9hud

Alpha-1-antitrypsin in the cleaved conformation in complex with a conformationally nonselective Fab fragment

Method: X-RAY DIFFRACTION Dmax: 169.9 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 heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 26–378 Chain B; UniProt 379–418 Not recorded FAB 9C5 heavy chain × 1 FAB 9C5 light chain × 1 EDO 1,2-ETHANEDIOL × 1 GLY GLYCINE × 2 CL CHLORIDE ION × 1 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;0.1M sodium HEPES, MOPS 0.1M DL-Glutamic acid monohydrate; 0.1M DL-Alanine; 0.1M Glycine; 0.1M DL-Lysine 40% v/v Glycerol; 20% w/v PEG 4000 Resolution 2.42 Å R-free 0.247
2 Protein heterocomplex Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain C; UniProt 26–378 Chain D; UniProt 379–418 Not recorded FAB 9C5 heavy chain × 1 FAB 9C5 light chain × 1 EDO 1,2-ETHANEDIOL × 5 GLY GLYCINE × 1 CL CHLORIDE ION × 1 NA SODIUM ION × 1 GOL GLYCEROL × 1 LYS LYSINE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;0.1M sodium HEPES, MOPS 0.1M DL-Glutamic acid monohydrate; 0.1M DL-Alanine; 0.1M Glycine; 0.1M DL-Lysine 40% v/v Glycerol; 20% w/v PEG 4000 Resolution 2.42 Å R-free 0.247

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 54 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A1AT_HUMAN
Isoform
PDB entities 1, 2
Chains and sequence ranges Author chain A; PDBConstruct 12–364; UniProt 26–378 Author chain C; PDBConstruct 12–364; UniProt 26–378 Author chain B; PDBConstruct 1–40; UniProt 379–418 Author chain D; PDBConstruct 1–40; UniProt 379–418

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 9hud

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9hud
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9hud
Deposition date deposition_date2024-12-22
最后修订 last_revision2025-11-26
Structure title titleAlpha-1-antitrypsin in the cleaved conformation in complex with a conformationally nonselective Fab fragment
Keywords keywords;Complex, Cleaved Alpha-1-antitrypsin, Alpha-1-antitrypsin, Antitrypsin, Fab, Fab fragment, Fragment antigen-binding region, Antibody antigen complex, 9C5, PROTEIN BINDING ;; PROTEIN BINDING
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier47.58
Radius of gyration Rg (electron density) rg_electron47.74
Forward intensity I(0) i0425850000.00
Molecular weight molecular_weight171060.0 kDa
Excluded volume excluded_volume214400 ų
Envelope volume envelope_volume297140 ų
Hydration-shell volume shell_volume56459 ų
Envelope diameter envelope_diameter178.9
Shell Rg shell_rg46.32
Envelope Rg envelope_rg48.17
Shape Rg shape_rg47.71
Total Rg total_rg47.79
Total atoms total_atoms12061
Residues n_residues1578
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 dmax169.9
Rg (real space) rg_real48.20
Rg uncertainty (real space) rg_real_error2.19
I(0) (real space) i0_real4.2590e+08
I(0) uncertainty (real space) i0_real_error8.9480e+06
Rg (reciprocal space) rg_reciprocal47.58
I(0) (reciprocal space) i0_reciprocal425500000.0000
Solution quality estimate total_estimate0.8096
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary51.5
Skewness Skewness skewness0.621
Kurtosis Kurtosis kurtosis0.076
Angular range angular_range— – 0.1650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha28060000.0000
Real-space data points n_real_points34
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.753; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.860; Smooth: 0.402

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (11)

8. Citations (2)

9. Files and Curves (10)