ライフサイエンスコーパス: guanosine triphosphate

1 hrough MyoII assembly via regulation of Rap1-guanosine triphosphate.

2 guanosine diphosphate-bound complex to eIF2-guanosine triphosphate.

3 ubunit to exchange guanosine diphosphate for guanosine triphosphate.

4 tated by binding to guanosine diphosphate or guanosine triphosphate.

5 osine monophosphate (AMP) in the presence of guanosine triphosphate.

6 eled, biotinylated, or cross-linker-modified guanosine triphosphates.

7 uanosine triphosphate (8-oxo-dGTP) and 8-oxo-guanosine triphosphate (8-oxo-GTP) from the nucleotide p

8 The loss of PI3K binding to Ras-guanosine triphosphate abolishes this PI3K activation, w

9 gnaling by converting active Ras is bound to guanosine triphosphate, activating Ras into inactive Ras

10 ll polarity in the context of elevated Cdc42-guanosine triphosphate activity, similar to nonmalignant

11 Guanosine triphosphate analog competition assays and mut

12 P, and ribo-GTP as well as the thymidine and guanosine triphosphate analogs ddTTP, ddGTP, and dITP.

13 the corneas were permeabilized to introduce guanosine triphosphate analogs into the corneal epitheli

14 an electrode containing the non-hydrolysable guanosine triphosphate analogue, guanosine 5'-thio-triph

15 App, and an associated depletion of cellular guanosine triphosphate and adenosine triphosphate pools,

16 30) catalyzes the reversible condensation of guanosine triphosphate and beta-l-fucose-1-phosphate to

17 the nucleotide-sugar GDP-beta-l-fucose from guanosine triphosphate and beta-l-fucose-1-phosphate.

18 G in a conformation intermediate between the guanosine triphosphate and guanosine diphosphate forms.

19 , and a new 1.45 A structure in complex with guanosine triphosphate and RNA cap analog.

20 e VPS15 pseudokinase domain binds tightly to guanosine triphosphate and stabilizes a web of interacti

21 entry site RNA, elongation factor eEF2, GTP (guanosine triphosphate), and sordarin, hygromycin B pref

22 s reaction, but also adenosine triphosphate, guanosine triphosphate, and cytidine triphosphate were s

23 Surprisingly, ADP, guanosine triphosphate, and the nonhydrolyzable ATP anal

24 Guanosine triphosphates are the prevalent oxidized nucle

25 = 0.0027], and mutations located within the guanosine triphosphate-ase region (odds ratio = 2.29, 95

26 utative Rap1 effector, colocalizes with Rap1-guanosine triphosphate at the leading edge and is requir

27 initiating NTP concentrations [adenosine or guanosine triphosphate (ATP or GTP), depending on the rr

28 (Gsalpha) of the stimulatory heterotrimeric guanosine triphosphate binding protein (G protein) Gs ac

29 The Vam2/6p complex then binds to Ypt7p, a guanosine triphosphate binding protein of the Rab family

30 ng or mutation of the SR-[Formula: see text] guanosine triphosphate binding site cause an N-glycosyla

31 Septins are conserved guanosine triphosphate-binding cytoskeletal proteins inv

32 A heterotrimeric guanosine triphosphate-binding protein (G protein)-coupl

33 utively activated stimulatory heterotrimeric guanosine triphosphate-binding protein alpha subunit (Ga

34 Mammalian nucleostemin (NS) is a nucleolar guanosine triphosphate-binding protein implicated in cel

35 ated protein kinases ERK-1 and ERK-2 and the guanosine triphosphate-binding protein p21ras were found

36 Activation of the guanosine triphosphate-binding protein Rac1, which was d

37 n activated nucleotide exchange on the small guanosine triphosphate-binding protein RhoA in seconds.

38 NRAS is a guanosine triphosphate-binding protein whose most well-c

39 A novel guanosine triphosphate-binding protein, chronic renal fa

40 The ras-like guanosine triphosphate-binding protein, rho, has recentl

41 predicted a protein with homology to several guanosine triphosphate-binding protein-coupled seven-tra

42 nd appeared to be mediated by heterotrimeric guanosine triphosphate-binding proteins (G proteins).

43 to identify alpha-subunits of heterotrimeric guanosine triphosphate-binding proteins in lens cell pop

44 The rho-subfamily of monomeric guanosine triphosphate-binding proteins is implicated in

45 We have shown previously that the guanosine triphosphate-binding proteins Rac and Rho link

46 Mammalian septins are a family of guanosine triphosphate-binding proteins thought to play

47 f at least four large families of regulatory guanosine triphosphate-binding proteins, including the A

48 septins, a conserved family of polymerizing guanosine triphosphate-binding proteins, localized to th

49 ion have been characterized, including small guanosine triphosphate-binding proteins, soluble N-ethyl

50 rotein is a member of the Ras superfamily of guanosine triphosphate-binding proteins.

51 a,l]P-induced hyperplasia, but the levels of guanosine triphosphate-bound (active) H-ras protein and

52 wnstream of Ras and cycle between the active guanosine triphosphate-bound and inactive guanosine diph

53 ec3 that are critical for its binding to the guanosine triphosphate-bound form of Cdc42.

54 ically interacting and coassembling with the guanosine triphosphate-bound form of Dnm1.

55 that EVI5 preferentially interacts with the guanosine triphosphate-bound form of Rab11, and in a GAP

56 process that depended on the presence of the guanosine triphosphate-bound form of the small guanosine

57 ed spatially and MglA only binds MreB in the guanosine triphosphate-bound form, the motility complexe

58 Guanosine triphosphate-bound Ran, but not guanosine diph

59 y been defined as an interaction surface for guanosine triphosphate-bound Ras, single amino acid subs

60 l-length Trio, led to increased abundance of guanosine triphosphate-bound RhoA (RhoA.GTP) in human ce

61 the small GTPases RalA and RalB to an active guanosine triphosphate-bound state.

62 uanosine monophosphate (cGMP) synthesis from guanosine triphosphate by RetGC1 in the presence of E6S/

63 -binding family of proteins that bind to the guanosine triphosphate cap at growing microtubule plus e

64 ap structures and found that an unmethylated guanosine triphosphate cap led to the lowest bias and hi

65 otein synthesis via assembly of the 7-methyl-guanosine triphosphate cap-dependent translation complex

66 properties, including the requirement for a guanosine triphosphate cofactor and the generation of lo

67 Additionally, we infer that the bound guanosine triphosphate cofactor interacts with the termi

68 yed a significantly increased stimulation by guanosine triphosphate compared with the E23/S1369 haplo

69 Crystal structures of a CTA1:ARF6-GTP (guanosine triphosphate) complex reveal that binding of t

70 ial cells (HBMECs) induces the expression of guanosine triphosphate cyclohydrolase (GCH1), the rate-l

71 ase, and no abnormality in the gene encoding guanosine triphosphate cyclohydrolase 1.

72 Guanosine triphosphate cyclohydrolase I (GTPCHI) is a cr

73 BH(4) and the activity of guanosine triphosphate cyclohydrolase I decreased in ihM

74 ATII increased vascular guanosine triphosphate cyclohydrolase I expression and b

75 nflammatory cell-dependent increase of iNOS, guanosine triphosphate cyclohydrolase I, tetrahydrobiopt

76 rate-limiting enzyme for BH(4) production is guanosine triphosphate cyclohydrolase-1 (GTPCH-1).

77 rahydrobiopterin (BH4) biosynthetic enzymes (guanosine triphosphate cyclohydrolase-1 and dihydrofolat

78 lease by either agonist, indicating that the guanosine triphosphate-dependent actions of VIP and carb

79 e-miRNAs directly and specifically, in a Ran guanosine triphosphate-dependent manner, but interacts o

80 ith and dissociate from donor membranes in a guanosine triphosphate-dependent manner, can also active

81 RNAs) are exported to the cytoplasm in a Ran.guanosine triphosphate-dependent manner.

82 gest that CRFG may be involved in regulating guanosine triphosphate-dependent nuclear events that are

83 c proteins including a guanosine diphosphate/guanosine triphosphate exchange factor for Sar1p have be

84 Type 2 nodes with protein Blt1p, guanosine triphosphate exchange factor Gef2p, and kinesi

85 te that Rab-activating guanosine diphosphate/guanosine triphosphate exchange factors (GEFs) display t

86 ), eukaryotic initiation factor (eIF) 2, and guanosine triphosphate form a ternary complex (TC).

87 (125)I-CCK-8 binding and [(35)S]guanosine triphosphate gamma S (GTP gamma S) binding stu

88 ver under both basal and agonist stimulated (guanosine triphosphate gamma S and forskolin) conditions

89 form of the Rho-associated protein (Rac) and guanosine triphosphate (GTP) (RacGTP) was immunolabeled

90 Ca2+ mobilization induced by guanosine triphosphate (GTP) analog guanosine 5'-0-(3 th

91 m extorquens MeaB bound to a nonhydrolyzable guanosine triphosphate (GTP) analog guanosine-5'-[(beta,

92 dels of the dynamin helical polymer bound to guanosine triphosphate (GTP) analogs define earlier stag

93 ger, cGAMP, is generated using intracellular guanosine triphosphate (GTP) and adenosine triphosphate

94 resence of 32P-alpha-adenosine triphosphate, guanosine triphosphate (GTP) and either carbachol or end

95 The interconversion of guanosine triphosphate (GTP) and guanosine diphosphate (

96 Guanosine triphosphate (GTP) and its non-hydrolyzable an

97 s have been hampered by the high affinity of guanosine triphosphate (GTP) and lack of allosteric regu

98 ps26/29/35 trimer specifically binds to Rab7-guanosine triphosphate (GTP) and localizes to Rab7-conta

99 ongation factor Tu (EF-Tu), which hydrolyzes guanosine triphosphate (GTP) and releases tRNA in respon

100 P-element transposase uses guanosine triphosphate (GTP) as a cofactor for transposi

101 Dynamin superfamily molecular motors use guanosine triphosphate (GTP) as a source of energy for m

102 ted by cell-surface receptors, which promote guanosine triphosphate (GTP) binding and dissociation of

103 nd maturing phagosomes, whereas inactivating guanosine triphosphate (GTP) binding blocks the dissocia

104 show that the causative mutation lies in the guanosine triphosphate (GTP) binding pocket of alpha-1 t

105 own as 1,3-beta-glucan synthase), requires a guanosine triphosphate (GTP) binding protein for activit

106 f CXCR4 and Rac-1 in lipid rafts facilitated guanosine triphosphate (GTP) binding/activation of Rac-1

107 guanosine triphosphatase Ran is loaded with guanosine triphosphate (GTP) by the chromatin-bound guan

108 seconds) and extensive (30% to 40% of total) guanosine triphosphate (GTP) charging of endogenous plat

109 tic chromosomes were surrounded by steep Ran guanosine triphosphate (GTP) concentration gradients, in

110 Guanosine triphosphate (GTP) cyclohydrolase I (GCH1) cat

111 of 6BH(4) de novo synthesis is controlled by guanosine triphosphate (GTP) cyclohydrolase I (GTPCHI) a

112 Vav, a guanosine diphosphate (GDP)-guanosine triphosphate (GTP) exchange factor for Rac tha

113 eotide-releasing factor C3G, which catalyzes guanosine triphosphate (GTP) exchange on Rap1.

114 naling), appears to function by facilitating guanosine triphosphate (GTP) exchange on the heterotrime

115 ation factor G (EF-G) hydrolyzes energy-rich guanosine triphosphate (GTP) for every amino acid incorp

116 anism is critical for spatial control of Ran-guanosine triphosphate (GTP) gradients that guide mitoti

117 Direct contacts between the RNA and CRM1/Ran-guanosine triphosphate (GTP) highlight the critical role

118 RAS proteins are conserved guanosine triphosphate (GTP) hydrolases (GTPases) that a

119 opsin (R*) and inactivation of transducin by guanosine triphosphate (GTP) hydrolysis are the leading

120 Finally, using guanosine triphosphate (GTP) hydrolysis assays, we demon

121 actions and by accelerating reactions of the guanosine triphosphate (GTP) hydrolysis cycle.

122 -bound, state of the oncoprotein and require guanosine triphosphate (GTP) hydrolysis for inhibition.

123 requires a functional Sar1 NH2 terminus and guanosine triphosphate (GTP) hydrolysis.

124 a defined catalytic residue for carrying out guanosine triphosphate (GTP) hydrolysis.

125 ,(7) a site that changes conformation during guanosine triphosphate (GTP) hydrolysis.(8) Consequently

126 n signaling 9 (RGS9)-catalyzed hydrolysis of guanosine triphosphate (GTP) in G protein-phosphodiester

127 embrane-associated rab3D significantly bound guanosine triphosphate (GTP) in overlay assays.

128 tyrosine kinase (RTK) ligands increase RhoA-guanosine triphosphate (GTP) in untransformed and transf

129 Addition of cytosol and the hydrolysis of guanosine triphosphate (GTP) induced caveolar fission.

130 Specifically, initiation with guanosine triphosphate (GTP) is required for efficient p

131 e ability of MLE to bind to ssRNA, ssDNA and guanosine triphosphate (GTP) less severely.

132 Contrastingly, guanosine triphosphate (GTP) levels always greatly excee

133 from Cdc42 and elevates intracellular Cdc42-guanosine triphosphate (GTP) levels in cells with inacti

134 nd controls rat sarcoma viral oncogene (RAS)-guanosine triphosphate (GTP) levels.

135 f rat hepatocytes with TDCA and TCA promoted guanosine triphosphate (GTP) loading of G(i1alpha), G(i2

136 binding to the integrin alphaIIbbeta3 and by guanosine triphosphate (GTP) loading of Galpha13.

137 s transiently transfected with empty vector, guanosine triphosphate (GTP) locked dominant active Rab4

138 es; beginning with the N(7) methylation of a guanosine triphosphate (GTP) molecule, followed by the c

139 ctly associates with the alpha-tubulin-bound guanosine triphosphate (GTP) molecule, impairing the int

140 n between Crm1 and Gcn4 requires neither Ran-guanosine triphosphate (GTP) nor the nuclear export sequ

141 les were attributed to the hydrolysis of the guanosine triphosphate (GTP) nucleotide bound to the bet

142 hosphorylation reduces intracellular GDP and guanosine triphosphate (GTP) pools and decreases mitogen

143 rtical motor complexes that depends on a Ran-guanosine triphosphate (GTP) signal [12], which is suffi

144 enase (IMPDH) is the rate-limiting enzyme in guanosine triphosphate (GTP) synthesis and assembles int

145 for guanosine diphosphate (GDP) relative to guanosine triphosphate (GTP) that is consistent with a 3

146 Here, we find that the binding of guanosine triphosphate (GTP) to one subunit inhibits the

147 Guanosine triphosphate (GTP) turnover, guanosine diphosp

148 expected allosteric activation of SOS by Ras-guanosine triphosphate (GTP) was conspicuously absent in

149 ent in vitro-selected RNA aptamers that bind guanosine triphosphate (GTP) with K(d)s ranging from 8 m

150 polymerization is coupled with hydrolysis of guanosine triphosphate (GTP) within beta-tubulin.

151 s), such as adenosine triphosphate (ATP) and guanosine triphosphate (GTP), are signaling and bioenerg

152 ne diphosphate ribosylation factor 1 (Arf-1)-guanosine triphosphate (GTP), cargo sorting signals, and

153 d the availability of ATP, which regenerates guanosine triphosphate (GTP), powers ribosomes, and prom

154 heir reduced intrinsic rate of hydrolysis of guanosine triphosphate (GTP), which results in their acc

155 ctivation by adenosine triphosphate (ATP) or guanosine triphosphate (GTP), with ATP favoring the inco

156 phagocytosis, we focused on the role of Rho-guanosine triphosphate (GTP)-ases.

157 olecules to the cleft between the N-terminal guanosine triphosphate (GTP)-binding and the C-terminal

158 and contains an adenosine triphosphate (ATP)/guanosine triphosphate (GTP)-binding motif that has homo

159 ning as a nucleotide exchange factor for the guanosine triphosphate (GTP)-binding protein Arf1p, is r

160 Here, the role of the small guanosine triphosphate (GTP)-binding protein CDC42Hs in

161 Raf-1 protein kinase is coupled to the small guanosine triphosphate (GTP)-binding protein Ras.

162 (MT) stabilization is regulated by the small guanosine triphosphate (GTP)-binding protein Rho and its

163 rm stress fibers and activation of the small guanosine triphosphate (GTP)-binding protein Rho.

164 diverse receptor subtypes includes the small guanosine triphosphate (GTP)-binding protein, p21ras.

165 We identified an HU-induced small guanosine triphosphate (GTP)-binding protein, secretion-

166 Guanosine triphosphate (GTP)-binding proteins are involv

167 in-treated cells showed translocation of ras guanosine triphosphate (GTP)-binding proteins from membr

168 The Rho subfamily of small guanosine triphosphate (GTP)-binding proteins, through t

169 CIITA contains motifs similar to guanosine triphosphate (GTP)-binding proteins.

170 he authors demonstrate that TBSV co-opts the guanosine triphosphate (GTP)-bound active form of the en

171 Ras proteins cycle between active, guanosine triphosphate (GTP)-bound and inactive, guanosi

172 ng podosome formation increased the level of guanosine triphosphate (GTP)-bound ARF1.

173 diphosphate (GDP)-bound form (RanGDP) and a guanosine triphosphate (GTP)-bound form (RanGTP) and pla

174 ant proteins, we show that Ypt31/32 in their guanosine triphosphate (GTP)-bound form interact directl

175 C2[E62K] displayed characteristics of active guanosine triphosphate (GTP)-bound RAC2 including enhanc

176 Quantification of activated guanosine triphosphate (GTP)-bound Ras protein and elect

177 n is initiated by the interaction of active, guanosine triphosphate (GTP)-bound Ras-related protein 1

178 0beta-Rab5 association maintains Rab5 in its guanosine triphosphate (GTP)-bound state and enhances th

179 leles encode proteins that accumulate in the guanosine triphosphate (GTP)-bound state.

180 Dominantly inherited guanosine triphosphate (GTP)-cyclohydrolase deficiency,

181 rnesyl-dependent, but neither palmitoyl- nor guanosine triphosphate (GTP)-dependent, fashion.

182 es are ultimately due to FtsZ's capacity for guanosine triphosphate (GTP)-dependent, reversible polym

183 activated and deactivated for assembly by a guanosine triphosphate (GTP)-driven reaction cycle, and

184 atrunculin A primed platelets for Ca(2+)- or guanosine triphosphate (GTP)-gamma-S-induced alpha-granu

185 aused lethality and perturbed binding to Ran guanosine triphosphate (GTP)-importin-beta, accumulation

186 aT) resides within a domain that undergoes a guanosine triphosphate (GTP)-induced conformational chan

187 , of VASH1/SVBP is much greater on mimics of guanosine triphosphate (GTP)-MTs than on guanosine dipho

188 nding protein-related protein 1L (ORP1L) are guanosine triphosphate (GTP)-Rab7 effectors that instiga

189 the density of elongated tubulin dimers like guanosine triphosphate (GTP)-tubulin.

190 lation of both substrates is opposed by Ypt7-guanosine triphosphate (GTP).

191 catalyzed by elongation factor G (EF-G) and guanosine triphosphate (GTP).

192 or without adenosine triphosphate (ATP) and guanosine triphosphate (GTP).

193 ed for ATP biosynthesis via ADSS in place of guanosine triphosphate (GTP).

194 embranes and the percentage of Rab7 bound to guanosine triphosphate (GTP).

195 dition, we demonstrated that OA induces Rho1 guanosine triphosphate (GTP)ase activation in the follic

196 GFP)-tagged dynamin, a large mechanochemical guanosine triphosphate (GTP)ase implicated in the libera

197 The mammalian guanosine triphosphate (GTP)ase-activating protein RanGA

198 on of force by phenylephrine, endothelin and guanosine triphosphate (GTP)gammaS, but did not inhibit

199 a unique complex in which hydrolyses of both guanosine triphosphates (GTP) are activated in a shared

200 hen Anillin is knocked down, active Rho (Rho-guanosine triphosphate [GTP]), F-actin, and myosin II ar

201 plicated in chromatin-stimulated nucleation, guanosine triphosphate(GTP)-bound Ran and its effector,

202 r 1 (ARF1) is proposed to be involved in the guanosine triphosphate- (GTP-) dependent, reversible ass

203 The growth and shortening of microtubules in guanosine triphosphate-(GTP-) mediated dynamic instabili

204 NF1 encodes neurofibromin, a Ras guanosine triphosphate (GTPase) activating protein that

205 This spatiotemporal regulation of Rab7 guanosine triphosphate/guanosine diphosphate cycling occ

206 The role of dynamin guanosine triphosphate hydrolase (GTPase) activity in co

207 tal organization and activity of Rho and Rac guanosine triphosphate hydrolase (GTPase) and Yes-associ

208 omain of transducin seems to move toward the guanosine triphosphate hydrolase (GTPase) domain.

209 biologic functions partly through the small guanosine triphosphate hydrolase (GTPase) Rac1 (ras-rela

210 ired for TLR-induced activation of the small guanosine triphosphate hydrolase (GTPase) Rac1 (ras-rela

211 Mutations in the small Rho-family guanosine triphosphate hydrolase RAC2, critical for acti

212 to the plasma membrane is regulated by small guanosine triphosphate hydrolases (GTPases) and is essen

213 sing number of assembly factors, among which guanosine triphosphate hydrolases (GTPases) are the most

214 ns associated with the Ras homolog family of guanosine triphosphate hydrolases (Rho GTPases), and cel

215 DOCK8 and DOCK11 activate CDC42, a Rho-guanosine triphosphate hydrolases involved in actin cyto

216 domain of PLC-beta3 subsequently accelerates guanosine triphosphate hydrolysis by Galpha(q), causing

217 ng of guanosine-5'-O-(3-thiotriphosphate) or guanosine triphosphate hydrolysis by the G protein.

218 egulates actin (dis-)assembly, and catalytic guanosine triphosphate hydrolysis is found in tubulin (d

219 ified as AS250) that directly stimulates the guanosine triphosphate hydrolysis of RalA.

220 th of immature myeloid cells by accelerating guanosine triphosphate hydrolysis on Ras proteins.

221 utes and remained stable for hours, required guanosine triphosphate hydrolysis, and recruited four GB

222 Dynamin-related protein 1 (Drp1) is a guanosine triphosphate-hydrolyzing mechanoenzyme importa

223 ore insertion required the generation of Ran guanosine triphosphate in the nuclear and cytoplasmic co

224 MP) in vitro from adenosine triphosphate and guanosine triphosphate in the presence of DNA but not RN

225 was performed using (35)S-GTPgammaS (GTP is guanosine triphosphate) in primate brains.

226 we show that FtsY-SecY complex formation is guanosine triphosphate independent but requires a phosph

227 ion of the rate constant for dissociation of guanosine triphosphate indicated that at pH 7.5 the rele

228 ite inhibited eukaryotic initiation factor 2-guanosine triphosphate-initiator methionyl transfer RNA

229 A Rag mutant that is constitutively bound to guanosine triphosphate interacted strongly with mTORC1,

230 Knockdown of Rap1-guanosine triphosphate-interacting adaptor molecule (RIA

231 cells have suggested a critical role of Rap1-guanosine triphosphate-interacting adaptor molecule (RIA

232 te cyclase (sGC) catalyzes the conversion of guanosine triphosphate into cyclic guanosine-3',5'-monop

233 served large GTPases (enzymes that hydrolyze guanosine triphosphate) involved in endocytosis and vesi

234 olves a complex rearrangement in which C8 of guanosine triphosphate is inserted between C2' and C3' o

235 alyzed exchange of guanosine diphosphate for guanosine triphosphate is proposed.

236 hate indicated that at pH 7.5 the release of guanosine triphosphate is rate-limiting.

237 small guanosine triphosphatases, binding to guanosine triphosphate leads to interaction with downstr

238 convenient synthetic routes to the oxidized guanosine triphosphate lesions spiroiminodihydantoin-2'-

239 evels correlating with heightened basal Rac1-guanosine triphosphate levels and increased reactivity.

240 ve Src alone was sufficient to stimulate Rit-guanosine triphosphate levels.

241 echanism of action may be related to altered guanosine triphosphate loading.

242 of hairpin proteins linked by hydrolysis of guanosine triphosphate nucleotides.

243 ng the exchange of guanosine diphosphate for guanosine triphosphate on Ras.

244 g, the enzyme exhibits strong preference for guanosine triphosphate over adenosine triphosphate as th

245 Mechanistically, we identified cellular guanosine triphosphate pool depletion as a key mediator

246 oteins normally using adenosine triphosphate/guanosine triphosphate, probably explains the disease.

247 BB, which are associated with CDC42, a small guanosine triphosphate protein linked to T-cell activati

248 m conversion of guanosine diphosphate-Rac to guanosine triphosphate-Rac following ITAM stimulation.

249 plasmic complex, an association regulated by guanosine triphosphate rac1 ([GTP]rac1) but not by [GTP]

250 s sustained by karyopherins (Kaps) and a Ran guanosine triphosphate (RanGTP) gradient that imports nu

251 d, and escort NLS-NCs through NPCs while Ran guanosine triphosphate (RanGTP) promotes their release f

252 or importinbeta1), to the cytoplasm in a Ran guanosine triphosphate (RanGTP)-mediated manner.

253 dle assembly by generating a gradient of Ran guanosine triphosphate (RanGTP).

254 n phosphoinositide-3 kinase (PI3K) and small guanosine triphosphate Ras signaling networks commonly d

255 rotein synthesis via tRNA aminoacylation and guanosine triphosphate regeneration.

256 ion of translation factor eIF-4E by 7-methyl guanosine triphosphate-Sepharose.

257 nteract with effector proteins when bound to guanosine triphosphate, stimulating downstream signaling

258 The NiRAN selectively binds guanosine triphosphate, strengthening proposals for the

259 t retain the intrinsic capacity to hydrolyze guanosine triphosphate, suggesting that the mechanism of

260 Resting and activated sGC enzyme converts guanosine triphosphate to an important second messenger

261 -A catalyzes the intracellular conversion of guanosine triphosphate to cGMP (cyclic 3',5'-guanosine m

262 1 is capable of catalyzing the conversion of guanosine triphosphate to cGMP.

263 the conformational change of EF-Tu from the guanosine triphosphate to guanine diphosphate conformati

264 by accelerating the hydrolysis of active Ras-guanosine triphosphate to inactive Ras-guanosine diphosp

265 Amino acids stimulate the binding of guanosine triphosphate to RagA and RagB but the factors

266 ency of spontaneous rescue unless patches of guanosine triphosphate tubulin are artificially embedded

267 at microtubules elongate by addition of bent guanosine triphosphate tubulin to the tips of curving pr