3okt

Mouse Plexin A2, extracellular domains 1-4

Method: X-RAY DIFFRACTION Dmax: 125.3 Å Quality: REASONABLE

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

Plexin-A2

Mus musculus

UniProt P70207

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 35–703 Fragment:residues 33-703, extracellular domains 1-4 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 5 CL CHLORIDE ION × 2 NA SODIUM ION × 1 GOL GLYCEROL × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;Polyethylene Glycol 6000 12.8% w/v, Magnesium Chloride 128mM, HEPES 64mM pH 7.0, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 2.30 Å R-free 0.251
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 35–703 Fragment:residues 33-703, extracellular domains 1-4 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 10 CL CHLORIDE ION × 4 NA SODIUM ION × 2 GOL GLYCEROL × 8 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;Polyethylene Glycol 6000 12.8% w/v, Magnesium Chloride 128mM, HEPES 64mM pH 7.0, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 2.30 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.

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

View Construct and Data Evidence
UniProt name PLXA2_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–672; UniProt 35–703

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 3okt

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3okt
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3okt
Deposition date deposition_date2010-08-25
Structure title titleMouse Plexin A2, extracellular domains 1-4
Keywords keywordsTransmembrane, receptor, sema-domain, Cell-cell signalling, Semaphorin-6A, SIGNALING PROTEIN; SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier34.79
Radius of gyration Rg (electron density) rg_electron34.84
Forward intensity I(0) i089773700.00
Molecular weight molecular_weight74589.0 kDa
Excluded volume excluded_volume93035 ų
Envelope volume envelope_volume123140 ų
Hydration-shell volume shell_volume32891 ų
Envelope diameter envelope_diameter129.5
Shell Rg shell_rg36.74
Envelope Rg envelope_rg35.85
Shape Rg shape_rg34.81
Total Rg total_rg35.10
Total atoms total_atoms5235
Residues n_residues656
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 dmax125.3
Rg (real space) rg_real35.35
Rg uncertainty (real space) rg_real_error1.63
I(0) (real space) i0_real8.9770e+07
I(0) uncertainty (real space) i0_real_error1.7810e+06
Rg (reciprocal space) rg_reciprocal35.00
I(0) (reciprocal space) i0_reciprocal89740000.0000
Solution quality estimate total_estimate0.7405
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary33.4
Skewness Skewness skewness0.711
Kurtosis Kurtosis kurtosis-0.195
Angular range angular_range— – 0.2250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7456000.0000
Real-space data points n_real_points46
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.441; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.519; Smooth: 0.781

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id3oktA01
Class class2 — Mainly Beta
Architecture architecture130 — 7 Propeller
Topology topology10 — Methylamine Dehydrogenase; Chain H
Homologous superfamily homologous superfamily10 — YVTN repeat-like/Quinoprotein amine dehydrogenase

8. Citations (1)

9. Files and Curves (10)