8cf4

SH3 domain solved by the exact solid-state method from the Bruker Dynamics Center using the combined correction method with PDB 2NUZ

Method: SOLID-STATE NMR Dmax: 46.0 Å Quality: GOOD

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

Spectrin alpha chain, non-erythrocytic 1

Gallus gallus

UniProt P07751

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 965–1025 Not recorded No other associated polymer SOLID-STATE NMR NMR measurement conditions:pH 7;298 K;Ionic strength (raw mmCIF value) 0;Pressure 1 NMR sample composition:1 na [U-100% 13C; U-100% 15N] SH3 of chicken alpha-spectrin, 100% H2O | 100% H2O Resolution not provided

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.

60 other PDB entries and 65 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SPTN1_CHICK
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–62; UniProt 965–1025

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 8cf4

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8cf4
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8cf4
Deposition date deposition_date2023-02-02
Structure title titleSH3 domain solved by the exact solid-state method from the Bruker Dynamics Center using the combined correction method with PDB 2NUZ
Keywords keywordssolid-state NMR spectroscopy, structure elucidation, integrated structural biology, protein dynamics, PEPTIDE BINDING PROTEIN; PEPTIDE BINDING PROTEIN
Experimental Method methodSOLID-STATE NMR

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

Radius of gyration Rg (Guinier) rg_guinier11.92
Radius of gyration Rg (electron density) rg_electron11.49
Forward intensity I(0) i071773000.00
Molecular weight molecular_weight72183.0 kDa
Excluded volume excluded_volume91185 ų
Envelope volume envelope_volume17800 ų
Hydration-shell volume shell_volume11180 ų
Envelope diameter envelope_diameter49.6
Shell Rg shell_rg19.55
Envelope Rg envelope_rg14.67
Shape Rg shape_rg11.41
Total Rg total_rg12.15
Total atoms total_atoms10200
Residues n_residues620
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 dmax46.0
Rg (real space) rg_real11.94
Rg uncertainty (real space) rg_real_error0.40
I(0) (real space) i0_real7.1770e+07
I(0) uncertainty (real space) i0_real_error8.1040e+05
Rg (reciprocal space) rg_reciprocal11.94
I(0) (reciprocal space) i0_reciprocal71770000.0000
Solution quality estimate total_estimate0.7668
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary15.2
Skewness Skewness skewness0.463
Kurtosis Kurtosis kurtosis0.319
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha143100.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.364; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.883; Smooth: 0.990

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

8. Citations (1)

9. Files and Curves (10)