[English] 日本語
![](img/lk-miru.gif)
- PDB-1g2a: THE CRYSTAL STRUCTURE OF E.COLI PEPTIDE DEFORMYLASE COMPLEXED WIT... -
+
Open data
-
Basic information
Entry | Database: PDB / ID: 1g2a | ||||||
---|---|---|---|---|---|---|---|
Title | THE CRYSTAL STRUCTURE OF E.COLI PEPTIDE DEFORMYLASE COMPLEXED WITH ACTINONIN | ||||||
![]() | POLYPEPTIDE DEFORMYLASE | ||||||
![]() | ![]() ![]() ![]() | ||||||
Function / homology | ![]() co-translational protein modification / ![]() ![]() ![]() ![]() ![]() ![]() ![]() Similarity search - Function | ||||||
Biological species | ![]() ![]() ![]() | ||||||
Method | ![]() ![]() | ||||||
![]() | Clements, J.M. / Beckett, P. / Brown, A. / Catlin, C. / Lobell, M. / Palan, S. / Thomas, W. / Whittaker, M. / Baker, P.J. / Rodgers, H.F. ...Clements, J.M. / Beckett, P. / Brown, A. / Catlin, C. / Lobell, M. / Palan, S. / Thomas, W. / Whittaker, M. / Baker, P.J. / Rodgers, H.F. / Barynin, V. / Rice, D.W. / Hunter, M.G. | ||||||
![]() | ![]() Title: Antibiotic activity and characterization of BB-3497, a novel peptide deformylase inhibitor. Authors: Clements, J.M. / Beckett, R.P. / Brown, A. / Catlin, G. / Lobell, M. / Palan, S. / Thomas, W. / Whittaker, M. / Wood, S. / Salama, S. / Baker, P.J. / Rodgers, H.F. / Barynin, V. / Rice, D.W. / Hunter, M.G. | ||||||
History |
|
-
Structure visualization
Structure viewer | Molecule: ![]() ![]() |
---|
-
Downloads & links
-
Download
PDBx/mmCIF format | ![]() | 129.8 KB | Display | ![]() |
---|---|---|---|---|
PDB format | ![]() | 100.2 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
---|
-Related structure data
-
Links
-
Assembly
Deposited unit | ![]()
| ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
1 | ![]()
| ||||||||||
2 | ![]()
| ||||||||||
3 | ![]()
| ||||||||||
Unit cell |
|
-
Components
#1: Protein | Mass: 19226.248 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() ![]() ![]() ![]() #2: Chemical | ![]() #3: Chemical | ![]() #4: Water | ChemComp-HOH / | ![]() |
---|
-Experimental details
-Experiment
Experiment | Method: ![]() |
---|
-
Sample preparation
Crystal | Density Matthews: 2.77 Å3/Da / Density % sol: 55.6 % | |||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Crystal grow![]() | Temperature: 290 K / Method: vapor diffusion, hanging drop / pH: 7.5 Details: 10mg/ml PDF, 20mM actinonin, 50mM HEPES, pH 7.5 + 25-32% PEG 4000, 0.1M sodium citrate, pH 5.6, 0.2M ammonium acetate, VAPOR DIFFUSION, HANGING DROP at 290K | |||||||||||||||||||||||||||||||||||
Crystal grow | *PLUS | |||||||||||||||||||||||||||||||||||
Components of the solutions | *PLUS
|
-Data collection
Diffraction | Mean temperature: 100 K |
---|---|
Diffraction source | Source: ![]() |
Detector | Type: MARRESEARCH / Detector: AREA DETECTOR / Date: Apr 28, 1999 / Details: MSC Yale Mirrors |
Radiation | Monochromator: msc yale mirrors / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength![]() |
Reflection | Resolution: 1.75→14 Å / Num. all: 62907 / Num. obs: 54729 / % possible obs: 0.87 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / Redundancy: 1.95 % / Rmerge(I) obs: 0.044 / Net I/σ(I): 13.6 |
Reflection shell | Resolution: 1.75→1.79 Å / Redundancy: 1.5 % / Rmerge(I) obs: 0.191 / % possible all: 86.8 |
Reflection | *PLUS % possible obs: 85.9 % |
Reflection shell | *PLUS % possible obs: 86.8 % / Num. unique obs: 3634 / Mean I/σ(I) obs: 3.9 |
-
Processing
Software |
| |||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Refinement | Method to determine structure![]() ![]()
| |||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.75→14 Å
| |||||||||||||||||||||||||
Refine LS restraints |
| |||||||||||||||||||||||||
Software | *PLUS Name: REFMAC / Classification: refinement | |||||||||||||||||||||||||
Refinement | *PLUS σ(F): 0 / % reflection Rfree: 5 % / Rfactor Rfree![]() ![]() | |||||||||||||||||||||||||
Solvent computation | *PLUS | |||||||||||||||||||||||||
Displacement parameters | *PLUS | |||||||||||||||||||||||||
Refine LS restraints | *PLUS
|