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- PDB-3l0c: Crystal structure of SCP1 phosphatase D206A mutant with trapped i... -
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Open data
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Basic information
Entry | Database: PDB / ID: 3l0c | ||||||
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Title | Crystal structure of SCP1 phosphatase D206A mutant with trapped inorganic phosphate | ||||||
![]() | Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 | ||||||
![]() | HYDROLASE / HAD superfamily / small C-terminal domain phosphatase / protein phosphatase / product-trapping | ||||||
Function / homology | ![]() RNA polymerase II CTD heptapeptide repeat phosphatase activity / myosin phosphatase activity / negative regulation of G1/S transition of mitotic cell cycle / protein-serine/threonine phosphatase / negative regulation of neuron differentiation / protein dephosphorylation / negative regulation of protein phosphorylation / negative regulation of neurogenesis / regulation of transcription by RNA polymerase II / extracellular exosome ...RNA polymerase II CTD heptapeptide repeat phosphatase activity / myosin phosphatase activity / negative regulation of G1/S transition of mitotic cell cycle / protein-serine/threonine phosphatase / negative regulation of neuron differentiation / protein dephosphorylation / negative regulation of protein phosphorylation / negative regulation of neurogenesis / regulation of transcription by RNA polymerase II / extracellular exosome / nucleoplasm / nucleus / metal ion binding Similarity search - Function | ||||||
Biological species | ![]() | ||||||
Method | ![]() ![]() ![]() | ||||||
![]() | Zhang, M. / Zhang, Y. | ||||||
![]() | ![]() Title: Structural and functional analysis of the phosphoryl transfer reaction mediated by the human small C-terminal domain phosphatase, Scp1. Authors: Zhang, M. / Liu, J. / Kim, Y. / Dixon, J.E. / Pfaff, S.L. / Gill, G.N. / Noel, J.P. / Zhang, Y. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 85.2 KB | Display | ![]() |
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PDB format | ![]() | 63.9 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 445.4 KB | Display | ![]() |
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Full document | ![]() | 450.1 KB | Display | |
Data in XML | ![]() | 15.2 KB | Display | |
Data in CIF | ![]() | 20 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 3l0bC ![]() 3l0yC ![]() 2ghqS C: citing same article ( S: Starting model for refinement |
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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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Components
#1: Protein | Mass: 21034.912 Da / Num. of mol.: 2 / Mutation: D206A Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() References: UniProt: Q9GZU7, protein-serine/threonine phosphatase #2: Chemical | #3: Chemical | #4: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 3.36 Å3/Da / Density % sol: 63.39 % |
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Crystal grow | Temperature: 298 K / Method: vapor diffusion, sitting drop / pH: 7 Details: 0.5M AMMONIUM SULFATE, 0.2M LITHIUM SULFATE, 100MM HEPES, pH 7.0. CRYSTAL TRANSFERRED TO 100MM MES, pH 6.5, 30% PEG8000, 20MM PNPP, AND 0.2M MAGNESIUM CHLORIDE, VAPOR DIFFUSION, SITTING DROP, temperature 298K |
-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: ![]() ![]() ![]() |
Detector | Type: ADSC QUANTUM 315 / Detector: CCD / Date: Oct 12, 2006 / Details: MIRRORS |
Radiation | Monochromator: GRAPHITE / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
Reflection | Resolution: 2.45→48.62 Å / Num. obs: 17693 / % possible obs: 95 % / Observed criterion σ(I): 0 / Redundancy: 3.3 % / Rsym value: 0.075 / Net I/σ(I): 13.4 |
Reflection shell | Resolution: 2.45→2.54 Å / Redundancy: 2.1 % / Mean I/σ(I) obs: 2.1 / Rsym value: 0.227 / % possible all: 53.2 |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: pdb entry 2GHQ Resolution: 2.45→39.25 Å / Cor.coef. Fo:Fc: 0.932 / Cor.coef. Fo:Fc free: 0.892 / SU B: 8.403 / SU ML: 0.19 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R: 0.397 / ESU R Free: 0.27 / 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: 1.4 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 37.48 Å2
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Refinement step | Cycle: LAST / Resolution: 2.45→39.25 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 2.45→2.52 Å / Total num. of bins used: 20
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