5c7g

Crystal Structure of the b1 Domain of Human Neuropilin-1 in complex with a bicine molecule

Method: X-RAY DIFFRACTION Dmax: 53.2 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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 273–427 Fragment:B1 DOMAIN, UNP residues 273-427 BCN BICINE × 1 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;25% PEG550 mme 5%, PEG 20 000, 60mM MgCl2, Na-Bicine 100 mM, pH 8.5 Resolution 1.45 Å R-free 0.172

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 7–161; UniProt 273–427

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 5c7g

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5c7g
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5c7g
Deposition date deposition_date2015-06-24
Structure title titleCrystal Structure of the b1 Domain of Human Neuropilin-1 in complex with a bicine molecule
Keywords keywordsNeuropilin-1, Human, Blood Coagulation Factors, Cell Adhesion, Binding sites, protein binding; PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.87
Radius of gyration Rg (electron density) rg_electron14.76
Forward intensity I(0) i05809040.00
Molecular weight molecular_weight17578.0 kDa
Excluded volume excluded_volume22065 ų
Envelope volume envelope_volume24182 ų
Hydration-shell volume shell_volume13744 ų
Envelope diameter envelope_diameter51.6
Shell Rg shell_rg20.78
Envelope Rg envelope_rg15.19
Shape Rg shape_rg14.72
Total Rg total_rg16.04
Total atoms total_atoms2444
Residues n_residues155
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 dmax53.2
Rg (real space) rg_real15.78
Rg uncertainty (real space) rg_real_error0.25
I(0) (real space) i0_real5.8090e+06
I(0) uncertainty (real space) i0_real_error6.5690e+04
Rg (reciprocal space) rg_reciprocal15.79
I(0) (reciprocal space) i0_reciprocal5809000.0000
Solution quality estimate total_estimate0.8725
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary51.8
Skewness Skewness skewness0.188
Kurtosis Kurtosis kurtosis-0.301
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1352000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.779; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 1.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd5c7ga_
Class classb — All beta proteins
Fold Fold foldb.18 — Galactose-binding domain-like
Superfamily Superfamily superfamilyb.18.1 — Galactose-binding domain-like
Family Family familyb.18.1.2 — Discoidin domain (FA58C, coagulation factor 5/8 C-terminal domain)

CATH v4.4 (1 domains)

Domain ID domain_id5c7gA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily260 — Galactose-binding domain-like

8. Citations (1)

9. Files and Curves (10)