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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
9 C-terminally truncated versions of Anabaena sensory rhodopsin (ASR) demonstrate that the charge move
11 rhodopsins characterized thus far, Anabaena sensory rhodopsin (ASR) is a photochromic sensor that in
13 ransmembrane helical photoreceptor, Anabaena sensory rhodopsin (ASR), prepared in the Escherichia col
14 igomeric integral membrane protein, Anabaena sensory rhodopsin (ASR), reconstituted in a lipid enviro
20 of Htr proteins interact with their cognate sensory rhodopsin cytoplasmic domains as part of the sig
22 compare the isomerization mechanisms of the sensory rhodopsin from the cyanobacterium Anabaena PCC 7
23 r complex containing the phototaxis receptor sensory rhodopsin I (SRI) and transducer protein HtrI (h
29 ch the C-terminus of Halobacterium salinarum sensory rhodopsin I (SRI) is connected by a flexible lin
30 hat transmits signals from the photoreceptor sensory rhodopsin I (SRI) to a cytoplasmic pathway contr
32 ducer HtrI [the halobacterial transducer for sensory rhodopsin I (SRI)] by site-specific mutagenesis.
33 omparison of SRII photoreactions to those of sensory rhodopsin I and bacteriorhodopsin, we interpret
34 protonated in the signal-transducing form of sensory rhodopsin I and is ionized and functions as the
35 rs of the dual-signaling phototaxis receptor sensory rhodopsin I and its transducer subunit (SRI-HtrI
38 from both low- and high-pH forms of purified sensory rhodopsin I reconstituted into lipid vesicles.
39 ignaling and impact our understanding of the sensory rhodopsin I signaling mechanism and the evolutio
41 HtrII has a common feature with HtrI, the sensory rhodopsin I transducer; like HtrI, HtrII possess
44 ic interaction with the phototaxis receptors sensory rhodopsins I and II (SRI and SRII), respectively
50 reference to the 2.4 A crystal structure of sensory rhodopsin II (NpSRII) from Natronobacterium phar
51 al rhodopsin family, the phototaxis receptor sensory rhodopsin II (NpSRII), which mediates blue-light
53 cytoplasmic loops of the phototaxis receptor sensory rhodopsin II (SRII) and the membrane-proximal cy
54 The phototaxis receptor complex composed of sensory rhodopsin II (SRII) and the transducer subunit H
56 studied the photochemical reaction cycle of sensory rhodopsin II (SRII) by flash photolysis of Halob
57 acteriorhodopsin and the phototaxis receptor sensory rhodopsin II (SRII) differ by 74% of their resid
60 Photostimulation of the repellent receptor sensory rhodopsin II (SRII) induced reversible demethyla
65 protein consisting of Natronomonas pharaonis sensory rhodopsin II (SRII), fused by a flexible linker
67 ic environment in the signaling state of the sensory rhodopsin II (SRII)-transducer (HtrII) complex.
70 ast side-chain dynamics of the alpha-helical sensory rhodopsin II and the beta-barrel outer membrane
71 nal protein phoborhodopsin (pR) (also called sensory rhodopsin II) is a specialized photoreceptor pig
79 two decades since the discovery of the first sensory rhodopsins in the archaeon Halobacterium salinar
81 membrane-embedded transducers, the Anabaena sensory rhodopsin may signal through a soluble cytoplasm
83 ducer interacts with its cognate photoactive sensory rhodopsin receptor, NpSRII, to mediate phototaxi
85 alobacterial cell, confirming that different sensory rhodopsins SRI and SRII in the same organism hav
89 e present crystal structures of the Anabaena sensory rhodopsin transducer (ASRT), a soluble cytoplasm
91 ysically and functionally with their cognate sensory rhodopsins via helix-helix contacts between thei