+Open data
-Basic information
Entry | Database: PDB / ID: 8c4y | |||||||||
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Title | SFX structure of FutA bound to Fe(III) | |||||||||
Components | Putative iron ABC transporter, substrate binding protein | |||||||||
Keywords | METAL BINDING PROTEIN / Periplasmic iron-binding protein / metal ion binding / iron homeostasis | |||||||||
Function / homology | Bacterial extracellular solute-binding protein / Ferric binding protein / iron ion transport / outer membrane-bounded periplasmic space / metal ion binding / : / Putative iron ABC transporter, substrate binding protein Function and homology information | |||||||||
Biological species | Prochlorococcus marinus subsp. pastoris str. CCMP1986 (bacteria) | |||||||||
Method | X-RAY DIFFRACTION / FREE ELECTRON LASER / MOLECULAR REPLACEMENT / Resolution: 1.6 Å | |||||||||
Authors | Bolton, R. / Tews, I. | |||||||||
Funding support | United Kingdom, 2items
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Citation | Journal: Proc.Natl.Acad.Sci.USA / Year: 2024 Title: A redox switch allows binding of Fe(II) and Fe(III) ions in the cyanobacterial iron-binding protein FutA from Prochlorococcus. Authors: Bolton, R. / Machelett, M.M. / Stubbs, J. / Axford, D. / Caramello, N. / Catapano, L. / Maly, M. / Rodrigues, M.J. / Cordery, C. / Tizzard, G.J. / MacMillan, F. / Engilberge, S. / von ...Authors: Bolton, R. / Machelett, M.M. / Stubbs, J. / Axford, D. / Caramello, N. / Catapano, L. / Maly, M. / Rodrigues, M.J. / Cordery, C. / Tizzard, G.J. / MacMillan, F. / Engilberge, S. / von Stetten, D. / Tosha, T. / Sugimoto, H. / Worrall, J.A.R. / Webb, J.S. / Zubkov, M. / Coles, S. / Mathieu, E. / Steiner, R.A. / Murshudov, G. / Schrader, T.E. / Orville, A.M. / Royant, A. / Evans, G. / Hough, M.A. / Owen, R.L. / Tews, I. #1: Journal: Biorxiv / Year: 2023 Title: A redox switch allows binding of Fe(II) and Fe(III) ions in the cyanobacterial iron binding protein FutA from Prochlorococcus; Authors: Bolton, R. / Machelett, M. / Stubbs, J. / Axford, D. / Caramello, N. / Catapano, L. / Maly, M. / Rodrigues, M. / Cordery, C. / Tizzard, G. / MacMillan, F. / Engilberge, S. / Stetten, D. / ...Authors: Bolton, R. / Machelett, M. / Stubbs, J. / Axford, D. / Caramello, N. / Catapano, L. / Maly, M. / Rodrigues, M. / Cordery, C. / Tizzard, G. / MacMillan, F. / Engilberge, S. / Stetten, D. / Tosha, T. / Sugimoto, H. / Worrall, J. / Webb, J. / Zubkov, M. / Coles, S. / Mathieu, E. / Steiner, R. / Murshudov, G. / Schrader, T. / Orville, A. / Royant, A. / Evans, G. / Hough, M. / Owen, R. / Tews, I. | |||||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8c4y.cif.gz | 81.7 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8c4y.ent.gz | Display | PDB format | |
PDBx/mmJSON format | 8c4y.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8c4y_validation.pdf.gz | 913.1 KB | Display | wwPDB validaton report |
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Full document | 8c4y_full_validation.pdf.gz | 914.4 KB | Display | |
Data in XML | 8c4y_validation.xml.gz | 13.3 KB | Display | |
Data in CIF | 8c4y_validation.cif.gz | 18.3 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/c4/8c4y ftp://data.pdbj.org/pub/pdb/validation_reports/c4/8c4y | HTTPS FTP |
-Related structure data
Related structure data | 8oeiC 8oemC 8oggC 8rk1C C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
#1: Protein | Mass: 35219.246 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Prochlorococcus marinus subsp. pastoris str. CCMP1986 (bacteria) Gene: futA,sfuA, idiA, PMM1164 / Plasmid: pET- 24b(+) / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: Q7V0T9 |
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#2: Chemical | ChemComp-FE / |
#3: Water | ChemComp-HOH / |
Has ligand of interest | Y |
Has protein modification | Y |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 2.06 Å3/Da / Density % sol: 40.27 % |
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Crystal grow | Temperature: 294 K / Method: batch mode Details: Purified protein, diluted crystal seeds, and crystallisation buffer were mixed at a 1:1.5:1.5 ratio. Crystallisation buffer was 25% PEG 3350, 200 mM sodium thiocyanate. Crystal seed stock ...Details: Purified protein, diluted crystal seeds, and crystallisation buffer were mixed at a 1:1.5:1.5 ratio. Crystallisation buffer was 25% PEG 3350, 200 mM sodium thiocyanate. Crystal seed stock was diluted 1:20 in 25% PEG 3350. |
-Data collection
Diffraction | Mean temperature: 298 K / Serial crystal experiment: Y |
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Diffraction source | Source: FREE ELECTRON LASER / Site: SACLA / Beamline: BL2 / Wavelength: 1.127 Å |
Detector | Type: MPCCD / Detector: CCD / Date: Jun 26, 2019 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.127 Å / Relative weight: 1 |
Reflection | Resolution: 1.6→30.1 Å / Num. obs: 37266 / % possible obs: 99.8 % / Redundancy: 618.7 % / Biso Wilson estimate: 12.09 Å2 / CC1/2: 0.99 / R split: 0.053 / Net I/σ(I): 12.1 |
Reflection shell | Resolution: 1.6→1.628 Å / Redundancy: 274.5 % / Mean I/σ(I) obs: 4.6 / Num. unique obs: 1877 / CC1/2: 0.91 / R split: 0.089 / % possible all: 100 |
Serial crystallography measurement | Pulse duration: 10 fsec. / XFEL pulse repetition rate: 30 Hz |
Serial crystallography sample delivery | Method: fixed target |
Serial crystallography sample delivery fixed target | Description: Silicon nitride chip / Details: 25600 apertures / Sample dehydration prevention: Sealed with a Mylar film |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.6→30.096 Å / Cor.coef. Fo:Fc: 0.946 / Cor.coef. Fo:Fc free: 0.941 / SU B: 1.831 / SU ML: 0.063 / Cross valid method: FREE R-VALUE / ESU R: 0.099 / ESU R Free: 0.091 Details: Hydrogens have been added in their riding positions
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Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK BULK SOLVENT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 17.084 Å2
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Refinement step | Cycle: LAST / Resolution: 1.6→30.096 Å
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Refine LS restraints |
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LS refinement shell |
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