ライフサイエンスコーパス: glycine

1 and d-allo-Thr along with d-amino acids and glycine.

2 t and endogenous synthesis from arginine and glycine.

3 ggered in response to certain bile acids and glycine.

4 fications, including a rare thioamidation of glycine.

5 scriminate between D-amino acids and achiral glycine.

6 by VEGF led to an increase in intracellular glycine.

7 made from calcite single crystals containing glycine (0-7 mol%) or aspartic acid (0-4 mol%), we eluci

8 PCP, 15 mg/kg/d by osmotic minipump), or PCP+glycine (16% by weight diet) interventions.

9 C1A protein had a shorter half-life than the glycine 482 variant when expressed in HepG2 cells.

10 ist at GluN1/2A (100% response compared with glycine), a partial agonist at GluN1/2B and GluN1/2D (10

11 n of the upper side chain (proton donor) and glycine acetamide of the lower side chain (proton accept

12 , which demonstrated ex vivo potentiation of glycine-activated current in mouse dorsal horn neurons f

13 ptors (iGluRs) that are distantly related to glycine-activated NMDA receptors and that bind glycine w

14 maximum value of 0.03 +/- 0.009 with aqueous glycine aerosol particles.

15 sed a significant reduction in glutamate and glycine agonist potency, whilst D731N was non-responsive

16 at a single nitrogen atom substitution for a glycine alpha-carbon increases the peptide's triple heli

17 s of d-xylose, d-arabinose and d-ribose with glycine, alpha-l- or beta-alanine and l-valine in pH 7.0

18 Its biosynthesis is reasoned to proceed via glycine-, alpha-hydroxyglycine-, glycyllysine-, and glyc

19 Glycine also caused a red shift in the OH stretch region

20 Synaptically released glycine also enhanced tonic glycinergic currents and res

21 Glycine amidinotransferase (GATM) catalyzes the rate-lim

22 svA is similar to that of the human arginine-glycine amidinotransferase in the creatine biosynthesis

23 ne, an N-methyl derivative of the amino acid glycine and a metabolic product of choline, plays an imp

24 at GluN2C-containing receptors compared with glycine and a partial agonist at GluN2B-containing recep

25 methyltransferse (SHMT) converts serine into glycine and a tetrahydrofolate-bound one-carbon unit.

26 Via a native N-terminal glycine and an added GGGGSLPETGG peptide at C-terminus o

27 sfAFP has low sequence complexity with 46% glycine and an interior filled only with backbone H-bond

28 ates at the polymer-water interface, whereas glycine and betaine are strongly depleted.

29 ations via a mechanism that is distinct from glycine and betaine.

30 ses of sarcosine and its natural precursors, glycine and choline, were performed from independent hum

31 hemistry and electrophysiology, we show that glycine and D-serine relative availability at rat hippoc

32 Receptor co-agonists, glycine and D-serine, have intriguingly emerged as poten

33 Glycine and GABA are both inhibitory neurotransmitters i

34 ggests that neurons in the VNLL release both glycine and GABA in the ICC, but functional evidence for

35 (1-deoxy-1-fructosylglycine) formation from glycine and glucose, varying temperature, water activity

36 ATPHI islets also exhibited increased serine/glycine and glutamine biosynthesis.

37 selectivity and yield: 40% yield for lauroyl glycine and less than 5% for dipeptide after 96h of synt

38 lerated by simple amino acids, in particular glycine and lysine.

39 The highest level of 2.0% for glycine and reduced glutathione favored protein extracta

40 not differ in their premature responding and glycine and serine levels in vmPFC during the performanc

41 ty is associated with reduced recruitment of glycine and serine neurotransmitters in the ventromedial

42 resent evidence that deficient activation of glycine and serine release in the ventral medial prefron

43 ed blunted task-related recruitment of vmPFC glycine and serine release, and the loss of an inverse r

44 ation of pentameric GlyR structures bound to glycine and strychnine have contributed to visualizing t

45 ylalanine, valine, GABA, glutamine, alanine, glycine and taurine were separated and detected at conce

46 A receptor in complex with the GluN1 agonist glycine and the GluN2A antagonist NVP-AAM077.

47 On the other hand, glycine and the higher concentrations of reduced glutath

48 Detection of glycine and thymopentin (separately) demonstrated the ma

49 ple helical collagen peptides containing aza-glycine and we demonstrate that minimal alteration to th

50 amylation, the posttranslational addition of glycines and glutamates to genetically encoded glutamate

51 uman serum albumin, neurotensin, creatinine, glycine, and alanine) were retained in the samples for s

52 list libraries biased with tyrosine, serine, glycine, and arginine to form binding surfaces for speci

53 significant stepwise increases of sarcosine, glycine, and choline tissue levels from benign prostate

54 three primary neurotransmitters (glutamate, glycine, and GABA) in the auditory brainstem of Fmr1 kno

55 -hydroxy-5-methyl-4-isoxazolepropionic acid, glycine, and gamma-aminobutyric acid-A receptors), were

56 s showed positive selection of tyrosines and glycines, and negative selection of leucines.

57 ine-glycine (GSG) index (glutamate/[serine + glycine]) and tested for an association with liver histo

58 The non-essential amino acids serine and glycine are used in multiple anabolic processes that sup

59 eneration from the allylic phosphate and the glycine aryl ester.

60 rs from readily accessible N,N-disubstituted glycine aryl esters and allylic phosphates.

61 These original results highlight glycine as a necessary mediator in VEGF signalling via t

62 plasticity and accessibility of the arginine-glycine-aspartic acid (RGD) binding site in FN, which, i

63 Cyclic arginine-glycine-aspartic acid (RGD) containing peptides are know

64 erally alphavbeta6, via a conserved arginine-glycine-aspartic acid (RGD) motif in the exposed, antige

65 mation beta5/beta3 integrins and an arginine-glycine-aspartic acid (RGD) sequence in the first extrac

66 l attachment to the high density of arginine-glycine-aspartic acid tripeptide present in DAPF.

67 d to mimic the tripeptide sequence (arginine-glycine-aspartic acid) of the natural ligands; however,

68 udy, we report the efficacy of RGD (arginine-glycine-aspartic acid) peptide-modified polylactic acid-

69 te bioinks containing cell adhesive Arginine-Glycine-Aspartic acid-Serene (RGDS) peptide and/or nanoc

70 Substitutions of a conserved glycine at the interface of adjacent protein layers dest

71 Introduction of bulky methionine for glycine at two points on this surface reduced catalytic

72 All six tryptophan indole and eight glycine backbone (15)N-(1)H NMR signals in A2AAR were in

73 essed in HEK cells, reduced the potencies of glycine, beta-alanine and taurine by 9-, 6- and 3-fold r

74 t, baseline levels of betaine, also known as glycine betaine (hazard ratio 0.84 per SD log metabolite

75 d osmotic homeostasis reestablishment due to glycine betaine accumulation.

76 ing choline, acetylcholine, L-carnitine, and glycine betaine effectively.The choline-binding protein

77 in the oligopeptide importer (oppABCDF) and glycine betaine importer (gbuABC) allowed DeltadacA muta

78 The subsequent uptake of glycine betaine returns SH3 to the stability observed wi

79 (Kd ) in the nanomolar range for choline and glycine betaine, micromolar Kd for stachydrine and trigo

80 line, glycerophosphocholine, phosphocholine, glycine betaine, N-methylproline, proline betaine (stach

81 of S. meliloti towards betonicine, choline, glycine betaine, stachydrine and trigonelline.

82 t oligopeptides act as osmolytes, similar to glycine betaine, to disrupt intracellular osmotic pressu

83 Results showed that glycine betaine, trigonelline, proline betaine, N(epsilo

84 in the presence and absence of the osmolyte, glycine betaine.

85 of NMDA receptor ion channel and kinetics of glycine binding with its ligand binding domain.

86 Most NMDA receptors comprise two glycine-binding GluN1 and two glutamate-binding GluN2 su

87 ne, a co-agonist of the NMDA receptor at the glycine-binding site, can be released by astrocytes in a

88 referential solvation arguments, betaine and glycine both increase the surface tension at the air-wat

89 ects can be mitigated by the transition from glycine bound to apo state of the GluN1 LBD.

90 an use cell wall precursors having different glycine branch lengths (penta-, tri-, or monoglycine), w

91 link peptidoglycan strands bearing different glycine branches.

92 he latter, common reagents like HCl, Na2CO3, glycine buffer, or SDS are employed.

93 Manipulation of extracellular glycine by blocking either, or both, the glial and neuro

94 Restriction of dietary serine and glycine can reduce tumour growth in xenograft and allogr

95 ncoding the LiaS protein with an arginine-to-glycine change at position 135 [liaS(R135G)]) recapitula

96 Glutamic acid, serine, and glycine concentrations are known to be altered in NAFLD.

97 C receptors in the presence of physiological glycine concentrations.

98 of collagen is unique due to its high (33%) glycine content.

99 GABA and glycine corelease is particularly common in the spinal c

100 ne in aqueous solution and the mechanisms of glycine crystallization.

101 ignificant amount of respiration, use serine-glycine cycle and produce ethanol in mitochondria as opp

102 -4-mercapto-4-methylpentan-2-one-l-cysteinyl-glycine (CysGly-4MMP) and S-4-mercapto-4-methylpentan-2-

103 ows for the measurement of NMDAR function in glycine/D-serine and/or glutamate sensitive modes.

104 rent subunit composition after activation by glycine/D-serine or glutamate and hence presents the fir

105 tes, suggesting DTD's key cellular role as a glycine deacylator.

106 pendent upon SHMT enzymatic activity to meet glycine demand.

107 methods, we identified this elusive phase as glycine dihydrate (GDH), representing the first report o

108 (3) Glycine directly bounded to voltage dependent anion chan

109 mutation, and demonstrate an increase in the glycine EC50 value.

110 In support of this finding, glycine enhances Akt activation in HEK293 cells over-exp

111 thranilate-derived amino ketones with an aza-glycine equivalent, chemoselective nitrogen functionaliz

112 Glycine ethyl ester (GEE) and ammonium chloride served a

113 Interestingly, the glycine-evoked currents in dissociated DRD1-positive MSN

114 water structure to the least extent, whereas glycine exerts the greatest influence on the water struc

115 ed polypeptides, which contain phenylalanine-glycine (FG) binding sites for nuclear transport recepto

116 e of molecules via hydrophobic phenylalanine-glycine (FG) domains on nucleoporins.

117 inds to polymeric forms of the phenylalanine:glycine (FG) repeat domain, which is shared by several p

118 ne-third of these Nups contain phenylalanine-glycine (FG)-rich repeats, forming a diffusion barrier,

119 ures of skepinone-L scaffold like inducing a glycine flip at the hinge region and occupying both hydr

120 y driven and can be reversed by substituting glycine for alanine in position 2, forming [YG(L)PAA+H](

121 s-specific glyS T-box controls the supply of glycine for both ribosomal translation and cell wall syn

122 We show corelease of GABA and glycine for the first time in the central nucleus of the

123 enesis and providing better understanding of glycine function in angiogenesis, which may provide valu

124 Here, we show that a single Arginine (R) to Glycine (G) mutation at position 76 in the refp17 backbo

125 spartate (NMDA) receptors are glutamate- and glycine-gated channels that flux Na(+) and Ca(2+) into p

126 ceptor family, GluN1/GluN3 receptors produce glycine-gated deeply desensitising currents that are ins

127 Remarkably, CDPK1 contains a small glycine gatekeeper residue in the ATP binding pocket mak

128 Small proteins characterized by a double-glycine (GG) secretion motif, typical of secreted bacter

129 ted more slowly than predicted, and proline, glycine, glutamate, lysine and arginine, which were all

130 n rejecting 98% of ascorbic acid and 100% of glycine, glutamic acid and uric acid.

131 m of GR (GRCl) was tested in the presence of glycine (GLY) and other selected amino acids.

132 was to quantify in vivo glutamate (Glu) and glycine (Gly) levels in patients with first-episode psyc

133 RyR1 S6 pore-lining helix has two conserved glycines, Gly-4934 and Gly-4941, that facilitate RyR1 ch

134 ubiquitinated proteins with trypsin yields a glycine-glycine remnant bound to the modified lysine res

135 llected samples of whole blood from codon 96 glycine/glycine, captive white-tailed deer that were ana

136 diffusion dynamics and synaptic trapping of glycine (GlyR) but not GABAA receptors.

137 ion x insulin), and the new glutamate-serine-glycine (GSG) index (glutamate/[serine + glycine]) and t

138 is, human myeloperoxidase was incubated with glycine, H2O2, malondialdehyde, and a lysine analog in P

139 installation of a (4-methylhexa-2,4-dienoyl)glycine handle across a hexadepsipeptide core contribute

140 Conservation of these glycine hinges among all class B GPCRs suggests their ge

141 ending of helices VI and VII around flexible glycine hinges.

142 hed-chain and aromatic amino acids (alanine, glycine, histidine, phenylalanine, leucine, isoleucine,

143 body TF2 (anti-CEA x anti-histamine-succinyl-glycine [HSG]) and the di-HSG-DOTA peptide IMP288.

144 ainst soybean cyst nematode (SCN, Heterodera glycines Ichinohe).

145 Thus, defective glycine import is a targetable metabolic deficiency of D

146 has important implications for the state of glycine in aqueous solution and the mechanisms of glycin

147 d that replacement of the strictly conserved glycine in collagen with aza-glycine provides a general

148 Our findings suggest roles for glycine in regulating neuronal excitability in the foreb

149 currents in response to exogenously applied glycine in these forebrain structures.

150 following dietary restriction of serine and glycine in these models was further improved by antagoni

151 ra amino acid residue at or near a conserved glycine in transmembrane segment 10.

152 eptide backbone conformation occurs with aza-glycine incorporation.

153 d conformational constraints provided by aza-glycine increases the thermal stability and rate of fold

154 However, GlyRalpha1 expression and glycine-induced currents are reduced in beta-cells from

155 Insertion of two glycines into the Rieske domain and substitution of tyro

156 vior of the centrosymmetric crystal of alpha-glycine is resolved by the discovery of a polar, several

157 Although glycine is the most effective co-germinant, other amino

158 ine, l-glutamine, l-threonine, l-arginine, l-glycine, l-proline, l-serine, l-alanine, and l-glutamic

159 transgenic plants such as aspartate, lysine, glycine, leucine and threonine with no changes in the am

160 ced toxicity in Escherichia coli even at low-glycine levels which is alleviated by alanine supplement

161 (+)-67 significantly elevated extracellular glycine levels within the medial prefrontal cortex (mPFC

162 iated with altered cortical myo-inositol and glycine levels, suggesting sleep loss-induced modificati

163 urea cycle metabolites and increased plasma glycine levels.

164 n N-methyl-D-aspartate (NMDA) modulator with glycine-like partial agonist properties; like the NMDA r

165 Synthesis of lauroyl glycine lipoaminoacid was carried out with a lipase from

166 itored the thermal formation of early ribose-glycine Maillard reaction products over time by ion cycl

167 Two types of resistant soybean (Glycine max (L.) Merr.) sources are widely used against

168 es along with expression studies in soybean [Glycine max (L.) Merr.] were leveraged to dissect the ge

169 Soybean (Glycine max [L.] Merr.) is one of the most important oil

170 gene families with those of fellow legumes, Glycine max and Phaseolus vulgaris, in addition to the m

171 ell characterized symbiosis between soybean (Glycine max L.

172 Soybean (Glycine max Merr.) is a widely grown oilseed crop and sh

173 ic analysis between Arabidopsis thaliana and Glycine max root hair genes reveals the evolution of the

174 sulfonate mutagenized population of soybean (Glycine max) 'Forrest' was screened to identify mutants

175 hemical capacity was measured in 67 soybean (Glycine max) accessions showing large variation in leaf

176 gh-antioxidant black legumes, black soybean (Glycine max) and black turtle bean (Phaseolus vulgaris),

177 sis (Arabidopsis thaliana) CPK4 and soybean (Glycine max) CDPKbeta are RcCDPK1 orthologs that effecti

178 The overexpression of AraEXLB8 in soybean (Glycine max) composite plants remarkably decreased the n

179 nd among-cultivar components across soybean (Glycine max) grown under both controlled and field condi

180 subgenomes in maize (Zea mays) and soybean (Glycine max) have followed different trajectories.

181 Soybean (Glycine max) is a major legume crop plant providing over

182 Soybean (Glycine max) is the most widely grown oilseed in the wor

183 The soybean (Glycine max) seed coat has distinctive, genetically prog

184 ce in the Peking-type resistance of soybean (Glycine max), which also requires the rhg1 gene.

185 bidopsis (Arabidopsis thaliana) and soybean (Glycine max).

186 virguliforme that are pathogenic to soybean (Glycine max).

187 wild-type roots of the crop legume soybean (Glycine max).

188 ductance (gs )) for legumes Cicer arietinum, Glycine max, Lupinus alba and Vicia faba, nonlegume dico

189 In addition, PV+ INs expressed robust glycine-mediated tonic currents; however, we found no ev

190 In spinal cord, glycine mediates synaptic inhibition through the activat

191 e inhibitor, DMOG [N-(2-Methoxy-2-oxoacetyl) glycine methyl ester], that can partially inhibit mangan

192 Importantly, AIS cases harbor mainly non-glycine missense mutations and lack the clinical feature

193 ownregulate expression of genes encoding the glycine modification machinery.

194 the net charge of their cell surface through glycine modification of lipid A.

195 acyltransferase known to produce an acylated glycine molecule called commendamide.

196 Precursor processing after the first di-glycine motif by the ubiquitin-specific proteases Ubp5 a

197 ry mediator in VEGF signalling via the GlyT1-glycine-mTOR-VDAC1 axis pathway.

198 Glycine N-methyltransferase (GNMT), a member of the fami

199 most widely studied member is N-arachidonoyl glycine (NAGly), which differs structurally from the end

200 both antibodies share a canonical asparagine-glycine (NG) motif in a structural loop, this is prone t

201 ysis of a series of (S)-N-(1-tert-butylethyl)glycine (Ns1tbe) peptoid homo-oligomers.

202 inding affinity of Kapbeta1 to phenylalanine-glycine nucleoporins (FG Nups), which is comparable with

203 trimethylamine N-oxide (TMAO), betaine, and glycine, on the hydrophobic collapse of an elastin-like

204 ificant differences in blood serum levels of glycine (P = 4.04 x 10(-6)) and serine (P = 2.48 x 10(-4

205 n assimilated into biomass via the reductive glycine pathway.

206 Antimicrobial N-substituted glycine (peptoid) oligomers ("ampetoids") are structural

207 ded mutation of a critical residue, F270, to glycine perturbs the Si site, allowing structural determ

208 vealing that in one case a single alanine to glycine point mutation suffices to more than double the

209 ic debridement, soft tissue curettage (STC), glycine powder air polishing (GPAP) and a repeated submu

210 ic debridement, soft tissue curettage (STC), glycine powder air polishing (GPAP), and a repeated subm

211 macologic inhibition of CSE with l-propargyl glycine prevented apneas in both HO-2(-/-) mice and SH r

212 ing amounts of gelatin increased circulating glycine, proline, hydroxyproline, and hydroxylysine, pea

213 As a functional consequence, glycine protects against excitotoxicity-induced neuronal

214 ictly conserved glycine in collagen with aza-glycine provides a general solution for stabilizing trip

215 d formaldehyde concentration and more robust glycine-quench conditions.

216 ies of AMPA channels with different arginine/glycine (R/G) editing and flip/flop status.

217 ng tfuA and/or ycaO revealed the presence of glycine, rather than thioglycine, supporting this hypoth

218 GLRB genes, which encode the alpha1 and beta glycine receptor (GlyR) subunits, are the major cause.

219 Analysis of the glycine receptor properties mediating inhibition of parv

220 1 and contactin-associated protein-like 2), glycine receptor, and gamma-aminobutyric acid-A receptor

221 Glycine receptors (GlyR) are inhibitory Cys-loop ion cha

222 Glycine receptors (GlyRs) are inhibitory ligand-gated io

223 Previous studies suggested that glycine receptors (GlyRs) are involved in the regulation

224 Glycine receptors (GlyRs) are major mediators of inhibit

225 Glycine receptors (GlyRs) are potentiated by ethanol and

226 bition through the activation of heteromeric glycine receptors (GlyRs) composed primarily of alpha1 a

227 irments or trafficking defects of inhibitory glycine receptors (GlyRs) have been linked to human hype

228 he shared stoichiometry for phasic and tonic glycine receptors suggests pharmacology is unlikely to b

229 on, such as ring-like structures composed of glycine receptors.

230 ition are mediated by heteromeric alpha/beta glycine receptors.

231 was to evaluate the ability of gallic acid, glycine, reduced glutathione and l-cysteine at 0.1, 0.5,

232 e less responsive to depletion of serine and glycine, reflecting an ability of activated Kras to incr

233 The glycine replacement mutants were devoid of transport act

234 Peptoids that are oligomers of N-substituted glycines represent a class of peptide mimics with great

235 A glycine residue above W583 might act as flexible linker

236 cereblon through a surface turn containing a glycine residue at a key position, interacting with both

237 ith a one-residue stagger to fit every third glycine residue in the inner core without disturbing the

238 ane helices II, IV, and V of subunit B, near glycine residues 140 and 141.

239 These two critical glycine residues form part of the structures that regula

240 cated adjacent to the substitution sensitive glycine residues play a role in blocking the pathway upo

241 It contains four symmetrically arranged glycine residues suggesting that flexibility is a key fe

242 ApOmpA), an adhesin that uses key lysine and glycine residues to interact with alpha2,3-sialylated an

243 Upon combinatorial substitution of these glycine residues to proline, functional and structural a

244 served when W69 was replaced with alanine or glycine residues.

245 that GABA co-release may speed the decay of glycine responses altering both temporal precision and s

246 el systems composed of adenine or adenosine, glycine, ribose and/or 2-furanmethanol (with and without

247 In addition, we identified variants of the glycine riboswitch class that no longer recognize this a

248 plex and the cytoskeletal-associated protein glycine-rich domain of Nip100/p150(glued) Our results su

249 ive site, including the hinge and tip of the glycine-rich flaps, and the rest of the protein.

250 lexes showed that the inhibitor stabilizes a glycine-rich loop conformation that shapes the ATP ribos

251 mbedded kinase by altering the dynamics of a glycine-rich motif that is critical for phosphotransfer

252 mple, the cardiac LIM protein, cysteine- and glycine-rich protein 3, is thought to mediate cardiac me

253 In addition, we show that GLYCINE-RICH PROTEIN 8 promotes hair cell fate while all

254 nes identified the At3g59640 gene encoding a glycine-rich protein as the putative PSS1 gene.

255 rtion of Aap contains a 135-aa-long, proline/glycine-rich region (PGR) that has not yet been characte

256 uN1 clamshell hinge is sufficient to control glycine sensitivity and activation efficacy.

257 ion also reduced cell-surface expression and glycine sensitivity.

258 ty is tightly controlled by their regulatory glycine-serine rich (GS) domain adjacent to the kinase d

259 on of SMRT, with recent implication of short glycine-serine-isoleucine (GSI) containing motifs.

260 34 and 1p12 loci have been implicated in the glycine/serine metabolic pathway.

261 In roots only glycine showed significant changes across all transgenic

262 Here we showed that (1) Glycine significantly promoted angiogenesis both in vitr

263 ole-2-carboxamido)propanoic acid (AICP) as a glycine site agonist with unique GluN2-dependent differe

264 l-exposed rats, and this was reliant on NMDA glycine site availability.

265 istration of d-cycloserine (DCS), which is a glycine site NMDA receptor agonist, can enhance extincti

266 3 is a putative NMDA receptor modulator with glycine-site partial agonist properties that produces ra

267 pe (S54) and a susceptible genotype (S67) of Glycine soja, the wild progenitor of soybean, to underst

268 sed RNA-Seq data from seven Glycine subgenus Glycine species (three recently formed allotetraploids a

269 impede the anti-tumour effect of serine and glycine starvation.

270 first report on the structure of a hydrated glycine structure.

271 We used RNA-Seq data from seven Glycine subgenus Glycine species (three recently formed

272 Here we show that aza-glycine substitution enhances the stability of an argini

273 Based on targeted glycine substitutions in the Env fusion machinery, we de

274 xA revealed allosteric cooperativity for its glycine substrate, but not O2 This is the first CTQ- or

275 A large amount of CO2 was detected from glycine-sucrose model system under coffee roasting condi

276 indicate that both enzymes favor the lauroyl glycine synthesis over the peptide synthesis, but the im

277 GDH may also be the form of glycine that comes to Earth from extraterrestrial source

278 Glycine, the simplest amino acid, is also the most polym

279 studies second stage juveniles of Heterodera glycines, the soybean cyst nematode (SCN), quickly migra

280 Heterodera glycines, the soybean cyst nematode, delivers effector p

281 ransfer of an amidino group from arginine to glycine to form ornithine and guanidinoacetate.

282 fer from S-adenosyl-l-methionine (AdoMet) to glycine to form S-adenosyl-l-homocysteine and sarcosine.

283 Administration of glycine transport inhibitor ALX5407 in the vmPFC allevia

284 Intra-vmPFC administration of the glycine transport inhibitor ALX5407 prevented excessive

285 (2) Activation of glycine transporter 1(GlyT1) induced by VEGF led to an i

286 ess disabled-1 (Dab1) but lack expression of glycine transporter-1 (GlyT-1).

287 av3 channels; and 4) inhibition of the GLYT2 glycine transporter.

288 urrents dominate, blocking neuronal or glial glycine transporters enhances tonic glycinergic currents

289 king either, or both, the glial and neuronal glycine transporters markedly decreased PV+ IN excitabil

290 PCP effects were prevented by concurrent glycine treatment (p<0.01 vs PCP alone).

291 of proteins, in particular those containing glycine/tyrosine repeats that mediate formation of highe

292 show that this effect is rooted in defective glycine uptake in DLBCL cell lines, rendering them uniqu

293 We find enrichment of glycine, valine, and arginine as both individual amino a

294 ts of five structurally variant amino acids, glycine, valine, methionine, phenylalanine and cysteine

295 Diazo compounds derived from (p-methylphenyl)glycine were screened for the ability to esterify the gr

296 amplitudes of current responses to exogenous glycine were significantly reduced.

297 ure determination of a long unknown phase of glycine, which was first reported by Pyne and Suryanaray

298 ycine-activated NMDA receptors and that bind glycine with unusually high affinity.

299 n be stabilized by substitution of C-capping glycines with d-Ala.

300 cteriocin-like proteins CdzC and CdzD harbor glycine-zipper motifs, often found in amyloids, and CdzC