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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

21 2,2'-1,3 benzyloxy tether that restricts the torsional angle between the two naphthalene subunits alo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 The required torsional angle is achieved by introduction of stericall

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 1a-c provided quantitative bond lengths and torsional angles to support the conclusion that the down

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

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