ライフサイエンスコーパス: biochemical property

1 MT bundles as a consequence of two inherent biochemical properties.

2 otein due to its outstanding biophysical and biochemical properties.

3 F, Y503F, and Y108F/Y503F, and studied their biochemical properties.

4 umber of physicochemical, environmental, and biochemical properties.

5 been postulated to contain distinct primary biochemical properties.

6 idance of certain protein mutations based on biochemical properties.

7 pecific sources of extrinsic variability and biochemical properties.

8 ases resulted in remarkable changes of their biochemical properties.

9 he Zea mays gene, At3g26430, and studied its biochemical properties.

10 ts other deubiquitinase and peptide cleavage biochemical properties.

11 ds, and examined their sequence features and biochemical properties.

12 is characterized by unique morphological and biochemical properties.

13 tion at position 172 and the analysis of its biochemical properties.

14 riants were identified on the basis of their biochemical properties.

15 er in their tissue distribution and in their biochemical properties.

16 tant derivatives of Gln91 and analyzed their biochemical properties.

17 However, little is known about its biochemical properties.

18 NUCB1) and characterized its biophysical and biochemical properties.

19 ferentially identify proteins based on their biochemical properties.

20 reviously noted changes in its antigenic and biochemical properties.

21 ntibiotic fredericamycin and investigate its biochemical properties.

22 ferent roles reflecting differences in their biochemical properties.

23 uce different variants in vivo have distinct biochemical properties.

24 ce-to-volume ratio and excellent optical and biochemical properties.

25 0) and FXN(81-210) have strikingly different biochemical properties.

26 from the Stat3 SH2 domain, replicates Stat3 biochemical properties.

27 for biological significance of these unique biochemical properties.

28 que structure and displays a unique array of biochemical properties.

29 to three biovars, based on physiological and biochemical properties.

30 al reaction, taking advantage of specialized biochemical properties.

31 unctionally important, yet generally unknown biochemical properties.

32 y of how an enzyme's sequence relates to its biochemical properties.

33 tissue distribution, expression levels, and biochemical properties.

34 However, little is known about its biochemical properties.

35 ing the growth environment modified both the biochemical properties and [PSI(+)]-inducing capabilitie

36 in yeast mitochondria showed that TbMCP5 has biochemical properties and ADP/ATP exchange kinetics sim

37 ally inactivated for Rad52 binding for their biochemical properties and also for functional interacti

38 Here we have characterized the biochemical properties and biological function of one of

39 rupted mutant Ago proteins and studied their biochemical properties and biological functionality in c

40 these species have very similar physical and biochemical properties and can cross-contaminate each ot

41 hly conserved in sequence, exhibit different biochemical properties and cellular roles.

42 Here we report the biochemical properties and crystal structures of both a

43 resents recent advances in understanding the biochemical properties and evolution of the primate orth

44 by transporting cholesterol to neurons, the biochemical properties and function of apoE secreted by

45 However, the biochemical properties and functional roles of putative

46 42-210) and FXN(81-210)) that have different biochemical properties and functional roles.

47 oadenosine phosphorylase (MTAP) based on its biochemical properties and mass spectrometry analysis.

48 Four mutants have biochemical properties and overall structures that are i

49 -syn intermediates in neuron function, their biochemical properties and pathobiological functions in

50 Based on unprecedented biochemical properties and phylogenetic analysis, we pro

51 ll, this work provides new insights into the biochemical properties and possible toxicity of coumarin

52 ch has allowed a better understanding of its biochemical properties and potential clinical benefits.

53 li by modulating a wide range of fundamental biochemical properties and processes, including the stab

54 structural insight for their biophysical and biochemical properties and reactivity.

55 ow a strong correlation between its in vitro biochemical properties and the aberrant intracellular fu

56 The biochemical properties and the HER2 binding affinity app

57 the actin cytoskeleton, we investigated the biochemical properties and the structural organization o

58 utations in the same gene may have different biochemical properties and thus different evolutionary c

59 a suite of aggregated conformers with unique biochemical properties and toxicities.

60 Combining the expression data, biochemical properties, and cellular features, we conclu

61 m, we analyzed the developmental expression, biochemical properties, and function of several glycosid

62 o evaluate protein expression, localization, biochemical properties, and function.

63 mber of the FKBP superfamily in terms of its biochemical properties, and it plays an important biolog

64 re the expression, subcellular localization, biochemical properties, and potential functions of LEA p

65 umented in many cases, but the identity, the biochemical properties, and the structure of the actual

66 tails, showing that these too exhibit unique biochemical properties--and are also likely to play a fu

67 al cardiac performance, information on cMLCK biochemical properties are limited.

68 the complete, four-subunit CPC and its basic biochemical properties are only beginning.

69 signaling mechanisms that exploit its unique biochemical properties as a free radical.

70 hese samples are commercialised due to their biochemical properties as ingredients of food supplement

71 c variation affects development, physiology, biochemical properties as well as mitochondrial transcri

72 wever, the specific cleavage site(s) and the biochemical properties as well as the functional consequ

73 to simultaneously map their biophysical and biochemical properties at sub-nanometer resolution.

74 plectin keratinocytes is not due to altered biochemical properties because, like full-length plectin

75 ndent of their absolute quantities and basic biochemical properties but is dictated by the compositio

76 rs200673353, MAF = 0.001), and studied their biochemical properties by magnetic tweezers-based superc

77 latory proteins permitted by their intrinsic biochemical properties can be effectively restricted in

78 gest that DNA polymerases with complementary biochemical properties can function cooperatively at rep

79 Currently, its biochemical property, cellular distribution and physiolo

80 These simple biochemical properties, combined with feedback control o

81 c connectivity have distinct topological and biochemical properties compared with static M-modules an

82 cule displayed improved production rates and biochemical properties compared with wild-type IgA.

83 d Methanosarcina acetivorans (MaTLP) display biochemical properties consistent with a prominent role

84 aldehyde substrates, respectively, and have biochemical properties consistent with those previously

85 rties, in conjunction with the corresponding biochemical properties could help to distinguish stem ce

86 er of LDCVs and affects their morphology and biochemical properties, due to impaired cargo sorting an

87 which multiple Galpha proteins with variable biochemical properties exist, plants have fewer, highly

88 We show that Exo70 has the biochemical properties expected of a direct effector for

89 ce of related scaffolds that display diverse biochemical properties for biotechnological applications

90 The possible importance of these biochemical properties for the regulation of Arabidopsis

91 Developing specific tools with defined biochemical properties for the reversible modulation of

92 namics of residues participating in the same biochemical property, for example, RNA binding, nucleoti

93 these animals showed mixed spectroscopic and biochemical properties from both parental and progeny se

94 at devices engineered by combining favorable biochemical properties from multiple known polymerases c

95 roteins, but their existence, structure, and biochemical properties have not been characterized exper

96 classified as A- or B-types on the basis of biochemical properties, have a conserved globular head,

97 These isoforms exhibit different biochemical properties; however, their function in sperm

98 d a series of Sry mutants, and studied their biochemical properties in cell lines and transgenic mous

99 and reveal evolutionary conservation of NatA biochemical properties in higher eukaryotes and uncover

100 sized relationship between functionality and biochemical properties in ligases, we have conducted stu

101 e HMR, which begins from Lys-58, retains its biochemical properties in phytochrome signaling.

102 terium tuberculosis (KATmt) show distinctive biochemical properties in terms of cAMP binding affinity

103 However, their biochemical properties in vitro have remained obscure.

104 se enzymes have been shown to possess common biochemical properties in vitro, including the ability t

105 How the biochemical properties including binding of dinucleotide

106 iral IAPs have common motifs, share multiple biochemical properties including oligomerization, and ac

107 tein expressed in HEK cells exhibited intact biochemical properties, inclusive trafficking into the p

108 a enterica lacking apbC have nutritional and biochemical properties indicative of defects in iron-sul

109 he C2 domains (most likely C2B, based on its biochemical properties) interacts with the membrane and

110 The knowledge of their biochemical properties is, however, limited, and the tra

111 Consistently, GLD-2 has distinct biochemical properties: It displays unusual specificity

112 The two biochemical properties known for ORF1p are high-affinity

113 canopy structural (leaf area index, LAI) and biochemical properties (leaf chlorophyll and nitrogen co

114 is associated with changes in four distinct biochemical properties likely crucial for LRRK2 function

115 h the subcellular location of HSFA1D and its biochemical properties, making it a key early component

116 Such biochemical properties might be exploited to reliably pr

117 with reference to their physicochemical and biochemical properties, moreover, the total free amino a

118 We focus on its biochemical properties, mRNA targets, and possible role

119 rational vaccine design, we interrogated the biochemical properties of 9,888 MHC class I peptides.

120 Ced-6 exhibits all the known biochemical properties of a clathrin-associated sorting

121 ytoplasmic domain of Nla28S has the in vitro biochemical properties of a histidine kinase protein: it

122 is toxin family, we studied the features and biochemical properties of a prototype M. tuberculosis Va

123 We analyzed the biochemical properties of a TF:S7 complex from Thermotog

124 However, the biochemical properties of A. aeolicus (Aa)-RNase III and

125 arried out to investigate the structural and biochemical properties of actomyosin under the influence

126 ide insight into the enzymatic mechanism and biochemical properties of AdPLA and LRAT-related protein

127 Here we investigated the biochemical properties of AID from a sea lamprey, nurse

128 rate, distribution of alpha-syn inclusions, biochemical properties of alpha-syn protein, demise and

129 f influenza when the scoring method based on biochemical properties of amino acids is employed in com

130 -containing assemblies that have optical and biochemical properties of amyloid.

131 e and function since the first report on the biochemical properties of an archaeal MCM protein in 199

132 Here we describe the structure and biochemical properties of an IgE-Fc mutant that is trapp

133 Although the cellular functions and biochemical properties of APE1 are well characterized, t

134 The structures and biochemical properties of avidin, biotin and their respe

135 vations highlight an important difference in biochemical properties of B. subtilis and E. coli RNA po

136 of information on the genetic regulation and biochemical properties of bacterial C4-dicarboxylate tra

137 me degradation, and to modulate physico- and biochemical properties of bioactive peptides as well as

138 ng NMR to study structural, biophysical, and biochemical properties of biological macromolecules.

139 ad bi-functional AbiE Abi-TA systems and the biochemical properties of both toxin and antitoxin prote

140 erein we review the genetic, structural, and biochemical properties of CAPN14 and its gene product CA

141 ructive CT-based methods to characterize the biochemical properties of cartilage using cationic contr

142 indings indicate that physical, chemical and biochemical properties of casein hydrolysates can be imp

143 This work illuminates how biochemical properties of cells differ in macro- and mic

144 ning across the animal kingdom; however, the biochemical properties of certain pathway components can

145 t a straightforward relationship between the biochemical properties of chromatin modifiers and the sp

146 The biochemical properties of CMY-32, a class C enzyme posse

147 d, significant differences exist between the biochemical properties of complex I prepared from ovine

148 However, the biochemical properties of CTRP12 and its naturally occur

149 with NDEL1 and how they change the inherent biochemical properties of DISC1.

150 ulation of this interplay could modulate the biochemical properties of Dna2 and thus license it to ca

151 The biochemical properties of DraRnl are compatible with its

152 length dystrophin cDNA and characterized the biochemical properties of each mutant protein.

153 unique expression pattern, localization, and biochemical properties of EhCP4 could be exploited as a

154 ailed characterization of the expression and biochemical properties of EMILIN-3 in mouse.

155 entation and its usefulness in revealing new biochemical properties of encoded proteins.

156 Changes in the biochemical properties of eNOS produced by combined phos

157 nt of pain and as tools to probe deeper into biochemical properties of FAAH.

158 ant to calpain proteolysis but retains other biochemical properties of FAK.

159 iew FET proteins with an emphasis on how the biochemical properties of FET proteins may relate to the

160 However, most work on the biochemical properties of fission yeast actin-binding pr

161 is Perspective, we review the structural and biochemical properties of FtsZ, its role in cell biochem

162 To characterize the biochemical properties of GIMAP6, we purified the recomb

163 Taken together, the biochemical properties of GLB-6 suggest that this neural

164 ly in RTs that may contribute to distinctive biochemical properties of group II intron RTs, and it pr

165 Here, we analyzed biochemical properties of human AGPAT2 and its close hom

166 We previously described the biochemical properties of human AID and found that it is

167 The physiological and biochemical properties of individual muscle fibers corre

168 reports novel results for distinguishing the biochemical properties of Isomerase I from those of Isom

169 DC, and describe the morphological and some biochemical properties of its neurons.

170 ed from clinal patterns of CHC variation and biochemical properties of lipids.

171 Some of the biochemical properties of malarial mitochondria also app

172 t-translational modification that alters the biochemical properties of many proteins.

173 ffort to probe the structure, mechanism, and biochemical properties of metallo-beta-lactamase Bla2 fr

174 vo, by studying the electrophysiological and biochemical properties of mouse rods in a new genetic mo

175 unexpected insights into the biophysical and biochemical properties of mutated contractile proteins a

176 We characterize the biochemical properties of NagZ and demonstrate its abili

177 Combining the unique structural and biochemical properties of native acellular scaffolds wit

178 This "occluded" structure may explain the biochemical properties of NbtG, specifically with regard

179 terface should mimic the biophysical and the biochemical properties of neural tissue.

180 In this report we compared the biochemical properties of P-gp in native membranes, dete

181 The model accounts for five biochemical properties of peptides: (i) hydrophobicity,

182 Whereas the biochemical properties of PFA0210c have been characteriz

183 Here we characterize the photochemical and biochemical properties of phot from the marine picoalga

184 ger than self-interactions, and based on the biochemical properties of PiSLF, we previously proposed

185 Here we describe the X-ray structures and biochemical properties of PMT orthologs from Plasmodium

186 Physical and biochemical properties of pressurised and pasteurised lo

187 Moreover, the deposition patterns and biochemical properties of protease-resistant form of PrP

188 It is unclear how the biochemical properties of PrP(Sc) influence its uptake,

189 in vivo and compared these results with the biochemical properties of recombinant proteins determine

190 Biochemical properties of recombinant SUN proteins were

191 The intrinsic biochemical properties of RetGC and GCAP determined in v

192 chain kinase in fast skeletal muscle, where biochemical properties of RLC kinase and phosphatase con

193 Our results better define the biochemical properties of some alpha globin variants and

194 ion patterns, subcellular localizations, and biochemical properties of some representative poplar (Po

195 However, the specific biochemical properties of SpAin1 and whether they are ta

196 The biochemical properties of Stu2 reported here account for

197 ently available methods and insight into the biochemical properties of such interactions in living ti

198 anslational modification that can change the biochemical properties of target proteins and mediate re

199 To confirm that the biochemical properties of TFM-4AS-1 confer tissue select

200 Here, we report the biochemical properties of the Ad-expressed full-length a

201 Biochemical properties of the associated transporter wer

202 asked whether the filament architecture and biochemical properties of the best-understood prokaryoti

203 to tailor independently the biophysical and biochemical properties of the cell culture microenvironm

204 ndividual lymphocytes, the morphological and biochemical properties of the cells are quantitatively r

205 In this study, we investigated the biochemical properties of the cerato-platanin protein EP

206 a 6-wk culture period, the biomechanical and biochemical properties of the constructs were measured.

207 Aminoacylation of membrane lipids alters the biochemical properties of the cytoplasmic membrane and e

208 However, little is known about the biochemical properties of the different complexes, and k

209 We investigate here the biochemical properties of the E. coli RadA protein and s

210 Chi activates recombination by changing the biochemical properties of the helicase-nuclease, transfo

211 Here, we report the biochemical properties of the homodimeric PFO of C. rein

212 to chromatin in human cells and describe the biochemical properties of the human CMG complex purified

213 ization of the mu-opioid receptor (MOR), the biochemical properties of the isolated receptor remain u

214 ent study we have comparatively assessed the biochemical properties of the J-protein paralogs in rela

215 omputer simulations based on the amounts and biochemical properties of the key proteins showed that t

216 nism's environment and the thermodynamic and biochemical properties of the metabolic pathways it empl

217 The physical and biochemical properties of the microenvironment regulate

218 ese specific interactions, which represented biochemical properties of the MOR-Gal1R heteromer, could

219 in a variety of human malignancies, but the biochemical properties of the mutant kinases and their r

220 ies among patients were not explained by the biochemical properties of the mutants.

221 long-running avenues of research, namely the biochemical properties of the PcG/TrxG system and the ap

222 with different sectors controlling different biochemical properties of the protein.

223 ity of HpHypB but had no effect on the other biochemical properties of the protein.

224 he transmissibility of prions as well as the biochemical properties of the PrPres generated.

225 ignificant effects on cell phenotype and the biochemical properties of the purified actins.

226 FabI(M99T) exhibited normal growth, and the biochemical properties of the purified protein were indi

227 t cells and compared the x-ray structure and biochemical properties of the purified protein with that

228 the required intramolecular interactions and biochemical properties of the R-spine and the newly iden

229 ter receptors, with a depth modulated by the biochemical properties of the receptor-gephyrin interact

230 which were significantly associated with the biochemical properties of the residue replaced.

231 In light of the cellular location and the biochemical properties of the two characterized beta-man

232 ined, despite the wealth of knowledge on the biochemical properties of the various oxygenases.

233 cal rescue assays were employed to study the biochemical properties of the wild-type enzyme and the m

234 participating microbial communities, and the biochemical properties of their cellulolytic enzymes hav

235 ate liprin scaffolds, but the structural and biochemical properties of these domains remain largely u

236 s comparably sensitive to azide but that the biochemical properties of these enzymes are subtly diffe

237 The biochemical properties of these factors, coupled with th

238 We further explore the biochemical properties of these isoforms, demonstrating

239 We investigated the biochemical properties of these mutants using an express

240 GluN1 revealed the mechanism underlying the biochemical properties of these mutants.

241 The biochemical properties of these proteins and their cross

242 0N, and D200H alleles parallel precisely the biochemical properties of these TREX1 dimers during dsDN

243 n the present study, the microbiological and biochemical properties of this food were examined follow

244 ith muscle cells; however, the structure and biochemical properties of this membrane protein have not

245 To explore the biochemical properties of this protein, we engineered tw

246 The biochemical properties of this RPA-interaction-deficient

247 Although the biochemical properties of this transport have been chara

248 Elucidating the structure and biochemical properties of this unique virus assembly int

249 basis of this architecture, we examined the biochemical properties of three Arabidopsis thaliana PMT

250 modifications fine-tune the biophysical and biochemical properties of transfer RNA (tRNA) so that it

251 f BphAE(LB400) and BphAE(p4) and examine the biochemical properties of two BphAE(LB400) variants with

252 In the current report, the biochemical properties of two endo-beta-1,4-mannanases (

253 Our result proposes a new biochemical property of a PR-10 protein.

254 This unique biochemical property of anionic trypsinogen explains the

255 o eradicate cancer based on this fundamental biochemical property of cancer cells.

256 Kinase activity is known as the key biochemical property of MAPKs.

257 Contiguous mutations are consistent with the biochemical property of pol zeta to extend a mismatch wi

258 f ORF1p to anneal RNA in vitro, an important biochemical property of the protein.

259 ntaining protein (VCP)/p97 is the only known biochemical property of the Ube4b domain.

260 Because of their structural and biochemical properties, oncogenic Ras proteins are excee

261 ealed robust SMURF2 E3 ligase activity, with biochemical properties previously restricted to the SMUR

262 These biochemical properties provide a framework for understan

263 Fungal decay, biochemical properties, quality and sensory attributes w

264 ishes DnaK's in vivo function, yet intrinsic biochemical properties remain largely intact.

265 s to ocean acidification, but the underlying biochemical properties remain unknown.

266 s of most copines are not understood and the biochemical properties required for their functions are

267 Analysis of their biochemical properties revealed that most of the sHsp su

268 Due to their unique and versatile biochemical properties, ruthenium-based compounds have e

269 These mutants were analyzed for their biochemical properties (self-interaction and DNA binding

270 Mutations that confer the loss of a single biochemical property (separation-of-function mutations)

271 ne encodes Shadoo (Sho), a glycoprotein with biochemical properties similar to the unstructured regio

272 eric complex is an active enzyme, displaying biochemical properties similar to those of gamma-secreta

273 aRPA has biochemical properties similar to those of the canonical

274 cinerea is a serine protease inhibitor with biochemical properties similar to those of the previousl

275 e have compared the association equilibrium, biochemical properties, stability, and chaperone activit

276 ing synthetic genes, characterized regarding biochemical properties, structural fold, and IgE reactiv

277 ury of research has not only illuminated the biochemical properties, structure, and conformational dy

278 These biochemical properties suggest that CARMILs play a varie

279 These biochemical properties suggest that Pol epsilon is a lik

280 versity of nuclease domains with distinctive biochemical properties suitable for genome-editing appli

281 lass of Dnmt-targeted molecular probes, with biochemical properties that allow it to distinguish betw

282 We have examined in vitro the basic biochemical properties that allow Pol delta-exo(-) to ca

283 It displays unique physiological as well as biochemical properties that are relevant in food-related

284 We found that Dia and Ena have distinct biochemical properties that contribute to the different

285 best understood ALP, ParM, has a core set of biochemical properties that contributes to its function,

286 upplementary, and tail regions-have distinct biochemical properties that explain the differences betw

287 atural polymer harboring unique physical and biochemical properties that make it an ideal biomaterial

288 oduced by the kidney tubule and has specific biochemical properties that mediate important functions

289 s reveal patterns of domain organization and biochemical properties that provide insight into mechani

290 Although the oligomers shared similar basic biochemical properties, those obtained from inclusion-be

291 On the basis of biochemical properties, tissue-specific expression patte

292 nosoma brucei, its SufCB protein has similar biochemical properties to its prokaryotic homologues, fu

293 Lys monooxygenase (NbtG), which has similar biochemical properties to mycobacterial homologs.

294 iated protein with the means to modulate its biochemical properties to promote different molecular pr

295 ural features, subcellular localization, and biochemical properties upon the PKA holoenzymes they for

296 (encoding Thg1-like proteins, TLPs), but the biochemical properties we associate here with these prot

297 To investigate these biochemical properties, we altered the evolutionarily co

298 Based on these distinct biochemical properties, we propose that rather than func

299 RecF point mutations with altered biochemical properties were constructed in the chromosom

300 Because IQDs share biochemical properties with scaffold proteins, we propos