9l40

kinase of ATR bound VE-822 state

Method: ELECTRON MICROSCOPY Dmax: 158.3 Å Quality: GOOD

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

Serine/threonine-protein kinase ATR

Homo sapiens

UniProt Q13535

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–2644 Chain B; UniProt 1–2644 Not recorded A1EIE VE-822 × 4 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.87 Å

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.

9 other PDB entries and 9 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ATR_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–2644; UniProt 1–2644 Author chain B; PDBConstruct 1–2644; UniProt 1–2644

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 9l40

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9l40
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9l40
Deposition date deposition_date2024-12-19
Structure title titlekinase of ATR bound VE-822 state
Keywords keywordsinhibitor, ATR, kinase, CELL CYCLE; CELL CYCLE
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier46.71
Radius of gyration Rg (electron density) rg_electron45.72
Forward intensity I(0) i01214040000.00
Molecular weight molecular_weight267600.0 kDa
Excluded volume excluded_volume324150 ų
Envelope volume envelope_volume493900 ų
Hydration-shell volume shell_volume87879 ų
Envelope diameter envelope_diameter165.4
Shell Rg shell_rg51.41
Envelope Rg envelope_rg45.97
Shape Rg shape_rg45.30
Total Rg total_rg47.24
Total atoms total_atoms35331
Residues n_residues2644
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 dmax158.3
Rg (real space) rg_real46.72
Rg uncertainty (real space) rg_real_error1.73
I(0) (real space) i0_real1.2140e+09
I(0) uncertainty (real space) i0_real_error2.3120e+07
Rg (reciprocal space) rg_reciprocal46.71
I(0) (reciprocal space) i0_reciprocal1214000000.0000
Solution quality estimate total_estimate0.8575
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary55.9
Skewness Skewness skewness0.417
Kurtosis Kurtosis kurtosis-0.142
Angular range angular_range— – 0.1700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha149300000.0000
Real-space data points n_real_points35
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.790; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.990; Smooth: 0.784

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)