6gv0

Insulin glulisine

Method: X-RAY DIFFRACTION Dmax: 48.1 Å Quality: GOOD

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

Insulin

Homo sapiens

UniProt P01308

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 × 12 PDB declaration: dodecameric(12) Consistent with protein copy count Chain B; UniProt 25–54 Chain D; UniProt 25–54 Chain G; UniProt 90–110 Chain I; UniProt 90–110 Not recorded ZN ZINC ION × 6 FMT FORMIC ACID × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;293 K;0.2-0.4M Mg-formate 0.1M BisTris buffer Resolution 1.26 Å R-free 0.152

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.

369 other PDB entries and 583 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name INS_HUMAN
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain G; PDBConstruct 1–21; UniProt 90–110 Author chain I; PDBConstruct 1–21; UniProt 90–110 Author chain B; PDBConstruct 1–30; UniProt 25–54 Author chain D; 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 6gv0

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6gv0
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6gv0
Deposition date deposition_date2018-06-20
Structure title titleInsulin glulisine
Keywords keywordsInsulin glulisine insulin analogue, HORMONE; HORMONE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier14.69
Radius of gyration Rg (electron density) rg_electron13.73
Forward intensity I(0) i02918680.00
Molecular weight molecular_weight11582.0 kDa
Excluded volume excluded_volume14241 ų
Envelope volume envelope_volume16167 ų
Hydration-shell volume shell_volume10504 ų
Envelope diameter envelope_diameter45.5
Shell Rg shell_rg18.77
Envelope Rg envelope_rg13.97
Shape Rg shape_rg13.69
Total Rg total_rg14.87
Total atoms total_atoms1539
Residues n_residues100
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 dmax48.1
Rg (real space) rg_real14.65
Rg uncertainty (real space) rg_real_error0.30
I(0) (real space) i0_real2.9190e+06
I(0) uncertainty (real space) i0_real_error2.9640e+04
Rg (reciprocal space) rg_reciprocal14.65
I(0) (reciprocal space) i0_reciprocal2919000.0000
Solution quality estimate total_estimate0.8746
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary46.9
Skewness Skewness skewness0.275
Kurtosis Kurtosis kurtosis-0.281
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha352300.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.804; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.957

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)