8sss

ZnFs 1-7 of CCCTC-binding factor (CTCF) Complexed with 23mer

Method: X-RAY DIFFRACTION Dmax: 102.6 Å Quality: GOOD

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

Transcriptional repressor CTCF

Homo sapiens

UniProt P49711

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–DNA Monomer Protein × 1 DNA 2 PDB declaration: trimeric(3) Consistent with all polymer counts Chain A; UniProt 263–465 Fragment:Zinc finger domains 1-7 DNA Strand (23mer) I × 1 DNA Strand (23mer) II × 1 ZN ZINC ION × 7 NA SODIUM ION × 1 EDO 1,2-ETHANEDIOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;292 K;26.5% PEG3350, 0.26M DL-Malic acid 7.0 Resolution 2.30 Å R-free 0.231
2 Protein–DNA Monomer Protein × 1 DNA 2 PDB declaration: trimeric(3) Consistent with all polymer counts Chain D; UniProt 263–465 Fragment:Zinc finger domains 1-7 DNA Strand (23mer) I × 1 DNA Strand (23mer) II × 1 ZN ZINC ION × 7 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;292 K;26.5% PEG3350, 0.26M DL-Malic acid 7.0 Resolution 2.30 Å R-free 0.231

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.

20 other PDB entries and 33 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CTCF_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–203; UniProt 263–465 Author chain D; PDBConstruct 1–203; UniProt 263–465

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 8sss

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8sss
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8sss
Deposition date deposition_date2023-05-08
Structure title titleZnFs 1-7 of CCCTC-binding factor (CTCF) Complexed with 23mer
Keywords keywords;PROTEIN-DNA COMPLEX, DNA BINDING PROTEIN, transcription factor, zinc fingers, insulator/chromatin architecture, transcription-dna complex, TRANSCRIPTION ;; TRANSCRIPTION/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier31.48
Radius of gyration Rg (electron density) rg_electron31.22
Forward intensity I(0) i0152889000.00
Molecular weight molecular_weight74340.0 kDa
Excluded volume excluded_volume82642 ų
Envelope volume envelope_volume121170 ų
Hydration-shell volume shell_volume33193 ų
Envelope diameter envelope_diameter102.3
Shell Rg shell_rg37.30
Envelope Rg envelope_rg30.67
Shape Rg shape_rg31.21
Total Rg total_rg31.67
Total atoms total_atoms5036
Residues n_residues487
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 dmax102.6
Rg (real space) rg_real31.41
Rg uncertainty (real space) rg_real_error0.77
I(0) (real space) i0_real1.5290e+08
I(0) uncertainty (real space) i0_real_error2.4350e+06
Rg (reciprocal space) rg_reciprocal31.44
I(0) (reciprocal space) i0_reciprocal152900000.0000
Solution quality estimate total_estimate0.8996
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary43.1
Skewness Skewness skewness0.168
Kurtosis Kurtosis kurtosis-0.530
Angular range angular_range— – 0.2500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7326000.0000
Real-space data points n_real_points51
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.914; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.954

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)