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1 nvolving the mitochondrial membrane NAD/NADP transhydrogenase.
2 it of the membrane-bound pyridine nucleotide transhydrogenase.
3 domains I and III from Rhodospirillum rubrum transhydrogenase.
4 d protein kinase and nicotinamide nucleotide transhydrogenase.
5 mbles the organization of nucleotides in the transhydrogenase active site in the crystal structure.
6                                  Oxidase and transhydrogenase activities are preserved in all mutants
7                              Mutants lacking transhydrogenase activity also have higher levels of glu
8                   For example, cells lacking transhydrogenase activity can utilize methanol as a sole
9                              Mutants lacking transhydrogenase activity have phenotypic and physiologi
10                                              Transhydrogenase activity is observed using NADH and thi
11 alpha-ketoglutarate, namely an FAD-dependent transhydrogenase activity using pyruvate as a hydrogen a
12 aerobic methanol resistance to cells lacking transhydrogenase activity.
13 is the only flavin cofactor required for the transhydrogenase activity.
14 notransferase [Got2] and hydroxyacid-oxoacid transhydrogenase [Adhfe1]).
15 h mitochondrial GSH is maintained largely by transhydrogenase and isocitrate dehydrogenase, the mecha
16 ion and purification of the Escherichia coli transhydrogenase and its reconstitution into liposomes,
17       NADPH-dependent peroxidase, NADH/NADP+ transhydrogenase, and glucose-6-phosphate dehydrogenase
18 at shock protein 60, nicotinamide nucleotide transhydrogenase, and superoxide dismutase.
19 itrobenzoic acid) (DTNB) reductase, oxidase, transhydrogenase, and, in the presence of AhpC, peroxide
20 the C-terminal end of Ec pyridine nucleotide transhydrogenase beta subunit.
21 mplex to that in the complete membrane-bound transhydrogenase, but the rates of forward and reverse t
22                                        Since transhydrogenase can be a major source of NADPH, loss of
23 xylases, hybrid cluster proteins, proteases, transhydrogenase, catalase, and several putative protein
24 lated dI and dIII from Rhodospirillum rubrum transhydrogenase catalyse a rapid, single-turnover burst
25                                              Transhydrogenase catalyses the transfer of reducing equi
26 )dIII(1) complex) from Rhodospirillum rubrum transhydrogenase catalyzes fast single-turnover hydride
27 doxin:NADP+ reductase family of flavoprotein transhydrogenases, catalyzes the NADH-dependent reductio
28 of the RC-LH1-PufX, ATP synthase and NAD(P)H transhydrogenase complexes, as well as showing that the
29                                              Transhydrogenase comprises three domains.
30 o enzyme data show that a not yet identified transhydrogenase could potentially reoxidize approximate
31                                              Transhydrogenase couples reversible hydride transfer fro
32                                              Transhydrogenase couples the redox (hydride-transfer) re
33                                              Transhydrogenase couples the redox reaction between NADH
34                                              Transhydrogenase couples the transfer of hydride-ion equ
35  preparation of a partially degraded E. coli transhydrogenase (ecbeta) was examined.
36         Large increases in pyridine cofactor transhydrogenase flux, correcting imbalanced production
37 rotonmotive force alters the affinity of the transhydrogenase for substrates, accelerates the rate of
38                                              Transhydrogenase, found in bacterial membranes and inner
39                  Here we introduce a soluble transhydrogenase from Escherichia coli (EcSTH) as a nove
40                                  The soluble transhydrogenase from Escherichia coli (SthA) has found
41                                Domain III of transhydrogenase from Rhodospirillum rubrum was expresse
42  studies and supports the notion that intact transhydrogenase functions by an alternating site mechan
43 ADH, were enabled by direct mutations to the transhydrogenase genes sthA and pntAB The phosphotransfe
44 ying NADP(+) reduction by dehydrogenases and transhydrogenases have been hypothesized as a plausible
45                         Recent structures of transhydrogenase holoenzymes suggest new mechanistic det
46 ent glutathione reductase, or the NADH/NADPH transhydrogenase, indicating that matrix GSH regeneratio
47                         We show that E. coli transhydrogenase is a reversible enzyme that can also wo
48 mitochondrial enzyme nicotinamide nucleotide transhydrogenase (Nnt) in pancreatic beta-cells.
49                      Nicotinamide nucleotide transhydrogenase (NNT) is a mitochondrial enzyme that tr
50                      Nicotinamide nucleotide transhydrogenase (NNT) is a mitochondrial redox-driven p
51                      Nicotinamide nucleotide transhydrogenase (NNT) is known to sustain mitochondrial
52 notype was mapped to nicotinamide nucleotide transhydrogenase (Nnt) on mouse chromosome 13, a nuclear
53 at the deficiency of nicotinamide nucleotide transhydrogenase (NNT) protein in C57BL/6J is responsibl
54  forward reaction of nicotinamide nucleotide transhydrogenase (NNT) reduces NADP(+) at the expense of
55 ox-regulating enzyme nicotinamide nucleotide transhydrogenase (NNT) resulted in cellular redox change
56 n, the gene encoding nicotinamide nucleotide transhydrogenase (Nnt) was found to be defective in C57B
57 We hypothesized that nicotinamide nucleotide transhydrogenase (Nnt), which utilizes the proton gradie
58             Although nicotinamide nucleotide transhydrogenase (NNT)-deficient C57BL/6J (6J) mice are
59  potential-dependent nicotinamide nucleotide transhydrogenase (NNT).
60 H provided mostly by nicotinamide nucleotide transhydrogenase (NNT).
61 mitochondrial enzyme Nicotinamide Nucleotide Transhydrogenase (NNT).
62 locator 1 (ANT1) and nicotinamide nucleotide transhydrogenase (NNT)], we selectively impaired mitocho
63 e energy-transducing nicotinamide nucleotide transhydrogenases of mammalian mitochondria and bacteria
64                  The nicotinamide nucleotide transhydrogenases of mitochondria and bacteria are proto
65                  The nicotinamide nucleotide transhydrogenases of mitochondria and bacteria are proto
66 modification of reduced AhpF does not affect transhydrogenase or oxidase activities.
67                          Pyridine nucleotide transhydrogenase (PntAB) is an integral membrane protein
68         Nicotinamide dinucleotide binding to transhydrogenase purified from Escherichia coli was inve
69               We define the mechanism of the transhydrogenase reaction as follows: NADPH binding, hyd
70                   P450 reductase catalyzes a transhydrogenase reaction between NADPH and oxidized nuc
71 , as demonstrated by a hydride ion exchange (transhydrogenase) reaction between NADPH and NADP(+) or
72 ever, the relatively simple structure of the transhydrogenase recommends it as a model for study of t
73                  Soluble pyridine nucleotide transhydrogenases (STHs) are flavoenzymes involved in th
74 ase (cb(5)r) and other members of the flavin transhydrogenase superfamily of oxidoreductases.
75       Membrane bound nicotinamide nucleotide transhydrogenase (TH) catalyses the hydride transfer fro
76                                              Transhydrogenase (TH) couples direct and stereospecific
77                         Proton-translocating transhydrogenase (TH) couples direct and stereospecific
78                                              Transhydrogenase (TH) is a dimeric integral membrane enz
79                      Nicotinamide nucleotide transhydrogenase (TH), a membrane enzyme present in both
80 redoxin oxidoreductase (NfnI), a bifurcating transhydrogenase that takes two electron pairs from NADP
81                    In intact, membrane-bound transhydrogenase, the substitution completely abolished
82 esting because most heterotrophs rely on the transhydrogenase, the TCA cycle, and the oxidative pento
83 ontent, rate constant for NADPH release, and transhydrogenase turnover rates allowed us to estimate t
84 del will be presented to explain the role of transhydrogenase under aerobic conditions when cells nee
85                               Detergent-free transhydrogenase was deposited as a thin film on an ATR
86  component (dI) of the Rhodospirillum rubrum transhydrogenase was substituted with Asn (to give dI.Q1
87 embrane protein Nnt (nicotinamide nucleotide transhydrogenase), we established an isogenic model of N
88 esidues of domain II of the Escherichia coli transhydrogenase were mutated, and the mutant enzymes we
89 nd to isolated dI from Rhodospirillum rubrum transhydrogenase with similar affinity to the physiologi
90 to the mechanism of energy transduction, the transhydrogenase works according to the same principles