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Open data
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Basic information
| Entry | Database: PDB / ID: 1zhc | ||||||
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| Title | Solution structure of HP1242 from Helicobacter pylori | ||||||
Components | hypothetical protein HP1242 | ||||||
Keywords | UNKNOWN FUNCTION / a-helical protein | ||||||
| Function / homology | Methane Monooxygenase Hydroxylase; Chain G, domain 1 - #50 / Protein of unknown function DUF465 / DUF465 superfamily / Protein of unknown function (DUF465) / Methane Monooxygenase Hydroxylase; Chain G, domain 1 / Helix non-globular / Special / DUF465 domain-containing protein Function and homology information | ||||||
| Biological species | ![]() | ||||||
| Method | SOLUTION NMR / simulated annealing, torsion angle dynamics | ||||||
Authors | Kang, S.J. / Park, S.J. / Jung, S.J. / Lee, B.J. | ||||||
Citation | Journal: Proteins / Year: 2005Title: Solution structure of HP1242 from Helicobacter pylori Authors: Kang, S.J. / Park, S.J. / Jung, S.J. / Lee, B.J. | ||||||
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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 | 1zhc.cif.gz | 490.4 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1zhc.ent.gz | 414.6 KB | Display | PDB format |
| PDBx/mmJSON format | 1zhc.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1zhc_validation.pdf.gz | 347.4 KB | Display | wwPDB validaton report |
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| Full document | 1zhc_full_validation.pdf.gz | 477 KB | Display | |
| Data in XML | 1zhc_validation.xml.gz | 30.3 KB | Display | |
| Data in CIF | 1zhc_validation.cif.gz | 48.5 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/zh/1zhc ftp://data.pdbj.org/pub/pdb/validation_reports/zh/1zhc | HTTPS FTP |
-Related structure data
| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| NMR ensembles |
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Components
| #1: Protein | Mass: 9130.293 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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-Experimental details
-Experiment
| Experiment | Method: SOLUTION NMR | ||||||||||||||||||||
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| NMR experiment |
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Sample preparation
| Details | Contents: U-15N, 13C; 50mM phosphate buffer, 100mM NaCl, 1mM EDTA, pH 6.8; 90% H2O, 10% D2O Solvent system: 90% H2O/10% D2O |
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| Sample conditions | Ionic strength: 100mm NaCl / pH: 6.8 / Pressure: ambient / Temperature: 303 K |
-NMR measurement
| NMR spectrometer | Type: Bruker DMX / Manufacturer: Bruker / Model: DMX / Field strength: 600 MHz |
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Processing
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| Refinement | Method: simulated annealing, torsion angle dynamics / Software ordinal: 1 Details: the structures are based on a total of 1040 restraints, 911 are NOE-derived distance constraints, 129 dihedral angle restraints | ||||||||||||||||||||
| NMR representative | Selection criteria: closest to the average | ||||||||||||||||||||
| NMR ensemble | Conformer selection criteria: structures with acceptable covalent geometry Conformers calculated total number: 100 / Conformers submitted total number: 20 |
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