5n62

Human TTR crystals soaked in manganese chloride.

Method: X-RAY DIFFRACTION Dmax: 61.2 Å Quality: REASONABLE

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

Transthyretin

OrganismNot specified

UniProt P02766

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 homooligomer Homooligomer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 30–146 Chain B; UniProt 30–146 Not recorded MN MANGANESE (II) ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 6;293 K;protein: 10 mg/ml Dialysed in 100 milli-M NaCl, 50 milli-M sodium acetate, pH 5.5 precipitant: 26% polyethylene glycol 4,000 (PEG4K), 0.16 M imidazole malate, pH 6.0 cryosoak: 40 % CM7 (12.5 % di-ethylene glycol + 12.5 % ethylene glycol + 12.5 % glycerol + 25 % 1,2-propanediol + 12.5 % DMSO), 25 % MPEG 5K, 5 mM MnCl2, 10 min soak. Resolution 1.80 Å R-free 0.244

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.

460 other PDB entries and 501 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TTHY_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–117; UniProt 30–146 Author chain B; PDBConstruct 1–117; UniProt 30–146

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 5n62

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5n62
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5n62
Deposition date deposition_date2017-02-14
Structure title titleHuman TTR crystals soaked in manganese chloride.
Keywords keywordsManganese complex, metal binding, Alzheimer beta-amyloid scavenging, 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_guinier18.98
Radius of gyration Rg (electron density) rg_electron17.58
Forward intensity I(0) i011430700.00
Molecular weight molecular_weight25416.0 kDa
Excluded volume excluded_volume31852 ų
Envelope volume envelope_volume36654 ų
Hydration-shell volume shell_volume17501 ų
Envelope diameter envelope_diameter62.3
Shell Rg shell_rg23.62
Envelope Rg envelope_rg17.79
Shape Rg shape_rg17.52
Total Rg total_rg18.69
Total atoms total_atoms1792
Residues n_residues232
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 dmax61.2
Rg (real space) rg_real18.87
Rg uncertainty (real space) rg_real_error0.31
I(0) (real space) i0_real1.1430e+07
I(0) uncertainty (real space) i0_real_error1.3690e+05
Rg (reciprocal space) rg_reciprocal18.88
I(0) (reciprocal space) i0_reciprocal11430000.0000
Solution quality estimate total_estimate0.7396
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary22.1
Skewness Skewness skewness0.154
Kurtosis Kurtosis kurtosis-0.408
Angular range angular_range— – 0.4200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2649000.0000
Real-space data points n_real_points73
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.850; Stabil: 1.000; Sysdev: 0.374; Positv: 1.000; Valcen: 0.998; Smooth: 0.942

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd5n62a_
Class classb — All beta proteins
Fold Fold foldb.3 — Prealbumin-like
Superfamily Superfamily superfamilyb.3.4 — Transthyretin (synonym: prealbumin)
Family Family familyb.3.4.1 — Transthyretin (synonym: prealbumin)
Domain ID domain_idd5n62b_
Class classb — All beta proteins
Fold Fold foldb.3 — Prealbumin-like
Superfamily Superfamily superfamilyb.3.4 — Transthyretin (synonym: prealbumin)
Family Family familyb.3.4.1 — Transthyretin (synonym: prealbumin)

8. Citations (1)

9. Files and Curves (10)