ライフサイエンスコーパス: ADP-ribosylation factor

1 ed with guanosine diphosphate (GDP) bound to ADP ribosylation factor 1 (ARF1) aligned in a liquid cry

2 din A or overexpression of dominant-negative ADP ribosylation factor 1 (ARF1) caused dissociation of

3 ily GTPase Arf79F, the Drosophila homolog of ADP ribosylation factor 1 (ARF1), essential for clathrin

4 of two subcomplexes: the membrane-targeting, ADP ribosylation factor 1 (Arf1):GTP-binding betagammade

5 -terminal fragment of adenosine diphosphate (ADP) ribosylation factor 1 (ARF1) is proposed to be invo

6 change protein that preferentially activates ADP-ribosylation factor 1 (ARF1) and ARF3.

7 ns, both reactions are greatly stimulated by ADP-ribosylation factor 1 (ARF1) but not by the GDP-boun

8 se-activating protein (GAP) that deactivates ADP-ribosylation factor 1 (ARF1) during the formation of

9 To investigate the role of ADP-ribosylation factor 1 (ARF1) in this process, a cDNA

10 ADP-ribosylation factor 1 (ARF1) is a key regulator of t

11 Although we have showed that the GTPase ADP-ribosylation factor 1 (ARF1) is overexpressed in hig

12 tudies defined the STAU1-binding site within ADP-ribosylation factor 1 (ARF1) mRNA as a 19-base-pair

13 pecifically associated with the small GTPase ADP-ribosylation factor 1 (Arf1) to mediate uniform dist

14 the finiteness of the cyclical activation of ADP-ribosylation factor 1 (Arf1), a fundamental step in

15 Finally, overexpression of ADP-ribosylation factor 1 (Arf1), a small GTPase essenti

16 ergic receptor (alpha(2B)-AR) interacts with ADP-ribosylation factor 1 (ARF1), a small GTPase involve

17 anner by protein kinase c-alpha (PKC-alpha), ADP-ribosylation factor 1 (ARF1), and Rho family members

18 FGAP1, a GTPase-activating protein (GAP) for ADP-ribosylation factor 1 (ARF1), couples to either BARS

19 and cell biological evidence for the role of ADP-ribosylation factor 1 (ARF1)-GTPase and its effector

20 4-phosphate (PtdIns(4)P) and a small GTPase ADP-ribosylation factor 1 (ARF1).

21 nd inhibits the GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1), suggesting that QS1

22 branes by expressing a constitutively active ADP-ribosylation factor 1 mutant arrests CFTR within dis

23 (GTPase-activating protein that inactivates ADP-ribosylation factor 1), reduces seizure threshold, a

24 release of HA was unaffected by depletion of ADP-ribosylation factor 1, a small GTPase that has been

25 FGAP1, a GTPase-activating protein (GAP) for ADP-Ribosylation Factor 1, also participate in vesicle f

26 ion was unaffected by cytosolic depletion of ADP-ribosylation factor 1, suggesting that HA sorting re

27 n is dependent on additional factors such as ADP-ribosylation factor-1 (ARF-1) and protein kinase Cal

28 Here we have investigated the role of the ADP-ribosylation factor-1 (ARF1) in this process to dete

29 ted guanine nucleotide-exchange proteins for ADP-ribosylation factors, 200-kDa BIG1 and 190-kDa BIG2,

30 ferentially with the activated form of human ADP-ribosylation factor 3 (ARF3) in two-hybrid assays.

31 the switch I and switch II regions of human ADP-ribosylation factor 3 (ARF3) were isolated from loss

32 In this study, we report that ADP-ribosylation factor 3p (Arf3p) acts as a regulator o

33 We report a novel role for the small GTPase ADP ribosylation factor 4 (Arf4) in controlling pattern

34 We found that ADP-ribosylation factor 4 (ARF4) interacts with the intr

35 ylinositol 3 kinase (PI3K)-dependent GTPase, ADP ribosylation factor 6 (ARF-6), to stimulate MHC-I in

36 ADP ribosylation factor 6 (Arf6) is a small GTPase known

37 ADP ribosylation factor 6 (ARF6) was recently identified

38 subsequent interaction with the host factor ADP ribosylation factor 6 (ARF6)-GTP.

39 The effects of binding of myristoylated ADP ribosylation factor 6 (myr-ARF6), an activator of ph

40 s clathrin and dynamin independent, requires ADP ribosylation factor 6, and traffics to lysosomes.

41 esult of signalling through the small GTPase ADP-ribosylation factor 6 (ARF6) and its activator ARF n

42 rian follicles is triggered by activation of ADP-ribosylation factor 6 (ARF6) and leads to uncoupling

43 Here we identify the ADP-ribosylation factor 6 (Arf6) as an important regulat

44 equires protein tyrosine phosphorylation and ADP-ribosylation factor 6 (ARF6) but is independent of p

45 ARs control the activity of the small GTPase ADP-ribosylation factor 6 (Arf6) by consecutively recrui

46 The ADP-ribosylation factor 6 (ARF6) GTPase has a dual funct

47 (2) mAChRs in HeLa cells and the role of the ADP-ribosylation factor 6 (Arf6) GTPase in regulating M(

48 Here, we report a novel role for the ADP-ribosylation factor 6 (ARF6) GTPase in the post-mito

49 X as a model system, we demonstrate that the ADP-ribosylation factor 6 (ARF6) GTPase is an important

50 rafficking through the clathrin-independent, ADP-ribosylation factor 6 (Arf6) GTPase-regulated endoso

51 dy, we have documented an essential role for ADP-ribosylation factor 6 (ARF6) in cell surface remodel

52 ADP-ribosylation factor 6 (ARF6) is a member of the Ras

53 ADP-ribosylation factor 6 (ARF6) is a small GTP-binding

54 udy shows that the small GTP-binding protein ADP-ribosylation factor 6 (ARF6) is an important regulat

55 Previous studies showed that ADP-ribosylation factor 6 (Arf6) is important for platel

56 The ADP-ribosylation factor 6 (Arf6) isoform and the exchang

57 The small G protein ADP-ribosylation factor 6 (Arf6) plays important roles i

58 The GTP-binding protein ADP-ribosylation factor 6 (Arf6) regulates endosomal mem

59 The ADP-ribosylation factor 6 (ARF6) small GTPase functions

60 ADP-ribosylation factor 6 (ARF6) small GTPase regulates

61 as a guanine nucleotide exchange factor for ADP-ribosylation factor 6 (ARF6) that promotes glut4 ves

62 ogic or genetic blockade of the small GTPase ADP-ribosylation factor 6 (arf6) that regulates integrin

63 The small GTPase ADP-ribosylation factor 6 (Arf6) was shown to regulate t

64 In this study, we report that ADP-ribosylation factor 6 (ARF6), a Ras superfamily smal

65 ceptor endocytosis through the activation of ADP-ribosylation factor 6 (ARF6), a small GTP-binding pr

66 We report that the small GTPase, ADP-ribosylation factor 6 (ARF6), is present only on the

67 host plasma membrane and interacts with host ADP-ribosylation factor 6 (Arf6).

68 y regulated by the small GTP-binding protein ADP-ribosylation factor 6 (Arf6).

69 ARF6 (ADP-ribosylation factor 6) is a small GTPase implicated

70 ARF6 (ADP-ribosylation factor 6) small GTP binding protein pla

71 equires the activation of small GTPase Arf6 (ADP-ribosylation factor 6), which regulates intracellula

72 ADP-ribosylation factor 6, a cytosolic eukaryotic protei

73 n active state, which is further enhanced by ADP-ribosylation factor 6, a host cofactor for CTA1.

74 proteinases, RNA, caveolin-1, and the GTPase ADP-ribosylation factor 6, and are biologically active t

75 m toxin substrate 1, p21-activated kinase 1, ADP-ribosylation factor 6, and cell division control pro

76 expression of a dominant inhibitory form of ADP-ribosylation factor 6, ARF6(T27N), in 3T3-L1 adipocy

77 copy to show that clathrin, dynamin, and the ADP-ribosylation factor 6, three components of the endoc

78 Another PLD1 activator, ADP-ribosylation factor 6, was involved in VWF secretion

79 on and/or facilitating its recycling via the ADP-ribosylation factor 6-dependent recycling pathway.

80 y of guanine nucleotide exchange factors for ADP-ribosylation factor 6.

81 ifferentially modulating PKCalpha, RhoA, and ADP-ribosylation factor 6.

82 osomes back to the surface in a small GTPase ADP ribosylation factor-6 (Arf6)-dependent manner.

83 T cells selectively express the small GTPase ADP-ribosylation factor-6 (ARF6), which is involved in m

84 es via a distinct pathway mediated by ARF-6 (ADP-ribosylation factor-6).

85 calize to the plasma membrane, caveolae, and ADP-ribosylation factor-6+ (Arf6+) endocytic compartment

86 tide exchange protein that activates class I ADP-ribosylation factors and as an AKAP for RIIbeta that

87 ADP-ribosylation factor appears to regulate the budding

88 nucleotide-exchange protein (BIG)2 activates ADP-ribosylation factors, approximately 20-kDa GTPase pr

89 aptor localization: a step that requires the ADP-ribosylation factor ARF, an ATP-dependent step that

90 ADP ribosylation factor (Arf) 6 anchors to the plasma me

91 s and the A subunit of cholera toxin bind to ADP ribosylation factor (ARF) and could modulate its act

92 The ADP ribosylation factor (Arf) and the coat protein compl

93 that functions as an exchange factor for the ADP ribosylation factor (ARF) family of guanosine tripho

94 ADP ribosylation factor (Arf) GTPases are key regulators

95 Here we focused on ADP ribosylation factor (Arf) GTPases, which orchestrate

96 d gamma-ear containing Arf-binding (GGA) and ADP ribosylation factor (Arf) proteins in retrovirus par

97 usly that RalA interacts with PLD activating ADP ribosylation factor (ARF) proteins.

98 anes is initiated by the GTP-binding protein ADP ribosylation factor (ARF), which generates high-affi

99 ng to the 3'-untranslated region (3'-UTR) of ADP ribosylation factor (ARF)1 mRNA has been shown to ta

100 TBC1D24 interacts with ADP ribosylation factor (ARF)6, a small GTPase crucial f

101 mma S) stimulation of adenosine diphosphate (ADP)-ribosylation factor (ARF) and Rho, stimulating rele

102 ide-exchange protein (BIG) 1 activates human ADP-ribosylation factor (ARF) 1 and 3 by accelerating th

103 n A (BFA), Exo1 induces the rapid release of ADP-ribosylation factor (ARF) 1 from Golgi membranes but

104 ADP-ribosylation factor (ARF) 6 regulates endosomal plas

105 ADP-ribosylation factor (Arf) 6 regulates the movement o

106 The ADP-ribosylation factor (ARF) 6 small GTPase regulates v

107 77 as an interactor with active small GTPase ADP-ribosylation factor (ARF) 6, but not ARF1.

108 ACAP1, a GTPase-activating protein (GAP) for ADP-ribosylation factor (ARF) 6, is part of a novel clat

109 ly sensitive to brefeldin A, an inhibitor of ADP-ribosylation factor (Arf) activation.

110 ADP-ribosylation factor (Arf) and Arf-like (Arl) protein

111 teps in the late secretory pathway requiring ADP-ribosylation factor (ARF) and clathrin.

112 nriched membranes by a process that requires ADP-ribosylation factor (ARF) and GTP but no other prote

113 f which seems to involve the small G protein ADP-ribosylation factor (ARF) and its physical associati

114 ynergistic manner by protein kinase C (PKC), ADP-ribosylation factor (ARF) and Rho family members.

115 ammalian cells to assess the requirement for ADP-ribosylation factor (ARF) binding to localization an

116 ino acid GTPase activating protein (GAP) for ADP-ribosylation factor (ARF) contains an amino-terminal

117 ADP-ribosylation factor (ARF) describes a family of GTPa

118 ein (AP)1 complexes and small GTPases of the ADP-ribosylation factor (ARF) family and to explore the

119 The ADP-ribosylation factor (Arf) family of GTP-binding prot

120 x-ray crystallography for two members of the ADP-ribosylation factor (ARF) family of regulatory GTPas

121 ADP-ribosylation factor (Arf) family of small GTP-bindin

122 Members of the ADP-ribosylation factor (Arf) family of small GTPases ar

123 e analyzed the role of ARF6, a member of the ADP-ribosylation factor (ARF) family of small GTPases, i

124 lite known to prevent normal function of the ADP-ribosylation factor (ARF) family of small GTPases.

125 e-activating proteins (GAPs) that act on the ADP-ribosylation factor (ARF) family of small GTPases.

126 was dependent on both its RING E3 ligase and ADP-ribosylation factor (ARF) GTPase activity.

127 otein-coupled receptor kinases and possesses ADP-ribosylation factor (ARF) GTPase-activating protein

128 At least six ADP-ribosylation factor (Arf) GTPase-activating proteins

129 icking using a functional screen, and report ADP-ribosylation factor (ARF) GTPases and p21-activated

130 The eukaryotic family of ADP-ribosylation factor (Arf) GTPases plays a key role i

131 nucleotide-exchange factors (GEFs) activate ADP-ribosylation factor (ARF) GTPases that recruit coat

132 otide-exchange proteins (GEPs) that activate ADP-ribosylation factor (ARF) GTPases, brefeldin A-inhib

133 NO, a guanine nucleotide exchange factor for ADP-ribosylation factor (ARF) GTPases, induces Madin-Dar

134 hange proteins (GEPs) BIG1 and BIG2 activate ADP-ribosylation factor (ARF) GTPases, which are require

135 GEP(100) (p100) was identified as an ADP-ribosylation factor (ARF) guanine nucleotide-exchang

136 The small GTP-binding protein ADP-ribosylation factor (ARF) has been shown to regulate

137 ADP-ribosylation factor (ARF) mediated recruitment of CO

138 s GTP-dependent, mimicked by the addition of ADP-ribosylation factor (ARF) nucleotide binding site op

139 investigated the participation of endogenous ADP-ribosylation factor (ARF) nucleotide-binding site op

140 The ADP-ribosylation factor (ARF) proteins initiate vesicula

141 The stoichiometry of the binding of GTP to ADP-ribosylation factor (ARF) proteins, normally quite l

142 Members of the ADP-ribosylation factor (ARF) small GTPase family regula

143 The ADP-ribosylation factor (ARF) subfamily of small GTPases

144 type IV transporter where it acts to recruit ADP-ribosylation factor (Arf) to pathogen-containing pha

145 Protein Kinase C, ADP-ribosylation factor (ARF), and Rho family members ac

146 guanine nucleotide-binding proteins, Rho and ADP-ribosylation factor (ARF), are involved in the regul

147 ly dependent on the protein cofactor, termed ADP-ribosylation factor (ARF), that is itself a 20 kDa r

148 Golgi-localized gamma-ear homology domain, ADP-ribosylation factor (ARF)-binding proteins (GGAs) fa

149 ough the phospholipase D (PLD) pathway in an ADP-ribosylation factor (ARF)-dependent manner that seem

150 essed in COS7 cells substantially utilize an ADP-ribosylation factor (ARF)-dependent route of PLD act

151 dy we investigate the roles of the cytohesin ADP-ribosylation factor (ARF)-guanine nucleotide exchang

152 Golgi-associated, gamma-adaptin homologous, ADP-ribosylation factor (ARF)-interacting proteins (GGAs

153 results in the sequential recruitment of the ADP-ribosylation factor (Arf)-like protein Arl1; the Arf

154 We found that silencing of the ADP-ribosylation factor (Arf)-like small GTPase Arl13b l

155 SRbeta is related to ADP-ribosylation factor (ARF)-type GTPases, and the rece

156 interacts with the 3'-untranslated region of ADP-ribosylation factor (Arf)1 mRNA.

157 enetic screen for IpaJ substrates identified ADP-ribosylation factor (ARF)1p and ARF2p, small molecul

158 Endocytosis of SNAP25 is regulated by ADP-ribosylation factor (ARF)6 (through phosphatidylinos

159 Previous studies indicated that ADP-ribosylation factor (ARF)6 and its GTP-exchange fact

160 or nucleotide-binding site opener (ARNO) and ADP-ribosylation factor (ARF)6 have important roles in t

161 hat catalyzes guanine nucleotide exchange on ADP-ribosylation factors (ARF) 1 and 5 as well as a plec

162 nge proteins (BIG) 1 and BIG2 activate human ADP-ribosylation factors (ARF) 1 and ARF3 by catalyzing

163 ASAP1 (ADP ribosylation factor [ARF]- GTPase-activating protein

164 We demonstrated the presence of ADP-ribosylation factor Arf1 and Arf6 in clonal beta-cel

165 G1, a guanine nucleotide exchange factor for ADP-ribosylation factor (Arf1), as a potential binding p

166 cleotide-exchange protein, activates class I ADP-ribosylation factors (ARF1-3) by catalyzing the repl

167 ADP-ribosylation factor, ARF1, triggers vesicle coat ass

168 a specific interaction with the small GTPase ADP-ribosylation factor (ARF5) in its active, GTP-bound

169 tide exchange factor of the small G proteins ADP ribosylation factors (Arfs) 1 and 6, and blocked by

170 ADP ribosylation factors (ARFs) are approximately 20-kDa

171 ADP ribosylation factors (Arfs) are members of a family

172 ADP ribosylation factors (Arfs) are small GTP-binding pr

173 ADP ribosylation factors (Arfs) are the central regulato

174 d BIG2 activate, through their Sec7 domains, ADP ribosylation factors (Arfs) by accelerating the repl

175 e-exchange protein (BIG) 1 activates class I ADP ribosylation factors (ARFs) by accelerating the repl

176 The predicted protein is related to ADP ribosylation factors (ARFs), members of the RAS fami

177 Host ADP-ribosylation factors (ARFs) act as in vitro alloster

178 ADP-ribosylation factors (Arfs) and Arf GTPase-activatin

179 Despite the 40-60% identity between ADP-ribosylation factors (ARFs) and ARF-like (ARL) prote

180 ADP-ribosylation factors (ARFs) and ARF-like proteins (A

181 f modular adaptor-related proteins that bind ADP-ribosylation factors (ARFs) and localize to the tran

182 ADP-ribosylation factors (ARFs) and their activating gua

183 ADP-ribosylation factors (Arfs) are 21-kDa GTPases that

184 ADP-ribosylation factors (ARFs) are critical in vesicula

185 The ADP-ribosylation factors (Arfs) are six proteins within

186 factors 1 and 2 (BIG1 or BIG2) that activate ADP-ribosylation factors (Arfs) by accelerating the repl

187 ADP-ribosylation factors (ARFs) have been reported to fu

188 ADP-ribosylation factors (ARFs) have crucial roles in ve

189 Activation of ADP-ribosylation factors (ARFs) is mediated by guanine n

190 t facilitates interaction with the cytosolic ADP-ribosylation factors (ARFs) that serve as allosteric

191 nucleotide exchange factors (GEFs) activate ADP-ribosylation factors (ARFs) to facilitate coating of

192 eaction is allosterically activated by human ADP-ribosylation factors (ARFs), a family of essential a

193 Activation of ADP-ribosylation factors (ARFs), approximately 20-kDa GT

194 Activation of ADP-ribosylation factors (ARFs), approximately 20-kDa gu

195 e nucleotide-exchange proteins that activate ADP-ribosylation factors (ARFs), critical components of

196 This is particularly true for the ADP-ribosylation factors (ARFs), GTPases that regulate v

197 A second class of GTPases, the ADP-ribosylation factors (ARFs), have also been implicat

198 s as a guanine nucleotide exchange factor of ADP-ribosylation factors (Arfs), is critical for Rickett

199 uanine nucleotide-exchange protein (GEP) for ADP-ribosylation factors (ARFs), named ARF-GEP(100), whi

200 Vesicular trafficking is controlled by ADP-ribosylation factors (ARFs), which are active in the

201 interaction with eukaryotic proteins termed ADP-ribosylation factors (ARFs).

202 perfamily comprises 5 subfamilies (Ras, Rho, ADP ribosylation factors [ARFs], Rab, and Ran) that act

203 rthermore, GRASP colocalized with endogenous ADP-ribosylation factors at the plasma membrane in trans

204 with Golgi-localized, gamma-ear-containing, ADP-ribosylation factor binding proteins (GGAs), and Arf

205 omer recruitment is a step that occurs after ADP-ribosylation factor binding to the membrane.

206 Golgi-localized, gamma-ear-containing, Arf (ADP-ribosylation factor)-binding (GGA) proteins are clat

207 olgi-localized, gamma adaptin-ear-containing ADP ribosylation factor-binding protein 3 (GGA3) interac

208 ocalized, gamma-adaptin ear domain homology, ADP ribosylation factor-binding protein 3), a multidomai

209 ocalized, gamma-adaptin ear domain homology, ADP ribosylation factor-binding proteins 1 and 2 (GGA1 a

210 GGAs (Golgi-localized, gamma ear-containing, ADP ribosylation factor-binding proteins) are multidomai

211 GGA (Golgi-associated, gamma-ear-containing, ADP-ribosylation factor-binding protein) on SG maturatio

212 Golgi-localized, gamma-Ear-containing, ADP-ribosylation factor-binding proteins (GGAs) and adap

213 ) and Golgi-localized, gamma ear-containing, ADP-ribosylation factor-binding proteins (GGAs) are both

214 The Golgi-associated gamma-adaptin-related ADP-ribosylation factor-binding proteins (GGAs) are crit

215 Human Golgi-localized, gamma-ear-containing, ADP-ribosylation factor-binding proteins (Ggas) bind dir

216 GGA (Golgi-localized, gamma-ear-containing, ADP-ribosylation-factor-binding) proteins.

217 afficking by accelerating the replacement of ADP-ribosylation factor-bound GDP with GTP.

218 e the binding protein modified activation of ADP ribosylation factor by cytohesin-1, we designate thi

219 uanine nucleotide-exchange proteins activate ADP-ribosylation factors by accelerating the replacement

220 s was recapitulated by expression of the Rho ADP-ribosylation factor (C3ADP) in combination with cons

221 n interaction motif immediately preceding an ADP-ribosylation factor domain at the C terminus, belong

222 acts as a GTPase-activating protein for the ADP-ribosylation factor domain of ARD1.

223 ADP-ribosylation factor domain protein 1 (ARD1) is a 64-

224 ARD1 (ADP-ribosylation factor domain protein 1), with a RING f

225 in (ARD1), a 64-kDa GTPase with a C-terminal ADP-ribosylation factor domain, is localized to lysosome

226 Nuf is a homologue of arfophilin-2, an ADP ribosylation factor effector that binds Rab11 and in

227 ARL13B is a member of the ADP ribosylation factor family of regulatory GTPases, bu

228 entified a GTPase-activating protein for the ADP ribosylation factor family of small GTP-binding prot

229 Arl13b, a ciliary protein within the ADP-ribosylation factor family and Ras superfamily of GT

230 TPase-activating protein, is a member of the ADP-ribosylation factor family encoded by a gene located

231 Arl2 is a member of the ADP-ribosylation factor family of 20-kDa GTPases that is

232 e guanine nucleotide exchange factor for the ADP-ribosylation factor family of proteins.

233 Arl13b belongs to the ADP-ribosylation factor family within the Ras superfamil

234 und a gene at 13q14, ARLTS1, a member of the ADP-ribosylation factor family, with properties of a tum

235 , BIG1 and BIG2, are important activators of ADP-ribosylation factors for vesicular trafficking.

236 ers of the cytohesin family, which are known ADP-ribosylation factors-GDP/GTP exchange factors, and i

237 calizing, gamma-adaptin ear homology domain, ADP-ribosylation factor (GGA)-binding motif affects the

238 e those regulated by GTP exchange factors on ADP-ribosylation factors GNOM-LIKE1 and HOPM INTERACTOR7

239 is a 64-kDa protein containing a functional ADP-ribosylation factor (GTP hydrolase, GTPase), GTPase-

240 ndicating that the responsible BFA-sensitive ADP ribosylation factor-GTP exchange factor (ARF-GEF) is

241 SFC encodes an ADP ribosylation factor GTPase activating protein (ARF-G

242 omology protein, and MTV4, which encodes the ADP ribosylation factor GTPase-activating protein nevers

243 o the guanine-nucleotide exchange factor for ADP-ribosylation factor GTPase (ARF-GEF) inhibitor brefe

244 both molecules at the TGN is dependent upon ADP-ribosylation factor GTPase activity.

245 Mutations in SFC/VAN3, an ADP-ribosylation factor GTPase-activating protein (ARF G

246 DEF-1/ASAP1 is an ADP-ribosylation factor GTPase-activating protein (ARF G

247 These studies identify the ADP-ribosylation factor GTPase-activating protein Centau

248 owers without functional NEVERSHED (NEV), an ADP-ribosylation factor GTPase-activating protein requir

249 Previously, we characterized an ADP-ribosylation factor GTPase-activating protein, NEVER

250 members of the AGAP subfamily of ASAP family ADP-ribosylation factor GTPase-activating proteins (Arf

251 l 3-kinase-sensitive and brefeldin-sensitive ADP-ribosylation factor GTPase-regulated mechanism.

252 two ankyrin repeats domains, and C-terminal ADP ribosylation factor-GTPase-activating protein activa

253 ms contain GTPase, pleckstrin homology (PH), ADP ribosylation factor-GTPase-activating protein, and t

254 report genetic evidence to suggest that two ADP ribosylation factor-GTPase-activating proteins (ARFG

255 ing were found to disrupt the function of an ADP-ribosylation factor-GTPase-activating protein (ARF-G

256 Cat-1) is a signaling scaffold as well as an ADP-ribosylation factor-GTPase-activating protein.

257 e proteins, BIG1 and BIG2, are activators of ADP-ribosylation factor GTPases that are essential for r

258 EFs (guanine-nucleotide exchange factors for ADP-ribosylation factor GTPases) are essential for vesic

259 cytic and recycling pathways mediated by the ADP ribosylation factor guanine nucleotide exchange fact

260 Pst) DC3000 infection of Arabidopsis, a host ADP ribosylation factor guanine nucleotide exchange fact

261 ther of two human genes, Filamin A (FLNA) or ADP-ribosylation factor guanine exchange factor 2 (ARFGE

262 evelopment associated with gene mutations in ADP-ribosylation factor guanine exchange factor 2 (ARFGE

263 Human mutations in the Filamin A (FLNA) and ADP-ribosylation factor guanine exchange factor 2 [ARFGE

264 Mutations in the vesicle transport ADP-ribosylation factor guanine exchange factor 2 gene (

265 me 20 and is caused by mutations in the gene ADP-ribosylation factor guanine nucleotide-exchange fact

266 HLB1 was found to interact with the ADP-ribosylation-factor guanine nucleotide exchange fact

267 UNC50 acted by recruiting GBF1, an ADP ribosylation factor-guanine nucleotide exchange fact

268 or the function of the brefeldin A-sensitive ADP-ribosylation factor-guanine exchange factors (ARF-GE

269 involvement of heterotrimeric G-proteins and ADP-ribosylation factor in the transport event(s).

270 GBF1 guanine nucleotide exchange factor for ADP-ribosylation factor inhibits CFTR trafficking to the

271 Here, we show that Drosophila ADP ribosylation factor like-2 (Arl2) and Msps, a known

272 Five conserved tubulin cofactors and ADP ribosylation factor-like 2 regulate the biogenesis a

273 RP2 has also been shown to interact with ADP ribosylation factor-like 3 (Arl3) in a nucleotide an

274 y, we find that RP2 interacts with GTP-bound ADP ribosylation factor-like 3 protein, providing a link

275 The gene for ADP ribosylation factor-like GTPase 13B (Arl13b) encodes

276 The ADP ribosylation factor-like proteins (Arls) are a famil

277 BBS3 (ARL6), an ADP ribosylation factor-like small GTPase, is not part o

278 PP5E is facilitated by another JBTS protein, ADP-ribosylation factor-like 13B (ARL13B), but not by AR

279 gulation of GliA and GliR: the cilia protein ADP-ribosylation factor-like 13b (Arl13b).

280 The ADP-ribosylation factor-like 2 (ARL2) GTPase and its bin

281 y of native tubulin, a reaction regulated by ADP-ribosylation factor-like 2 protein.

282 ADP-ribosylation factor-like 3 (Arl3) is a member of a s

283 The small GTPase, ADP-ribosylation factor-like 3 (ARL3), has been proposed

284 The ADP-ribosylation factor-like 4C (Arl4C) small GTPase act

285 One of these genes, ADP-ribosylation factor-like 6 (ARL6), contains a homozy

286 tin, the product of the mouse cpk locus, and ADP-ribosylation factor-like 6, the product of the human

287 report the crucial role of the small GTPase ADP-ribosylation factor-like 8b (Arl8b) in MHC II presen

288 re, we identify a small GTP-binding protein, ADP-ribosylation factor-like 8b (Arl8b), as a critical f

289 Herein, we investigated the protein ADP-ribosylation factor-like GTPase 13b (ARL13b) as a mo

290 Small G-proteins of the ADP-ribosylation-factor-like (Arl) subfamily have been s

291 Arf activation by GTP and ADP ribosylation factor nucelotide-binding site opener p

292 CGR-dependent desensitization is mimicked by ADP ribosylation factor nucleotide-binding site opener,

293 nucleotide exchange factors (GEFs), such as ADP-ribosylation factor nucleotide binding site opener (

294 hat an Arf-nucleotide exchange factor, ARNO (ADP-ribosylation factor nucleotide site opener) as well

295 l imaging of green fluorescent protein (GFP) ADP-ribosylation factor nucleotide-binding site opener (

296 ADP-ribosylation factor nucleotide-binding site opener (

297 g the Golgi membrane/cytosol partitioning of ADP-ribosylation factor proteins.

298 ion of a Golgi-associated phospholipase D by ADP-ribosylation factor results in the hydrolysis of pho

299 ble components, including COPI (coatomer and ADP-ribosylation factor), results in the release of retr

300 sociation of the activated lipase, RhoA, and ADP-ribosylation factor with the actin-based membrane sk