ライフサイエンスコーパス: nonequivalent

1 ary components of the ligand-binding site is nonequivalent.

2 domains in these two halves are functionally nonequivalent.

3 posal that these two halves are functionally nonequivalent.

4 fact that DNA strands are complementary and nonequivalent.

5 ogous halves of the ArsA may be functionally nonequivalent.

6 nit of CPS are functionally and structurally nonequivalent.

7 PLP sites in cystathionine beta-synthase are nonequivalent.

8 t isotherms and indicates that the hemes are nonequivalent.

9 n this region are important for function and nonequivalent.

10 exonic and intronic replacements between two nonequivalent 5'splice sites in the 469 nt long rbcS3A i

11 roceeds with high selectivity between subtly nonequivalent acetal oxygen atoms.

12 l muscle acetylcholine receptor contains two nonequivalent acetylcholine binding sites, one each at t

13 dition reactions involving 1,3-disubstituted nonequivalent allene dienophiles were studied, and some

14 sition alpha2 beta gamma delta are formed by nonequivalent alpha-gamma and alpha-delta subunit interf

15 elements in the HTLV-1 LTR are functionally nonequivalent and suggest that Sp1 can influence HTLV-1

16 ions are all contributors to activation, are nonequivalent, and are additive.

17 rtzite CdS nanorods are crystallographically nonequivalent, asymmetric heterostructures can be produc

18 a spectroscopic characterization of the two nonequivalent beta-carotene molecules in the photosystem

19 For tobramycin, two nonequivalent binding sites were found with K(D1) = 352

20 potential nucleotide binding sites that are nonequivalent both in the absence and in the presence of

21 causes development of healthy, functionally nonequivalent brain hemispheres.

22 ffluxing pump Anabaena AztA are functionally nonequivalent, but only with respect to zinc resistance.

23 body rely on interactions among distinct and nonequivalent cell types.

24 and precursors for graphenic C phases, five nonequivalent CO species have been distinguished, eviden

25 eries, and nonrandomized experiments using a nonequivalent comparison group.

26 ts of 60 copies each of P1(A) and P1(B), two nonequivalent conformers of the P1 protein.

27 hium atoms in all crystal structures adopt a nonequivalent coordination protocol and exist in two dif

28 ht to be essential in binding one of the two nonequivalent copper atoms.

29 interactions of the 180-subunit capsid plus nonequivalent CP-CP interactions.

30 s in situ, we show that these enzymes act as nonequivalent decision gates, determining context-depend

31 remia with same species was also analyzed as nonequivalent dependent controls.

32 We identify two nonequivalent DNA-binding sites and propose a model in w

33 ctions are the result of binding of multiple nonequivalent domains.

34 translocating potential are cooperative and nonequivalent due to the interaction-dependent reorganiz

35 rified that 32 (74%) of the 43 patients with nonequivalent durations of response (> 30 days differenc

36 supramolecular species composed of a pair of nonequivalent Dy(III)-radical complexes exhibits single-

37 ension of this approach to proteins with two nonequivalent EF-hand Ca(2+)-binding sites--rat beta par

38 ach such dimer contains two CPs in distinct, nonequivalent environments, in contrast to the quasi-equ

39 al and rotational behavior because its three nonequivalent equilibrium structures have nearly identic

40 ws five distinct peaks for each magnetically nonequivalent exchangeable proton in the molecule.

41 nated receptors or by incorporating multiple nonequivalent fluorine atoms in a single receptor.

42 The styrene methylene protons were nonequivalent for both adducts, suggesting hydrogen bond

43 interactions with corepressor components are nonequivalent for these otherwise similar oncoproteins,

44 subtle differences in MAPK signaling confer nonequivalent functions that influence tumor spectra ind

45 Mutants carrying double mutations in nonequivalent genes (i.e., motA motD or motB motC) retai

46 drogen-bonded to a wide set of energetically nonequivalent groups.

47 The two hydrogen bonds were found to be nonequivalent, having different directions and different

48 The problems posed by the presence of nonequivalent hydrogen bond acceptor sites in molecular

49 tion for molecular structures with multiple, nonequivalent hydrogen bond acceptors are presented.

50 peats bind distinct regions of RAD51 and are nonequivalent in their mode of interaction.

51 indications that the two domains of CFTR are nonequivalent in their nucleotide interactions.

52 Thus, signal sequences are functionally nonequivalent in vivo, with intrinsic inefficiency of th

53 americ structure as a "dimer of dimers" with nonequivalent interactions between subunits.

54 cisternae at equivalent levels, but none at nonequivalent levels.

55 We found nonequivalent lipid panel test results between Theranos

56 The duplex assay detected nonequivalent molar ratios as high as 100-fold.

57 classes studied relies on interactions with nonequivalent N-H bonds that break symmetry.

58 an ATP dependent manner by utilizing its two nonequivalent nucleotide binding domains (NBDs) to bind

59 an ATP-dependent manner by utilizing its two nonequivalent nucleotide binding domains (NBDs) to bind

60 nd that CaMKIIgamma and -delta isoforms have nonequivalent, opposing functions.

61 rms the presence of a radical containing two nonequivalent oxygens as required for a superoxide in ma

62 domains in the elongated Gag subunits, whose nonequivalent packing is reflected in subtly different m

63 ylene protons of the hydroxymethyl group are nonequivalent protons and the hydroxymethyl group is not

64 d rearrangement of disulfide bonds using two nonequivalent redox active-sites, located in two differe

65 Our studies reveal that MyoR contains two nonequivalent repression domains.

66 rboxylate ligands (both crystallographically nonequivalent), resulting in a 173.3-angstrom cubic unit

67 d sites on the proteasome and play specific, nonequivalent roles in the asymmetric assembly and activ

68 Here, we demonstrate the nonequivalent roles of the C termini of six AAA subunits

69 However, the two glutamates are nonequivalent since EbrA E15 is required for substrate b

70 These stems are connected by two nonequivalent single-stranded loops.

71 Wnt-dependent reiterative switch to generate nonequivalent sister cells that are born by anterior-pos

72 ing the differential nuclear POP-1 levels in nonequivalent sister cells.

73 " by a novel strand-specific imprint so that nonequivalent sister chromatids are produced.

74 hile the asymmetric distribution of POP-1 in nonequivalent sisters apparently requires a 124-amino-ac

75 hGH has two nonequivalent sites, called site 1 and site 2, that bind

76 ers when the bridging carbon substitution is nonequivalent (X not equal Y).

77 g sites on PLD2 was found to be functionally nonequivalent: Y(169) serves to modulate the activity of