ライフサイエンスコーパス: enzymological

1 Through enzymological and biophysical analysis, we further show

2 Here, we utilize enzymological and biophysical studies, including NMR mea

3 A classic set of enzymological and crystallographic studies by Baldwin an

4 We present enzymological and crystallographic studies of the mechan

5 Contrary to a previous report, our enzymological and genetic studies indicate that ytkD is

6 Taking both enzymological and molecular approaches, we demonstrate h

7 , recombinant P69 was expressed and used for enzymological and structural investigations.

8 In agreement with previous enzymological and structural studies, our thermodynamic

9 We present enzymological and x-ray structural data for hamster chym

10 nine kinase family that exhibits structural, enzymological, and regulatory features distinct from tho

11 so discussed is the failure of the classical enzymological approach to polyketide biosynthesis.

12 ing a combination of immunoprecipitation and enzymological approaches, we show that the plasma membra

13 entified in the Arabidopsis genome by direct enzymological assays and functional expression in yeast.

14 (the E9 DNase) shares many of the same basic enzymological characteristics as sequence-specific H-N-H

15 eports the first heterologous expression and enzymological characterization of a human QSOX1 isoform.

16 This work presents the first enzymological characterization of human lfALR.

17 The current work presents a structural and enzymological characterization of the human R194H mutant

18 arent homogeneity, and performed a classical enzymological characterization.

19 Such fundamental enzymological constants are key to determining substrate

20 ative label-free approach to obtaining basic enzymological constants will facilitate the study of pro

21 disulfide-generating flavoenzymes to provide enzymological context for investigation of the physiolog

22 re of metabolic self-inhibition, we surveyed enzymological data accrued from a century of experimenta

23 lar recombination frequency does not reflect enzymological differences.

24 torial biosynthesis, which would explore the enzymological flexibilities of polyketide biosynthesis.

25 donor analogues to obtain new structural and enzymological information for a representative blood gro

26 Despite decades of enzymological investigation, structural evidence definin

27 ed the Nem1-Spo7 phosphatase complex for its enzymological, kinetic, and regulatory properties with p

28 yeast and characterized with respect to its enzymological, kinetic, and regulatory properties.

29 n further clarified at both the cellular and enzymological levels.

30 cofactor, biotin has a critical role in the enzymological mechanism of a number of enzymes that are

31 ic interactions play essential roles in many enzymological mechanisms, often facilitating formation o

32 Enzymological paradigms have shifted recently to acknowl

33 ly quantified for both types of enzymes, and enzymological parameters could be determined within minu

34 No enzymological precedent exists for an UQ-protein thiolat

35 The enzymological properties (pH optimum, dependence on magn

36 ate in unrelated biological processes, their enzymological properties are decidedly similar.

37 e of dephosphorylating Dol-P and PA, several enzymological properties distinguish this lipid phosphom

38 Other enzymological properties of RGSZ1, brain Gz GAP, and RET

39 id not significantly alter the molecular and enzymological properties of the laccase.

40 To understand the enzymological properties of the protein, we purified and

41 cerate dehydrogenase from M. maripaludis had enzymological properties similar to those of its bacteri

42 wever, SPP1 has some significantly different enzymological properties than the LPPs: the aliphatic ca

43 nt PA phosphatase enzyme and showed that its enzymological properties were very similar to those of t

44 rane fractions that were used to examine its enzymological properties.

45 size and show similar, but distinguishable, enzymological properties.

46 The enzymological results reported here are thus strongly su

47 ifferent classes of substrate is not only of enzymological significance, but in addition, this findin

48 Despite enzymological similarities between eukaryotic R(D,E,C*)-

49 In this study we identified the potential enzymological source of the amine moiety as a pyridoxal

50 expression as determined by a combination of enzymological, structural, and genetic methodologies.

51 dimethylallyl diphosphate (DMAPP) useful for enzymological studies are reported.

52 Two LovC cocrystal structures and enzymological studies help elucidate the molecular basis

53 ght into the substrate specificity of vOTUs, enzymological studies were conducted on vOTUs from Dugbe

54 lier prediction but consistent with in vitro enzymological studies, FKBP38 peptidylprolyl cis/trans i

55 ensive method that could be a useful tool in enzymological studies.

56 s and that has been a paradigm for classical enzymological studies.

57 ), a commonly used fluorescent substrate for enzymological studies.

58 us subtilis, based on the operon context and enzymological studies; these enzymes are presumed to be

59 n mediating DNA transactions in a variety of enzymological systems.

60 genesis, coupled with calorimetric, NMR, and enzymological techniques, to define the key interactions

61 selves formed colloids, by both physical and enzymological tests.

62 We also describe how proteomic and enzymological tools can be used to identify and quantify