9c9i

Structure of the TSC1:WIPI3 complex

Method: X-RAY DIFFRACTION Dmax: 113.3 Å Quality: EXCELLENT

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

WD repeat domain phosphoinositide-interacting protein 3

Homo sapiens

UniProt Q5MNZ6

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 12–344 Not recorded Hamartin × 1 (Q92574) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 12–344 Not recorded Hamartin × 1 (Q92574) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255
3 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain E; UniProt 12–344 Not recorded Hamartin × 2 (Q92574) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255
4 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain G; UniProt 12–344 Not recorded Hamartin × 1 (Q92574) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255

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.

4 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name WIPI3_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 8–316; UniProt 12–344 Author chain C; PDBConstruct 8–316; UniProt 12–344 Author chain E; PDBConstruct 8–316; UniProt 12–344 Author chain G; PDBConstruct 8–316; UniProt 12–344

Hamartin

Homo sapiens

UniProt Q92574

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 648–681 Not recorded WD repeat domain phosphoinositide-interacting protein 3 × 1 (Q5MNZ6) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 648–681 Not recorded WD repeat domain phosphoinositide-interacting protein 3 × 1 (Q5MNZ6) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255
3 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain F; UniProt 648–681 Chain X; UniProt 648–681 Not recorded WD repeat domain phosphoinositide-interacting protein 3 × 1 (Q5MNZ6) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255
4 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain H; UniProt 648–681 Not recorded WD repeat domain phosphoinositide-interacting protein 3 × 1 (Q5MNZ6) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2 M ammonium tartrate, 20 % PEG3350, and 0.25 M sodium acetate. Resolution 3.18 Å R-free 0.255

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.

4 other PDB entries and 6 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TSC1_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–34; UniProt 648–681 Author chain D; PDBConstruct 1–34; UniProt 648–681 Author chain F; PDBConstruct 1–34; UniProt 648–681 Author chain H; PDBConstruct 1–34; UniProt 648–681 Author chain X; PDBConstruct 1–34; UniProt 648–681

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 9c9i

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9c9i
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id9c9i
Deposition date deposition_date2024-06-14
最后修订 last_revision2024-12-04
Structure title titleStructure of the TSC1:WIPI3 complex
Keywords keywordsTSC, Tuberous sclerosis complex, TSC1, TSC2, TBC1D7, WIPI3, end-some, MTOR, cell growth, GENE REGULATION; GENE REGULATION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier35.98
Radius of gyration Rg (electron density) rg_electron35.65
Forward intensity I(0) i0311734000.00
Molecular weight molecular_weight143900.0 kDa
Excluded volume excluded_volume180490 ų
Envelope volume envelope_volume231070 ų
Hydration-shell volume shell_volume53662 ų
Envelope diameter envelope_diameter121.9
Shell Rg shell_rg42.26
Envelope Rg envelope_rg35.41
Shape Rg shape_rg35.65
Total Rg total_rg36.11
Total atoms total_atoms10118
Residues n_residues1304
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 dmax113.3
Rg (real space) rg_real35.83
Rg uncertainty (real space) rg_real_error0.79
I(0) (real space) i0_real3.1170e+08
I(0) uncertainty (real space) i0_real_error5.1210e+06
Rg (reciprocal space) rg_reciprocal35.93
I(0) (reciprocal space) i0_reciprocal311800000.0000
Solution quality estimate total_estimate0.9040
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary48.9
Skewness Skewness skewness0.155
Kurtosis Kurtosis kurtosis-0.553
Angular range angular_range— – 0.2200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha127000000.0000
Real-space data points n_real_points45
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.937; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.938

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)