ライフサイエンスコーパス: aromatic amino acid

1 sequence enriched in positively charged and aromatic amino acids.

2 and contained multiple large hydrophobic and aromatic amino acids.

3 norepinephrine and for the hydroxylation of aromatic amino acids.

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

5 B. hydrogenotrophica targets aliphatic and aromatic amino acids.

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

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

8 tCM shows that *MtCM is not regulated by the aromatic amino acids.

9 is the substitution of this residue with non-aromatic amino acids.

10 ight- and branched-aliphatic amino acids and aromatic amino acids.

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

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

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

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

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

16 spiratory nitrogen cycle and accumulation of aromatic amino acids.

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

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

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

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

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

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

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

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

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

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

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

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

29 PC12 cells, it is transported by both the l-aromatic amino acid and the dopamine transporters.

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

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

32 resonance energy transfer between PPAR alpha aromatic amino acids and bound corresponding naturally o

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

34 The aromatic amino acids and carotenoids are the major contr

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

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

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

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

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

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

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

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

43 d to determine the structures of the neutral aromatic amino acids and their complexes to Na(+) and K(

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

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

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

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

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

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

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

51 Aromatic amino acids are characterized by an additional

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

53 phate (DKFP) pathway for the biosynthesis of aromatic amino acids (AroAAs) and p-aminobenzoic acid (P

54 Aromatic amino acids (AroAAs) are biosynthesized in this

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

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

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

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

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

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

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

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

63 se-1-phosphate (DKFP), a precursor sugar for aromatic amino acid biosynthesis in Methanocaldococcus j

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

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

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

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

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

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

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

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

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

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

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

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

76 required only for germination in response to aromatic amino acid cogerminants.

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

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

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

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

81 Coinfusion of the aromatic amino acid decarboxylase (AADC) inhibitor m-hyd

82 Aromatic amino acid decarboxylase (AADC) then converts d

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

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

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

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

87 s metabolized by the concerted action of the aromatic amino acid decarboxylase and monoamine oxidase.

88 rat neurons, which was also prevented by an aromatic amino acid decarboxylase inhibitor.

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

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

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

92 in the presence of NSD-1015, an inhibitor of aromatic amino acid decarboxylase.

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

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

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

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

97 -12-independent Th1 differentiation, whereas aromatic amino acid-derived AHR ligands were selectively

98 This loss in aromatic amino-acid discrimination in vivo revealed that

99 The contribution of editing to aromatic amino-acid discrimination is less well understo

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

101 In pocket 9, DQ0604 preferred aromatic amino acids due to the beta9 and beta30 polymor

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

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

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

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

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

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

108 yrosine decarboxylase (TDC), a member of the aromatic amino acid family, but this enzyme has not been

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 e synthase, a key enzyme in the synthesis of aromatic amino acids in plants, fungi, and bacteria.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

155 onBs appear to form a single cluster of 8-10 aromatic amino acids, including those found at opposite

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

157 Substituting an aromatic amino acid into the chelator approximately doub

158 ing homologous alanine substitutions for two aromatic amino acids involved in DNA melting.

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

160 w reaction observed between radicals a-c and aromatic amino acids is the addition of the radical to t

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

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

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

164 e first two steps in the biosynthesis of the aromatic amino acids leading to 3-dehydroquinate (DHQ).

165 ientation, is sequestered within a basic and aromatic amino acid-lined cleft between the La and RRM1

166 carbon metabolism, pigment biosynthesis and aromatic amino acid metabolism, were significantly modif

167 d multifaceted intercompartmental effects on aromatic amino acid metabolism.

168 mbiont Clostridium sporogenes that generates aromatic amino acid metabolites.

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

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

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

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

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

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

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

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

177 Aromatic amino acids of membrane proteins are enriched a

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

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

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

181 pplied this framework to the analysis of the aromatic amino acid pathways and discovered almost 75,00

182 The aromatic amino acid Phe is required for protein synthesi

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

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

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

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

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

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

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

190 The aromatic amino acids phenylalanine and tyrosine represen

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

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

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

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

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

196 hrough a defined pathway involving conserved aromatic amino acids (R2: Y122, W48, Y356; R1: Y731, Y73

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 and replacing Phe(6) and Trp(8) with bulkier aromatic amino acid residues is very important for selec

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

218 Two conserved aromatic amino acid residues located on the intracellula

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

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

221 oring bands (particularly those derived from aromatic amino acid residues) as well as the relatively

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

223 ubstrates, implying changing environments of aromatic amino acid residues.

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

225 Here, we characterize an aromatic amino acid rich region within the ectodomain of

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

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

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

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

230 molecular base-stacking interactions between aromatic amino acid side chains and the substrate.

231 Aromatic amino acid side chains have a rich role within

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

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

234 Aromatic amino acid side chains mediate most coat-intern

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

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

237 consists of a deep cleft, heavily lined with aromatic amino acid side-chains but bounded by numerous

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

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

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

241 We also show that aromatic amino acid-stimulated [Ca(2+)](i) oscillations

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

243 IL4I1 has preference for aromatic amino acid substrates, having highest specific

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

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

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

247 ion of the aromatic residue with a different aromatic amino acid, such as W653Y or Y1302W, did not af

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

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

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

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

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

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

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

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

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

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

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

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

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

261 Aromatic amino acids, the well-known osmoprotectant beta

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

263 Overrepresentation of conserved aromatic amino acids through 20 herpesviruses homologues

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

265 r the transmembrane segment using charged or aromatic amino acids, thus limiting the peptides' abilit

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

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

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

269 lar 3-nitrotyrosine is transported via the l-aromatic amino acid transporter in nondopaminergic NT2 c

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

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

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

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

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

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

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

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

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

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

280 15 A distant from the chromophore by another aromatic amino acid, W389F, restores native Pr --> Pfr p

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

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

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

284 more, [Ca(2+)](i) oscillations stimulated by aromatic amino acids were also abolished by inhibition o

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

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

287 t the [Ca(2+)](i) oscillations stimulated by aromatic amino acids were selectively abolished by TRPC1

288 ng the aroA gene (necessary for synthesizing aromatic amino acids) were able to establish GI coloniza

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

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

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

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

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

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

295 ds to extracellular Ca(2+) ([Ca(2+)](o)) and aromatic amino acids with the production of different pa

296 illations that integrates its stimulation by aromatic amino acids with TRPC1 regulation by PKC and ca

297 sponds to two different agonists, Ca(2+) and aromatic amino acids, with the production of sinusoidal

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

299 acid replacements involving arginine and/or aromatic amino acids within the final five C-terminal re

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