1ah1

CTLA-4, NMR, 20 STRUCTURES

Method: SOLUTION NMR Dmax: 65.2 Å Quality: GOOD

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

CTLA-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 Other combination Monomer Protein × 1 其他Polymer 2 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 37–161 Fragment:EXTRACELLULAR N-TERMINAL IMMUNOGLOBULIN V-LIKE ;beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[beta-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose ; × 1 ;beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose ; × 1 SOLUTION NMR NMR measurement conditions:pH 7;303 K Resolution not provided

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 CTL4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–125; UniProt 37–161

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 1ah1

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1ah1
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id1ah1
Deposition date deposition_date1997-04-11
Structure title titleCTLA-4, NMR, 20 STRUCTURES
Keywords keywordsIMMUNORECEPTOR, T CELL RECEPTOR, IMMUNE RESPONSE, IMMUNOGLOBULIN; IMMUNORECEPTOR
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier16.96
Radius of gyration Rg (electron density) rg_electron16.78
Forward intensity I(0) i01349070000.00
Molecular weight molecular_weight305400.0 kDa
Excluded volume excluded_volume379510 ų
Envelope volume envelope_volume51617 ų
Hydration-shell volume shell_volume21096 ų
Envelope diameter envelope_diameter72.3
Shell Rg shell_rg27.66
Envelope Rg envelope_rg21.98
Shape Rg shape_rg16.77
Total Rg total_rg16.98
Total atoms total_atoms41980
Residues n_residues2580
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 dmax65.2
Rg (real space) rg_real17.12
Rg uncertainty (real space) rg_real_error0.62
I(0) (real space) i0_real1.3490e+09
I(0) uncertainty (real space) i0_real_error1.8340e+07
Rg (reciprocal space) rg_reciprocal17.10
I(0) (reciprocal space) i0_reciprocal1349000000.0000
Solution quality estimate total_estimate0.7616
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary18.0
Skewness Skewness skewness0.686
Kurtosis Kurtosis kurtosis0.348
Angular range angular_range— – 0.4700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1252000.0000
Real-space data points n_real_points77
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.431; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.615; Smooth: 0.989

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1ah1a_
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_id1ah1A00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily10 — Immunoglobulins

8. Citations (1)

9. Files and Curves (10)