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Yorodumi- PDB-3mh3: Mutagenesis of p38 MAP kinase establishes key roles of Phe169 in ... -
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Basic information
| Entry | Database: PDB / ID: 3mh3 | |||||||||
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| Title | Mutagenesis of p38 MAP kinase establishes key roles of Phe169 in function and structural dynamics and reveals a novel DFG-out state | |||||||||
 Components | Mitogen-activated protein kinase 14 | |||||||||
 Keywords | TRANSFERASE / SIGNALING PROTEIN | |||||||||
| Function / homology |  Function and homology informationstress-activated protein kinase signaling cascade / positive regulation of cyclase activity / Activation of PPARGC1A (PGC-1alpha) by phosphorylation / regulation of synaptic membrane adhesion / stress-induced premature senescence / cell surface receptor protein serine/threonine kinase signaling pathway / CD163 mediating an anti-inflammatory response / 3'-UTR-mediated mRNA stabilization / KSRP (KHSRP) binds and destabilizes mRNA / positive regulation of myoblast fusion ...stress-activated protein kinase signaling cascade / positive regulation of cyclase activity / Activation of PPARGC1A (PGC-1alpha) by phosphorylation / regulation of synaptic membrane adhesion / stress-induced premature senescence / cell surface receptor protein serine/threonine kinase signaling pathway / CD163 mediating an anti-inflammatory response / 3'-UTR-mediated mRNA stabilization / KSRP (KHSRP) binds and destabilizes mRNA / positive regulation of myoblast fusion / cellular response to UV-B / cartilage condensation / mitogen-activated protein kinase p38 binding / positive regulation of muscle cell differentiation / Platelet sensitization by LDL / Myogenesis / positive regulation of myotube differentiation / NFAT protein binding / regulation of cytokine production involved in inflammatory response / Activation of the AP-1 family of transcription factors / D-glucose import / p38MAPK cascade / ERK/MAPK targets / response to dietary excess / fatty acid oxidation / cellular response to lipoteichoic acid / response to muramyl dipeptide / Regulation of MITF-M-dependent genes involved in pigmentation / MAP kinase kinase activity / signal transduction in response to DNA damage / regulation of ossification / MAP kinase activity / cellular response to vascular endothelial growth factor stimulus / RHO GTPases Activate NADPH Oxidases / mitogen-activated protein kinase / chondrocyte differentiation / vascular endothelial growth factor receptor signaling pathway / negative regulation of hippo signaling / positive regulation of myoblast differentiation / stress-activated MAPK cascade / skeletal muscle tissue development / positive regulation of cardiac muscle cell proliferation / p38MAPK events / positive regulation of brown fat cell differentiation / striated muscle cell differentiation / response to muscle stretch / positive regulation of interleukin-12 production / osteoclast differentiation / positive regulation of erythrocyte differentiation / lipopolysaccharide-mediated signaling pathway / DNA damage checkpoint signaling / placenta development / tumor necrosis factor-mediated signaling pathway / cellular response to ionizing radiation / positive regulation of D-glucose import / activated TAK1 mediates p38 MAPK activation / stem cell differentiation / negative regulation of inflammatory response to antigenic stimulus / negative regulation of canonical Wnt signaling pathway / NOD1/2 Signaling Pathway / response to insulin / bone development / cellular response to virus / platelet activation / positive regulation of protein import into nucleus / VEGFA-VEGFR2 Pathway / glucose metabolic process / cell morphogenesis / positive regulation of reactive oxygen species metabolic process / chemotaxis / spindle pole / osteoblast differentiation / ADP signalling through P2Y purinoceptor 1 / cellular senescence / MAPK cascade / cellular response to lipopolysaccharide / angiogenesis / secretory granule lumen / protein phosphatase binding / Oxidative Stress Induced Senescence / Regulation of TP53 Activity through Phosphorylation / ficolin-1-rich granule lumen / transcription by RNA polymerase II / cell surface receptor signaling pathway / intracellular signal transduction / nuclear speck / protein serine kinase activity / protein serine/threonine kinase activity / apoptotic process / Neutrophil degranulation / positive regulation of gene expression / regulation of transcription by RNA polymerase II / glutamatergic synapse / enzyme binding / signal transduction / positive regulation of transcription by RNA polymerase II / mitochondrion / extracellular region / nucleoplasm / ATP binding Similarity search - Function  | |||||||||
| Biological species |  Homo sapiens (human) | |||||||||
| Method |  X-RAY DIFFRACTION /  SYNCHROTRON /  MOLECULAR REPLACEMENT / Resolution: 2.2 Å  | |||||||||
 Authors | Namboodiri, H.V. / Karpusas, M. / Bukhtiyarova, M. / Springman, E.B. | |||||||||
 Citation |  Journal: Biochemistry / Year: 2007Title: Mutagenesis of p38alpha MAP kinase establishes key roles of Phe169 in function and structural dynamics and reveals a novel DFG-OUT state. Authors: Bukhtiyarova, M. / Karpusas, M. / Northrop, K. / Namboodiri, H.V. / Springman, E.B.  | |||||||||
| History | 
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Structure visualization
| Structure viewer | Molecule:  Molmil Jmol/JSmol | 
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Downloads & links
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Download
| PDBx/mmCIF format |  3mh3.cif.gz | 81.7 KB | Display |  PDBx/mmCIF format | 
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| PDB format |  pdb3mh3.ent.gz | 60.7 KB | Display |  PDB format | 
| PDBx/mmJSON format |  3mh3.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  3mh3_validation.pdf.gz | 639.5 KB | Display |  wwPDB validaton report | 
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| Full document |  3mh3_full_validation.pdf.gz | 647.1 KB | Display | |
| Data in XML |  3mh3_validation.xml.gz | 15.3 KB | Display | |
| Data in CIF |  3mh3_validation.cif.gz | 20.5 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/mh/3mh3 ftp://data.pdbj.org/pub/pdb/validation_reports/mh/3mh3 | HTTPS FTP  | 
-Related structure data
| Related structure data | ![]() 3mgyC ![]() 3mh0C ![]() 3mh1C ![]() 3mh2C ![]() 1zyjS 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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| Unit cell | 
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Components
| #1: Protein |   Mass: 41353.215 Da / Num. of mol.: 1 / Mutation: F169R Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Homo sapiens (human) / Gene: CSBP, CSBP1, CSBP2, CSPB1, MAPK14, MXI2 / Plasmid: DE3 / Production host: ![]() References: UniProt: Q16539, mitogen-activated protein kinase  | 
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| #2: Sugar |  ChemComp-BOG /  | 
| #3: Water |  ChemComp-HOH /  | 
-Experimental details
-Experiment
| Experiment | Method:  X-RAY DIFFRACTION / Number of used crystals: 1  | 
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Sample preparation
| Crystal | Density Matthews: 2.26 Å3/Da / Density % sol: 45.57 % | 
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| Crystal grow | Temperature: 295 K / Method: vapor diffusion, sitting drop / pH: 6  Details: 10-20% PEG 4000, 0.1 M cacodylic acid, 50 mM n-octyl-beta-D-glucoside, pH 6.0, VAPOR DIFFUSION, SITTING DROP, temperature 295K  | 
-Data collection
| Diffraction | Mean temperature: 93 K | 
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| Diffraction source | Source:  SYNCHROTRON / Site:  NSLS   / Beamline: X4A / Wavelength: 0.98 Å | 
| Detector | Type: ADSC QUANTUM 4 / Detector: CCD / Date: Aug 16, 2004 / Details: Mirrors | 
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | 
| Radiation wavelength | Wavelength: 0.98 Å / Relative weight: 1 | 
| Reflection | Resolution: 2.2→40 Å / Num. obs: 19105 / % possible obs: 96.7 % / Rmerge(I) obs: 0.083 / Rsym value: 0.055 / Net I/σ(I): 7.1 | 
| Reflection shell | Resolution: 2.2→2.37 Å / Rmerge(I) obs: 0.441 / Mean I/σ(I) obs: 2 / Num. unique all: 3740 / Rsym value: 0.426 / % possible all: 96.2 | 
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Processing
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| Refinement | Method to determine structure:  MOLECULAR REPLACEMENTStarting model: PDB ENTRY 1ZYJ Resolution: 2.2→23.99 Å / Cor.coef. Fo:Fc: 0.92 / Cor.coef. Fo:Fc free: 0.881 / SU B: 7.694 / SU ML: 0.195 / Cross valid method: THROUGHOUT / ESU R: 0.38 / ESU R Free: 0.277 / Stereochemistry target values: MAXIMUM LIKELIHOOD 
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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: 29.034 Å2
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| Refinement step | Cycle: LAST / Resolution: 2.2→23.99 Å
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| Refine LS restraints | 
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| LS refinement shell | Resolution: 2.195→2.252 Å / Total num. of bins used: 20 
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Homo sapiens (human)
X-RAY DIFFRACTION
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