9eou

Crystal Structure of the b1b2 domains from Human Neuropilin-1 in complex with a peptide.

Method: X-RAY DIFFRACTION Dmax: 80.5 Å Quality: GOOD

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

Neuropilin-1

Homo sapiens

UniProt O14786

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 273–586 Not recorded Osteopontin × 1 (P10451) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;295 K;0.1 M sodium malonate pH 6.0, 9% w/v PEG 3350 Resolution 1.55 Å R-free 0.202

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.

24 other PDB entries and 41 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NRP1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 5–318; UniProt 273–586

Osteopontin

OrganismNot specified

UniProt P10451

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain P; UniProt 153–168 Not recorded Neuropilin-1 × 1 (O14786) X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;295 K;0.1 M sodium malonate pH 6.0, 9% w/v PEG 3350 Resolution 1.55 Å R-free 0.202

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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name OSTP_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain P; PDBConstruct 1–15; UniProt 153–168

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 9eou

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9eou
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9eou
Deposition date deposition_date2024-03-15
Structure title titleCrystal Structure of the b1b2 domains from Human Neuropilin-1 in complex with a peptide.
Keywords keywordsangiogenesis, Neuropilin-1, STRUCTURAL PROTEIN; STRUCTURAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier23.35
Radius of gyration Rg (electron density) rg_electron22.48
Forward intensity I(0) i022168500.00
Molecular weight molecular_weight35658.0 kDa
Excluded volume excluded_volume44550 ų
Envelope volume envelope_volume52734 ų
Hydration-shell volume shell_volume20587 ų
Envelope diameter envelope_diameter82.0
Shell Rg shell_rg28.20
Envelope Rg envelope_rg22.67
Shape Rg shape_rg22.48
Total Rg total_rg23.23
Total atoms total_atoms2507
Residues n_residues313
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 dmax80.5
Rg (real space) rg_real23.46
Rg uncertainty (real space) rg_real_error0.52
I(0) (real space) i0_real2.2170e+07
I(0) uncertainty (real space) i0_real_error3.0290e+05
Rg (reciprocal space) rg_reciprocal23.43
I(0) (reciprocal space) i0_reciprocal22170000.0000
Solution quality estimate total_estimate0.8606
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.5
Skewness Skewness skewness0.460
Kurtosis Kurtosis kurtosis-0.321
Angular range angular_range— – 0.3400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3866000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.771; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.884; Smooth: 0.985

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)