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Yorodumi- PDB-4rvy: Serial Time resolved crystallography of Photosystem II using a fe... -
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Basic information
| Entry | Database: PDB / ID: 4rvy | ||||||||||||
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| Title | Serial Time resolved crystallography of Photosystem II using a femtosecond X-ray laser. The S state after two flashes (S3) | ||||||||||||
Components |
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Keywords | OXIDOREDUCTASE / Photosystem II / Time resolved / Free electron laser / ELECTRON TRANSPORT / Membrane | ||||||||||||
| Function / homology | Function and homology informationphotosystem II oxygen evolving complex / photosystem II assembly / oxygen evolving activity / photosystem II stabilization / photosystem II reaction center / photosystem II / oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor / photosynthetic electron transport chain / photosystem II / response to herbicide ...photosystem II oxygen evolving complex / photosystem II assembly / oxygen evolving activity / photosystem II stabilization / photosystem II reaction center / photosystem II / oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor / photosynthetic electron transport chain / photosystem II / response to herbicide / extrinsic component of membrane / chlorophyll binding / plasma membrane-derived thylakoid membrane / photosynthetic electron transport in photosystem II / : / phosphate ion binding / photosynthesis, light reaction / photosynthesis / respiratory electron transport chain / electron transfer activity / protein stabilization / iron ion binding / heme binding / metal ion binding Similarity search - Function | ||||||||||||
| Biological species | ![]() Thermosynechococcus elongatus (bacteria) | ||||||||||||
| Method | X-RAY DIFFRACTION / FREE ELECTRON LASER / MOLECULAR REPLACEMENT / Resolution: 5.5 Å | ||||||||||||
Authors | Kupitz, C. / Basu, S. / Grotjohann, I. / Fromme, R. / Zatsepin, N. / Rendek, K.N. / Hunter, M. / Shoeman, R.L. / White, T.A. / Wang, D. ...Kupitz, C. / Basu, S. / Grotjohann, I. / Fromme, R. / Zatsepin, N. / Rendek, K.N. / Hunter, M. / Shoeman, R.L. / White, T.A. / Wang, D. / James, D. / Yang, J.-H. / Cobb, D.E. / Reeder, B. / Sierra, R.G. / Liu, H. / Barty, A. / Aquila, A. / Deponte, D. / Kirian, R. / Bari, S. / Bergkamp, J.J. / Beyerlein, K. / Bogan, M.J. / Caleman, C. / Chao, T.-C. / Conrad, C.E. / Davis, K.M. / Fleckenstein, H. / Galli, L. / Hau-Riege, S.P. / Kassemeyer, S. / Laksmono, H. / Liang, M. / Lomb, L. / Marchesini, S. / Martin, A.V. / Messerschmidt, M. / Milathianaki, D. / Nass, K. / Ros, A. / Roy-Chowdhury, S. / Schmidt, K. / Seibert, M. / Steinbrener, J. / Stellato, F. / Yan, L. / Yoon, C. / Moore, T.A. / Moore, A.L. / Pushkar, Y. / Williams, G.J. / Boutet, S. / Doak, R.B. / Weierstall, U. / Frank, M. / Chapman, H.N. / Spence, J.C.H. / Fromme, P. | ||||||||||||
Citation | Journal: Nature / Year: 2014Title: Serial time-resolved crystallography of photosystem II using a femtosecond X-ray laser. Authors: Kupitz, C. / Basu, S. / Grotjohann, I. / Fromme, R. / Zatsepin, N.A. / Rendek, K.N. / Hunter, M.S. / Shoeman, R.L. / White, T.A. / Wang, D. / James, D. / Yang, J.H. / Cobb, D.E. / Reeder, B. ...Authors: Kupitz, C. / Basu, S. / Grotjohann, I. / Fromme, R. / Zatsepin, N.A. / Rendek, K.N. / Hunter, M.S. / Shoeman, R.L. / White, T.A. / Wang, D. / James, D. / Yang, J.H. / Cobb, D.E. / Reeder, B. / Sierra, R.G. / Liu, H. / Barty, A. / Aquila, A.L. / Deponte, D. / Kirian, R.A. / Bari, S. / Bergkamp, J.J. / Beyerlein, K.R. / Bogan, M.J. / Caleman, C. / Chao, T.C. / Conrad, C.E. / Davis, K.M. / Fleckenstein, H. / Galli, L. / Hau-Riege, S.P. / Kassemeyer, S. / Laksmono, H. / Liang, M. / Lomb, L. / Marchesini, S. / Martin, A.V. / Messerschmidt, M. / Milathianaki, D. / Nass, K. / Ros, A. / Roy-Chowdhury, S. / Schmidt, K. / Seibert, M. / Steinbrener, J. / Stellato, F. / Yan, L. / Yoon, C. / Moore, T.A. / Moore, A.L. / Pushkar, Y. / Williams, G.J. / Boutet, S. / Doak, R.B. / Weierstall, U. / Frank, M. / Chapman, H.N. / Spence, J.C. / Fromme, P. | ||||||||||||
| History |
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 4rvy.cif.gz | 1.2 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb4rvy.ent.gz | 1 MB | Display | PDB format |
| PDBx/mmJSON format | 4rvy.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 4rvy_validation.pdf.gz | 18.1 MB | Display | wwPDB validaton report |
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| Full document | 4rvy_full_validation.pdf.gz | 18.7 MB | Display | |
| Data in XML | 4rvy_validation.xml.gz | 255.4 KB | Display | |
| Data in CIF | 4rvy_validation.cif.gz | 304.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/rv/4rvy ftp://data.pdbj.org/pub/pdb/validation_reports/rv/4rvy | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 4pbuC ![]() 3arc S: Starting model for refinement C: citing same article ( |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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Components
-Photosystem II ... , 16 types, 32 molecules AaBbCcDdHhIiJjKkLlMmOoTtUuXxYyZz
| #1: Protein | Mass: 37029.234 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: P0A444, photosystem II#2: Protein | Mass: 55939.562 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DIQ1#3: Protein | Mass: 50287.500 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DIF8#4: Protein | Mass: 38404.949 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8CM25, photosystem II#7: Protein | Mass: 7227.559 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DJ43#8: Protein/peptide | Mass: 4410.245 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DJZ6#9: Protein/peptide | Mass: 4105.908 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: P59087#10: Protein/peptide | Mass: 4101.911 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q9F1K9#11: Protein/peptide | Mass: 4299.044 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DIN8#12: Protein/peptide | Mass: 3807.517 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DHA7#13: Protein | Mass: 26523.578 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: P0A431#14: Protein/peptide | Mass: 3620.369 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DIQ0#15: Protein | Mass: 10966.317 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q9F1L5#17: Protein/peptide | Mass: 4077.873 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q9F1R6#18: Protein/peptide | Mass: 3098.921 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DJI1#19: Protein | Mass: 6766.187 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DHJ2 |
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-Cytochrome b559 subunit ... , 2 types, 4 molecules EeFf
| #5: Protein | Mass: 9321.515 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DIP0#6: Protein/peptide | Mass: 3868.611 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: Q8DIN9 |
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-Protein / Sugars , 2 types, 12 molecules Vv

| #16: Protein | Mass: 15148.255 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / Strain: BP-1 / References: UniProt: P0A386#31: Sugar | ChemComp-DGD / |
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-Non-polymers , 14 types, 156 molecules 


























| #20: Chemical | | #21: Chemical | #22: Chemical | ChemComp-CLA / #23: Chemical | ChemComp-PHO / #24: Chemical | ChemComp-BCR / #25: Chemical | ChemComp-SQD / #26: Chemical | ChemComp-CL / #27: Chemical | #28: Chemical | ChemComp-PL9 / #29: Chemical | ChemComp-LMG / #30: Chemical | ChemComp-CA / #32: Chemical | ChemComp-LHG / #33: Chemical | ChemComp-HEM / #34: Chemical | |
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-Details
| Has protein modification | Y |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 18772 |
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Sample preparation
| Crystal | Density Matthews: 4.1 Å3/Da / Density % sol: 70.02 % |
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| Crystal grow | Temperature: 283 K / Method: free interface diffusion / pH: 7 Details: 100 mM Pipes pH 7.0, 5 mM CaCl2, 10 mM tocopherol, and 10-17% PEG 2000 , Free interface diffusion, temperature 283K, temperature 283.0K |
-Data collection
| Diffraction | Mean temperature: 283 K | |||||||||||||||||||||||||||||||||||||||
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| Diffraction source | Source: FREE ELECTRON LASER / Site: SLAC LCLS / Beamline: CXI / Wavelength: 2.05 Å | |||||||||||||||||||||||||||||||||||||||
| Detector | Type: CS-PAD CXI-1 / Detector: PIXEL / Date: Jan 25, 2012 | |||||||||||||||||||||||||||||||||||||||
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | |||||||||||||||||||||||||||||||||||||||
| Radiation wavelength | Wavelength: 2.05 Å / Relative weight: 1 | |||||||||||||||||||||||||||||||||||||||
| Reflection | Resolution: 5.5→102.295 Å / Num. all: 33992 / Num. obs: 32066 / % possible obs: 99.88 % | |||||||||||||||||||||||||||||||||||||||
| Reflection shell |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 3ARC ![]() 3arc Resolution: 5.5→102.295 Å / σ(F): 1.35
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| Refinement step | Cycle: LAST / Resolution: 5.5→102.295 Å
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| LS refinement shell |
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Thermosynechococcus elongatus (bacteria)
X-RAY DIFFRACTION
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