ライフサイエンスコーパス: trans form

1 ization of the 11-cis chromophore to its all-trans form.

2 le, uninhibited conformation promoted by the trans form.

3 hydes inhibiting productive binding of the S-trans-form.

4 re much more difficult to stabilize than the trans forms.

5 ed a general treatment covering both cis and trans forms.

6 chromophores isomerized by light to the all-trans form be replaced with 11-cis retinal to regenerate

7 (Gly-Pro-Hyp)(4) sequence, which must be in trans form before the monomer is competent to initiate t

8 wavelength of light, with the visible-light (trans) form being more hydrophobic and, thus, inducing a

9 photoisomerization, with the visible-light (trans) form being more hydrophobic than the UV-light (ci

10 uced isomerization of cis-retinal to the all trans form breaks this rhodopsin salt bridge leading to

11 it blocks voltage-gated ion channels in the trans form but not the cis form.

12 The energetically stable trans form can be completely converted to the cis form w

13 osomal deletions, rather than breakpoints in trans, forming chromosomal translocations.

14 er rate of thermal isomerization back to the trans form compared to that of AzoAMP-1.

15 phosphorylated tau (cis P-tau), but not the trans form, contributes to tau pathology and functional

16 bound 11- cis-retinal isomerizes to the all- trans form, enabling rhodopsin to activate transducin, i

17 As a consequence, the trans form exhibits enhanced interaction with the protei

18 -handed all-cis (Form I) and left-handed all-trans (Form II), were determined in the crystalline stat

19 Initiation of the catalyst from the inert trans-form into the active cis-form occurs through a dis

20 However, the trans form is stabilized by favorable stacking interacti

21 The initial all-trans-form isomerized to the 13-cis isomer more rapidly

22 borhood of retinal upon stabilization of the trans form, local structural rearrangements in the adjoi

23 two conformers, namely, Z6 and Z8, while the trans-form manifests uniquely as an H8 structure.

24 Model docking revealed that the trans form of AAPF does not fit into the active site.

25 fied chromatographically as an epimer of the trans form of alpha-(N2-deoxyguanosinyl)tamoxifen, and t

26 Simulations suggest that the all-trans form of polyproline is relatively stiff, with pers

27 pulation may be unfolded subtilisin with the trans form of proline 168, which must isomerize to the c

28 eoarthritis mediator IL-1 beta, with the all-trans form of retinoic acid (ATRA), which promotes endoc

29 geometric isomer is intended to mimic the s-trans form of the AAIs, while the Z geometric isomer is

30 ds an interesting shift of preference to the trans form of the mercaptosulfonamides was observed with

31 d the enhanced dynamics of lysozyme with the trans form of the photosurfactant.

32 enhanced protein flexibility induced by the trans form of the surfactant relative to the native prot

33 M/MM incorporation of PSB11, 6-s-cis and 6-s-trans forms of 3,4-dehydro-PSB11, and 3,4-dehydro-5,6-di

34 further our understanding of cis as well as trans forms of enhancer-promoter communication.

35 l response seen the presence of both cis and trans forms of GFR alpha-1.

36 tions that arise from populations of cis and trans forms of proline.

37 Cross-links in cis and trans forms of the antigenomic RNA were generated using

38 ntirely, by differing frequencies of cis and trans forms of the double heterokaryotypes and their com

39 of the transition state (TS) and the cis and trans forms of the ground state (GS), when bound to CyP

40 iated with different combinations of cis and trans forms of the three proline residues.

41 ition of the equilibrium between the cis and trans forms of the Xxx116-Pro117 peptide bond in the fol

42 For example, mixed cis and trans forms of triacylglycerols and phosphatidylcholines

43 wavelength of light, with the visible-light (trans) form of the surfactant being more hydrophobic tha

44 Baseline separation of the cis- and trans- forms of both hydroxyproline and fluoroproline wa

45 Trans-forms of dG-N(2)-TAM and dG-N(2)-N-desTAM adducts

46 cis-forms of dG-N2-tamoxifen, but not at the trans-forms of dG-N2-tamoxifen.

47 rrect base, opposite the lesions; one of the trans-forms of dG-N2-tamoxifens only promoted incorporat

48 -isomerisation of the chromophore to its all-trans form, that involves pivoting movements of kinked h

49 When the linker is in the trans form, the peptide favors a more helical structure

50 yme were detected with the surfactant in the trans form through NSE measurements of the Q-dependent e

51 distance on (photo)switching from the linear trans-form to the bulky cis-form of the photochromes.

52 rometry (UPLC-MS/MS), and lycopene (cis- and trans-forms) was analysed using high-performance liquid

53 eported that </=40% of ALA can be present as trans forms.We aimed to evaluate the associations betwee