+Open data
-Basic information
Entry | Database: PDB / ID: 2okr | ||||||
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Title | Crystal Structure of the P38a-MAPKAP kinase 2 Heterodimer | ||||||
Components |
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Keywords | TRANSFERASE / Kinase / NLS / NES / heterodimer / docking groove | ||||||
Function / homology | Function and homology information macropinocytosis / CREB phosphorylation / calcium-dependent protein serine/threonine kinase activity / Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA / leukotriene metabolic process / Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA / Synthesis of Leukotrienes (LT) and Eoxins (EX) / regulation of tumor necrosis factor production / regulation of tumor necrosis factor-mediated signaling pathway / stress-activated protein kinase signaling cascade ...macropinocytosis / CREB phosphorylation / calcium-dependent protein serine/threonine kinase activity / Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA / leukotriene metabolic process / Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA / Synthesis of Leukotrienes (LT) and Eoxins (EX) / regulation of tumor necrosis factor production / regulation of tumor necrosis factor-mediated signaling pathway / stress-activated protein kinase signaling cascade / positive regulation of cyclase activity / calcium/calmodulin-dependent protein kinase activity / mitogen-activated protein kinase binding / Activation of PPARGC1A (PGC-1alpha) by phosphorylation / regulation of interleukin-6 production / CD163 mediating an anti-inflammatory response / positive regulation of macrophage cytokine production / regulation of synaptic membrane adhesion / stress-induced premature senescence / cell surface receptor protein serine/threonine kinase signaling pathway / 3'-UTR-mediated mRNA stabilization / KSRP (KHSRP) binds and destabilizes mRNA / cartilage condensation / toll-like receptor signaling pathway / positive regulation of myoblast fusion / cellular response to UV-B / Platelet sensitization by LDL / mitogen-activated protein kinase p38 binding / positive regulation of muscle cell differentiation / positive regulation of myotube differentiation / NFAT protein binding / Myogenesis / D-glucose import / regulation of cytokine production involved in inflammatory response / Activation of the AP-1 family of transcription factors / ERK/MAPK targets / p38MAPK cascade / Regulation of MITF-M-dependent genes involved in pigmentation / fatty acid oxidation / MAP kinase kinase activity / cellular response to lipoteichoic acid / response to muramyl dipeptide / response to dietary excess / inner ear development / RHO GTPases Activate NADPH Oxidases / MAP kinase activity / regulation of ossification / Regulation of HSF1-mediated heat shock response / cellular response to vascular endothelial growth factor stimulus / signal transduction in response to DNA damage / mitogen-activated protein kinase / negative regulation of hippo signaling / positive regulation of myoblast differentiation / chondrocyte differentiation / vascular endothelial growth factor receptor signaling pathway / positive regulation of cardiac muscle cell proliferation / lipopolysaccharide-mediated signaling pathway / regulation of cellular response to heat / stress-activated MAPK cascade / skeletal muscle tissue development / p38MAPK events / striated muscle cell differentiation / regulation of mRNA stability / response to muscle stretch / positive regulation of interleukin-12 production / positive regulation of brown fat cell differentiation / positive regulation of erythrocyte differentiation / osteoclast differentiation / response to cytokine / DNA damage checkpoint signaling / activated TAK1 mediates p38 MAPK activation / positive regulation of D-glucose import / stem cell differentiation / cellular response to ionizing radiation / negative regulation of inflammatory response to antigenic stimulus / Regulation of TNFR1 signaling / NOD1/2 Signaling Pathway / response to insulin / bone development / negative regulation of canonical Wnt signaling pathway / cell morphogenesis / placenta development / cellular response to virus / platelet activation / VEGFA-VEGFR2 Pathway / spindle pole / positive regulation of protein import into nucleus / osteoblast differentiation / ADP signalling through P2Y purinoceptor 1 / chemotaxis / glucose metabolic process / positive regulation of reactive oxygen species metabolic process / cellular senescence / positive regulation of tumor necrosis factor production / MAPK cascade / cellular response to tumor necrosis factor / peptidyl-serine phosphorylation / cellular response to lipopolysaccharide / protein phosphatase binding / angiogenesis Similarity search - Function | ||||||
Biological species | Homo sapiens (human) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2 Å | ||||||
Authors | Ter Haar, E. | ||||||
Citation | Journal: J.Biol.Chem. / Year: 2007 Title: Crystal structure of the P38alpha-MAPKAP kinase 2 heterodimer. Authors: ter Haar, E. / Prabakhar, P. / Liu, X. / Lepre, C. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 2okr.cif.gz | 158.2 KB | Display | PDBx/mmCIF format |
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PDB format | pdb2okr.ent.gz | 123.4 KB | Display | PDB format |
PDBx/mmJSON format | 2okr.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 2okr_validation.pdf.gz | 461.3 KB | Display | wwPDB validaton report |
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Full document | 2okr_full_validation.pdf.gz | 489.4 KB | Display | |
Data in XML | 2okr_validation.xml.gz | 31.5 KB | Display | |
Data in CIF | 2okr_validation.cif.gz | 43.9 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ok/2okr ftp://data.pdbj.org/pub/pdb/validation_reports/ok/2okr | HTTPS FTP |
-Related structure data
Related structure data | 2onlC 1lezS C: citing same article (ref.) S: Starting model for refinement |
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Similar structure data |
-Links
-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: 41998.938 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: MAPK14, CSBP, CSBP1, CSBP2, MXI2 / Plasmid: pVL1392 / Production host: Spodoptera frugiperda (fall armyworm) References: UniProt: Q16539, mitogen-activated protein kinase #2: Protein/peptide | Mass: 2812.511 Da / Num. of mol.: 2 / Fragment: residues 370-393 / Source method: obtained synthetically Details: This sequence occurs naturally in Homo sapiens (Humans) References: UniProt: P49137, non-specific serine/threonine protein kinase #3: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 2.6 Å3/Da / Density % sol: 52.67 % |
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Crystal grow | Temperature: 298 K / Method: vapor diffusion, hanging drop / pH: 7.2 Details: 25% Peg 3350, 250 mM Sodium Formate, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 298K |
-Data collection
Diffraction | Mean temperature: 95 K |
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Diffraction source | Source: SYNCHROTRON / Site: ALS / Beamline: 5.0.2 / Wavelength: 1 Å |
Detector | Type: ADSC QUANTUM 210 / Detector: CCD / Date: Apr 8, 2005 |
Radiation | Monochromator: Si 111 CHANNEL / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
Reflection | Resolution: 2→40.78 Å / Num. obs: 60104 / % possible obs: 98.6 % / Observed criterion σ(F): 1 / Observed criterion σ(I): 1 / Redundancy: 3.06 % / Biso Wilson estimate: 31.6 Å2 / Rmerge(I) obs: 0.059 / Χ2: 0.97 / Net I/σ(I): 9 / Scaling rejects: 1391 |
Reflection shell | Resolution: 2→2.07 Å / Redundancy: 2.48 % / Rmerge(I) obs: 0.364 / Mean I/σ(I) obs: 2.2 / Num. measured all: 13657 / Num. unique all: 5517 / Χ2: 1.15 / % possible all: 90.7 |
-Phasing
Phasing MR |
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-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: PDB entry 1LEZ Resolution: 2→8.48 Å / Isotropic thermal model: anisotropic / Cross valid method: THROUGHOUT / σ(F): 0 / σ(I): 0 / Stereochemistry target values: Engh & Huber
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Displacement parameters | Biso mean: 16.049 Å2
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Refine analyze | Luzzati coordinate error obs: 0.2895 Å | ||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 2→8.48 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 2→2.12 Å
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