ライフサイエンスコーパス: amino acid level

1 o FtsY (47% identical and 67% similar at the amino acid level).

2 % at the nucleotide level, and 96-99% at the amino acid level).

3 esent a wide range of identity values at the amino acid level.

4 s exhibiting significant conservation at the amino acid level.

5 pa6 and Epa7, which are 92% identical at the amino acid level.

6 ynthetic modules, at both the nucleotide and amino acid level.

7 than 50% identity and 65% similarity at the amino acid level.

8 MPK1 and MPK2 are 95% identical at the amino acid level.

9 EL) domains that are highly conserved at the amino acid level.

10 omology shared by them at the nucleotide and amino acid level.

11 a1a.2, which shared only 48% identity at the amino acid level.

12 .2% at the nucleotide level and 14.8% at the amino acid level.

13 en BoNT serotypes differ by up to 70% at the amino acid level.

14 T/A1 and BoNT/A2, which differ by 10% at the amino acid level.

15 A and D copies could only be observed at the amino acid level.

16 y with human, bovine, and mouse RDH10 at the amino acid level.

17 consistent with a potential function at the amino acid level.

18 a Monte Carlo code which is specific at the amino acid level.

19 tively, with their human counterparts at the amino acid level.

20 entical with their human counterparts at the amino acid level.

21 genes are approximately 36% identical at the amino acid level.

22 he strong conservation of this domain at the amino acid level.

23 respectively, at the nucleotide and deduced amino acid level.

24 OG1 at the nucleotide level and 97.8% at the amino acid level.

25 3A and MUC3B mucins are 91% conserved at the amino acid level.

26 the nucleotide level and 96% identity at the amino acid level.

27 rain of human HEV by approximately 5% at the amino acid level.

28 , but are not excessively polymorphic at the amino acid level.

29 these two siglecs share 47% identity at the amino acid level.

30 ST-2 (40.1%) than to Gal3ST-1 (38.0%) at the amino acid level.

31 ent to ALF5 and 83% identical to ALF5 at the amino acid level.

32 ical to each other at the nucleotide and the amino acid level.

33 examples at the nucleotide level or 9 at the amino acid level.

34 the nucleotide level and 99% identity at the amino acid level.

35 and hPPTG3 89% identical with hPPTG1 at the amino acid level.

36 ctural changes in the permease at the single amino acid level.

37 om human heart, is identical to pNBC1 at the amino acid level.

38 s 27% at the nucleotide level and 15% at the amino acid level.

39 redict this probability of generation at the amino acid level.

40 ins and were from 26 to 53% identical at the amino acid level.

41 quences revealed 83% overall identity at the amino acid level.

42 alpha9 is 73% identical to rat alpha9 at the amino acid level.

43 D enzymes that are only 57% identical at the amino acid level.

44 dentity and 77% similarity at the translated amino acid level.

45 ortion of SV40, yielding 84% homology at the amino acid level.

46 an forms of P450c17 are 69% identical at the amino acid level.

47 ene sequences ranged from 0.1 to 7.2% at the amino acid level.

48 e nucleotide level and 90% similarity at the amino acid level.

49 ty at the nucleotide and 91% identity at the amino acid level.

50 thway its capacity to respond rapidly to the amino acid level.

51 and PtD14b that are over 95% similar at the amino acid level.

52 tch2 locus leading to a Q2319X change at the amino acid level.

53 shift site consistent with a function at the amino acid level.

54 ins was low and ranged from 16 to 27% at the amino acid level.

55 nding the resolution of labeled sites at the amino acid level.

56 y trade off in enzyme function at the single amino acid level.

57 s, while others differ by up to 13.2% at the amino acid level.

58 all adenovirus-encoded gene products at the amino acid level.

59 ) that is 79% identical to human NHE1 at the amino acid level.

60 nt accessibility at the peptide and even the amino-acid level.

61 s the determination of contact interfaces at amino-acid level.

62 ins with the potential for resolution at the amino-acid level.

63 rected mutagenesis experiments at the single-amino-acid level.

64 MoSMN, which is 82% identical to SMN at the amino-acid level.

65 ns focus on either the entire-gene or single amino-acid level.

66 sing inhibition that may result from lowered amino acid levels.

67 agy, which can be triggered by a decrease in amino acid levels.

68 subspecies and strains at the nucleotide and amino acid levels.

69 omology to human UDG2 at both nucleotide and amino acid levels.

70 equence identity at both the genomic and the amino acid levels.

71 mology with human PSCA at the nucleotide and amino acid levels.

72 um, phorbol myristate acetate, and increased amino acid levels.

73 of identity with each other at both DNA and amino acid levels.

74 31.6 and 30.7% identity with HNK-1ST at the amino acid levels.

75 33.8% identity with C2GnT-L and IGnT at the amino acid levels.

76 ral inhibition of macropinocytosis decreases amino acid levels.

77 ndbreaking research may result from elevated amino acid levels.

78 l nutrient transporters, and decreases fetal amino acid levels.

79 succinate followed a similar pattern as the amino acid levels.

80 erglycemia was significantly associated with amino acid levels.

81 sons at the gene, rather than the individual amino acid, level.

82 e monkey putamen while L-DOPA rescues both D-amino acids levels.

83 expedite the decay of Y-linked genes at the amino acid level?

84 ble to convergent or parallel changes at the amino acid level?

85 CAX4 is 53% identical to CAX1 at the amino acid level, 42% identical to CAX2, and 54% identic

86 the gene product is highly conserved at the amino acid level (98 to 100% identity), and Western blot

87 In contrast, at the amino acid level all three loci show strong evidence of

88 to simulate the evolution of proteins at the amino acid level, allowing the analysis of their sequenc

89 computational metrics at both nucleotide and amino acid levels along with multiple protein sequence/s

90 ha(5) and alpha(V) are >50% identical at the amino acid level, alpha(5)beta(1) and alpha(V)beta(1) sh

91 rming the cavity are highly conserved at the amino acid level among all Spn1 family members, suggesti

92 was highly conserved at both nucleotide and amino acid levels among all ASFV field isolates examined

93 nary conservation of the PAX6 protein at the amino acid level amongst vertebrates predicts that patho

94 in tomato fruit did not significantly alter amino acid levels, an expression quantitative trait locu

95 f the Pasteuria bacterium and have performed amino acid level analyses of 33 bacterial species (inclu

96 We then perform the same amino acid-level analysis individually for 24 protein fu

97 t, and mouse PRL-1 are 100% conserved at the amino acid level and 55% identical to a newly identified

98 the human sequence, with 95% identity at the amino acid level and a perfect conservation of all the r

99 a, -IId, and -IIb, are >93% identical at the amino acid level and are broadly expressed in numerous m

100 rabidopsis thaliana are 85% identical at the amino acid level and are of equal length, but they posse

101 se co-transporters share 57% homology at the amino acid level and are pharmacologically inhibited by

102 hich share approximately 84% identity at the amino acid level and can compensate for each other for m

103 MchA1 and MchA2 are 74% identical at the amino acid level and diverge only in the C-terminal regi

104 d for quantitating label distribution at the amino acid level and explores the nature and basis for a

105 al to GTF2I at the nucleotide and 97% at the amino acid level and generates several alternatively spl

106 otein that is 71% identical to mCCCAP at the amino acid level and has the same predicted secondary st

107 t share significant sequence homology at the amino acid level and mediate a number of different biolo

108 us to human STEAP at both the nucleotide and amino acid levels and contains six potential membrane-sp

109 of permease activity in response to elevated amino acid levels and provide a physiological explanatio

110 n of TPPII in mammalian cells is to maintain amino acid levels and that TPPII-deficient cells compens

111 Instead, reduced amino acid levels and the consequent increase in uncoupl

112 defensin-1 gene at both the nucleic acid and amino acid levels and was termed rat beta-defensin-1 (RB

113 vels, prevented the effect of bafilomycin on amino acids levels and completely reversed its inhibitio

114 o virus (segment 2; approximately 74% at the amino acid level) and a more distant relationship to Dho

115 (87% at the nucleotide level and 80% at the amino acid level) and clone 2 was identical to a region

116 highly related to one another (79-91% at the amino acid level) and showed significant similarity to o

117 quence divergence on both the nucleotide and amino acid levels) and were more closely related to othe

118 RhaS is 30% identical to RhaR at the amino acid level, and both are members of the AraC/XylS

119 n isolated, shown to be 70% identical at the amino acid level, and functionally expressed.

120 sequences lack significant similarity at the amino acid level, and the linear organizations of the P2

121 s within people over time is associated with amino acid levels, and differences across people are ass

122 of the tricarboxylic acid cycle, changes in amino acid levels, and elevated metabolism of abscisic a

123 , improved fatty acid composition, increased amino acid levels, and heightened antioxidant levels.

124 significantly reduced insulin and essential amino acid levels, and increased glucose levels within m

125 other, but were unrelated to carbohydrates, amino acid levels, and total protein.

126 extra-membrane protein surfaces, even at the amino-acid level, and to illuminate intrinsic membrane p

127 While constraints acting at the amino acid level are expected, the silent polymorphisms

128 erative handgrip strength and branched chain amino acid levels are associated with longer ICU stays a

129 When internal amino acid levels are low, Gap1p is localized to the pla

130 or defined time periods until the targeted d-amino acid levels are obtained.

131 esis are greatly accelerated, and low plasma amino acid levels are probably at least partly responsib

132 This study, therefore, measured amino acid levels, arginase activity, and nitric oxide m

133 s were >99% concordant at the nucleotide and amino acid levels, as well as for resistance-associated

134 baseline fumarate levels and lower baseline amino acid levels-asparagine and glutamine-correlate wit

135 irst molecular contact site mapped to single amino acid level between these two proteins.

136 Although not apparent at the amino acid level, BipA is also similar to Int and Inv in

137 ation between the positions is strong at the amino acid level but weak at the codon level.

138 P similar to current avian strain NPs at the amino acid level but with many synonymous nucleotide dif

139 coding sequences, both at the nucleotide and amino acid level, but has lower homology with the chicke

140 nd are nearly identical to each other at the amino acid level, but play distinct intracellular roles.

141 hy individuals increased plasma glucagon and amino acid levels, but did not change circulating Angptl

142 d effects orchestrate cellular adaptation to amino acid levels, but how their activities are coordina

143 ference lines revealed increased organic and amino acid levels, but reduced sugar levels, implying th

144 TOR signaling pathway in plants responds to amino acid levels by eliciting regulatory effects on res

145 ights into genetic influences on circulating amino acid levels by integrating -omic technologies in a

146 Donor-recipient HLA mismatch at the amino acid level can now be determined.

147 relatively conserved at the nucleic acid and amino acid level compared to human, mouse, and rat ortho

148 NA translation, whereas larger reductions in amino acid levels control translation through eIF2A.

149 which is highly homologous to DvABCB1 at the amino acid level, did not reduce the sensitivity of WCR

150 We find that these amino acid-level differences can drive the formation of

151 hrough many heterogeneous pathways by way of amino acid-level dynamics biased toward selecting native

152 differing on average by 19 mutations) and at amino acid level (each having experienced three amino ac

153 Plasma and tissue amino acid levels, enzyme activities, and metabolic inte

154 ough both sequences are 96% identical on the amino acid level, excluding the amino-terminal end, a fr

155 The output is presented at the amino acid level for the user-selected PTM types.

156 space at the rotamer level instead of at the amino acid level further improved the efficiency by redu

157 GluR1(o) and GluR3(o) are homologous at the amino acid level, GluR3(o) desensitizes approximately th

158 ing transgenes in planta, including modified amino acid levels, have been seen but without the identi

159 Basal monoamine and amino acid levels (home cage) were assessed in experimen

160 eases are approximately 55% identical at the amino acid level; however, their substrate and peptide b

161 STTV1 has only weak amino acid level identities (25%) to chicken anemia viru

162 Despite being highly divergent at the amino acid level, IFITM3 proteins of birds and mammals c

163 40 and 77% identical to VAV and VAV2 at the amino acid level in all identified functional motifs.

164 gnificant sequence similarity at the deduced amino acid level in both the N-terminal and C-terminal h

165 Each ingredient affected plasma amino acid levels in a singular manner when fed individu

166 Essential amino acid levels in all insect species were comparable

167 ne deiminase (ADI-PEG 20) depletes essential amino acid levels in argininosuccinate synthetase 1 (ASS

168 t are mobilized to new growth, we tested the amino acid levels in center and outer leaf blades.

169 For these studies, we measured the amino acid levels in dams from two mouse models for IUGR

170 emia, hyperaminoacidemia, and no lowering of amino acid levels in response to high levels of glucagon

171 The amino acid levels in serum were measured serially.

172 zymes was determined by measuring growth and amino acid levels in the aat mutants.

173 there may be substantial genetic effects on amino acid levels in the general population that may und

174 ary administration of high protein increases amino acid levels in the gut and promotes pathogen colon

175 iants for hyperglycemia/type 2 diabetes with amino acid levels in the population-based Metabolic Synd

176 We measured amino acid levels in the yeast deletion collection, a se

177 N supply had a variable effect on individual amino acid levels in young cobs and spikelets, with Asn

178 similarity and >74% identity at the deduced amino acid levels) in all Bb sensu lato strains tested,

179 pes that exhibit up to 30% divergence at the amino acid level, including challenges with genotype 4,

180 Amino acid levels increased immediately from birth and r

181 This study thus provides, at the amino acid level, information for rational structural en

182 atrixes, the analysis of urine with elevated amino acid levels is used as a model system where the el

183 95% homology with the ROD10 envelope at the amino acid level, is unable to enhance viral particle re

184 ggest that mTORC1/2 inhibition, regulated by amino acid levels, is causal for diapause metabolism and

185 ence indicates that ureagenesis, and thereby amino acid levels, is critically controlled by glucagon.

186 mology with any known genes; however, at the amino acid level, it had 50% similarity and 29% identity

187 eEF2 from other organisms (about 42% at the amino acid level), key regulatory sequences that are inv

188 At the amino acid level, KLHL3 shares 77% similarity with Droso

189 At the amino acid level, Krct is most closely related to four p

190 Whole genome sequence analysis of amino acid levels may establish a paradigm for analyzing

191 rtly acting through changes in intracellular amino acid levels mediated by amino acid transporters.

192 Although there are no differences at the amino acid level near the active site metal ion, signifi

193 e of 30 min at 95 degrees C will lead to a d-amino acid level of 1-5%, while 6 h at 95 degrees C prov

194 tigates the SLE-MHC associations down to the amino acid level of major HLA genes in 5,342 unrelated K

195 showed Tat to be the least conserved at the amino acid level of nine proteins encoded by the virus,

196 each genus, both in gene content and at the amino acid level of the encoded proteins.

197 ean evolutionary rates at the nucleotide and amino acid levels of between 1 x 10(-5) and 1.3 x 10(-3)

198 Essential amino acid levels of the gastrocnemius muscle did not re

199 hat leads to the recovery of cell volume and amino acid levels once extracellular amino acid availabi

200 At the amino acid level, OV-SA00 is 94% identical to OV-IA82 an

201 However, despite 70% homology on the amino acid level, overexpression of a foreign Microvirid

202 ns were associated with lower branched chain amino acid levels (P<0.01 and <0.001, respectively).

203 andgrip strength (P<0.01) and lower aromatic amino acid levels (P<0.01).

204 At physiologically relevant amino acid levels, parasite growth became defective in A

205 Despite considerable diversity at the amino acid level, PCPs for both proteins were well conse

206 iling, PhastCons) did not perform as well as amino acid-level prediction algorithms (Polyphen-2, SIFT

207 ion inhibitor known to augment intracellular amino acid levels, prevented the effect of bafilomycin o

208 n-genotype variability at the nucleotide and amino acid levels ranged from 6.5 to 8.6% and 2.2 to 3.8

209 trategies typically do not provide a direct, amino acid level readout of covalent activity for comple

210 entity on nucleotide and 66% identity on the amino acid level, respectively.

211 63% identical to cd59a at the nucleotide and amino acid level, respectively.

212 ctrin (betaSpIIsigma1) at the nucleotide and amino acid level, respectively.

213 86% identical to HMG1 at the nucleotide and amino acid level, respectively.

214 by up to 5.3% and 5.8% at the nucleotide and amino acid levels, respectively, and genotype 1a had sig

215 and 90 to 98% identity at the nucleotide and amino acid levels, respectively.

216 e 80 and 89% identical at the nucleotide and amino acid levels, respectively.

217 58% sequence identity at the nucleotide and amino acid levels, respectively.

218 deletion or insertion on the nucleotide and amino acid levels, respectively.

219 7 to 93% and 90 to 98% at the nucleotide and amino acid levels, respectively.

220 75 and 85% identities at the nucleotide and amino acid levels, respectively.

221 91% and 92% identical at the nucleotide and amino-acid levels, respectively.

222 of foldons predisposes the thermally driven amino acid-level search to form an initial foldon and su

223 at it no longer gives an accurate measure of amino acid level selection pressure?

224 the products of a conserved gene and at the amino acid level share 82% identity.

225 urthermore, we show that small reductions in amino acid levels signal through different mTOR-dependen

226 Amino acid-level signal-to-noise analysis was performed.

227 An increase in extracellular amino acid levels, similar to the increase observed afte

228 wn organisms at the nucleotide level; at the amino acid level, six predicted proteins had distant mat

229 e current approach from being able to obtain amino acid level structural information within the disul

230 by 15.7 to 23.0% but only 0.4 to 5.6% at the amino acid level, suggesting that this genotype most lik

231 bited differences at both the nucleotide and amino acid levels, suggesting that these chimeras may al

232 arbors two HKs that are 98% identical at the amino acid level, T. brucei hexokinase 1 (TbHK1) and TbH

233 At the amino acid level, Tc-1 displayed 95% and 99% identity to

234 ankyrin-B and both Cav2.1 and Cav2.2 at the amino acid level that is necessary for proper Cav2.1 and

235 ation becomes essential to maintain critical amino acids levels that uphold protein synthesis early d

236 To determine at the amino acid level the reason for the apparent distinction

237 At the amino acid level, the coding regions of CKbeta4GT-I and

238 Notably, at the amino acid level, the extracellular domain of the bovine

239 At the amino acid level, the human HIWI protein was 52% homolog

240 though neither gene is well conserved at the amino acid level, the predicted secondary structure of C

241 vidence of its importance in regulating seed amino acid levels, the full BCAA catabolic network is no

242 t although these proteins are diverse at the amino acid level, their exon-intron boundaries are conse

243 ycin complex 1 (mTORC1) senses intracellular amino acid levels through an intricate machinery, which

244 eratively refines the mapping results at the amino acid level to achieve 99-100% four-digit typing ac

245 CE2FT-1 has very low identity (5-10%) at the amino acid level to alpha1,2FT sequences in humans, rabb

246 es indicate that DSA3 is most similar at the amino acid level to an in-chain fatty acid hydroxylase w

247 eading frame with over 55% similarity at the amino acid level to archaeal class I-type lysyl-tRNA syn

248 The cDNA is 83% homologous at the amino acid level to human and mouse TaxREB107 and contai

249 he nucleotide level and 98% identical at the amino acid level to human RHOA and maps to mouse Chromos

250 ess using mouse Ube2g2 (E2; identical at the amino acid level to human Ube2g2) and human gp78 (E3), a

251 g (UL) region, and it is most similar at the amino acid level to MDV2, herpesvirus of turkeys (HVT),

252 luenzae strain G622 was 99% identical at the amino acid level to that of the H. influenzae type b str

253 Adh8a is 82, 73, 72, and 72% similar at the amino acid level to the Baltic cod ADH8 (previously name

254 Adh8b is 77, 68, 67, and 66% similar at the amino acid level to the Baltic cod ADH8, the human ADH1B

255 LIP-50 because of its high similarity at the amino acid level to the C-terminal region of the microtu

256 ins are 27% identical and 53% similar at the amino acid level to the Drosophila melanogaster and Dros

257 , is 87% identical at the nucleotide and the amino acid level to the hyaluronan synthase, pmHAS, from

258 e N methyltransferase is most similar at the amino acid level to the plastidic gamma-tocopherol C met

259 oyl domains and is only 33% identical at the amino acid level to the smaller isoform.

260 d that they were 91 and 92% identical at the amino acid level to their human homologues, respectively

261 e describe a role for FTO in the coupling of amino acid levels to mammalian target of rapamycin compl

262 ship (46% identity and 61% similarity at the amino acid level) to that of the avian leukosis-sarcoma

263 roups of early-harvest varieties with higher amino acid levels; two groups of mid- and late-harvest v

264 which simulates the evolution process at the amino acid level using site-specific substitution matric

265 genetically predicted difference of 1 SD in amino acid level was associated with an odds ratio for t

266 Selective pressure at the amino acid level was measured by using the nonsynonymous

267 and the EPEC and EHEC LEEs at the predicted amino acid level was observed for the components of the

268 apamycin (both molecules involved in sensing amino acid levels) was assessed in response to different

269 nucleotide level and 59.6% at the predicted amino acid level), was found.

270 most pronounced conservation at the primary amino acid level, we have focused on determining whether

271 dynamic coupling at a site-specific, single-amino-acid level, we provide evidence that the migration

272 xtra-large HDL levels and decreased VLDL and amino acid levels were associated with increased complem

273 particles from inclusions declined as medium amino acid levels were further reduced.

274 Correspondingly, amino acid levels were increased 2 weeks after tendon re

275 The amino acid levels were much lower in MF-N. siegelii and

276 etabolic reprogramming in which increases in amino acid levels were partially compromised in atg muta

277 rosine fluxes, leucine oxidation, and plasma amino acid levels were similar in all groups, although p

278 bon content was reduced while the total free amino acid levels were strongly increased.

279 Extracellular amino-acid levels were also affected by KORs, as U69,593

280 ormed an in depth analysis on the individual amino acid level which showed that G8 rotaviruses were m

281 cted to diversify these PAG molecules at the amino acid level, which in turn suggests that these mole

282 This differed from the amino acid levels, which decreased in heart failure but

283 ed for an average of 1.8% of the variance in amino acid levels, which ranged from 0.4 to 9.7%.

284 has 78% homology to the mouse SPPase at the amino acid level with 6-8 possible transmembrane domains

285 anio rerio) Abcd1 is highly conserved at the amino acid level with human ABCD1, and during developmen

286 a cDNA that exhibited 99.6% identity at the amino acid level with human ILK-1.

287 cted protein that shares 80% identity at the amino acid level with Msk, is located.

288 These 2 proteins are 30% identical at the amino acid level with remarkable similarity in the N-ter

289 el with the fur gene and 79% homology at the amino acid level with the iron uptake regulator (Fur) pr

290 e of AAAV displays 50 to 54% identity at the amino acid level with the other AAVs, with most of the d

291 V) nitrogenases, with an 80% identity at the amino acid level with the vnfD gene product from Anabaen

292 hKCa4 shares 41-42% similarity at the amino acid level with three small conductance calcium-ac

293 Although 60% identical to SodCII at the amino acid level with very similar enzymatic properties,

294 nsurate drop in starch levels, elevated free amino acid levels with a corresponding reduction in inta

295 nvestigated transcriptomes using RNA-seq and amino acid levels with N treatment in tea (Camellia sine

296 rain was observed at both the nucleotide and amino acid level, with 2010 strains clustering separate

297 that supervillin is highly conserved at the amino acid level, with 79.2% identity of the NH2-terminu

298 and NORE1 share almost 60% homology, at the amino acid level, with RASSF1.

299 macropinocytosis supports the maintenance of amino acid levels within pancreatic tumors.

300 are quite similar at both the nucleotide and amino acid level, yet they are very divergent in their b