2x44

Structure of a strand-swapped dimeric form of CTLA-4

Method: X-RAY DIFFRACTION Dmax: 107.5 Å Quality: REASONABLE

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

CYTOTOXIC T-LYMPHOCYTE PROTEIN 4

HOMO SAPIENS

UniProt P16410

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 36–161 Fragment:RESIDUES 36-161 Mutation:YES No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 7.5;0.02 M MAGNESIUM CHLORIDE, 0.1 M HEPES PH 7.5, 22 % W/V POLYACRYLIC ACID 5100 SODIUM SALT, 0.4 M NDSB-256 (OR 6 % 1,6-DIAMINOHEXANE). Resolution 2.60 Å R-free 0.245

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.

21 other PDB entries and 32 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CTLA4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain D; PDBConstruct 2–127; UniProt 36–161

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 2x44

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2x44
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2x44
Deposition date deposition_date2010-01-28
Structure title titleStructure of a strand-swapped dimeric form of CTLA-4
Keywords keywordsIMMUNE SYSTEM, AMYLOIDOGENIC, SYSTEMIC LUPUS ERYTHEMATOSUS, IMMUNOGLOBULIN DOMAIN, MEMBRANE, GLYCOPROTEIN, TRANSMEMBRANE; IMMUNE SYSTEM
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.84
Radius of gyration Rg (electron density) rg_electron24.13
Forward intensity I(0) i03346600.00
Molecular weight molecular_weight12998.0 kDa
Excluded volume excluded_volume16229 ų
Envelope volume envelope_volume24468 ų
Hydration-shell volume shell_volume11247 ų
Envelope diameter envelope_diameter106.2
Shell Rg shell_rg23.47
Envelope Rg envelope_rg30.03
Shape Rg shape_rg24.28
Total Rg total_rg23.58
Total atoms total_atoms906
Residues n_residues121
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 dmax107.5
Rg (real space) rg_real23.84
Rg uncertainty (real space) rg_real_error2.35
I(0) (real space) i0_real3.3470e+06
I(0) uncertainty (real space) i0_real_error7.2530e+04
Rg (reciprocal space) rg_reciprocal23.44
I(0) (reciprocal space) i0_reciprocal3346000.0000
Solution quality estimate total_estimate0.6129
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary17.6
Skewness Skewness skewness1.477
Kurtosis Kurtosis kurtosis1.704
Angular range angular_range— – 0.3650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1129000.0000
Real-space data points n_real_points68
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.001; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.000; Smooth: 0.962

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2x44d_
Class classb — All beta proteins
Fold Fold foldb.1 — Immunoglobulin-like beta-sandwich
Superfamily Superfamily superfamilyb.1.1 — Immunoglobulin
Family Family familyb.1.1.1 — V set domains (antibody variable domain-like)

CATH v4.4 (1 domains)

Domain ID domain_id2x44D01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins

8. Citations (1)

9. Files and Curves (10)