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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 emarkably, Borg genes encoding nanowire-like electron-transferring cytochromes and cell surface prote
8 to the properties of redox proteins and many electron-transferring enzymes, allowing investigations o
9 , reduction of both EtfABs depleted of their electron-transferring FAD by NADH was monophasic with a
10 se that represents the slow reduction of the electron-transferring FAD to FADH(-), with reduction of
11 ction of the replete proteins containing the electron-transferring FAD was multiphasic, consisting of
12 between the reactivities of the flavins: the electron transferring flavin ((ET)flavin) was calculated
13 h both proteins, we find that removal of the electron-transferring flavin adenine dinucleotide (FAD)
14 t interaction formed between Arg-alpha237 in electron transferring flavoprotein (ETF) and Tyr-442 in
15         Here we characterize the bifurcating electron transferring flavoprotein (EtfAf) and butyryl-C
16  studies of the trimethylamine dehydrogenase-electron transferring flavoprotein (TMADH-ETF) electron
17                                         When electron transferring flavoprotein and porcine dimethylg
18 microm for the dimethylglycine dehydrogenase-electron transferring flavoprotein and short chain acyl-
19 signal for the dimethylglycine dehydrogenase.electron transferring flavoprotein complex decreased, in
20 cular mass corresponding to the flavoprotein.electron transferring flavoprotein complex was observed,
21 e or closely overlapping binding motif(s) on electron transferring flavoprotein for dehydrogenase int
22 otein and short chain acyl-CoA dehydrogenase-electron transferring flavoprotein interactions, respect
23 bated with dimethylglycine dehydrogenase and electron transferring flavoprotein, the microelectrospra
24 sarcosine dehydrogenase family for access to electron transferring flavoprotein.
25 ss spectrometry was used to directly observe electron transferring flavoprotein.flavoprotein dehydrog
26                                              Electron-transferring flavoprotein (Etf) and butyryl-CoA
27                                              Electron-transferring flavoprotein (ETF) and its dehydro
28 ers trimethylamine dehydrogenase (TMADH) and electron-transferring flavoprotein (ETF) from Methylophi
29                                          The electron-transferring flavoprotein (ETF) from Methylophi
30 at LYRM5 interacts with and deflavinates the electron-transferring flavoprotein that shuttles electro
31 onstant of 3-7 microM for the interaction of electron-transferring flavoprotein with two equivalent a
32 x partners, trimethylamine dehydrogenase and electron-transferring flavoprotein, has been characteriz
33                                          The electron-transferring flavoprotein-menaquinone oxidoredu
34 with the transfer of reducing equivalents to electron-transferring flavoprotein.
35                                  Bifurcating electron transferring flavoproteins (Bf-ETFs) tune chemi
36                   From the outset, canonical electron transferring flavoproteins (ETFs) earned a repu
37 fixing organisms, is a member of a family of electron-transferring flavoproteins that catalyze electr
38 rk function of carbon nanotubes modulated by electron transferring from P3HT to SWNTs is proposed to
39        Moreover, this heterojunction impedes electrons transferring from BiCuSeO to Cu(2) Se, obstruc
40 hat pseudoazurin binds closely enough to the electron-transferring heme of the peroxidase to perturb
41 f a single cytochrome lies above the exposed electron-transferring heme of the peroxidase.
42 of solutions that were situated close to the electron-transferring heme with Cu-Fe distances of about
43 ter turnover are delivered one-by-one to the electron-transferring heme.
44 re observed in the properties of the second, electron transferring, Heme 2.
45 e proteins that harbor seven bis-His ligated electron-transferring hemes and one 5-coordinate catalyt
46 ylogenetically diverse group of complexes of electron-transferring membrane proteins, most familiarly
47 ying the evolution and prevalence of diverse electron-transferring microorganisms and in determining
48 cells do not express MtrF but rather MtrC as electron transferring outer membrane cytochrome.
49            Although molecular, spectral, and electron transferring properties of recombinant His(6) P
50 ficial electron acceptors indicated that the electron-transferring properties of both the FAD- and FM
51 ies of Pdr, to characterize its spectral and electron-transferring properties, and to investigate the
52 rane-bound cytochromes P450 (CYPs) and their electron transferring protein partners, cytochrome P450
53 tate dehydrogenase (Ldh) in concert with the electron-transferring proteins EtfA and EtfB.
54 duction, FMN serves as a redox centre in the electron-transferring system by mediating the electron t