9ni8

Cryo-EM structure of the Class 2 PI3K alpha/KRas complex on POPC/POPS nanodiscs

Method: ELECTRON MICROSCOPY Dmax: 127.0 Å Quality: GOOD

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

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

Homo sapiens

UniProt P42336

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–1068 Not recorded Phosphatidylinositol 3-kinase regulatory subunit alpha × 1 (P27986) Isoform 2B of GTPase KRas × 1 (P01116) A1AZD tert-butyl [2-(2-{[(2P)-2-{4-[4-(2-amino-2-oxoethyl)-2-fluoroanilino]thieno[2,3-d]pyridazin-7-yl}phenyl]oxy}ethoxy)ethyl]carbamate × 1 MG MAGNESIUM ION × 1 GNP PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5;50 mM Tris-HCL, 150 mM NaCl, 1mM TCEP cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.23 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.

134 other PDB entries and 145 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PK3CA_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 29–1096; UniProt 1–1068

Phosphatidylinositol 3-kinase regulatory subunit alpha

Homo sapiens

UniProt P27986

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 1–724 Not recorded Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform × 1 (P42336) Isoform 2B of GTPase KRas × 1 (P01116) A1AZD tert-butyl [2-(2-{[(2P)-2-{4-[4-(2-amino-2-oxoethyl)-2-fluoroanilino]thieno[2,3-d]pyridazin-7-yl}phenyl]oxy}ethoxy)ethyl]carbamate × 1 MG MAGNESIUM ION × 1 GNP PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5;50 mM Tris-HCL, 150 mM NaCl, 1mM TCEP cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.23 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.

103 other PDB entries and 116 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name P85A_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–724; UniProt 1–724

Isoform 2B of GTPase KRas

Homo sapiens

UniProt P01116

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 1–188 Not recorded Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform × 1 (P42336) Phosphatidylinositol 3-kinase regulatory subunit alpha × 1 (P27986) A1AZD tert-butyl [2-(2-{[(2P)-2-{4-[4-(2-amino-2-oxoethyl)-2-fluoroanilino]thieno[2,3-d]pyridazin-7-yl}phenyl]oxy}ethoxy)ethyl]carbamate × 1 MG MAGNESIUM ION × 1 GNP PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5;50 mM Tris-HCL, 150 mM NaCl, 1mM TCEP cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.23 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.

445 other PDB entries and 804 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RASK_HUMAN
Isoform P01116-2
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 2–189; UniProt 1–188

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 9ni8

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9ni8
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9ni8
Deposition date deposition_date2025-02-25
Structure title titleCryo-EM structure of the Class 2 PI3K alpha/KRas complex on POPC/POPS nanodiscs
Keywords keywordslipid kinase, GTPase, ONCOPROTEIN, Transferase-Hydrolase complex; Transferase/Hydrolase
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier37.91
Radius of gyration Rg (electron density) rg_electron37.23
Forward intensity I(0) i0290866000.00
Molecular weight molecular_weight139670.0 kDa
Excluded volume excluded_volume175470 ų
Envelope volume envelope_volume234900 ų
Hydration-shell volume shell_volume53784 ų
Envelope diameter envelope_diameter128.5
Shell Rg shell_rg42.46
Envelope Rg envelope_rg36.92
Shape Rg shape_rg37.20
Total Rg total_rg37.68
Total atoms total_atoms19576
Residues n_residues1189
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 dmax127.0
Rg (real space) rg_real37.91
Rg uncertainty (real space) rg_real_error1.02
I(0) (real space) i0_real2.9090e+08
I(0) uncertainty (real space) i0_real_error4.8700e+06
Rg (reciprocal space) rg_reciprocal37.91
I(0) (reciprocal space) i0_reciprocal290900000.0000
Solution quality estimate total_estimate0.8853
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary45.4
Skewness Skewness skewness0.344
Kurtosis Kurtosis kurtosis-0.347
Angular range angular_range— – 0.2100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha41590000.0000
Real-space data points n_real_points43
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.866; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.907

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)