ライフサイエンスコーパス: amino

1 disclose an efficacious hybrid molecule 4-(5-Amino-1,2,3-oxadiazol-3-yl)-2,2,6,6-tetramethyl-1-piperi

2 lators of the ligand-binding domain of (S)-2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propanoic acid

3 statement: dendritic spine morphology, alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMP

4 ld-type mice, these compounds blocking alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA

5 receptors and decreased expression of alpha-amino-3-hydroxy-5-methylisoxazole-4-proprionic acid (AMP

6 incorporates three key features: (a) a bis(4-amino-3-hydroxyphenyl)squaraine core with bright deep-re

7 ent compound of the present series, sodium 1-amino-4-[4-(2,4-dimethylphenylthio)phenylamino]-9,10-dio

8 gned and developed a one-step synthesis of 5-amino-4-carboxamidothiazoles 1 by an yttrium-triflate-ca

9 radiation of a photo-crosslinkable unnatural amino acid (UAA) cotranslationally incorporated into the

10 Moreover, the observed polymorphism on amino acid 186 between H3N8 and H3N2 CIVs might be the r

11 peptides composed of natural and non-natural amino acid analogs, thereby enabling screens in a much d

12 y coupled plasma mass spectrometry (ICP-MS), amino acid analysis, and spectroscopy (ATR-IR, Raman).

13 A novel amino acid and metabolomics signature in mice overexpres

14 The macaque A2*05 allotype prefers the basic amino acid arginine at the second position of the peptid

15 codons when aminoacylated (charged) with an amino acid at its 3' end.

16 ds not more than 3 residues after the anchor amino acid at POmega, which enabled them to open the F p

17 ing reverse genetics, we found that a single amino acid at position 158 of the hemagglutinin (HA) pro

18 These findings thus demonstrate that amino acid availability controls lysosome positioning th

19 noacyl-tRNA with a PTC and subsequently, the amino acid becomes incorporated into the nascent polypep

20 Enzymes of amino acid biosynthesis were higher in coculture than in

21 regulation of translation, fermentation, and amino acid biosynthesis.

22 en proposed to specifically recognize a four-amino acid CAAX C-terminal sequence within their substra

23 lian target of rapamycin, suggesting reduced amino acid catabolism in MS patients.

24 ses our knowledge of the role branched-chain amino acid catabolism plays in seed development and amin

25 in response to different stimuli modulating amino acid catabolism, as were cytokine secretion levels

26 h a recombinant pH1N1 virus encoding these 6 amino acid changes (pH1N1/NSs-6mut) induced lower levels

27 ome sequence signature analysis identified 3 amino acid changes, 16 synonymous nucleotide changes, an

28 essed VH and VL genes and by influencing the amino acid composition of the Ag binding site.

29 n vitro could be predicted entirely based on amino acid composition.

30 Fractions showed different amino acid compositions and angiotensin I-converting enz

31 mbody a "cholesterol recognition/interaction amino acid consensus" motif.

32 spite often minute concentrations in vivo, d-amino acid containing peptides (DAACPs) are crucial to m

33 be recovered only by covalent attachment of amino acid deactivation agents to residual activated car

34 ied new potential bacterial taxa involved in amino acid degradation.

35 logs of 43 compounds, including amino acids, amino acid derivatives, and organic acids, was performed

36 s time, however, the assays utilize only one amino acid each.

37 was identical with the first, except for an amino acid exchange in the stalk region abolishing the N

38 rs the chemical synthesis of the fluorogenic amino acid Fmoc-Trp(C2-BODIPY)-OH (3-4 d), the preparati

39 cid catabolism plays in seed development and amino acid homeostasis.

40 fficacy of a fixed combination of pepsin and amino acid hydrochloride for the treatment of patients w

41 Average nucleotide and amino acid identities revealed that the four Ca.

42 encodes a predicted protease with 54 to 68% amino acid identity to torovirus (ToV) papain-like prote

43 tified a missense mutation, which encodes an amino acid in the tetratricopeptide repeat, in OGT (759G

44 disease, respectively, using the small nine amino acid influenza hemagglutinin tag.

45 Furthermore, amino acid infusion likely results in a further breakdow

46 resolution for each pairwise combination of amino acid ions.

47 ophilic (Ser-109) or a hydrophobic (Ile-305) amino acid is mutated instead.

48 is a chiral ligand derived from the natural amino acid l-histidine, are replaced by CH3NH3(+).

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

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

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

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

53 Specific loss of the 9000 amino acid long isoform results in vesicle clustering de

54 ulating biochemical pathways associated with amino acid metabolism and redox status.

55 the liver is a major handler of protein and amino acid metabolism as it is responsible for the major

56 metabolism, the citric acid (TCA) cycle, and amino acid metabolism.

57 ons of major pathways for central carbon and amino acid metabolisms to biofilm pH homeostasis.

58 d/l-Amino acid mixtures play a key role in human physiology

59 Single amino acid modifications identified a novel peptide, DII

60 Mutational analysis of a cyclin F-specific amino acid motif in the C-terminal region of Vif indicat

61 This virus has an amino acid mutation in VP1, which is the enzyme responsi

62 The extracellular, active 180 amino acid Nogo-A region, named Nogo-A-Delta20, binds to

63 gen peroxide and nutrient stresses caused by amino acid or glucose withdrawal.

64 trategy for the reversible immobilization of amino acid or peptide derivatives on carbon nanomaterial

65 The unnatural amino acid p-Benzoylphenylalanine was successfully incor

66 It is a 35-amino acid peptide cross-linked by two disulfide bridges

67 rate-transport elicited endocytosis of other amino acid permeases similarly involves unmasking of a c

68 effects of hyperaccumulation of the aromatic amino acid phenylalanine (Phe) in animals, known as phen

69 lar, we show that peptides incorporating the amino acid phenylalanine, a functional group that is con

70 The nonprotein amino acid pipecolic acid (Pip) regulates plant systemic

71 show that the largest effect is caused by an amino acid polymorphism that arose when an ancestral thr

72 , which suggests important roles of specific amino acid polymorphisms in the antigen-binding clefts.

73 tuted glutamic acid (E) for glutamine (Q) at amino acid position 623 (E623Q) displayed a titration cu

74 post-translational labeling at the specific amino acid positions.

75 y imputing classical alleles and polymorphic amino acid positions.

76 VEGFxxxa isoforms (VEGF165a, 165 for the 165 amino acid product) and antiangiogenic VEGFxxxb (VEGF165

77 s of selection and assessments of changes in amino acid properties provide evidence of positive selec

78 cently developed silk dating technique using amino acid racemization (AAR) in conjunction with capill

79 dichloramines, depending on the chlorine to amino acid ratio (Cl:AA).

80 hough pharmacologic modulation of excitatory amino acid receptors is well studied, minimal considerat

81 The effects of amino acid replacements on lipid association of the C-te

82 allele knock-in of the most commonly mutated amino acid residue, tyrosine 537, in the estrogen-respon

83 Five highly represented signature amino acid residues (37A, 95K, 224N, and 242N in the M1

84 sults show that interactions between charged amino acid residues are important both to directly stabi

85 t Glu(446) and Arg(447) cooperate with other amino acid residues in the GERAMT-binding site for prope

86 ge equilibria to measure the propensities of amino acid residues to participate in helical secondary

87 that involves just 7-8 out of a total of 148 amino acid residues was clearly detected.

88 egatively charged DNA and positively charged amino acid residues, the translocation speed of DNA can

89 ences of the two isozymes only differ at six amino acid residues.

90 hemical property and occurrence frequency of amino acid residues.

91 l and yet accounts for 90 of the toxin's 387 amino acid residues.

92 y limited to a peptide resolution of 5 to 20 amino acid residues.

93 (+/-) mice displayed an amplification of the amino acid response and ER stress response transcription

94 Selenoproteins contain the amino acid selenocysteine (Sec), co-translationally inse

95 ic code allows for UGA codons to specify the amino acid selenocysteine (Sec).

96 links messenger RNA nucleotide sequence with amino acid sequence during protein synthesis.

97 proteins also display extreme divergence in amino acid sequence identity between STs (i.e., 59%-61%

98 in domain organization they display just 31% amino acid sequence identity.

99 n at multiple sites along the spectrin-betaV amino acid sequence in the lineage leading to mammals, t

100 s of decoy peptides derived from the primary amino acid sequence in the SOD2-binding site in hsp70.

101 Substance P (SP) [SP + 3H](3+) ion (SP(3+); amino acid sequence RPKPQQFFGLM-NH2).

102 actin are nearly indistinguishable in their amino acid sequence, but are encoded by different genes

103 At the level of entry, differences in the amino acid sequences between the human and mouse ortholo

104 Analysis of amino acid sequences of three bZIPs does not identify in

105 ifferent enzyme kinetic profiles and primary amino acid sequences.

106 ely, which differ solely in their N-terminal amino acid sequences.

107 Principal component analysis showed a serum amino acid signature composed of arginine, leucine/isole

108 ntains an amphipathic helix and exhibits 42% amino acid similarity with SM N100.

109 tions or PTEN deletion to grow using diverse amino acid sources.

110 titutively active and resistant to serum and amino acid starvation.

111 f the missense polymorphism resulting in the amino acid substitution Glu326Lys.

112 Amino acid substitution mutations within a PMS2 C-termin

113 ealed that some escape mutants possessing an amino acid substitution other than K166Q showed superior

114 lysis of the two iNK TCR types with a single amino acid substitution revealed that the staining inten

115 We used an unbiased D-amino acid substitution strategy to determine structure-

116 the effect of the shaker-1 mutation, a R502P amino acid substitution, on the motor function is unclea

117 A single amino acid substitution-based adaptive coevolution of th

118 activation because trimming the Phe by small amino acid substitutions abolished alphaLbeta2 binding w

119 head subdomain, which is highly tolerant of amino acid substitutions and continual addition of glyco

120 follows: experimentally evaluated effects of amino acid substitutions at toggle positions are binary,

121 populations possessed mutations that caused amino acid substitutions from ClO2-labile to ClO2-stable

122 tructural assessment predicted that the five amino acid substitutions have damaging effects on DNA bi

123 Together, these findings demonstrate that amino acid substitutions in Fn-binding repeat-9 can sign

124 and growth selection approach, we identified amino acid substitutions in human and mouse Ctr2 protein

125 The amino acid substitutions lie in two highly conserved loo

126 the Galpha:RGS protein pair based on single amino acid substitutions.

127 nction; 13 pathways including branched chain amino acid synthesis were significantly enriched in base

128 luorescence-based biorthogonal non-canonical amino acid tagging (BONCAT) - for studying the activity

129 Here, we adapt bioorthogonal noncanonical amino acid tagging (BONCAT) to interrogate protein synth

130 These neurons also release the amino acid transmitter GABA, which can inhibit downstrea

131 epithelia, where it has an important role in amino acid transport.

132 ndent trafficking of the neuronal excitatory amino acid transporter 3 (EAAT3) blocks potentiation, su

133 aracter is dependent on vesicular inhibitory amino acid transporter-mediated signaling.

134 such as induction of potassium channels and amino acid transporters, derepression of genes marked wi

135 HLA association was the previously reported amino acid variant located at position 71, within the pe

136 at incorporates a photoreactive, non-natural amino acid, p-benzoyl-l-phenylalanine, into various posi

137 incorporation of a fluorescent noncanonical amino acid, we show that there is a rearrangement in the

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

139 to overcome this obstacle by utilizing the 6-amino-acid (CCPGCC) tetracysteine (TC) tag and FlAsH-EDT

140 ing of nascent proteins with a non-canonical amino-acid and click chemistry.

141 Hence, the puzzle remains: how a single-amino-acid difference between the ApoE3 and ApoE4 sequen

142 human L-asparaginase 1 (hASNase1) share 70% amino-acid identity, we decided to humanize gpASNase1 by

143 ty is dependent on both the presence of a 22-amino-acid N-terminal 'loop' region and its catalytic ac

144 ion of biosensor which is based on fructosyl amino-acid oxidase (FAO) immobilized nitrogen-doped grap

145 We combine a 97-amino-acid peptide of human origin that binds hyaluronan

146 th the estimated surface areas, we derive an amino-acid propensity scale that enables prediction of a

147 TaADF4 encodes a 139-amino-acid protein containing five F-actin-binding sites

148 ied eukaryotes possess a tandemly repeated 7-amino-acid sequence, called the canonical CTD, which orc

149 A protocol for mapping amino-acid sequences to coarse-grained beads enables the

150 Here we identified a two-amino-acid substitution in RORgammat (RORgammat(M)) that

151 For M. smegmatis TopoI-CTD, a 27-amino-acid tail that is rich in basic residues at the C-

152 d phosphinothricin over the 20 proteinogenic amino acids (1) , indirect effects of BAR-containing tra

153 nd requires the replacement of the canonical amino acids (4R)-hydroxyproline and proline by cysteine

154 nched-chain amino acids (BCAAs) and aromatic amino acids (AAAs) have been shown to be associated with

155 Plasma concentrations of amino acids (AAs), in particular, branched chain AAs (BC

156 Circulating branched-chain amino acids (BCAAs) and aromatic amino acids (AAAs) have

157 anding protein chemistries with noncanonical amino acids (ncAAs) and genetically isolating synthetic

158 The use of genetically encoded noncanonical amino acids (ncAAs) to construct crosslinks within or be

159 (PCET) steps along a pathway of redox active amino acids (Y122beta <--> [W48beta?] <--> Y356beta <-->

160 esidue Y745 and, essentially, the N-terminal amino acids 1-800.

161 bind to the same three A3G tryptic peptides (amino acids 181-194, 314-320, and 345-374) that form par

162 tricted CD4 T cell epitope, corresponding to amino acids 37-47 in the PVM matrix protein (M37-47).

163 wnstream of the S2' cleavage site is the FP (amino acids 798-818 SFIEDLLFNKVTLADAGFMKQY for SARS-CoV,

164 ted a recombinant virus (DeltaXX) that lacks amino acids 87 to 106, a portion of the previously descr

165 starting from diamines derived from natural amino acids and commercially available aminoalkyl polyst

166 isotopes, compound specific analyses (e.g., amino acids and fatty acids), and both biodiversity and

167 ing substrate depletion from a mixture of 19 amino acids and glucose by two Pseudomonas and one Bacil

168 actions with HIV-1 protease (PR) active-site amino acids and is bulkier with a larger contact surface

169 orms of a protein with specific sequences of amino acids and localized post-translational modificatio

170 These findings suggest that amino acids and organic cations may interact with the tr

171 Herein, we use two unnatural aromatic amino acids and several spectroscopic techniques to exam

172 adsorbed on the graphene as well as charged amino acids associated with the immobilized protein.

173 LDAH alternative-splicing variant missing 90 amino acids at C-terminus does not promote LD fusion or

174 on of the peptide, and hydrophobic and polar amino acids at the C-terminal end.

175 f N,N'-disubstituted hydantoin bearing alpha-amino acids by improving yields, reducing the time and n

176 to the degeneracy of the genetic code, most amino acids can be encoded by multiple synonymous codons

177 ate that IQF substrates containing unnatural amino acids can be used to investigate protease activiti

178 Chlorination of amino acids can result in the formation of organic monoc

179 ined by intrinsic local interactions between amino acids close to each other in the protein sequence.

180 iations of physical activity and circulating amino acids concentration in peripubertal girls.

181 ructose transport after introduction of four amino acids derived from GLUT5.

182 nce, specifically C(x)3X sequences with four amino acids downstream of the cysteine.

183 range of unique proteins), the processing of amino acids for energy, and disposal of nitrogenous wast

184 identified a small conopeptide of only four amino acids from the venom of Conus textile that strongl

185 HCF222 encodes a protein of 99 amino acids in Arabidopsis (Arabidopsis thaliana) that h

186 ncy of a small number of linear motifs three amino acids in length can accurately identify a CD4 T ce

187 C I molecules typically bind peptides with 9 amino acids in length with both ends tucked inside the m

188 ed, site-specific incorporation of unnatural amino acids in regions essential for activation, followe

189 Molecular modeling suggested a number of amino acids in RRM1 likely to be involved in interaction

190 ion likely results in a further breakdown of amino acids in the liver, mediated by increased glucagon

191 t pTRS1 inhibits PKR by binding to conserved amino acids in the PKR eIF2alpha binding site and blocki

192 , we have explored the use of phosphorylated amino acids in which the phosphate moiety bears a chemic

193 oth the concentration and d/l composition of amino acids is very promising for the study of biologica

194 nt antigenic clusters, we inferred a few key amino acids mutation driving the 11 historical antigenic

195 he C terminus (POmega) and contained charged amino acids not more than 3 residues after the anchor am

196 here that a region as small as the first 32 amino acids of Swi1 (Swi11-32) can decorate [SWI(+)] agg

197 mouse strain in which the substitution of 2 amino acids of the endogenous TTP protein renders it con

198 Most of the amino acids presented the highest concentrations when th

199 95 substitution matrices reflecting various amino acids properties in predicting the antigenicity of

200 Although positively charged amino acids result in the Tyr-84 swing, amino acids that

201 ication of a single H7 epitope by changing 3 amino acids so that it is homologous with a known H3 imm

202 ic prediction method relies on the choice of amino acids substitution matrices.

203 Consumption of amino acids such as arginine and tryptophan by immunoreg

204 ermined that the charge type and identity of amino acids surrounding FG sequences impact the structur

205 o were the most abundant and rapidly labeled amino acids synthesized.

206 alized form of autophagy, providing critical amino acids that activate mTOR and enable the metabolic

207 rged amino acids result in the Tyr-84 swing, amino acids that are negatively charged induce a not pre

208 that it is controlled by a set of conserved amino acids that couple RNA and ATP binding to the prote

209 1) is a central growth regulator that senses amino acids through a pathway that converges on the Rag

210 n flux toward the shikimate-derived aromatic amino acids tyrosine and tryptophan.

211 confirmed the functional relevance of these amino acids using a targeted mutagenesis strategy.

212 CO2, and N2O were measured for the 20 common amino acids using low-pressure, ambient-temperature ion

213 ies, we measured DeltaDeltaGsc(o) for all 20 amino acids using the transmembrane beta-barrel E. coli

214 Only natural amino acids were used as probes, and thus possible struc

215 the STING protein define a novel cluster of amino acids with functional importance in the regulation

216 esent, especially for individual derivatized amino acids with increasing acyl chain lengths.

217 drates, amino acids, bacterial biomarkers (D-amino acids), and plant protein biomarkers (hydroxyproli

218 installed in a range of molecules, including amino acids, a monosaccharide, a fluorophore, and an ana

219 13)C] isotopologs of 43 compounds, including amino acids, amino acid derivatives, and organic acids,

220 nic BAR indeed converts two plant endogenous amino acids, aminoadipate and tryptophan, to their respe

221 mentarity-determining region 3 (CDRH3) of 25 amino acids, among the shortest known for this class of

222 gh consumption of lipids, carbohydrates, and amino acids, as well as governing systemic signaling net

223 periods using measurements of carbohydrates, amino acids, bacterial biomarkers (D-amino acids), and p

224 duced the lysosomal efflux of most essential amino acids, converting the lysosome into a cellular dep

225 peptides containing only one or two types of amino acids, here we used modern mass spectrometry (MS)-

226 exes regulate the Rag GTPases in response to amino acids, including GATOR1, a GTPase activating prote

227 (.) CF3 reacts with 18 of the 20 common amino acids, including Gly, Ala, Ser, Thr, Asp, and Glu,

228 ance of the volatile compounds produced from amino acids, including the sulfur-containing compounds a

229 reconstitution test, proximate composition, amino acids, minerals and electrophoresis] were determin

230 , and the release of soluble molecules (free amino acids, proteins and glucidic colloids), but the ef

231 cular disease risk (including branched-chain amino acids, select unsaturated lipid species, and trime

232 elements, such as K, Ca and P, and essential amino acids, such as tryptophan, valine, and threonine,

233 f a flexible loop region containing aromatic amino acids, the caveolin-binding motif.

234 ntly catalyze peptide bond synthesis by most amino acids, the imino acid proline is a poor substrate

235 proteins containing unmodified proteinogenic amino acids, which can be altered readily by site-direct

236 ntain local structures not accessible with l-amino acids.

237 g site, supporting a hierarchy of vulnerable amino acids.

238 des containing post-translationally modified amino acids.

239 additional compounds that were unrelated to amino acids.

240 of arginines adjacent to M6CK-phosphorylated amino acids.

241 e change in telomere length, and circulating amino acids.

242 s of total cellular protein and several free amino acids.

243 hydantoins and unsaturated alpha-quaternary amino acids.

244 using UPLC-MS/MS identified sixteen peptides/amino acids.

245 ce as human A3C S188I, but through different amino acids.

246 mbered and densely functionalized quaternary amino acids.

247 enamides toward the synthesis of cis vicinal amino alcohols and tetrasubstituted alpha-borylamido com

248 llenylation reactions of N-protected l-alpha-amino aldehydes is reported.

249 in transfected cells, we determined that the amino and carboxyl termini reside in the extracellular s

250 ich correlates well with their downregulated amino and fatty acid metabolism.

251 A series of amino and phenoxy analogues have been synthesized, and a

252 ides allowed expedient preparations of alpha-amino boronic acids, often with high stereoselectivity,

253 CPP-115, a next-generation gamma-amino butyric acid (GABA)-aminotransferase (AT) inhibito

254 s characterized in vitro by delivering gamma-amino butyric acid to a target solution, and demonstrate

255 ivative 2 was converted to a cyclic (alkyl) (amino)carbene (cAAC) via 1,2-hydrogen migration triggere

256 r the synthesis of storable bicyclic (alkyl)(amino)carbenes (BICAACs), which feature enhanced sigma-d

257 ng properties compared to monocyclic (alkyl)(amino)carbenes (CAACs).

258 is a powerful method for accessing the beta-amino carbonyl motif that remains underdeveloped.

259 -glutamine to pyroglutamic acid, the typical amino-carbonyl reaction was slowed down.

260 ination reaction proceeds via a nucleophilic amino cyclization followed by an intermolecular C-N bond

261 a blend of biodegradable polymer, poly(beta-amino ester) (PBAE), with PBAE conjugated with 5kDa poly

262 ach also afforded (Z)-alpha,beta-unsaturated amino esters in moderate to good yields.

263 to synthesize novel non-proteinogenic alpha-amino esters.

264 s substituted with an equatorial hydroxyl or amino group in the newly formed ring are considerably mo

265 d that the PRNTase domain recognizes the C-2-amino group, but not the C-6-oxo group, N-1-hydrogen, or

266 he highest pKa values ever reported for this amino group, providing a rational for the observed need

267 ile transfer of primary (-NH2) and secondary amino groups (-NHR) to heteroaryl- as well as arylcuprat

268 aphene oxide (GO) and GO functionalized with amino groups (GONH2) on 15 immune cell populations, inte

269 asurement of the rotation rate of individual amino groups could give insight into the dynamic process

270 In this novel biosensor matrix, amino groups in HKCN were used for the enzyme immobiliza

271 eals a distinct approach to install aromatic amino groups in metabolites and raises questions about t

272 ium(II)-aryl complex and a weak base, lysine amino groups underwent C-N bond formation at room temper

273 Inhibition of NOS2 and COX2 using amino-guanidine and aspirin/indomethacin yielded an addi

274 4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)hexadecanoic acid (13b) decreased proliferation an

275 levels of diastereocontrol, leading to beta-amino ketones in high yields.

276 ive binding of both an acetato ligand and an amino ligand to zinc occurs in distinct confined environ

277 ic synthesis, the direct transfer of primary amino (-NH2) and hydroxyl (-OH) groups to arylmetals in

278 f reducing sugars, ethanol, acetic acid, and amino nitrogen did not differ significantly (p<0.05) bet

279 n of substrates with 2'-azido, 2'-chloro, 2'-amino, or arabinose sugars.

280 For secondary amino ozonides, additional functional groups had variabl

281 boxy-5-[(6-(18)F-fluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-p entanedioic acid) and more rece

282 y against a hepatic surface protein, leucine amino peptidase (LAP).

283 ortholog responsible for the transfer of the amino-residue phosphoethanolamine (pEtN) to the lipid A

284 llowed incorporation of functionalized alpha-amino substituents appropriate for enhancement of antibi

285 assumptions that the tau torsion of the meta-amino-substituted BDI systems leads to a zwitterionic tw

286 based and high-throughput screens against an amino-sugar acetyltransferase enzyme, PglD, involved in

287 ncorporation of extraneous nitrogen (N) into amino sugars (AS) could reflect the contribution of micr

288 of FGF2, whereas IGF1 displayed homogeneous amino-terminal cleavage with complete removal of the bom

289 The FliG amino-terminal domain is organized in a regular array wi

290 The amino-terminal domain with a fold distinct among known T

291 phorylation sites to the otherwise divergent amino-terminal extensions on these pollen sPPases.

292 previously characterized viruses expressing amino-terminal fusions, this virus expresses more VP26 f

293 lue of serial measurement of soluble ST2 and amino-terminal pro-B-type natriuretic peptide to clinica

294 hat MLO homooligomerization, mediated by the amino-terminal region of the protein, and carboxyl-termi

295 findings demonstrate that the occurrence of amino-terminal structural homogeneity may be associated

296 erogeneity of signal peptide cleavage at the amino terminus of FGF2, whereas IGF1 displayed homogeneo

297 CD11(+) DCs, the mutant virus that lacks the amino terminus of gamma134.5 undergoes temporal replicat

298 Fluorescent protein fusions to the amino terminus of small capsid protein VP26 are the most

299 Loss of alpha-amino trimethylation causes a reduction in the CENP-T an

300 Installation of the radical trap 3-amino tyrosine (NH2Y) by amber codon suppression at posi