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1 wever, in species of Pseudomonas, Rhizobium, Paracoccus and Legionella, mutations in ccm genes result
2 cloned vbs genes, plus rpoI, to Rhodobacter, Paracoccus and Sinorhizobium conferred the ability to ma
4 state of cytochrome c550 for its binding to Paracoccus cytochrome c peroxidase and its delivery of t
5 icans can accommodate horse cytochrome c and Paracoccus cytochrome c(550) at different sites on its m
6 pH 6.0, I = 0.026) but only one molecule of Paracoccus cytochrome c-550 with a K(d) of 2.8 microM, m
8 on (PDB code 1occ) and of the soil bacterium Paracoccus denitrificans (1arl) include a dicopper cente
10 igands to the native type I copper center of Paracoccus denitrificans amicyanin was replaced with the
11 g with antibodies raised against subunits of Paracoccus denitrificans and against synthetic peptides
16 acter sphaeroides is specifically related to Paracoccus denitrificans and Rc. gelatinosa is related t
17 t is a novel inhibitor of the F1FO-ATPase of Paracoccus denitrificans and related alpha-proteobacteri
18 lly simpler bacterial counterpart (NDH-1) in Paracoccus denitrificans and Thermus thermophilus HB-8 c
20 in the dimeric cytochrome bc(1) complex from Paracoccus denitrificans by characterizing the kinetics
21 previous papers, cytochrome c peroxidase of Paracoccus denitrificans can accommodate horse cytochrom
24 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans consists of at least 14 unlike
26 chemical changes in the P(M) intermediate of Paracoccus denitrificans cytochrome c oxidase have been
27 The structure of the P(M) intermediate of Paracoccus denitrificans cytochrome c oxidase was invest
28 es of P(M) and F intermediates of bovine and Paracoccus denitrificans cytochrome c oxidase were inves
31 he three-dimensional structures of human and Paracoccus denitrificans ETFs determined by X-ray crysta
32 Our work with the model denitrifying strain Paracoccus denitrificans further shows that ligand-enhan
33 ic quinohemoprotein amine dehydrogenase from Paracoccus denitrificans has been determined at 2.05-A r
34 quinoprotein methylamine dehydrogenase from Paracoccus denitrificans has been refined at 1.75 A reso
35 ccinate:ubiquinone oxidoreductase (SQR) from Paracoccus denitrificans have been undertaken in the pur
36 residue in both Saccharomyces cerevisiae and Paracoccus denitrificans have indicated that mutations a
37 of these ligands in supporting the growth of Paracoccus denitrificans in a low-iron environment and t
38 he zinc-specific SBP AztC from the bacterium Paracoccus denitrificans in the zinc-bound and apo-state
40 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of 14 different sub
41 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of 14 different sub
42 e- (NADH-) quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of at least 14 diff
43 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of at least 14 subu
44 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of at least 14 unli
49 1-14, encode subunits homologous to those of Paracoccus denitrificans NDH-1, respectively, and are ar
50 Molecular properties of the NQO9 subunit of Paracoccus denitrificans NDH-1, which is predicted to co
51 reported for the homologous D477A mutant of Paracoccus denitrificans or for bovine COX (K(d) = 1-3 m
52 dicted from the known processing site of the Paracoccus denitrificans oxidase, does not produce the s
56 sis of methylamine dehydrogenase (MADH) from Paracoccus denitrificans requires four genes in addition
57 sis of methylamine dehydrogenase (MADH) from Paracoccus denitrificans requires four genes in addition
58 alculations on the cytochrome c oxidase from Paracoccus denitrificans revealed an unexpected coupling
59 he amino acid sequence of cytochrome c550 of Paracoccus denitrificans strain LMD 52.44 was determined
62 based on the biological reduction of N2O by Paracoccus denitrificans using methanol as a carbon/elec
63 of electron transfer flavoprotein (ETF) from Paracoccus denitrificans was determined and refined to a
64 of the Type I copper protein, amicyanin from Paracoccus denitrificans was determined at 1.8 A resolut
69 unction, as revealed by the structure of the Paracoccus denitrificans zeta-subunit in complex with AD
70 oxidases, the equivalent tryptophan (W121 in Paracoccus denitrificans) has been identified as the "el
71 y dependent on haem-iron as a cofactor (e.g. Paracoccus denitrificans) or a Nir that is solely depend
72 ms from methane-acclimated sludge (including Paracoccus denitrificans) to facilitate electron transfe
75 with structures of Rhodobacter sphaeroides, Paracoccus denitrificans, and bovine CcO derived by crys
76 ic to a bacterium related to R. sphaeroides, Paracoccus denitrificans, and is lethal to R. sphaeroide
77 Atp11p from Candida glabrata and Atp12p from Paracoccus denitrificans, and we show that some features
78 ATP synthase from the alpha-proteobacterium Paracoccus denitrificans, inhibited by its natural regul
79 dditionally conserved in Pichia pastoris and Paracoccus denitrificans, suggesting that they are funct
81 f this putative accessory factor (AztD) from Paracoccus denitrificans, we have analyzed its transcrip
82 ria (from Bos taurus) and from the bacterium Paracoccus denitrificans, we show that four protons are
83 , also observed in cytochrome c oxidase from Paracoccus denitrificans, were similarly associated with
84 species, such as Rhodobacter sphaeroides and Paracoccus denitrificans, which contain an additional mi
85 ing NADH-quinone oxidoreductase (NDH-1) from Paracoccus denitrificans, which is composed of the NQO1
97 y reacted with a single band (11 kDa) of the Paracoccus membranes and cross-reacted with Rhodobactor
98 ubunit was not able to be extracted from the Paracoccus membranes by NaI or alkaline treatment, unlik
99 qo10 subunit could not be extracted from the Paracoccus membranes by NaI or alkaline treatment, which
100 thylamino)propyl]carbodiimide (EDC), and the Paracoccus membranes were used, and the cross-linked pro
105 in SY is phylogenetically closely related to Paracoccus niistensis with a 16S rRNA gene similarity of
111 modification techniques, the topology of the Paracoccus NQO7 subunit in the membranes has been examin
114 ratory reduction of nitrate to dinitrogen in Paracoccus pantotrophus is catalyzed by the quinol-nitra
115 erize a sirohydrochlorin-ferrochelatase from Paracoccus pantotrophus that catalyses the last step of
116 embrane-bound nitrate reductase (narGHJI) in Paracoccus pantotrophus there is a fusion of two genes,
117 single site on cytochrome c peroxidase from Paracoccus pantotrophus with a K(d) of 16.4 microM at 25
120 ide direct evidence for As(III) oxidation by Paracoccus species and suggest that these species may pl
121 results indicate that EO-2 represents a new Paracoccus species, the first isolated from human clinic
125 m the P. laminosum plastocyanin gene and the Paracoccus versutus cytochrome c-550 gene), much higher
127 ltage-dependent Na(+) channels (Na(V)PZ from Paracoccus zeaxanthinifaciens and Na(V)SP from Silicibac
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