9mzl

CryoEM structure of GluK2 bound to glutamate in the transition state

Method: ELECTRON MICROSCOPY Dmax: 180.6 Å Quality: GOOD

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

Glutamate receptor ionotropic, kainate 2

Rattus norvegicus

UniProt P42260

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Homooligomer Protein × 4 其他Polymer 1 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1–908 Chain B; UniProt 1–908 Chain C; UniProt 1–908 Chain D; UniProt 1–908 Not recorded beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 9 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 4.02 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.

91 other PDB entries and 106 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name GRIK2_RAT
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–908; UniProt 1–908 Author chain B; PDBConstruct 1–908; UniProt 1–908 Author chain C; PDBConstruct 1–908; UniProt 1–908 Author chain D; PDBConstruct 1–908; UniProt 1–908

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 9mzl

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9mzl
Deposition date deposition_date2025-01-23
Structure title titleCryoEM structure of GluK2 bound to glutamate in the transition state
Keywords keywordsglutamate, cryoEM, STRUCTURAL PROTEIN; STRUCTURAL PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier55.41
Radius of gyration Rg (electron density) rg_electron55.70
Forward intensity I(0) i01503060000.00
Molecular weight molecular_weight335260.0 kDa
Excluded volume excluded_volume423690 ų
Envelope volume envelope_volume622780 ų
Hydration-shell volume shell_volume93428 ų
Envelope diameter envelope_diameter180.6
Shell Rg shell_rg58.98
Envelope Rg envelope_rg54.16
Shape Rg shape_rg55.72
Total Rg total_rg55.73
Total atoms total_atoms23592
Residues n_residues2963
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 dmax180.6
Rg (real space) rg_real55.33
Rg uncertainty (real space) rg_real_error2.00
I(0) (real space) i0_real1.5030e+09
I(0) uncertainty (real space) i0_real_error3.2250e+07
Rg (reciprocal space) rg_reciprocal55.46
I(0) (reciprocal space) i0_reciprocal1503000000.0000
Solution quality estimate total_estimate0.8710
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary71.0
Skewness Skewness skewness0.210
Kurtosis Kurtosis kurtosis-0.462
Angular range angular_range— – 0.1400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha90240000.0000
Real-space data points n_real_points29
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.925; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.545

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)