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1 rase/adenylyl cyclase/FhlA (GAF) domain from Thermosynechococcus elongatus (Te) PixJ, a member of the
2  of PSII from a thermophilic cyanobacterium, Thermosynechococcus elongatus , on a nanostructured indi
3 onomeric and trimeric PS I core complexes of Thermosynechococcus elongatus and Arthrospira platensis,
4  the dimeric and monomeric form of PSII from Thermosynechococcus elongatus and spinach PSII.
5 ystal structures of cyanobacterial PORs from Thermosynechococcus elongatus and Synechocystis sp. in t
6  domain from the cyanobacteriochrome PixJ in Thermosynechococcus elongatus assembled with phycocyanob
7 e crystal structure of CyanoP (Tlr2075) from Thermosynechococcus elongatus at 2.8 A.
8  the structure of PSII of the cyanobacterium Thermosynechococcus elongatus at 3.5 angstrom resolution
9 onstructed by substituting sequence from the Thermosynechococcus elongatus b and b' genes in the E. c
10                                   PBP-A from Thermosynechococcus elongatus belongs to a cyanobacteria
11 ercomplexes isolated from the cyanobacterium Thermosynechococcus elongatus BP-1 cultured under iron-s
12 complex from the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1 enabled characterizat
13 lectron microscopy study of S. elongatus and Thermosynechococcus elongatus BP-1 KaiA-KaiC complexes.
14 her one observed in strains belonging to the Thermosynechococcus elongatus BP-1 lineage, in which Ca-
15 nctiforme, Anabaena sp. strain PCC 7120, and Thermosynechococcus elongatus BP-1), and apparent orthol
16  isolated from the hopane-producing bacteria Thermosynechococcus elongatus BP-1, Bradyrhizobium japon
17 complex from the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1, obtained by single-p
18 KaiC-derived peptide from the cyanobacterium Thermosynechococcus elongatus BP-1.
19 of KaiA from the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1.
20 lant-like Te-Rubisco from the cyanobacterium Thermosynechococcus elongatus BP1 identified two large s
21 re the 1.35- angstrom structure of the first Thermosynechococcus elongatus CcmM(S) domain, revealing
22     Here we present the crystal structure of Thermosynechococcus elongatus Gun4 at 1.5 A, describe th
23  is very similar to the native S(2) state of Thermosynechococcus elongatus in terms of spin state ene
24 for crystals of photosystem II isolated from Thermosynechococcus elongatus indicates that a calcium i
25  a cyanobacterial photosystem II (PSII) from Thermosynechococcus elongatus on a mesoporous indium-tin
26  experiments on PSII nano/microcrystals from Thermosynechococcus elongatus performed with the recentl
27 othermophilus thermolysin (2.2-A structure), Thermosynechococcus elongatus photosystem II (<3-A diffr
28 oint potentials (E(m) ) of Q(B) in PSII from Thermosynechococcus elongatus using electron paramagneti
29 fer processes in PSI complexes isolated from Thermosynechococcus elongatus via conventional n-dodecyl
30 t time, we obtained a structure of PSII from Thermosynechococcus elongatus without the Mn4CaO5-cluste
31 PSI complexes are present in thylakoids from Thermosynechococcus elongatus, Synechococcus sp PCC 7002
32 , ChlH, from the thermophilic cyanobacterium Thermosynechococcus elongatus.
33 gous sequences from the b and b' subunits of Thermosynechococcus elongatus.
34 D) structure of PSII from the cyanobacterium Thermosynechococcus elongatus.
35 Tlr0924 from the thermophilic cyanobacterium Thermosynechococcus elongatus.
36 (O5) of Ca-PSII core complexes isolated from Thermosynechococcus vestitus has, within experimental co
37 etry analysis of isolated, functional intact Thermosynechococcus vulcanus PBS, as well as functional
38 stic models of a native cyanobacterial form (Thermosynechococcus vulcanus) and a chimeric spinach-lik