7pvu

Crystal structure of p38alpha C162S in complex with CAS2094511-69-8, P 1 21 1

Method: X-RAY DIFFRACTION Dmax: 102.4 Å Quality: GOOD

1. Protein Identity and Related Structures Protein Identity & Related Structures

Mitogen-activated protein kinase 14

Mus musculus

UniProt P47811

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–359 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.8;293 K;27% PEG 3350, 0,1M BIS-TRIS pH 6.8 Resolution 2.15 Å R-free 0.239
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 1–359 Not recorded 8DI N-(2-cyclobutyl-1H-1,3-benzodiazol-5-yl)-2-fluorobenzene-1-sulfonamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.8;293 K;27% PEG 3350, 0,1M BIS-TRIS pH 6.8 Resolution 2.15 Å R-free 0.239

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

127 other PDB entries and 136 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MK14_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–359; UniProt 1–359 Author chain B; PDBConstruct 1–359; UniProt 1–359

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 7pvu

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7pvu
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7pvu
Deposition date deposition_date2021-10-05
Structure title titleCrystal structure of p38alpha C162S in complex with CAS2094511-69-8, P 1 21 1
Keywords keywordskinase, enzyme, inhibitor, ligand, ONCOPROTEIN; ONCOPROTEIN
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier31.74
Radius of gyration Rg (electron density) rg_electron31.08
Forward intensity I(0) i090780300.00
Molecular weight molecular_weight77341.0 kDa
Excluded volume excluded_volume97680 ų
Envelope volume envelope_volume127720 ų
Hydration-shell volume shell_volume34736 ų
Envelope diameter envelope_diameter106.7
Shell Rg shell_rg37.71
Envelope Rg envelope_rg30.54
Shape Rg shape_rg31.05
Total Rg total_rg31.78
Total atoms total_atoms5457
Residues n_residues673
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax102.4
Rg (real space) rg_real31.75
Rg uncertainty (real space) rg_real_error0.65
I(0) (real space) i0_real9.0780e+07
I(0) uncertainty (real space) i0_real_error1.3680e+06
Rg (reciprocal space) rg_reciprocal31.75
I(0) (reciprocal space) i0_reciprocal90780000.0000
Solution quality estimate total_estimate0.8964
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary38.9
Skewness Skewness skewness0.294
Kurtosis Kurtosis kurtosis-0.463
Angular range angular_range— – 0.2500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha30190000.0000
Real-space data points n_real_points51
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.933; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.991; Smooth: 0.857

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id7pvuA01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology510 — Transferase(Phosphotransferase); domain 1
Homologous superfamily homologous superfamily10 — Transferase(Phosphotransferase) domain 1
Domain ID domain_id7pvuB01
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology510 — Transferase(Phosphotransferase); domain 1
Homologous superfamily homologous superfamily10 — Transferase(Phosphotransferase) domain 1

8. Citations (1)

9. Files and Curves (10)