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- PDB-2ih2: Crystal structure of the adenine-specific DNA methyltransferase M... -
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Open data
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Basic information
Entry | Database: PDB / ID: 2ih2 | ||||||
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Title | Crystal structure of the adenine-specific DNA methyltransferase M.TaqI complexed with the cofactor analog AETA and a 10 bp DNA containing 5-methylpyrimidin-2(1H)-one at the target base partner position | ||||||
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![]() | TRANSFERASE/DNA / DNA / DNA methyltransferase / target base partner / 5-methylpyrimidin-2(1H)-one / base flipping / nucleotide flipping / TRANSFERASE-DNA COMPLEX | ||||||
Function / homology | ![]() site-specific DNA-methyltransferase (adenine-specific) / site-specific DNA-methyltransferase (adenine-specific) activity / DNA restriction-modification system / methylation / DNA binding Similarity search - Function | ||||||
Biological species | ![]() ![]() | ||||||
Method | ![]() ![]() ![]() | ||||||
![]() | Lenz, T. / Scheidig, A.J. / Weinhold, E. | ||||||
![]() | ![]() Title: Influence of the target base partner on the methylation rate of the adenine-specific DNA methyltransferase M.TaqI Authors: Lenz, T. / Scheidig, A.J. / Weinhold, E. #1: ![]() Title: Structure of the N6-adenine DNA methyltransferase M.TaqI in complex with DNA and a cofactor analog Authors: Goedecke, K. / Pignot, M. / Goody, R.S. / Scheidig, A.J. / Weinhold, E. #2: ![]() Title: Differential binding of s-adenosylmethionine, s-adenosylhomocysteine and sinefungin to the adenine-specific DNA methyltransferase M.TaqI Authors: Schluckebier, G. / Kozak, M. / Bleimling, N. / Weinhold, E. / Saenger, W. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 232.7 KB | Display | ![]() |
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PDB format | ![]() | 177.2 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 1.1 MB | Display | ![]() |
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Full document | ![]() | 1.1 MB | Display | |
Data in XML | ![]() | 47 KB | Display | |
Data in CIF | ![]() | 73.8 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 2ih4C ![]() 2ih5C ![]() 1g38S S: Starting model for refinement C: citing same article ( |
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Similar structure data |
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Links
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Assembly
Deposited unit | ![]()
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1 | ![]()
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2 | ![]()
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Unit cell |
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Details | The asymmetric unit contains two independent biological assemblies, each consisting of M.TaqI, DNA and cofactor analog AETA. |
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Components
-DNA chain , 2 types, 4 molecules BECF
#1: DNA chain | Mass: 3051.001 Da / Num. of mol.: 2 / Source method: obtained synthetically / Details: Solid-phase DNA synthesis #2: DNA chain | Mass: 3036.047 Da / Num. of mol.: 2 / Source method: obtained synthetically / Details: Solid-phase DNA synthesis |
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-Protein , 1 types, 2 molecules AD
#3: Protein | Mass: 47931.195 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() ![]() References: UniProt: P14385, site-specific DNA-methyltransferase (adenine-specific) |
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-Non-polymers , 3 types, 1420 molecules ![](data/chem/img/GOL.gif)
![](data/chem/img/NEA.gif)
![](data/chem/img/HOH.gif)
![](data/chem/img/NEA.gif)
![](data/chem/img/HOH.gif)
#4: Chemical | ChemComp-GOL / #5: Chemical | #6: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.15 Å3/Da / Density % sol: 42.66 % | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / pH: 7.3 Details: 3 microliters crystallization buffer (10 mM Tris/HCl, 300 mM NaCl, pH 7.3) containing the complex plus 1 microliter reservoir solution (100 mM KCl, 100 mM MgCl2, 6% isopropanol, 50 mM sodium ...Details: 3 microliters crystallization buffer (10 mM Tris/HCl, 300 mM NaCl, pH 7.3) containing the complex plus 1 microliter reservoir solution (100 mM KCl, 100 mM MgCl2, 6% isopropanol, 50 mM sodium cacodylate, pH 6.0), VAPOR DIFFUSION, HANGING DROP, temperature 293K | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Components of the solutions |
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-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: ![]() ![]() ![]() |
Detector | Type: ADSC QUANTUM 105 / Detector: CCD / Date: Feb 10, 2003 / Details: ID14-2 (mirror) |
Radiation | Monochromator: ID14-2 (mirror) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.934 Å / Relative weight: 1 |
Reflection | Resolution: 1.6→19.66 Å / Num. all: 121645 / Num. obs: 116532 / % possible obs: 95.8 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / Redundancy: 7.2 % / Biso Wilson estimate: 18.55 Å2 / Rmerge(I) obs: 0.117 / Rsym value: 0.117 / Net I/σ(I): 11.95 |
Reflection shell | Resolution: 1.6→1.65 Å / Redundancy: 3.92 % / Rmerge(I) obs: 0.34 / Mean I/σ(I) obs: 3.58 / Num. unique all: 10668 / Rsym value: 0.34 / % possible all: 58.6 |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: PDB ENTRY 1G38 Resolution: 1.61→19.64 Å / Cor.coef. Fo:Fc: 0.962 / Cor.coef. Fo:Fc free: 0.942 / SU B: 1.464 / SU ML: 0.053 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R: 0.089 / ESU R Free: 0.09 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
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Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 14.678 Å2
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Refinement step | Cycle: LAST / Resolution: 1.61→19.64 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 1.613→1.654 Å / Total num. of bins used: 20
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