ライフサイエンスコーパス: component protein

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

2 sential gene that encodes a putative exosome component protein.

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

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

5 cture, exposing novel interfaces between the component proteins.

6 necessary for maturation of the nitrogenase component proteins.

7 -S clusters contained within the nitrogenase component proteins.

8 initial steps of recognizing the nitrogenase component proteins.

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

10 precise docking of crystal structures of the component proteins.

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

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

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

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

15 ociated with mutations in genes encoding the component proteins.

16 lex by promoting differential endocytosis of component proteins.

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

18 independent of changes in expression of Ptf1 component proteins.

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

20 based on defined local concentrations of the component proteins.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 eripheral localization of nucleolar granular component protein B23.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 The nitrogenase component proteins in an Azotobacter strain bearing the

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

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

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

83 How component protein interactions control catalysis, howeve

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 The DPOR component proteins share significant overall similaritie

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

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

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

127 capable of building complexes from putative component protein structures?

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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