메뉴 건너뛰기




Volumn 10, Issue 8, 2003, Pages 663-668

Anticipatory active-site motions and chromophore distortion prime photoreceptor PYP for light activation

Author keywords

[No Author keywords available]

Indexed keywords

PHOTOACTIVE YELLOW PROTEIN;

EID: 0043125483     PISSN: 10728368     EISSN: None     Source Type: Journal    
DOI: 10.1038/nsb958     Document Type: Article
Times cited : (114)

References (28)
  • 1
    • 0027324441 scopus 로고
    • The eubacterium Ectothiorhodospira halophila is negatively phototactic, with a wavelength dependence that fits the absorption spectrum of the photoactive yellow protein
    • Sprenger, W.W., Hoff, W.D., Armitage, J.P. & Hellingwerf, K.J. The eubacterium Ectothiorhodospira halophila is negatively phototactic, with a wavelength dependence that fits the absorption spectrum of the photoactive yellow protein. J. Bacteriol. 175, 3096-3104 (1993).
    • (1993) J. Bacteriol. , vol.175 , pp. 3096-3104
    • Sprenger, W.W.1    Hoff, W.D.2    Armitage, J.P.3    Hellingwerf, K.J.4
  • 2
    • 0033575370 scopus 로고    scopus 로고
    • Bacterial photoreceptor with similarity to photoactive yellow protein and plant phytochromes
    • Jiang, Z. et al. Bacterial photoreceptor with similarity to photoactive yellow protein and plant phytochromes. Science 285, 406-409 (1999).
    • (1999) Science , vol.285 , pp. 406-409
    • Jiang, Z.1
  • 3
    • 0032809454 scopus 로고    scopus 로고
    • Femtosecond spectroscopic observations of initial intermediates in the photocycle of the photoactive yellow protein from Ectothiorhodospira halophila
    • Devanathan, S. et al. Femtosecond spectroscopic observations of initial intermediates in the photocycle of the photoactive yellow protein from Ectothiorhodospira halophila. Biophys. J. 77, 1017-1023 (1999).
    • (1999) Biophys. J. , vol.77 , pp. 1017-1023
    • Devanathan, S.1
  • 4
    • 0035807935 scopus 로고    scopus 로고
    • Spectroscopic characterization of the photocycle intermediates of photoactive yellow protein
    • Imamoto, Y., Mihara, K., Tokunaga, F. & Kataoka, M. Spectroscopic characterization of the photocycle intermediates of photoactive yellow protein. Biochemistry 40, 14336-14343 (2001).
    • (2001) Biochemistry , vol.40 , pp. 14336-14343
    • Imamoto, Y.1    Mihara, K.2    Tokunaga, F.3    Kataoka, M.4
  • 5
    • 0029110488 scopus 로고
    • 1.4 Å structure of photoactive yellow protein, a cytosolic photoreceptor: Unusual fold, active site, and chromophore
    • Borgstahl, G.E., Williams, D.R. & Getzoff, E.D. 1.4 Å structure of photoactive yellow protein, a cytosolic photoreceptor: unusual fold, active site, and chromophore. Biochemistry 34, 6278-6287 (1995).
    • (1995) Biochemistry , vol.34 , pp. 6278-6287
    • Borgstahl, G.E.1    Williams, D.R.2    Getzoff, E.D.3
  • 6
    • 0031039399 scopus 로고    scopus 로고
    • Structure of a protein photocycle intermediate by millisecond time-resolved crystallography
    • Genick, U.K. et al. Structure of a protein photocycle intermediate by millisecond time-resolved crystallography. Science 275, 1471-1475 (1997).
    • (1997) Science , vol.275 , pp. 1471-1475
    • Genick, U.K.1
  • 7
    • 0032510475 scopus 로고    scopus 로고
    • Structure at 0.85 Å resolution of an early protein photocycle intermediate
    • Genick, U.K., Soltis, S.M., Kuhn, P., Canestrelli, I.L. & Getzoff, E.D. Structure at 0.85 Å resolution of an early protein photocycle intermediate. Nature 392, 206-209 (1998).
    • (1998) Nature , vol.392 , pp. 206-209
    • Genick, U.K.1    Soltis, S.M.2    Kuhn, P.3    Canestrelli, I.L.4    Getzoff, E.D.5
  • 8
    • 0034727659 scopus 로고    scopus 로고
    • Probing the nature of the blue-shifted intermediate of photoactive yellow protein in solution by NMR: Hydrogen-deuterium exchange data and pH studies
    • Craven, C.J. et al. Probing the nature of the blue-shifted intermediate of photoactive yellow protein in solution by NMR: hydrogen-deuterium exchange data and pH studies. Biochemistry 39, 14392-14399 (2000).
    • (2000) Biochemistry , vol.39 , pp. 14392-14399
    • Craven, C.J.1
  • 9
    • 0035923399 scopus 로고    scopus 로고
    • A molecular movie at 1.8 Å resolution displays the photocycle of photoactive yellow protein, a eubacterial blue-light receptor from nanoseconds to seconds
    • Ren, Z. et al. A molecular movie at 1.8 Å resolution displays the photocycle of photoactive yellow protein, a eubacterial blue-light receptor from nanoseconds to seconds. Biochemistry 40, 13788-13801 (2001).
    • (2001) Biochemistry , vol.40 , pp. 13788-13801
    • Ren, Z.1
  • 10
    • 0037197689 scopus 로고    scopus 로고
    • Resonance Raman spectroscopy and quantum chemical calculations reveal structural changes in the active site of photoactive yellow protein
    • Unno, M., Kumauchi, M., Sasaki, J., Tokunaga, F. & Yamauchi, S. Resonance Raman spectroscopy and quantum chemical calculations reveal structural changes in the active site of photoactive yellow protein. Biochemistry 41, 5668-5674 (2002).
    • (2002) Biochemistry , vol.41 , pp. 5668-5674
    • Unno, M.1    Kumauchi, M.2    Sasaki, J.3    Tokunaga, F.4    Yamauchi, S.5
  • 11
    • 0038344081 scopus 로고    scopus 로고
    • Photoisomerization and proton transfer in photoactive yellow protein
    • Thompson, M.J., Bashford, D., Noodleman, L. & Getzoff, E.D. Photoisomerization and proton transfer in photoactive yellow protein. J. Am. Chem. Soc. 125, 8186-8194 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 8186-8194
    • Thompson, M.J.1    Bashford, D.2    Noodleman, L.3    Getzoff, E.D.4
  • 12
    • 0028577744 scopus 로고
    • Complete chemical structure of photoactive yellow protein: Novel thioester-linked 4-hydroxycinnamyl chromophore and photocycle chemistry
    • Baca, M. et al. Complete chemical structure of photoactive yellow protein: novel thioester-linked 4-hydroxycinnamyl chromophore and photocycle chemistry. Biochemistry 33, 14369-14377 (1994).
    • (1994) Biochemistry , vol.33 , pp. 14369-14377
    • Baca, M.1
  • 13
    • 0028918464 scopus 로고
    • Photoinduced volume change and energy storage associated with the early transformations of the photoactive yellow protein from Ectothiorhodospira halophila
    • van Brederode, M.E., Gensch, T., Hoff, W.D., Hellingwerf, K.J. & Braslavsky, S.E. Photoinduced volume change and energy storage associated with the early transformations of the photoactive yellow protein from Ectothiorhodospira halophila. Biophys. J. 68, 1101-1109 (1995).
    • (1995) Biophys. J. , vol.68 , pp. 1101-1109
    • Van Brederode, M.E.1    Gensch, T.2    Hoff, W.D.3    Hellingwerf, K.J.4    Braslavsky, S.E.5
  • 14
    • 0023152468 scopus 로고
    • Properties of a water-soluble, yellow protein isolated from a halophilic phototrophic bacterium that has photochemical activity analogous to sensory rhodopsin
    • Meyer, T.E., Yakali, E., Cusanovich, M.A. & Tollin, G. Properties of a water-soluble, yellow protein isolated from a halophilic phototrophic bacterium that has photochemical activity analogous to sensory rhodopsin. Biochemistry 26, 418-423 (1987).
    • (1987) Biochemistry , vol.26 , pp. 418-423
    • Meyer, T.E.1    Yakali, E.2    Cusanovich, M.A.3    Tollin, G.4
  • 15
    • 0028832513 scopus 로고
    • Resonance Raman evidence that the thioester-linked 4-hydroxycinnamyl chromophore of photoactive yellow protein is deprotonated
    • Kim, M., Mathies, R.A., Hoff, W.D. & Hellingwerf, K.J. Resonance Raman evidence that the thioester-linked 4-hydroxycinnamyl chromophore of photoactive yellow protein is deprotonated. Biochemistry 34, 12669-12672 (1995).
    • (1995) Biochemistry , vol.34 , pp. 12669-12672
    • Kim, M.1    Mathies, R.A.2    Hoff, W.D.3    Hellingwerf, K.J.4
  • 16
    • 0034619501 scopus 로고    scopus 로고
    • Coupling of hydrogen bonding to chromophore conformation and function in photoactive yellow protein
    • Brudler, R. et al. Coupling of hydrogen bonding to chromophore conformation and function in photoactive yellow protein. Biochemistry 39, 13478-13486 (2000).
    • (2000) Biochemistry , vol.39 , pp. 13478-13486
    • Brudler, R.1
  • 17
    • 0034620544 scopus 로고    scopus 로고
    • Protonation states and pH titration in the photocycle of photoactive yellow protein
    • Demchuk, E., Genick, U.K., Woo, T.T., Getzoff, E.D. & Bashford, D. Protonation states and pH titration in the photocycle of photoactive yellow protein. Biochemistry 39, 1100-1113 (2000).
    • (2000) Biochemistry , vol.39 , pp. 1100-1113
    • Demchuk, E.1    Genick, U.K.2    Woo, T.T.3    Getzoff, E.D.4    Bashford, D.5
  • 18
    • 0033613812 scopus 로고    scopus 로고
    • Visualizing and quantifying molecular goodness-of-fit: Small-probe contact dots with explicit hydrogen atoms
    • Word, J.M. et al. Visualizing and quantifying molecular goodness-of-fit: small-probe contact dots with explicit hydrogen atoms. J. Mol. Biol. 285, 1711-1733 (1999).
    • (1999) J. Mol. Biol. , vol.285 , pp. 1711-1733
    • Word, J.M.1
  • 19
    • 0002466550 scopus 로고    scopus 로고
    • Ab initio molecular dynamics study of cis-trans photoisomerization in ethylene
    • Ben-Nun, M. & Martinez, T.J. Ab initio molecular dynamics study of cis-trans photoisomerization in ethylene. Chem. Phys. Lett. 298, 57-65 (1998).
    • (1998) Chem. Phys. Lett. , vol.298 , pp. 57-65
    • Ben-Nun, M.1    Martinez, T.J.2
  • 20
    • 0035969547 scopus 로고    scopus 로고
    • Real-time spectroscopy of transition states in bacteriorhodopsin during retinal isomerization
    • Kobayashi, T., Saito, T. & Ohtani, H. Real-time spectroscopy of transition states in bacteriorhodopsin during retinal isomerization. Nature 414, 531-534 (2001).
    • (2001) Nature , vol.414 , pp. 531-534
    • Kobayashi, T.1    Saito, T.2    Ohtani, H.3
  • 21
    • 0037022785 scopus 로고    scopus 로고
    • Themodynamic and transport properties of intermediate states of the photocyclic reaction of photoactive yellow protein
    • Takeshita, K., Imamoto, Y., Kataoka, M., Tokunaga, F. & Terazima, M. Themodynamic and transport properties of intermediate states of the photocyclic reaction of photoactive yellow protein. Biochemistry 41, 3037-3048 (2002).
    • (2002) Biochemistry , vol.41 , pp. 3037-3048
    • Takeshita, K.1    Imamoto, Y.2    Kataoka, M.3    Tokunaga, F.4    Terazima, M.5
  • 22
    • 0020648847 scopus 로고
    • The role of mobility in the substrate binding and catalytic machinery of enzymes
    • Alber, T., Gilber, W.A., Ponzi, B.R. & Petzko, G.A. The role of mobility in the substrate binding and catalytic machinery of enzymes. Ciba Found. Symp. 93, 4-24 (1983).
    • (1983) Ciba Found. Symp. , vol.93 , pp. 4-24
    • Alber, T.1    Gilber, W.A.2    Ponzi, B.R.3    Petzko, G.A.4
  • 24
    • 0037012441 scopus 로고    scopus 로고
    • Identification of a protein-promoting vibration in the reaction catalyzed by horse liver alcohol dehydrogenase
    • Caratzoulas, S., Mincer, J.S. & Schwartz, S.D. Identification of a protein-promoting vibration in the reaction catalyzed by horse liver alcohol dehydrogenase. J. Am. Chem. Soc. 124, 3270-3276 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3270-3276
    • Caratzoulas, S.1    Mincer, J.S.2    Schwartz, S.D.3
  • 25
    • 0032790081 scopus 로고    scopus 로고
    • XtalView/XFIT - A versatile program for manipulation of atomic coordinates and electron density
    • McRee, D.E. XtalView/XFIT - a versatile program for manipulation of atomic coordinates and electron density. J. Struct. Biol. 125, 156-165 (1999).
    • (1999) J. Struct. Biol. , vol.125 , pp. 156-165
    • McRee, D.E.1
  • 26
  • 28
    • 0030815133 scopus 로고    scopus 로고
    • Raster3D: Photorealistic molecular graphics
    • Merritt, E.A. & Bacon, D.J. Raster3D: photorealistic molecular graphics. Methods Enzymol. 277, 505-524 (1997).
    • (1997) Methods Enzymol. , vol.277 , pp. 505-524
    • Merritt, E.A.1    Bacon, D.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.