ライフサイエンスコーパス: intrinsic protein

1 f the fiber cell-specific protein MIP (major intrinsic protein).

2 a membrane intrinsic proteins from tonoplast intrinsic proteins.

3 re not present in any of the known tonoplast intrinsic proteins.

4 a) and plants overexpressing plasma membrane intrinsic protein 1;4 (PIP1;4) and PIP2;5.

5 al sites (Ser280, Ser283) of PLASMA MEMBRANE INTRINSIC PROTEIN 2;1 (AtPIP2;1), a major plasma membran

6 thaliana plants lacking the Plasma membrane Intrinsic Protein 2;1 (PIP2;1) aquaporin have a defect i

7 cluded expression of crystallins, lens major intrinsic protein 26 (MIP26), CP49, and filensin and mor

8 a protein of unknown function known as Major Intrinsic Protein 26.

9 eptide antibodies specific for the tonoplast intrinsic proteins alpha-TIP, gamma-TIP, and delta-TIP i

10 e that antibodies to two different tonoplast intrinsic proteins, alpha-TIP and TIP-Ma27, label vacuol

11 bidopsis aquaporin, delta-TIP (for tonoplast intrinsic protein), and show that it is located in the t

12 ase), phosphoenolpyruvate carboxylase, major intrinsic protein, and alpha-tubulin were amplified by p

13 e directly from the ER; a specific tonoplast intrinsic protein; and a novel receptor-like RING-H2 pro

14 tis vinifera) VvPIP2;4N (for Plasma membrane Intrinsic Protein) aquaporin gene.

15 Nodulin 26, a member of the major intrinsic protein/aquaporin (AQP) channel family, is a m

16 cript abundance of Zea maize Plasma Membrane Intrinsic Protein aquaporins.

17 In contrast, the granule-intrinsic proteins are prone to covalent modification, b

18 belong to family of NIP2s (Nod26-like major intrinsic protein), bona fide silicon transporters, wher

19 The intrinsic protein characteristics of globular proteins w

20 urfaces are readily patternable, incorporate intrinsic protein charge into the film, and able to cont

21 s critically dependent on chloride ions, and intrinsic protein charges also play a role.

22 In green plants, several intrinsic protein components of the photosystem II (PS I

23 ess of specific cuts of meat, based on their intrinsic protein composition.

24 The stem cell intrinsic proteins controlling this switch are largely u

25 Vavouri et al. find that intrinsic protein disorder and promiscuous molecular int

26 We found that accounting for intrinsic protein disorder and the unbiased mass spectro

27 hich the structural flexibility conferred by intrinsic protein disorder can be functionally advantage

28 lex showed that environmental control of the intrinsic protein disorder could in principle explain th

29 Intrinsic protein disorder is functionally implicated in

30 The contribution of intrinsic protein disorder to the nature and function of

31 structural and functional information about intrinsic protein disorder, aggregating annotations from

32 43%) and highlights functional importance of intrinsic protein disorder.

33 Since ligand binding may be influenced by intrinsic protein dynamical properties, we have characte

34 ucture and function and, more recently, that intrinsic protein dynamics at different time scales enab

35 substrate-induced conformational change and intrinsic protein dynamics.

36 We conclude that individual granule intrinsic proteins exist as monomers and are not deposit

37 anogaster, we show that 4 genes of the major intrinsic protein family are expressed at a very high le

38 efine a new evolutionary branch of the major intrinsic protein family of aquaporin proteins and descr

39 n (BIB) has sequence identity with the major intrinsic protein family that includes the water- and io

40 emical and biophysical descriptors uncovered intrinsic protein features that account for ~15% of secr

41 aration of specimens of adequate quality and intrinsic protein flexibility, rather than imaging or im

42 pha-lactalbumin (alpha-LA) has been shown by intrinsic protein fluorescence and electron spin resonan

43 Altered intrinsic protein fluorescence and highly cooperative bi

44 e change is accompanied by a decrease of the intrinsic protein fluorescence and is essential to creat

45 resolving changes in the label fluorescence, intrinsic protein fluorescence as well as in the absorpt

46 we have taken advantage of the quenching of intrinsic protein fluorescence by bound metal ions to co

47 and van't Hoff enthalpy changes derived from intrinsic protein fluorescence changes were in agreement

48 The quenching of intrinsic protein fluorescence confirmed that the curcum

49 he kinetic profiles for the quenching of the intrinsic protein fluorescence during the course of the

50 bodies, this study investigates the observed intrinsic protein fluorescence emission spectra as a fun

51 as well as a 20 % weaker, 10 nm red-shifted intrinsic protein fluorescence emission spectrum.

52 trate that assaying leuprolide release using intrinsic protein fluorescence in a 96-well format requi

53 3 muM as assessed by changes in DREAM/KChIP3 intrinsic protein fluorescence in the presence of CaM.

54 This suggests that solid state, intrinsic protein fluorescence measurements using the Ca

55 strated to contribute to the large change in intrinsic protein fluorescence observed when the enzyme

56 riophage T7 by monitoring alterations in the intrinsic protein fluorescence of RNA polymerase in stop

57 nto an EC as monitored by alterations in the intrinsic protein fluorescence of the core polymerase re

58 kinetic studies involving alterations in the intrinsic protein fluorescence of the core polymerase up

59 calculated from data in which changes in the intrinsic protein fluorescence of the enzyme associated

60 ration is followed either by a change in the intrinsic protein fluorescence on ligand release, or by

61 Further experience with the intrinsic protein fluorescence quenching approach to mon

62 IT purified as a monomer and, as measured by intrinsic protein fluorescence quenching, bound Fe(2+) i

63 bining and automating circular dichroism and intrinsic protein fluorescence spectroscopy.

64 Intrinsic protein fluorescence studies were consistent w

65 s was monitored by following the increase in intrinsic protein fluorescence that occurs upon ligand d

66 n derivatives of ArsD exhibited quenching of intrinsic protein fluorescence upon binding of As(III) o

67 tifying the time-dependent increase in total intrinsic protein fluorescence was assessed.

68 The intrinsic protein fluorescence was attributed primarily

69 The effect of As(III) or Sb(III) on intrinsic protein fluorescence was used to examine the p

70 (BIP)(2)B quenched NS3 intrinsic protein fluorescence with an apparent dissocia

71 ditions using a combination of solution NMR, intrinsic protein fluorescence, and chromophoric chelato

72 were determined by monitoring changes in the intrinsic protein fluorescence, in the fluorescence of f

73 uench fluorophores that are red-shifted from intrinsic protein fluorescence, such as acridone.

74 e Glu-98 or on its potential contribution to intrinsic protein fluorescence.

75 the enzyme with concomitant quenching of the intrinsic protein fluorescence.

76 xtend the use of in vitro phasor analysis to intrinsic protein fluorescence.

77 g far UV circular dichroism spectroscopy and intrinsic protein fluorescence.

78 change is associated with a repositioning of intrinsic protein fluorophores from a hydrophobic to a s

79 al features that distinguish plasma membrane intrinsic proteins from tonoplast intrinsic proteins.

80 the tonoplast aquaporin gamma-TIP (tonoplast intrinsic protein) from Arabidopsis.

81 tein stability, subcellular localization, or intrinsic protein function.

82 ive spatiotemporal expression and not by its intrinsic protein functions.

83 a green fluorescent protein-delta tonoplast intrinsic protein fusion.

84 Here, three plasma membrane intrinsic protein genes, SlPIP2;1, SlPIP2;7 and SlPIP2;5

85 ; thus, the tonoplast marker delta-tonoplast intrinsic protein-green fluorescent protein delineates c

86 e selectivity for the barley Nodulin 26-like Intrinsic Protein (HvNIP2;1) embedded in liposomes and e

87 Aquaporin 0 (AQP0) is the major intrinsic protein in the lens and is essential for estab

88 Aquaporin-0 (AQP0) is the most prevalent intrinsic protein in the plasma membrane of lens fiber c

89 disease and may hold promise as a potential intrinsic protein inhibitor.

90 These data establish intrinsic protein instability as the generalizable, prim

91 The process of insertion of intrinsic proteins into phospholipid membranes conjures

92 xamer containing 24 +/- 3 helices, the major intrinsic protein is a tetramer containing 24 +/- 3 heli

93 s expressing fluorescently labeled tonoplast intrinsic protein isoforms reveal an altered tonoplast m

94 issue-specific localization of two tonoplast intrinsic protein isoforms, the small leaf vacuoles were

95 phosphorylated form of Chk1 possessed higher intrinsic protein kinase activity and eluted more quickl

96 Here we report that VprBP possesses an intrinsic protein kinase activity and is capable of phos

97 largest subunit of TFIID, TAF1, possesses an intrinsic protein kinase activity and is important for c

98 Immunoprecipitated ATM had intrinsic protein kinase activity and phosphorylated p53

99 We report here that yeast TOR1 has an intrinsic protein kinase activity capable of phosphoryla

100 We now report that PIKfyve possesses an intrinsic protein kinase activity inseparable from its l

101 rylation, demonstrating that hSMG-1 exhibits intrinsic protein kinase activity.

102 d preparations, only CBP2 exhibited apparent intrinsic protein kinase activity.

103 of the receptor guanylate cyclase family has intrinsic protein kinase activity.

104 solvent, resulting in overestimation of the intrinsic protein-ligand binding contribution to the app

105 vTIP3;1 (alpha-TIP) is a member of the Major Intrinsic Protein membrane channel family.

106 lens differentiation marker proteins, major intrinsic protein (MIP) and delta-crystallin, was also i

107 hown the involvement of the members of major intrinsic protein (MIP) family in controlling B transpor

108 - to 29-kD proteins that belong to the major intrinsic protein (MIP) family of channels.

109 gnificant similarity to members of the major intrinsic protein (MIP) family of membrane transporters.

110 The NIPs belong to major intrinsic protein (MIP) family, members of which form ch

111 The major intrinsic protein (MIP) from bovine lens fibre membranes

112 uaporin-1 (AQP1) is a member of the membrane intrinsic protein (MIP) gene family and is known to prov

113 and the exon-intron borders of the membrane intrinsic protein (MIP) gene.

114 l protein alpha-TIP is a member of the major intrinsic protein (MIP) membrane channel family.

115 The major intrinsic protein (MIP) of the vertebrate eye lens is th

116 Expression of the major intrinsic protein (MIP) PIP1 in Xenopus laevis oocytes r

117 Aquaporins (AQP) are members of the major intrinsic protein (MIP) superfamily of integral membrane

118 Major intrinsic protein (MIP), also called aquaporin-0, is ess

119 Major intrinsic protein (MIP), also known as aquaporin-0 (AQP0

120 Lens major intrinsic protein (MIP), exclusive to the vertebrate len

121 quaporin-0 (AQP0), previously known as major intrinsic protein (MIP), is the only water pore protein

122 rt of mouse chromosome 10 close to the major intrinsic protein (Mip), which is expressed only in cell

123 oding lens water channel protein AQP0 (major intrinsic protein, MIP).

124 growth factor receptor 1 (FGFR1), and major intrinsic protein (MIP26) in exponential growth.

125 Major intrinsic proteins (MIPs) are a diverse class of integra

126 Major intrinsic proteins (MIPs) are a family of membrane chann

127 ave characterized transcripts for nine major intrinsic proteins (MIPs), some of which function as wat

128 ns are members of the larger family of major intrinsic proteins (MIPs).

129 antiphage signalling system (CBASS) uses its intrinsic protein modification system to regulate the nu

130 Human lens fiber membrane intrinsic protein MP20 is the second most abundant membr

131 The nodulin 26-like intrinsic protein (NIP) subfamily in Arabidopsis can be

132 analyses, we identified two NODULIN 26-LIKE INTRINSIC PROTEIN (NIP)-encoding genes, NIP1;1 and NIP6;

133 Plant nodulin-26 intrinsic proteins (NIPs) are members of the aquaporin s

134 Nodulin 26 intrinsic proteins (NIPs) are plant-specific, highly con

135 rbed as silicic acid through nodulin 26-like intrinsic proteins (NIPs).

136 the first ADC locus on chromosome 12; major intrinsic protein of lens fiber (MIP) is a candidate gen

137 mammalian aquaporins (AQP) 1-5 and the major intrinsic protein of lens fiber (MIP).

138 Aquaporin-0 (AQP0) is the major intrinsic protein of lens fiber cells and the founder me

139 Aquaporin 0 (AQP0), also known as major intrinsic protein of lens, is the most abundant membrane

140 Insig-1 is an intrinsic protein of the endoplasmic reticulum (ER) that

141 Aquaporin 0 (AQP0), the major intrinsic protein of the eye lens, plays a vital role in

142 n of the first mutations affecting the major intrinsic protein of the lens, MIP, encoded by the gene

143 calized zeins of 10 to 27 kD and the granule-intrinsic proteins of 32 kD or higher.

144 the EAA loop sequence that defines membrane-intrinsic proteins of ABC transporters.

145 e suggests that high concentrations of major intrinsic proteins on membranes provide interaction and

146 conserved transcriptional coactivators with intrinsic protein phosphatase activity.

147 oscopy and expression of six plasma membrane intrinsic protein (PIP) aquaporin genes (VvPIP1;1, VvPIP

148 ss-induced redistribution of plasma membrane intrinsic protein (PIP) aquaporins from the plasma membr

149 tributed by finely regulated Plasma membrane Intrinsic Protein (PIP) aquaporins.

150 hat members of the aquaporin plasma membrane intrinsic protein (PIP) subfamily are expressed in these

151 The plant aquaporin plasma membrane intrinsic proteins (PIP) subfamily represents one of the

152 The plasma membrane intrinsic protein PIP2;5 is the most highly expressed aq

153 Plasma membrane intrinsic proteins (PIPs) are aquaporins facilitating th

154 Plant plasma membrane intrinsic proteins (PIPs) are aquaporins that facilitate

155 Plasma membrane intrinsic proteins (PIPs) are involved in the adjustment

156 Plasma membrane intrinsic proteins (PIPs) are known to be major facilita

157 In plants so-called plasma membrane intrinsic proteins (PIPs) are major water channels gover

158 out plants showed that three plasma membrane intrinsic proteins (PIPs) sharing expression in veins (P

159 ally homologous subfamilies: plasma membrane intrinsic proteins (PIPs), tonoplast intrinsic proteins

160 intrinsic proteins (TIPs) or plasma membrane intrinsic proteins (PIPs).

161 Both plasma membrane intrinsic protein (PMIP) subgroups partitioned identical

162 Heat treatment altered the intrinsic protein profile on the oil bodies' surface, su

163 yields large-scale data sets that can reveal intrinsic protein properties, protein behavior within ce

164 PROTACs harness the cell-intrinsic protein recycling infrastructure, the ubiquiti

165 e 17 and 23 kDa extrinsic proteins and other intrinsic proteins remaining bound to the reaction cente

166 Here the intrinsic protein S-glutathionylation (PrSSG) at the 70-

167 Transmembrane receptors with intrinsic protein serine kinase activity bind ligand in

168 wo conserved sequences associated with major intrinsic proteins (SGxHxNPA at residues 78 to 85, NPA r

169 ic membrane proteins (NIPs), and small basic intrinsic proteins (SIPs).

170 ) storage tissue contain two prominent major intrinsic protein species of 31 and 27 kD.

171 teractions within the catalytic domain alter intrinsic protein stability, nucleotide/inhibitor bindin

172 tion than to make a positive contribution to intrinsic protein stability.

173 r understanding of the basic determinants of intrinsic protein structure and dynamics.

174 3 and AtTIP5;1, two members of the Tonoplast Intrinsic Protein subfamily of aquaporins.

175 ngs to the nodulin-like members of the major intrinsic protein superfamily branch of the aquaporin (m

176 n superfamily branch of the aquaporin (major intrinsic protein) superfamily.

177 hat the two highly conserved plasma membrane intrinsic protein surface loops are structural features

178 Nodulin 26 (nod26) is a major intrinsic protein that constitutes the major protein com

179 Aquaporin-1 (AQP1) is a major intrinsic protein that facilitates flux of water and oth

180 soluble phycobiliproteins (PBP) and membrane-intrinsic proteins that bind chlorophylls (Chls) and car

181 Trg-31 belongs to a family of membrane intrinsic proteins that play a role in facilitating inte

182 50 hemi-channel; a water channel, the major intrinsic protein (the aquaporin 0); and a cotransporter

183 coincident with insertion of a new tonoplast intrinsic protein (TIP), delta-TIP, into their membranes

184 re marked by the presence of alpha-tonoplast intrinsic protein (TIP), whereas lytic vacuoles (LV) are

185 A comparison of the NIPs and tonoplast-intrinsic proteins (TIP) shows that the H2 residue can p

186 Tonoplast intrinsic proteins (TIPs) have been implicated in the pr

187 uaporins are categorized as either tonoplast intrinsic proteins (TIPs) or plasma membrane intrinsic p

188 mbrane containing alpha- and delta-tonoplast intrinsic proteins (TIPs), markers for protein storage v

189 embrane intrinsic proteins (PIPs), tonoplast intrinsic proteins (TIPs), nodulin 26-like intrinsic mem

190 ace has been eludicated in a recent study of intrinsic protein transport signals within potassium cha

191 epidermal growth factor receptor (EGFR), the intrinsic protein tyrosine kinase (PTK) activity of one

192 F), which act through receptors that possess intrinsic protein tyrosine kinase activity, raising ques

193 through cell surface receptors that possess intrinsic protein tyrosine kinase activity.

194 Although neither receptor contains an intrinsic protein tyrosine kinase, such activity has bee

195 s and in vitro indicate that Eyes absent has intrinsic protein tyrosine phosphatase activity and can

196 r suppressor function may associate with its intrinsic protein tyrosine phosphatase activity and its

197 ture motif, and we show that it possesses an intrinsic protein tyrosine phosphatase activity.

198 g protein-protein interactions and possesses intrinsic protein tyrosine phosphatase activity.

199 efficient at MHC-II presentation due to poor intrinsic protein uptake capability.

200 heat shock proteins, chaperonins, and major intrinsic proteins, were the largest class of genes regu

201 Cox25 is an inner mitochondrial membrane intrinsic protein with a hydrophilic C terminus protrudi

202 X-Intrinsic Proteins (XIP) were recently identified in a n

203 uses on the maize (Zea mays) plasma membrane intrinsic protein (ZmPIP) aquaporin subfamily, which is