2le4

Solution structure of the HMG box DNA-binding domain of human stem cell transcription factor Sox2

Method: SOLUTION NMR Dmax: 43.3 Å Quality: REASONABLE

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

Transcription factor SOX-2

Homo sapiens

UniProt P48431

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 39–118 Fragment:HMG box DNA binding residues 39-118 No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.7;298 K;Ionic strength (raw mmCIF value) 100 mM;Pressure AMBIENT NMR sample composition:0.7 mM [U-100% 13C; U-100% 15N] Sox2, 7 % DTT, 95% H2O, 5% D2O | 95% H2O/5% D2O 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.

12 other PDB entries and 13 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SOX2_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–81; UniProt 39–118

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 2le4

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2le4
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2le4
Deposition date deposition_date2011-06-06
Structure title titleSolution structure of the HMG box DNA-binding domain of human stem cell transcription factor Sox2
Keywords keywordsStructural Genomics, Protein Structure Initiative, PSI, Center for Eukaryotic Structural Genomics, TRANSCRIPTION, CESG; TRANSCRIPTION
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier16.17
Radius of gyration Rg (electron density) rg_electron16.28
Forward intensity I(0) i0602074000.00
Molecular weight molecular_weight198150.0 kDa
Excluded volume excluded_volume245930 ų
Envelope volume envelope_volume57176 ų
Hydration-shell volume shell_volume21733 ų
Envelope diameter envelope_diameter77.0
Shell Rg shell_rg29.08
Envelope Rg envelope_rg24.03
Shape Rg shape_rg16.25
Total Rg total_rg16.79
Total atoms total_atoms28300
Residues n_residues1620
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 dmax43.3
Rg (real space) rg_real14.98
Rg uncertainty (real space) rg_real_error0.08
I(0) (real space) i0_real5.7240e+08
I(0) uncertainty (real space) i0_real_error4.8270e+06
Rg (reciprocal space) rg_reciprocal16.41
I(0) (reciprocal space) i0_reciprocal602100000.0000
Solution quality estimate total_estimate0.6871
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary17.2
Skewness Skewness skewness0.333
Kurtosis Kurtosis kurtosis-0.355
Angular range angular_range— – 0.4900 −1
Current regularization parameter α current_alpha3.1120
Highest regularization parameter α highest_alpha206700.0000
Real-space data points n_real_points79
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.004; Oscil: 0.988; Stabil: 0.990; Sysdev: 0.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd2le4a1
Class classa — All alpha proteins
Fold Fold folda.21 — HMG-box
Superfamily Superfamily superfamilya.21.1 — HMG-box
Family Family familya.21.1.1 — HMG-box
Domain ID domain_idd2le4a2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (1 domains)

Domain ID domain_id2le4A00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology30 — DNA Binding (I), subunit A
Homologous superfamily homologous superfamily10 — High mobility group box domain

8. Citations (1)

9. Files and Curves (10)