+Open data
-Basic information
Entry | Database: PDB / ID: 1tif | ||||||
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Title | TRANSLATION INITIATION FACTOR 3 N-TERMINAL DOMAIN | ||||||
Components | TRANSLATION INITIATION FACTOR 3 | ||||||
Keywords | RIBOSOME BINDING FACTOR / IF3 N-TERMINAL DOMAIN | ||||||
Function / homology | Function and homology information ribosome disassembly / translation initiation factor activity / ribosome binding / membrane / cytosol Similarity search - Function | ||||||
Biological species | Geobacillus stearothermophilus (bacteria) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / Resolution: 1.8 Å | ||||||
Authors | Biou, V. / Shu, F. / Ramakrishnan, V. | ||||||
Citation | Journal: EMBO J. / Year: 1995 Title: X-ray crystallography shows that translational initiation factor IF3 consists of two compact alpha/beta domains linked by an alpha-helix. Authors: Biou, V. / Shu, F. / Ramakrishnan, V. #1: Journal: Biochemistry / Year: 1995 Title: Prokaryotic Translation Initiation Factor If3 is an Elongated Protein Consisting of Two Crystallizable Domains Authors: Kycia, J.H. / Biou, V. / Shu, F. / Gerchman, S.E. / Graziano, V. / Ramakrishnan, V. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 1tif.cif.gz | 33.2 KB | Display | PDBx/mmCIF format |
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PDB format | pdb1tif.ent.gz | 22.3 KB | Display | PDB format |
PDBx/mmJSON format | 1tif.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 1tif_validation.pdf.gz | 379.2 KB | Display | wwPDB validaton report |
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Full document | 1tif_full_validation.pdf.gz | 378.8 KB | Display | |
Data in XML | 1tif_validation.xml.gz | 3.1 KB | Display | |
Data in CIF | 1tif_validation.cif.gz | 4.2 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ti/1tif ftp://data.pdbj.org/pub/pdb/validation_reports/ti/1tif | HTTPS FTP |
-Related structure data
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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Atom site foot note | 1: CIS PROLINE - PRO 54 |
-Components
#1: Protein | Mass: 9114.607 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Geobacillus stearothermophilus (bacteria) Gene: T7 / Plasmid: T7 VECTOR PET13A / Gene (production host): T7 / Production host: Escherichia coli (E. coli) / References: UniProt: P03000 | ||||
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#2: Chemical | ChemComp-PBM / | ||||
#3: Chemical | #4: Water | ChemComp-HOH / | Nonpolymer details | NOTE THAT SOME SOLVENT MOLECULES HAVE AN OCCUPANCY GREATER THAN 1.0. IF IT IS SIGNIFICANTLY GREATER ...NOTE THAT SOME SOLVENT MOLECULES HAVE AN OCCUPANCY GREATER THAN 1.0. IF IT IS SIGNIFICAN | |
-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: 37.08 % Description: THE WAVELENGHT FOR DATA COLLECTION IS THE PB EDGE | |||||||||||||||
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Crystal grow | *PLUS pH: 7.4 / Method: unknown | |||||||||||||||
Components of the solutions | *PLUS
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-Data collection
Diffraction source | Source: SYNCHROTRON / Site: NSLS / Beamline: X12C / Wavelength: 0.95 Å |
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Detector | Type: MARRESEARCH / Detector: IMAGE PLATE AREA DETECTOR / Date: Apr 1, 1994 |
Radiation | Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.95 Å / Relative weight: 1 |
Reflection | Num. obs: 6646 / % possible obs: 95.9 % / Observed criterion σ(I): 0 / Redundancy: 7.2 % / Rmerge(I) obs: 0.039 |
Reflection | *PLUS Rmerge(I) obs: 0.039 |
-Processing
Software |
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Refinement | Resolution: 1.8→10 Å / σ(F): 0
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Refinement step | Cycle: LAST / Resolution: 1.8→10 Å
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Software | *PLUS Name: X-PLOR / Classification: refinement | |||||||||||||||
Refinement | *PLUS | |||||||||||||||
Solvent computation | *PLUS | |||||||||||||||
Displacement parameters | *PLUS | |||||||||||||||
Refine LS restraints | *PLUS
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