+Open data
-Basic information
Entry | Database: PDB / ID: 1hha | ||||||||||||
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Title | Decaplanin first P6122-Form | ||||||||||||
Components | DECAPLANIN | ||||||||||||
Keywords | ANTIBIOTIC / GLYCOPEPTIDE | ||||||||||||
Function / homology | Decaplanin / 4-epi-vancosamine / : Function and homology information | ||||||||||||
Biological species | UNCULTURED ACTINOMYCETE (environmental samples) | ||||||||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MAD / Resolution: 1.9 Å | ||||||||||||
Authors | Lehmann, C. / Vertessy, L. / Sheldrick, G.M. / Dauter, Z. / Dauter, M. | ||||||||||||
Citation | Journal: Helv.Chim.Acta / Year: 2003 Title: Structures of Four Crystal Forms of Decaplanin Authors: Lehmann, C. / Debreczeni, J.E. / Bunkoczi, G. / Dauter, M. / Dauter, Z. / Vertesy, L. / Sheldrick, G.M. | ||||||||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 1hha.cif.gz | 22.9 KB | Display | PDBx/mmCIF format |
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PDB format | pdb1hha.ent.gz | 19.5 KB | Display | PDB format |
PDBx/mmJSON format | 1hha.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 1hha_validation.pdf.gz | 1.5 MB | Display | wwPDB validaton report |
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Full document | 1hha_full_validation.pdf.gz | 1.5 MB | Display | |
Data in XML | 1hha_validation.xml.gz | 6.3 KB | Display | |
Data in CIF | 1hha_validation.cif.gz | 7.3 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/hh/1hha ftp://data.pdbj.org/pub/pdb/validation_reports/hh/1hha | HTTPS FTP |
-Related structure data
-Links
-Assembly
Deposited unit |
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1 |
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2 |
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Unit cell |
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Components on special symmetry positions |
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Noncrystallographic symmetry (NCS) | NCS oper:
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-Components
#1: Protein/peptide | #2: Polysaccharide | alpha-L-rhamnopyranose-(1-2)-beta-D-glucopyranose Source method: isolated from a genetically manipulated source Details: DECAPLANIN IS A TRICYCLIC GLYCOPEPTIDE. THE SCAFFOLD IS A HEPTAPEPTIDE WITH THE CONFIGURATION D-D-L-D-D-L-L, GLYCOSYLATED References: Decaplanin #3: Sugar | ChemComp-ERE / Type: L-saccharide, alpha linking, Glycopeptide / Class: Antibiotic / Mass: 161.199 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Formula: C7H15NO3 Details: DECAPLANIN IS A TRICYCLIC GLYCOPEPTIDE. THE SCAFFOLD IS A HEPTAPEPTIDE WITH THE CONFIGURATION D-D-L-D-D-L-L, GLYCOSYLATED References: Decaplanin #4: Chemical | #5: Water | ChemComp-HOH / | Compound details | DECAPLANIN IS A TRICYCLIC GLYCOPEPTIDE. HERE, DECAPLANIN IS REPRESENTED BY GROUPING TOGETHER THE ...DECAPLANIN | |
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-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 3.93 Å3/Da / Density % sol: 57.61 % |
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Crystal grow | pH: 8.5 / Details: 0.1M TRIS, PH=8.5, 44% MGSO4, pH 8.50 |
-Data collection
Diffraction | Mean temperature: 100 K | |||||||||
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Diffraction source | Source: SYNCHROTRON / Site: NSLS / Beamline: X9B / Wavelength: 0.98000,0.98500 | |||||||||
Detector | Type: CHESS / Detector: CCD / Date: Oct 15, 1999 | |||||||||
Radiation | Protocol: MAD / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | |||||||||
Radiation wavelength |
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Reflection | Resolution: 1.9→23.23 Å / Num. obs: 8592 / % possible obs: 99.5 % / Redundancy: 10.5 % / Rmerge(I) obs: 0.0382 / Net I/σ(I): 26.2 | |||||||||
Reflection shell | Resolution: 1.9→2 Å / Redundancy: 10.7 % / Rmerge(I) obs: 0.1031 / Mean I/σ(I) obs: 7.28 / % possible all: 99.8 |
-Processing
Software |
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Refinement | Method to determine structure: MAD / Resolution: 1.9→23.23 Å / Num. parameters: 2176 / Num. restraintsaints: 1843 / Cross valid method: THROUGHOUT / σ(F): 0 / Stereochemistry target values: ENGH AND HUBER
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Solvent computation | Solvent model: MOEWS & KRETSINGER, J.MOL.BIOL.91(1973)201-228 | |||||||||||||||||||||||||||||||||
Refine analyze | Num. disordered residues: 9 / Occupancy sum hydrogen: 432.9 / Occupancy sum non hydrogen: 521.8 | |||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.9→23.23 Å
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Refine LS restraints |
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