+Open data
-Basic information
Entry | Database: PDB / ID: 8btu | ||||||
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Title | Structure of D179N BlaC from Mycobacterium tuberculosis | ||||||
Components | Beta-lactamase | ||||||
Keywords | HYDROLASE | ||||||
Function / homology | Function and homology information beta-lactam antibiotic catabolic process / beta-lactamase activity / beta-lactamase / periplasmic space / response to antibiotic / extracellular region Similarity search - Function | ||||||
Biological species | Mycobacterium tuberculosis (bacteria) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.8 Å | ||||||
Authors | Chikunova, A. / Bruenle, S. / Ubbink, M. | ||||||
Funding support | Netherlands, 1items
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Citation | Journal: Febs J. / Year: 2023 Title: Asp179 in the class A beta-lactamase from Mycobacterium tuberculosis is a conserved yet not essential residue due to epistasis. Authors: van Alen, I. / Chikunova, A. / van Zanten, D.B. / de Block, A.A. / Timmer, M. / Brunle, S. / Ubbink, M. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8btu.cif.gz | 69.7 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8btu.ent.gz | 48.6 KB | Display | PDB format |
PDBx/mmJSON format | 8btu.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8btu_validation.pdf.gz | 420.1 KB | Display | wwPDB validaton report |
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Full document | 8btu_full_validation.pdf.gz | 421.5 KB | Display | |
Data in XML | 8btu_validation.xml.gz | 13.3 KB | Display | |
Data in CIF | 8btu_validation.cif.gz | 19.4 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/bt/8btu ftp://data.pdbj.org/pub/pdb/validation_reports/bt/8btu | HTTPS FTP |
-Related structure data
Related structure data | 8btvC 8btwC 8bv4C 2gdnS S: Starting model for refinement 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: 28328.789 Da / Num. of mol.: 1 / Mutation: D179N Source method: isolated from a genetically manipulated source Source: (gene. exp.) Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (bacteria) Gene: blaC, blaA, MT2128 / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: P9WKD2, beta-lactamase |
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#2: Water | ChemComp-HOH / |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 1.95 Å3/Da / Density % sol: 37.01 % |
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, sitting drop / pH: 5.5 Details: 0.1 M ammonium acetate; 0.1 M BIS-TRIS buffer; 17% w/v PEG 10K |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: SYNCHROTRON / Site: Diamond / Beamline: I04-1 / Wavelength: 0.9795 Å |
Detector | Type: DECTRIS PILATUS 6M-F / Detector: PIXEL / Date: Dec 2, 2020 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.9795 Å / Relative weight: 1 |
Reflection | Resolution: 1.8→38.34 Å / Num. obs: 20045 / % possible obs: 98.4 % / Redundancy: 1.8 % / CC1/2: 0.988 / Rpim(I) all: 0.091 / Net I/σ(I): 5.2 |
Reflection shell | Resolution: 1.8→1.84 Å / Mean I/σ(I) obs: 1.2 / Num. unique obs: 1404 / CC1/2: 0.591 / Rpim(I) all: 0.427 / % possible all: 97.7 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: 2GDN Resolution: 1.8→38.34 Å / Cor.coef. Fo:Fc: 0.959 / Cor.coef. Fo:Fc free: 0.927 / SU B: 4.69 / SU ML: 0.132 / Cross valid method: THROUGHOUT / ESU R: 0.155 / ESU R Free: 0.15 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 18.087 Å2
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Refinement step | Cycle: 1 / Resolution: 1.8→38.34 Å
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