9l3r

Human PI3KDELTA in complex with Zandelisib

Method: X-RAY DIFFRACTION Dmax: 111.3 Å Quality: GOOD

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

Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform

Homo sapiens

UniProt O00329

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–1044 Not recorded Phosphatidylinositol 3-kinase regulatory subunit alpha × 1 (P23727) A1L62 Zandelisib × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.8;283.15 K;10% PEG 4000, 100 mM KCl, 1 mM TCEP neutral pH, 10 mM CaCl2, 100 mM MES pH 5.8 Resolution 2.50 Å R-free 0.278

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.

17 other PDB entries and 18 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PK3CD_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–1044; UniProt 1–1044

Phosphatidylinositol 3-kinase regulatory subunit alpha

Bos taurus

UniProt P23727

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 431–600 Non-standard monomer:Yes (specific site not provided by mmCIF) Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform × 1 (O00329) A1L62 Zandelisib × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.8;283.15 K;10% PEG 4000, 100 mM KCl, 1 mM TCEP neutral pH, 10 mM CaCl2, 100 mM MES pH 5.8 Resolution 2.50 Å R-free 0.278

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.

27 other PDB entries and 36 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name P85A_BOVIN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 3–172; UniProt 431–600

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 9l3r

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9l3r
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id9l3r
Deposition date deposition_date2024-12-19
Structure title titleHuman PI3KDELTA in complex with Zandelisib
Keywords keywordsInhibitor, TRANSFERASE, TRANSFERASE-INHIBITOR complex; TRANSFERASE/INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier33.99
Radius of gyration Rg (electron density) rg_electron33.41
Forward intensity I(0) i0475671000.00
Molecular weight molecular_weight117530.0 kDa
Excluded volume excluded_volume113750 ų
Envelope volume envelope_volume208650 ų
Hydration-shell volume shell_volume51369 ų
Envelope diameter envelope_diameter119.5
Shell Rg shell_rg40.75
Envelope Rg envelope_rg33.37
Shape Rg shape_rg33.41
Total Rg total_rg33.81
Total atoms total_atoms8889
Residues n_residues1104
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 dmax111.3
Rg (real space) rg_real33.88
Rg uncertainty (real space) rg_real_error0.88
I(0) (real space) i0_real4.7570e+08
I(0) uncertainty (real space) i0_real_error8.0530e+06
Rg (reciprocal space) rg_reciprocal33.95
I(0) (reciprocal space) i0_reciprocal475700000.0000
Solution quality estimate total_estimate0.8878
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary42.6
Skewness Skewness skewness0.248
Kurtosis Kurtosis kurtosis-0.292
Angular range angular_range— – 0.2350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha43610000.0000
Real-space data points n_real_points48
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.858; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.962

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)