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Yorodumi- PDB-3akh: Crystal structure of exo-1,5-alpha-L-arabinofuranosidase complexe... -
+Open data
-Basic information
Entry | Database: PDB / ID: 3akh | |||||||||
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Title | Crystal structure of exo-1,5-alpha-L-arabinofuranosidase complexed with alpha-1,5-L-arabinofuranotriose | |||||||||
Components | Putative secreted alpha L-arabinofuranosidase II | |||||||||
Keywords | HYDROLASE / FIVE-BLADED BETA PROPELLER / BETA-TREFOIL | |||||||||
Function / homology | Function and homology information arabinan catabolic process / L-arabinose metabolic process / non-reducing end alpha-L-arabinofuranosidase / alpha-L-arabinofuranosidase activity / extracellular region Similarity search - Function | |||||||||
Biological species | Streptomyces avermitilis (bacteria) | |||||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.7 Å | |||||||||
Authors | Fujimoto, Z. / Ichinose, H. / Kaneko, S. | |||||||||
Citation | Journal: J.Biol.Chem. / Year: 2010 Title: Crystal Structure of an Exo-1,5-{alpha}-L-arabinofuranosidase from Streptomyces avermitilis Provides Insights into the Mechanism of Substrate Discrimination between Exo- and Endo-type Enzymes ...Title: Crystal Structure of an Exo-1,5-{alpha}-L-arabinofuranosidase from Streptomyces avermitilis Provides Insights into the Mechanism of Substrate Discrimination between Exo- and Endo-type Enzymes in Glycoside Hydrolase Family 43. Authors: Fujimoto, Z. / Ichinose, H. / Maehara, T. / Honda, M. / Kitaoka, M. / Kaneko, S. #1: Journal: Acta Crystallogr.,Sect.F / Year: 2008 Title: Crystallization and preliminary crystallographic analysis of exo-alpha-1,5-L-arabinofuranosidase from Streptomyces avermitilis NBRC14893. Authors: Fujimoto, Z. / Ichinose, H. / Kaneko, S. #2: Journal: Appl.Microbiol.Biotechnol. / Year: 2008 Title: Characterization of a modular enzyme of exo-1,5-alpha-L-arabinofuranosidase and arabinan binding module from Streptomyces avermitilis NBRC14893. Authors: Ichinose, H. / Yoshida, M. / Fujimoto, Z. / Kaneko, S. | |||||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 3akh.cif.gz | 119.2 KB | Display | PDBx/mmCIF format |
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PDB format | pdb3akh.ent.gz | 88.1 KB | Display | PDB format |
PDBx/mmJSON format | 3akh.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ak/3akh ftp://data.pdbj.org/pub/pdb/validation_reports/ak/3akh | HTTPS FTP |
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-Related structure data
Related structure data | 3akfSC 3akgC 3akiC S: Starting model for refinement C: citing same article (ref.) |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
-Protein , 1 types, 1 molecules A
#1: Protein | Mass: 51937.340 Da / Num. of mol.: 1 / Fragment: UNP RESIDUES 28-481 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Streptomyces avermitilis (bacteria) / Strain: MA-4680 / Gene: abfA, SAV1043, SAV_1043 / Plasmid: pET30 / Production host: Escherichia coli (E. coli) / Strain (production host): BL21 Gold (DE3) References: UniProt: Q82P90, non-reducing end alpha-L-arabinofuranosidase |
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-Sugars , 2 types, 4 molecules
#2: Polysaccharide | Source method: isolated from a genetically manipulated source #5: Sugar | ChemComp-AHR / | |
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-Non-polymers , 4 types, 582 molecules
#3: Chemical | ChemComp-CL / | ||
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#4: Chemical | ChemComp-NA / | ||
#6: Chemical | #7: 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: 2.52 Å3/Da / Density % sol: 51.26 % |
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, sitting drop / pH: 7 Details: 0.8M sodium citrate, 0.2M sodium chloride, 0.1M Tris, pH 7.0, VAPOR DIFFUSION, SITTING DROP, temperature 293K |
-Data collection
Diffraction | Mean temperature: 95 K |
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Diffraction source | Source: SYNCHROTRON / Site: Photon Factory / Beamline: BL-17A / Wavelength: 0.97 Å |
Detector | Type: ADSC QUANTUM 270 / Detector: CCD / Date: Jun 26, 2007 |
Radiation | Monochromator: Numerical link type Si(111) double crystal monochromator Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.97 Å / Relative weight: 1 |
Reflection | Resolution: 1.7→39.47 Å / Num. obs: 56484 / % possible obs: 97.9 % / Observed criterion σ(F): 0 / Observed criterion σ(I): -3 / Redundancy: 14.6 % / Biso Wilson estimate: 22.2 Å2 / Rmerge(I) obs: 0.055 / Rsym value: 0.055 / Net I/σ(I): 53.7 |
Reflection shell | Resolution: 1.7→1.76 Å / Redundancy: 14.4 % / Rmerge(I) obs: 0.257 / Mean I/σ(I) obs: 9.53 / Num. unique all: 5492 / Rsym value: 0.257 / % possible all: 97 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: PDB ENTRY 3AKF Resolution: 1.7→39.47 Å / Cor.coef. Fo:Fc: 0.96 / Cor.coef. Fo:Fc free: 0.947 / SU B: 2.109 / SU ML: 0.071 / Cross valid method: THROUGHOUT / ESU R Free: 0.107 / Stereochemistry target values: MAXIMUM LIKELIHOOD
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Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 22.698 Å2
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Refine analyze | Luzzati coordinate error obs: 0.0398 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.7→39.47 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 1.7→1.744 Å / Total num. of bins used: 20
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