8roi

Human cohesin SMC3-HD(EQ)/RAD21-N complex - ADP-bound conformation

Method: X-RAY DIFFRACTION Dmax: 107.9 Å Quality: GOOD

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

Structural maintenance of chromosomes protein 3

Homo sapiens

UniProt Q9UQE7

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 1–211 Chain A; UniProt 979–1217 Mutation:E1144Q Double-strand-break repair protein rad21 homolog × 1 (O60216) ADP ADENOSINE-5'-DIPHOSPHATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Na/K phosphate pH 7.5; 0.1 M HEPES pH 7.5; 15% v/v PEG Smear High; 10% v/v ethylene glycol Resolution 2.45 Å R-free 0.239

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.

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

View Construct and Data Evidence
UniProt name SMC3_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–211; UniProt 1–211 Author chain A; PDBConstruct 224–462; UniProt 979–1217

Double-strand-break repair protein rad21 homolog

Homo sapiens

UniProt O60216

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 B; UniProt 1–102 Not recorded Structural maintenance of chromosomes protein 3 × 1 (Q9UQE7) ADP ADENOSINE-5'-DIPHOSPHATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Na/K phosphate pH 7.5; 0.1 M HEPES pH 7.5; 15% v/v PEG Smear High; 10% v/v ethylene glycol Resolution 2.45 Å R-free 0.239

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.

35 other PDB entries and 41 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RAD21_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–102; UniProt 1–102

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 8roi

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8roi
Deposition date deposition_date2024-01-11
Structure title titleHuman cohesin SMC3-HD(EQ)/RAD21-N complex - ADP-bound conformation
Keywords keywords3D genome organization, Chromatin, Cohesin, ATPase activity, ATPase cycle, NUCLEAR PROTEIN; NUCLEAR PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier29.33
Radius of gyration Rg (electron density) rg_electron28.99
Forward intensity I(0) i049314400.00
Molecular weight molecular_weight56010.0 kDa
Excluded volume excluded_volume70781 ų
Envelope volume envelope_volume88910 ų
Hydration-shell volume shell_volume27652 ų
Envelope diameter envelope_diameter111.5
Shell Rg shell_rg33.29
Envelope Rg envelope_rg29.64
Shape Rg shape_rg28.99
Total Rg total_rg29.45
Total atoms total_atoms3938
Residues n_residues484
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 dmax107.9
Rg (real space) rg_real29.68
Rg uncertainty (real space) rg_real_error1.02
I(0) (real space) i0_real4.9310e+07
I(0) uncertainty (real space) i0_real_error7.3760e+05
Rg (reciprocal space) rg_reciprocal29.53
I(0) (reciprocal space) i0_reciprocal49310000.0000
Solution quality estimate total_estimate0.8010
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.0
Skewness Skewness skewness0.701
Kurtosis Kurtosis kurtosis0.154
Angular range angular_range— – 0.2700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha11070000.0000
Real-space data points n_real_points55
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.595; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.698; Smooth: 0.926

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)