ライフサイエンスコーパス: packing arrangement

1 ins through a hydrophobic "knobs-into-holes" packing arrangement.

2 osely packed bundle with an altered AS2/AS2' packing arrangement.

3 tly to achieve the most favored superhelical packing arrangement.

4 unit cell, compared to a uniformly eclipsed packing arrangement.

5 ealed that high order existed in the surface packing arrangement.

6 ed intrachain hydrogen bonds and a hexagonal packing arrangement.

7 to the thermodynamically most stable crystal packing arrangement.

8 ight into their molecular structures and the packing arrangement.

9 e because of the large number of alternative packing arrangements.

10 ar materials depend on the molecules' mutual packing arrangements.

11 ns, secondary structure content and tertiary packing arrangements.

12 rve ordered arrays of TBPB in three distinct packing arrangements.

13 nitrates, all of which adopt centrosymmetric packing arrangements.

14 sp. molischianum-were simulated in different packing arrangements.

15 four structural subclasses based on internal packing arrangements.

16 can adopt multiple conformations and diverse packing arrangements.

17 isomer and differ only in their solid-state packing arrangements.

18 ween microscopic morphologies and nanoscopic packing arrangements.

19 here to test possible sheet and microfibril packing arrangements.

20 At the same time, the different molecular packing arrangements after charge screening led to diffe

21 ructurally elucidated and show variations in packing arrangements and host-guest interactions.

22 . Structural analysis reveals that different packing arrangements and orientational disorder of the s

23 th hydrophobic cores, varying supramolecular packing arrangements and surface charge.

24 The observed synergy between the packing arrangements and the extended hydration network

25 ther symmetrically to identify complementary packing arrangements, and low-energy protein-protein int

26 X-ray diffraction data to determine crystal packing arrangements, and the excited state dynamics of

27 eoretical calculations, revealing that their packing arrangements are governed by distinct pai-pai-st

28 tice; however, for other toroids alternative packing arrangements are observed.

29 lactose all exhibit the same 12 nm hexagonal packing arrangement, array size and other structural par

30 cleosomes display differential diffusion and packing arrangements as chromatin density increases wher

31 arc structures that follow the same subunit packing arrangements as found in isolation.

32 Highly ordered packing arrangement at the column wall is seen for packe

33 embrane proteins by constraining helix-helix packing arrangements at particular positions predicted f

34 tive of the CsCl lattice type and an unusual packing arrangement based on the double-hexagonal close-

35 Strikingly, the overall packing arrangement between the two DEDs of MC159 resemb

36 same class often share a secondary structure packing arrangement but differ in how the secondary stru

37 fibrils had an electron-lucent core but the packing arrangement comprised five or six protofilaments

38 sts as a dimer in the crystals, but adopts a packing arrangement considerably different from that of

39 ly result in NtQ22P10 fibrils that possess a packing arrangement consistent with the common amyloid s

40 f just a few cells, establishing the correct packing arrangements (contacts) between cells is essenti

41 We relate the molecular packing arrangement derived from the crystal structure o

42 interesting base pairing of enantiomers and packing arrangements directed by the chiral F substituen

43 The novel packing arrangement displayed by the T3-785 structure, c

44 e ALIgnment), can efficiently find conserved packing arrangements, even if they are non-sequentially

45 n-sequential alignments shows that recurrent packing arrangements exist in topologically different st

46 r surface of the monomeric protein suggest a packing arrangement for the oligomeric protein in the F0

47 ns: (i) fewer than 0.2% of all possible core packing arrangements have high folding stabilities; (ii)

48 ifferences appear to be dictated by distinct packing arrangements (i.e. steric zipper interfaces) wit

49 e C60 prefers to adopt a face-centered cubic packing arrangement in the solid state, it has been demo

50 We found that the lateral packing arrangement in the vicinity of the inner sub-dom

51 From the packing arrangement in two crystal structures of differe

52 h form filaments that share a conserved haem packing arrangement in which haems are coordinated by hi

53 tions in proteins, we compare the side-chain packing arrangements in native proteins to those found i

54 morphology due to differences in side-chain packing arrangements, intermolecular driving forces, seq

55 is crystallized from solution a head-to-tail packing arrangement is formed, but during reintroduction

56 at the lowest deposition rate, the new local packing arrangement is present only for deposition tempe

57 Importantly, their disparate packing arrangements lead to very different dynamic magn

58 ciation and are predicated on intermolecular packing arrangements observed in crystal structures of f

59 coils from the great majority of helix-helix packing arrangements observed in globular domains.

60 phobic core, thereby creating an alternating packing arrangement of leucine and hFLeu, leads to very

61 To gain insights into the TMS packing arrangement of NCX1, we performed cysteine cross

62 example demonstrated here, we determine the packing arrangement of our nanocrystalline GB1 preparati

63 ic subunits together with information on the packing arrangement of subunit c in a ring of 12 subunit

64 We propose a model for the packing arrangement of surface protein dimers in the tub

65 on seen in other bacterial T4P and share the packing arrangement of the archaeal T4P.

66 that activation causes large changes in the packing arrangement of the arrays, up to and including t

67 echanisms, the molecular architecture and/or packing arrangement of the chromophores are vital for th

68 h class of these reactions requires a unique packing arrangement of the corresponding monomers for th

69 The lateral packing arrangement of the human immunodeficiency virus

70 Then, it follows that if we modify the packing arrangement of the individual molecules within t

71 tion STM images revealed the orientation and packing arrangement of the molecular adlayers.

72 hnique from being able to uniquely solve the packing arrangement of the molecules.

73 e crystal, the formation of a honeycomb-like packing arrangement of the simplest isotrianglimine was

74 The packing arrangement of the voltage-sensing region as det

75 rived from eag and Shaker specify the unique packing arrangement of transmembrane segments S2, S3, an

76 terpretation of the tomogram in terms of the packing arrangement of Tsr using constraints derived fro

77 kbone structures to supersecondary-structure packing arrangements of a-helices and B-strands.

78 ntation-dependent potential derived from the packing arrangements of aliphatic side-chain pairs disti

79 deuterium mass spectrometry revealed altered packing arrangements of beta-sheets that encompass resid

80 Here we explore the packing arrangements of DNA, RNA, and DNA/RNA hybrid mol

81 placement of the helix points to alternative packing arrangements of native-like beta-structure, in w

82 ns between tRNA and the ribosome, and of the packing arrangements of ribosomal RNA (rRNA) helices in

83 tal polymorphism, characterized by different packing arrangements of the same compound, strongly ties

84 Although structurally similar, the packing arrangements of the three complexes are consider

85 the dimensionality and directionality of the packing arrangements on charge transport in organic semi

86 ntacts, helix-helix interactions and helical packing arrangement predictions in both plain text and g

87 V and I/II pairs exemplify the T-shaped heme packing arrangement, prevalent in multiheme cytochromes,

88 Global conformational searches to generate packing arrangements rapidly are carried out with a Mont

89 ouse alpha-synuclein fibrils display altered packing arrangements, reduced hydrophobicity, and height

90 sufficient for them to switch to a vertical packing arrangement that increases surface tip density w

91 dent phases and with the different molecular packing arrangements that would necessarily apply to reg

92 dels exhibit a distinct transmembrane domain packing arrangement to that of canonical GPCRs, establis

93 sues of Arabidopsis do not conform to random packing arrangements to varying degrees.

94 , each in a distinct space group and lattice packing arrangement, together with the existing structur

95 Two subunit packing arrangements were identified: one has rings of f

96 nondelipidated protein, displayed an unusual packing arrangement wherein RPE65 is embedded in a lipid

97 terials that typically exhibit high-symmetry packing arrangements, which optimize the interactions be

98 ructures reveals that they possess different packing arrangements, which results in different nanosca

99 two transmembrane helices form a left-handed packing arrangement with a crossing angle of 24 degrees

100 s highly sensitive to the specific molecular packing arrangement within a noncentrosymmetric lattice,

101 vels of protein structure: the intra-helical packing arrangements within secondary structure that per

102 ss involves a dramatic reorganization of the packing arrangements within the ribonucleoprotein core w

103 e protein-zinc ion recognition and the helix-packing arrangements would contribute to the conformatio

104 Z = 2; [2]2Be, P2(1)/c, Z = 4) with distinct packing arrangements, yet we are able to isolate crystal