3bx7

Engineered Human Lipocalin 2 (LCN2) in Complex with the Extracellular Domain of Human CTLA-4

Method: X-RAY DIFFRACTION Dmax: 82.2 Å Quality: GOOD

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

CYTOTOXIC T-LYMPHOCYTE-ASSOCIATED ANTIGEN 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 heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain C; UniProt 38–161 Not recorded ENGINEERED HUMAN LIPOCALIN 2 × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.4;293.15 K;1.4 M Na-malonate, pH 8.4, VAPOR DIFFUSION, SITTING DROP, temperature 293.15K Resolution 2.10 Å R-free 0.226

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 C; PDBConstruct 1–124; UniProt 38–161

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 3bx7

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3bx7
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3bx7
Deposition date deposition_date2008-01-11
Structure title titleEngineered Human Lipocalin 2 (LCN2) in Complex with the Extracellular Domain of Human CTLA-4
Keywords keywords;PROTEIN DESIGN, PROTEIN-PROTEIN COMPLEX, GLYCOPROTEIN, IMMUNOGLOBULIN DOMAIN, POLYMORPHISM, TRANSMEMBRANE PROTEIN, DE NOVO PROTEIN, PROTEIN BINDING ;; DE NOVO PROTEIN, PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.62
Radius of gyration Rg (electron density) rg_electron20.59
Forward intensity I(0) i017988200.00
Molecular weight molecular_weight32517.0 kDa
Excluded volume excluded_volume40849 ų
Envelope volume envelope_volume48407 ų
Hydration-shell volume shell_volume20309 ų
Envelope diameter envelope_diameter84.8
Shell Rg shell_rg26.46
Envelope Rg envelope_rg21.21
Shape Rg shape_rg20.56
Total Rg total_rg21.50
Total atoms total_atoms2287
Residues n_residues293
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 dmax82.2
Rg (real space) rg_real21.70
Rg uncertainty (real space) rg_real_error0.70
I(0) (real space) i0_real1.7990e+07
I(0) uncertainty (real space) i0_real_error2.2600e+05
Rg (reciprocal space) rg_reciprocal21.69
I(0) (reciprocal space) i0_reciprocal17990000.0000
Solution quality estimate total_estimate0.7952
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary25.4
Skewness Skewness skewness0.558
Kurtosis Kurtosis kurtosis0.239
Angular range angular_range— – 0.3700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4917000.0000
Real-space data points n_real_points69
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.517; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.799; Smooth: 0.983

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3bx7a_
Class classb — All beta proteins
Fold Fold foldb.60 — Lipocalins
Superfamily Superfamily superfamilyb.60.1 — Lipocalins
Family Family familyb.60.1.1 — Retinol binding protein-like
Domain ID domain_idd3bx7c_
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 (2 domains)

Domain ID domain_id3bx7A00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology128 — Lipocalin
Homologous superfamily homologous superfamily20 — Calycin beta-barrel core domain
Domain ID domain_id3bx7C00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins

8. Citations (1)

9. Files and Curves (10)