ライフサイエンスコーパス: adenine nucleotide

1 ude more slowly than excitations in a single adenine nucleotide.

2 release and subsequent dephosphorylation of adenine nucleotides.

3 or the binding of both Ca(2+)/calmodulin and adenine nucleotides.

4 it confers energy sensor function by binding adenine nucleotides.

5 imulated the reaction only in the absence of adenine nucleotides.

6 ondrial distress by regulating the levels of adenine nucleotides.

7 described so far with unique specificity for adenine nucleotides.

8 rmed by AK into a cytotoxic mixture of three adenine nucleotides.

9 104 functions at the physiological levels of adenine nucleotides.

10 suppress depurination during the addition of adenine nucleotides.

11 GRK2 largely reflects its lower affinity for adenine nucleotides.

12 odulated by a number of regulators including adenine nucleotides.

13 ines, the enzyme was unable to interact with adenine nucleotides.

14 ntracellular NAD, the metabolic precursor of adenine nucleotide 2nd messengers implicated in TRPM2 ga

15 ly through the actions of a related group of adenine nucleotide 2nd messengers.

16 N) ring conformation of the ribose moiety of adenine nucleotide 3',5'-bisphosphate antagonists of P2Y

17 igo(U) tail by reading the position of a key adenine nucleotide (A102) and pausing 5 uridine residues

18 acers strands comprised of phosphorothioated adenine nucleotides (A15*).

19 lass of herbicides and strongly suggest that adenine nucleotide accumulation is a metabolic trigger f

20 e binding assays show that SAM competes with adenine nucleotide activation of RyR2, and the effects o

21 Mitochondrial adenine nucleotide (AdN) content is regulated through th

22 h as phenylephrine show an increase in their adenine nucleotide (AdN) content, respiratory activity,

23 -BCL2 protein family, cyclophilin D, and the adenine nucleotide (ADP/ATP) translocators (ANTs).

24 The rapid loss of adenine nucleotides after PHx generates early stress sig

25 These studies demonstrate that 2-substituted adenine nucleotides allosterically inhibit basal and lig

26 Extracellular adenine nucleotides also serve as precursors for adenosi

27 he A5 bulge, which consists of five unpaired adenine nucleotides, alters the direction of the helical

28 (HPLC-ESI-MS/MS) to simultaneously quantify adenine nucleotides (AMP, ADP, and ATP), pyridine dinucl

29 Adenine nucleotide (AN) was measured by P nuclear magnet

30 P-site inhibitors are adenosine and adenine nucleotide analogues that inhibit adenylyl cycla

31 to a 2-A shift in the bound position of the adenine nucleotide and bringing it near the bicarbonate

32 he RYR1 was dependent on the presence of the adenine nucleotide and calmodulin and reflected a select

33 and NADPH (the reduced forms of nicotinamide adenine nucleotide and nicotinamide adenine dinucleotide

34 ts demonstrate transcription coordination of adenine nucleotide and nucleoside signaling at the vascu

35 the central pore protein ANT is regulated by adenine nucleotide and the activity of mitochondrial res

36 hydrolysis of the peptidoglycan cortex, but adenine nucleotides and 3-phosphoglycerate were not.

37 Lung tissue levels of adenine nucleotides and cAMP were measured by HPLC.

38 /3 complex cocrystallized with various bound adenine nucleotides and cations.

39 ding constants and specificity of RPAI-1 for adenine nucleotides and its functional significance.

40 In series 3, AICAR increased ileal tissue adenine nucleotides and metabolites during the shock per

41 se findings indicate that in the presence of adenine nucleotides and Mg2+,Ca2+-induced PTP in non-syn

42 Adenine nucleotides and nucleosides act on purinoceptors

43 ctivity; loosening of binding as a result of adenine nucleotides and phosphorylation may instigate mo

44 review the regulation of the KATP channel by adenine nucleotides and present an equilibrium allosteri

45 edly diminished capacity to phosphohydrolyze adenine nucleotides and regulate platelet reactivity, su

46 and substrate-binding domain) in response to adenine nucleotides and substrates.

47 The level of major adenine nucleotides and their related compounds was dete

48 llular metabolism to the membrane by sensing adenine nucleotides, and are thus instrumental in mediat

49 ative action on other cell types, adenosine, adenine nucleotides, and related analogs may also repres

50 arginase 1, asymmetric dimethylarginine, and adenine nucleotides are all products of hemolysis that p

51 also indicate that MMS-induced mutations at adenine nucleotides are significantly enriched on the no

52 Erythrocyte adenine nucleotides are the source of the purine precurs

53 tral to the mechanism by which adenosine and adenine nucleotides arrest proliferation in these cells.

54 ity, suggesting a failure to maintain matrix adenine nucleotides as a cause for premature delayed Ca(

55 P-binding site on Kir6.2, we used a range of adenine nucleotides as molecular measuring sticks to map

56 Individuals who were homozygous for an adenine nucleotide at position 519 of the gene for the i

57 tagenized a leucine residue that contacts an adenine nucleotide at the site of cleavage.

58 eased sensitivity to 2-thioether-substituted adenine nucleotides at the canine receptor.

59 The adenine nucleotides ATP and cAMP block the channel with

60 phy (HPLC) determination of tissue levels of adenine nucleotides (ATP, ADP, and AMP) and their interr

61 Adenine nucleotides bind to the CBS domains in CBS-PPase

62 As in other adenine nucleotide binding cassette (ABC) proteins the n

63 form include quinone (capsaicin), copper and adenine nucleotide binding domains, and two cysteines es

64 cyte glucose transport protein (GluT1) is an adenine nucleotide binding protein.

65 within the Mdm2 RING, we mapped the specific adenine nucleotide binding region of Mdm2 to residues 42

66 d whether SAM exerts its effects through the adenine nucleotide binding sites on the RyR2 channel.

67 e determined the functional relevance of two adenine nucleotide binding sites through site-directed m

68 models, both subunits are predicted to have adenine nucleotide binding sites.

69 uctures from eukaryotic Pfk revealed several adenine nucleotide binding sites.

70 mainly used AMP-PNP to focus on the role of adenine nucleotide binding to retGC.

71 ry subunit regulates phosphorylation through adenine nucleotide binding.

72 egral membrane glycoprotein, a member of the adenine nucleotide-binding cassette (ABC) transporter fa

73 quinone-binding domain of complex I, flavin adenine nucleotide-binding moiety and quinone-binding po

74 ar adenosine and hydrolysis of extracellular adenine nucleotides by CD73.

75 sed-phase HPLC method by which separation of adenine nucleotides can be performed rapidly, allowing m

76 te that a bacterial actin, when activated by adenine nucleotides, can modify the length distribution

77 wo motors, a phosphate carrier (PIC), and an adenine nucleotide carrier (ANC).

78 Levels of adenine nucleotides change rapidly after reperfusion and

79 ulated reperfusion model, a similar trend in adenine nucleotide changes was observed.

80 inct supercoiling reactions depending on the adenine nucleotide cofactor that is present in the react

81 synthetase from Thermatoga maritima and the adenine nucleotide complexes of the synthetase from Sacc

82 osphotransferases that regulate the cellular adenine nucleotide composition and play a critical role

83 Adenine nucleotide concentrations were derived at variou

84 e 4B (PDE4B) without affecting intracellular adenine nucleotide concentrations.

85 receptor antagonists of acyclic analogues of adenine nucleotides, containing two phosphate groups on

86 We reported that acyclic analogues of adenine nucleotides, containing two phosphate groups on

87 on 1 (ERO1) is a conserved eukaryotic flavin adenine nucleotide-containing enzyme that promotes disul

88 uctions in the concentrations of cytoplasmic adenine nucleotide, creatine, and phosphate pools that o

89 Respiratory substrates and adenine nucleotides cross the mitochondrial outer membra

90 shes that exploits the intrinsic affinity of adenine nucleotides (dA) for gold surfaces.

91 advantage of the preferential adsorption of adenine nucleotides (dA) on gold, as previously demonstr

92 obe DNA with a lateral spacer, a strand of k adenine nucleotides, (dA)(k).

93 ide DNA probe sequence that has additional m adenine nucleotides, (dA)(m), at the 5' end.

94 i's disease erythrocytes exhibit accelerated adenine nucleotide depletion in response to an increase

95 e changes in cell energy status that control adenine nucleotide distribution.

96 ng different sensitivity to block by various adenine nucleotides (EC(50) of 0.79 microm for [ATP](i),

97 function of this activity, we have examined adenine nucleotide effects on interactions of Escherichi

98 Selective enzyme cleavage required bound adenine nucleotide, either ATP or ADP, in the presence o

99 the PCA via a novel mechanism that involves adenine nucleotide-evoked adenosine release and the subs

100 s presumably associated with a modulation of adenine nucleotide exchange between mitochondria and cyt

101 tic inhibitors of mitochondrial AACs blocked adenine nucleotide exchange by the Neocallimastix protei

102 ation disrupts the gene Sil1 that encodes an adenine nucleotide exchange factor of BiP, a crucial ER

103 SIL1 is an adenine nucleotide exchange factor of the essential ER l

104 delivery, metabolic inhibition, the rate of adenine nucleotide exchange, and Ca(2+).

105 a small subset of these processes requiring adenine nucleotide exchange.

106 Here, we show that guanine and adenine nucleotides exert positive and negative effects,

107 of islet loss in culture, quantification of adenine nucleotides, flow cytometric measurement of viab

108 The mechanism by which ubiquitous adenine nucleotide-gated K(IR)6.0(4)/SUR(4) channels lin

109 at diffusional anisotropy may lead to modest adenine nucleotide gradients in the myoplasm under physi

110 ortant autocrine/paracrine functions for the adenine nucleotides have been proposed in several tissue

111 TP versus ADP) thereby dominantly disturbing adenine nucleotide homeostasis in mitochondria.

112 mmalian ciliary and flagellar beating via an adenine nucleotide homeostasis module.

113 ssue concentrations of creatine phosphate or adenine nucleotides; however, it did correlate with incr

114 e nucleotides in the stem and an unusual syn adenine nucleotide in the loop.

115 nzyme that contributes to the homeostasis of adenine nucleotides in eukaryotic and prokaryotic cells.

116 Substitution of conserved adenine nucleotides in mgtM abolished the response to AT

117 idely recognized activation of the enzyme by adenine nucleotides in plants is mediated in this manner

118 rain estimates of diffusional anisotropy for adenine nucleotides in the cardiac myofibril, using homo

119 ous enzyme that regulates the homeostasis of adenine nucleotides in the cell.

120 of inflammation, multiple cell types release adenine nucleotides in the form of ATP, ADP, 5'-AMP, and

121 ility (hypoxia), multiple cell types release adenine nucleotides in the form of ATP, ADP, and AMP.

122 efined structure including unpaired, stacked adenine nucleotides in the stem and an unusual syn adeni

123 sults in complete loss of interrupting (LOI) adenine nucleotides in this region [(CAG)n-CAG-CAG].

124 ious studies demonstrated that 2-substituted adenine nucleotides, including 2-methylthioATP (2MeSATP)

125 Adenine nucleotides induce danger signals in T cells via

126 biochemical techniques, we demonstrate that adenine nucleotides induce large asymmetric conformation

127 Similarly, 2-substituted adenine nucleotides inhibited those enzymes when Mn2+, w

128 he kinetic and thermodynamic consequences of adenine nucleotide interaction with the low-affinity and

129 (AK2), a mitochondrial enzyme that regulates adenine nucleotide interconversion within the intermembr

130 ular adenosine involves phosphohydrolysis of adenine nucleotide intermediates, and is regulated by th

131 Cells release adenine nucleotides into the extracellular space, where

132 Mitochondrial ATP-Mg/Pi carriers import adenine nucleotides into the mitochondrial matrix and ex

133 ously reported and that a preincubation with adenine nucleotide is essential for the large activation

134 the suggestion that allosteric inhibition by adenine nucleotides is a general characteristic of the f

135 The specificity of the catalytic site for adenine nucleotides is established by specific hydrogen

136 assembly and outer membrane permeability for adenine nucleotides leading to energy deficit, 2) excess

137 at mechanisms that do not involve changes in adenine nucleotide levels can activate AMPK.

138 e extraction procedure given that changes in adenine nucleotide levels take place very quickly when A

139 annels) are designed as exquisite sensors of adenine nucleotide levels that signal changes in glucose

140 The hepatic energy state, defined by adenine nucleotide levels, couples metabolic pathways wi

141 embrane-trafficking machinery, and increased adenine nucleotide levels.

142 e tissue's energy state were determined from adenine nucleotide levels.

143 homo-dimers, but the translocation pore for adenine nucleotides lies in the center of the molecule a

144 Consistent with the effects on adenine nucleotides, maximal mitochondrial respiration w

145 ed that conformational changes, modulated by adenine nucleotides, mediate the interactions of MutL al

146 hypoxia signaling at several steps along the adenine nucleotide metabolism and adenosine receptor sig

147 e hypothesized that adenosine production via adenine nucleotide metabolism at the vascular surface tr

148 hat extracellular adenosine produced through adenine nucleotide metabolism during hypoxia is a potent

149 uggest that T cells express multiple NAD and adenine nucleotide-metabolizing activities that together

150 ractions between Kir6.2 positive charges and adenine nucleotide negative phosphate groups.

151 nd stored at 4 degrees C for 10days prior to adenine nucleotide (nmol/gw/w) profile determination.

152 dration; i.e., percentage solids) and sputum adenine nucleotide/nucleoside concentrations.

153 enzyme in complex with CoA and show that the adenine nucleotide of this cofactor is bound in a distin

154 study examined the effects of 2-substituted adenine nucleotides on crude and purified sGC.

155 e (ecto-AK) contributes to the metabolism of adenine nucleotides on human airway epithelial surfaces

156 We examined the effects of adenine nucleotides on K(ATP) channels containing wild-t

157 ynthesis DNA polymerase that readily inserts adenine nucleotides opposite photoproducts involving thy

158 ss of UV-induced pyrimidine dimers inserting adenine nucleotides opposite these lesions.

159 a cancer-associated ENOX (tNOX or ENOX2) as adenine nucleotide or copper binding along with essentia

160 Adenosine may be formed intracellularly from adenine nucleotides or extracellularly through sequentia

161 diseases, where multiple cell types release adenine-nucleotides (particularly adenosine triphosphate

162 that adenosine, formed extracellularly from adenine nucleotides, plays a major role in the pathogene

163 point corresponds to reductions in the total adenine nucleotide pool (TAN) of approximately 30%, corr

164 anges in high-energy phosphate and the total adenine nucleotide pool are considered to be the critica

165 e latter two comprising >90% of the released adenine nucleotide pool as cells transitioned from the e

166 DF (150 nm) to produce growth inhibition and adenine nucleotide pool expansion comparable to that obs

167 chanisms that function to maintain the total adenine nucleotide pool in mature erythrocytes, which ar

168 -regulated to control the size of the matrix adenine nucleotide pool in response to cellular energeti

169 Adenylate kinase 2 (AK2), which balances adenine nucleotide pool, is a multi-functional protein.

170 Central to remodeling are changes in the adenine nucleotide pool.

171 g and loss of membrane ion gradients and the adenine nucleotide pool; (3) repair of damaged cell orga

172 in intracellular coenzyme A (CoA) esters and adenine nucleotide pools in microbial cells is described

173 t are triggered by Ca2+ and are modulated by adenine nucleotides, possibly from the matrix side of th

174 unctional ligands of GroEL such as Mg(2+) or adenine nucleotides produced differences in the observed

175 /ADP ratio, indicative of an energy-depleted adenine nucleotide profile.

176 Ischemia-induced changes in metabolism (adenine nucleotides, purines, lactate, and amino acids)

177 These include calcium, serotonin, adenine nucleotides, pyrophosphate, and polyphosphate, w

178 Indeed, total adenine nucleotide release, like UDP-glucose release, di

179 blood, is generated by phosphohydrolysis of adenine nucleotides released from cells and catabolized

180 ar space or it may form extracellularly from adenine nucleotides released from injured cells.

181 ssing chamber studies of chloride secretion, adenine nucleotides released from the host by EPEC also

182 and hydropathy, and examined the effects on adenine nucleotide sensitivity in the absence and presen

183 nnel by Ca2+ and the block of the channel by adenine nucleotides show a mild voltage dependence, whic

184 a-ATP)) and exhibits sensitivity to block by adenine nucleotides similar to that of sulfonylurea rece

185 sparks may reflect reduced occupancy of the adenine nucleotide site on the SR Ca(2+) channel.

186 We determined the expression and function of adenine nucleotide-specific P2Y receptors on cord blood-

187 s with competing reactions that interconvert adenine nucleotides such as in permeabilized cells that

188 onin, or maintain outer membrane exchange of adenine nucleotide, such as Bcl-x(L), restored ADP-depen

189 In the airways, adenine nucleotides support a complex signaling network

190 The molecular mechanism involved in this adenine nucleotide switch is unclear.

191 Total adenine nucleotide (TAN) levels correlated with Kfc in n

192 AMP), resulting in a marked decline in total adenine nucleotides (TAN).

193 Total adenine nucleotides tended to be highest in the phenylep

194 All of the adenine nucleotides tested bound to Lon on the order of

195 various phosphorylated or non-phosphorylated adenine nucleotides that may even be better agonists tha

196 nse granule components such as serotonin and adenine nucleotides though near-normal numbers of dense

197 e of cellular activities; many of these bind adenine nucleotides through a conserved motif that is al

198 The diffusion of adenine nucleotides through the myofilament lattice has

199 alyze the extracellular dephosphorylation of adenine nucleotides to adenosine.

200 The ability of adenine nucleotides to prevent reaction of the introduce

201 It is inhibited by the binding of adenine nucleotides to subunit Kir6.2, which closes the

202 DNA was sequence independent, and binding of adenine nucleotides to the protein induced the formation

203 its of ATP synthase and the liver isoform of adenine nucleotide transferase.

204 ctivity was insensitive to inhibitors of the adenine nucleotide translocase (ANT) and of the voltage-

205 een mitochondrial creatine kinase (MtCK) and adenine nucleotide translocase (ANT) can play an importa

206 Adenine nucleotide translocase (Ant) catalyzes ADP/ATP e

207 Adenine nucleotide translocase (ANT) exchanges ADP/ATP t

208 Members of the adenine nucleotide translocase (ANT) family exchange ADP

209 nding puzzle is that in permeabilized cells, adenine nucleotide translocase (ANT) is less accessible

210 Adenine nucleotide translocase (Ant) is the most abundan

211 oside and bongkrekic acid, inhibitors of the adenine nucleotide translocase (ANT) that lock the trans

212 mely voltage-dependent anion channel (VDAC), adenine nucleotide translocase (ANT), and hexokinase II

213 was attenuated by knockdown or inhibition of adenine nucleotide translocase (ANT), cyclophilin D (Cyp

214 trometry analysis identified this protein as adenine nucleotide translocase (ANT), represented by two

215 or alpha induced RIP-dependent inhibition of adenine nucleotide translocase (ANT)-conducted transport

216 ibits all ADP-ATP-using reactions except the adenine nucleotide translocase (ANT)-mediated mitochondr

217 by carboxyatractyloside, an inhibitor of the adenine nucleotide translocase (ANT).

218 oupling proteins UCP1, UCP2 and UCP3 and the adenine nucleotide translocase (ANT).

219 d increased proton transport activity of the adenine nucleotide translocase (dependent on fatty acids

220 hondria is known to be cardioprotective, and adenine nucleotide translocase 1 (ANT1) is a key mediato

221 Adenine nucleotide translocase 1 (Ant1) is a mitochondri

222 ondria, to interact with and dephosphorylate adenine nucleotide translocase 1 (ANT1), a central molec

223 nd several mitochondrial proteins, including adenine nucleotide translocase 1 (ANT1), were more oxidi

224 olve saturated fatty acid stimulation of the adenine nucleotide translocase 2 (ANT2), an inner mitoch

225 Proteomics screening identified adenine nucleotide translocase 3 (ANT3) as a previously

226 increased oxygen consumption independent of adenine nucleotide translocase and uncoupling proteins,

227 Suppression of adenine nucleotide translocase content may be a key fact

228 cle depended on electron transport chain and adenine nucleotide translocase functionality, but it was

229 This study provides evidence for a role of adenine nucleotide translocase in the mechanism underlyi

230 The adenine nucleotide translocase inhibitor bongkrekic acid

231 ation, increased levels of the mitochondrial adenine nucleotide translocase stress-sensitive B (SesB)

232 the voltage-dependent anion channel and the adenine nucleotide translocase were similar in the two m

233 n pore (ie, voltage-dependent anion channel, adenine nucleotide translocase, cyclophilin D).

234 ction of both the F(1)F(O)-ATPase and of the adenine nucleotide translocase, which delivers nucleotid

235 ation/knockdown-induced dysregulation in the adenine nucleotide translocase, which results in a slowe

236 els of cytochrome oxidase, cytochrome c, and adenine nucleotide translocase-1.

237 ds, these mitochondria also showed a greater adenine nucleotide translocase-catalysed proton conducta

238 This was due to an increase in the amount of adenine nucleotide translocase.

239 source, ATP depletion, or inhibition of the adenine nucleotide translocase.

240 The ADP/ATP translocator (or adenine nucleotide translocase; ANT) is thought to play

241 The adenine nucleotide translocases (Ant) facilitate the tra

242 rt (alpha-cyano-4-hydroxycinnamate, 0.5 mM), adenine nucleotide translocation (atractyloside, 0.3 mM)

243 The adenine nucleotide translocator (ANT) and F1-ATPase resp

244 Unexpectedly, we find that the adenine nucleotide translocator (ANT) complex is require

245 We have identified the adenine nucleotide translocator (ANT) isoforms ANT1 and

246 d by the MPT because it was blocked with the adenine nucleotide translocator (ANT) ligand bongkrekic

247 e for cytosolic ADP(3-) via the electrogenic adenine nucleotide translocator (ANT) located in the mit

248 The authors hypothesized that mitochondrial adenine nucleotide translocator (ANT) reverses its activ

249 the voltage-dependent anion channel (VDAC), adenine nucleotide translocator (ANT), and cyclophilin D

250 ays, we demonstrate that CyPD binding to the adenine nucleotide translocator (ANT), which is consider

251 parallel with accumulation of mitochondrial adenine nucleotide translocator (ANT), which provides a

252 e c oxidase subunit I (COI)] or nuclear DNA [adenine nucleotide translocator 1 (ANT1) and nicotinamid

253 Mutations in the heart and muscle isoform of adenine nucleotide translocator 1 (ANT1) are associated

254 n heavy chain-alpha, cardiac troponin-I, and adenine nucleotide translocator 1 (ANT1), have been iden

255 led inwardly rectifying K channel 2 (GIRK2), adenine nucleotide translocator 2 (ANT-2) and the growth

256 oteins and mPTP-regulatory elements, such as adenine nucleotide translocator and cyclophilin D (possi

257 e mechanisms of such degradation involve the adenine nucleotide translocator and mitochondrial permea

258 ealed GSH-adducted peptides corresponding to adenine nucleotide translocator and the alpha-subunit of

259 t by interacting with mitochondrial proteins adenine nucleotide translocator and voltage-dependent an

260 proach to "state 4" could be mimicked by the adenine nucleotide translocator inhibitor bongkrekic aci

261 rmed in mice in which the heart-muscle-brain adenine nucleotide translocator isoform 1 (ANT1) was ina

262 ltage-dependent anion channel protein or the adenine nucleotide translocator protein could not be dem

263 ucleotides were abolished by blockade of the adenine nucleotide translocator with carboxyatractylosid

264 d downstream (e.g., the respiratory chain or adenine nucleotide translocator).

265 The mPT pore is thought to consist of the adenine nucleotide translocator, a voltage-dependent ani

266 ssette protein 1 (mABC1), phosphate carrier, adenine nucleotide translocator, and ATP synthase] assoc

267 ipitating proteins (succinate dehydrogenase, adenine nucleotide translocator, ATP synthase, inorganic

268 t contain voltage-dependent anion channel or adenine nucleotide translocator, were reconstituted into

269 Ten homozygous null (adenine nucleotide translocator-1(-/-)) patients monitor

270 ch codes for the heart-muscle isoform of the adenine nucleotide translocator-1.

271 the voltage-dependent anion channel, or the adenine nucleotide translocator.

272 This assay requires adenine nucleotide transport across the outer but not th

273 Both proteomics and adenine nucleotide transport data suggest that GSK regul

274 The adenine nucleotide transporter (ANT) is implicated in mi

275 oltage-dependent anion channel (VDAC) and/or adenine nucleotide transporter (ANT) or to inhibition of

276 microsequencing identified the protein as an adenine nucleotide transporter (ANT).

277 The adenine nucleotide transporter 1 gene (ANT1) encodes an

278 serve a down-regulation of the mitochondrial adenine nucleotide transporter and suggest that this may

279 mitochondrial permeability transition pore, adenine nucleotide transporter and voltage-dependent ani

280 This protein and the adenine nucleotide transporter move ATP, newly synthesiz

281 lophilin D, voltage-dependent anion channel, adenine nucleotide transporter, and ATP synthase.

282 voltage-dependent anion channel, and/or the adenine nucleotide transporter, or by direct inhibition

283 Binding of an adenine nucleotide triggered release of Hep1 and folding

284 inhibitors or by SCaMC-3 activity promoting adenine nucleotide uptake into mitochondria.

285 A rapid shift toward higher energy adenine nucleotides was observed following clinical repe

286 The effects of adenine nucleotides were abolished by blockade of the ad

287 he MMC/PTP, and were inhibited by Mg(2+) and adenine nucleotides, which also inhibit the PTP.

288 ased mucosal perfusion, and increased tissue adenine nucleotides, which is consistent with preserved

289 ters a large part of the plastidial pools of adenine nucleotides, which limits photophosphorylation,

290 diated vesicle priming could be regulated by adenine nucleotides, which might provide a link between

291 residues had small effects on inhibition by adenine nucleotide, while substitution with neutral or n

292 y, TIP48 formed oligomers in the presence of adenine nucleotides, whilst TIP49 did not.

293 The interaction of adenine nucleotides with glycyl-tRNA synthetase was exam

294 Interaction of adenine nucleotides with Kir6.2 positively charged amino

295 constrained (N)-methanocarba modification of adenine nucleotides with other functionalities known to

296 ibition is mediated by direct interaction of adenine nucleotides with sGC, likely at the catalytic do

297 ly member with high sequence homology, binds adenine nucleotides with similar affinity and specificit

298 bolism, altering regulation of extracellular adenine nucleotides, with a resultant protective influen

299 om dephosphorylation was highly specific for adenine nucleotides, with ADP being the most effective l

300 dent changes in the intracellular pattern of adenine nucleotides, with AMP release dominating in the