7ac4

Structure of insulin collected by rotation serial crystallography on a COC membrane at a synchrotron source

Method: X-RAY DIFFRACTION Dmax: 38.1 Å Quality: GOOD

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

Insulin

Sus scrofa

UniProt P01315

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 88–108 Chain B; UniProt 25–54 Not recorded PGR R-1,2-PROPANEDIOL × 1 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;50mM Na2HPO4, 10mM EDTA pH 10.8 Resolution 1.46 Å R-free 0.180

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.

41 other PDB entries and 126 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name INS_PIG
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 1–21; UniProt 88–108 Author chain B; PDBConstruct 1–30; UniProt 25–54

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 7ac4

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7ac4
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7ac4
Deposition date deposition_date2020-09-09
Structure title titleStructure of insulin collected by rotation serial crystallography on a COC membrane at a synchrotron source
Keywords keywordshormone; HORMONE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier11.23
Radius of gyration Rg (electron density) rg_electron9.83
Forward intensity I(0) i0812446.00
Molecular weight molecular_weight5822.0 kDa
Excluded volume excluded_volume7233 ų
Envelope volume envelope_volume7676 ų
Hydration-shell volume shell_volume6943 ų
Envelope diameter envelope_diameter35.3
Shell Rg shell_rg15.05
Envelope Rg envelope_rg10.19
Shape Rg shape_rg9.85
Total Rg total_rg11.29
Total atoms total_atoms781
Residues n_residues51
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 dmax38.1
Rg (real space) rg_real11.18
Rg uncertainty (real space) rg_real_error0.24
I(0) (real space) i0_real8.1240e+05
I(0) uncertainty (real space) i0_real_error8.0210e+03
Rg (reciprocal space) rg_reciprocal11.18
I(0) (reciprocal space) i0_reciprocal812400.0000
Solution quality estimate total_estimate0.8694
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary14.4
Skewness Skewness skewness0.189
Kurtosis Kurtosis kurtosis-0.195
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha89700.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.782; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.997; Smooth: 0.956

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)