9c3g

human cGAS core domain (K427E/K428E) bound to Cladophorol A

Method: X-RAY DIFFRACTION Dmax: 67.7 Å Quality: EXCELLENT

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

Cyclic GMP-AMP synthase

Homo sapiens

UniProt Q8N884

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 152–522 Fragment:residues 152-522 Mutation:K427E, K428E A1AVI cladophorol A × 1 ZN ZINC ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.2;295.15 K;100 mM MES/Sodium Hydroxide pH 7.2, 1% PEG 20000 Resolution 2.75 Å R-free 0.258

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.

106 other PDB entries and 132 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CGAS_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–373; UniProt 152–522

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 9c3g

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9c3g
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9c3g
Deposition date deposition_date2024-05-31
最后修订 last_revision2025-03-05
Structure title titlehuman cGAS core domain (K427E/K428E) bound to Cladophorol A
Keywords keywordscGAS, cGAMP, cyclic GMP-AMP synthase, DNA BINDING PROTEIN, TRANSFERASE-INHIBITOR complex; DNA BINDING PROTEIN,TRANSFERASE/INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.83
Radius of gyration Rg (electron density) rg_electron20.77
Forward intensity I(0) i053404900.00
Molecular weight molecular_weight38160.0 kDa
Excluded volume excluded_volume36981 ų
Envelope volume envelope_volume62052 ų
Hydration-shell volume shell_volume24457 ų
Envelope diameter envelope_diameter68.5
Shell Rg shell_rg27.66
Envelope Rg envelope_rg20.82
Shape Rg shape_rg20.71
Total Rg total_rg21.52
Total atoms total_atoms2896
Residues n_residues350
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 dmax67.7
Rg (real space) rg_real21.67
Rg uncertainty (real space) rg_real_error0.29
I(0) (real space) i0_real5.3400e+07
I(0) uncertainty (real space) i0_real_error6.3490e+05
Rg (reciprocal space) rg_reciprocal21.70
I(0) (reciprocal space) i0_reciprocal53410000.0000
Solution quality estimate total_estimate0.9047
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.3
Skewness Skewness skewness0.128
Kurtosis Kurtosis kurtosis-0.505
Angular range angular_range— – 0.3650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10150000.0000
Real-space data points n_real_points68
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.921; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.999

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (3)

9. Files and Curves (10)