戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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 can adopt multiple conformations and diverse packing arrangements.
7 ns, secondary structure content and tertiary packing arrangements.
8 rve ordered arrays of TBPB in three distinct packing arrangements.
9 nitrates, all of which adopt centrosymmetric packing arrangements.
10 sp. molischianum-were simulated in different packing arrangements.
11 four structural subclasses based on internal packing arrangements.
12  isomer and differ only in their solid-state packing arrangements.
13 ween microscopic morphologies and nanoscopic packing arrangements.
14  here to test possible sheet and microfibril packing arrangements.
15 e because of the large number of alternative packing arrangements.
16    At the same time, the different molecular packing arrangements after charge screening led to diffe
17 ructurally elucidated and show variations in packing arrangements and host-guest interactions.
18             The observed synergy between the packing arrangements and the extended hydration network
19 ther symmetrically to identify complementary packing arrangements, and low-energy protein-protein int
20  X-ray diffraction data to determine crystal packing arrangements, and the excited state dynamics of
21 tice; however, for other toroids alternative packing arrangements are observed.
22 lactose all exhibit the same 12 nm hexagonal packing arrangement, array size and other structural par
23                               Highly ordered packing arrangement at the column wall is seen for packe
24 embrane proteins by constraining helix-helix packing arrangements at particular positions predicted f
25 tive of the CsCl lattice type and an unusual packing arrangement based on the double-hexagonal close-
26                      Strikingly, the overall packing arrangement between the two DEDs of MC159 resemb
27 same class often share a secondary structure packing arrangement but differ in how the secondary stru
28  fibrils had an electron-lucent core but the packing arrangement comprised five or six protofilaments
29 sts as a dimer in the crystals, but adopts a packing arrangement considerably different from that of
30 ly result in NtQ22P10 fibrils that possess a packing arrangement consistent with the common amyloid s
31                      We relate the molecular packing arrangement derived from the crystal structure o
32  interesting base pairing of enantiomers and packing arrangements directed by the chiral F substituen
33                                    The novel packing arrangement displayed by the T3-785 structure, c
34 e ALIgnment), can efficiently find conserved packing arrangements, even if they are non-sequentially
35 n-sequential alignments shows that recurrent packing arrangements exist in topologically different st
36 r surface of the monomeric protein suggest a packing arrangement for the oligomeric protein in the F0
37 ns: (i) fewer than 0.2% of all possible core packing arrangements have high folding stabilities; (ii)
38 ifferences appear to be dictated by distinct packing arrangements (i.e. steric zipper interfaces) wit
39 e C60 prefers to adopt a face-centered cubic packing arrangement in the solid state, it has been demo
40                    We found that the lateral packing arrangement in the vicinity of the inner sub-dom
41                                     From the packing arrangement in two crystal structures of differe
42 tions in proteins, we compare the side-chain packing arrangements in native proteins to those found i
43  morphology due to differences in side-chain packing arrangements, intermolecular driving forces, seq
44 is crystallized from solution a head-to-tail packing arrangement is formed, but during reintroduction
45 at the lowest deposition rate, the new local packing arrangement is present only for deposition tempe
46                 Importantly, their disparate packing arrangements lead to very different dynamic magn
47 ciation and are predicated on intermolecular packing arrangements observed in crystal structures of f
48 coils from the great majority of helix-helix packing arrangements observed in globular domains.
49 phobic core, thereby creating an alternating packing arrangement of leucine and hFLeu, leads to very
50                To gain insights into the TMS packing arrangement of NCX1, we performed cysteine cross
51  example demonstrated here, we determine the packing arrangement of our nanocrystalline GB1 preparati
52 ic subunits together with information on the packing arrangement of subunit c in a ring of 12 subunit
53                   We propose a model for the packing arrangement of surface protein dimers in the tub
54  that activation causes large changes in the packing arrangement of the arrays, up to and including t
55                                  The lateral packing arrangement of the human immunodeficiency virus
56 tion STM images revealed the orientation and packing arrangement of the molecular adlayers.
57 hnique from being able to uniquely solve the packing arrangement of the molecules.
58                                          The packing arrangement of the voltage-sensing region as det
59 rived from eag and Shaker specify the unique packing arrangement of transmembrane segments S2, S3, an
60 terpretation of the tomogram in terms of the packing arrangement of Tsr using constraints derived fro
61 ntation-dependent potential derived from the packing arrangements of aliphatic side-chain pairs disti
62 deuterium mass spectrometry revealed altered packing arrangements of beta-sheets that encompass resid
63                          Here we explore the packing arrangements of DNA, RNA, and DNA/RNA hybrid mol
64 placement of the helix points to alternative packing arrangements of native-like beta-structure, in w
65 ns between tRNA and the ribosome, and of the packing arrangements of ribosomal RNA (rRNA) helices in
66           Although structurally similar, the packing arrangements of the three complexes are consider
67 the dimensionality and directionality of the packing arrangements on charge transport in organic semi
68 ntacts, helix-helix interactions and helical packing arrangement predictions in both plain text and g
69   Global conformational searches to generate packing arrangements rapidly are carried out with a Mont
70 dent phases and with the different molecular packing arrangements that would necessarily apply to reg
71 dels exhibit a distinct transmembrane domain packing arrangement to that of canonical GPCRs, establis
72 , each in a distinct space group and lattice packing arrangement, together with the existing structur
73                                  Two subunit packing arrangements were identified: one has rings of f
74 nondelipidated protein, displayed an unusual packing arrangement wherein RPE65 is embedded in a lipid
75 terials that typically exhibit high-symmetry packing arrangements, which optimize the interactions be
76 ructures reveals that they possess different packing arrangements, which results in different nanosca
77 two transmembrane helices form a left-handed packing arrangement with a crossing angle of 24 degrees
78 vels of protein structure: the intra-helical packing arrangements within secondary structure that per
79 ss involves a dramatic reorganization of the packing arrangements within the ribonucleoprotein core w
80 e protein-zinc ion recognition and the helix-packing arrangements would contribute to the conformatio
81 Z = 2; [2]2Be, P2(1)/c, Z = 4) with distinct packing arrangements, yet we are able to isolate crystal

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。