9ifx

Beta-hairpin macrocyclic peptide in complex with STAT1

Method: X-RAY DIFFRACTION Dmax: 132.0 Å Quality: REASONABLE

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

Signal transducer and activator of transcription 1-alpha/beta

Homo sapiens

UniProt P42224

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 132–684 Not recorded OPG024 protein × 1 (P17356) OXE ORTHO-XYLENE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;Crystallisation condition: 4% v/v TacsimateTM pH 5.0 12% w/v Polyethylene glycol 3,350 Protein:peptide complex: 5 mg /ml 20 mM Tris pH 8.0, 300 mM NaCl Resolution 3.64 Å R-free 0.271

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.

9 other PDB entries and 16 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name STAT1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–545; UniProt 132–684

OPG024 protein

OrganismNot specified

UniProt P17356

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 C; UniProt 11–31 Not recorded Signal transducer and activator of transcription 1-alpha/beta × 1 (P42224) OXE ORTHO-XYLENE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;Crystallisation condition: 4% v/v TacsimateTM pH 5.0 12% w/v Polyethylene glycol 3,350 Protein:peptide complex: 5 mg /ml 20 mM Tris pH 8.0, 300 mM NaCl Resolution 3.64 Å R-free 0.271

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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PG024_VACCW
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 1–21; UniProt 11–31

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 9ifx

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9ifx
Deposition date deposition_date2025-02-18
最后修订 last_revision2026-02-18
Structure title titleBeta-hairpin macrocyclic peptide in complex with STAT1
Keywords keywordsSTAT1, 018, poxvirus, TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier33.97
Radius of gyration Rg (electron density) rg_electron34.22
Forward intensity I(0) i059582900.00
Molecular weight molecular_weight63403.0 kDa
Excluded volume excluded_volume80276 ų
Envelope volume envelope_volume99553 ų
Hydration-shell volume shell_volume27445 ų
Envelope diameter envelope_diameter138.9
Shell Rg shell_rg35.58
Envelope Rg envelope_rg35.03
Shape Rg shape_rg34.19
Total Rg total_rg34.42
Total atoms total_atoms4465
Residues n_residues546
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 dmax132.0
Rg (real space) rg_real34.50
Rg uncertainty (real space) rg_real_error2.11
I(0) (real space) i0_real5.9580e+07
I(0) uncertainty (real space) i0_real_error1.1320e+06
Rg (reciprocal space) rg_reciprocal34.17
I(0) (reciprocal space) i0_reciprocal59570000.0000
Solution quality estimate total_estimate0.7134
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary25.3
Skewness Skewness skewness0.718
Kurtosis Kurtosis kurtosis0.075
Angular range angular_range— – 0.2350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha14490000.0000
Real-space data points n_real_points48
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.394; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.143; Smooth: 0.946

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)