ライフサイエンスコーパス: guanosine triphosphatase

1 ic factors were shown to be activated by Ran guanosine triphosphatase.

2 ntestinal epithelia and are regulated by Rho guanosine triphosphatase.

3 where aPKC is activated by Rho family small guanosine triphosphatases.

4 that it requires activity of one or more Rho guanosine triphosphatases.

5 keletal changes induced by the Rho family of guanosine triphosphatases.

6 pparatus and physically interacts with small guanosine triphosphatases.

7 we show that the Insert B domain of the Dnm1 guanosine triphosphatase (a DRP) contains a novel motif

8 We have identified a Rho guanosine triphosphatase activating protein (RhoGAP), PA

9 d to and phosphorylated spine-associated Rap guanosine triphosphatase activating protein (SPAR), a po

10 and dispersed at the lagging pole where the guanosine triphosphatase activating protein MglB disrupt

11 ere evidence that neurofibromin, via its Ras guanosine triphosphatase -activating activity, controls

12 the MKlp1-CYK4 centralspindlin complex is a guanosine triphosphatase-activating protein (GAP) for Ra

13 p190Rho-guanosine triphosphatase-activating protein (GAP) is kno

14 Here, we show that the Cdc42 guanosine triphosphatase-activating protein (GAP) Rga1 e

15 Here, we identify a Rap1 guanosine triphosphatase-activating protein (GAP; RapGAP

16 me 2q31 that encodes alpha2-chimaerin, a Rac guanosine triphosphatase-activating protein (RacGAP) sig

17 and Plk3 interact with spine-associated Rap guanosine triphosphatase-activating protein (SPAR), a re

18 pecifically binds to the IQ motif-containing guanosine triphosphatase-activating protein 1 (IQGAP1) s

19 hat Epo1p binds simultaneously to the Cdc42p guanosine triphosphatase-activating protein Bem3p.

20 ucleotide-exchange factor ECT-2, and the Rho guanosine triphosphatase-activating protein CYK-4 modula

21 yonic closure events, independent of the Rho guanosine triphosphatase-activating protein domain.

22 Gcs1p was previously characterized as a guanosine triphosphatase-activating protein for the smal

23 ng the genes small ARF GAP1 (SMAP1), an ARF6 guanosine triphosphatase-activating protein that functio

24 is by regulating the expression level of Ras guanosine triphosphatase-activating protein.

25 ional activity for p120RasGAP (RASA1), a Ras guanosine triphosphatase-activating protein.

26 human Tre-2/Bub2/Cdc16 domain-containing Rab guanosine triphosphatase-activating proteins (GAPs) and

27 signaling through their ability to serve as guanosine triphosphatase-activating proteins (GAPs).

28 Two Rab guanosine triphosphatases-activating proteins (GAPs) hav

29 downstream signaling to engage small GTPase (guanosine triphosphatase) activation and AMPAR synaptic

30 ion that is altered by inhibition of dynamin guanosine triphosphatase activity and is temporally dist

31 Both Rab18 guanosine triphosphatase activity and isoprenylation are

32 We hypothesized that the guanosine triphosphatase activity encoded in the HCV NS4

33 ling (RGS) proteins accelerate the intrinsic guanosine triphosphatase activity of heterotrimeric G-pr

34 ulin and it inhibited the colchicine-induced guanosine triphosphatase activity of tubulin, indicating

35 ing of the mutant ftsZ84, which has 1/10 the guanosine triphosphatase activity of wild-type FtsZ in v

36 merization, suppression of PDGF-induced Rac1 guanosine triphosphatase activity, and Akt and extracell

37 treadmilling predominantly determined by its guanosine triphosphatase activity.

38 e kidney (MDCK) cells and identified the rho-guanosine triphosphatase adaptor and scaffolding protein

39 The loss of the small guanosine triphosphatase ADP-ribosylation factor 1 (Arf1

40 e proteins, inhibition of filamentous septin guanosine triphosphatases alleviates constriction defect

41 many membrane proteins, including the Ypt7p guanosine triphosphatase and a "SNARE complex" with Vam3

42 FtsZ is an essential bacterial guanosine triphosphatase and homolog of mammalian beta-t

43 We identified Arf6 guanosine triphosphatase and its activators, cytohesins,

44 s the only known exchange factor for the Ran guanosine triphosphatase and performs essential roles in

45 t it was soluble and stable, did not bind to guanosine triphosphatases and bound more tightly to the

46 ormation requires the function of Rho family guanosine triphosphatases and reorganization of the acti

47 nse proteins, including interferon-inducible guanosine triphosphatases and the antimicrobial cathelic

48 ell adhesion molecules that activate RAS/RHO guanosine triphosphatases and their effector mitogen-act

49 importance and activates mTORC1 via the Rag guanosine triphosphatases and their regulators GATOR1 an

50 echanistically distinct enzymes (a kinase, a guanosine triphosphatase, and a ubiquitin protein hydrol

51 gulate protein levels of MIG-2, a Rho family guanosine triphosphatase, and/or down-regulate INA-1, an

52 d into motility signaling proteins (kinases, guanosine triphosphatases, and guanine exchange factors)

53 ons in members of the RAS subfamily of small guanosine triphosphatases are found in > 30% of all huma

54 The Rho guanosine triphosphatases are well known regulators of c

55 We found that HIV-1 Nef and the guanosine triphosphatase Arf1 induced trimerization and

56 is issue, Rafiq et al. reveal that the small guanosine triphosphatase ARF1, a well-known orchestrator

57 phosphatase-activating protein for the small guanosine triphosphatase Arf1, and gcs1 mutants displaye

58 d Kinesin-6 (which carries activators of Rho guanosine triphosphatase) at the cell cortex using total

59 ranes into an ER network is dependent on the guanosine triphosphatase atlastin (ATL).

60 For Rac and other small guanosine triphosphatases, binding to guanosine triphosp

61 Protein release factor 3 (RF3), a guanosine triphosphatase, binds to ribosome after releas

62 gine off switch by sensing mitochondrial Rho guanosine triphosphatase-Ca(2+) and as a brake by anchor

63 We show that the Rac1 guanosine triphosphatase can bind to and regulate STAT3

64 Here, we examine the function of Rho guanosine triphosphatase CDC-42 in AJ formation and regu

65 e cortical PAR proteins (including the small guanosine triphosphatase CDC-42) have an active role in

66 In FRLalpha, the Rho family guanosine triphosphatase Cdc42 relieves the autoinhibiti

67 report a positive feedback loop between the guanosine triphosphatase Cdc42, a central determinant in

68 ndicating that PAKs are effectors of the Rho-guanosine triphosphatase Cdc42.

69 ves localization of the conserved Rho-family guanosine triphosphatase, Cdc42, to the cortical region

70 es (PAKs), downstream effectors of the small guanosine triphosphatase, Cdc42p.

71 pathway between the decoding center and the guanosine triphosphatase center of EF-Tu.

72 The Rab subfamily of small guanosine triphosphatases controls these processes by ac

73 a heterodimer composed of a conserved 54-kDa guanosine triphosphatase (cpSRP54) and a unique 43-kDa s

74 aintain a basal state of activation of small guanosine triphosphatases critical for normal T cell mot

75 uitment to the TASCC was amino acid- and Rag guanosine triphosphatase-dependent, and disruption of mT

76 uitment and assembly of some dynamin-related guanosine triphosphatases depends on adaptor proteins re

77 ino acid positions (p.G488R, p.A495V) in the guanosine triphosphatase domain, each segregating with a

78 pression of a dominant-active Drosophila Rho guanosine triphosphatase, Drac1, rescued photoreceptor m

79 The dynamin-related guanosine triphosphatase Drp1 mediates the division of m

80 is paper, we provide evidence that the large guanosine triphosphatase dynamin2 and its partner, endot

81 ociation factor Tif6 by the translocase-like guanosine triphosphatase Efl1 is a critical late maturat

82 on is a multistep process facilitated by the guanosine triphosphatase elongation factor (EF)-Tu.

83 es bound to tRNAs, nascent polypeptides, the guanosine triphosphatase elongation factors mtEF-Tu and

84 sion cycle 42 (Cdc42) is a member of the Rho guanosine triphosphatase family and has pivotal function

85 mber of a newly emerging 47-kilodalton (p47) guanosine triphosphatase family, LRG-47, that acts indep

86 s well as adherens junction proteins and Rho guanosine triphosphatase from the cell periphery to the

87 eractions of the ancient outer transmembrane guanosine triphosphatase, Fzo1, were required to promote

88 de exchange factor (GEF) for Tem1, the small guanosine triphosphatase governing activity of the Sacch

89 Rho guanosine triphosphatases (GT-Pases) are recognized as c

90 Rho family guanosine triphosphatase (GTPase) 3 (Rnd3), a member of

91 in complex 1 (mTORC1) protein kinase via its guanosine triphosphatase (GTPase) activating protein (GA

92 des Rop (RHO-like small G protein of plants) guanosine triphosphatase (GTPase) activating protein 4 (

93 ors (GEFs) and by RGS proteins, which act as guanosine triphosphatase (GTPase) activating proteins (G

94 n with increased MLC phosphorylation and Rho guanosine triphosphatase (GTPase) activation.

95 action of SRP and SR, which stimulates their guanosine triphosphatase (GTPase) activities, leading to

96 s reveal the critical link between intrinsic guanosine triphosphatase (GTPase) activity and downstrea

97 ide-binding proteins (G proteins) that lacks guanosine triphosphatase (GTPase) activity in NIH-3T3 ce

98 eins are constitutively active because their guanosine triphosphatase (GTPase) activity is disabled.

99 ctivation of the G protein by increasing its guanosine triphosphatase (GTPase) activity.

100 In this study, we show that the small guanosine triphosphatase (GTPase) adenosine diphosphate

101 ich repeat kinase 2 (LRRK2) protein has both guanosine triphosphatase (GTPase) and kinase activities,

102 LRRK2 has guanosine triphosphatase (GTPase) and kinase activities,

103 This process requires Rab9 guanosine triphosphatase (GTPase) and the putative tethe

104 erestingly, ciliary trafficking of the small guanosine triphosphatase (GTPase) Arl13b, loss of which

105 SKIP binds to the small guanosine triphosphatase (GTPase) ARL8 on the lysosomal

106 with Bnip-2, a protein that binds the small guanosine triphosphatase (GTPase) Cdc42 and a negative r

107 The Rho guanosine triphosphatase (GTPase) Cdc42 regulates sequen

108 The Ran guanosine triphosphatase (GTPase) controls nucleocytopla

109 Two structurally homologous guanosine triphosphatase (GTPase) domains interact direc

110 During mitochondrial division, the mechano-guanosine triphosphatase (GTPase) dynamin-related protei

111 ot involve the exocyst complex, a common Ral guanosine triphosphatase (GTPase) effector.

112 mal subunit rotation and is catalyzed by the guanosine triphosphatase (GTPase) elongation factor G (E

113 The guanosine triphosphatase (GTPase) elongation factor G (E

114 Protein synthesis requires several guanosine triphosphatase (GTPase) factors, including elo

115 in RAB23, which encodes a member of the RAB guanosine triphosphatase (GTPase) family of vesicle tran

116 and constitutively active member of the Rho guanosine triphosphatase (GTPase) family, has been impli

117 The Rac1 guanosine triphosphatase (GTPase) has been implicated in

118 of mTORC1 by amino acids is mediated by Rag guanosine triphosphatase (GTPase) heterodimers on the ly

119 w that TIP47 also bound directly to the Rab9 guanosine triphosphatase (GTPase) in its active, GTP-bou

120 ecause activation of Rap1, an abundant small guanosine triphosphatase (GTPase) in platelets, contribu

121 uring cotranslational protein targeting, two guanosine triphosphatase (GTPase) in the signal recognit

122 Here, we investigated whether Rap1, a small guanosine triphosphatase (GTPase) known to promote integ

123 s targeting KRAS(G12C), a mutant form of the guanosine triphosphatase (GTPase) KRAS, are a promising

124 enic mutation in the gene encoding the small guanosine triphosphatase (GTPase) NRAS.

125 ornavirus infection was a large set encoding guanosine triphosphatase (GTPase) of immunity-associated

126 Deregulation of Rho guanosine triphosphatase (GTPase) pathways plays an impo

127 The Cdc42 guanosine triphosphatase (GTPase) plays a central role i

128 We identified the Arabidopsis small guanosine triphosphatase (GTPase) protein AtRac1 as a ce

129 ently manipulating the activity of the small guanosine triphosphatase (GTPase) Rab1.

130 The guanosine triphosphatase (GTPase) Rab32 coordinates a ce

131 The small guanosine triphosphatase (GTPase) Rab7 has been implicat

132 hibits eotaxin-induced activation of the Rho-guanosine triphosphatase (GTPase) Rac, and Rac2-deficien

133 ration and cell migration, whereas the small guanosine triphosphatase (GTPase) Rac1 mediates cell mig

134 abrogated PDGF-mediated activation of small guanosine triphosphatase (GTPase) Rac1, a member of the

135 The small guanosine triphosphatase (GTPase) Rap1 is an important r

136 ayed but not early ERK activation, the small guanosine triphosphatase (GTPase) Rap1 was considered as

137 The retinitis pigmentosa guanosine triphosphatase (GTPase) regulator (RPGR) is es

138 activation bioprobe), we revealed that Cdc42 guanosine triphosphatase (GTPase) remains inactive withi

139 on of an activated form of Cdc42, a Rho-type guanosine triphosphatase (GTPase) required for cell pola

140 lular factors to activation of the monomeric guanosine triphosphatase (GTPase) Rho control cytoskelet

141 In yeast and animal cytokinesis, the small guanosine triphosphatase (GTPase) Rho1/RhoA has an estab

142 During cytokinesis, the guanosine triphosphatase (GTPase) RhoA orchestrates cont

143 ly of heterotrimeric G proteins to the small guanosine triphosphatase (GTPase) RhoA, enabling Galpha(

144 Etd1 activates the guanosine triphosphatase (GTPase) Spg1 to trigger signal

145 y as part of a 43-member IFN-gamma-inducible guanosine triphosphatase (GTPase) superfamily in mouse a

146 Elongation factor G (EF-G) is a guanosine triphosphatase (GTPase) that plays a crucial r

147 e we show that transcripts for RhoA, a small guanosine triphosphatase (GTPase) that regulates the act

148 ly active (ca) or dominant negative (dn) Rho guanosine triphosphatase (GTPase) vectors.

149 kinase G (PKG), protein kinase A (PKA), Rho guanosine triphosphatase (GTPase), and MLC phosphatase w

150 ein synthesis, elongation factor G (EF-G), a guanosine triphosphatase (GTPase), binds to the ribosoma

151 ivity is regulated by Rheb, a Ras-like small guanosine triphosphatase (GTPase), in response to growth

152 The small guanosine triphosphatase (GTPase), Rab5, was first found

153 udy was to investigate the role of the small guanosine triphosphatase (GTPase), Rho, in the corneal e

154 osphorylation, we identified the RAB35 small guanosine triphosphatase (GTPase)-a protein previously i

155 They are basically the guanosine triphosphatase (GTPase)-accelerating proteins

156 sequence(s) of regulation of Ras activity by guanosine triphosphatase (GTPase)-activating proteins (G

157 re its Raptor subunit interacts with the Rag guanosine triphosphatase (GTPase)-Ragulator complex.

158 ic cells involves membrane-localized and Rac guanosine triphosphatase (GTPase)-regulated reduced nico

159 on of tubules mediated by the atlastin (ATL) guanosine triphosphatase (GTPase).

160 is a disease-associated RAS subfamily small guanosine triphosphatase (GTPase).

161 te plasma membrane-associated ROPs [Rho-like guanosine triphosphatases (GTPase) from plants], leading

162 chromosome [SRPX], and retinitis pigmentosa guanosine triphosphatase [GTPase] regulator [RPGR]) are

163 ownstream target of Rho (a Ras-related small guanosine triphosphatase [GTPase]), is associated with l

164 idues in switch region I of immunity-related guanosine triphosphatases (GTPases) (IRGs), a family of

165 The Rag guanosine triphosphatases (GTPases) activate mTORC1 in r

166 C1 is activated on lysosomes by Rag and Rheb guanosine triphosphatases (GTPases) and drives biosynthe

167 nucleotide exchange factors specific for Rho guanosine triphosphatases (GTPases) and invariably posse

168 ide exchange factors (GEFs) specific for Rho guanosine triphosphatases (GTPases) and invariably posse

169 membrane protein that interacts with the Rag guanosine triphosphatases (GTPases) and Ragulator in an

170 (mTORC1) is recruited to the lysosome by Rag guanosine triphosphatases (GTPases) and regulates anabol

171 phatidylinositol 4-kinases (PI4Ks) and small guanosine triphosphatases (GTPases) are essential for pr

172 Rho guanosine triphosphatases (GTPases) are implicated in TE

173 Rho guanosine triphosphatases (GTPases) are master regulator

174 Rab guanosine triphosphatases (GTPases) are pivotal regulato

175 The guanosine triphosphatases (GTPases) Arf, Sar1, and dynam

176 yclical activation and inactivation of small guanosine triphosphatases (GTPases) by their specific gu

177 ns, this process is mediated by dynamin-like guanosine triphosphatases (GTPases) called atlastins (AT

178 The Rho guanosine triphosphatases (GTPases) control cell shape a

179 Rab guanosine triphosphatases (GTPases) control cellular tra

180 Rho guanosine triphosphatases (GTPases) control the cytoskel

181 The Rho family of guanosine triphosphatases (GTPases) is composed of membe

182 The guanosine triphosphatases (GTPases) of the immunity-asso

183 creasing the activity of the recycling small guanosine triphosphatases (GTPases) Rab4 or Rab11 was su

184 ses whose activity is regulated by the small guanosine triphosphatases (GTPases) Rac and Cdc42.

185 The Rho guanosine triphosphatases (GTPases) Rac1 and Rac2 are cr

186 The Rag guanosine triphosphatases (GTPases) recruit the master k

187 al cells, signaling pathways involving small guanosine triphosphatases (GTPases) regulate cell polari

188 Rho guanosine triphosphatases (GTPases) regulate multiple as

189 st cells, signaling pathways involving small guanosine triphosphatases (GTPases) regulate polarized o

190 Ras guanosine triphosphatases (GTPases) regulate signaling p

191 r-bundle morphogenesis whereby different Rho guanosine triphosphatases (GTPases) regulate the initiat

192 Rab guanosine triphosphatases (GTPases) regulate vesicle tra

193 histicated mechanisms to modulate Rho family guanosine triphosphatases (GTPases) to mediate specific

194 uding amino acids, which act through the Rag guanosine triphosphatases (GTPases) to promote mTORC1 tr

195 Nutrients signal via the Rag guanosine triphosphatases (GTPases) to promote the local

196 Activation of Rho guanosine triphosphatases (GTPases) to the guanine triph

197 e an interferon (IFN)-inducible subfamily of guanosine triphosphatases (GTPases) with well-establishe

198 involving the Ragulator complex and the Rag guanosine triphosphatases (GTPases), causing release of

199 The Rho family of small guanosine triphosphatases (GTPases), including Rac and C

200 e group of proteins, the Rho family of small guanosine triphosphatases (GTPases), is critical for thi

201 ce of RIT1 to other members of the Ras small guanosine triphosphatases (GTPases), mutations affecting

202 Many of those factors are guanosine triphosphatases (GTPases), proteins that catal

203 ner thought to be dependent on the Rag small guanosine triphosphatases (GTPases), the Ragulator compl

204 These processes all involve Rho family small guanosine triphosphatases (GTPases), which are regulated

205 Amino acids activate the Rag guanosine triphosphatases (GTPases), which promote the t

206 y the activation of Ras homolog (Rho) family guanosine triphosphatases (GTPases), which regulate the

207 Rag proteins--a family of four related small guanosine triphosphatases (GTPases)--interact with mTORC

208 of the actin cytoskeleton by inhibiting Rho guanosine triphosphatases (GTPases).

209 the ADP ribosylation factor (ARF) family of guanosine triphosphatases (GTPases).

210 tment to the surface of lysosomes by the Rag guanosine triphosphatases (GTPases).

211 action of various kinases, phosphatases, and guanosine triphosphatases (GTPases).

212 Amino acids signal to mTORC1 through the Rag guanosine triphosphatases (GTPases).

213 Activation of the small guanosine triphosphatase H-Ras by the exchange factor So

214 ular, we focus on the role of the Rho family guanosine triphosphatases in endothelial function and va

215 Deletion of Rac1, a Rho guanosine triphosphatase, in adult mouse epidermis stimu

216 nin regulates the activity of the Rho family guanosine triphosphatases (including RhoA and Rac1) in a

217 We found that the murine Irgm1 (LRG-47) guanosine triphosphatase induced autophagy and generated

218 le protein 42 (Cdc42Hs) is a small, Rho-type guanosine triphosphatase involved in multiple cellular p

219 cation, unlike those missing the related p47 guanosine triphosphatases IRG-47 or IGTP.

220 Immunity-related p47 guanosine triphosphatases (IRG) play a role in defense a

221 The Cdc42 guanosine triphosphatase is essential for cell polarizat

222 a genetically encoded, photoactivatable Rac guanosine triphosphatase is sufficient to direct migrati

223 The Rab family of small guanosine triphosphatases is evolutionarily conserved an

224 ere, we show that dynamin1 (Dyn1), the large guanosine triphosphatase, is an interacting partner of I

225 Ran, a small guanosine triphosphatase, is suggested to have additiona

226 Cdc42, a Rho guanosine triphosphatase, is thought to orchestrate crit

227 Interestingly, Rap1, but not Rho family guanosine triphosphatases, is required for the response

228 idermal growth factor receptor (EGFR) or the guanosine triphosphatase KRAS.

229 Inhibition of Cdc42 and related Rho guanosine triphosphatases may be a general feature of cy

230 An intrinsic guanosine triphosphatase mediates a contact between the

231 The mammalian dynamin-related guanosine triphosphatases Mfn1,2 and Opa1 are required f

232 e show that the mitochondrial outer membrane guanosine triphosphatase mitofusin (Mfn) 2 mediates Park

233 Rho guanosine triphosphatases (molecular switches that contr

234 OPA1, a dynamin-related guanosine triphosphatase mutated in dominant optic atrop

235 Proteolytic cleavage of the dynamin-like guanosine triphosphatase OPA1 in mitochondria is emergin

236 Cdc42, a member of Rho GTPases (guanosine triphosphatases), participates in cytokine- an

237 However, constitutively active Rag guanosine triphosphatases prevented TFEB translocation d

238 IC4 and RIC3 pathways downstream of the ROP1 guanosine triphosphatase promoting actin assembly and di

239 The guanosine triphosphatase Rab1 regulates the transport of

240 The small guanosine triphosphatase Rab13 functions in exocytic ves

241 tis elegans homologue of the mammalian small guanosine triphosphatase Rab2.

242 and is regulated by Wnt5a through the small guanosine triphosphatases Rab4 and RhoB.

243 In this study, we demonstrate that the guanosine triphosphatase Rab7 contributes to this recrui

244 The small guanosine triphosphatase Rab7 regulates late endocytic t

245 ine nucleotide exchange factor for the small guanosine triphosphatase Rab8, to promote recruitment of

246 volvement of G(i)alpha subunit and the small guanosine triphosphatase Rac, respectively.

247 toward PDGF and also activation of the small guanosine triphosphatase Rac, which is essential for pro

248 f serum, where it colocalizes with the small guanosine triphosphatase Rac-1.

249 es (Paks), downstream effectors of the small guanosine triphosphatases Rac and Cdc42, biochemically c

250 leton dynamics and the activity of the small guanosine triphosphatases Rac and Cdc42.

251 PIX and decreasing the activity of the small guanosine triphosphatase Rac1 and Cdc42.

252 high degree of sequence similarity, the Rho guanosine triphosphatases Rac1 and Rac2 regulate distinc

253 ionally enhanced by signaling from the small guanosine triphosphatase, Rac1.

254 nal display analysis, to show that the small guanosine triphosphatase Rac2 is expressed selectively i

255 ly was mediated by chromosomes and the small guanosine triphosphatase Ran in a process requiring ~16

256 The small guanosine triphosphatase Ran is loaded with guanosine tr

257 The guanosine triphosphatase Ran stimulates assembly of micr

258 were assembled around beads coated with the guanosine triphosphatase Ran, forming pseudo-nuclei that

259 anosine triphosphate-bound form of the small guanosine triphosphatase Ran.

260 The small guanosine triphosphatase Rap1 regulates LFA-1 adhesivene

261 diated activation of the integrin regulatory guanosine triphosphatase Rap1 via the recruitment and ac

262 is an active process that requires the small guanosine triphosphatase Rap1.

263 uncaging to image the activity of the small guanosine triphosphatase Ras after NMDA receptor activat

264 mTOR is directly activated by the small guanosine triphosphatase Ras homolog enriched in brain (

265 l adhesion reduction by activating the small guanosine triphosphatase Ras homolog family member J by

266 Rab guanosine triphosphatases regulate intracellular membran

267 inhibition of p75NTR signaling to the small guanosine triphosphatase Rho resulted in impaired HSC di

268 uanine exchange factor for the Rho family of guanosine triphosphatases (Rho GEF GTPases), as a protei

269 , and CTNNB1 (encoding beta-catenin) and RHO guanosine triphosphatase [RHO GTPase, RHO], two signalin

270 In many organisms, the small guanosine triphosphatase RhoA controls assembly and cont

271 rotein kinase c-Src and stimulated the small guanosine triphosphatase RhoA, consequently inhibiting c

272 f early growth response 3 (EGR3) and the Rho guanosine triphosphatase RhoA.

273 on factor FoxF directly upregulate the small guanosine triphosphatase RhoDF, which synergizes with Cd

274 is IpgB1, a mimic of the human Ras-like Rho guanosine triphosphatase RhoG.

275 show that mouse embryos that lack the small guanosine triphosphatase RSG1 die at embryonic day 12.5,

276 The guanosine triphosphatase Sar1 controls the assembly and

277 d by pleiotropic perturbations to Rho family guanosine triphosphatase signaling and myosin II activit

278 Dynamin guanosine triphosphatases support the scission of clathr

279 eIF2 is a guanosine triphosphatase that becomes activated by eIF2B

280 -membrane receptor for DRP1, the cytoplasmic guanosine triphosphatase that catalyzes mitochondrial fi

281 duced activation of Rap1A, a phox-associated guanosine triphosphatase that is regulated by cAMP.

282 KRIT-1 binds to Rap1, a guanosine triphosphatase that maintains the integrity of

283 ynamin-related protein 1 (Drp1), a cytosolic guanosine triphosphatase that polymerizes and constricts

284 protein kinases and the regulation of small guanosine triphosphatases that control cellular movement

285 s based on the activity of Rho and Rap small guanosine triphosphatases that control integrin activati

286 2 (SEPT2), a member of the septin family of guanosine triphosphatases that form a diffusion barrier

287 Dynamins are 100-kilodalton guanosine triphosphatases that participate in the format

288 Rabs are monomeric guanosine triphosphatases that regulate membrane traffic

289 Fzo1 and Mgm1 are conserved guanosine triphosphatases that reside in the outer and i

290 For Cdc42 and other guanosine triphosphatases, the subcellular location of a

291 Dynamin 1 is a neuron-specific guanosine triphosphatase thought to be critically requir

292 ganelles universally require dynamin-related guanosine triphosphatases to divide.

293 Competitive binding of small guanosine triphosphatases to the IS domain disrupts the

294 on factor 4 (EF4/LepA) is a highly conserved guanosine triphosphatase translation factor.

295 Small guanosine triphosphatases, typified by the mammalian Ras

296 ture-sensitive allele of the shibire dynamin guanosine triphosphatase, which is required for synaptic

297 in the appressorium by means of four septin guanosine triphosphatases, which polymerize into a dynam

298 The activation of Rho guanosine triphosphatases within the extending growth co

299 tioning at this same step, including the Rab guanosine triphosphatase Ypt1p, which associated with cy

300 like other organelles, requires a Rab-family guanosine triphosphatase (Ypt7p), a Rab effector and Sec