lipid oxidation (e.g., alcohol dehydrogenase) are considerably higher in PE-fed

159 nanotubes as electron transfer accelerator, alcohol dehydrogenase as biocatalyst and polydiallyldime

160 e P450 2A6, glutathione S transferase P, and alcohol dehydrogenases as specialized indicators of hepa

161 s are the highest currently reported for the alcohol dehydrogenase bioanodes operating utilizing a di

162 centration is elevated and there is adequate alcohol dehydrogenase blockade, extracorporeal treatment

163 500 mg/L or 15.6 mmol/L in the absence of an alcohol dehydrogenase blocker; in the absence of a metha

164 ied the functions of members of the cinnamyl alcohol dehydrogenase (CAD) and cinnamoyl-CoA reductase

165 s cinnamoyl-CoA reductase (CCR) and cinnamyl alcohol dehydrogenase (CAD) catalyze the two key reducti

166 Cinnamyl alcohol dehydrogenase (CAD) catalyzes the conversion of

167 Cinnamyl alcohol dehydrogenase (CAD) catalyzes the final step in

168 Silencing two CINNAMYL ALCOHOL DEHYDROGENASE (CAD) genes in Nicotiana attenuata

169 the Arabidopsis genome database as cinnamyl alcohol dehydrogenase (CAD) homologues, an in silico ana

170 recursors synthesized by the enzyme cinnamyl alcohol dehydrogenase (CAD).

171 Although SAD and classical cinnamyl alcohol dehydrogenases (CADs) catalyze the same reaction

172 cation and characterization of four cinnamyl alcohol dehydrogenases (CADs) from cucumber (Cucumis sat

173 nal dynamics in the proton transfer steps of alcohol dehydrogenase catalysis.

174 yme-linked immunosorbent assay (ELISA) using alcohol dehydrogenase-catalyzed gold nanoparticle seed-m

175 efficient and inexpensive biocatalysts (i.e. alcohol dehydrogenases, cellulases and esterases) that a

176 es (CCoAOMT and COMT) and a form of cinnamyl alcohol dehydrogenase (ChCAD4) with preference for conif

177 olution, the beta(1)beta(1) isoform of human alcohol dehydrogenase complexed with N-benzylformamide a

178 structure of the alphaalpha isoform of human alcohol dehydrogenase complexed with N-cyclopentyl-N-cyc

179 Structures of horse liver alcohol dehydrogenase complexed with NAD(+) and unreacti

180 Inhibition of alcohol dehydrogenase, cytochrome P450 2E1, and catalase

181 The results show that in alcohol dehydrogenase, dynamic protein motion is in fact

182 thanol tolerant and that alcohol upregulates alcohol dehydrogenase E (AdhE) and potentiates pneumolys

183 oryzae (AspRedAm) was combined with a single alcohol dehydrogenase (either metagenomic ADH-150, an AD

184 Glucose 6-phospatase, alcohol dehydrogenase, elongation factor-TU, methylgluta

185 ells induce the expression of an alternative alcohol dehydrogenase encoded by the adh4 gene.

186 The study was performed using the alcohol dehydrogenase enzyme immobilised by covalent bin

187 of an ethanol biosensor based on the coupled alcohol dehydrogenase enzyme(ADH).

188 ics the catalytic activity similar to enzyme alcohol dehydrogenase for ETB.

189 A tetrameric thermophilic alcohol dehydrogenase from Bacillus stearothermophilus (

190 The crystal structure of NAD(+)-dependent alcohol dehydrogenase from Bacillus stearothermophilus s

191 ilic enzyme (55% identity), NAD(+)-dependent alcohol dehydrogenase from Escherichia coli.

192 acid reductase from Nocardia iowensis and an alcohol dehydrogenase from Leifsonia sp. strain S749.

193 iopure (S)-alcohols in high yields using the alcohol dehydrogenase from Rhodococcus ruber (ADH-A), wh

194 ductase from Candida magnoliae ( CMCR) or an alcohol dehydrogenase from Saccharomyces cerevisiae ( Ym

195 y alcohols was achieved with W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicu

196 used to reduce NADP(+) to R-[4-3H]NADPH with alcohol dehydrogenase from Thermoanaerobium brockii at 4

197 d relies on a combination of two enzymes: an alcohol dehydrogenase (from Aromatoleum sp., Lactobacill

198 nd 10 unpreferred codons into the Drosophila alcohol dehydrogenase gene (Adh).

199 e to a mutated bifunctional acetaldehyde-CoA/alcohol dehydrogenase gene (adhE), hypothesize based on

200 dies examining this zinc-dependent switch in alcohol dehydrogenase gene expression, we isolated an ad

201 higher prevalence of ADH2*2, an allele of an alcohol dehydrogenase gene that protects against heavy d

202 ment containing the promoter of a Drosophila alcohol dehydrogenase gene, several translational positi

203 ADH (alcohol dehydrogenase) gene expression, enzyme activity,

204 Humans have seven alcohol dehydrogenase genes (ADH) falling into five clas

205 the clinically significant enzymes including alcohol dehydrogenase, glucose 6-phosphate dehydrogenase

206 The logic network composed of three enzymes (alcohol dehydrogenase, glucose dehydrogenase, and glucos

207 lycinin, glycinin, Kunitz trypsin inhibitor, alcohol dehydrogenase, Gly m Bd 28K allergen, and sucros

208 yl-CoA dehydrogenase type II/amyloid binding alcohol dehydrogenase (HADH II/ABAD), a mitochondrial ox

209 al decades the hydride transfer catalyzed by alcohol dehydrogenase has been difficult to understand.

210 s into a gene annotated as encoding cinnamyl alcohol dehydrogenase, here designated M. truncatula CAD

211 , glucosidase, MYB transcription factor, and alcohol dehydrogenase, highly regulated due to insect in

212 ross-correlation analysis of the horse liver alcohol dehydrogenase HLADH.NAD(+).PhCH(2)O(-) complex h

213 ely resembles that of mesophilic horse liver alcohol dehydrogenase (HLADH).

214 sted as inhibitors of purified Class I liver alcohol dehydrogenases: horse (EqADH E), human (HsADH1C*

215 nvestigated in two mutants of a thermophilic alcohol dehydrogenase (ht-ADH): Y25A (at the dimer inter

216 catalyzed by a series of mutant thermophilic alcohol dehydrogenases (ht-ADH), presenting evidence for

217 the thermophilic Bacillus stearothermophilus alcohol dehydrogenase (HtADH) closely resembles that of

218 s in relation to the homologous thermophilic alcohol dehydrogenase (htADH) from Bacillus stearothermo

219 deuterium (H/D) exchange of the thermophilic alcohol dehydrogenase (htADH) has been studied by using

220 binase A (RecA) and Saccharomyces cerevisiae alcohol dehydrogenase-I (YADH-I).

221 Bacteria were engineered such that alcohol dehydrogenase II (ADHII) was surface displayed.

222 nt distances from the NAD(+) binding site in alcohol dehydrogenase II was performed.

223 ia through a surface displayed redox enzyme, alcohol dehydrogenase II.

224 ith unfounded claims for a so-called sinapyl alcohol dehydrogenase in angiosperms.

225 ydride transfer reactions catalyzed by liver alcohol dehydrogenase in calculated energy profile and r

226 nthetic cinnamoyl CoA reductase and cinnamyl alcohol dehydrogenase in not only the lignifying TEs but

227 0 2E1 activity but increased the activity of alcohol dehydrogenase in the liver, without affecting th

228 ult of low aldehyde reductase activity (i.e. alcohol dehydrogenase in the reverse reaction) of CsCAD

229 lization of horseradish peroxidase and yeast alcohol dehydrogenase in these glasses.

230 atocytes were incubated with antioxidants or alcohol dehydrogenase inhibitor prior to alcohol exposur

231 alone or in combination with ranitidine (an alcohol dehydrogenase inhibitor) while the biosensor sig

232 d efficiency in the chaperoning ability with alcohol dehydrogenase, insulin, and citrate synthase as

233 hable electrode concept by immobilisation of alcohol dehydrogenase into vapour-phase polymerised poly

234 S-Nitrosoglutathione reductase (GSNOR) is an alcohol dehydrogenase involved in the regulation of S-ni

235 at the D-2HG-producing mitochondrial enzyme, alcohol dehydrogenase, iron-containing protein 1 (ADHFE1

236 Horse liver alcohol dehydrogenase is a homodimer, the protomer havin

237 Binding of NAD+ to wild-type horse liver alcohol dehydrogenase is strongly pH-dependent and is li

238 We found that ADH3, the major mitochondrial alcohol dehydrogenase, is regulated in a manner similar

239 ted potent and selective inhibition of human alcohol dehydrogenase isoenzymes.

240 Oxidation processes with three of them, alcohol dehydrogenases isolated from horse liver (HLADH)

241 n system for Sulfolobus solfataricus ADH-10 (Alcohol Dehydrogenase isozyme 10) and its use in the dyn

242 ADH2, encoding the alcohol dehydrogenase isozyme required for ethanol oxida

243 For horse liver alcohol dehydrogenase, it was confirmed that the functio

244 e diversity are analyzed for three duplicate alcohol dehydrogenase loci (adh1-adh3) within a species-

245 is of associations between haplotypes at the Alcohol Dehydrogenase locus in Drosophila melanogaster t

246 mechanism of the zinc-dependent medium chain alcohol dehydrogenase (MDR) superfamily remain contentio

247 Here, we report an alcohol dehydrogenase-mediated cyclization step in the b

248 ith the incorporation of glucose oxidase and alcohol dehydrogenase/NAD(+) within the three-dimensiona

249 The cognate cDNA, with similarity to alcohol dehydrogenases (NtADH2) was expressed in E. coli

250 mall but important class of radical-mediated alcohol dehydrogenases operate.

251 alphaA-crystallin or alphaB-crystallin with alcohol dehydrogenase or citrate synthase by applying th

252 r fumarate concentrations are measured using alcohol dehydrogenase or fumarase plus malic dehydrogena

253 ecombinant from Escherichia coli and primary alcohol dehydrogenase (PADH I), were characterized by th

254 ion of alcohol metabolism through either the alcohol dehydrogenase pathway or the cytochrome P450 sys

255 The psychrophilic alcohol dehydrogenase (psADH) cloned from Antarctic Mora

256 Highly abundant short-chain alcohol dehydrogenases (RDHs) in the retina were assumed

257 ding stabilization effect on the T.S. of the alcohol dehydrogenase reactions.

258 rad NSYK motif in the C-terminal short-chain alcohol dehydrogenase/reductase (SDR) domain, which may

259 ified was Hep27, a member of the short-chain alcohol dehydrogenase/reductase (SDR) family of enzymes.

260 er of a vast protein family, the short-chain alcohol dehydrogenase/reductase (SDR) family.

261 Together WOX1 binds Tau via its short-chain alcohol dehydrogenase/reductase domain and is likely to

262 bound Tau via its COOH-terminal short-chain alcohol dehydrogenase/reductase domain.

263 6), a conserved component of the short chain alcohol dehydrogenase/reductase superfamily active site

264 a highly conserved member of the short chain alcohol dehydrogenase/reductase superfamily with a repor

265 In this study, a short chain alcohol dehydrogenase/reductase that co-expresses with t

266 ) from Candida parapsilosis is a short-chain alcohol dehydrogenase/reductase.

267 Only one short-chain alcohol dehydrogenase/reductases (SDRs), which has been

268 nd product yields of eight other short-chain alcohol dehydrogenases/reductases.

269 regions of the Alcohol dehydrogenase (Adh), Alcohol dehydrogenase related (Adhr), Glucose dehydrogen

270 ilum PM1 (mdh2) predicted to encode a type I alcohol dehydrogenase related to the characterized metha

271 aliana) CAD5 and Populus tremuloides sinapyl alcohol dehydrogenase, respectively.

272 e the three-dimensional structure of sinapyl alcohol dehydrogenase (SAD) from Populus tremuloides (as

273 (Triticum aestivum) germin, maize (Zea mays) alcohol dehydrogenase, satellite tobacco necrosis virus

274 t requires CsgA, a member of the short-chain alcohol dehydrogenase (SCAD) family of proteins.

275 Short-chain alcohol dehydrogenases (SCADHs) synthesize a variety of

276 Expression of alcohol dehydrogenase sensitized Caco-2 cells to ethanol

277 to be metabolized, which requires functional alcohol dehydrogenase sodh-1.

278 sis, support the inclusion of SAD in a plant alcohol dehydrogenase subfamily that includes cinnamalde

279 nally, we report CIU-ECD experiments for the alcohol dehydrogenase tetramer, demonstrating improved s

280 ADH1 encodes the major zinc-dependent alcohol dehydrogenase that is utilized during fermentati

281 Five of these (phosphoglycerate mutase, alcohol dehydrogenase, thioredoxin peroxidase, catalase,

282 The use of purified and overexpressed alcohol dehydrogenases to synthesize enantiopure fluorin

283 nes including two alkane monooxygenases, two alcohol dehydrogenases, two aldehyde dehydrogenases, a f

284 protein of S. enterica is an iron-dependent alcohol dehydrogenase used for 1,2-PD catabolism.

285 Mutants of Lactobacillus kefir short-chain alcohol dehydrogenase, used here as ketoreductases (KRED

286 genes (HRG) PYRUVATE DECARBOXYLASE (VvPDC), ALCOHOL DEHYDROGENASE (VvADH2), SUCROSE SYNTHASE (VvSUSY

287 emperature in two variants of a thermophilic alcohol dehydrogenase: W87F and W87F:H43A.

288 tic activities of pyruvate decarboxylase and alcohol dehydrogenase were increased significantly compa

289 of serum albumin, streptavidin, avidin, and alcohol dehydrogenase were probed using cation-to-anion

290 lphaB crystallin when beta(L) crystallin and alcohol dehydrogenase were the chaperone substrates and

291 ol and its substituted analogues mediated by alcohol dehydrogenases were compared to the oxidations b

292 In the first method, eight alcohol dehydrogenases were investigated as biocatalysts

293 as AtCAD7 and 8 (highest homology to sinapyl alcohol dehydrogenase) were catalytically less active ov

294 d alcohols (up to 99% ee) was achieved using alcohol dehydrogenases, whereas chiral transition-metal

295 The first was Thermoanaerobium brockii alcohol dehydrogenase, which stereospecifically catalyze

296 ation is similar to that of ADH that encodes alcohol dehydrogenase, which we have reported previously

297 biotransformation of the aldol adduct by an alcohol dehydrogenase without the need for intermediate

298 Results suggest that in the alcohol dehydrogenases without a Zn(II) cofactor in the

299 y large isotope effect associated with yeast alcohol dehydrogenase (YADH) catalyzed oxidation of etha

300 yde dehydrogenase (Bldh) and NADPH-dependent alcohol dehydrogenase (YqhD) increased 1-butanol product