7bn1

Clathrin heavy chain N-terminal domain complexed with peptide from Protein mu-NS of Reovirus type 1

Method: X-RAY DIFFRACTION Dmax: 108.0 Å Quality: GOOD

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

Clathrin heavy chain 1

Homo sapiens

UniProt Q00610

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 1–364 Not recorded Protein mu-NS from Reovirus type 1 × 1 PG4 TETRAETHYLENE GLYCOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;297 K;30% PEG 550 MME; PEG 20K, 0.12M Monosaccharides (D-Glucose; D-Mannose; D-Galactose; L-Fucose; D-Xylose; N-Acetyl-D-Glucosamine) and 0.1M Sodium HEPES; MOPS (acid) pH-7.5 Resolution 1.97 Å R-free 0.215
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 1–364 Not recorded Protein mu-NS from Reovirus type 1 × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;297 K;30% PEG 550 MME; PEG 20K, 0.12M Monosaccharides (D-Glucose; D-Mannose; D-Galactose; L-Fucose; D-Xylose; N-Acetyl-D-Glucosamine) and 0.1M Sodium HEPES; MOPS (acid) pH-7.5 Resolution 1.97 Å R-free 0.215

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 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CLH1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–364; UniProt 1–364 Author chain B; PDBConstruct 1–364; UniProt 1–364

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 7bn1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7bn1
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7bn1
Deposition date deposition_date2021-01-21
Structure title titleClathrin heavy chain N-terminal domain complexed with peptide from Protein mu-NS of Reovirus type 1
Keywords keywordsCLTC-NTD, Clathrin-Box motif, Viral Replication protein E1, HPV, TRANSPORT PROTEIN; TRANSPORT PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier31.46
Radius of gyration Rg (electron density) rg_electron30.92
Forward intensity I(0) i0105004000.00
Molecular weight molecular_weight82092.0 kDa
Excluded volume excluded_volume103210 ų
Envelope volume envelope_volume128620 ų
Hydration-shell volume shell_volume35786 ų
Envelope diameter envelope_diameter113.3
Shell Rg shell_rg36.67
Envelope Rg envelope_rg31.02
Shape Rg shape_rg30.90
Total Rg total_rg31.49
Total atoms total_atoms5767
Residues n_residues738
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 dmax108.0
Rg (real space) rg_real31.60
Rg uncertainty (real space) rg_real_error0.85
I(0) (real space) i0_real1.0500e+08
I(0) uncertainty (real space) i0_real_error1.6060e+06
Rg (reciprocal space) rg_reciprocal31.54
I(0) (reciprocal space) i0_reciprocal105000000.0000
Solution quality estimate total_estimate0.8608
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary32.4
Skewness Skewness skewness0.463
Kurtosis Kurtosis kurtosis-0.372
Angular range angular_range— – 0.2500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha20000000.0000
Real-space data points n_real_points51
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.756; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.950; Smooth: 0.969

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)