9un2

native NMDAR receptor-GluN1/N2B in the inactive state

Method: ELECTRON MICROSCOPY Dmax: 179.1 Å Quality: GOOD

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

Glutamate receptor ionotropic, NMDA 1

OrganismNot specified

UniProt P35438

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 26–844 Chain C; UniProt 26–844 Not recorded Glutamate receptor ionotropic, NMDA 2B × 2 (Q01097) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 17 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 4.30 Å

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.

14 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NMDZ1_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–819; UniProt 26–844 Author chain C; PDBConstruct 1–819; UniProt 26–844

Glutamate receptor ionotropic, NMDA 2B

OrganismNot specified

UniProt Q01097

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain B; UniProt 34–842 Chain D; UniProt 34–842 Not recorded Glutamate receptor ionotropic, NMDA 1 × 2 (P35438) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 17 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 4.30 Å

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.

7 other PDB entries and 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NMDE2_MOUSE
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–809; UniProt 34–842 Author chain D; PDBConstruct 1–809; UniProt 34–842

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 9un2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9un2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9un2
Deposition date deposition_date2025-04-23
Structure title titlenative NMDAR receptor-GluN1/N2B in the inactive state
Keywords keywordsnative, NMDA receptor, ionotropic ion channel, excitatory neurotransmitter, MEMBRANE PROTEIN; MEMBRANE PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier53.92
Radius of gyration Rg (electron density) rg_electron53.97
Forward intensity I(0) i01339500000.00
Molecular weight molecular_weight310000.0 kDa
Excluded volume excluded_volume389510 ų
Envelope volume envelope_volume602770 ų
Hydration-shell volume shell_volume96609 ų
Envelope diameter envelope_diameter180.4
Shell Rg shell_rg54.38
Envelope Rg envelope_rg52.01
Shape Rg shape_rg53.97
Total Rg total_rg54.01
Total atoms total_atoms21861
Residues n_residues3156
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 dmax179.1
Rg (real space) rg_real53.88
Rg uncertainty (real space) rg_real_error1.48
I(0) (real space) i0_real1.3400e+09
I(0) uncertainty (real space) i0_real_error2.3980e+07
Rg (reciprocal space) rg_reciprocal53.95
I(0) (reciprocal space) i0_reciprocal1340000000.0000
Solution quality estimate total_estimate0.8703
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary61.8
Skewness Skewness skewness0.280
Kurtosis Kurtosis kurtosis-0.400
Angular range angular_range— – 0.1450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha103800000.0000
Real-space data points n_real_points30
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.900; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.993; Smooth: 0.616

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)