ライフサイエンスコーパス: esterase

1 ceptor-destroying sialate-O-acetylesterase ("esterase").

2 rough binding the ColQ tail of acetylcholine esterase.

3 minal domain of calmodulin into an efficient esterase.

4 2 is not a potent inhibitor of acetylcholine esterase.

5 tion affecting the catalytic activity of the esterase.

6 , but is efficiently removed by an exogenous esterase.

7 ability to inhibit the enzyme acetylcholine esterase.

8 on the oligomeric assembly of hemagglutinin-esterase.

9 with no significant change in acetylcholine esterase.

10 ied cells that express a substrate-selective esterase.

11 r hydrolysis reactions catalyzed by a serine esterase.

12 of any previously reported de novo designed esterases.

13 as well as controlled deactivation by plasma esterases.

14 esidue peptides that act as Zn(2+)-dependent esterases.

15 of additional not yet characterized lipases/esterases.

16 he consensus motif "GXSXG" characteristic of esterases.

17 Sulfonyl fluorides are known to inhibit esterases.

18 t enzymatically active member of a family of esterases.

19 D-39-type apyrase, adenosine deaminases, and esterases.

20 for the differences in activities in the two esterases.

21 structure of AF-Est2 with the human carboxyl esterase 1, which has CoA thioesterase activity, reveals

22 main with the typical fold of a carbohydrate esterase 4 and an N-terminal domain unique for this fami

23 eta-xylosidase/alpha-arabinosidase, feruloyl esterase, acetylxylan esterase, and a Xanthomonas oryzae

24 Using the Ellman assay to measure ACh esterase (AChE) activity that breaks down ACh, the secon

25 accumulation of Abeta, reduced acetylcholine esterase (AChE) activity, and accelerated deterioration

26 e a highly potent inhibitor of acetylcholine esterase (AChE) and unsuitable for development.

27 used to follow the activity of acetylcholine esterase, AChE, and to probe its inhibition.

28 The esterase active-site residues are located at the apical

29 SsE(M28) possesses much lower esterase activities against triglycerides and other este

30 he mutant strain lost most of its lipase and esterase activities and displayed reduced virulence in c

31 In S. invicta, male alates had the highest esterase activities followed by workers then female alat

32 Esterase activities in S. invicta were always significan

33 petitive inhibition of the dehydrogenase and esterase activities of the enzyme.

34 Specific esterase activities were determined each 2 days over a p

35 Esterase activities were measured for workers and male a

36 erted into the active species 2c by secreted esterase activities.

37 ae1A and BiFae1B, were functionally assigned esterase activities.

38 both endo-beta-1,4-xylanase and ferulic acid esterase activities.

39 eviously observed to have either high or low esterase activity against artificial substrates.

40 esidues are positively correlated with fecal esterase activity and acetate level of human diabetes.

41 Here we explore the minimal requirements for esterase activity by computationally designing artificia

42 he xylanase domain (E280S), the ferulic acid esterase activity increased threefold, which suggests th

43 es in the esterase domain suggested that the esterase activity is derived from a tetrad composed of S

44 MeSA esterase activity is required in distal, healthy tissue

45 We have validated the esterase activity of 80 selected genes, which belong to

46 Notably, the classical esterase activity of AChE is dispensable for this activi

47 opied the DeltahfsH mutant and abolished the esterase activity of HfsH.

48 , although each showed a higher ferulic acid esterase activity on methyl-ferulate.

49 binding or provide the protease, lipase, or esterase activity required for entry of the virus into a

50 ly higher levels of variation about the mean esterase activity than S. invicta.

51 more invasive S. invicta would have a higher esterase activity than S. richteri.

52 However, survival measured by esterase activity was higher for C. auris than C. paraps

53 able microorganisms exhibiting intracellular esterase activity were detected on >90% of both NC types

54 s seem to exhibit no significant protease or esterase activity when tested against analogous substrat

55 Optimized conjugate 16 was designed so that esterase activity will liberate 5 and cathepsin K cleava

56 m stems of these species exhibit only a weak esterase activity with caffeoyl shikimate.

57 le, fluorogenic probe was developed to sense esterase activity with single-molecule resolution.

58 hosphatidylserine, DNA breaks, intracellular esterase activity, and activation of caspase-8, -9, and

59 Intracellular esterase activity, sub-G(1) cell cycle arrest, and caspa

60 As indicated by assays that measure esterase activity, sub-G(1) fractions, mitochondrial act

61 are bifunctional enzymes containing a trans-esterase activity, which is responsible for nicking the

62 ic microenvironment, which shows significant esterase activity.

63 ls high in esterases over fibroblasts low in esterase activity.

64 proposed biosensor was obtained using 0.5 U esterase activity.

65 ters are apparently important markers of LAB esterase activity.

66 sed to reconstruct a super-resolved image of esterase activity.

67 d, how does the L29P substitution change the esterase activity?

68 s, we identified GDSL1, a member of the GDSL esterase/acylhydrolase family of plant proteins.

69 A new carboxyl esterase, AF-Est2, from the hyperthermophilic archaeon A

70 activity of GH5 and GH26 mannanases and CE2 esterases against intact plant cell walls.

71 The lipase/esterase also elicited a hypersensitive response in grap

72 The activity of pectin methyl esterase and beta-glucosidase was enhanced in ET-treated

73 y of biomass from plants expressing feruloyl esterase and beta-xylosidase/alpha-arabinosidase.

74 , temperature and substrate conditions using esterase and caseinolytic activity assays and time cours

75 cies, suggesting that high expression of the esterase and consequent low ester content may provide an

76 terplay of the virion-attached hemagglutinin-esterase and fusion glycoproteins.

77 TI, a negative dipstick result for leukocyte esterase and nitrites excludes infection.

78 characterized a novel periplasmic trilactone esterase and suggested a new model of FeEnt acquisition

79 er hydrolysis reaction catalyzed by a serine esterase and, therefore, one no longer can simply assume

80 ester groups are processed by intracellular esterases and accumulate in cells.

81 tible to the sequential actions of bacterial esterases and sialidases.

82 rabinosidase, feruloyl esterase, acetylxylan esterase, and a Xanthomonas oryzae putative a-L: -arabin

83 ding an absence of protein, blood, leukocyte esterase, and nitrites.

84 e ester group and thus its susceptibility to esterase, and structural features critical to the lacton

85 ion and activity of the enzyme pectin methyl-esterase, and the chelation of calcium by pectic acids.

86 EGG pathway profiling predicts that kinases, esterases, and hydrolases may contribute to venom activi

87 rolases, polysaccharide lyases, carbohydrate esterases, and lytic polysaccharide monooxygenases.

88 Esterase- and phosphatase-sensitive H2S2 prodrugs with t

89 O-acetylation, and an O-acetylpeptidoglycan esterase (ape1) for de-O-acetylation.

90 ibition of pancreatic lipase and cholesterol esterase, as well as cholesterol micelle formation and b

91 ses, polysaccharide lyases, and carbohydrate esterases, as well as accessory, redox-active enzymes fo

92 paradigm pimeloyl-ACP methyl ester carboxyl-esterase, BioH.

93 lysis but is a highly reactive substrate for esterases both in vitro and in cellulo, yielding a brigh

94 or their capacities to inhibit acetylcholine esterase but, in contrast to the predictions from dockin

95 r masking motif that is stable to endogenous esterases, but is efficiently removed by an exogenous es

96 The sulfocoumarins were hydrolyzed by the esterase CA activity to 2-hydroxyphenyl-vinylsulfonic ac

97 Unlike coumarins which are hydrolyzed by the esterase CA activity to the corresponding 2-hydroxy-cinn

98 knockdown approach, we identified a specific esterase, carboxylesterase 1, whose function had a clear

99 on until entry into a cell, where endogenous esterases catalyze the hydrolysis of the masking groups,

100 tified a mutant G4C/S10C/T172R/G173Q cocaine esterase (CCRQ CocE) with an in vitro duration of action

101 hat is a member of the family 4 carbohydrate esterases (CE4s) and a domain structurally similar to gl

102 arrel common to the family four carbohydrate esterases (CE4s) with the canonical motifs circularly pe

103 analysis identified a unique Ent trilactone esterase Cee (Cj1376) in C. jejuni.

104 The esterase Chath_Est1 from the anaerobic risk 1 strain Clo

105 ssay for total cholesterol using cholesterol esterase/cholesterol oxidase coupled with the luminol-H2

106 thrombin inhibitor as a single, macrocyclic esterase-cleavable (acyloxy)alkoxy prodrug.

107 polyethylene glycol (PEG)ylated lipids with esterase-cleavable linkers (e.g., ME42) to promote intra

108 Rhodococcal cocaine esterase (CocE) is an attractive potential treatment for

109 Bacterial cocaine esterase (CocE) is the fastest known native enzyme that

110 d that administration of a cocaine hydrolase/esterase (CocH/CocE) can considerably decrease the cocai

111 four members but lacks the canonical lipase/esterase consensus catalytic sequences, and their enzyma

112 oxil bisphosphonate esters enter cells where esterases convert them to their active acids.

113 ave previously identified caffeoyl shikimate esterase (CSE) as an enzyme in the monolignol biosynthes

114 Caffeoyl shikimate esterase (CSE) was recently shown to play an essential r

115 -5-hydroxylase (F5H), and caffeoyl shikimate esterase (CSE), were targeted by MYB31 or MYB42, but in

116 of E. coli H1187 (fepA-) or the enterobactin esterase-deficient derivative of E. coli K-12 JW0576 (fe

117 Although CE2 esterases display similar specificities against acetylat

118 we have developed a mutant bacterial cocaine esterase (DM-CocE), which has been previously shown to r

119 inds to a conserved epitope in the vestigial esterase domain of hemagglutinin (HA) and blocks HA-medi

120 highly conserved active-site residues in the esterase domain suggested that the esterase activity is

121 Sequence alignments of the esterase domains in BiFae1B with the feruloyl esterase f

122 in the Sia-binding sites of both lectin and esterase domains.

123 y modest architectural changes in lectin and esterase domains; and (iii) a single, inconspicuous Ala-

124 articles are fully degradable in response to esterases due to an embedded ester cross-linker in the p

125 due to the activity of beta-glucosidase and esterase during the first months of storage and then a s

126 enes S85 Axe6B (FSUAxe6B) is an acetyl xylan esterase encoded in the genome of this rumen bacterium.

127 ame enzyme acting in concert with a putative esterase encoded upstream.

128 o samples were quantified with a cholesterol esterase enzymatic reaction.

129 The decarboxylase and esterase enzymes that effect this valuable transformatio

130 Unlike warfarin, it is metabolized by esterases, escaping metabolism by the cytochrome P450 sy

131 the first structure of a full-length AT, the esterase EstA from Pseudomonas aeruginosa, at a resoluti

132 Two purified esterases (EstA2 and EstB28) synthesised ethyl butanoate

133 Here, we describe a generalizable esterase-ester pair capable of targeted delivery of smal

134 of glutathione-S-transferase (GST), general esterases (ESTs) and phenol oxidase (PO) decreased in th

135 All of the new VoltageFluors targeted by esterase expression (VF-EXs) report single spikes in cul

136 The carbohydrate esterases family 1 (CE1s) is a diverse group of enzymes

137 sterase domains in BiFae1B with the feruloyl esterase from Clostridium thermocellum suggest that both

138 Here, we show that exposure to an esterase from Mycobacterium smegmatis (Msmeg_1529), hydr

139 O-Acetylpeptidoglycan esterase from Neisseria gonorrhoeae functions to release

140 ion catalyzed by the versatile lipase/sterol esterase from the ascomycete fungus O. piceae.

141 A chlorogenic acid esterase from this basidiomycete was expressed in good y

142 rain bacteriuria (from 7% to 69%), leukocyte esterase (from 31% to 64%), and symptoms (from 3% to 43%

143 of eight aliphatic polyesters by two fungal esterases (FsC and Rhizopus oryzae lipase) at different

144 Secreted esterases further hydrolyze the adhesive polymer, exposi

145 ce in cells expressing tobacco pectin methyl esterase fused to green fluorescent protein (PME-GFP).

146 Molecular modeling of the hemagglutinin esterase fusion protein of D/3-13 identified a mutation

147 y a chimeric influenza C virus hemagglutinin/esterase/fusion (HEF) segment carrying the HA packaging

148 hat the recently characterized acetylcholine esterase gene, choE (PA4921), is also regulated by GbdR.

149 n(2+) bimetallo core is an effective mono/di-esterase generalist and that the bimetallo cores were no

150 tudy provides evidence that purified O. oeni esterases have the ability to both synthesise and hydrol

151 It is also unclear whether hemagglutinin-esterase (HE) protein plays a role in viral entry.

152 hCoV-HKU1 encodes a hemagglutinin-esterase (HE) protein that is unique to the group a beta

153 The hemagglutinin esterase (HE) protein was truncated, and reverse transcr

154 complex of the ISAV F and ISAV hemagglutinin esterase (HE) proteins in an unknown stoichiometry prior

155 Hemagglutinin-esterases (HEs) are bimodular envelope proteins of ortho

156 Hog liver esterase (HLE) hydrolyzed chlorogenic acid lactones (CQA

157 Both purified esterases hydrolysed ethyl butanoate, ethyl hexanoate an

158 fferences were observed and strains with low esterase hydrolysis activity against artificial substrat

159 QALs, FQALs) selectively, while chlorogenate esterase hydrolyzed all chlorogenic acids (CQAs, FQAs) a

160 f alcohol acyl-transferase EEB1 and the acyl esterase IAH1.

161 Exposure to the esterase immediately releases free mycolic acids, while

162 rface and two effectors, glucose oxidase and esterase, immobilized on the Au face.

163 t drug 1 in vivo by alkaline phosphatase and esterase in a stepwise manner, providing higher exposure

164 ly suggested that Cee is the sole trilactone esterase in C. jejuni.

165 etic peptide-derived cGMP hydrolysis by this esterase in diseased heart myocardium.

166 Interestingly, expression of the esterase in normal fibroblasts or endothelial cells had

167 s, suggesting the presence of a TDM-specific esterase in this pathogen.

168 usceptible to enzymatic hydrolysis by plasma esterases in a controllable manner, while their metaboli

169 Detailed characterization of this esterase including elucidation of the crystal structure

170 bsequently screened to establish the SAR for esterase inhibition.

171 ts received intravenous recombinant human C1 esterase inhibitor (50 IU/kg; maximum 4200 IU) twice wee

172 cks of hereditary angioedema (HAE) due to C1 esterase inhibitor (C1-INH) deficiency (C1-INH-HAE) incl

173 C1 esterase inhibitor (C1-INH) is a soluble regulator of co

174 Recombinant human C1 esterase inhibitor (C1INH) serves as a promising future

175 To explore whether C1 esterase inhibitor (C1INH), an endogenous inhibitor of t

176 fusion of C1-esterase inhibitor increased C1-esterase inhibitor (p < .005 vs. control on days 2, 3, a

177 ngioedema (HAE) in the presence of normal C1 esterase inhibitor activity (FXII-HAE).

178 study, patients in the lowest quartile of C1-esterase inhibitor activity in combination with high C-r

179 Quartile analysis of C1-esterase inhibitor activity in sepsis subjects revealed

180 study assesses the influence of high-dose C1-esterase inhibitor administration on systemic inflammato

181 Hereditary angioedema with normal C1 esterase inhibitor and mutations in the F12 gene (HAE-FX

182 Infusions of plasma-derived C1 esterase inhibitor deter attacks of hereditary angio-oed

183 assess the efficacy of recombinant human C1 esterase inhibitor for prophylaxis of hereditary angio-o

184 urvival implications for individuals with C1-esterase inhibitor functional deficiency.

185 prophylactic effect of recombinant human C1 esterase inhibitor has not been rigorously studied.

186 Overall, infusion of C1-esterase inhibitor increased C1-esterase inhibitor (p <

187 In general, high-dose C1-esterase inhibitor infusion down-regulated the systemic

188 Simultaneously, C1-esterase inhibitor infusion in sepsis patients was assoc

189 randomized to receive either 12,000 U of C1-esterase inhibitor infusions in addition to conventional

190 4200 IU) twice weekly, recombinant human C1 esterase inhibitor once weekly and placebo once weekly,

191 ATION: Prophylaxis with recombinant human C1 esterase inhibitor provided clinically relevant reductio

192 n hIL1ra(Ast)(+/+) mice, the cholinergic ACh esterase inhibitor pyridostigmine increases ACh levels a

193 These normal-level C1-esterase inhibitor sepsis patients nevertheless displaye

194 XII-driven coagulation and the ability of C1-esterase inhibitor to bind and inhibit activated FXII we

195 nificantly reduced with recombinant human C1 esterase inhibitor twice weekly (2.7 attacks [SD 2.4]) a

196 ents given twice-weekly recombinant human C1 esterase inhibitor, 13 (45%) of 29 patients given the on

197 nt or conventional treatment only (n = 41 C1-esterase inhibitor, 20 controls).

198 C1-esterase inhibitor, an endogenous acute-phase protein, r

199 y plasmin, escape from inhibition through C1 esterase inhibitor, and elicit excessive bradykinin form

200 lated to treatment with recombinant human C1 esterase inhibitor, but both resolved without additional

201 Blood samples for measurement of C1-esterase inhibitor, complement components C3 and C4, and

202 rmacokinetic profile of recombinant human C1 esterase inhibitor, our results suggest that efficacy of

203 ery 60 s while neostigmine, an acetylcholine esterase inhibitor, was infused into the medial prefront

204 We hypothesized that application of C1-esterase-inhibitor (C1-INH) in LTX-recipients showing ea

205 unctional proteome analysis using lipase and esterase inhibitors revealed a subset of candidate genes

206 bled eight copies of a C3-symmetric trimeric esterase into a well-defined octahedral protein cage by

207 shown that high expression of a non-specific esterase is critical for the low overall ester content o

208 shown that high expression of a non-specific esterase is critical for the low overall ester content o

209 The usefulness of wild-type (wt) cocaine esterase is hampered by its inactivation at 37 degrees C

210 falciparum Prodrug Activation and Resistance Esterase) is required for activation of esterified pepst

211 sly determined a crystal structure of the JH esterase (JHE) of the tobacco hornworm Manduca sexta (Ms

212 io-3-oxobutyl groups have been introduced as esterase-labile phosphodiester protecting groups that ad

213 ized and tested as a substrate for leukocyte esterase (LE), an enzyme produced by leukocytes (white b

214 the Xf secretome revealed a putative lipase/esterase (LesA) that was abundantly secreted in bacteria

215 mal UA finding (greater-than-trace leukocyte esterase level, positive nitrite test result, or pyuria)

216 n-regulated genes including juvenile hormone esterase-like protein et al.

217 This study demonstrates that ABH is an esterase/lipase with catalytic Ser-His-Asp triad.

218 YTYL ESTER SYNTHASE1 [PES1] and PES2) of the esterase/lipase/thioesterase family of acyltransferases

219 ty of catalytic tandem reactions that employ esterases, lipases or alcohol dehydrogenases and gold(I)

220 Prodrugs that release hydrogen sulfide upon esterase-mediated cleavage of an ester group followed by

221 Importantly, we also demonstrate that the esterase-mediated rapid lysis of M. tuberculosis signifi

222 crystal structure of the metal-ion dependent esterase MGS0169 from the amidohydrolase superfamily rev

223 water-soluble p-nitrophenolate catalyzed by esterase-mimic SAE.

224 circularly permuted family four carbohydrate esterase motifs.

225 ch is cleaved by a novel TDM-specific serine esterase, Msmeg_1529.

226 Parasites with esterase mutations are resistant to pepstatin esters and

227 g protein 6, also known as neuropathy target esterase (NTE), which is the target of toxic organophosp

228 that LipC is a novel cell surface-associated esterase of M. tuberculosis that is highly immunogenic a

229 The esterases of pimelate moiety synthesis show remarkable g

230 e similarity to the family CE-3 carbohydrate esterases of the CAZy classification system.

231 ophytic fungus Eupenicillium shearii FREI-39 esterase on halloysite, using graphite powder, multi-wal

232 ons identified by staining for acetylcholine esterase or conjugated alpha-bungarotoxin binding.

233 stick analyses for the presence of leukocyte esterase or nitrites, microscopic analysis for white blo

234 ding reactivity, inhibition of acetylcholine esterase or uncoupling of oxidative phosphorylation.

235 on level of specific enzymes like proteases, esterases or glycosidases is often higher in tumor cells

236 DA-ZP1-TPP is insensitive to intracellular esterases over a 2-h period and is impervious to proton-

237 gene expression in the cancer cells high in esterases over fibroblasts low in esterase activity.

238 t in TraB proteins, but also in erythromycin esterase (Pfam ID: PF05139), DUF399 (domain of unknown f

239 9P, in Pseudomonas fluorescens (SIK WI) aryl esterase (PFE) increased the specificity constant of PFE

240 nt parasite mutants, we find that a parasite esterase, PfPARE (P. falciparum Prodrug Activation and R

241 with the surface glycoprotein hemagglutinin esterase phylogeny, were observed between the two lineag

242 Esterases play a crucial role in toxic tolerance of inse

243 (2-ethyl)norleucinate (4) with porcine liver esterase (PLE) immobilized on Sepabeads.

244 an be removed by the action of porcine liver esterase (PLE) to reveal the bright unmodified VoltageFl

245 he methyl-transferase LCMT-1, and the methyl-esterase PME-1.

246 esterification via decreasing pectin methyl esterase (PME) activity in roots and leaves under unstre

247 The inactivation kinetics of pectin methyl esterase (PME) during the shelf life (4 degrees C-180 da

248 ntially demethyl esterified by pectin methyl esterase (PME) to strengthen or loosen plant cell walls

249 ppressed by a null allele of a pectin methyl esterase (PME3) whose activity normally leads to cross-l

250 gues seem the sole pimeloyl-ACP methyl ester esterase present in the Helicobacter species and their o

251 We recently reported that the secreted esterase produced by serotype M1 GAS (SsE(M1)) reduces n

252 Importantly, ISAV hemagglutinin-esterase receptor engagement does not initiate conformat

253 probable 9-O-acetyl N-acetylneuraminic acid esterase required for E. coli to grow on this alternativ

254 An esterase-responsive charge-reversal polymer mediates sel

255 hydrophilic polyethylene glycol (PEG) and an esterase-responsive hydrophobic dendron, to prepare and

256 is insertion causes higher expression of the esterase, resulting in the reduced levels of multiple es

257 click chemistry", to develop new fluorogenic esterase sensors.

258 the CovRS-controlled secreted streptococcal esterase (SsE).

259 Whether examined by esterase staining, phosphatidyl-serine staining, DNA bre

260 counts were examined by using chloroacetate esterase staining.

261 eal a conserved epitope in the HA1 vestigial esterase subdomain that is some distance from the recept

262 How the switch in esterase substrate specificity was realized remained unr

263 core of the transition in lectin ligand and esterase substrate specificity; (ii) in consequence, the

264 were seen or if either nitrates or leukocyte esterase testing was positive.

265 ed by a combination of nitrite and leukocyte esterase tests can be used.

266 Nitrite, leukocyte esterase tests, and urine microscopy alone were of poor

267 es were evaluated with nitrite and leukocyte esterase tests, using urine culture and/or dipslide with

268 ble antimalarial; (2) PfPARE is a functional esterase that is capable of activating prodrugs; (3) Mut

269 er of JH is hydrolyzed in many insects by an esterase that shows high specificity for JH.

270 work has shown that Oenococcus oeni produces esterases that are capable of hydrolysing artificial sub

271 ilarity to a class of proteins that includes esterases, the heme-binding protein ChaN, and an unchara

272 ast to previously described chlorogenic acid esterases, the reUmChlE was also active towards feruloyl

273 When treated with hog liver esterase, these groups were removed by enzymatic deacyla

274 he persulfide prodrug can be activated by an esterase to generate a "hydroxymethyl persulfide" interm

275 f taurine and D-peptide allows intracellular esterase to trigger intracellular self-assembly of the D

276 a xylan binding CBM reduced the capacity of esterases to deacetylate xylan in tobacco walls.

277 Sacubitril is converted by esterases to LBQ657, which inhibits neprilysin, the enzy

278 posure) and b) can be metabolized by porcine esterases to TBMEHP, which c) elicited maternal thyrotox

279 TBPH was metabolized by purified porcine esterases to TBMEHP.

280 uorescent probe are cleaved by intracellular esterases to yield the corresponding negatively charged,

281 rability and efficacy of a novel cholesterol esterase transfer protein (CETP) inhibitor TA-8995 in pa

282 Exogenous pectin methyl esterase treatment of pollen tubes, which demethoxylates

283 After esterase treatment, micelle-delivered beta-lap-dC3 and -

284 the crystal structures of ISAV hemagglutinin-esterase unbound and complexed with receptor.

285 of carbofuran pesticide by inhibition of the esterase using square-wave voltammetry (SWV).

286 conserved protein domain carrying an acetyl esterase was found to be associated with at least one ta

287 rgistic combination of xylanase and feruloyl esterase was found to be the most efficient enzymatic tr

288 tyl Neu5Ac by lentiviral transduction of the esterase was lethal to ALL cells in vitro even in the pr

289 HbA1c but no association with acetylcholine esterase was noticed.

290 e, by expressing an intracellular form of JH esterase, we demonstrate that JH must enter the cell in

291 Cholesterol oxidase and cholesterol esterase were assembled on the surface of graphene by in

292 creted glycoside hydrolases and carbohydrate esterases were identified in the genome, revealing a div

293 ALE: Phosphodiesterase 2 is a dual substrate esterase, which has the unique property to be stimulated

294 Phosphodiesterase 2 is a dual substrate esterase, which has the unique property to be stimulated

295 nascent esters are substrates for endogenous esterases, which regenerate native protein.

296 or CB receptors and is deactivated by plasma esterases while the respective acid metabolite is inacti

297 It has been demonstrated to be a serine esterase with sequence similarity to the family CE-3 car

298 egrating cholesterol oxidase and cholesterol esterase with the hybrid material.

299 Here we show that carboxylesterase 1/esterase-x (Ces1/Es-x) plays a regulatory role in hepati

300 encode a bifunctional xylanase-ferulic acid esterase (xyn10D-fae1A) and expressed the recombinant pr