2hrj

NMR solution structure of the F2 subdomain of talin

Method: SOLUTION NMR Dmax: 40.1 Å Quality: REASONABLE

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

Talin-1

Gallus gallus

UniProt P54939

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 189–309 Fragment:F2 subdomain No other associated polymer SOLUTION NMR NMR measurement conditions:pH 6.5;298 K;Pressure ambient NMR measurement conditions:pH 6.5;310 K;Pressure ambient 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.

10 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TLN1_CHICK
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–121; UniProt 189–309

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 2hrj

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2hrj
Deposition date deposition_date2006-07-20
Structure title titleNMR solution structure of the F2 subdomain of talin
Keywords keywordsACBP-like, talin, STRUCTURAL PROTEIN; STRUCTURAL PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier15.90
Radius of gyration Rg (electron density) rg_electron16.12
Forward intensity I(0) i01710020000.00
Molecular weight molecular_weight353630.0 kDa
Excluded volume excluded_volume443980 ų
Envelope volume envelope_volume78696 ų
Hydration-shell volume shell_volume26978 ų
Envelope diameter envelope_diameter93.7
Shell Rg shell_rg31.65
Envelope Rg envelope_rg26.45
Shape Rg shape_rg16.08
Total Rg total_rg16.59
Total atoms total_atoms49775
Residues n_residues3025
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 dmax40.1
Rg (real space) rg_real14.65
Rg uncertainty (real space) rg_real_error0.05
I(0) (real space) i0_real1.6130e+09
I(0) uncertainty (real space) i0_real_error1.3770e+07
Rg (reciprocal space) rg_reciprocal16.07
I(0) (reciprocal space) i0_reciprocal1710000000.0000
Solution quality estimate total_estimate0.6876
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary16.8
Skewness Skewness skewness0.193
Kurtosis Kurtosis kurtosis-0.451
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha3.1450
Highest regularization parameter α highest_alpha604300.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.033; Oscil: 0.994; Stabil: 0.988; Sysdev: 0.000; Positv: 1.000; Valcen: 0.994; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2hrja_
Class classa — All alpha proteins
Fold Fold folda.11 — Acyl-CoA binding protein-like
Superfamily Superfamily superfamilya.11.2 — Second domain of FERM
Family Family familya.11.2.1 — Second domain of FERM

CATH v4.4 (1 domains)

Domain ID domain_id2hrjA01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology80 — Acyl-CoA Binding Protein
Homologous superfamily homologous superfamily10

8. Citations (1)

9. Files and Curves (10)