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1 first FTIR spectra of L intermediates among sensory rhodopsins.
2 sory receptor as do the related haloarchaeal sensory rhodopsins.
3 pigment a candidate for one of the G. theta sensory rhodopsins.
4 d residues at the donor position as in known sensory rhodopsins.
5 unction of the two rhodopsins, Chlamydomonas sensory rhodopsins A and B (CSRA and CSRB), as phototaxi
8 C-terminally truncated versions of Anabaena sensory rhodopsin (ASR) demonstrate that the charge move
10 rhodopsins characterized thus far, Anabaena sensory rhodopsin (ASR) is a photochromic sensor that in
12 ransmembrane helical photoreceptor, Anabaena sensory rhodopsin (ASR), prepared in the Escherichia col
13 igomeric integral membrane protein, Anabaena sensory rhodopsin (ASR), reconstituted in a lipid enviro
19 of Htr proteins interact with their cognate sensory rhodopsin cytoplasmic domains as part of the sig
21 compare the isomerization mechanisms of the sensory rhodopsin from the cyanobacterium Anabaena PCC 7
22 r complex containing the phototaxis receptor sensory rhodopsin I (SRI) and transducer protein HtrI (h
28 ch the C-terminus of Halobacterium salinarum sensory rhodopsin I (SRI) is connected by a flexible lin
29 hat transmits signals from the photoreceptor sensory rhodopsin I (SRI) to a cytoplasmic pathway contr
31 ducer HtrI [the halobacterial transducer for sensory rhodopsin I (SRI)] by site-specific mutagenesis.
32 omparison of SRII photoreactions to those of sensory rhodopsin I and bacteriorhodopsin, we interpret
33 protonated in the signal-transducing form of sensory rhodopsin I and is ionized and functions as the
34 rs of the dual-signaling phototaxis receptor sensory rhodopsin I and its transducer subunit (SRI-HtrI
37 from both low- and high-pH forms of purified sensory rhodopsin I reconstituted into lipid vesicles.
38 ignaling and impact our understanding of the sensory rhodopsin I signaling mechanism and the evolutio
40 HtrII has a common feature with HtrI, the sensory rhodopsin I transducer; like HtrI, HtrII possess
43 ic interaction with the phototaxis receptors sensory rhodopsins I and II (SRI and SRII), respectively
49 reference to the 2.4 A crystal structure of sensory rhodopsin II (NpSRII) from Natronobacterium phar
50 al rhodopsin family, the phototaxis receptor sensory rhodopsin II (NpSRII), which mediates blue-light
51 cytoplasmic loops of the phototaxis receptor sensory rhodopsin II (SRII) and the membrane-proximal cy
52 The phototaxis receptor complex composed of sensory rhodopsin II (SRII) and the transducer subunit H
54 studied the photochemical reaction cycle of sensory rhodopsin II (SRII) by flash photolysis of Halob
55 acteriorhodopsin and the phototaxis receptor sensory rhodopsin II (SRII) differ by 74% of their resid
58 Photostimulation of the repellent receptor sensory rhodopsin II (SRII) induced reversible demethyla
63 protein consisting of Natronomonas pharaonis sensory rhodopsin II (SRII), fused by a flexible linker
65 ic environment in the signaling state of the sensory rhodopsin II (SRII)-transducer (HtrII) complex.
68 nal protein phoborhodopsin (pR) (also called sensory rhodopsin II) is a specialized photoreceptor pig
76 two decades since the discovery of the first sensory rhodopsins in the archaeon Halobacterium salinar
78 membrane-embedded transducers, the Anabaena sensory rhodopsin may signal through a soluble cytoplasm
80 ducer interacts with its cognate photoactive sensory rhodopsin receptor, NpSRII, to mediate phototaxi
82 alobacterial cell, confirming that different sensory rhodopsins SRI and SRII in the same organism hav
86 e present crystal structures of the Anabaena sensory rhodopsin transducer (ASRT), a soluble cytoplasm
88 ysically and functionally with their cognate sensory rhodopsins via helix-helix contacts between thei
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