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Open data
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Basic information
| Entry | Database: PDB / ID: 1s5l | ||||||||||||
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| Title | Architecture of the photosynthetic oxygen evolving center | ||||||||||||
Components |
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Keywords | PHOTOSYNTHESIS / photosystem / oxygen-evolving / tetra-manganese / 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 / SYNCHROTRON / MIR / Resolution: 3.5 Å | ||||||||||||
Authors | Ferreira, K.N. / Iverson, T.M. / Maghlaoui, K. / Barber, J. / Iwata, S. | ||||||||||||
Citation | Journal: Science / Year: 2004Title: Architecture of the Photosynthetic Oxygen-Evolving Center Authors: Ferreira, K.N. / Iverson, T.M. / Maghlaoui, K. / Barber, J. / Iwata, S. | ||||||||||||
| History |
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| Remark 999 | SEQUENCE Because the electron density for the two N chains was poor, the authors were unable to ...SEQUENCE Because the electron density for the two N chains was poor, the authors were unable to assign side chains. | ||||||||||||
| Remark 600 | HETEROGEN Ligand PL9 is missing two isoprenoids due to disorder in the electron density. |
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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 | 1s5l.cif.gz | 1.1 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb1s5l.ent.gz | 966 KB | Display | PDB format |
| PDBx/mmJSON format | 1s5l.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1s5l_validation.pdf.gz | 16.6 MB | Display | wwPDB validaton report |
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| Full document | 1s5l_full_validation.pdf.gz | 17.2 MB | Display | |
| Data in XML | 1s5l_validation.xml.gz | 287 KB | Display | |
| Data in CIF | 1s5l_validation.cif.gz | 344 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/s5/1s5l ftp://data.pdbj.org/pub/pdb/validation_reports/s5/1s5l | HTTPS FTP |
-Related structure data
| Related structure data | |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| 1 | ![]()
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| 2 | ![]()
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| Unit cell |
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| Details | the biological unit is a dimer, which is present in the asymmetric unit |
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Components
-Protein , 2 types, 4 molecules AaVv
| #1: Protein | Mass: 38265.625 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: P0A444#16: Protein | Mass: 15148.255 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: P0A386 |
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-Photosystem II ... , 15 types, 30 molecules BbCcDdHhIiJjKkLlMmOoTtUuXxNnZz
| #2: Protein | Mass: 56656.457 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8DIQ1#3: Protein | Mass: 51666.094 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8DIF8#4: Protein | Mass: 39388.156 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8CM25#7: Protein | Mass: 7358.754 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / 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) / 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) / 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) / 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) / References: UniProt: Q8DIN8#12: Protein/peptide | Mass: 3981.673 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8DHA7#13: Protein | Mass: 26851.965 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: P0A431#14: Protein/peptide | Mass: 3878.728 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8DIQ0#15: Protein | Mass: 15030.986 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q9F1L5#17: Protein/peptide | Mass: 5235.296 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q9F1R6#18: Protein/peptide | Mass: 3166.895 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria)#19: Protein | Mass: 6766.187 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8DHJ2 |
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-Cytochrome b559 ... , 2 types, 4 molecules EeFf
| #5: Protein | Mass: 9580.840 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8DIP0#6: Protein/peptide | Mass: 5067.900 Da / Num. of mol.: 2 / Source method: isolated from a natural source / Source: (natural) ![]() Thermosynechococcus elongatus (bacteria) / References: UniProt: Q8DIN9 |
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-Sugars , 1 types, 2 molecules 
| #26: Sugar |
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-Non-polymers , 8 types, 106 molecules 














| #20: Chemical | | #21: Chemical | ChemComp-BCT / #22: Chemical | #23: Chemical | ChemComp-CLA / #24: Chemical | ChemComp-PHO / #25: Chemical | ChemComp-PL9 / #27: Chemical | ChemComp-BCR / #28: Chemical | ChemComp-HEC / |
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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: 1 |
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Sample preparation
| Crystal | Density Matthews: 3.92 Å3/Da / Density % sol: 68.64 % | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Crystal grow | Temperature: 291 K / Method: pseudo-batch hanging drop / pH: 7.5 Details: 100mM HEPES, 100mM (NH4)2SO4, PEG 4000, C12E8, trimethyl lead acetate, pH 7.5, pseudo-batch hanging drop, temperature 291K | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Crystal grow | *PLUS Temperature: 18 ℃ / pH: 6.5 / Method: vapor diffusion, hanging drop | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Components of the solutions | *PLUS
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-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: SLS / Beamline: X06SA / Wavelength: 1 Å |
| Detector | Type: MARRESEARCH / Detector: CCD / Date: Jan 25, 2003 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
| Reflection | Resolution: 3.5→20 Å / Num. all: 117866 / Num. obs: 103604 / % possible obs: 87.9 % / Observed criterion σ(F): 2 / Observed criterion σ(I): 2 |
| Reflection shell | Resolution: 3.5→3.52 Å / % possible all: 80.9 |
| Reflection | *PLUS Lowest resolution: 40 Å / % possible obs: 87.3 % / Redundancy: 2.88 % / Num. measured all: 298731 / Rmerge(I) obs: 0.08 |
| Reflection shell | *PLUS % possible obs: 80.9 % / Rmerge(I) obs: 0.43 / Mean I/σ(I) obs: 2 |
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Processing
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| Refinement | Method to determine structure: MIR / Resolution: 3.5→20 Å / Cross valid method: THROUGHOUT / σ(F): 0 / Stereochemistry target values: Engh & Huber
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| Refinement step | Cycle: LAST / Resolution: 3.5→20 Å
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| Refine LS restraints |
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| Refinement | *PLUS Num. reflection all: 103485 / % reflection Rfree: 1 % / Rfactor Rfree: 0.346 / Rfactor Rwork: 0.303 | ||||||||||||||||||||
| Solvent computation | *PLUS | ||||||||||||||||||||
| Displacement parameters | *PLUS | ||||||||||||||||||||
| Refine LS restraints | *PLUS
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| LS refinement shell | *PLUS Highest resolution: 3.5 Å / Lowest resolution: 3.56 Å / Rfactor Rfree: 0.384 / Rfactor Rwork: 0.34 |
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Thermosynechococcus elongatus (bacteria)
X-RAY DIFFRACTION
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