9pav

Antibody (1B2) Bound Rifamycin Synthetase Module 1 in the Elongation Mode

Method: ELECTRON MICROSCOPY Dmax: 188.9 Å Quality: GOOD

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

6-deoxyerythronolide-B synthase

Amycolatopsis mediterranei

UniProt O54666

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 × 7 PDB declaration: heptameric(7) Consistent with protein copy count Chain A; UniProt 631–2179 Chain B; UniProt 631–2179 Chain C; UniProt 631–2179 Non-standard monomer:Yes (specific site not provided by mmCIF) Antibody Fragment 1B2 Heavy Chain × 2 Antibody Fragment 1B2 Light Chain × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.2;100 mM citric acid, 10 mM HEPES, pH 7.2 (NaOH) cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.22 Å

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.

3 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name O54666_AMYMD
Isoform
PDB entities 3, 4
Chains and sequence ranges Author chain A; PDBConstruct 32–1580; UniProt 631–2179 Author chain B; PDBConstruct 32–1580; UniProt 631–2179 Author chain C; PDBConstruct 32–1580; UniProt 631–2179

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 9pav

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9pav
Deposition date deposition_date2025-06-25
Structure title titleAntibody (1B2) Bound Rifamycin Synthetase Module 1 in the Elongation Mode
Keywords keywordsPolyketide Synthase Module, Antibody (Fab), Transferase-Immune System complex; Transferase/Immune System
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier57.18
Radius of gyration Rg (electron density) rg_electron57.11
Forward intensity I(0) i01955450000.00
Molecular weight molecular_weight364060.0 kDa
Excluded volume excluded_volume453840 ų
Envelope volume envelope_volume725710 ų
Hydration-shell volume shell_volume108550 ų
Envelope diameter envelope_diameter194.4
Shell Rg shell_rg57.30
Envelope Rg envelope_rg55.35
Shape Rg shape_rg57.10
Total Rg total_rg57.13
Total atoms total_atoms25647
Residues n_residues3464
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 dmax188.9
Rg (real space) rg_real57.08
Rg uncertainty (real space) rg_real_error1.51
I(0) (real space) i0_real1.9550e+09
I(0) uncertainty (real space) i0_real_error3.8060e+07
Rg (reciprocal space) rg_reciprocal57.24
I(0) (reciprocal space) i0_reciprocal1956000000.0000
Solution quality estimate total_estimate0.8827
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary70.0
Skewness Skewness skewness0.237
Kurtosis Kurtosis kurtosis-0.495
Angular range angular_range— – 0.1350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha88360000.0000
Real-space data points n_real_points28
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.875; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.997; Smooth: 0.848

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)