ライフサイエンスコーパス: torsional angle

1 a remarkably large dependence on the C=C-C-C torsional angle.

2 h a high antibase conformation and a +sc C-5 torsional angle.

3 al intersection seam that persists along all torsional angles.

4 istance only requires a very small change in torsional angles.

5 DFT) calculations reproduce the experimental torsional angles and also establish a correlation indica

6 The analysis of the glycosidic torsional angles and the pair interaction energy between

7 s of fluctuations in backbone and side chain torsional angles, and averaged (1)H chemical shifts are

8 SSNMR constraints including chemical shifts, torsional angles, and interatomic distances.

9 een the pyrrolidine ring pucker, phi and psi torsional angles, and peptide bond trans/cis ratio of su

10 effect of polarization of ribosyl hydroxyls, torsional angles, and the effect of base orientation on

11 Calculated helical parameters and backbone torsional angles, and the observed 31P chemical shifts,

12 mental photon energies near 1.0 eV, when the torsional angle approaches 104 degrees.

13 tein complexes, both anti and syn glycosidic torsional angles are found.

14 imately 40 degrees variations of interdomain torsional angle, are revealed.

15 In the solid state, the torsional angles around the C-C bonds between the four p

16 easing the thermally driven root-mean-square torsional angle between adjacent filament subunits from

17 l-angle X-ray scattering and MD, the average torsional angle between DNA-binding domains is approxima

18 ies indicate the potential importance of the torsional angle between the 1-phenyl "A" ring and 4-phen

19 he lowest triplet state at all values of the torsional angle between the allyl subunits.

20 olor, the major structural difference is the torsional angle between the ester group and the aromatic

21 the swallowtail porphyrins indicate that the torsional angle between the proton on the alkyl carbon a

22 2,2'-1,3 benzyloxy tether that restricts the torsional angle between the two naphthalene subunits alo

23 thyl groups were used to calculate effective torsional angles between different planes of unsaturatio

24 gous series of compounds, an increase in the torsional angles between the planar molecular core and t

25 thyl groups were used to calculate effective torsional angles between the three different planes that

26 Alterations include torsional angle changes in the loop between helix I and

27 ges near C(5), which could be low bond order torsional angle changes.

28 logen series, the N2-C2a bond length and the torsional angle chi(1) smoothly increase with the increa

29 ctra were converted into 604 distance and 48 torsional angle constraints for structure calculations.

30 this stability, with induced changes in the torsional angle delta (C5'-C4'-C3'-O3) and phosphate-pho

31 A comparison of the phi and psi torsional angle differences between the crystal structur

32 d by conformational dynamics that impact the torsional angle distribution between the porphyrin-porph

33 The backbone torsional angles fall in a narrow range, except for the

34 As the NDI-T2 backbone torsional angle falls the LUMO energy rises.

35 tron diffraction (MicroED) data show a large torsional angle for meta-phenylenes relative to para-phe

36 nction of the phi, psi, omega, chi1 and chi2 torsional angles for all 20 naturally occurring amino ac

37 Consideration of the allowable torsional angles for the side chains introduced by the m

38 A comparison of these values with the torsional angles found for the inhibited enzyme from cry

39 hanges attributed to a change in the PDI-PDI torsional angle from ca. 20 degrees in the Franck-Condon

40 l population that results from variations of torsional angles in the O-(C=O)-C=C=NH-C skeleton.

41 ies, are the tools for classifying rotamers (torsional angles) in a way that reflect their frequency

42 The required torsional angle is achieved by introduction of stericall

43 and 4 were obtained as BF(4)(-) salts, where torsional angles larger than 80 degrees were observed be

44 phene, the resulting SBT systems are planar (torsional angle <1 degrees ) and highly pi-conjugated.

45 ergy curve for the singlet state occurs at a torsional angle near 45 degrees , in contrast to previou

46 each of which the phenyl-porphyrin bonds had torsional angles near 90 degrees.

47 itterion, corresponding to a H1'-C1'-C2'-H2' torsional angle of 33 degrees.

48 fluorenyl rings are cis to each other with a torsional angle of 59 degrees and a long C-C single bond

49 Single crystal X-ray analysis shows that the torsional angle of the carboxylate group and the C-CO(2)

50 is accompanied by a change in the main chain torsional angles of Asp402, a conserved residue located

51 ta-turn are defined according to Phi and Psi torsional angles of the backbone for residues i + 1 and

52 rge transfer process depends on the relative torsional angles of the donor and acceptor groups where

53 lactam ring to restrict two of the six free torsional angles of TRH and constrain the X-Pro-NH2 pept

54 The backbone torsional angles, phi and psi, were shown to correlate w

55 itivity provides a new route for determining torsional angles plus other molecular structural details

56 Given by chi torsional angles, rotamers describe the side-chain confo

57 s all increase with decreasing values of the torsional angle that C(1)-Li makes with respect to the a

58 y 90%; and (ii) provide a set of (chi1/chi2) torsional angles that leads to optimal agreement between

59 liability of the provided set of (chi1/chi2) torsional angles, the side chains of all reported confor

60 1a-c provided quantitative bond lengths and torsional angles to support the conclusion that the down

61 that use of the provided set of (chi1/chi2) torsional angles together with other observables, such a

62 Then, we extracted torsional angles via the Bio3D module in R language.

63 w of their interglycosidic linkages and the torsional angle w of their side chain along the C5-C6 bo

64 The classification of torsional angles was also done in R according to the pen

65 es, as evidenced by the decreased end-to-end torsional angles, was confirmed by X-ray crystallography

66 distinct topological profiles with inducible torsional angles when bound to different HAs.