ライフサイエンスコーパス: enzymatic property

1 onal change that may account for its altered enzymatic properties.

2 and, after purification, investigated their enzymatic properties.

3 li, purified the protein, and determined its enzymatic properties.

4 PDEs 9A5 and 9A1 have similar enzymatic properties.

5 t multiple facets of myosin's mechanical and enzymatic properties.

6 lization of complex IV and alteration of its enzymatic properties.

7 ease of the pancreas with novel physical and enzymatic properties.

8 fied altered Acr2p proteins exhibited normal enzymatic properties.

9 1 RNase H enzymes, yet both possess similar enzymatic properties.

10 a, because, in vitro, they have very similar enzymatic properties.

11 y distinct substrate specificities and other enzymatic properties.

12 d intracellular Ndk and demonstrates similar enzymatic properties.

13 inity copper transporters but share distinct enzymatic properties.

14 in distinct Na,K-ATPase isozymes with unique enzymatic properties.

15 way or to the formation of proteins with new enzymatic properties.

16 ity assays despite some differences in their enzymatic properties.

17 roteases that was screened for four distinct enzymatic properties.

18 ns that modulate TL function and thus pol II enzymatic properties.

19 intimate electronic insight into functional enzymatic properties.

20 gions I and II in determining their distinct enzymatic properties.

21 eir distinct substrate specificity and other enzymatic properties.

22 o they encode E1s with dramatically distinct enzymatic properties.

23 human factor XI have similar structural and enzymatic properties.

24 observed species differences in ecto-ATPase enzymatic properties.

25 yeast and from mammalian cells had identical enzymatic properties.

26 s that may contribute to the known divergent enzymatic properties.

27 systematically characterized their in vitro enzymatic properties.

28 no terminus and exhibit similar yet distinct enzymatic properties.

29 LC3 are partly redundant but differ in their enzymatic properties.

30 on plant lines were consistent with in vitro enzymatic properties.

31 f the system rather than regulating its core enzymatic properties.

32 er of substitutions that can confer specific enzymatic properties.

33 rms of NEIL1 are shown here to have distinct enzymatic properties.

34 deficiency, we characterized their effect on enzymatic properties.

35 y be matched to a biological context through enzymatic properties.

36 decreased ssDNA-binding affinity and altered enzymatic properties.

37 cules require Mg(2+) for their structure and enzymatic properties.

38 Enzymatic properties and acceptor specificity of native

39 In contrast S236A has nearly normal enzymatic properties and actin-translocating activity.

40 Remodeling and exchange have different enzymatic properties and apparently occur in different s

41 families, which have distinct structural and enzymatic properties and are essentially unrelated in se

42 anscripts along with detailed studies of the enzymatic properties and cell biological behavior of hum

43 Taking into account enzymatic properties and coenzyme preferences, a case ca

44 We report here the enzymatic properties and crystal structures of neuramini

45 The enzymatic properties and expression pattern of RalR1 in

46 omains of PKG1alpha (GFP-G1C) to examine the enzymatic properties and intracellular location.

47 Echerichia coli endonuclease IV, both in its enzymatic properties and its amino acid sequence.

48 The enzymatic properties and kinetic parameters of dimeric r

49 s are nearly identical with respect to their enzymatic properties and mass of the deglycosylated prot

50 While the enzymatic properties and physiological functions of NADK

51 The enzymatic properties and quaternary structures of these

52 cytosolic carboxypeptidases share identical enzymatic properties and redundant biological functions.

53 in domain, yet little is known regarding the enzymatic properties and regulation of the kinase cataly

54 Based on enzymatic properties and sequence information, a functio

55 sP-5-OH kinases, or PIP(5)Ks) based on their enzymatic properties and sequence similarities'.

56 egulates the localization of proteins, their enzymatic properties and their interaction with ligands.

57 they provide detailed understanding of their enzymatic properties and their proposed role in a number

58 sence of which confers alterations to pol II enzymatic properties and transcription fidelity.

59 n families distinctions occur with regard to enzymatic properties and type of activity against carboh

60 hylretinol appear to be a consequence of the enzymatic properties, and binding affinities of the isom

61 protease IV in terms of its biochemical and enzymatic properties, and found it to be a unique extrac

62 HoSF and HuHF, consistent with their having enzymatic properties, and is facilitated by higher pH (7

63 recent H1N1 vaccine strain and compared for enzymatic properties, antigenicity, stability, and prote

64 c subunits (STT3A versus STT3B) and distinct enzymatic properties are coexpressed in mammalian cells.

65 terization of native JHDK are described; its enzymatic properties are examined; and its role in cellu

66 However, the extent to which these enzymatic properties are important for the in vivo funct

67 otubularin and MTMR2 demonstrates that their enzymatic properties are indistinguishable, indicating t

68 tryptophan fluorescence, suggesting that the enzymatic properties are normal.

69 GTPases; however, its cellular function and enzymatic properties are poorly understood.

70 reticulum/Golgi apparatus where its putative enzymatic properties as a lipase or acyltransferase, pre

71 Because of its chromosomal position, its enzymatic properties as a receptor phosphatase, which mi

72 ) is highly homologous with and has the same enzymatic properties as its human orthologue.

73 vate kinase displayed identical physical and enzymatic properties as the authentic enzyme.

74 sly expressed human (h)EndoV, share the same enzymatic properties as the recombinant protein and clea

75 is studies provide not only insight into the enzymatic properties but also guidelines for design of P

76 ifferent targeting ranges, specificities and enzymatic properties, but many of them are inactive in m

77 es demonstrate that SERCA Ca2+ transport and enzymatic properties can be accurately measured in mouse

78 synthetic materials display biophysical and enzymatic properties comparable to the biologically expr

79 two recombinant chimeras that have enhanced enzymatic properties compared with the naturally occurri

80 in E. coli and partially purified and their enzymatic properties compared.

81 Biocompatible nanomaterials with enzymatic properties could play a crucial role in the tr

82 We found that the enzymatic properties differ between rNAs containing the

83 rtantly, this model allows the prediction of enzymatic properties directly from cellular growth rates

84 Despite the common enzymatic properties, discrete expression of both isofor

85 the following: (1) ADPR-cyclase in VSMCs has enzymatic properties distinct from "classic" CD38 ADPR-c

86 It is suggested that VanA has different enzymatic properties due to a change in binding specific

87 perimental and computational tools to tailor enzymatic properties, equipping enzyme engineers with th

88 pattern of molecular vibrations, and thus on enzymatic properties, even if the overall amplitudes of

89 tary activity of their unique structures and enzymatic properties for appropriate control of chromati

90 vergent cohorts of transcription factors and enzymatic properties for each RNA polymerase system.

91 ctopyranoside residues and possessed a novel enzymatic property for a family 42 beta-galactosidase.

92 gene) is distinct in sequence, structure and enzymatic properties from both the long-known bacterial

93 owever, the detailed characterization of its enzymatic properties has been lacking.

94 NA molecules stored information and acquired enzymatic properties, has been proposed to have preceded

95 However, their gene expression profiles and enzymatic properties have not been experimentally define

96 oplasma acidophilum has been elucidated, its enzymatic properties have not been explored in depth.

97 iogenesis in Saccharomyces cerevisiae, their enzymatic properties have remained largely biochemically

98 eme oxygenase mutants have spectroscopic and enzymatic properties identical to those of wild type.

99 wever, the two polymerases exhibit different enzymatic properties in vitro.

100 ylate H3 Lys9 displayed remarkably different enzymatic properties in vivo.

101 owever, S198T, caused several alterations in enzymatic properties including shifting the pH optimum f

102 However, evidence on its enzymatic properties, including its substrates, has been

103 cleotide (NAD(+))-dependent deacetylase with enzymatic properties indistinguishable from the yeast en

104 NIR-RIT-treated patients and to analyze the enzymatic properties, inhibitor susceptibility, and stru

105 derstanding the kinetic mechanism of its two enzymatic properties is critical for the discovery of in

106 died extensively, direct comparison of their enzymatic properties is difficult because studies are of

107 Because of their remarkable enzymatic properties, it has been of interest to find ne

108 We show that Pol delta3 has altered enzymatic properties: it is less able to perform transle

109 onstitutes telomerase activity that exhibits enzymatic properties like those of the native enzyme.

110 h these IKKs are structurally similar, their enzymatic properties may provide insights into their uni

111 ing the same reaction and displaying similar enzymatic properties, MJ0883 and bacterial TrmD are comp

112 In addition to its enzymatic properties, murine CD38 has been shown to act

113 We describe physicochemical and enzymatic properties of 5' bridging phosphorothioester l

114 sion programs by binding to and altering the enzymatic properties of a different sensor.

115 Here we describe the primary structure and enzymatic properties of a second secreted variant, terme

116 To characterize the enzymatic properties of ACK, we have expressed and purif

117 The enzymatic properties of actomyosin VIIb are suited for g

118 The enzymatic properties of alpha4beta1 and alpha4beta3 are,

119 To determine the enzymatic properties of BACE2, two variants of its pro-p

120 The enzymatic properties of bcTopo IIIbeta differ substantia

121 e biological role (pigment biosynthesis) and enzymatic properties of BpUGAT are significantly differe

122 is study provides valuable insights into the enzymatic properties of BvPelB and its potential industr

123 The enzymatic properties of CaN heterodimers comprised of th

124 vation process involves an alteration in the enzymatic properties of caspase-8; while procaspase-8 mo

125 We have analyzed the putative enzymatic properties of CCR4 and have found that it cont

126 The spatiotemporal expression pattern and enzymatic properties of class IV ADH are thus consistent

127 Here, we report the first analysis of the enzymatic properties of class VIII myosin.

128 ons between cd(1)NiR and cNOR that influence enzymatic properties of cNOR and oligomerization propert

129 The force-generating and enzymatic properties of conventional kinesin have been e

130 Examining the enzymatic properties of CSB revealed that p53 excludes C

131 The enzymatic properties of cytosolic phospholipase A(2)gamm

132 To investigate the enzymatic properties of Dbh, we characterized the errors

133 Based on marked differences in the enzymatic properties of diacylglycerols compared with ph

134 computational biosensing systems due to the enzymatic properties of DNAzymes and the ligand-inducibl

135 r understand their function, we examined the enzymatic properties of Dpb8, a DExD/H box protein previ

136 fects of these mutations on the physical and enzymatic properties of dynamin have been not examined.

137 in does not significantly modulate the basal enzymatic properties of eEF1A; however, actin may still

138 The enzymatic properties of Est30 and Est55 reported here wa

139 Here we analyze the enzymatic properties of five class I HDAC complexes: CoR

140 y (PHTH) module of Btk, we have compared the enzymatic properties of full-length Btk and a Btk mutant

141 We initially investigated the enzymatic properties of GO(x) by varying glucose and rut

142 t on the effects of Mn(2+) and Mg(2+) on the enzymatic properties of human DNA polymerase iota (pol i

143 Despite 52% identity in primary structures, enzymatic properties of human E-NTPDase 8 expressed in H

144 Direct examination of the motor and enzymatic properties of human MYO3A and MYO3B revealed t

145 activity with a pattern consistent with the enzymatic properties of IDE, whereas inhibitors of acid

146 recombinant Atp1al1-betaHK complex exhibits enzymatic properties of K(+)-dependent ATPase sensitive

147 se is expressed in keratinocytes and has the enzymatic properties of keratinocyte RE hydrolase.

148 Further studies of the enzymatic properties of Kvbeta seem to favor the role of

149 l signaling, but it has been unclear how the enzymatic properties of LGP2 regulate its biological res

150 gether, our studies provide insight into the enzymatic properties of MarP, its substrate preference,

151 had little effect on secretion, sorting, or enzymatic properties of meprin.

152 s study, we identified and characterized the enzymatic properties of MG_186, a calcium-dependent Myco

153 Our results provide insights into the enzymatic properties of MGME1 and a rationale for the co

154 st this hypothesis we have characterized the enzymatic properties of MI(130) using steady-state and s

155 y is increased by mutations that improve the enzymatic properties of Moloney murine leukemia virus re

156 To improve our understanding of the enzymatic properties of mTOR alone and mTOR in its compl

157 The enzymatic properties of MV 1IQ FlAsH were similar to tho

158 The enzymatic properties of myosin VIIB provide a kinetic ba

159 used transient kinetics to characterize the enzymatic properties of N348I RT and determine the bioch

160 Our in vitro studies validate the multi-enzymatic properties of nanoceria, enabling the transiti

161 Here, we compared the enzymatic properties of neuraminidases from two influenz

162 Comparison of the enzymatic properties of NG PBP 4 with other DD-carboxype

163 Investigation of the physical and enzymatic properties of NUDT9 indicates that it is funct

164 ssion of the Stt3p homologs suggest that the enzymatic properties of oligosaccharyltransferase are re

165 n provides insights into the biochemical and enzymatic properties of plasma kallikrein and paves the

166 To begin to define the enzymatic properties of PLC-eta2 and its potential direc

167 The enzymatic properties of poliota appear consistent with t

168 Studies of the enzymatic properties of purified P(4)-ATPase.Cdc50 compl

169 Analysis of the enzymatic properties of purified ParB indicated that the

170 l survival and in parallel characterized the enzymatic properties of purified recombinant Nna1.

171 In this study, the enzymatic properties of rat dynamin II and of D746, a dy

172 vious studies on structural organization and enzymatic properties of rat FDH suggest that the overall

173 tering the DNA regulatory sequence, chi, the enzymatic properties of RecBCD enzyme are altered.

174 The enzymatic properties of recombinant bovine prRDH closely

175 Therefore, the enzymatic properties of recombinant IspC from M. tubercu

176 We demonstrate that the enzymatic properties of recombinant shewasin D are stron

177 In this study the enzymatic properties of retinol dehydratase were examine

178 tical role in many biological processes, the enzymatic properties of RHBDL4 remain largely unknown.

179 We used the assay to study enzymatic properties of ricin such as pH and temperature

180 hotolabeling did not significantly alter the enzymatic properties of S1.

181 ance in T. goesingense, we characterized the enzymatic properties of SATs from T. goesingense.

182 gy to measure SR Ca2+ transport function and enzymatic properties of SR Ca2+ ATPase (SERCA) in indivi

183 Further characterization of the enzymatic properties of synaptojanin now shows that it h

184 tened telomeres in vivo but altered specific enzymatic properties of telomerase in vitro, including i

185 Detailed characterization of the enzymatic properties of telomerase using epimatigote-sta

186 ormation and expand our understanding of the enzymatic properties of telomerase.

187 Both the architecture and enzymatic properties of the 20S proteasome are relativel

188 We have studied the enzymatic properties of the 5'-3' exonuclease, both as a

189 tion will facilitate characterization of the enzymatic properties of the ACD and contribute to our kn

190 Characterization of the enzymatic properties of the alpha4beta1 and alpha4beta3

191 the LF domain of Dbh with that of Dpo4, the enzymatic properties of the chimeric enzyme are more Dpo

192 e larger catalytic subunit and influence the enzymatic properties of the DNA polymerase.

193 tarch biosynthesis was due to differences in enzymatic properties of the enzyme from potato and tomat

194 lly pathological inflammatory reactions, the enzymatic properties of the enzymes responsible for this

195 mensional structures and the biophysical and enzymatic properties of the four gene products.

196 Comparison of the enzymatic properties of the four murine NDSTs revealed s

197 The enzymatic properties of the FP subcomplex, reconstituted

198 he protease on the helicase by comparing the enzymatic properties of the full-length NS3 protein with

199 In this study, we compared the enzymatic properties of the full-length NS5B (FL-NS5B) a

200 To study the enzymatic properties of the intermediates we have mutate

201 inant IpeOMT enzymes with integration of the enzymatic properties of the IpeGlu1 revealed that emetin

202 eters in controlling the electrochemical and enzymatic properties of the LBL films.

203 Enzymatic properties of the liver membrane ecto-ATPDase

204 autocatalytic processing of the proform and enzymatic properties of the mature protease.

205 In this respect, the enzymatic properties of the mixed-linkage beta-glucan sy

206 hough none of the FP tags interfere with the enzymatic properties of the motor, four of the tags (EGF

207 This system is exquisitely tuned through the enzymatic properties of the myosin motor, its lever arm

208 Further characterization of enzymatic properties of the new peptidase was performed.

209 Collectively, these data show that the enzymatic properties of the Pols have diverged over the

210 he AC inhibition, provides insights into the enzymatic properties of the protein, and is a great aid

211 The distinct yet overlapping enzymatic properties of the PS1 gamma-secretase complex

212 The enzymatic properties of the purified catalytic subunit w

213 urified, partially sequenced, and determined enzymatic properties of the rat liver mitochondrial form

214 The enzymatic properties of the re-proteins and their inhibi

215 The enzymatic properties of the RECQ1 helicase and strand an

216 The newly found enzymatic properties of the RECQ1 helicase may have impo

217 By combining these models with the measured enzymatic properties of the Toc GTPases, we provide new

218 r catalytic activity, possibly affecting the enzymatic properties of these isoforms.

219 om two methanogenic archaea and measured the enzymatic properties of these proteins.

220 The differences in the structural and enzymatic properties of these three variants are discuss

221 However, the enzymatic properties of this complex are incompatible wi

222 there is no information about structural and enzymatic properties of this enzyme.

223 The enzymatic properties of this novel ecSOD may have import

224 ral propagation, a full understanding of the enzymatic properties of this protein is lacking.

225 To evaluate enzymatic properties of this protein, a soluble 170-kDa

226 y degraded by the active site of subtilisin, enzymatic properties of this site differ significantly b

227 As the enzymatic properties of this type of RubisCO have not be

228 cones was investigated by examination of the enzymatic properties of three recombinant Fragaria vesca

229 These studies demonstrate that selective enzymatic properties of thrombin can be dissociated by s

230 The enzymatic properties of TM1, TM7, and TM8 mutants were s

231 Membrane binding and enzymatic properties of two double-site mutants (W245A/W

232 This study reports the enzymatic properties of various kinetoplastid PDECs and

233 ta portal that summarizes and contextualizes enzymatic properties of widely used Cas enzymes, equippi

234 (AML) and chondrosarcomas, and share a novel enzymatic property of producing 2-hydroxyglutarate (2HG)

235 s C higher thermostability with no change in enzymatic properties or in the active-site configuration

236 ng affinity to DNA rather than affecting the enzymatic properties per se.

237 The two families of kinases have distinct enzymatic properties, raising the question of how they m

238 M and examined drug susceptibility in vitro, enzymatic properties, replication efficiency, and transm

239 trinsic Ser/Thr protein kinase activity with enzymatic properties similar to Raf-1.

240 lyze all three 4-phosphatase substrates with enzymatic properties similar to the original enzyme.

241 ructure of the AgaA(A355E) mutant, which has enzymatic properties similar to those of AgaB.

242 d molecular weight with O-FucT-1 kinetic and enzymatic properties similar to those of O-FucT-1 purifi

243 n contrast, Ala202CPE or Gly202CPE exhibited enzymatic properties similar to those of wild-type CPE a

244 Two of the mutant proteins exhibited enzymatic properties similar to those of wild-type gluta

245 II at the amino acid level with very similar enzymatic properties, SodCI is dimeric, protease resista

246 re that provided for the molecular tuning of enzymatic properties such as single-base termination and

247 ed by very low fluorescence and has specific enzymatic properties suggesting the existence of a high

248 is enzyme displays substrate specificity and enzymatic properties that are remarkably similar to thos

249 e during polymerization and indicate unusual enzymatic properties that bear on the Ty1 replication pa

250 Each protease is endowed with specific enzymatic properties that determine both substrate choic

251 rat vascular smooth muscle cells (VSMCs) has enzymatic properties that differ from the well-character

252 these data demonstrate that Ube2w has novel enzymatic properties that direct ubiquitination of the N

253 he Src family possess common physical and/or enzymatic properties that enable them to potentiate sign

254 sin II isoforms thus appear to have distinct enzymatic properties that may be of importance in carryi

255 es, by taking advantage of the vast array of enzymatic properties that nature has evolved, as well as

256 ction resolving enzymes, and it has distinct enzymatic properties that suggest it uses a novel enzyma

257 Based on its enzymatic properties, the relationship of the chicken ov

258 ut distinct functions and possess dissimilar enzymatic properties, their catalytic N-terminal domain

259 mone biosynthesis as a result of the diverse enzymatic properties they have evolved.

260 The theory relates dynein's enzymatic properties to its mechanical force production.

261 oduction of Poldelta, which was identical in enzymatic properties to Poldelta isolated from a wild-ty

262 utations and measurement of their effects on enzymatic properties to test mechanistic hypotheses.

263 des for a cytoplasmic AP-P with very similar enzymatic properties to those of mammalian AP-P, and we

264 isoforms GOX1 and GOX2, which share similar enzymatic properties, use glycolate with much higher eff

265 te mutants of human PDE2A and identify their enzymatic properties using a wheat germ in vitro transla

266 hydrolase (EC 3.6.1.29) on the basis of its enzymatic properties we report here.

267 T298C YPK was isolated and purified, and its enzymatic properties were characterized.

268 al pectate lyases were discovered, and their enzymatic properties were characterized.

269 s of three proteins were purified, and their enzymatic properties were characterized.

270 NOS enzymatic properties were defined for rat heart preparat

271 Domains 1B and 2 were purified, and the enzymatic properties were examined.

272 nsient expression system in plants and their enzymatic properties were investigated.

273 erichia coli exhibited essentially identical enzymatic properties which were also similar to those of

274 Human RNase H1 shares many enzymatic properties with Escherichia coli RNase H1.

275 man (rh)IKK-i and rhTBK-1 and compared their enzymatic properties with those of rhIKK-2.

276 rogenase expressed in rat liver had distinct enzymatic properties; yet ethanol inhibited cytosolic re