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

1 ntestinal epithelia and are regulated by Rho guanosine triphosphatase.

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

3 pparatus and physically interacts with 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 where aPKC is activated by Rho family 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 hat Epo1p binds simultaneously to the Cdc42p guanosine triphosphatase-activating protein Bem3p.

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

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

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

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

23 GAIP is a GAP or guanosine triphosphatase-activating protein that was ini

24 ppressor protein functions as a Ras-specific guanosine triphosphatase-activating protein, but the ide

25 oliferation by functioning as a Ras-specific guanosine triphosphatase-activating protein.

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

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

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

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

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

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

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

33 Both Rab18 guanosine triphosphatase activity and isoprenylation are

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

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

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

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

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

39 treadmilling predominantly determined by its guanosine triphosphatase activity.

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

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

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

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

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

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

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

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

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

52 The Rho guanosine triphosphatases are well known regulators of c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 By contrast, mutations in the guanosine triphosphatase consensus sequence had no effec

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 gnaling (RGS) family stimulate the intrinsic guanosine triphosphatase (GTPase) activity of the alpha

96 Several members of this group stimulate the guanosine triphosphatase (GTPase) activity of various G

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

98 of Pseudomonas aeruginosa showing intrinsic guanosine triphosphatase (GTPase) activity.

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

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

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

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

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

104 The Rho guanosine triphosphatase (GTPase) Cdc42 regulates sequen

105 The Ran guanosine triphosphatase (GTPase) controls nucleocytopla

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 It also binds to the guanosine triphosphatase (GTPase) Ran in its guanosine d

127 croinjection studies revealed a role for the guanosine triphosphatase (GTPase) Ran in NES-mediated ex

128 rt that is dependent on the ras-like nuclear guanosine triphosphatase (GTPase) Ran-TC4 and its associ

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

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

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

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

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

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

135 e (ADP)-ribosylates and thus inactivates the guanosine triphosphatase (GTPase) Rho.

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

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

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

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

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

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

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

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

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

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

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

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

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

149 by more than 90 percent its response to the guanosine triphosphatase (GTPase)-accelerating activity

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 Rho guanosine triphosphatases (GTPases) are implicated in TE

166 Rab guanosine triphosphatases (GTPases) are pivotal regulato

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

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

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

170 Rab guanosine triphosphatases (GTPases) control cellular tra

171 Rho guanosine triphosphatases (GTPases) control the cytoskel

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

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

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

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

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

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

178 Rho guanosine triphosphatases (GTPases) regulate multiple as

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

180 Ras guanosine triphosphatases (GTPases) regulate signaling p

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

182 Rab guanosine triphosphatases (GTPases) regulate vesicle tra

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

202 Members of the Rho family of small guanosine triphosphatases have emerged as key regulators

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

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

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

206 proteolytic activation of PAK2 represents a guanosine triphosphatase-independent mechanism of PAK re

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

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

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

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

211 The Cdc42 guanosine triphosphatase is essential for cell polarizat

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

213 between phosphatidylinositol metabolites and guanosine triphosphatases is an important feature of the

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

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

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

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

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

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

220 An intrinsic guanosine triphosphatase mediates a contact between the

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

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

223 N-terminal domain (N-domain) or the central guanosine triphosphatase module (GTPase-domain) also con

224 Rho guanosine triphosphatases (molecular switches that contr

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

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

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

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

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

230 Each member of the rab guanosine triphosphatase protein family assists in the r

231 The guanosine triphosphatase Rab1 regulates the transport of

232 The small guanosine triphosphatase Rab13 functions in exocytic ves

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

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

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

236 The small guanosine triphosphatase Rab7 regulates late endocytic t

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

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

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

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

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

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

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

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

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

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

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

248 The small guanosine triphosphatase Ran is loaded with guanosine tr

249 The guanosine triphosphatase Ran stimulates assembly of micr

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

251 repeat motifs and four binding sites for the guanosine triphosphatase Ran, is localized at the cytopl

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

253 t partly consumed by the action of the small guanosine triphosphatase Ran.

254 The small guanosine triphosphatase Rap1 regulates LFA-1 adhesivene

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

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

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

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

259 Rab guanosine triphosphatases regulate intracellular membran

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

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

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

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

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

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

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

267 The guanosine triphosphatase Sar1 controls the assembly and

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

269 Dynamin guanosine triphosphatases support the scission of clathr

270 f the Sec1-Sly1 protein family, and by small guanosine triphosphatases termed Rabs.

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

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

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

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

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

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

277 2 (SEPT2), a member of the septin family of guanosine triphosphatases that form a diffusion barrier

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

279 Rabs are monomeric guanosine triphosphatases that regulate membrane traffic

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

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

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

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

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

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

286 Small guanosine triphosphatases, typified by the mammalian Ras

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

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

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

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

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