2jgl

Crystal structure of mouse acetylcholinesterase inhibited by aged VX and sarin

Method: X-RAY DIFFRACTION Dmax: 133.3 Å Quality: GOOD

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

ACETYLCHOLINESTERASE

MUS MUSCULUS

UniProt P21836

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 32–574 Fragment:CATALYTIC DOMAIN, RESIDUES 32-574 Non-standard monomer:Yes (specific site not provided by mmCIF) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 PGE TRIETHYLENE GLYCOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;28% PEG 750MME, 0.1 M HEPES PH7.0, pH 7.00 Resolution 2.60 Å R-free 0.240
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 32–574 Fragment:CATALYTIC DOMAIN, RESIDUES 32-574 Non-standard monomer:Yes (specific site not provided by mmCIF) PGE TRIETHYLENE GLYCOL × 1 P4G 1-ETHOXY-2-(2-ETHOXYETHOXY)ETHANE × 1 P6G HEXAETHYLENE GLYCOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;28% PEG 750MME, 0.1 M HEPES PH7.0, pH 7.00 Resolution 2.60 Å R-free 0.240

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.

97 other PDB entries and 114 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ACES_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–543; UniProt 32–574 Author chain B; PDBConstruct 1–543; UniProt 32–574

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 2jgl

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2jgl
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2jgl
Deposition date deposition_date2007-02-13
Structure title titleCrystal structure of mouse acetylcholinesterase inhibited by aged VX and sarin
Keywords keywords;GLYCOPROTEIN, SERINE ESTERASE, ACETYLCHOLINESTERASE, ALTERNATIVE SPLICING, NEUROTRANSMITTER DEGRADATION, VX, SARIN, AGING, SYNAPSE, MEMBRANE, HYDROLASE ;; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier37.94
Radius of gyration Rg (electron density) rg_electron37.81
Forward intensity I(0) i0207811000.00
Molecular weight molecular_weight118880.0 kDa
Excluded volume excluded_volume149340 ų
Envelope volume envelope_volume181830 ų
Hydration-shell volume shell_volume41938 ų
Envelope diameter envelope_diameter142.1
Shell Rg shell_rg41.62
Envelope Rg envelope_rg37.71
Shape Rg shape_rg37.78
Total Rg total_rg38.14
Total atoms total_atoms8406
Residues n_residues1067
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 dmax133.3
Rg (real space) rg_real38.34
Rg uncertainty (real space) rg_real_error1.39
I(0) (real space) i0_real2.0780e+08
I(0) uncertainty (real space) i0_real_error3.6440e+06
Rg (reciprocal space) rg_reciprocal38.09
I(0) (reciprocal space) i0_reciprocal207800000.0000
Solution quality estimate total_estimate0.7965
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary34.9
Skewness Skewness skewness0.512
Kurtosis Kurtosis kurtosis-0.494
Angular range angular_range— – 0.2100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha57260000.0000
Real-space data points n_real_points43
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.555; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.777; Smooth: 0.910

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 5 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd2jgla_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.69 — alpha/beta-Hydrolases
Superfamily Superfamily superfamilyc.69.1 — alpha/beta-Hydrolases
Family Family familyc.69.1.1 — Acetylcholinesterase-like
Domain ID domain_idd2jglb1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.69 — alpha/beta-Hydrolases
Superfamily Superfamily superfamilyc.69.1 — alpha/beta-Hydrolases
Family Family familyc.69.1.1 — Acetylcholinesterase-like
Domain ID domain_idd2jglb2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (2 domains)

Domain ID domain_id2jglA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1820 — Alpha/Beta hydrolase fold, catalytic domain
Domain ID domain_id2jglB00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1820 — Alpha/Beta hydrolase fold, catalytic domain

8. Citations (1)

9. Files and Curves (10)