ライフサイエンスコーパス: component protein

1 etitively inhibited by recombinant secretory component protein.

2 s ESCRT-III heteropolymers by affecting each component protein.

3 sential gene that encodes a putative exosome component protein.

4 lex by promoting differential endocytosis of component proteins.

5 ort, as well as the interactions between the component proteins.

6 independent of changes in expression of Ptf1 component proteins.

7 s of multiple copies of its approximately 20 component proteins.

8 based on defined local concentrations of the component proteins.

9 terms of high-resolution X-ray models of the component proteins.

10 nding by the fusion protein, compared to its component proteins.

11 necessary for maturation of the nitrogenase component proteins.

12 -S clusters contained within the nitrogenase component proteins.

13 initial steps of recognizing the nitrogenase component proteins.

14 ts to gate electron transfer between the two component proteins.

15 e of MOIT response than those based on serum component proteins.

16 f electron donor (BchL) and acceptor (BchNB) component proteins.

17 cture, exposing novel interfaces between the component proteins.

18 precise docking of crystal structures of the component proteins.

19 ational changes of the complex and/or of its component proteins.

20 tein, lack the interactions amongst the four component proteins.

21 uster of co-evolving dynamic residues in two-component proteins.

22 mplex that is monomeric for each of the four component proteins.

23 ociated with mutations in genes encoding the component proteins.

24 O(2)-resistant complex with the nitrogenase component proteins(11,12).

25 e are one-component systems, followed by two-component proteins (26%), chemotaxis (6%), and finally E

26 The component protein, AbpA, shows homology, both at the seq

27 argeted to only one component epitope or one component protein Ag of a diverse autoimmune response.

28 The impact of individual components (protein, alginate and oil) as well as the ef

29 roperties and known complexes of nitrogenase component proteins allow us to propose a model of the co

30 articles (protein complexes carrying ciliary component proteins) along the axoneme to facilitate the

31 upon existing knowledge of the structures of component proteins and computational analyses of protein

32 Based on crystal structures of component proteins and homology modeling, we constructed

33 react with the transient complex of the two component proteins and nucleotide.

34 toad Xenopus laevis, immunogold labeling of component proteins and subsequent visualization by field

35 Due to the high molecular masses of the component proteins and the complexes, we employ a hierar

36 hermodynamic redox properties of nitrogenase component proteins and their complexes, as well as on ne

37 , a complex of viral L (large, the enzymatic component) protein and P (phosphoprotein, a cofactor com

38 repared three solutions containing different components: proteins and ions [natural saliva (NS)], min

39 of specific (s)IgE and sIgG(4) to peanut and component proteins, and 50 esIgE and esIgG(4) were quant

40 tion; the operational complex must have five component proteins, and the last process in the sequence

41 Component protein APH-1 serves as a scaffold, anchoring

42 These component proteins are as follows: component I, a homohe

43 s protein assemblies-i.e., those wherein the component proteins are expressed at endogenous levels in

44 The domains of two-component proteins are modular and can be integrated int

45 As molecular electronic components, proteins are distinguished by a remarkably l

46 ved when other APA regulators, such as CFIIm component proteins, are depleted.

47 s bound to the RNA-induced silencing complex component protein Argonaute 2.

48 etent for in vitro maturation of nitrogenase component proteins, as evidenced by rapid transfer of [4

49 (84.8%), twice the performance of the serum component proteins assayed by UniCAP (41.9%).

50 p a hierarchical approach to designing multi-component protein assemblies from two classes of modular

51 tion that is coupled to MgATP hydrolysis and component protein association and dissociation.

52 ntly better than models using standard serum component proteins (average area under the curve, >97% v

53 t is facilitated and controlled by the third component, protein B (MMOB).

54 eripheral localization of nucleolar granular component protein B23.

55 n campaign was launched in SLSJ, using the 4-component protein-based meningococcal vaccine (MenB-4C).

56 Here, we present a two-component protein-based nanoparticle vaccine that displa

57 In September 2015, the four-component, protein-based meningococcal serogroup B vacci

58 doreductase contains two [4Fe-4S]-containing component proteins (BchL and BchNB) that assemble upon A

59 this process by DNA damage, and transport of component proteins between cytoplasm and nucleus.

60 noncovalent and could be separated into its component proteins by anion-exchange chromatography.

61 mulated 3T3-L1 adipocytes and identified the component proteins by mass spectrometry.

62 itrogenase requires the participation of two component proteins called the Fe protein and the MoFe pr

63 ch knowledge of previously characterized two-component proteins can be applied to newly discovered sy

64 wever, that the cytoplasmic tails of the IRV component proteins carry targeting information to this c

65 movements and to explain why defects in the component proteins cause disease.

66 study macromolecular assemblies by detecting component proteins' characteristic high-resolution proje

67 ed for rosette biomass, levels of structural components (protein, chlorophyll), total phenols and maj

68 The possibility to integrate all components (proteins, cofactor, mediator) in the sol-gel

69 sMMO is a water-soluble three-component protein complex consisting of a hydroxylase wi

70 ata suggest that Bright functions as a three-component protein complex in the immunoglobulin locus an

71 Here, we identified an eight-core-component protein complex, the TPLATE complex, essential

72 sed in terms of surface compatibility of the component proteins, complex formation, overall charges,

73 es through nucleating the formation of multi-component protein complexes involved in the regulation o

74 The NTA monooxygenase activity requires two component proteins, component A and component B, but the

75 taining assemblies are consistent with multi-component protein condensates with roles to promote cell

76 This CGRP receptor component protein confers CGRP-specific activation to th

77 Chromoplasts contained the thylakoid Sec component protein, cpSecA, at levels comparable to chlor

78 ow variations in local concentrations of the component proteins create GTPase-cycle modules with dist

79 Here we show that absence of the core clock component protein cryptochrome (CRY) leads to constituti

80 an be detected by covariance analyses of two-component protein databases.

81 strongly express genes encoding translation components, protein degradation machinery, and some nodu

82 me involves the transient interaction of two component proteins, designated the iron (Fe) protein and

83 uctural information concerning the different components (protein, detergent molecules) of detergent-s

84 by providing the binding sites for two other component proteins, dihydrolipoamide dehydrogenase (E3)

85 One of these components, protein disulphide isomerase (PDI), facilita

86 ng method was used to systematically analyse component protein-DNA interactions that govern promoter

87 protein conformational changes that control component protein docking, interprotein electron transfe

88 n to reveal the molecular basis by which two-component proteins evolve.

89 l increases in mRNA levels encoding all AP-1 component proteins, except c-fos, were also noted.

90 n mice increased calcium/calcineurin pathway component protein expression and calcineurin activity.

91 CF MDMs generally have increased total NADPH component protein expression, they demonstrate decreased

92 inhibitor of nitrogenase that requires both component proteins (Fe-protein and MoFe-protein) and nuc

93 alization with the nucleolar dense fibrillar component protein fibrillarin closely matched the level

94 terial genomes typically encode multiple two-component proteins for distinct signalling pathways, the

95 ygenase requires complexes between its three component proteins for efficient catalysis.

96 expected to be conserved among different two-component proteins from those that are expected to diffe

97 ystematically identified 69 270 two- and one-component proteins in 365 bacterial and archaeal genomes

98 The nitrogenase component proteins in an Azotobacter strain bearing the

99 e ratio of the fibrillar center and granular component proteins in the nucleolus and nucleoplasm.

100 em for which structural information for core component proteins, in this case KaiA, KaiB and KaiC, is

101 genases reduce dinitrogen to NH(3) using two component proteins, in which electrons and protons are d

102 The progeny virions also lack certain virion component proteins, including ORF45.

103 large set of genes that encode a variety of component proteins, including those involved in meiotic

104 How component protein interactions control catalysis, howeve

105 ic resolution crystallographic structures of component proteins into an 11-A resolution cryoelectron

106 dization demonstrated that the CGRP receptor component protein is expressed in outer hair cells of th

107 The interaction between the two component proteins is mediated by a distinct C-terminal

108 lex, although the interface area between the component proteins is small.

109 In this study, we show that a MEN component, protein kinase Dbf2-Mob1, promotes transfer o

110 A full appreciation of all the exosomal components (proteins, lipids, and RNA content) will be i

111 at includes a P450 and a putative hybrid two-component protein located downstream of the terpene synt

112 eflects a complex choreography involving two component proteins, MgATP and reductant.

113 s laser heating method is applied to a three-component protein mixture to demonstrate the ability to

114 allel ion parking is demonstrated with a six-component protein mixture, which shows the potential app

115 ltaneous and efficient separation of a three-component protein mixture.

116 ate the ability to work label-free for three-component protein mixtures.

117 multielectron redox process, the nitrogenase component proteins, MoFe-protein (MoFeP) and Fe-protein

118 nanostructures; however, the design of multi-component protein nanomaterials with high accuracy remai

119 Here, we use two-component protein nanoparticles consisting of trimeric a

120 Specialized bacteria produce discrete multi-component protein networks called cellulosomes to effect

121 roduction of active forms of the nitrogenase component proteins, NifH and NifDK.

122 esent the design and characterization of two-component protein NPs displaying 20 stabilized SOSIP tri

123 ions of an HIV-1 Gag molecule with all three components (protein, nucleic acid, and membrane) are req

124 We determined the crystal structure of a component protein of a synthetic BMC shell, which inform

125 epared a monoclonal antibody against a novel component protein of Glut4 vesicles and have identified

126 r 4 (Glut4) and sortilin, represents a major component protein of the insulin-responsive vesicles (IR

127 PSD-95, a component protein of the PSD, plays an essential role in

128 Among the 29 component proteins of 18 kinds, ATP6 and ATP8 are mitoch

129 is that altered expression of connexins, the component proteins of gap junctions, is a determinant of

130 elineates the interactions of FXN with other component proteins of the complex.

131 TFI in a manner that required several of the component proteins of the COUP-TFI complex.

132 mutants has revealed the identities of many component proteins of the terminal organelle as well as

133 t differentially regulates the expression of component proteins of TJs in the cerebral cortex of fetu

134 cus furiosus genome encodes three proteasome component proteins: one alpha protein (PF1571) and two b

135 hibit a novel localization distinct from the component proteins or fragments.

136 ndicate that the recombinant T. maritima two-component proteins overexpressed in E. coli are stable a

137 enine dinucleotide phosphate (NADPH) oxidase component protein p47phox.

138 ieberkuhn in the small intestine where their component proteins participate in mucosal immunity.

139 ing cassette transporter PstSCAB and the two-component proteins PhoR and PhoB, is absolutely required

140 gh resolution X-ray crystal structure of the component protein pilin, combined with available biophys

141 ts suggest that luminal interactions between component proteins play an important role in the process

142 hen induces the degradation of critical ND10 component protein PML and therefore the release and disp

143 ovides exhaustive removal of unwanted medium components (proteins, polar molecules, and apolar/neutra

144 chine through the self-assembly of its three component proteins--protective antigen (PA), lethal fact

145 tide signal transduction pathway involved in component protein-protein dissociation.

146 reflect specific interactions between viral components (protein-protein, protein-RNA, or RNA-RNA) an

147 Assembled pertussis toxin and the secretion component proteins PtlC through PtlH are too large to di

148 at this accessory protein, the CGRP-receptor component protein (RCP), is expressed in CGRP responsive

149 phrocytes showed internalized slit diaphragm component proteins, reduced autophagy, increased endopla

150 is uncertain if the behavior of an isolated component protein reflects that of the protein in this m

151 diated by plasmid-directed expression of the component proteins required for replication and transcri

152 tivity modifying protein 1 and CGRP-receptor component protein, required for ligand specificity and s

153 gments (i.e., coarse-grained beads) for each component protein sequence.

154 The DPOR component proteins share significant overall similaritie

155 d extraction using AAA+ enzymes and targeted component proteins should be broadly applicable to the s

156 d resonance Raman (SERR) amplifiers in a two-component protein solution.

157 One of its component proteins, SPARC (osteonectin/BM-40), binds cal

158 capable of building complexes from putative component protein structures?

159 im to combine these traits to create a three-component Protein Subunit vaccine on Microneedle Arrays

160 These enzymes utilize a two-component protein system and a series of iron-sulfur clu

161 LF(N)-Acr/PA is a nontoxic, two-component protein system derived from anthrax toxin, whe

162 Steady-state kinetic analysis of the two-component protein system of Azotobacter vinelandii (Av)

163 identification of the first prokaryotic two-component protein system related to the eukaryotic NOX f

164 the complex completely disassembled into its component proteins that migrated at their monomer molecu

165 donor (L-protein) and acceptor (NB-protein) component proteins that transiently form a complex in th

166 The DPOR holoenzyme is comprised of two component proteins, the dimeric BchL protein and the het

167 transient association of the two nitrogenase component proteins, the Fe protein and the MoFe protein.

168 ctions require electron transfer between two component proteins, the iron (Fe) protein and the molybd

169 Mo nitrogenase consists of two component proteins: the Fe protein, which contains a [Fe

170 ombinant polyprotein Leish-111f or its three component proteins, thiol-specific antioxidant (TSA), Le

171 rates of transcription of genes encoding the component proteins, thus allowing control of this proces

172 Surprisingly, MEFs lacking the AVG component protein TIA-1 supported increased replication

173 orce (PMF) as the energy source to transport component proteins to the distal growing end.

174 Anthrax toxin, a three-component protein toxin secreted by Bacillus anthracis,

175 Among WNT/PCP components, protein tyrosine kinase 7 (PTK7) is a tyrosi

176 Expression of NADPH oxidase component protein was detected by means of immunoblottin

177 nover in the periplasm and that the FliE rod component protein was required for efficient FlgE-Bla se

178 ty maps with the amino acid sequences of the component proteins, we advocate peptide-based difference

179 at across the lateral extent of single PSDs, component proteins were differentially distributed, and

180 uble-gradient ultracentrifugation, and their component proteins were resolved by sodium dodecyl sulfa

181 e density gradient centrifugation, and their component proteins were separated by denaturing polyacry

182 e outer-sphere reorganization energy of both component proteins which arise due to solvent exclusion