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Yorodumi- PDB-9wfz: Cryo-EM structure of PSII PsbA3-S264V from Thermosynechococcus ve... -
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Basic information
| Entry | Database: PDB / ID: 9wfz | |||||||||
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| Title | Cryo-EM structure of PSII PsbA3-S264V from Thermosynechococcus vestitus BP-1 (local refinement) | |||||||||
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Keywords | PHOTOSYNTHESIS / PSII mutation / local refinement | |||||||||
| Function / homology | Function and homology informationoxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor / photosystem II oxygen evolving complex / photosystem II assembly / response to herbicide / oxygen evolving activity / photosystem II stabilization / photosystem II reaction center / photosystem II / photosynthetic electron transport chain / photosystem II ...oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor / photosystem II oxygen evolving complex / photosystem II assembly / response to herbicide / oxygen evolving activity / photosystem II stabilization / photosystem II reaction center / photosystem II / photosynthetic electron transport chain / photosystem II / extrinsic component of membrane / photosynthetic electron transport in photosystem II / chlorophyll binding / plasma membrane-derived thylakoid membrane / photosynthesis, light reaction / photosynthesis / respiratory electron transport chain / electron transfer activity / iron ion binding / heme binding Similarity search - Function | |||||||||
| Biological species | ![]() Thermosynechococcus vestitus BP-1 (bacteria) | |||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.08 Å | |||||||||
Authors | Fan, S.B. / Nakajima, Y. / Shen, J.R. | |||||||||
| Funding support | 1items
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Citation | Journal: Biochim Biophys Acta Bioenerg / Year: 2026Title: Structural and functional analysis of a photosystem II mutant PsbA3-S264V. Authors: Songbo Fan / Yoshiki Nakajima / Koji Kato / Haowei Jiang / Pi-Cheng Tsai / Anqi Jia / Miwa Sugiura / Jian-Ren Shen / ![]() Abstract: Photosystem II (PSII) catalyzes water oxidation and oxygen evolution by a light-induced electron transfer chain, leading to the generation of electrons, protons and dioxygen. D1-S264 is a residue ...Photosystem II (PSII) catalyzes water oxidation and oxygen evolution by a light-induced electron transfer chain, leading to the generation of electrons, protons and dioxygen. D1-S264 is a residue located close to the Q-binding site, and mutation of this residue has been shown to bring significant effects on the electron transfer and oxygen-evolving activities. Here we analyzed the structure of a Thermosynechococcus elongatus mutant PsbA3-S264V by cryo-electron microscopy at 1.96 Å resolution, which showed significant changes in the structure surrounding the bicarbonate and Q-binding region. Due to change of Ser to Val, the hydrogen-bond between the Q carbonyl oxygen and S264 is altered, which changed the protonation pathway of Q from the original route of D1-H252 through D1-S264 to Q, to a new, longer and less efficient route of D1-H252 through D1-F265 to Q. Two residues, D1-E244 and D2-E242, changed their side chain orientations significantly. Among them, D2-E242 adopted two conformations, and both are largely deviated from the original structure. All these changes led to alterations in hydrogen-bonding networks of two channels, channel A and channel B, that connect the stromal surface to Q and may function to transport protons to protonate Q. Furthermore, isothermal titration calorimetry experiments showed a diminished 3-(3,4-dichlorophenyl)-1, 1-dimethylurea (DCMU) binding affinity of the mutated PSII, which may be explained by a structural rotation of D1-F255 in the mutant based on structural analysis of DCMU-bound PSII. These findings offer valuable insights into the functions of D1-S264 in Q protonation and function, as well as in the DCMU-binding. | |||||||||
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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 | 9wfz.cif.gz | 506.5 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9wfz.ent.gz | 377.2 KB | Display | PDB format |
| PDBx/mmJSON format | 9wfz.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/wf/9wfz ftp://data.pdbj.org/pub/pdb/validation_reports/wf/9wfz | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 65941MC ![]() 9w5bC ![]() 9w7dC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-Photosystem II ... , 16 types, 17 molecules IKTVYABbCDJLMOUXZ
| #1: Protein/peptide | Mass: 4410.245 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DJZ6 | ||||||||||||||||||
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| #2: Protein/peptide | Mass: 5028.083 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q9F1K9 | ||||||||||||||||||
| #3: Protein/peptide | Mass: 3878.728 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DIQ0 | ||||||||||||||||||
| #4: Protein | Mass: 18046.943 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: P0A386 | ||||||||||||||||||
| #5: Protein/peptide | Mass: 5039.143 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DJI1 | ||||||||||||||||||
| #6: Protein | Mass: 39792.391 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DIV4, photosystem II | ||||||||||||||||||
| #7: Protein | Mass: 56656.457 Da / Num. of mol.: 2 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DIQ1 #8: Protein | | Mass: 50287.500 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DIF8 #9: Protein | | Mass: 39388.156 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8CM25, photosystem II #12: Protein/peptide | | Mass: 4105.908 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: P59087 #13: Protein/peptide | | Mass: 4299.044 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DIN8 #14: Protein/peptide | | Mass: 3981.673 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DHA7 #15: Protein | | Mass: 29637.443 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: P0A431 #16: Protein | | Mass: 15030.986 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q9F1L5 #17: Protein/peptide | | Mass: 4322.226 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q9F1R6 #18: Protein | | Mass: 6766.187 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DHJ2 |
-Cytochrome b559 subunit ... , 2 types, 2 molecules EF
| #10: Protein | Mass: 9580.840 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DIP0 |
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| #11: Protein/peptide | Mass: 5067.900 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() Thermosynechococcus vestitus BP-1 (bacteria)References: UniProt: Q8DIN9 |
-Sugars , 2 types, 7 molecules 


| #21: Sugar | | #33: Sugar | ChemComp-DGD / |
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-Non-polymers , 15 types, 497 molecules 


























| #19: Chemical | ChemComp-UNL / Num. of mol.: 6 / Source method: obtained synthetically #20: Chemical | ChemComp-BCR / #22: Chemical | ChemComp-HEC / | #23: Chemical | ChemComp-OEX / | #24: Chemical | ChemComp-FE2 / | #25: Chemical | #26: Chemical | ChemComp-CLA / #27: Chemical | #28: Chemical | #29: Chemical | ChemComp-BCT / | #30: Chemical | ChemComp-LHG / #31: Chemical | #32: Chemical | #34: Chemical | ChemComp-HEM / | #35: Water | ChemComp-HOH / | |
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-Details
| Has ligand of interest | N |
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| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: Cryo-EM structure of PSII PsbA3-S264V from Thermosynechococcus vestitus BP-1 (local refinement) Type: COMPLEX / Entity ID: #1-#18 / Source: NATURAL |
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| Source (natural) | Organism: ![]() Thermosynechococcus vestitus BP-1 (bacteria) |
| Buffer solution | pH: 6.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE / Humidity: 100 % |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: TFS KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 1000 nm / Nominal defocus min: 200 nm |
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||
| 3D reconstruction | Resolution: 2.08 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 93573 / Symmetry type: POINT |
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Thermosynechococcus vestitus BP-1 (bacteria)
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