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1 mbination of protein semisynthesis, NMR, and enzymological analysis to characterize structural featur
2                             Here, we combine enzymological analysis with x-ray crystallography to inv
3                                      Through enzymological and biophysical analysis, we further show
4                             Here, we utilize enzymological and biophysical studies, including NMR mea
5                             A classic set of enzymological and crystallographic studies by Baldwin an
6                                   We present enzymological and crystallographic studies of the mechan
7           Contrary to a previous report, our enzymological and genetic studies indicate that ytkD is
8                                  Taking both enzymological and molecular approaches, we demonstrate h
9                                     Genetic, enzymological and structural experiments revealed that P
10 , recombinant P69 was expressed and used for enzymological and structural investigations.
11                   In agreement with previous enzymological and structural studies, our thermodynamic
12                                   We present enzymological and x-ray structural data for hamster chym
13 nine kinase family that exhibits structural, enzymological, and regulatory features distinct from tho
14                Here, we report a structural, enzymological, and virological study of KHNYN's essentia
15 so discussed is the failure of the classical enzymological approach to polyketide biosynthesis.
16 ing a combination of immunoprecipitation and enzymological approaches, we show that the plasma membra
17 entified in the Arabidopsis genome by direct enzymological assays and functional expression in yeast.
18 apenem and penem structural classes, gave an enzymological basis for the effectiveness of the first a
19                       Using a combination of enzymological, cell-culture, and in vivo approaches, we
20 (the E9 DNase) shares many of the same basic enzymological characteristics as sequence-specific H-N-H
21 eports the first heterologous expression and enzymological characterization of a human QSOX1 isoform.
22                 This work presents the first enzymological characterization of human lfALR.
23                                              Enzymological characterization of Rim11 showed that its
24   The current work presents a structural and enzymological characterization of the human R194H mutant
25 arent homogeneity, and performed a classical enzymological characterization.
26                             Such fundamental enzymological constants are key to determining substrate
27 ative label-free approach to obtaining basic enzymological constants will facilitate the study of pro
28 disulfide-generating flavoenzymes to provide enzymological context for investigation of the physiolog
29 re of metabolic self-inhibition, we surveyed enzymological data accrued from a century of experimenta
30              Here, we present structural and enzymological data showing that SAMHD1 utilises an activ
31    Here, crystal and cryo-EM structures, and enzymological data, demonstrate that a conserved tetrame
32                                              Enzymological details of AOA nitrogen metabolism are bro
33 lar recombination frequency does not reflect enzymological differences.
34 torial biosynthesis, which would explore the enzymological flexibilities of polyketide biosynthesis.
35 donor analogues to obtain new structural and enzymological information for a representative blood gro
36                           Despite decades of enzymological investigation, structural evidence definin
37 ed the Nem1-Spo7 phosphatase complex for its enzymological, kinetic, and regulatory properties with p
38  yeast and characterized with respect to its enzymological, kinetic, and regulatory properties.
39 n further clarified at both the cellular and enzymological levels.
40 dards allow next-generation sequencing-based enzymological measurements, reveal the extent of editing
41  cofactor, biotin has a critical role in the enzymological mechanism of a number of enzymes that are
42 ic interactions play essential roles in many enzymological mechanisms, often facilitating formation o
43                                              Enzymological paradigms have shifted recently to acknowl
44 ly quantified for both types of enzymes, and enzymological parameters could be determined within minu
45                                           No enzymological precedent exists for an UQ-protein thiolat
46                                          The enzymological properties (pH optimum, dependence on magn
47 ate in unrelated biological processes, their enzymological properties are decidedly similar.
48 e of dephosphorylating Dol-P and PA, several enzymological properties distinguish this lipid phosphom
49                                        Other enzymological properties of RGSZ1, brain Gz GAP, and RET
50 id not significantly alter the molecular and enzymological properties of the laccase.
51                            To understand the enzymological properties of the protein, we purified and
52 cerate dehydrogenase from M. maripaludis had enzymological properties similar to those of its bacteri
53 wever, SPP1 has some significantly different enzymological properties than the LPPs: the aliphatic ca
54  of human and murine CADs and compared their enzymological properties to CAD from A. terreus Recombin
55 nt PA phosphatase enzyme and showed that its enzymological properties were very similar to those of t
56 CC was distinct from Pah1 in the protein and enzymological properties, which include overexpression t
57 rane fractions that were used to examine its enzymological properties.
58  size and show similar, but distinguishable, enzymological properties.
59 eterotetramers that combine their individual enzymological properties.
60  synthetic reactions shed light on potential enzymological reactivity, including the role of epoxide
61                                          The enzymological results reported here are thus strongly su
62 ifferent classes of substrate is not only of enzymological significance, but in addition, this findin
63                                      Despite enzymological similarities between eukaryotic R(D,E,C*)-
64    In this study we identified the potential enzymological source of the amine moiety as a pyridoxal
65 expression as determined by a combination of enzymological, structural, and genetic methodologies.
66 dimethylallyl diphosphate (DMAPP) useful for enzymological studies are reported.
67            Two LovC cocrystal structures and enzymological studies help elucidate the molecular basis
68 ght into the substrate specificity of vOTUs, enzymological studies were conducted on vOTUs from Dugbe
69 tudies, as well as from classical and recent enzymological studies, are addressed, and open questions
70 lier prediction but consistent with in vitro enzymological studies, FKBP38 peptidylprolyl cis/trans i
71 ensive method that could be a useful tool in enzymological studies.
72 s and that has been a paradigm for classical enzymological studies.
73 ), a commonly used fluorescent substrate for enzymological studies.
74 us subtilis, based on the operon context and enzymological studies; these enzymes are presumed to be
75 n mediating DNA transactions in a variety of enzymological systems.
76 genesis, coupled with calorimetric, NMR, and enzymological techniques, to define the key interactions
77 selves formed colloids, by both physical and enzymological tests.
78           We also describe how proteomic and enzymological tools can be used to identify and quantify