9ggp

Alpha-1-antitrypsin in complex with the Fab fragment of an anti-polymer antibody

Method: X-RAY DIFFRACTION Dmax: 118.5 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 26–418 Chain B; UniProt 26–418 Not recorded Fab fragment heavy chain of 2C1 monoclonal antibody × 1 Fab fragment light chain of 2C1 monoclonal antibody × 1 EDO 1,2-ETHANEDIOL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.1;293 K;0.2 M Ammonium citrate dibasic 20% w/v Polyethylene glycol 3,350 pH 5.1 Resolution 1.84 Å R-free 0.206

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 12–404; UniProt 26–418 Author chain B; PDBConstruct 12–404; UniProt 26–418

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 9ggp

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9ggp
Deposition date deposition_date2024-08-13
最后修订 last_revision2025-05-14
Structure title titleAlpha-1-antitrypsin in complex with the Fab fragment of an anti-polymer antibody
Keywords keywordsSerpin, Fab fragment, monoclonal antibody, selective binding, epitope, 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_guinier34.37
Radius of gyration Rg (electron density) rg_electron34.02
Forward intensity I(0) i0114108000.00
Molecular weight molecular_weight86911.0 kDa
Excluded volume excluded_volume109230 ų
Envelope volume envelope_volume140350 ų
Hydration-shell volume shell_volume35965 ų
Envelope diameter envelope_diameter123.1
Shell Rg shell_rg38.85
Envelope Rg envelope_rg33.82
Shape Rg shape_rg33.98
Total Rg total_rg34.50
Total atoms total_atoms6132
Residues n_residues787
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 dmax118.5
Rg (real space) rg_real34.59
Rg uncertainty (real space) rg_real_error1.13
I(0) (real space) i0_real1.1410e+08
I(0) uncertainty (real space) i0_real_error1.9510e+06
Rg (reciprocal space) rg_reciprocal34.45
I(0) (reciprocal space) i0_reciprocal114100000.0000
Solution quality estimate total_estimate0.8527
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary33.5
Skewness Skewness skewness0.491
Kurtosis Kurtosis kurtosis-0.325
Angular range angular_range— – 0.2300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha20200000.0000
Real-space data points n_real_points47
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.803; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.876; Smooth: 0.796

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (3)

9. Files and Curves (10)