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Yorodumi- PDB-3mpa: Conformational plasticity of p38 MAP kinase DFG motif mutants in ... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 3mpa | ||||||
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| Title | Conformational plasticity of p38 MAP kinase DFG motif mutants in response to inhibitor binding | ||||||
Components | Mitogen-activated protein kinase 14 | ||||||
Keywords | TRANSFERASE | ||||||
| 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: 2.1 Å | ||||||
Authors | Namboodiri, H.V. / Karpusas, M. / Bukhtiyarova, M. / Springman, E.B. | ||||||
Citation | Journal: TO BE PUBLISHEDTitle: Conformational plasticity of p38 MAP kinase DFG motif mutants in response to inhibitor binding Authors: Namboodiri, H.V. / Springman, E.B. / Karpusas, M. / Bukhtiyarova, M. / Ramcharan, J. | ||||||
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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 | 3mpa.cif.gz | 85.6 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb3mpa.ent.gz | 62.5 KB | Display | PDB format |
| PDBx/mmJSON format | 3mpa.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 3mpa_validation.pdf.gz | 889.2 KB | Display | wwPDB validaton report |
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| Full document | 3mpa_full_validation.pdf.gz | 898.4 KB | Display | |
| Data in XML | 3mpa_validation.xml.gz | 16.6 KB | Display | |
| Data in CIF | 3mpa_validation.cif.gz | 23.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/mp/3mpa ftp://data.pdbj.org/pub/pdb/validation_reports/mp/3mpa | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 3o8pC ![]() 3o8tC ![]() 3o8uC ![]() 3obgC ![]() 3objC ![]() 3oc1C ![]() 1zyjS 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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| Unit cell |
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Components
| #1: Protein | Mass: 41285.160 Da / Num. of mol.: 1 / Mutation: D168G Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: CSBP, CSBP1, CSBP2, CSPB1, MAPK14, MXI2References: UniProt: Q16539, mitogen-activated protein kinase |
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| #2: Chemical | ChemComp-SB2 / |
| #3: Sugar | ChemComp-BOG / |
| #4: 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: 2.27 Å3/Da / Density % sol: 45.79 % |
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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 / 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: 2.1→40 Å / Num. obs: 22530 / % possible obs: 95 % / Observed criterion σ(I): 1 / Rmerge(I) obs: 0.042 / Rsym value: 0.031 / Net I/σ(I): 31 |
| Reflection shell | Resolution: 2.1→2.18 Å / Redundancy: 2.4 % / Rmerge(I) obs: 0.266 / Mean I/σ(I) obs: 2.9 / Num. unique all: 1755 / Rsym value: 0.236 / % possible all: 79.6 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: PDB ENTRY 1ZYJ Resolution: 2.1→30.34 Å / Cor.coef. Fo:Fc: 0.933 / Cor.coef. Fo:Fc free: 0.905 / SU B: 5.969 / SU ML: 0.164 / Cross valid method: THROUGHOUT / ESU R Free: 0.238 / 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: 1.2 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 36.33 Å2
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| Refinement step | Cycle: LAST / Resolution: 2.1→30.34 Å
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| Refine LS restraints |
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| LS refinement shell | Resolution: 2.101→2.156 Å / Total num. of bins used: 20
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Homo sapiens (human)
X-RAY DIFFRACTION
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