2y54

Fragment growing induces conformational changes in acetylcholine- binding protein: A structural and thermodynamic analysis - (Fragment 1)

Method: X-RAY DIFFRACTION Dmax: 88.1 Å Quality: EXCELLENT

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

SOLUBLE ACETYLCHOLINE RECEPTOR

APLYSIA CALIFORNICA

UniProt Q8WSF8

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 homooligomer Homooligomer Protein × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain A; UniProt 20–236 Chain B; UniProt 20–236 Chain C; UniProt 20–236 Chain D; UniProt 20–236 Chain E; UniProt 20–236 Fragment:RESIDUES 20-236 V63 [(1R,5S)-8-AZABICYCLO[3.2.1]OCTAN-3-YL] BENZOATE × 5 SO4 SULFATE ION × 2 CL CHLORIDE ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7.5;0.1M MMT PH7.5, 0.9M AMMONIUM SULPHATE Resolution 3.65 Å R-free 0.217

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.

85 other PDB entries and 120 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q8WSF8_APLCA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–217; UniProt 20–236 Author chain B; PDBConstruct 1–217; UniProt 20–236 Author chain C; PDBConstruct 1–217; UniProt 20–236 Author chain D; PDBConstruct 1–217; UniProt 20–236 Author chain E; PDBConstruct 1–217; UniProt 20–236

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 2y54

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2y54
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2y54
Deposition date deposition_date2011-01-12
Structure title titleFragment growing induces conformational changes in acetylcholine- binding protein: A structural and thermodynamic analysis - (Fragment 1)
Keywords keywordsRECEPTOR; RECEPTOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.31
Radius of gyration Rg (electron density) rg_electron30.61
Forward intensity I(0) i0224376000.00
Molecular weight molecular_weight117790.0 kDa
Excluded volume excluded_volume146830 ų
Envelope volume envelope_volume197150 ų
Hydration-shell volume shell_volume51133 ų
Envelope diameter envelope_diameter95.0
Shell Rg shell_rg39.85
Envelope Rg envelope_rg29.69
Shape Rg shape_rg30.61
Total Rg total_rg31.49
Total atoms total_atoms8281
Residues n_residues1025
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 dmax88.1
Rg (real space) rg_real31.94
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real2.2440e+08
I(0) uncertainty (real space) i0_real_error2.9530e+06
Rg (reciprocal space) rg_reciprocal32.10
I(0) (reciprocal space) i0_reciprocal224400000.0000
Solution quality estimate total_estimate0.9072
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary43.1
Skewness Skewness skewness-0.110
Kurtosis Kurtosis kurtosis-0.601
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha59870000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.958; Stabil: 0.996; Sysdev: 1.000; Positv: 1.000; Valcen: 0.980; Smooth: 0.945

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 5 domains

CATH v4.4 (5 domains)

Domain ID domain_id2y54A00
Class class2 — Mainly Beta
Architecture architecture70 — Distorted Sandwich
Topology topology170 — Acetylcholine Binding Protein; Chain: A,
Homologous superfamily homologous superfamily10 — Neurotransmitter-gated ion-channel ligand-binding domain
Domain ID domain_id2y54B00
Class class2 — Mainly Beta
Architecture architecture70 — Distorted Sandwich
Topology topology170 — Acetylcholine Binding Protein; Chain: A,
Homologous superfamily homologous superfamily10 — Neurotransmitter-gated ion-channel ligand-binding domain
Domain ID domain_id2y54C00
Class class2 — Mainly Beta
Architecture architecture70 — Distorted Sandwich
Topology topology170 — Acetylcholine Binding Protein; Chain: A,
Homologous superfamily homologous superfamily10 — Neurotransmitter-gated ion-channel ligand-binding domain
Domain ID domain_id2y54D00
Class class2 — Mainly Beta
Architecture architecture70 — Distorted Sandwich
Topology topology170 — Acetylcholine Binding Protein; Chain: A,
Homologous superfamily homologous superfamily10 — Neurotransmitter-gated ion-channel ligand-binding domain
Domain ID domain_id2y54E00
Class class2 — Mainly Beta
Architecture architecture70 — Distorted Sandwich
Topology topology170 — Acetylcholine Binding Protein; Chain: A,
Homologous superfamily homologous superfamily10 — Neurotransmitter-gated ion-channel ligand-binding domain

8. Citations (1)

9. Files and Curves (10)