ライフサイエンスコーパス: aromatic amino acid

1 ed in vivo activity, and were preferred over aromatic amino acids.

2 ributed to overlapping pi-pi orbitals of key aromatic amino acids.

3 rt assays show that PhpCAT exports all three aromatic amino acids.

4 in the Acanthamoeba spp. that synthesize the aromatic amino acids.

5 spiratory nitrogen cycle and accumulation of aromatic amino acids.

6 of the Tyr9 residue with different unnatural aromatic amino acids.

7 norepinephrine and for the hydroxylation of aromatic amino acids.

8 ritical branch point in the synthesis of the aromatic amino acids.

9 B. hydrogenotrophica targets aliphatic and aromatic amino acids.

10 ands of promoters through a conserved set of aromatic amino acids.

11 binds peptides that have a high fraction of aromatic amino acids.

12 hosphate, which is required for synthesis of aromatic amino acids.

13 C domains is reliant upon widely distributed aromatic amino acids.

14 gher activity with IA derived from L-Glu and aromatic amino acids.

15 (ubiquinone biosynthesis), menaquinone, and aromatic amino acids.

16 sequence enriched in positively charged and aromatic amino acids.

17 and contained multiple large hydrophobic and aromatic amino acids.

18 attributed to overlapping pi-pi orbitals of aromatic amino acids.

19 in the visible range even in the absence of aromatic amino acids.

20 Using a combination of an aromatic amino acid, a homoserine side chain, and a d-am

21 ge of other metabolites including those from aromatic amino acid (AAA) fermentation.

22 ating branched-chain amino acids (BCAAs) and aromatic amino acids (AAAs) have been shown to be associ

23 Based on recent studies, fluorophores-mainly aromatic amino acids (AAAs) in proteins-might be respons

24 ch as branched-chain amino acids (BCAAs) and aromatic amino acids (AAAs), have been associated with d

25 Circulating branched-chain and aromatic amino acids (alanine, glycine, histidine, pheny

26 The unique properties of aromatic amino acids allow them to play specialized role

27 lack of redox sites and the trace amounts of aromatic amino acids also eliminate the possibility that

28 ptome identified a phylogenetically distinct aromatic amino acid aminotransferase (ArAT), designated

29 uences of these organisms for members of the aromatic amino acid ammonia lyase family.

30 C6S-binding peptides where A represents any aromatic amino acid and B any basic amino acid.

31 n the antioxidant activity as well as on the aromatic amino acid and carotenoid contents in ordinary

32 aled differences in the microbiota-sensitive aromatic amino acid and secondary bile acid metabolism.

33 ge with particular carbon sources, including aromatic amino acids and acyclic terpenes, suggesting a

34 In conclusion, the levels of branched-chain, aromatic amino acids and alanine increased and the level

35 that Pal is a versatile surrogate to natural aromatic amino acids and can be employed as an alternati

36 The aromatic amino acids and carotenoids are the major contr

37 in) using commercially available fluorinated aromatic amino acids and fluorinated precursors as examp

38 viously reported markers, branched-chain and aromatic amino acids and glutamine/glutamate, were assoc

39 llular bacterium that is auxotrophic for the aromatic amino acids and histidine, causes scrub typhus,

40 An intermolecular interaction between aromatic amino acids and imino acids within the triple h

41 color parameters and fluorescence spectra of aromatic amino acids and nucleic acids (AAA + NA), trypt

42 s drawn into biosynthetic pathways that form aromatic amino acids and other important metabolites, in

43 In some cases, the PTM domain is rich in aromatic amino acids and plays an important role in memb

44 enzyme such that they grew on media lacking aromatic amino acids and produced GA in vitro.

45 nabling rapid 1D NMR spectral acquisition on aromatic amino acids and proteins bearing aromatic resid

46 ne and glutamate, which act as precursors to aromatic amino acids and salicylic acid, respectively.

47 Herein, we use two unnatural aromatic amino acids and several spectroscopic technique

48 Isolated aromatic amino acids and short peptides provide benchmar

49 ectron capture mass spectra of aliphatic and aromatic amino acids and their methyl esters show intens

50 o make erythrose-4-phosphate, a precursor of aromatic amino acids and vitamins.

51 that the proteinaceous binder degrades into aromatic amino acids and/or fatty acids after exposure t

52 molecules such as chlorophyll, carotenoids, aromatic amino-acids and prenylquinones.

53 irst reaction of the biosynthetic pathway of aromatic amino acids, and a chorismate mutase (CM), func

54 cribe fluorinated versions of alkyl, cyclic, aromatic amino acids, and also nickel-complexes to acces

55 lasses and particle size, branched-chain and aromatic amino acids, and inflammation-related glycoprot

56 the role of a surface-accessible cluster of aromatic amino acids, and purified mutant proteins were

57 dia but do not grow in defined media lacking aromatic amino acids, and the growth defect is rescued b

58 rostatic and conformational perturbations of aromatic amino acids are associated with metal cluster a

59 Spectral contributions from aromatic amino acids are observed through UV resonance e

60 GH3 proteins can use metabolic precursors of aromatic amino acids as substrates.

61 hat is responsible for regulating the use of aromatic amino acids as the nitrogen source.

62 ence, with a net positive charge and several aromatic amino acids, as a putative membrane-interacting

63 A key hydrophobic aromatic amino acid at one position was functionally sub

64 lectivity for N-protected dipeptides with an aromatic amino acid at the carboxylic terminus, which pr

65 ter family, Cleomaceae, naturally bear a non-aromatic amino acid at this position.

66 aled strong evidence that branched-chain and aromatic amino acids (BCAAs and AAAs) are closely associ

67 d intracellular levels of branched-chain and aromatic amino acids (BCAAs and ARO AAs, respectively) a

68 ays for H2O2 resistance included DNA repair, aromatic amino acid biosynthesis (aroBK), Fe-S cluster b

69 elated with metabolites of the shikimate and aromatic amino acid biosynthesis (SA) pathways (upstream

70 nt set of genes coding for shikimic acid and aromatic amino acid biosynthesis enzymes, leading to the

71 naerobic respiration, nitrate metabolism and aromatic amino acid biosynthesis genes among down-regula

72 osphate synthase (DAH7PS), at the gateway to aromatic amino acid biosynthesis in Mycobacterium tuberc

73 at allows complex control of the pathway for aromatic amino acid biosynthesis in the pathogen Mycobac

74 s that B. thailandensis, when exposed to the aromatic amino acid biosynthesis inhibitor glyphosate, i

75 We also used our module to control flux into aromatic amino acid biosynthesis to increase titers of s

76 Vi capsule, lipopolysaccharide (LPS), and aromatic amino acid biosynthesis were essential for viru

77 The first enzyme of the aromatic amino acid biosynthesis, 3-deoxy-D-arabino-hept

78 olite in the established shikimic pathway of aromatic amino acid biosynthesis, are absent in most eur

79 M. tuberculosis provide exquisite control of aromatic amino acid biosynthesis, not only controlling f

80 or branched-chain amino acid degradation and aromatic amino acid biosynthesis.

81 tase converts chorismate into prephenate for aromatic amino acid biosynthesis.

82 Ceramides, lysolipids, aromatic amino acids, branched chain amino acids, and st

83 ers (except C(3)) in this unusual tetrahydro-aromatic amino acid building block, giving insights into

84 Aromatic amino acids buried at a protein's core are ofte

85 orter can excrete fusel acids (byproducts of aromatic amino acid catabolism) and this role is shared

86 nits (phhA, hpd, hmgA, and dhcA) involved in aromatic amino acid catabolism; however, genes involved

87 utative binding sites are identified for the aromatic amino acid cofactors.

88 olate high-affinity oligonucleotides against aromatic amino acids complexed in situ with a nonspecifi

89 Plant aromatic amino acid decarboxylase (AAAD) enzymes are cap

90 synthesis, tryptophan hydroxylase (TPH) and aromatic amino acid decarboxylase (AADC) are expressed i

91 arginine to glutamine substitution in the L-aromatic amino acid decarboxylase (AADC) enzyme was repl

92 synthesizes dopamine through the actions of aromatic amino acid decarboxylase (AADC) in the proximal

93 Aromatic amino acid decarboxylase (AADC) then converts d

94 mainly attributed to its decarboxylation by aromatic amino acid decarboxylase (AADC), an enzyme over

95 Tracers for dopamine transporter (DAT), aromatic amino acid decarboxylase (AADC), or vesicular m

96 bstrate of the dopamine-synthesizing enzyme, aromatic amino acid decarboxylase (AADC).

97 e used mice with proximal tubule deletion of aromatic amino acid decarboxylase (ptAADC(-/-)).

98 The cell death was reversed by caspases and aromatic amino acid decarboxylase and monoamine oxidase

99 Although a drug that targets host aromatic amino acid decarboxylase does not prevent gut m

100 ro-l-m-tyrosine ([(18)F]FMT; a substrate for aromatic amino acid decarboxylase), baseline D2/3 recept

101 thesis enzymes tyrosine hydroxylase (TH) and aromatic amino acid decarboxylase, providing a novel mec

102 zing enzymes glutamic acid decarboxylase and aromatic amino acid decarboxylase.

103 emonstrated that Hsc70 interacts with TH and aromatic amino acid decarboxylase.

104 e Catharanthus roseus and Papaver somniferum aromatic amino acid decarboxylases changes the enzymes d

105 Glutamine, alanine, and aromatic amino acids decreased from non-failing to faili

106 e with phenylalanine but not other large and aromatic amino acids, demonstrating its molecular specif

107 MAGE (CoS-MAGE) to optimize biosynthesis of aromatic amino acid derivatives by combinatorially inser

108 The FTIR spectra revealed the presence of aromatic amino acids derived from QF.

109 -12-independent Th1 differentiation, whereas aromatic amino acid-derived AHR ligands were selectively

110 dy it has been shown how incorporation of an aromatic amino acid drastically improves selective antib

111 protein (IFABP) by incorporating fluorinated aromatic amino acids during synthesis in Escherichia col

112 and charging of tRNAs for branched chain and aromatic amino acids (e.g. leucine and tryptophan), the

113 res, conformation of disulphide bridges, and aromatic amino acid environment, depended on the fibres

114 y matrix of key intrinsic fluorophores, like aromatic amino acids, enzyme cofactors, and vitamins.

115 ikimate pathway leads to the biosynthesis of aromatic amino acids essential for protein biosynthesis

116 nd receptor signaling, (ii) substitutions of aromatic amino acids F295 and F296 in TM6 with alanine a

117 ith a corresponding decrease in the usage of aromatic amino acids, favoring formation of IDR structur

118 d by mutating it to other hydrophobic and/or aromatic amino acids, followed by voltage-clamp experime

119 ritical for assembly, the substitution of an aromatic amino acid for D111 produced a lethal phenotype

120 The substitution of any aromatic amino acid for Leu256 had similar effects in th

121 alanine biosynthetic pathways to supply more aromatic amino acids for secondary metabolism.

122 Branched-chain and aromatic amino acids, gluconeogenesis intermediates, ket

123 VLDL-triglycerides, VLDL-diameter, branched/aromatic amino acids, glycoprotein acetyls, and triglyce

124 There, a tight web of aromatic amino acids grips the substrate in a sequence-p

125 rrelated with loss of pi-pi stacking between aromatic amino acids H84 and Y83, which removes a wall s

126 Five branched-chain and aromatic amino acids had highly significant associations

127 rged amino acids and clusters of hydrophobic/aromatic amino acids have been assessed.

128 en luminescence in amyloid systems devoid of aromatic amino acids have not been resolved.

129 by which plants maintain intercompartmental aromatic amino acid homeostasis, and provide critical in

130 biopterin (BH(4)), an essential cofactor for aromatic amino acid hydrolases including tyrosine hydrox

131 ccessful knockout and complementation of the aromatic amino acid hydroxylase AAH2 gene, with no obser

132 e wild type hTPH2, like other members of the aromatic amino acid hydroxylase superfamily, exists as a

133 ) is a pterin-dependent mononuclear non-heme aromatic amino acid hydroxylase that catalyzes the conve

134 nases, namely, tetrahydrobiopterin-dependent aromatic amino acid hydroxylase, 2-oxoglutarate-dependen

135 dely distributed among eukaryotes, including aromatic amino acid hydroxylases (AAAHs), nitric oxide s

136 Tetrahydropterin-dependent aromatic amino acid hydroxylases (AAHs) are known from a

137 cycle oxidized pterin cofactors generated by aromatic amino acid hydroxylases (AAHs).

138 erall, these results are consistent with the aromatic amino acid hydroxylases all sharing the same ch

139 Additionally, expression levels of the two aromatic amino acid hydroxylases were negligible both in

140 st dopamine pathways due to parasite-encoded aromatic amino acid hydroxylases.

141 ), an obligate cofactor for NO synthases and aromatic amino acid hydroxylases.

142 ctivity of the iron center for the family of aromatic amino acid hydroxylases.

143 the reactivities of bacterial and eukaryotic aromatic amino acid hydroxylases.

144 e, Orf13 is novel in its ability to catalyze aromatic amino acid hydroxylation with hydrogen peroxide

145 oles in enzymatic nitric oxide synthesis and aromatic amino acid hydroxylation.

146 Ggamma5 was found due to the presence of an aromatic amino acid in its Ca(1)a(2)X motif.

147 For Ddc1, we identify two essential aromatic amino acids in a hydrophobic environment that w

148 erefore asserts a recognition preference for aromatic amino acids in a variety of sequence configurat

149 acking interactions between heterocycles and aromatic amino acids in biological systems, our ability

150 ore provide a rationale for the abundance of aromatic amino acids in fibril-forming peptides and esta

151 to deoxyhexoses used for the biosynthesis of aromatic amino acids in methanogens.

152 lution imaging reveals an unexpected role of aromatic amino acids in promoting protein-mHtt aggregate

153 C 7002, through site-directed mutagenesis of aromatic amino acids in the binding niche of the chlorop

154 gen-bond interactions between carotenoid and aromatic amino acids in the binding pocket.

155 Two conserved aromatic amino acids in the C terminus of Dpb11 are crit

156 Site-directed mutagenesis of two aromatic amino acids in the G domain demonstrated that t

157 The use of natural abundance aromatic amino acids in the growth media facilitated the

158 The aromatic amino acids in the JMD of the SARS-CoV S glycop

159 Specifically, aromatic amino acids in the peptides stack with bases at

160 The role of aromatic amino acids in the self-assembly of triple-heli

161 C-terminal, aromatic amino acids in the varphiX174 internal scaffold

162 me 10% of predicted prenylated proteins have aromatic amino acids in their Ca(1)a(2)X sequence and wo

163 The basis of the low PPII propensities of aromatic amino acids in this context was significant cis

164 and enzyme catalysis, and the involvement of aromatic amino acids in this process is of much interest

165 In this review we focus on cyclic aromatic amino acids in which the side chain is connecte

166 The presence of other aromatic amino acids, including l-tyrosine, l-phenylalan

167 Conversely, aromatic amino acid-induced CaR activation does not stim

168 Substituting an aromatic amino acid into the chelator approximately doub

169 he change in His-heme loop stability for the aromatic amino acids is caused by a slowdown in the rate

170 ly complex dynamic allostery: three distinct aromatic amino acids jointly communicate occupancy to th

171 t enzyme that catalyzes the hydroxylation of aromatic amino acid l-phenylalanine (L-Phe) to l-tyrosin

172 der Caryophyllales, are synthesized from the aromatic amino acid l-tyrosine (Tyr) and replaced the ot

173 IE) by altering extracellular [Ca(2+)] or by aromatic amino acid, L-phenylalanine (L-Phe, endogenous

174 es successful forward engineering of complex aromatic amino acid metabolism in yeast, with the best m

175 d multifaceted intercompartmental effects on aromatic amino acid metabolism.

176 mbiont Clostridium sporogenes that generates aromatic amino acid metabolites.

177 had reduced urine levels of methylamines and aromatic amino acids metabolites.

178 ontains a large amount of a toxic nonprotein aromatic amino acid, mimosine, and also an enzyme, mimos

179 to binding energy are heavily biased toward aromatic amino acids near the center of the binding surf

180 s contributes to regulating flux through the aromatic amino-acid network.

181 us most closely related to SARS-CoV, employs aromatic amino acid-nucleobase stacking interactions wit

182 ition, but the site has moved to a different aromatic amino acid of the agonist-binding site dependin

183 a strong cation-pi interaction to a specific aromatic amino acid of the receptor, TrpB.

184 No (13)C was incorporated into aromatic amino acids of cell wall proteins in the dark,

185 Aromatic amino acids of membrane proteins are enriched a

186 etion of a 21-amino acid segment enriched in aromatic amino acids on the C-terminal side of Cys-739 a

187 lementation of infected hMDMs with the three aromatic amino acids or with Trp alone rescues the intra

188 radicals was the four-amino-acid chain with aromatic amino acids, P#2 (LQKW).

189 icant stabilization of residual structure by aromatic amino acids, particularly Trp and Phe, and mini

190 suring transcriptional regulation of MAA and aromatic amino acid pathways in the filamentous cyanobac

191 The aromatic amino acid Phe is required for protein synthesi

192 for the shikimate pathway that generates the aromatic amino acids Phe, Trp, and Tyr.

193 d applications for cyclized analogues of the aromatic amino acids Phe, Tyr, Trp, and His within pepti

194 Asn, protonated Asp, Ser, Thr, and Cys), and aromatic amino acids (Phe, Tyr, and Trp).

195 of COX-2 is also aided by partitioning of 4 aromatic amino acids, Phe(59), Phe(66), Tyr(76), and Phe

196 the temporal and spatial interchange of the aromatic amino acid phenylalanine (Phe) between human re

197 rimental effects of hyperaccumulation of the aromatic amino acid phenylalanine (Phe) in animals, know

198 benzenoids/phenylpropanoids derived from the aromatic amino acid phenylalanine.

199 The aromatic amino acids phenylalanine and tyrosine represen

200 e first steps of hydration of the protonated aromatic amino acids phenylalanine, tryptophan, and tyro

201 These genes encode enzymes involved in aromatic amino acid, phenylpropanoid, camalexin, and sph

202 Different structural data suggest that aromatic amino acids play a particular role in the stabi

203 in stark contrast to the general belief that aromatic amino acids play a prominent role in multidrug

204 D-amino acids include N-methyl amino acids, aromatic amino acids, polar amino acids, and hydrophobic

205 not through later shikimate intermediates or aromatic amino acid precursors.

206 initiation involves a pathway of transient, aromatic amino acid radical intermediates, including Y73

207 tic determinant of branched-chain amino acid/aromatic amino acid ratio on changes in body weight and

208 he C allele of the branched-chain amino acid/aromatic amino acid ratio-associated variant rs1440581 m

209 We genotyped the branched-chain amino acid/aromatic amino acid ratio-associated variant rs1440581 n

210 ers another level of complexity in the plant aromatic amino acid regulatory network, unveiling new ta

211 l-Tyrosine is an essential aromatic amino acid required for the synthesis of protei

212 udies also revealed that viperin requires an aromatic amino acid residue at its C terminus for proper

213 demonstrated a remarkable preference for an aromatic amino acid residue in the P3 position.

214 revealed that the introduction of the large aromatic amino acid residue tryptophan at position 940 p

215 ns near-UV CD signals from its complement of aromatic amino acid residues (one Trp, eight Tyr, and 13

216 ia long-range radical transport (RT) through aromatic amino acid residues (Y122 left arrow over right

217 detected the partial solvent exposure of Pet aromatic amino acid residues at 37 degrees C, and a cell

218 In particular, the relative positioning of aromatic amino acid residues at positions 100 and 107 de

219 hat different cations affected structures of aromatic amino acid residues differently, which indicate

220 Interestingly, one or more aromatic amino acid residues have been identified as cri

221 se mutations revealed functionally important aromatic amino acid residues in four locations: at the i

222 vealed alteration of the microenvironment of aromatic amino acid residues in mutant proteins.

223 ing with ASLV(C) glycoproteins, at least two aromatic amino acid residues in the IgV domain of Tvc, T

224 thologues exhibited exclusive preference for aromatic amino acid residues in the P2 position, and for

225 ite-directed mutagenesis of highly conserved aromatic amino acid residues in the SPATE family resulte

226 is interface identified two highly conserved aromatic amino acid residues located in the H-I loop and

227 Two conserved aromatic amino acid residues located on the intracellula

228 mine oxidases A and B (MAO A and MAO B) show aromatic amino acid residues oriented approximately perp

229 lly possess an "aromatic box," where several aromatic amino acid residues surround the bound ligand.

230 ion by UVR8 is based on intrinsic tryptophan aromatic amino acid residues, with tryptophan-285 as the

231 e present study investigates the role of the aromatic amino acid-responsive regulator PhhR in mediati

232 er, these results, along with the lack of an aromatic amino acid-rich region in CdtC similar to that

233 The juxtamembrane domain (JMD) of S is an aromatic amino acid-rich region proximal to the transmem

234 nscriptional activation of genes involved in aromatic amino acid, S-adenosyl methionine (SAM) and fol

235 Using SCFM, we provide evidence that aromatic amino acids serve as nutritional cues that infl

236 Aromatic amino acid side chains have a rich role within

237 1)H enrichment of a single ortho position of aromatic amino acid side chains in an otherwise perdeute

238 t involve the site-specific intercalation of aromatic amino acid side chains into genomic DNA.

239 n protein-stabilizing interactions involving aromatic amino acid side chains make significant contrib

240 Aromatic amino acid side chains mediate most coat-intern

241 associated benzene rings (a simple model of aromatic amino acid side chains) can switch inherent dyn

242 e the strength of stacking interactions with aromatic amino acid side chains, follow predictable tren

243 Interactions between carbohydrates and aromatic amino acid side chains, however, are supplement

244 t such interactions are possible for all the aromatic amino acid side-chains.

245 elative concentrations of branched-chain and aromatic amino acids significantly increased in the free

246 lectron transfer (PCET) through a network of aromatic amino acids spanning the two subunits.

247 roxylase catalyze the hydroxylation of their aromatic amino acid substrates using a tetrahydropterin

248 ation-deamination on various combinations of aromatic amino acid substrates.

249 ipal functions, BAL can slowly decarboxylate aromatic amino acids such as benzoylformic acid.

250 changes in Raman vibrations corresponding to aromatic amino acids such as phenylalanine and tryptopha

251 (18)F- and (11)C-labeled neutral aromatic amino acids, such as l-3,4-dihydroxy-6-(18)F-fl

252 beta-sheet areas are rich in cysteine and aromatic amino acids, such as phenylalanine and tyrosine

253 gation in mutated pili that were missing key aromatic amino acids, suggest that the pili of G. sulfur

254 etes, such as branched chain amino acids and aromatic amino acids, suggesting they report on a distin

255 In addition, acidic, hydrophobic, or aromatic amino acids surrounding the p(S/T)Q sequence ha

256 m tumefaciens, and two experimental systems, aromatic amino acid synthesis and DNA transfer in bacter

257 emphasized the genetics and biochemistry of aromatic amino acid synthesis and the characterization o

258 H), a shikimate pathway enzyme essential for aromatic amino acid synthesis, is also required for GA p

259 veal the existence of a fourth, more distant aromatic amino acid that serves as a terminal electron d

260 el provides insight into the organization of aromatic amino acids that are important for electrical c

261 tions were generated for the six C-terminal, aromatic amino acids that mediate most coat-internal sca

262 amino acids, exhibited impaired transport of aromatic amino acids that require a large binding site v

263 resence of a flexible loop region containing aromatic amino acids, the caveolin-binding motif.

264 ist binding sites have the same core of five aromatic amino acids, the fetal site has approximately 3

265 Aromatic amino acids, the well-known osmoprotectant beta

266 A number of aromatic amino acids thought to be near the agonist-bind

267 Overrepresentation of conserved aromatic amino acids through 20 herpesviruses homologues

268 mide intermediate was stabilized by adjacent aromatic amino acids through ring-ring stacking interact

269 itionally, exchange of the respective fourth aromatic amino acid to redox-inactive phenylalanines sti

270 nvolving the obligatory binding of essential aromatic amino acids to Mec1, followed by an enhancement

271 on caused by the affinity of hydrophobic and aromatic amino acids toward these surfaces leads to elec

272 nvolved in monapterin biosynthesis(8-10) and aromatic amino acid transamination,(11) respectively, we

273 e addition of aspartate and expression of an aromatic amino acid transporter, as well as a tyrosine-s

274 olar, hydrophobic side chains, including one aromatic amino acid (Trp-31).

275 Intriguingly, the large, aromatic amino acid tryptophan has a high propensity to

276 ino acids (valine, leucine, and isoleucine), aromatic amino acids (tryptophan and phenylalanine), and

277 All three aromatic amino acids (tryptophan, phenylalanine and tyro

278 en quantum yields generated by excited state aromatic amino acids (tryptophan, tyrosine, phenylalanin

279 In addition to the aromatic amino acids, two acidic residues, D111 and E113

280 urthermore, replacing Trp-248 with a smaller aromatic amino acid (Tyr/Phe) impaired the beta-arrestin

281 of carbon flux toward the shikimate-derived aromatic amino acids tyrosine and tryptophan.

282 esis was used to assess the contributions of aromatic amino acids (tyrosine and phenylalanine) to rec

283 ormation of Hb S fibers in real time through aromatic amino acid vibrational modes.

284 15 A distant from the chromophore by another aromatic amino acid, W389F, restores native Pr --> Pfr p

285 no-acid (aa) PTM domain of AcMNPV GP64 lacks aromatic amino acids, we asked whether this region might

286 mutase, a key enzyme in the biosynthesis of aromatic amino acids, we demonstrate the design of natur

287 Focusing on aromatic amino acids, we predict metabolic products that

288 show that only substitutions of Tyr(511) to aromatic amino acids were able to mimic, albeit partiall

289 Aromatic amino acids were detected by means of the FTIR

290 stream open reading frames encoding multiple aromatic amino acids were found 5' of the translation in

291 Circulating branched-chain amino acids and aromatic amino acids were recently related to insulin re

292 There is little perturbation of other aromatic amino acids when Y122* is reduced.

293 ar capsules based on oligoamide sequences of aromatic amino acids which are capable of binding tartar

294 growth defect is rescued by inclusion of the aromatic amino acids, which are essential for production

295 dified Dulbecco's medium, a medium richer in aromatic amino acids, which give rise to AhR agonists, c

296 recruited to stress granules, and found that aromatic amino acids, which have previously been linked

297 vidual and simultaneous replacement of these aromatic amino acids with aliphatic residues.

298 cs suggest multiple stacking arrangements of aromatic amino acids with the nucleobases at the junctio

299 s work from our laboratory demonstrated that aromatic amino acids within CF lung secretions (sputum)

300 posed to involve a hopping mechanism through aromatic amino acids (Y(122) --> W(48) --> Y(356) in bet