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1 hat they could provide a route for iron into bacterioferritin.
2 ied within the four-helix bundle, similar to bacterioferritin.
3 cinate dehydrogenase), and a gene encoding a bacterioferritin.
4 xidase center and the iron storage cavity of bacterioferritin.
5 atios of several mammalian ferritins and one bacterioferritin.
6 alpha and beta, of the iron-binding protein, bacterioferritin.
7 xidation and hydrolysis chemistry in E. coli bacterioferritin.
8 es was not impaired by deletion of the alpha-bacterioferritin.
9 ls (DPS)-like protein than to the 24-subunit bacterioferritins.
11 the recombinant M. smegmatis strain exported bacterioferritin, a large (approximately 500-kDa), leade
12 nucleation centers for the mineral cores in bacterioferritins and indicate that these proteins are n
13 acterial two-hybrid system screen identified bacterioferritins and the heme-containing subunit NarI o
15 chocystis sp. PCC 6803 (Synechocystis 6803), bacterioferritins are responsible for the storage of as
17 Escherichia coli and Rhodobacter capsulatus bacterioferritins are unable to associate into 24-meric
18 eroxidase, the heat shock protein GroEL, and bacterioferritin as measured by splenic lymphocyte proli
19 as aeruginosa suggested the possibility of a bacterioferritin assembled from two different subunits.
20 presence of a "regulator", the apo form of a bacterioferritin-associated ferredoxin (apo Pa Bfd).
21 BfrB, FPR, and the apo form of P. aeruginosa bacterioferritin-associated ferredoxin (apo-Bfd) results
22 dehydratase (fumC), bacterioferritin (bfr), bacterioferritin-associated ferredoxin (bfd), and multip
23 a bacterioferritin (Pa-BfrB) in complex with bacterioferritin-associated ferredoxin (Pa-Bfd) at 2.0 A
26 ucture of recombinant Pseudomonas aeruginosa bacterioferritin B (Pa BfrB) has been determined from cr
28 onstrated specific complex formation between bacterioferritin (Bfr) and this NIFU-like [2Fe-2S] prote
31 smutase (sodA), fumarate dehydratase (fumC), bacterioferritin (bfr), bacterioferritin-associated ferr
32 e fluorescence intensity of Escherichia coli bacterioferritin (BFR), due to the presence of two trypt
34 often coexist in bacteria, the heme binding bacterioferritins (Bfr) and the non-heme binding bacteri
36 many other cyanobacterial species, have two bacterioferritins, BfrA and BfrB, in which either the he
37 eroxiredoxins (alkylhydroperoxide reductase, bacterioferritin co-migratory protein and a thiol-peroxi
40 ecently reclassified one such peroxiredoxin, bacterioferritin comigratory protein (BCP) of Escherichi
41 0 in the catalytic cycle of Escherichia coli bacterioferritin comigratory protein (BCP), a previous s
46 oxidized di-Fe(3+) site of Escherichia coli bacterioferritin (EcBFR) is stable and therefore does no
50 Although the structures consist of a typical bacterioferritin fold comprised of a nearly spherical 24
52 n open reading frame located upstream of the bacterioferritin gene in Escherichia coli encodes a hypo
54 ext, the thus far mysterious role of heme in bacterioferritins has been brought to the front by recon
57 l iron, thus demonstrating a central role of bacterioferritins in iron homeostasis in these photosynt
58 heteromultimeric structure of Synechocystis bacterioferritin, in which one subunit ligates a di-iron
60 r cytochrome with such a ligand arrangement, bacterioferritin, is too large to be studied by current
61 g from the exterior surface of SsDPSL to the bacterioferritin-like dimetal binding site, possibly all
66 of the product of the bfrB gene as a genuine bacterioferritin (Pa BfrB), indicate the coexistence of
67 crystal structure of Pseudomonas aeruginosa bacterioferritin (Pa-BfrB) in complex with bacterioferri
70 es and the iron-activated genes encoding two bacterioferritins (PSPTO_0653 and PSPTO_4160), a ParA pr
71 oli (E. coli) multifunctional single subunit bacterioferritin recognized two proteins in the Pp extra
73 quired to maintain iron homeostasis, whereas bacterioferritin seems to be dispensable for this functi
76 ) forms of the native Azotobacter vinelandii bacterioferritin to 2.7 and 2.0 A resolution, respective
77 H(2)O(2), consistent with the ability of the bacterioferritin to facilitate the pairwise oxidation of
78 te of the virulent clinical isolate, whereas bacterioferritin was more abundant in the culture filtra
79 34, Glu-66, Asp-132, and Asp-139) of E. coli bacterioferritin were substituted to determine if they a
80 e transcripts of the two bfr genes (encoding bacterioferritin) were found to be constitutively up-reg
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