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1 arious dehydrogenases, and we found that its electron transferring ability was diminished by AtMETTL2
2 ic P450cam and retained ca. 20% of the first electron transferring ability.
3 ly to Zn(2+), resulting in a decrease in the electron transferring activity without changing drastica
4 ype of reductive activator distinct from the electron-transferring ATPases found to reduce the MoFe-n
5  A Rieske-type [2Fe-2S] cluster serves as an electron-transferring cofactor, and a mononuclear iron s
6 nation of cardiolipin from two mitochondrial electron-transferring complexes was achieved using a rap
7 t interaction formed between Arg-alpha237 in electron transferring flavoprotein (ETF) and Tyr-442 in
8         Here we characterize the bifurcating electron transferring flavoprotein (EtfAf) and butyryl-C
9  studies of the trimethylamine dehydrogenase-electron transferring flavoprotein (TMADH-ETF) electron
10                                         When electron transferring flavoprotein and porcine dimethylg
11 microm for the dimethylglycine dehydrogenase-electron transferring flavoprotein and short chain acyl-
12 signal for the dimethylglycine dehydrogenase.electron transferring flavoprotein complex decreased, in
13 cular mass corresponding to the flavoprotein.electron transferring flavoprotein complex was observed,
14 e or closely overlapping binding motif(s) on electron transferring flavoprotein for dehydrogenase int
15 otein and short chain acyl-CoA dehydrogenase-electron transferring flavoprotein interactions, respect
16 bated with dimethylglycine dehydrogenase and electron transferring flavoprotein, the microelectrospra
17 sarcosine dehydrogenase family for access to electron transferring flavoprotein.
18 ss spectrometry was used to directly observe electron transferring flavoprotein.flavoprotein dehydrog
19                                              Electron-transferring flavoprotein (Etf) and butyryl-CoA
20                                              Electron-transferring flavoprotein (ETF) and its dehydro
21 ers trimethylamine dehydrogenase (TMADH) and electron-transferring flavoprotein (ETF) from Methylophi
22                                          The electron-transferring flavoprotein (ETF) from Methylophi
23 at LYRM5 interacts with and deflavinates the electron-transferring flavoprotein that shuttles electro
24 onstant of 3-7 microM for the interaction of electron-transferring flavoprotein with two equivalent a
25 x partners, trimethylamine dehydrogenase and electron-transferring flavoprotein, has been characteriz
26 with the transfer of reducing equivalents to electron-transferring flavoprotein.
27 rk function of carbon nanotubes modulated by electron transferring from P3HT to SWNTs is proposed to
28 hat pseudoazurin binds closely enough to the electron-transferring heme of the peroxidase to perturb
29 f a single cytochrome lies above the exposed electron-transferring heme of the peroxidase.
30 of solutions that were situated close to the electron-transferring heme with Cu-Fe distances of about
31 ter turnover are delivered one-by-one to the electron-transferring heme.
32 ylogenetically diverse group of complexes of electron-transferring membrane proteins, most familiarly
33 cells do not express MtrF but rather MtrC as electron transferring outer membrane cytochrome.
34            Although molecular, spectral, and electron transferring properties of recombinant His(6) P
35 ficial electron acceptors indicated that the electron-transferring properties of both the FAD- and FM
36 ies of Pdr, to characterize its spectral and electron-transferring properties, and to investigate the
37 rane-bound cytochromes P450 (CYPs) and their electron transferring protein partners, cytochrome P450
38 duction, FMN serves as a redox centre in the electron-transferring system by mediating the electron t

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