ライフサイエンスコーパス: peripheral membrane protein

1 rotein confirmed that SA0422 is an acylated, peripheral membrane protein.

2 epresented 9% of total SUS and occurred as a peripheral membrane protein.

3 n studies demonstrated that P31(LipL45) is a peripheral membrane protein.

4 Biochemical studies revealed that Apg2 is a peripheral membrane protein.

5 H solutions, which indicates that NBCCV is a peripheral membrane protein.

6 y salt or carbonate, indicating that it is a peripheral membrane protein.

7 ergent Triton X-114 indicated that BtpA is a peripheral membrane protein.

8 compartment depends on Vps35p, a hydrophilic peripheral membrane protein.

9 and at least a portion of it behaves like a peripheral membrane protein.

10 lized to the FBPase-containing vesicles as a peripheral membrane protein.

11 cated on the inner face of the membrane as a peripheral membrane protein.

12 ion with 0.8 M NaCl, suggesting that it is a peripheral membrane protein.

13 suggests that A-FABP behaves like a typical peripheral membrane protein.

14 x g membrane fraction and is associated as a peripheral membrane protein.

15 The results show that Naa60 is a peripheral membrane protein.

16 blackout, which we found was a palmitoylated peripheral membrane protein.

17 ordingly, we provide evidence that AGO1 is a peripheral membrane protein.

18 raft, localization, even when expressed as a peripheral membrane protein.

19 ure can serve as a cue for localization of a peripheral membrane protein.

20 RS in intact retina is a peripheral membrane protein.

21 ane at high pH, which is characteristic of a peripheral membrane protein.

22 s resistant to treatments that would release peripheral membrane proteins.

23 Rab1 effectors p115 and GM130 but not other peripheral membrane proteins.

24 ch for investigating the binding geometry by peripheral membrane proteins.

25 tructures that contain specific membrane and peripheral membrane proteins.

26 function in the context of both integral and peripheral membrane proteins.

27 ecialized lipid domains in axonal sorting of peripheral membrane proteins.

28 alt and high-pH treatments that release most peripheral membrane proteins.

29 ct with 1.0 M NaCl, suggesting that they are peripheral membrane proteins.

30 to the mode of interaction for this class of peripheral membrane proteins.

31 tions alter the localization and function of peripheral membrane proteins.

32 ATP hydrolysis, and depends on cytosolic and peripheral membrane proteins.

33 of a lipid bilayer studded with integral and peripheral membrane proteins.

34 ic protein-lipid code for the recruitment of peripheral membrane proteins.

35 et of structurally diverse transmembrane and peripheral membrane proteins.

36 Drosophila to explore lysine acetylation in peripheral membrane proteins.

37 uding many GPCRs, receptors/ion channels and peripheral membrane proteins.

38 ation of NM2s with membrane-bound F-actin or peripheral membrane proteins.

39 is a critical function of many integral and peripheral membrane proteins.

40 ated here may be extended to a wide range of peripheral membrane proteins.

41 out the membrane-attachment mechanics of any peripheral membrane proteins.

42 actions and can be readily adapted for other peripheral membrane proteins.

43 hanges in the membrane docking geometries of peripheral membrane proteins.

44 can alter location and enzymatic function of peripheral membrane proteins.

45 functionally diverse and important class of peripheral membrane proteins.

46 ties and their interaction with integral and peripheral membrane proteins.

47 ws that H. somnus has two IgBPs, including a peripheral membrane protein and a fibrillar surface netw

48 Tim44p is an essential mitochondrial peripheral membrane protein and a major component of TIM

49 e kinase from an integral to a tightly bound peripheral membrane protein and abrogates its catalytic

50 KPP is a peripheral membrane protein and is phosphorylated in pol

51 model accounts for weak membrane binding of peripheral membrane proteins and a leaky connecting cili

52 These two properties, a reliance on peripheral membrane proteins and a structurally distinct

53 inus associates with a group of integral and peripheral membrane proteins and glycoproteins that are

54 Over 30 other peripheral membrane proteins and over 30 transmembrane p

55 ficult to analyze with other methods such as peripheral membrane proteins and peptides that interact

56 ment also containing chromatin, integral and peripheral membrane proteins, and large structures such

57 Water dynamics in the hydration shell of the peripheral membrane protein annexin B12 were studied usi

58 the phosphate level, as demonstrated with a peripheral membrane protein, annexin B12.

59 In neurons, peripheral membrane proteins are enriched in subcellular

60 Several peripheral membrane proteins are known to form membrane

61 Peripheral membrane proteins are targeted to the cytopla

62 subcellular localizations and activities of peripheral membrane proteins, are fundamentally importan

63 anding the organization of ankyrin and other peripheral membrane proteins around band 3.

64 receptor (AChR) requires rapsyn, a synaptic peripheral membrane protein, as well as protein-tyrosine

65 ocusing on transcripts encoding secreted and peripheral membrane proteins, as well as mesenchymal tra

66 Conversely, subpopulations of peripheral membrane proteins, as well as transmembrane o

67 onation experiments indicated that AFL1 is a peripheral membrane protein associated with both plasma

68 ow in 3T3-L1 fibroblasts that tankyrase is a peripheral membrane protein associated with the Golgi.

69 Dematin and protein 4.2 are peripheral membrane proteins associated with the cytopla

70 We demonstrate that VPS13A is a peripheral membrane protein, associated with mitochondri

71 ast two-hybrid-based screen and identified a peripheral membrane protein, Atg11, that interacts with

72 ue was also used to monitor association of a peripheral membrane protein, Bacillus thuringiensis phos

73 This is especially true for peripheral membrane proteins, because they, unlike integ

74 has proven successful for quantification of peripheral membrane protein binding to the PM in living

75 DrrA, a peripheral membrane protein, binds ATP in a UV-catalyzed

76 data confirmed that Pcs60p is a peroxisomal peripheral membrane protein but the protein is also loca

77 rizing atomic details of membrane binding of peripheral membrane proteins by molecular dynamics (MD)

78 Peripheral membrane proteins can be targeted to specific

79 App1 and Pah1 are peripheral membrane proteins catalyzing an Mg(2+)-depend

80 findings indicate that hSec34p is part of a peripheral membrane protein complex localized on cis/med

81 pends on its exchange factor, Ric1p-Rgp1p, a peripheral membrane protein complex restricted to the Go

82 Retromer is a peripheral membrane protein complex that coordinates mul

83 The retromer is a cytosolic/peripheral membrane protein complex that mediates the re

84 onserved oligomeric Golgi (COG) complex is a peripheral membrane protein complex which orchestrates t

85 atasets of 44 transmembrane complexes and 92 peripheral membrane protein complexes, of which it succe

86 b8ip is present both in the cytosol and as a peripheral membrane protein concentrated in the Golgi re

87 Recognition of membrane curvature by peripheral membrane proteins could be a general strategy

88 ytoplasm and at the plasma membrane, such as peripheral membrane proteins, create stratified fluoresc

89 been used to investigate the behavior of the peripheral membrane protein, cytochrome c, covalently te

90 Here we report that localization of the peripheral membrane protein DivIVA is determined in whol

91 A comparison with other peripheral membrane proteins elucidates common and speci

92 1 inhibitor, namely the C2 domain-containing peripheral membrane protein ENHANCED BENDING1 (EHB1).

93 tion of the peptide caused delocalization of peripheral membrane proteins essential for respiration a

94 croscopy, we find that functional Prm3p is a peripheral membrane protein exposed on the cytoplasmic f

95 The structures reveal that Ndi1 is a peripheral membrane protein forming an intimate dimer, i

96 und in association with several integral and peripheral membrane proteins, forming a complex known as

97 pallidin was distributed in both soluble and peripheral membrane protein fractions.

98 membrane system induced by the presence of a peripheral membrane protein from human myelin.

99 Extraction of peripheral membrane proteins from the postnuclear membra

100 prevented cytochrome c, a well characterized peripheral membrane protein, from binding to membranes.

101 h CRBP-I was able to prevent cytochrome c, a peripheral membrane protein, from binding, whereas CRBP-

102 The peripheral membrane protein GAD65 is an autoantigen in h

103 controlling membrane targeting of a typical peripheral membrane protein, Galpha(z), we directed its

104 Analysis of 50 peripheral membrane proteins harboring BAR, PX, C2, or E

105 The S-acylation of peripheral membrane proteins has been proposed to occur

106 Recent studies have implicated the peripheral membrane protein HID-1 in neuropeptide sortin

107 localized on the endoplasmic reticulum as a peripheral membrane protein in a complex with Erf2p, an

108 alized to the intermembrane space (IMS) as a peripheral membrane protein in a multimeric complex.

109 contrary to this belief, CPR can exist as a peripheral membrane protein in the absence of NADPH and

110 cytoplasmic domain (Src-LAT) localized as a peripheral membrane protein in the PM, but outside lipid

111 ctroscopy of a site-selectively spin-labeled peripheral membrane protein in the presence and absence

112 reasons: (i) it binds to and regulates many peripheral membrane proteins in bacteria and mitochondri

113 tal techniques can assess the orientation of peripheral membrane proteins in their native environment

114 prisingly revealed its regulatory roles as a peripheral membrane protein instead of a predicted cell

115 which dynamic intracellular localization of peripheral membrane proteins is achieved by highly selec

116 advance understanding of how S-acylation of peripheral membrane proteins is handled by Golgi zDHHC e

117 ocalization and signaling of S-palmitoylated peripheral membrane proteins is sustained by an acylatio

118 PBP 5, as a representative peripheral membrane protein, is anchored to the cytoplas

119 if the target autoantigen is an integral or peripheral membrane protein, islet cell CM were treated

120 A peripheral membrane protein kinase cdr2p has properties

121 In this way, we identified p115, a peripheral membrane protein known to be involved in memb

122 ne-bound and cytoplasmic concentrations of a peripheral membrane protein labeled by the enhanced gree

123 d physiological consequences associated with peripheral membrane protein localization, only a rudimen

124 In addition, many peripheral membrane proteins localize to the AJC.

125 bsence of detergent suggesting that it was a peripheral membrane protein localized on the cytosolic f

126 Upon starvation, Grh1, a peripheral membrane protein located at endoplasmic retic

127 gral membrane proteins, MalF and MalG, and a peripheral membrane protein, MalK.

128 All peripheral membrane proteins must negotiate unique const

129 (CPE) is a prohormone-processing enzyme and peripheral membrane protein of endocrine/neuroendocrine

130 Rapsyn, a peripheral membrane protein of skeletal muscle, clusters

131 Rapsyn, a 43-kDa peripheral membrane protein of skeletal muscle, is essen

132 Rapsyn, a peripheral membrane protein of skeletal muscle, is neces

133 Myelin protein P2 is a peripheral membrane protein of the fatty acid-binding pr

134 vealed DSP21 is localized to the matrix as a peripheral membrane protein of the inner membrane.

135 8 is located in the intermembrane space as a peripheral membrane protein of the inner membrane.

136 We now demonstrate that Kes1p is a peripheral membrane protein of the yeast Golgi complex,

137 the presence in ROS membranes "stripped" of peripheral membrane proteins of numerous ubiquitin-prote

138 Peripheral membrane proteins of the Bin/amphiphysin/Rvs

139 Syntrophins, a family of intracellular peripheral membrane proteins of the dystrophin-associate

140 Syntrophins are cytoplasmic peripheral membrane proteins of the dystrophin-associate

141 e coil-coil (CC) domain of Grp1 engaging two peripheral membrane proteins of the recycling endosome.

142 nd the applications of the method to include peripheral membrane proteins of the S-layer and amyloid

143 umour cells) and co-stimulation by B7-1&2 (a peripheral membrane protein on dendritic cells).

144 is also no consensus on whether tubulin is a peripheral membrane protein or is integrated into the ou

145 embrane, and can be applied to virtually any peripheral membrane protein or membrane-like structure.

146 proteins LipL32, LipL36, and LipL41; and the peripheral membrane protein P31(LipL45).

147 egion that is modeled as the complex being a peripheral membrane protein partially embedded in the me

148 The enzymatic activity of the peripheral membrane protein, phosphatidylinositol-specif

149 Peripheral membrane proteins (PMPs) include a wide varie

150 tigate polarized targeting of lipid-anchored peripheral membrane proteins, postsynaptic density-95 (P

151 Our findings reveal 45 integral and 51 peripheral membrane proteins re-routed by golgin-97, evi

152 ovel neural/endocrine-specific cytosolic and peripheral membrane protein required for the Ca2+-regula

153 o known as CADPS) is a 145-kDa cytosolic and peripheral membrane protein required for vesicle docking

154 studies suggest that dynein binds to a Golgi peripheral membrane protein(s) that resists extraction b

155 with Sam35 in precursor recognition, and the peripheral membrane protein Sam37.

156 n of either the salt-extracted mitochondrial peripheral membrane proteins (SE), or a protein fraction

157 ity of tER sites in P. pastoris requires the peripheral membrane protein Sec16.

158 s remained at their normal levels, the major peripheral membrane proteins spectrin, adducin, and acti

159 We found that the peripheral membrane protein SpoVM (VM) recognizes a geom

160 ne receptors (nAChRs) and other integral and peripheral membrane proteins such as beta-dystroglycan a

161 timized the anchor-away method, which allows peripheral membrane proteins such as COPI to be sequeste

162 acting proteins, actin binding proteins, and peripheral membrane proteins such as F-BAR proteins.

163 Peripheral membrane proteins such as these GEFs are ofte

164 technique to investigate the binding of two peripheral membrane protein systems for which previous z

165 is present in purified Golgi membranes as a peripheral membrane protein, targeted by its globular ta

166 In this paper, we find that SPK1 is a peripheral membrane protein that accumulates at, and pro

167 AtVPS45p is a peripheral membrane protein that associates with microso

168 Rapsyn, an intracellular peripheral membrane protein that binds AChRs, is essenti

169 We show here that supervillin (SV), a peripheral membrane protein that binds F-actin and myosi

170 We show that supervillin (SV)--a peripheral membrane protein that binds myosin II and F-a

171 rotein thought to be involved is gephyrin, a peripheral membrane protein that binds to the inhibitory

172 Cvt19 is a peripheral membrane protein that binds to the precursor

173 Dsl1p is an ER-localized peripheral membrane protein that can be extracted from t

174 RAPSN encodes rapsyn, a 43 kDa postsynaptic peripheral membrane protein that clusters the nicotinic

175 The RGS9-1 kinase is a peripheral membrane protein that co-purifies with rhodop

176 In summary, SYT7 is a peripheral membrane protein that controls multiple modes

177 p205 is a tightly bound peripheral membrane protein that cosediments with endoge

178 ts in the case of the fourth enzyme, LpxH, a peripheral membrane protein that hydrolyzes UDP-2,3-diac

179 The addition of MinD, a peripheral membrane protein that interacts with MinC, re

180 lar fractions and established that HMW1 is a peripheral membrane protein that is antibody accessible

181 Thus, Jsn1p is a peripheral membrane protein that is associated with the

182 Dok7 is a peripheral membrane protein that is associated with the

183 ver of its interaction with rapsyn, a 43 kDa peripheral membrane protein that is closely associated w

184 ue fractionation revealed that CRHSP-28 is a peripheral membrane protein that is highly enriched in s

185 A peripheral membrane protein that is interactive with lym

186 contrast to previous suggestions, RPM1 is a peripheral membrane protein that likely resides on the c

187 2, the ABA receptor in mammalian cells, is a peripheral membrane protein that localizes at the intrac

188 ssociates with both Tor1p and Tor2p and is a peripheral membrane protein that localizes to endosomal

189 Coq6p is a peripheral membrane protein that localizes to the matrix

190 We also demonstrate that ARG1 is a peripheral membrane protein that may share some subcellu

191 gA glycosyltransferase (also called TarA), a peripheral membrane protein that produces the conserved

192 lagen-like protein (Lcl) is an extracellular peripheral membrane protein that recognises sulphated gl

193 We also demonstrate that Atg23 is a peripheral membrane protein that requires the presence o

194 ensity-95 (PSD-95/SAP-90) is a palmitoylated peripheral membrane protein that scaffolds ion channels

195 c oxide synthase (eNOS) is a dually acylated peripheral membrane protein that targets to the Golgi re

196 They are peripheral membrane proteins that are encoded in operons

197 n stomatin-domain genes, all of which encode peripheral membrane proteins that can modulate ion chann

198 l and biochemical data showing that CARs are peripheral membrane proteins that functionally cluster o

199 is mid1p (anillin-like protein), which is a peripheral-membrane protein that forms a broad cortical

200 The method is applied to two peripheral membrane proteins, the early endosome antigen

201 ins, the Vo sector, attached to a complex of peripheral membrane proteins, the V1 sector.

202 e G protein cascade of vision depends on two peripheral membrane proteins: the G protein, transducin

203 helices in a helical hairpin while CetB is a peripheral membrane protein tightly associated with the

204 when expressed in CHO cells and behaves as a peripheral membrane protein, tightly associated with the

205 It is well established that an essential peripheral membrane protein, Tim44, tethers mitochondria

206 s a cytosolic protein, AFABP may behave as a peripheral membrane protein to help target fatty acids t

207 acid sequence that specifies targeting of a peripheral membrane protein to the basolateral membrane

208 -protein interaction controls targeting of a peripheral membrane protein to the proper compartment, w

209 The Rab GTPases recruit peripheral membrane proteins to intracellular organelles

210 They can anchor peripheral membrane proteins to the membrane, be attache

211 Peripheral membrane proteins utilize a variety of mechan

212 nteract with a variety of other integral and peripheral membrane proteins via a diversity of protein-

213 Putative peroxisomal peripheral membrane proteins were isolated by successive

214 drolases like CPY and PrA, while Vps35p is a peripheral membrane protein which cofractionates with me

215 Syntrophins are peripheral membrane proteins which have been found assoc

216 domains are lipid-binding modules present in peripheral membrane proteins which interact with phospha

217 This model may be operational in other peripheral membrane proteins with an unprecedented impac

218 Cavins are cytosolic peripheral membrane proteins with negatively charged int

219 very little is known about the targeting of peripheral membrane proteins within these cells.

220 scarinic receptor subtypes M1 and M3 and the peripheral membrane protein ZO-1 were analyzed by immuno