+Open data
-Basic information
Entry | Database: PDB / ID: 1pnl | ||||||
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Title | PENICILLIN ACYLASE HAS A SINGLE-AMINO-ACID CATALYTIC CENTRE | ||||||
Components | (PENICILLIN AMIDOHYDROLASE) x 2 | ||||||
Keywords | ANTIBIOTIC RESISTANCE | ||||||
Function / homology | Function and homology information penicillin amidase activity / penicillin amidase / antibiotic biosynthetic process / periplasmic space / response to antibiotic / metal ion binding Similarity search - Function | ||||||
Biological species | Escherichia coli (E. coli) | ||||||
Method | X-RAY DIFFRACTION / Resolution: 2.5 Å | ||||||
Authors | Duggleby, H.J. / Moody, P.C.E. | ||||||
Citation | Journal: Nature / Year: 1995 Title: Penicillin acylase has a single-amino-acid catalytic centre. Authors: Duggleby, H.J. / Tolley, S.P. / Hill, C.P. / Dodson, E.J. / Dodson, G. / Moody, P.C. #1: Journal: Protein Eng. / Year: 1990 Title: Expression, Purification and Crystallisation of Penicillin G Acylase from Escherichia Coli Atcc 11105 Authors: Hunt, P.D. / Tolley, S.P. / Ward, R.J. / Hill, C.P. / Dodson, G.G. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 1pnl.cif.gz | 171.6 KB | Display | PDBx/mmCIF format |
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PDB format | pdb1pnl.ent.gz | 132.3 KB | Display | PDB format |
PDBx/mmJSON format | 1pnl.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 1pnl_validation.pdf.gz | 395.4 KB | Display | wwPDB validaton report |
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Full document | 1pnl_full_validation.pdf.gz | 426.5 KB | Display | |
Data in XML | 1pnl_validation.xml.gz | 20 KB | Display | |
Data in CIF | 1pnl_validation.cif.gz | 32.3 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/pn/1pnl ftp://data.pdbj.org/pub/pdb/validation_reports/pn/1pnl | HTTPS FTP |
-Related structure data
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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Atom site foot note | 1: CIS PROLINE - PRO B 29 / 2: CIS PROLINE - PRO B 366 / 3: CIS PROLINE - PRO B 505 |
-Components
#1: Protein | Mass: 23838.824 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Escherichia coli (E. coli) / Strain: ATCC 11105 / References: UniProt: P06875, penicillin amidase |
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#2: Protein | Mass: 62429.496 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Escherichia coli (E. coli) / Strain: ATCC 11105 / References: UniProt: P06875, penicillin amidase |
#3: Chemical | ChemComp-CA / |
#4: Chemical | ChemComp-PAC / |
#5: Water | ChemComp-HOH / |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION |
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-Sample preparation
Crystal | Density Matthews: 2.55 Å3/Da / Density % sol: 51.84 % | ||||||||||||||||||||
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Crystal grow | *PLUS Temperature: 20 ℃ / pH: 7.2 / Method: batch method | ||||||||||||||||||||
Components of the solutions | *PLUS
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-Data collection
Radiation | Scattering type: x-ray |
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Radiation wavelength | Relative weight: 1 |
Reflection | *PLUS Highest resolution: 2.5 Å / % possible obs: 95.3 % / Rmerge(I) obs: 0.061 |
-Processing
Software | Name: PROLSQ / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Refinement | Resolution: 2.5→6 Å /
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Refinement step | Cycle: LAST / Resolution: 2.5→6 Å
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Refine LS restraints |
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Refinement | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Solvent computation | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | *PLUS Biso mean: 28.28 Å2 |