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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 i demonstrated green/red photoswitching with phytochromobilin, a chromophore endogenous to plants, bu
5 codes the key protein in the biosynthesis of phytochromobilin, a cofactor of photoconvertible phytoch
6 rom dark-adapted algal cells, while the (3E)-phytochromobilin adduct displayed red-shifted absorption
8 nt conversions of biliverdin IXalpha to (3Z)-phytochromobilin and (3Z)-phytochromobilin to (3Z)-phyco
9 ana fail to make the phytochrome-chromophore phytochromobilin and therefore are deficient in a wide r
12 yn, 10(Z)syn, 15(Z)anti configuration of the phytochromobilin chromophore buried within the cGMP phos
14 nobilin:ferredoxin oxidoreductase (PcyA), 3Z-phytochromobilin:ferredoxin oxidoreductase (HY2) from Ar
15 BV to the phytochrome chromophore precursor phytochromobilin, genes encoding putative bilin reductas
16 strain producing phycobiliproteins carrying phytochromobilin grew much more slowly at low light inte
17 ase (BVR) is able to functionally inactivate phytochromobilin in vitro, this investigation was undert
19 Whereas incorporation of the native bilin phytochromobilin into PhyB confers robust Pfr --> Pr the
20 biosynthesis of the phytochrome chromophore phytochromobilin involves the oxidative cleavage of heme
21 green algal phytochrome chromophore and that phytochromobilin is an intermediate in its biosynthesis
22 n etiolated ho2-1 seedlings, suggesting that phytochromobilin is limiting in this mutant, even in the
23 s demonstrate that the ability to synthesize phytochromobilin is not restricted to photosynthetic org
24 lue shift is due to a chromophore other than phytochromobilin or reflects a different protein environ
25 E. coli strains produced phycocyanobilin, phytochromobilin, or phycoerythrobilin when they express
27 family member may uniquely contribute to the phytochromobilin pool needed to assemble holo-phytochrom
32 unable to convert biliverdin IX alpha to 3Z-phytochromobilin, preventing synthesis of the phytochrom
37 response due to a lesion in a gene encoding phytochromobilin synthase that severely compromises the
38 The hypothesis that P. pastoris contains phytochromobilin synthase, the enzyme that converts bili