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- PDB-1hjg: Alteration of the co-substrate selectivity of deacetoxycephalospo... -
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Open data
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Basic information
Entry | Database: PDB / ID: 1hjg | |||||||||
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Title | Alteration of the co-substrate selectivity of deacetoxycephalosporin C synthase: The role of arginine-258 | |||||||||
![]() | DEACETOXYCEPHALOSPORIN C SYNTHASE | |||||||||
![]() | OXIDOREDUCTASE / ALTERNATIVE 2-OXOACIDS / CEPHEM ANTIBIOTIC BIOSYNTHESIS / CHEMICAL COSUBSTRATE RESCUE / CO-SUBSTRATE SELECTIVITY / 2- OXOGLUTARATE-DEPENDENT OXYGENASE | |||||||||
Function / homology | ![]() deacetoxycephalosporin-C synthase / deacetoxycephalosporin-C synthase activity / L-ascorbic acid binding / antibiotic biosynthetic process / iron ion binding Similarity search - Function | |||||||||
Biological species | ![]() | |||||||||
Method | ![]() ![]() ![]() | |||||||||
![]() | Lee, H.J. / Lloyd, M.D. / Clifton, I.J. / Harlos, K. / Dubus, A. / Baldwin, J.E. / Frere, J.M. / Schofield, C.J. | |||||||||
![]() | ![]() Title: Alteration of the 2-Oxoacid Cosubstrate Selectivity in Deacetoxycephalosporin C Synthase: The Role of Arginine-258 Authors: Lee, H.J. / Lloyd, M.D. / Harlos, K. / Clifton, I.J. / Baldwin, J.E. / Schofield, C.J. #1: Journal: J.Mol.Biol. / Year: 1999 Title: Studies on the Active Site of Deacetoxycephalosporin C Synthase Authors: Lloyd, M.D. / Lee, H.J. / Harlos, K. / Zhang, Z.H. / Baldwin, J.E. / Schofield, C.J. / Charnock, J.M. / Garner, C.D. / Hara, T. / Van Scheltinga, A.C.T. / Valegard, K. / Viklund, J.A.C. / ...Authors: Lloyd, M.D. / Lee, H.J. / Harlos, K. / Zhang, Z.H. / Baldwin, J.E. / Schofield, C.J. / Charnock, J.M. / Garner, C.D. / Hara, T. / Van Scheltinga, A.C.T. / Valegard, K. / Viklund, J.A.C. / Hajdu, J. / Andersson, I. / Danielsson, A. / Bhikhabhai, R. | |||||||||
History |
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Remark 285 | TEXT TO EXPLAIN UNUSUAL UNIT-CELL DATA: R3 SPACE GROUP INDEX IN HEXAGONAL SETTING |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 72.7 KB | Display | ![]() |
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PDB format | ![]() | 51.5 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 449.9 KB | Display | ![]() |
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Full document | ![]() | 456.5 KB | Display | |
Data in XML | ![]() | 14.2 KB | Display | |
Data in CIF | ![]() | 20.2 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 1hjfC ![]() 1rxgS 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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1 | ![]()
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Unit cell |
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Components
#1: Protein | Mass: 34562.574 Da / Num. of mol.: 1 / Mutation: YES Source method: isolated from a genetically manipulated source Details: IRON(II) AND ALPHA-KETOISOVALERATE COMPLEX OF MUTANT ENZYME Source: (gene. exp.) ![]() Description: RECOMBINANT ENZYME OF S. CLAVULIGERUS ENZYME. R258Q MUTANT ENZYME Gene: CEFE, R258Q MUTANT / Plasmid: PET24A / Production host: ![]() ![]() |
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#2: Chemical | ChemComp-FE2 / |
#3: Chemical | ChemComp-KIV / |
#4: Water | ChemComp-HOH / |
Compound details | CHAIN A ENGINEERED MUTATION ARG258GLN DAOCS CATALYZES THE REACTION FROM PENICILLIN N TO DEACETOXY- ...CHAIN A ENGINEERED |
Sequence details | RESIDUE A50 BUILT AS ILE (AS REPORTED IN PATENT) NOT LEU (AS REPORTED IN PAPER) SIDECHAIN OF GLN- ...RESIDUE A50 BUILT AS ILE (AS REPORTED IN PATENT) NOT LEU (AS REPORTED IN PAPER) SIDECHAIN OF GLN-258 DISORDERED |
-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.39 Å3/Da / Density % sol: 48.2 % | ||||||||||||||||||||||||||||||
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / pH: 7 Details: HANGING DROP AT 20 DEGREES C. 100 MM HEPES-NAOH, PH 7.0, 3% (W/V) GLYCEROL, 5 MM 2-OXO-3-METHYLBUTANOATE, 1.5-1.7 M AMMONIUM SULPHATE. CRYSTALS SOAKED IN 5 MM IRON(II) SULPHATE IN MOTHER ...Details: HANGING DROP AT 20 DEGREES C. 100 MM HEPES-NAOH, PH 7.0, 3% (W/V) GLYCEROL, 5 MM 2-OXO-3-METHYLBUTANOATE, 1.5-1.7 M AMMONIUM SULPHATE. CRYSTALS SOAKED IN 5 MM IRON(II) SULPHATE IN MOTHER LIQUOR UNDER ANAEROBIC CONDITIONS BEFORE DATA COLLECTION. | ||||||||||||||||||||||||||||||
Crystal grow | *PLUS Temperature: 14 ℃ / 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: ![]() ![]() ![]() |
Detector | Type: ADSC QUANTUM 4 / Detector: CCD / Date: May 11, 1999 |
Radiation | Monochromator: SILICON 111 / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.87 Å / Relative weight: 1 |
Reflection | Resolution: 1.5→100 Å / Num. obs: 38283 / % possible obs: 88.8 % / Observed criterion σ(I): 1.4 / Redundancy: 2.9 % / Biso Wilson estimate: 22.9 Å2 / Rmerge(I) obs: 0.057 / Net I/σ(I): 6.86 |
Reflection shell | Resolution: 1.5→1.51 Å / Redundancy: 2.4 % / Rmerge(I) obs: 0.542 / Mean I/σ(I) obs: 1.4 / % possible all: 90.9 |
Reflection | *PLUS Lowest resolution: 100 Å / Num. measured all: 175826 |
Reflection shell | *PLUS % possible obs: 90.9 % |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: PDB ENTRY 1RXG Resolution: 1.5→19.4 Å / Rfactor Rfree error: 0.006 / Data cutoff high absF: 1934787.09 / Isotropic thermal model: RESTRAINED / Cross valid method: THROUGHOUT / σ(F): 0 / Details: DATA DETWINNED BEFORE REFINEMENT
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Solvent computation | Solvent model: FLAT MODEL / Bsol: 66.9078 Å2 / ksol: 0.438466 e/Å3 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 25.6 Å2
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Refine analyze |
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Refinement step | Cycle: LAST / Resolution: 1.5→19.4 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 1.5→1.59 Å / Rfactor Rfree error: 0.021 / Total num. of bins used: 6
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Xplor file |
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Software | *PLUS Name: CNS / Version: 0.5 / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refine LS restraints | *PLUS
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LS refinement shell | *PLUS Rfactor Rfree: 0.35 |