2qug

Crystal structure of alpha-1-antitrypsin, crystal form A

Method: X-RAY DIFFRACTION Dmax: 77.1 Å Quality: GOOD

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

Alpha-1-antitrypsin

Homo sapiens

UniProt P01009

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 25–418 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;295 K;29% PEG 3350, 400 mM NaF, vapor diffusion, hanging drop, temperature 295K Resolution 2.00 Å R-free 0.275

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.

45 other PDB entries and 55 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A1AT_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–394; UniProt 25–418

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 2qug

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2qug
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id2qug
Deposition date deposition_date2007-08-05
Structure title titleCrystal structure of alpha-1-antitrypsin, crystal form A
Keywords keywords;antitrypsin, polymerisation, protein aggregation, protein unfolding, serpin, Acute phase, Disease mutation, Glycoprotein, Protease inhibitor, Secreted, Serine protease inhibitor ;; Protease Inhibitor
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.93
Radius of gyration Rg (electron density) rg_electron21.61
Forward intensity I(0) i027205600.00
Molecular weight molecular_weight41514.0 kDa
Excluded volume excluded_volume52668 ų
Envelope volume envelope_volume62450 ų
Hydration-shell volume shell_volume24087 ų
Envelope diameter envelope_diameter80.5
Shell Rg shell_rg28.63
Envelope Rg envelope_rg22.01
Shape Rg shape_rg21.56
Total Rg total_rg22.67
Total atoms total_atoms2928
Residues n_residues368
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 dmax77.1
Rg (real space) rg_real22.89
Rg uncertainty (real space) rg_real_error0.55
I(0) (real space) i0_real2.7210e+07
I(0) uncertainty (real space) i0_real_error3.5420e+05
Rg (reciprocal space) rg_reciprocal22.90
I(0) (reciprocal space) i0_reciprocal27210000.0000
Solution quality estimate total_estimate0.7967
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary27.3
Skewness Skewness skewness0.343
Kurtosis Kurtosis kurtosis-0.255
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha7195000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.786; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.997; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2quga_
Class classe — Multi-domain proteins (alpha and beta)
Fold Fold folde.1 — Serpins
Superfamily Superfamily superfamilye.1.1 — Serpins
Family Family familye.1.1.1 — Serpins

CATH v4.4 (2 domains)

Domain ID domain_id2qugA01
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology497 — Antithrombin; Chain I, domain 2
Homologous superfamily homologous superfamily10 — Antithrombin, subunit I, domain 2
Domain ID domain_id2qugA02
Class class2 — Mainly Beta
Architecture architecture30 — Roll
Topology topology39 — Alpha-1-antitrypsin; domain 1
Homologous superfamily homologous superfamily10 — Alpha-1-antitrypsin, domain 1

8. Citations (1)

9. Files and Curves (10)