ライフサイエンスコーパス: unligated

1 ay junctions of the repair intermediates are unligated.

2 1S rRNA accumulates in those cells; instead, unligated 21S rRNA exons appear.

3 When unligated, a salt bridge between Arg(287) and Glu(317) i

4 ents in the vicinity of the binding site for unligated AChBP that can be influenced selectively by li

5 The analysis of unligated and AMP-bound subunits of M.voltae suggests th

6 rence spectra of cytochrome c oxidase in the unligated and cyanide-ligated states.

7 tly the change in domain orientation between unligated and dual ligated subdomains of the SH(32) segm

8 ts were 1.7 +/- 1.3 and 14.5 +/- 3.5 MPa for unligated and ligated fibers, respectively.

9 hat the change in domain orientation between unligated and ligated forms can be measured directly in

10 Structures of unligated and ligated MHC class-I-restricted TCRs with d

11 rtate, were similar to that observed for the unligated and N-phosphonacetyl-L-aspartateligated wild-t

12 Unligated animals served as controls.

13 ithin a dimer is in a decoupled state in the unligated Apo state of the receptor.

14 sitioning of conformationally activated, but unligated, beta1 integrins along the leading edge of fib

15 The unligated (boryl)iminomethane BIM is also synthetically

16 n the TLR9(-/-) ligated mice compared to the unligated controls.

17 follow closely the data curve predicted for unligated CRP in the open form, whereas the cAMP-ligated

18 rmine molecular and electronic structures of unligated (deoxy), CO-inhibited (carboxy), and O2-bound

19 me in the R state tetramer and the number of unligated deoxyheme sites necessary for nitrite binding,

20 ric effectors and hemoglobin in not only the unligated derivative but also the fully ligated form has

21 Both for unligated (empty) and ligated enzyme samples a single sp

22 ational changes of up to 9 A relative to the unligated enzyme occur in loops that bind to Mg2+, GDP,

23 hemoglobins which are hexacoordinate in the unligated, ferrous state.

24 ylated N terminus has been determined in its unligated form (apo-GK) as well as in complex with GMP (

25 man normal hemoglobin (Hb A) in the deoxy or unligated form in the absence and presence of an alloste

26 The ferrous unligated form of VCA0720 is 5-coordinate, high-spin.

27 AL-57 in complex with IA, as well as in its unligated form.

28 iginating from the host cell and also in the unligated form.

29 periments carried out with their ligated and unligated forms in the absence and presence of effectors

30 elaxation pathway common to both ligated and unligated forms of Hb* (photolyzed heme), in which the e

31 quely blocked adaptors along with removal of unligated genomic DNA by exonuclease III digestion.

32 Accordingly, we solved the structure of the unligated HA1.7 TCR and compared it to both complex stru

33 ncreased from 0.08 to 0.7 M, whereas that of unligated Hb is practically insensitive to changes in [N

34 Binding CO to unligated HbI crystals results in a structure that appro

35 state decay mechanisms for both ligated and unligated hemes.

36 Small angle x-ray scattering analysis of the unligated hybrid indicated that the enzyme was in a new

37 Surprisingly, unligated integrin or beta integrin tails recruit caspas

38 Apoptosis was initiated by unligated integrins by means of a process known as integ

39 In poorly metastatic cells, unligated integrins were found to trigger activation of

40 atrix undergo apoptosis due to expression of unligated integrins, the beta subunit cytoplasmic domain

41 OX protein from Shewanella oneidensis in the unligated, intermediate six-coordinate and activated fiv

42 Assays in which gap-filled but unligated intermediates were trapped using dideoxynucleo

43 ally, Pro25 is predominantly in trans in the unligated low-pH unfolded protein, but is constrained in

44 This study reveals that, in solution, unligated Ly49A adopts a symmetric, open-state, homodime

45 is of distinct crystal forms for ligated and unligated molecules.

46 moglobin molecules in the monomer phase with unligated ones in the polymer phase.

47 The unligated open form of RBP is stabilized by conformation

48 hereas the two Fe2+ subunits either are both unligated or both ligated with O2, CO, or CN.

49 lls had comparable ATP levels; that decoy of unligated or scrambled sequence was ineffective; that HS

50 Comparison with the unligated P. aeruginosa catabolic OTCase structure indic

51 The data suggest that unligated p53 in unstressed cells should be predominantl

52 photolysis to initiate the reaction from the unligated, pentacoordinate form of the heme protein.

53 thinking about how structural information on unligated peptide/MHC complexes should be best used when

54 tructural features in the heme pocket of the unligated protein function to maintain the heme distorte

55 hanges reflect the intrinsic dynamics of the unligated proteins.

56 hanced the probability of collisions between unligated receptors and promoted their clustering.

57 compare with our previous measurements with unligated Rep monomer (P).

58 minimal mechanism for ATP hydrolysis by the unligated Rep subunit of the cis dimer: E + ATP <==> E-A

59 ly of RNAs requiring uridylate (U) deletion; unligated RNAs cleaved at U-deletion sites accumulated.

60 The T(2) values were much shorter than for unligated samples, consistent with full opening and clos

61 where cobalt-substituted hemes comprise the unligated sites.

62 measured for binding of the same ssDNA to an unligated SSB tetramer to form a singly ligated complex.

63 d from analysis of HbI crystals grown in the unligated state.

64 Fe(II)-NO ligation state, but not the Fe(II) unligated state; and (v) consistent with the Hnox1 regul

65 evaluate its structures in both ligated and unligated states in solution.

66 sociated with conversion between ligated and unligated states, we have conducted time-resolved Laue d

67 , is more sensitive to the DFT analog on the unligated strand whereas the ATP-dependent T4 ligase is

68 gle x-ray scattering studies showed that the unligated structure of the mutant enzymes, and the struc

69 site, thereby allowing determination of the unligated structure.

70 nated subunits (FeO(2)), in combination with unligated subunits containing zinc-substituted hemes (Zn

71 ConDNA binding to the unligated T127L and CRP* mutants was observed as well as

72 which ligated TCR may be differentiated from unligated TCR and selectively down-modulated.

73 Characterization of the dynamics of unligated TCR shows how binding loop motion can influenc

74 /or estrogen deficiency decreased TBA in the unligated teeth and reduced BH after tooth extraction.

75 igher bone loss values in ligated molars and unligated teeth in the control group than the RESV group

76 ted a greater number of TRAP(+) cells around unligated teeth than the control group (P <0.05).

77 cells than the control group around ligated/unligated teeth.

78 hat TRUSS was constitutively associated with unligated TNF-R1 and that the complex was relatively ins

79 Both metal-substituted subunits are unligated, whereas the two Fe2+ subunits either are both

80 tution were evaluated in all combinations of unligated Zn/Fe hybrid tetramers.