6rrc

Crystal structure of the N-terminal region of human cohesin subunit STAG1 in complex with RAD21 peptide

Method: X-RAY DIFFRACTION Dmax: 108.7 Å Quality: GOOD

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

Cohesin subunit SA-1

Homo sapiens

UniProt Q8WVM7

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 86–420 Not recorded Double-strand-break repair protein rad21 homolog × 1 (O60216) SO4 SULFATE ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.3;277 K;2.1 M Ammonium Sulfate, 0.1 M MES pH 6.3 Resolution 2.37 Å R-free 0.248
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 86–420 Not recorded Double-strand-break repair protein rad21 homolog × 1 (O60216) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.3;277 K;2.1 M Ammonium Sulfate, 0.1 M MES pH 6.3 Resolution 2.37 Å R-free 0.248

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.

19 other PDB entries and 48 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name STAG1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 5–339; UniProt 86–420 Author chain C; PDBConstruct 5–339; UniProt 86–420

Double-strand-break repair protein rad21 homolog

OrganismNot specified

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 321–345 Not recorded Cohesin subunit SA-1 × 1 (Q8WVM7) SO4 SULFATE ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.3;277 K;2.1 M Ammonium Sulfate, 0.1 M MES pH 6.3 Resolution 2.37 Å R-free 0.248
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 321–345 Not recorded Cohesin subunit SA-1 × 1 (Q8WVM7) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6.3;277 K;2.1 M Ammonium Sulfate, 0.1 M MES pH 6.3 Resolution 2.37 Å R-free 0.248

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 40 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 1–25; UniProt 321–345 Author chain D; PDBConstruct 1–25; UniProt 321–345

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 6rrc

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6rrc
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6rrc
Deposition date deposition_date2019-05-17
Structure title titleCrystal structure of the N-terminal region of human cohesin subunit STAG1 in complex with RAD21 peptide
Keywords keywordsCohesin, SA-1, chromosome segregation, GENE REGULATION; GENE REGULATION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.77
Radius of gyration Rg (electron density) rg_electron32.15
Forward intensity I(0) i0103231000.00
Molecular weight molecular_weight79874.0 kDa
Excluded volume excluded_volume99693 ų
Envelope volume envelope_volume133560 ų
Hydration-shell volume shell_volume35752 ų
Envelope diameter envelope_diameter110.1
Shell Rg shell_rg37.81
Envelope Rg envelope_rg31.90
Shape Rg shape_rg32.15
Total Rg total_rg32.62
Total atoms total_atoms5594
Residues n_residues690
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 dmax108.7
Rg (real space) rg_real32.84
Rg uncertainty (real space) rg_real_error0.87
I(0) (real space) i0_real1.0320e+08
I(0) uncertainty (real space) i0_real_error1.5970e+06
Rg (reciprocal space) rg_reciprocal32.82
I(0) (reciprocal space) i0_reciprocal103200000.0000
Solution quality estimate total_estimate0.8911
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary36.2
Skewness Skewness skewness0.346
Kurtosis Kurtosis kurtosis-0.463
Angular range angular_range— – 0.2400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha12210000.0000
Real-space data points n_real_points49
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.907; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.955; Smooth: 0.903

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)