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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

19 RS in intact retina is a peripheral membrane protein.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 functionally diverse and important class of peripheral membrane proteins.

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

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

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

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

41 tructures that contain specific membrane and peripheral membrane proteins.

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

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

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

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

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

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

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

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

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

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

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

53 Peripheral membrane proteins are targeted to the cytopla

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 Peripheral membrane proteins can be targeted to specific

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 Extraction of peripheral membrane proteins from the postnuclear membra

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

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

87 The peripheral membrane protein GAD65 is an autoantigen in h

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 A peripheral membrane protein kinase cdr2p has properties

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

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

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

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

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

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

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

111 All peripheral membrane proteins must negotiate unique const

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

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

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

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

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

117 8 is located in the intermembrane space as a peripheral membrane protein of the inner membrane.

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

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

120 Peripheral membrane proteins of the Bin/amphiphysin/Rvs

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 Peripheral membrane proteins such as these GEFs are ofte

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

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

143 AtVPS45p is a peripheral membrane protein that associates with microso

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 A peripheral membrane protein that is interactive with lym

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

161 2, the ABA receptor in mammalian cells, is a peripheral membrane protein that localizes at the intrac

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

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

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

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

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

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

168 They are peripheral membrane proteins that are encoded in operons

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

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

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

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

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

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

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

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

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

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

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

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

181 The Rab GTPases recruit peripheral membrane proteins to intracellular organelles

182 Peripheral membrane proteins utilize a variety of mechan

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

184 Putative peroxisomal peripheral membrane proteins were isolated by successive

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

186 Syntrophins are peripheral membrane proteins which have been found assoc

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

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

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