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 AF/I (25% identity and 47% similarity at the amino acid level).

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

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

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

7 .2% at the nucleotide level and 14.8% at the amino acid level.

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

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

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

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

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

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

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

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

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

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

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

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

20 3A and MUC3B mucins are 91% conserved at the amino acid level.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

46 th mouse: 91% at both the nucleotide and the amino acid level.

47 have between 88.7 and 96.6% identity at the amino acid level.

48 kDa, respectively, with 90% homology at the amino acid level.

49 nia chrysanthemi, with 47.2% identity at the amino acid level.

50 iversification of the mature defensin at the amino acid level.

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

52 cleotide level and 90 to 95% homology at the amino acid level.

53 eported sequence at either the nucleotide or amino acid level.

54 the average of 50% identity to human APC at amino acid level.

55 ty and 98% similarity to polycystin-2 at the amino acid level.

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

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

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

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

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

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

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

63 s exhibiting significant conservation at the amino acid level.

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

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

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

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

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

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

70 ndbreaking research may result from elevated amino acid levels.

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

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

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

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

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

76 31.6 and 30.7% identity with HNK-1ST at the amino acid levels.

77 33.8% identity with C2GnT-L and IGnT at the amino acid levels.

78 s are highly conserved at the nucleotide and amino acid levels.

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

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

81 erglycemia was significantly associated with amino acid levels.

82 ral inhibition of macropinocytosis decreases amino acid levels.

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

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

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

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

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

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

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

90 d hamster enzymes at both the nucleotide and amino acid levels (92 and 95%, respectively).

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

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

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

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

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

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

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

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

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

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

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

102 entity at the nucleotide level, 67.7% at the amino acid level and 85.5% within the seven zinc finger

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

104 terium tuberculosis have 71% identity at the amino acid level and are both highly homologous with Sal

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

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

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

108 TIGA and ERp38 show 66% identity at the amino acid level and are putative ER proteins.

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

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

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

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

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

114 t the first complete MIP sequence map at the amino acid level and identify the single major phosphory

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

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

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

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

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

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

121 hat is dissimilar to SBL at both the DNA and amino acid levels and we suggest that it is this lectin

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

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

124 (87% at the nucleotide level and 80% at the amino acid level) and clone 2 was identical to a region

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 The sequence is highly conserved at the amino acid level between chicken, mouse (99%), human (99

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 versification of the mature defensins at the amino acid level has been selectively favored.

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

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

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

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

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

166 40 and 77% identical to VAV and VAV2 at the amino acid level in all identified functional motifs.

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

168 bcl-2, bcl-x, and bax, share homology at the amino acid level in the BH1 and BH2 domains, through whi

169 Essential amino acid levels in all insect species were comparable

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

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

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

173 The amino acid levels in serum were measured serially.

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

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

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

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

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

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

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

181 Amino acid levels increased immediately from birth and r

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

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

184 95% homology with the ROD10 envelope at the amino acid level, is unable to enhance viral particle re

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

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

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

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

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

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

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

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

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

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

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

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

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

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

207 63% identical to cd59a at the nucleotide and amino acid level, respectively.

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

209 86% identical to HMG1 at the nucleotide and amino acid level, respectively.

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

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

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

213 58% sequence identity at the nucleotide and amino acid levels, respectively.

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

215 7 to 93% and 90 to 98% at the nucleotide and amino acid levels, respectively.

216 75 and 85% identities at the nucleotide and amino acid levels, respectively.

217 entical to the murine gene at nucleotide and amino acid levels, respectively.

218 91% and 92% identical at the nucleotide and amino-acid levels, respectively.

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

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

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

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

223 At the amino acid level, significantly elevated diversity was d

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

240 tical at the cDNA level and identical at the amino acid level to a previously described murine riboso

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

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

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

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

245 transporter gene products are related on the amino acid level to bacterial sugar transporters and pro

246 helatase-II), which was 69% identical at the amino acid level to ferrochelatase-I.

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

248 The linking region had a 79% identity at the amino acid level to human cardiac titin.

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 cDNA encoding a protein 85% identical at the amino acid level to mammalian Rab7 has been cloned from

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

284 nucleotide level and 90-92% identity at the amino acid level with human HEV strains.

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

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

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

288 .3% at the nucleotide level and 85.7% at the amino acid level with the Escherichia coli purA gene.

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

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

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

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

298 e 91% identical to the human receptor at the amino acid level, with sequence differences concentrated

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