ライフサイエンスコーパス: crystallographic analyses

1 ce using site-directed mutagenesis and x-ray crystallographic analyses.

2 ructure on the basis of proton NMR and X-ray crystallographic analyses.

3 e identified from other studies, with recent crystallographic analyses.

4 of 1 were studied by spectroscopic and X-ray crystallographic analyses.

5 on on protein crystals, complementary to the crystallographic analyses.

6 these modifications were confirmed by x-ray crystallographic analyses.

7 ter was addressed through elegantly designed crystallographic analyses.

8 in solution as suggested by 1H NMR and X-ray crystallographic analyses.

9 c (1)H and (13)C NMR spectroscopic and X-ray crystallographic analyses.

10 t of the active site), as supported by X-ray crystallographic analyses.

11 vable in typical medium- and high-resolution crystallographic analyses.

12 sis and chemical cross-linking, coupled with crystallographic analyses.

13 ed conformations identified in earlier X-ray crystallographic analyses.

14 K and characterized by biochemical and X-ray crystallographic analyses.

15 armony with previous comparisons obtained by crystallographic analyses.

16 e enzyme is known from high resolution x-ray crystallographic analyses.

17 SA*+ are probed by the combination of X-ray crystallographic analyses and density functional theoret

18 We report crystallographic analyses and ligand-binding experiments

19 -free P protein required for high resolution crystallographic analyses and may be useful for the prep

20 Both crystallographic analyses and quantum mechanical calcula

21 tor to InhA, as shown by enzymatic and X-ray crystallographic analyses, and establishes InhA as the p

22 y, NOE experiments, mass spectrometry, X-ray crystallographic analyses, and isothermal titration calo

23 ed by solution and solid-state NMR and X-ray crystallographic analyses, and provided insight into the

24 The results of single-crystal X-ray crystallographic analyses are given for four of the comp

25 e unusual interactions are documented, X-ray crystallographic analyses are reported, and theoretical

26 Crystallographic analyses confirm that 1 and 2 adopt C(2

27 ar magnetic resonance spectroscopy and X-ray crystallographic analyses confirm that a Tyr8 to Phe mut

28 X-ray crystallographic analyses confirm that the side chains o

29 Peptide maps and crystallographic analyses confirm the presence of the 10

30 ar magnetic resonance spectroscopy and X-ray crystallographic analyses demonstrate that the covalent

31 Crystallographic analyses demonstrate that the surface a

32 tudies, mass spectrometric measurements, and crystallographic analyses demonstrate that these inhibit

33 the BtuCD and BtuF preparations used in the crystallographic analyses for both ATPase and transport

34 Based on crystallographic analyses for others RTKs, TrkB tyrosine

35 Crystallographic analyses have been unsuccessful in reso

36 yme complexes may be more flexible than most crystallographic analyses have implied.

37 High resolution x-ray crystallographic analyses have shown that, remarkably, t

38 ent issue of PLOS Biology reveal by means of crystallographic analyses how the Rap proteins of bacill

39 REAP combined with crystallographic analyses identified 35 sites where repl

40 Previous x-ray crystallographic analyses identified distinct binding si

41 X-ray crystallographic analyses identify the consistent format

42 Crystallographic analyses of 11 PelC-Ca(2+) complexes, f

43 lpha-substituted tropanes, as shown by X-ray crystallographic analyses of 11, 12, and 19.

44 Here we report physiological and crystallographic analyses of a calcium selectivity filte

45 We report here the first X-ray crystallographic analyses of a Fab fragment from a rat a

46 tion, have been largely revealed by detailed crystallographic analyses of a number of haemoglobin mol

47 Crystallographic analyses of a shared HSPG-CSPG binding

48 Subsequent crystallographic analyses of AChE complexes with the TZ2

49 Crystallographic analyses of CocE-L169K/G173Q, determine

50 Evidence for such a mechanism comes from crystallographic analyses of fragments of VP4, the rotav

51 By carrying out crystallographic analyses of full-length H6N6-NS1 (A/blu

52 F-RNA we carried out thermodynamic and X-ray crystallographic analyses of fully and partially 2'-F-mo

53 Previous crystallographic analyses of GlpG, a bacterial rhomboid

54 Crystallographic analyses of H-2K(b)-peptide complexes s

55 Crystallographic analyses of HA from the recent H1N1 vir

56 nscription complexes of a bacterial RNAP and crystallographic analyses of its backtracked and Gre-fac

57 A series of crystallographic analyses of Leishmania major PTR1 are r

58 Comparative X-ray crystallographic analyses of MDMX and of pTyr99 MDMX in

59 e phosphatase activity of NSP2, we performed crystallographic analyses of native NSP2 and a functiona

60 Crystallographic analyses of product and substrate compl

61 mapping in a human helminth parasite, while crystallographic analyses of protein-drug interactions i

62 X-ray crystallographic analyses of Q425 in the presence of Ca(

63 Crystallographic analyses of Ras bound to the catalytic

64 X-ray crystallographic analyses of ribosomal complexes have re

65 eraction at the atomic level, we carried out crystallographic analyses of Sp-Nup37 alone and in a com

66 The crystallographic analyses of such enzyme-DNA complexes h

67 We performed x-ray crystallographic analyses of the 6-aminohexanoate oligom

68 X-ray crystallographic analyses of the 8-, 9-, and 10-membered

69 IR spectral and X-ray crystallographic analyses of the [ArH,NO+] complexes rev

70 Crystallographic analyses of the antibodies, in many cas

71 Structural as well as crystallographic analyses of the cross-linked species, B

72 Kinetic and crystallographic analyses of the EcoRV E45A mutant enzym

73 d-containing bacteriophage PM2 determined by crystallographic analyses of the entire approximately 45

74 molecule-1, have been investigated by X-ray crystallographic analyses of the individual components a

75 Here, we describe crystallographic analyses of the mechanism of inhibition

76 X-ray crystallographic analyses of the new cores were used to

77 Crystallographic analyses of the paired-end complex (PEC

78 However, recent high-resolution X-ray crystallographic analyses of the protein from Escherichi

79 putational model of the nucleosome, based on crystallographic analyses of the structure and elasticit

80 NMR and X-ray crystallographic analyses of the tetrafluorinated methyl

81 X-ray crystallographic analyses of the three parent ligands (1

82 Here we present crystallographic analyses of the virally hijacked form o

83 Crystallographic analyses of this construct show the bas

84 X-ray crystallographic analyses of three different examples ha

85 Spectroscopic and atomic resolution crystallographic analyses of three representatives, mOra

86 ally different from that proposed from x-ray crystallographic analyses of two-domain fragments, in wh

87 ased on solution fluorescence, kinetics, and crystallographic analyses of wild-type and mutant polyme

88 Our kinetic and crystallographic analyses offer the molecular basis for

89 line with important conclusions of previous crystallographic analyses, particularly the ZZEssa confi

90 Electron crystallographic analyses provide little information abo

91 Crystallographic analyses reveal inhibition by 2OG cosub

92 Detailed crystallographic analyses reveal quantitively the flexib

93 Crystallographic analyses reveal that the N-terminal dom

94 Biochemical and X-ray crystallographic analyses reveal that the properties of

95 Crystallographic analyses reveal that the UTY(KDM6C) act

96 While the crystallographic analyses revealed only one structure, I

97 Biochemical and crystallographic analyses revealed that hormone binding

98 X-ray crystallographic analyses revealed that the phase transi

99 Crystallographic analyses revealed two binding modes for

100 We report cellular, biochemical, and crystallographic analyses revealing that Pseudomonas pro

101 ese enzymes are homologous, and recent X-ray crystallographic analyses show the active sites of the t

102 Previous x-ray crystallographic analyses showed that the GAT region is

103 The results support crystallographic analyses showing the importance of hydr

104 sis experiments, enzymatic assays, and x-ray crystallographic analyses suggest that His(49) functions

105 Amide hydrogen exchange studies and crystallographic analyses suggest that this substrate-bi

106 Atomic resolution crystallographic analyses suggest that two important fac

107 We show in biochemical and crystallographic analyses that PHF2 recognizes histone H

108 2+ and the MIDAS region have been defined by crystallographic analyses, the role of cation in I domai

109 richia coli genome, has been solved by X-ray crystallographic analyses to a resolution of 1.85 A for

110 nary complexes have been determined by X-ray crystallographic analyses to high resolution.

111 Here, through crystallographic analyses we show that the SUMO E2 Ubc9

112 X-ray crystallographic analyses were performed on ureas 1, 3,

113 for the inhibition of elastase, kinetic and crystallographic analyses were undertaken to identify th

114 erminal domain of RNase E is consistent with crystallographic analyses, which indicate that the tetra

115 Crystallographic analyses with succinate, fumarate, L-ma