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Open data
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Basic information
| Entry | Database: PDB / ID: 2eng | |||||||||
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| Title | ENDOGLUCANASE V | |||||||||
Components | ENDOGLUCANASE V | |||||||||
Keywords | HYDROLASE (ENDOGLUCANASE) / CELLULOSE DEGRADATION / GLYCOSIDASE | |||||||||
| Function / homology | Function and homology information | |||||||||
| Biological species | Humicola insolens (fungus) | |||||||||
| Method | X-RAY DIFFRACTION / Resolution: 1.5 Å | |||||||||
Authors | Davies, G.J. / Schulein, M. | |||||||||
Citation | Journal: Biochemistry / Year: 1995Title: Structures of oligosaccharide-bound forms of the endoglucanase V from Humicola insolens at 1.9 A resolution. Authors: Davies, G.J. / Tolley, S.P. / Henrissat, B. / Hjort, C. / Schulein, M. #1: Journal: Nature / Year: 1993Title: Structure and Function of Endoglucanase V Authors: Davies, G.J. / Dodson, G.G. / Hubbard, R.E. / Tolley, S.P. / Dauter, Z. / Wilson, K.S. / Hjort, C. / Mikkelsen, J.M. / Rasmussen, G. / Schulein, M. | |||||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 2eng.cif.gz | 56.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb2eng.ent.gz | 40.6 KB | Display | PDB format |
| PDBx/mmJSON format | 2eng.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 2eng_validation.pdf.gz | 389.6 KB | Display | wwPDB validaton report |
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| Full document | 2eng_full_validation.pdf.gz | 390.4 KB | Display | |
| Data in XML | 2eng_validation.xml.gz | 6.4 KB | Display | |
| Data in CIF | 2eng_validation.cif.gz | 10 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/en/2eng ftp://data.pdbj.org/pub/pdb/validation_reports/en/2eng | HTTPS FTP |
-Related structure data
| 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: 22545.969 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Humicola insolens (fungus) / References: UniProt: P43316, cellulase | ||
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| #2: Water | ChemComp-HOH / | ||
| Compound details | ENDOGLUCAN| Has protein modification | Y | |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION |
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Sample preparation
| Crystal | Density Matthews: 2.05 Å3/Da / Density % sol: 40.01 % | ||||||||||||||||||||||||
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| Crystal grow | *PLUS Method: vapor diffusion, hanging drop | ||||||||||||||||||||||||
| 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: 1.48 Å |
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Processing
| Software | Name: SHELXL / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||||||
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| Refinement | Resolution: 1.5→10 Å Details: THE SECOND (LESSER) CONFORMATION FOR THE SIDE CHAIN OF ASP 121 MAKES A STERIC CLASH WITH THE SIDE CHAIN OF HIS 119. HIS 119 HAS THEREFORE BEEN REFINED WITH A PARTIAL OCCUPANCY OF 0.6. THE ...Details: THE SECOND (LESSER) CONFORMATION FOR THE SIDE CHAIN OF ASP 121 MAKES A STERIC CLASH WITH THE SIDE CHAIN OF HIS 119. HIS 119 HAS THEREFORE BEEN REFINED WITH A PARTIAL OCCUPANCY OF 0.6. THE ISOTROPIC TEMPERATURE FACTORS GIVEN ARE CALCULATED BY CONVERSION FROM THE ANISOTROPIC DISPLACEMENT PARAMETERS. A COORDINATE SET WITH ANISOTROPIC DISPLACEMENT PARAMETERS WILL BE SUBMITTED SOON.
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| Refinement step | Cycle: LAST / Resolution: 1.5→10 Å
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| Software | *PLUS Name: SHELX / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||||||
| Refinement | *PLUS Rfactor Rwork: 0.105 | ||||||||||||||||||||||||||||||||||||||||||||
| Solvent computation | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | *PLUS |
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Humicola insolens (fungus)
X-RAY DIFFRACTION
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