9l4b

Kinase domain of ATR bound with RP-3500

Method: ELECTRON MICROSCOPY Dmax: 157.3 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 A1EIK Camonsertib × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.20 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 9l4b

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9l4b
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9l4b
Deposition date deposition_date2024-12-20
Structure title titleKinase domain of ATR bound with RP-3500
Keywords keywordsATR inhibitor, CELL CYCLE; CELL CYCLE
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier46.41
Radius of gyration Rg (electron density) rg_electron45.94
Forward intensity I(0) i01282330000.00
Molecular weight molecular_weight293470.0 kDa
Excluded volume excluded_volume364830 ų
Envelope volume envelope_volume490180 ų
Hydration-shell volume shell_volume87578 ų
Envelope diameter envelope_diameter168.1
Shell Rg shell_rg51.35
Envelope Rg envelope_rg45.65
Shape Rg shape_rg45.80
Total Rg total_rg46.60
Total atoms total_atoms40343
Residues n_residues2669
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 dmax157.3
Rg (real space) rg_real46.42
Rg uncertainty (real space) rg_real_error1.60
I(0) (real space) i0_real1.2820e+09
I(0) uncertainty (real space) i0_real_error2.3230e+07
Rg (reciprocal space) rg_reciprocal46.41
I(0) (reciprocal space) i0_reciprocal1282000000.0000
Solution quality estimate total_estimate0.8574
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary55.5
Skewness Skewness skewness0.415
Kurtosis Kurtosis kurtosis-0.136
Angular range angular_range— – 0.1700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha154800000.0000
Real-space data points n_real_points35
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.792; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.990; Smooth: 0.777

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)