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Dive into the research topics where Yasue Murata is active.

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Featured researches published by Yasue Murata.


Journal of Biological Chemistry | 2006

Assembly of Synthetic Locked Chromophores with Agrobacterium Phytochromes Agp1 and Agp2

Katsuhiko Inomata; Steffi Noack; Mostafa A. S. Hammam; Htoi Khawn; Hideki Kinoshita; Yasue Murata; Norbert Michael; Patrick Scheerer; Norbert Krauss; Tilman Lamparter

Phytochromes are photoreceptors with a bilin chromophore in which light triggers the conversion between the red-absorbing form Pr and the far-red-absorbing form Pfr. Agrobacterium tumefaciens has two phytochromes, Agp1 and Agp2, with antagonistic properties: in darkness, Agp1 converts slowly from Pfr to Pr, whereas Agp2 converts slowly from Pr to Pfr. In a previous study, we have assembled Agp1 with synthetic locked chromophores 15Za, 15Zs, 15Ea, and 15Es in which the C15=C16 double bond is fixed in either the E or Z configuration and the C14–C15 single bond is fixed in either the syn (s) or anti (a) conformation. In the present study, the locked chromophores 5Za and 5Zs were used for assembly with Agp1; in these chromophores, the C4=C5 double bond is fixed in the Z configuration, and the C5–C6 single bond is fixed in either the syn or anti conformation. All locked chromophores were also assembled with Agp2. The data showed that in both phytochromes the Pr chromophore adopts a C4=C5 Z C5–C6 syn C15=C16 Z C14–C15 anti stereochemistry and that in the Pfr chromophore the C15=C16 double bond has isomerized to the E configuration, whereas the C14–C15 single bond remains in the anti conformation. Photoconversion shifted the absorption maxima of the 5Zs adducts to shorter wavelengths, whereas the 5Za adducts were shifted to longer wavelengths. Thus, the C5–C6 single bond of the Pfr chromophore is rather in an anti conformation, supporting the previous suggestion that during photoconversion of phytochromes, a rotation around the ring A-B connecting single bond occurs.


Journal of Biological Chemistry | 2005

Sterically locked synthetic bilin derivatives and phytochrome Agp1 from Agrobacterium tumefaciens form photoinsensitive Pr- and Pfr-like adducts

Katsuhiko Inomata; Mostafa A. S. Hammam; Hideki Kinoshita; Yasue Murata; Htoi Khawn; Steffi Noack; Norbert Michael; Tilman Lamparter


Bulletin of the Chemical Society of Japan | 1978

Preparation and Diels-Alder Reactions of 3-Substituted 3-Sulfolenes

Katsuhiko Inomata; Hideki Kinoshita; Hisayo Takemoto; Yasue Murata; Hiroshi Kotake


Chemistry Letters | 1993

Convenient and Regioselective Syntheses of 3,4-Disubstituted Δ3-Pyrrolin-2-one Derivatives Starting from 2-Tosyl-3,4-Disubstituted Pyrroles

Hideki Kinoshita; Yoshio Hayashi; Yasue Murata; Katsuhiko Inomata


Bulletin of the Chemical Society of Japan | 2006

Syntheses of biliverdin derivatives sterically locked at the CD-ring components

Mostafa A. S. Hammam; Hiroshi Nakamura; Yukari Hirata; Htoi Khawn; Yasue Murata; Hideki Kinoshita; Katsuhiko Inomata


Bulletin of the Chemical Society of Japan | 1983

A convenient method for the synthesis of acyclic ketones. Synthesis of sex pheromone of Douglas fir tussock moth

Yasue Murata; Katsuhiko Inomata; Hideki Kinoshita; Hiroshi Kotake


Chemistry Letters | 2004

Synthesis of the Sterically Fixed Biliverdin Derivative Bearing the Z-anti C/D-Ring Component

Mostafa A. S. Hammam; Yasue Murata; Hideki Kinoshita; Katsuhiko Inomata


Bulletin of the Chemical Society of Japan | 1996

Syntheses of 3,4-Disubstituted 2-Tosylpyrroles and 5-Tosyl-1,5-dihydro-2H-pyrrol-2-ones Starting from Ethyl 3,4-Disubstituted 2-Pyrrolecarboxylates

Yasue Murata; Hideki Kinoshita; Katsuhiko Inomata


Chemistry Letters | 1985

1,3-Rearrangement of allylic p-tolyl sulfones catalyzed by [Pd(PPh3)4] and its application to the synthesis of α,β-unsaturated ketones

Katsuhiko Inomata; Yasue Murata; Hisatoyo Kato; Yuhko Tsukahara; Hideki Kinoshita; Hiroshi Kotake


Bulletin of the Chemical Society of Japan | 1965

The Ionization Constants of Organic Compounds. I. The Microscopic Ionization Constants of Tyrosine and Related Compounds

Futaba Yamazaki; Kiyoko Fujiki; Yasue Murata

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Norbert Michael

Technical University of Berlin

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Steffi Noack

Free University of Berlin

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Tilman Lamparter

Karlsruhe Institute of Technology

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