9s2x

Crystal structure of the human RAGE ectodomain in complex with murine S100A6 mutant Y84C

Method: X-RAY DIFFRACTION Dmax: 129.0 Å Quality: REASONABLE

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

Advanced glycosylation end product-specific receptor

Homo sapiens

UniProt Q15109

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 23–323 Fragment:V, C1 and C2 domains (VC1C2 module), full-length ectodomain, UNP residues 23-323 Protein S100-A6 × 2 (P14069) ZN ZINC ION × 12 CL CHLORIDE ION × 8 ACT ACETATE ION × 8 CA CALCIUM ION × 4 NA SODIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;277 K;0.2 M Zn acetate, 0.1 M Na cacodylate pH 6.5, 9% isopropanol Resolution 2.35 Å R-free 0.235

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.

31 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RAGE_HUMAN
Isoform Q15109-10
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–304; UniProt 23–323

Protein S100-A6

Mus musculus

UniProt P14069

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain B; UniProt 1–89 Mutation:Y84C Advanced glycosylation end product-specific receptor × 2 (Q15109) ZN ZINC ION × 12 CL CHLORIDE ION × 8 ACT ACETATE ION × 8 CA CALCIUM ION × 4 NA SODIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.5;277 K;0.2 M Zn acetate, 0.1 M Na cacodylate pH 6.5, 9% isopropanol Resolution 2.35 Å R-free 0.235

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.

1 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name S10A6_MOUSE
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 3–91; UniProt 1–89

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 9s2x

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9s2x
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9s2x
Deposition date deposition_date2025-07-23
最后修订 last_revision2026-05-13
Structure title titleCrystal structure of the human RAGE ectodomain in complex with murine S100A6 mutant Y84C
Keywords keywordssignaling complex, S100 alarmin, RAGE receptor, homodimerization, disulfide crosslinking, SIGNALING PROTEIN; SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier35.33
Radius of gyration Rg (electron density) rg_electron36.26
Forward intensity I(0) i031045100.00
Molecular weight molecular_weight43205.0 kDa
Excluded volume excluded_volume53852 ų
Envelope volume envelope_volume76778 ų
Hydration-shell volume shell_volume21233 ų
Envelope diameter envelope_diameter125.7
Shell Rg shell_rg34.88
Envelope Rg envelope_rg36.18
Shape Rg shape_rg36.29
Total Rg total_rg36.05
Total atoms total_atoms3006
Residues n_residues390
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 dmax129.0
Rg (real space) rg_real36.00
Rg uncertainty (real space) rg_real_error1.35
I(0) (real space) i0_real3.1050e+07
I(0) uncertainty (real space) i0_real_error5.5930e+05
Rg (reciprocal space) rg_reciprocal35.59
I(0) (reciprocal space) i0_reciprocal31030000.0000
Solution quality estimate total_estimate0.6618
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary22.9
Skewness Skewness skewness0.621
Kurtosis Kurtosis kurtosis-0.395
Angular range angular_range— – 0.2250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1417000.0000
Real-space data points n_real_points46
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.460; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.218; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

8. Citations (1)

9. Files and Curves (10)