8t5f

De novo design of high-affinity protein binders to bioactive helical peptides

Method: X-RAY DIFFRACTION Dmax: 70.5 Å Quality: GOOD

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

Parathyroid hormone

OrganismNot specified

UniProt P01270

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 32–65 Chain B; UniProt 32–65 Chain C; UniProt 32–65 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.5;293 K;0.2 M Sodium chloride, 0.1 M Sodium acetate pH 4.5, and 1.26 M Ammonium sulfate Resolution 1.99 Å R-free 0.251

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.

25 other PDB entries and 26 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PTHY_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–34; UniProt 32–65 Author chain B; PDBConstruct 1–34; UniProt 32–65 Author chain C; PDBConstruct 1–34; UniProt 32–65

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 8t5f

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8t5f
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8t5f
Deposition date deposition_date2023-06-13
Structure title titleDe novo design of high-affinity protein binders to bioactive helical peptides
Keywords keywordsAlpha-helical peptides, protein design, diffusion, deep learning, DE NOVO PROTEIN; DE NOVO PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.50
Radius of gyration Rg (electron density) rg_electron18.08
Forward intensity I(0) i03185550.00
Molecular weight molecular_weight12158.0 kDa
Excluded volume excluded_volume15124 ų
Envelope volume envelope_volume20270 ų
Hydration-shell volume shell_volume10819 ų
Envelope diameter envelope_diameter69.4
Shell Rg shell_rg21.63
Envelope Rg envelope_rg18.60
Shape Rg shape_rg18.18
Total Rg total_rg18.52
Total atoms total_atoms853
Residues n_residues101
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 dmax70.5
Rg (real space) rg_real18.62
Rg uncertainty (real space) rg_real_error0.79
I(0) (real space) i0_real3.1860e+06
I(0) uncertainty (real space) i0_real_error4.1830e+04
Rg (reciprocal space) rg_reciprocal18.60
I(0) (reciprocal space) i0_reciprocal3186000.0000
Solution quality estimate total_estimate0.8139
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary18.3
Skewness Skewness skewness0.445
Kurtosis Kurtosis kurtosis-0.214
Angular range angular_range— – 0.4300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha258100.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.662; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.594; Smooth: 0.997

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)