ライフサイエンスコーパス: GTP-binding protein

1 on the surface of proteins, but it is also a GTP binding protein.

2 known regulators or target/effectors of this GTP binding protein.

3 d alpha-subunit (Galpha) of a heterotrimeric GTP binding protein.

4 ASA1), a negative regulator of the Ras small GTP-binding protein.

5 t which signaling events regulate this small GTP-binding protein.

6 kinase Syk and those that operate through a GTP-binding protein.

7 ng the transcriptional activation of a small GTP-binding protein.

8 E. coli Era is an essential GTP-binding protein.

9 represents a novel fold for an effector of a GTP-binding protein.

10 transduction initiated through the Ras small GTP-binding protein.

11 accelerates nucleotide exchange of eEF1A2, a GTP-binding protein.

12 cts as a negative regulator of the Ras small GTP-binding protein.

13 d revealing a distinct mode of control for a GTP-binding protein.

14 0(-11)), a variant of ARL15, which encodes a GTP-binding protein.

15 Gem/Kir) subfamily of the Ras superfamily of GTP binding proteins.

16 s of the Rab subfamily of small Ras-like GDP/GTP binding proteins.

17 y conserved motif characteristic of ATP- and GTP-binding proteins.

18 eb is a unique member of the Ras superfamily GTP-binding proteins.

19 he RAS superfamily of small-molecular-weight GTP-binding proteins.

20 ge of GDP for GTP on the Arf family of small GTP-binding proteins.

21 ns comprise a family of 13 genes that encode GTP-binding proteins.

22 ated RGK (Rad, Gem, and Kir) family of small GTP-binding proteins.

23 (GEF) for the Arf family of eukaryotic small GTP-binding proteins.

24 d for the prenylation and normal function of GTP-binding proteins.

25 spite lacking structural homology with other GTP-binding proteins.

26 ange factors for the Rho/Rac family of small GTP-binding proteins.

27 Mgm1 is a member of the dynamin family of GTP-binding proteins.

28 s, a process that has a requirement for some GTP-binding proteins.

29 proper function and activation of the small GTP-binding proteins.

30 o the plasma membrane, in concert with small GTP-binding proteins.

31 inositol phosphates, ubiquitin, cyclin, and GTP-binding proteins.

32 oduct (TTN5) is related to the ARL2 class of GTP-binding proteins.

33 c42 and not via PTX-sensitive heterotrimeric GTP-binding proteins.

34 e Akt did not increase activity of other Rho GTP-binding proteins.

35 inates between K-Ras G12C and other cellular GTP-binding proteins.

36 g between the V-ATPase, cytohesin-2, and Arf GTP-binding proteins.

37 is a member of the RAS superfamily of small GTP-binding proteins.

38 The 136-SNP region contained the sheep ATP/GTP-binding protein 1 (AGTPBP1) gene.

39 the newly identified small GTPase, Nucleolar GTP-binding protein 1 (NOG1), functions for plant immuni

40 ations in GTPBP3, encoding the mitochondrial GTP-binding protein 3.

41 osome Ag-1-positive endosomes to RAS-related GTP-binding protein 7 (Rab7)-associated late endosomes c

42 mplex and with the small GTPases Ras-related GTP-binding protein A (RagA) and RagC.

43 Here we show that the Ras-related Rin GTP-binding protein, a GTPase that is expressed predomin

44 ction from osmotic stress, a stress response GTP-binding protein, a response regulator, a sensor kina

45 Rho small GTP-binding proteins activate mammalian diaphanous-relat

46 This study shows that the small GTP-binding protein ADP-ribosylation factor 6 (ARF6) is

47 n-independent pathway regulated by the small GTP-binding protein ADP-ribosylation factor 6 (Arf6).

48 Here, we identify a small GTP-binding protein, ADP-ribosylation factor-like 8b (Ar

49 This GTP-binding protein affects dopamine-mediated signaling

50 n assays, to characterize comprehensively (S)GTP-binding proteins along with the specific binding sit

51 n between the SRP guanosine-5'-triphosphate (GTP) binding protein and its receptor FtsY in classical

52 Era is a small GTP-binding protein and essential for cell growth in Esc

53 Arabidopsis NSN1 encodes a nucleolar GTP-binding protein and is required for flower developme

54 probes facilitated the identification of 100 GTP-binding proteins and 206 kinases with the use of low

55 A into target cells to inactivate Rho family GTP-binding proteins and block immune responses.

56 d the role of several Golgi-associated small GTP-binding proteins and found that Rab43 differentially

57 is a member of the Ras superfamily of small GTP-binding proteins and has 2 isoforms, Rap1a and Rap1b

58 is a member of the Ras superfamily of small GTP-binding proteins and is localized on pancreatic zymo

59 The Ras family of small GTP-binding proteins and their downstream effectors are

60 Ca(2+) fluxes, and ending with host cell Rab GTP-binding proteins and their effectors.

61 ted current by noradrenaline was mediated by GTP binding proteins, and was highly dependent on calciu

62 eins, C. maxima phloem protein 16, C. maxima GTP-binding protein, and C. maxima phosphoinositide-spec

63 are thought to represent a distinct class of GTP-binding proteins, and conformational switching in ga

64 ssion of transforming growth factor beta and GTP-binding proteins, and generation of reactive oxygen

65 probes are important tools for the study of GTP-binding proteins, and proteomic profiling is a power

66 s (including cytoskeletal proteins, kinases, GTP-binding proteins, and their effectors) bind lipids t

67 The Rho family of GTP binding proteins are important upstream mediators of

68 The Obg subfamily of bacterial GTP-binding proteins are biochemically distinct from Ras

69 Small GTP-binding proteins are key regulators of these process

70 Heterotrimeric GTP-binding proteins are membrane-associated molecular s

71 Septins, a family of GTP-binding proteins, are key regulators of spatial comp

72 The small GTP binding protein ARF has been implicated in budding c

73 tion in membrane traffic by inactivating the GTP binding protein Arf1.

74 RIBEYE competes with the GTP-binding protein Arf1 for binding to ArfGAP3.

75 omplex that is recruited to membranes by the GTP-binding protein Arf1.

76 hange factor for the guanosine triphosphate (GTP)-binding protein Arf1p, is required to recruit Chs5p

77 ary for transport to the cilia including the GTP-binding protein Arf4 and the two G proteins of the R

78 Several studies have implicated the small GTP-binding protein ARF6 in tumor cell invasion, althoug

79 The small GTP-binding protein Arf6 is known to be an important reg

80 we show that cellular depletion of the small GTP-binding protein ARF6 promotes the formation of inver

81 ine nucleotide exchange factor for the small GTP-binding protein Arf6 that localizes to the postsynap

82 tivating protein in hair cells for the small GTP-binding protein ARF6, known to participate in actin

83 g axis involving sustained activation of the GTP-binding protein, ARF6, that provokes dramatic change

84 iRNA knockdown experiments, we find that the GTP-binding protein, Arfrp1, and the clathrin adaptor co

85 hese 93 were genes encoding: 1) the Ras-like GTP-binding proteins Arl1p and Arl3p, 2) actin-related p

86 The small GTP-binding proteins Arl2 and Arl3, which are close homo

87 functional profiles establish the Rho family GTP-binding proteins as integral to the hallmark invasiv

88 Rab3A, a small GTP-binding protein attached to synaptic vesicles, has b

89 In another case, the GTP-binding protein bound to an effector is the substrat

90 e facilitated identification of a variety of GTP-binding proteins by mass spectrometry, such as small

91 The betagamma subunit complex of large GTP-binding proteins, by interacting with PAK, stimulate

92 activation for PI3K-C2alpha and that a small GTP-binding protein can activate a class II PI3K isoform

93 The effectors of monomeric GTP-binding proteins can influence interactions with GTP

94 cate that members of the Rho family of small GTP-binding proteins can provoke the concomitant stimula

95 r (EGF) promotes the activation of the small GTP-binding protein Cdc42, as well as its phosphorylatio

96 In this report, the role of the Rho family GTP-binding protein Cdc42, in the mastoparan stimulus-se

97 e coat protein, coatomer, and the regulatory GTP-binding protein Cdc42.

98 that facilitate the activation of the small GTP-binding proteins Cdc42, Rac, and Rho.

99 namic distributions of a family of nucleolar GTP-binding proteins, consisting of nucleostemin (NS), g

100 Ras-related small GTP-binding proteins control a wide range of cellular pr

101 In every organism, GTP-binding proteins control many aspects of cell signal

102 on of beta-adrenergic receptors, classically GTP-binding proteins coupled receptors, influence the mi

103 otective effect of stimulating an astrocytic GTP-binding protein-coupled receptor (P2Y1Rs) following

104 ticulum Ca(2+) handling, IP3 production, and GTP-binding protein-coupled receptor signaling was devel

105 lso known as PI3Kgamma) links heterotrimeric GTP-binding protein-coupled receptors to these pathways.

106 One of the new proteins is a novel GTP binding protein, DAP3, that has been implicated in a

107 Here, we demonstrated that a pro-apoptotic GTP-binding protein, DAP3 (death-associated protein 3),

108 roarray analysis reveals that RAB38, a small GTP binding protein, demonstrates a similar expression p

109 Smo recruits a heterotrimeric GTP-binding protein-dependent pathway and engages both i

110 A unique GTP-binding protein, Der contains two consecutive GTP-bi

111 Here, we identify a novel GTP-binding protein, dubbed NGB (referring to NF2-associ

112 probe will be a useful tool for the study of GTP-binding proteins, especially when targets of interes

113 Nucleostemin (NS) is a nucleolar GTP-binding protein essential for ribosomal biogenesis,

114 med Rin, an incompletely characterized small GTP-binding protein expressed only in neurons.

115 veral genes including HBS1L, a member of the GTP-binding protein family that is expressed in erythroi

116 , a subunit of the ubiquitous heterotrimeric GTP-binding protein family, and AtIRE1A/AtIRE1B independ

117 n particle family guanosine 5c-triphosphate (GTP)-binding protein FlhF is required for the correct lo

118 eEF1A2 is an essential GTP-binding protein for protein synthesis.

119 GEFs) that stimulate the activation of small GTP-binding proteins from the Rho family.

120 Rab GTPase family comprises approximately 70 GTP-binding proteins, functioning in vesicle formation,

121 via heterotrimeric guanosine 5-triphosphate (GTP)-binding protein G(q), and the platelet ADP receptor

122 denylyl cyclase (P2Y(12)) via heterotrimeric GTP-binding protein G(i).

123 alling is the activation of a heterotrimeric GTP binding protein (G protein) by an agonist-occupied r

124 is mediated by a prototypical heterotrimeric GTP-binding protein (G protein) and mitogen-activated pr

125 n phosphatase 2C (PP2C) and a heterotrimeric GTP-binding protein (G protein) in Arabidopsis.

126 sion of the expression of the heterotrimeric GTP-binding protein (G protein) transducin, and suppress

127 The GTP-binding protein (G protein), transducin, serves as a

128 ail of the DOR as a candidate heterotrimeric GTP-binding protein (G protein)-coupled receptor-associa

129 Here, we identify two heterotrimeric GTP-binding protein (G protein)-coupled receptors (GPCRs

130 ignaling cascade through a specific membrane GTP-binding protein (G-protein)-coupled receptor in a G-

131 Heterotrimeric GTP-binding proteins (G proteins) are involved in direct

132 Signaling by heterotrimeric GTP-binding proteins (G proteins) drives numerous cellul

133 nd signaling proteins such as heterotrimeric GTP-binding proteins (G proteins).

134 Oxytocin receptor (OTR) activates the GTP-binding protein Galpha(q).

135 tate GTPase activity of the alpha subunit of GTP-binding protein (Galpha(s)) but do not alter its int

136 atypical beta subunit of the heterotrimeric GTP-binding proteins (Gbeta5).

137 gulated by the interaction of heterotrimeric GTP-binding protein Gbetagamma subunits or cytosolic act

138 that inhibits the stimulatory heterotrimeric GTP-binding protein Gs.

139 (CRF1) is sex biased whereby coupling to its GTP-binding protein, Gs, is greater in females, whereas

140 Here, we report that the GTP binding protein, H-Ras in the nucleus accumbens (NAc

141 ell as proliferation, the role of this small GTP-binding protein has not been addressed in the contex

142 The superfamily of small GTP-binding proteins has expanded dramatically in recent

143 Cdc42, a Ras-related GTP-binding protein, has been implicated in the regulati

144 Cdc42, a member of the Rho family of GTP-binding proteins, has been implicated in a variety o

145 Nucleostemin (NS) encodes a nucleolar GTP-binding protein highly enriched in the stem cells an

146 s genome contains 93 genes that encode small GTP-binding protein homologs.

147 Structural studies of GTP-binding proteins identified the Switch I and Switch

148 dii in astrocytes via an IFN-gamma-inducible GTP-binding protein (IGTP)-dependent mechanism.

149 ation of a variety of proteins such as small GTP binding proteins implicated in intracellular signali

150 Septins are GTP binding proteins important for cytokinesis in many e

151 The septins are conserved, GTP-binding proteins important for cytokinesis, membrane

152 signaling demonstrates a novel role for this GTP-binding protein in apoptosis induction caused by cel

153 Rac, a small, GTP-binding protein in the Rho family, regulates several

154 are valuable for the analysis of individual GTP-binding proteins in complex systems.

155 a subfamily of the Ras-superfamily of small GTP-binding proteins in the development of various disea

156 s to enrich, identify, and quantify ATP- and GTP-binding proteins in the entire human proteome.

157 hosphorylation, and membrane localization of GTP-binding proteins in trabecular meshwork (TM) cells,

158 lpha/beta and IFN-gamma, as were a number of GTP-binding proteins, including GTPases with known antiv

159 tested the hypothesis that RhoA, a monomeric GTP-binding protein, induces association of inositol tri

160 mplex, and Cdc42, a member of the Rho family GTP-binding proteins, interacted with the M1 protein via

161 tous and brain-specific ERCs bind to Rab6, a GTP-binding protein involved in membrane traffic at the

162 Septins are filament-forming GTP-binding proteins involved in important cellular even

163 Septins are filament-forming GTP-binding proteins involved in many essential cellular

164 Septins are conserved GTP-binding proteins involved in membrane compartmentali

165 This small GTP-binding protein is a member of the Ras superfamily w

166 In one case, effector and GAP binding to the GTP-binding protein is mutually exclusive.

167 Activation of the Ras small GTP-binding protein is necessary for normal T cell devel

168 icate that stabilizing the switch domains of GTP-binding proteins is an important part of GAP-stimula

169 The Rho family of GTP-binding proteins is involved in cytoskeletal remodel

170 nd thereby decreased function of one or more GTP-binding proteins is provided.

171 eotide exchange factor for the Arf family of GTP-binding proteins, is a major component of the PSD.

172 Rap2B, a member of GTP-binding proteins, is widely upregulated in many type

173 ADP ribosylation factors (Arfs) are small GTP-binding proteins known for their role in vesicular t

174 upport the concept that dysfunction of small GTP-binding proteins lead to statin-induced muscle damag

175 ypeptidase inhibitor that interacts with ATP/GTP binding protein-like 2 (AGBL2), a cytoplasmic carbox

176 Deletion of the GTP-binding protein-like domain affected lipid dependenc

177 o the Arf GAP domain, these proteins contain GTP-binding protein-like, ankyrin repeat and pleckstrin

178 nt alleles of MSS1, encoding a mitochondrial GTP-binding protein, manifest a respiratory-deficient ph

179 The Rho subfamily of small GTP-binding proteins mediates many fundamental cellular

180 nucleotide-binding protein-like 3 (GNL3L), a GTP-binding protein most similar to nucleostemin, as a n

181 RAS is a small GTP binding protein mutated in approximately 30% human c

182 and expression in HeLa cells of the putative GTP-binding protein NGB/CRFG demonstrated it to be a nov

183 Nucleolar GTP-binding protein (NGP-1) is overexpressed in various

184 and an interacting partner of the nucleolar GTP-binding protein Nog1.

185 afficking is regulated by small Ras-like GDP/GTP binding proteins of the Rab subfamily (Rab GTPases)

186 The stimulatory GTP-binding protein of adenylyl cyclase (AC) regulates h

187 Ran is a small GTP-binding protein of the Ras superfamily regulating fu

188 Rab3B, Rab3C, and Rab3D are closely related GTP-binding proteins of synaptic vesicles that may funct

189 Low molecular weight GTP-binding proteins of the Rheb and Rag families are ke

190 The small GTP-binding proteins of the Rho family and its regulator

191 but that result from the activation of small GTP-binding proteins of the Rho family and their downstr

192 yltransferase domain into the cytosol, where GTP-binding proteins of the Rho/Ras family are mono-O-gl

193 These findings implicate small GTP-binding proteins of the Ypt/Rab family in a signal c

194 ad, Gem/Kir) family of Ras-related monomeric GTP-binding proteins, on the function of the skeletal mu

195 The GTP-binding proteins or GTPases comprise a superfamily o

196 scular cell adhesion molecule 1 [VCAM1], and GTP binding protein overexpressed in skeletal muscle [GE

197 ine nucleotide exchange factor (GEF) for its GTP-binding protein partner eIF2 via interaction with eI

198 ARF6 (ADP-ribosylation factor 6) small GTP binding protein plays critical roles in actin cytosk

199 DP-ribosylation factor (Arf) family of small GTP-binding proteins plays a central role in membrane tr

200 Cdc42, a Rho-related small GTP binding protein, plays pivotal roles in actin cytosk

201 Rem2, Rad, and Gem/Kir (RGK) family of small GTP-binding proteins potently inhibits high voltage-acti

202 The RGK family of monomeric GTP-binding proteins potently inhibits high voltage-acti

203 NOG1 is a nucleolar GTP-binding protein present in eukaryotes ranging from t

204 Death-associated protein-3 (DAP3) is a GTP binding protein previously implicated in both intram

205 LRG-47 is an IFN-inducible GTP-binding protein previously shown to be required for

206 ad, Rem, Rem2, Gem/Kir (RGK) family of small GTP-binding proteins profoundly inhibit L-type Ca(2+) ch

207 contrast, to H-Ras, a closely related small GTP-binding protein R-Ras has the opposite activity, and

208 The small GTP-binding protein Rab12 plays an important role in the

209 nd that activation of the low-molecular-mass GTP-binding protein Rab27a, involved in the regulation o

210 es, and is regulated by the synaptic vesicle GTP-binding protein Rab3 that binds to RIM and to rabphi

211 ); translation-initiation factor 2 (6%); and GTP-binding protein, Rab38 (15%).

212 The four closely related small GTP-binding proteins Rab3A, Rab3B, Rab3C, and Rab3D are

213 Previous studies have indicated that the GTP-binding protein, Rab3A, plays a mechanistic role in

214 nt of the NADPH oxidase complex is the small GTP-binding protein Rac.

215 as the early growth response 1 (Egr1), small GTP binding protein Rac1 (Rac1), neurogranin (Nrgn), sod

216 Inhibition of the small GTP-binding protein Rac1 ameliorated post-SCI changes in

217 oduction during ischemia, and that the small GTP-binding protein Rac1 and reactive oxygen species (RO

218 s of TRPC5 prevented activation of the small GTP-binding protein Rac1 and stabilized synaptopodin.

219 Translocation of the small GTP-binding protein Rac1 to the cell plasma membrane is

220 The small GTP-binding protein Rac1, a member of the Rho family of

221 preventing the activation of the Rho family GTP-binding protein Rac1.

222 mice harboring a conditional deletion of the GTP-binding protein, Rac1, in macrophages are protected

223 ffects partly through binding of (S)GTP to a GTP-binding protein, Rac1.

224 l transduction pathway mediated by the small GTP-binding proteins RalA and RhoA but independent of Ra

225 s the effect of high glucose (HG) on a small GTP-binding protein, Rap1b, expression and activation, a

226 In this study, we identified the small GTP-binding protein Rap2a as a common target of both miR

227 We now show that the small GTP-binding protein Rap2A is the obligate effector for,

228 Small GTP binding proteins regulate diverse biological process

229 Small GTP-binding proteins regulate diverse processes in eukar

230 ing proteins, especially protein kinases and GTP-binding proteins, remain challenging.

231 OOT HAIR DEFECTIVE3) gene encodes a putative GTP-binding protein required for appropriate cell enlarg

232 ue nucleotide-binding motifs for kinases and GTP-binding proteins, respectively, and the characteriza

233 oreover, the Ser(863) mutant prevented small GTP-binding protein Rheb from enhancing the phosphorylat

234 by insulin or by overexpression of the small GTP-binding protein RheB under nutrient starvation.

235 yphosphate 5'-phosphatase E (INPP5E) and the GTP-binding protein (Rheb) that cargo sorting depends on

236 gulated by the small guanosine triphosphate (GTP)-binding protein Rho and its effector, mammalian hom

237 rs activate TRPC3 channels through the small GTP-binding protein Rho and subsequent phospholipase D s

238 ctor, glucosylates and inactivates the small GTP-binding proteins Rho, Rac, and Cdc42.

239 Pase-activating protein domain for the small GTP-binding protein, Rho.

240 In particular, inhibition of small GTP-binding proteins, Rho, Ras, and Rac, whose proper me

241 The small GTP-binding protein, Rho1/RhoA plays a central role in c

242 The small guanine nucleotide triphosphate (GTP)-binding protein RhoA stimulates type II myosin cont

243 the authors determined S1P activation of the GTP-binding proteins, RhoA and Rac (1,2,3).

244 directly induces the expression of the small GTP-binding protein Rnd2 in newly generated mouse cortic

245 c reticulum and the Golgi requires the small GTP-binding proteins Sar1 and Arf1 and that its glycosyl

246 an HU-induced small guanosine triphosphate (GTP)-binding protein, secretion-associated and RAS-relat

247 trategy for capturing and characterizing ATP/GTP-binding proteins should be generally applicable for

248 anism where neuroglial physiology, involving GTP-binding protein signaling pathways, links rhythmic c

249 s of activation that involves heterotrimeric GTP-binding protein subunits betagamma to regulate membr

250 the post-translational prenylation of small GTP-binding proteins such as Rho and Rac, and their down

251 by inhibition of isoprenylation of the small GTP-binding proteins such as Rho GTPase.

252 rons by inducing the expression of the small GTP-binding proteins such as Rnd2 and Rnd3.

253 The localization of the GTP-binding protein TC10 to lipid raft microdomains has

254 idylinositol 3-kinase (PI 3-K) and the small GTP-binding protein TC10, respectively.

255 Gh is a GTP binding protein that couples to the thromboxane rece

256 Arf1 is a GTP binding protein that functions at a number of cellul

257 illus subtilis Obg is a ribosome-associating GTP binding protein that is needed for growth, sporulati

258 Ran is a small GTP binding protein that was originally identified as a

259 namin and dynamin-related proteins are large GTP binding proteins that are involved in membrane traff

260 GGAP2/PIKE-A is a GTP-binding protein that can enhance Akt activity.

261 transglutaminase (tTG) is an acyltransferase/GTP-binding protein that contributes to the development

262 Gem is a small GTP-binding protein that has a ras-like core and extende

263 he synaptic vesicle protein Rab3A is a small GTP-binding protein that interacts with rabphilin and RI

264 tumor suppressor gene, encodes a M(r) 26,000 GTP-binding protein that is 60% homologous to ras and ra

265 Rac1, a small GTP-binding protein that is activated upon LPS stimulati

266 RhoB is a small GTP-binding protein that is involved in apoptotic signal

267 FoxO1 increased expression of Rab7, a small GTP-binding protein that mediates late autophagosome-lys

268 Rheb is a GTP-binding protein that promotes cell survival and medi

269 ranscription initiation factor I (TIF-IA), a GTP-binding protein that recruits RNA polymerase I to th

270 ADP-ribosylation factor 6 (ARF6) is a small GTP-binding protein that regulates peripheral vesicular

271 Nucleostemin (NS) is a nucleolar GTP-binding protein that was first identified in neural

272 ell division cycle 42) is a Rho family small GTP-binding protein that works as a molecular switch to

273 GBPs), a second family of interferon-induced GTP-binding proteins that also function in innate immuni

274 Septins belong to a family of polymerizing GTP-binding proteins that are important for cytokinesis

275 nd GTP affinity probes, we identified 165 (S)GTP-binding proteins that are involved in several differ

276 Septins are conserved GTP-binding proteins that assemble into heteromeric comp

277 Septins are conserved, GTP-binding proteins that assemble into higher order str

278 Septins are a conserved family of GTP-binding proteins that assemble into symmetric linear

279 itide 3-kinase enhancer (PIKE) is a group of GTP-binding proteins that belong to the subgroup of cent

280 n septins constitute a family of at least 12 GTP-binding proteins that can form hetero-oligomers and

281 Septins are GTP-binding proteins that form filaments and higher-orde

282 Septins are GTP-binding proteins that form ordered, rod-like multime

283 Septins comprise a family of GTP-binding proteins that oligomerize into higher-order

284 Septins are GTP-binding proteins that polymerize into heteromeric fi

285 Cdc42Hs, a member of the Ras superfamily of GTP-binding proteins, that facilitates cellular transfor

286 Mammalian septins are GTP-binding proteins the functions of which are not well

287 d Rad are members of another family of small GTP binding proteins (the Rad, Gem, and Kir family) for

288 dies indicate that Cdc42 could be a putative GTP-binding protein thought to be involved in the mastop

289 o the widely conserved YqeH subfamily [2] of GTP-binding proteins thought to play a role in ribosome

290 s makes it only the second of over 100 small GTP-binding proteins to be identified in the nucleus, an

291 alk between two distinct regulators of small GTP-binding proteins using structural and biochemical me

292 es of cell shape rearrangement involve small GTP-binding proteins, we examined the contribution of Rh

293 Cdc42 is a small GTP-binding protein which has been implicated in a numbe

294 as is a novel member of the Ras subfamily of GTP-binding proteins which has a unique expression patte

295 ein, dubbed NGB (referring to NF2-associated GTP binding protein), which binds to merlin.

296 The ARL15 gene encodes a small GTP-binding protein whose function is currently unknown.

297 tumor suppressor gene that encodes a 26 kDa GTP-binding protein with high homology to Ras and Rap.

298 Xanthine nucleotide-selective small GTP-binding proteins with an Asp/Asn mutation are valuab

299 Rnd proteins are Rho family GTP-binding proteins with cellular functions that antago

300 dopsis thaliana genome has three extra-large GTP-binding protein (XLG)-encoding genes: XLG1 (At2g2346

301 has three related proteins: the extra-large GTP-binding proteins XLG1, XLG2, and XLG3.