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1  of the linear tetrapyrrole prosthetic group phytochromobilin.
2 n is converted to both 3E- and 3Z-isomers of phytochromobilin.
3 chiral center at C2, thus becoming 2(R),3(E)-phytochromobilin, a chemistry more similar to that propo
4 codes the key protein in the biosynthesis of phytochromobilin, a cofactor of photoconvertible phytoch
5 rom dark-adapted algal cells, while the (3E)-phytochromobilin adduct displayed red-shifted absorption
6 lgal apophytochrome was undertaken with (3E)-phytochromobilin and (3E)-phycocyanobilin.
7 nt conversions of biliverdin IXalpha to (3Z)-phytochromobilin and (3Z)-phytochromobilin to (3Z)-phyco
8 ana fail to make the phytochrome-chromophore phytochromobilin and therefore are deficient in a wide r
9               Whereas plant phytochromes use phytochromobilin as the chromophore, BphPs assemble with
10                  These results indicate that phytochromobilin can functionally substitute for phycocy
11 yn, 10(Z)syn, 15(Z)anti configuration of the phytochromobilin chromophore buried within the cGMP phos
12 he geometry of the C15 methine bridge of the phytochromobilin chromophore.
13 nobilin:ferredoxin oxidoreductase (PcyA), 3Z-phytochromobilin:ferredoxin oxidoreductase (HY2) from Ar
14  BV to the phytochrome chromophore precursor phytochromobilin, genes encoding putative bilin reductas
15  strain producing phycobiliproteins carrying phytochromobilin grew much more slowly at low light inte
16 ase (BVR) is able to functionally inactivate phytochromobilin in vitro, this investigation was undert
17  affect an enzyme that converts heme to this phytochromobilin intermediate.
18    Whereas incorporation of the native bilin phytochromobilin into PhyB confers robust Pfr --> Pr the
19  biosynthesis of the phytochrome chromophore phytochromobilin involves the oxidative cleavage of heme
20 green algal phytochrome chromophore and that phytochromobilin is an intermediate in its biosynthesis
21 n etiolated ho2-1 seedlings, suggesting that phytochromobilin is limiting in this mutant, even in the
22 s demonstrate that the ability to synthesize phytochromobilin is not restricted to photosynthetic org
23 lue shift is due to a chromophore other than phytochromobilin or reflects a different protein environ
24    E. coli strains produced phycocyanobilin, phytochromobilin, or phycoerythrobilin when they express
25 hment of the linear tetrapyrrole chromophore phytochromobilin (P Phi B) for photoactivity.
26 family member may uniquely contribute to the phytochromobilin pool needed to assemble holo-phytochrom
27  only FDBR in flowering plants producing the phytochromobilin (PPhiB) for phytochromes.
28  accumulation of the phytochrome chromophore phytochromobilin (PPhiB) was employed.
29  synthesis of the phytochrome chromophore 3E-phytochromobilin (PPhiB).
30  the linear tetrapyrrole (bilin) chromophore phytochromobilin (PPhiB).
31  unable to convert biliverdin IX alpha to 3Z-phytochromobilin, preventing synthesis of the phytochrom
32 ects a different protein environment for the phytochromobilin prosthetic group.
33 the conclusion that this species possesses a phytochromobilin prosthetic group.
34  the overproduction of phycoerythrobilin and phytochromobilin, respectively.
35                By exploiting the sequence of phytochromobilin synthase (HY2) of Arabidopsis, an enzym
36  response due to a lesion in a gene encoding phytochromobilin synthase that severely compromises the
37     The hypothesis that P. pastoris contains phytochromobilin synthase, the enzyme that converts bili
38 O (designated AtHO1) responsible for much of phytochromobilin synthesis recently was identified.
39  the second HO subfamily also contributes to phytochromobilin synthesis.
40                            Overproduction of phytochromobilin, synthesized by the Arabidopsis thalian
41 in IXalpha to (3Z)-phytochromobilin and (3Z)-phytochromobilin to (3Z)-phycocyanobilin.
42  enzyme that converts biliverdin IX alpha to phytochromobilin, was also addressed in this study.

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