ライフサイエンスコーパス: heteropolymer

1 izobium etli CE3 O antigen is a fixed-length heteropolymer.

2 by perturbing the chemical structure of the heteropolymer.

3 inued metabolism of this essential cell wall heteropolymer.

4 extension of a short A-tail into a long A/U-heteropolymer.

5 , likely due to stabilization of the keratin heteropolymer.

6 aining the free energy of a typical designed heteropolymer.

7 at is structurally related to UMOD but forms heteropolymers.

8 ion of two simplified models of protein-like heteropolymers.

9 ncovalent type I (K18, K19) and type II (K8) heteropolymers.

10 s which are assemblies of specific ESCRT-III heteropolymers.

11 DW-135/Y) have been identified to form these heteropolymers.

12 ent mutants reveal that FtsZ1 and FtsZ2 form heteropolymers.

13 nd select mRNAs and contributes U's into A/U heteropolymers.

14 nover of FtsZ2 and FtsZA, respectively, from heteropolymers.

15 o its ligands, resulting in the formation of heteropolymers.

16 n predicting the functional utility of novel heteropolymers.

17 (s) and the formation of high molecular mass heteropolymers.

18 While suberin is an insoluble heteropolymer, a number of soluble lipids can be extract

19 The resulting heteropolymer adopts a dramatically different structure

20 hase molecular recognition (CoPhMoRe) uses a heteropolymer adsorbed onto and templated by a nanoparti

21 The infused heteropolymers also facilitated rapid and quantitative b

22 osed during this transfer reaction, but both heteropolymer and CR1 are removed from the erythrocytes

23 The Langevin dynamics of a random heteropolymer and its dynamic glass transition are studi

24 primarily through interaction with FtsZ2 in heteropolymers and suggest that ARC3 activity is spatial

25 xical in light of what is known about random heteropolymers and the sensitivity of their properties t

26 Keratins are obligate heteropolymers and, similarly to other IFs, they contain

27 ing that like mammalian NFs, lamprey NFs are heteropolymers, and that additional NF subunits may exis

28 then cross-linked bispecific mAb complexes (heteropolymers, anti-CR1 x anti-phi X174) were infused i

29 Heteropolymers are important examples of self-assembling

30 As a result, folded heteropolymers are predicted to display the kind of clos

31 being a universal feature of all designable heteropolymers, as it is present also in natural protein

32 Mammalian neurofilaments are obligate heteropolymers assembled from three polypeptides, neurof

33 terface, consistent with roles in modulating heteropolymer assembly.

34 ular crowding that favors coalescence of the heteropolymer at the insert site and thus closure of the

35 This allows water to penetrate into folded heteropolymers at high pressure and break apart their hy

36 Spirocyclic adducts, in both homo- and heteropolymer background single-stranded DNA sequences,

37 rgy transfer to demonstrate the formation of heteropolymers between S and Z alpha1-antitrypsin.

38 ow information varies with activity in other heteropolymers, both biological and synthetic, may lead

39 dicate that not only may mixed variants form heteropolymers, but that this can causally lead to the d

40 4A suggesting that it disassembles ESCRT-III heteropolymers by affecting each component protein.

41 d 2, induces the postediting addition of A/U heteropolymers by KPAP1 poly(A) polymerase and RET1 term

42 sing two litter types that possessed similar heteropolymer chemistry, but different proportions of la

43 We revisit a heteropolymer collapse theory originally introduced to e

44 sic information about protein sequence using heteropolymer collapse theory.

45 from elementary sequence information using a heteropolymer collapse theory.

46 specific short and long range interactions (heteropolymer collapse).

47 We have constructed tri-molecular heteropolymer complexes consisting of b-mAb 9B9, SA, and

48 It is often described as a heteropolymer comprised of polyaliphatic and polyaromati

49 gest that both these models (homopolymer and heteropolymer) could be applicable depending on the solu

50 Because the integrity of NF heteropolymers depends upon maintaining properly balance

51 ently linked to the FctA- and Cpa-containing heteropolymer derived from cell extracts.

52 They act by disassembling ESCRT-III heteropolymers during or after their proposed function i

53 Incubation of the erythrocyte-heteropolymer-E. coli complexes with freshly isolated hu

54 insert mutants to assess the strength of the heteropolymer-encoded folding signals that facilitate lo

55 Amylovoran, a high molecular weight acidic heteropolymer exopolysaccharide, is a virulent factor of

56 pleen ferritin (HoSF), a naturally occurring heteropolymer ferritin of H and L-subunits (approximatel

57 recombinant H- and L-subunit homopolymer and heteropolymer ferritins and several site-directed H-subu

58 elps to explain the widespread occurrence of heteropolymer ferritins in tissues of vertebrates.

59 two-state co-operative transition following heteropolymer formalism, whereas secondary structure for

60 The regiocontrol of heteropolymer formation derives from the inability of th

61 the adult axon, the neurofilaments (NFs) are heteropolymers formed from the low (NFL), middle (NFM),

62 ucophytes, chloroplast division involves two heteropolymer-forming FtsZ isoforms: FtsZ1 and FtsZ2 in

63 nt structural studies indicate that a tektin heteropolymer forms a unique protofilament of flagellar

64 Suberin is a lipid and phenolic cell wall heteropolymer found in the roots and other organs of all

65 tests of the validity of REM as a model for heteropolymer freezing, freezing transition of random se

66 ghtly to the beta-1,4-linked glucose-mannose heteropolymer glucomannan.

67 mers, unlike the triplet, which are obligate heteropolymers, have supported a widely held view that a

68 mers, unlike the triplet, which are obligate heteropolymers, have supported a widely held view that p

69 (CR1) on E using a bispecific mAb complex, a heteropolymer (HP).

70 Monoclonal antibody (MAb)-based heteropolymers (HP) were used to simulate immune adheren

71 Lignin is a phenylpropanoid-derived heteropolymer important for the strength and rigidity of

72 lants is the presence of the phenolic lignin heteropolymer in xylem and other sclerified cell types.

73 t as in mammals, NFs in lamprey are obligate heteropolymers, in which NF-L is a required subunit.

74 ess, the short A-tails are extended as (A/U) heteropolymers into structures previously thought to be

75 ss-linking of the cartilage type II collagen heteropolymer is an integral, early process in fibril as

76 The folding of a protein-like heteropolymer is studied by using direct simulation of a

77 hile the collapse of homopolymers and random heteropolymers is continuous and multi-phasic.

78 ion, which is a three-legged pinwheel-shaped heteropolymer, is a major component in the protein coats

79 Here we show that a more sophisticated heteropolymer Ising model can be constructed and fitted

80 is clathrin, which appears as a three-legged heteropolymer (known as a triskelion) that assembles int

81 dded to guide RNAs and rRNAs, while long A/U heteropolymers mark 3' ends of most mRNAs.

82 Keratins 8 and 18 (K8/18) heteropolymers may regulate cell signaling via the known

83 The folding mechanism of a 125-bead heteropolymer model for proteins is investigated with Mo

84 mputer simulations of a well-studied lattice heteropolymer model, the first systematic test of this o

85 Numerical calculations on lattice heteropolymer models are presented to illustrate the key

86 s that the otherwise rapid folding of simple heteropolymer models becomes "glassy"-dominated by multi

87 this phenomenon, we report three examples of heteropolymer-nanotube recognition complexes for ribofla

88 Unlike random heteropolymers, natural proteins fold into unique ordere

89 As obligate heteropolymers, NF assembly requires interactions betwee

90 homopolymer common antigen (A band) and the heteropolymer O antigen (B band), which impart serospeci

91 demands at each phase of regeneration for NF heteropolymers of differing composition in regrowing axo

92 toskeletal polymers of vertebrate axons, are heteropolymers of multiple NF subunit proteins.

93 In the serogroups W and Y, these are heteropolymers of the repeating units (-->6)-alpha-d-Gal

94 Keratin intermediate filaments are heteropolymers of type I and type II polypeptides that c

95 Here, we show that synthetic heteropolymers, once constrained onto a single-walled ca

96 It should now be possible to extend the heteropolymer paradigm to a live pathogen in a primate m

97 etween the inserted homopolymer and flanking heteropolymer portions of the unfolded protein.

98 lyketides are a class of biologically active heteropolymers produced by assembly line-like multiprote

99 The 24-subunit ferritin heteropolymer protein shell consists of light (L) and he

100 These unusual heteropolymers represent unique examples of a conjugatio

101 Assembled as obligate heteropolymers requiring NF-L and substoichiometric amou

102 that rodent neurofilaments (NF) are obligate heteropolymers requiring NF-L plus either NF-M or NF-H f

103 accommodate the use of both homopolymer and heteropolymer RNA templates lacking uridylates and can b

104 We have generated bispecific mAb complexes (heteropolymer(s), HP), which contain a mAb specific for

105 gnificantly more foldable than purely random heteropolymer sequences.

106 Lignins, complex aromatic heteropolymers, stiffen and fortify secondary cell walls

107 hage previously cleared to the liver via the heteropolymer system was phagocytosed and destroyed.

108 Lignin is a phenolic heteropolymer that is deposited in secondary-thickened c

109 Septin monomers form heteropolymers that in turn associate into a variety of

110 ent in their molecular mass assemble to form heteropolymers that produce a structure-providing intrac

111 ared cross-linked, bispecific mAb complexes (heteropolymers) that facilitate rapid and quantitative b

112 However, in the design of artificial heteropolymers the control over the single chain self-as

113 ytoplasmic membrane with a net-like, elastic heteropolymer, the peptidoglycan sacculus, to protect th

114 tional evidence for the potential utility of heteropolymers to facilitate the safe and rapid clearanc

115 tained predominantly B-type homopolymers and heteropolymers up to 12-mers (3400 Da).

116 ade in previous in vivo experiments in which heteropolymers were used to facilitate clearance of inno

117 proteins can produce beta-linked glucomannan heteropolymers when supplied both GDP-mannose and GDP-gl

118 ormation generation from random sequences of heteropolymers, where unfavorable Shannon entropy is ove

119 formational mobility of peptides and related heteropolymers while simultaneously altering their prope

120 izobium etli CE3 O antigen is a fixed-length heteropolymer with O methylation being the predominant t

121 nant O-polysaccharide (OPS) is an unbranched heteropolymer with repeating d-glucose and 6-deoxy-l-tal

122 In addition, FctA formed a heteropolymer with the putative collagen-binding protein

123 ynthetically accessible and provides (AB)(n) heteropolymers with an alternating backbone and alternat

124 an be a powerful tool in the design of novel heteropolymers with tuned stereochemical properties.