9qgy

Structure of the YbjP lipoprotein bound to the MacAB-TolC tripartite efflux pump

Method: ELECTRON MICROSCOPY Dmax: 227.8 Å Quality: GOOD

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

Outer membrane protein TolC

Escherichia coli

UniProt P02930

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 × 14 PDB declaration: 14-meric(14) Consistent with protein copy count Chain A; UniProt 23–493 Chain B; UniProt 23–493 Chain C; UniProt 23–493 Not recorded Uncharacterized lipoprotein YbjP × 3 (P75818) Macrolide export protein MacA × 6 (P75830) Macrolide export ATP-binding/permease protein MacB × 2 (P75831) CL CHLORIDE ION × 3 Z41 (2S)-3-hydroxypropane-1,2-diyl dihexadecanoate × 3 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.48 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.

19 other PDB entries and 19 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TOLC_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–471; UniProt 23–493 Author chain B; PDBConstruct 1–471; UniProt 23–493 Author chain C; PDBConstruct 1–471; UniProt 23–493

Uncharacterized lipoprotein YbjP

Escherichia coli

UniProt P75818

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 × 14 PDB declaration: 14-meric(14) Consistent with protein copy count Chain D; UniProt 19–171 Chain E; UniProt 19–171 Chain F; UniProt 19–171 Not recorded Outer membrane protein TolC × 3 (P02930) Macrolide export protein MacA × 6 (P75830) Macrolide export ATP-binding/permease protein MacB × 2 (P75831) CL CHLORIDE ION × 3 Z41 (2S)-3-hydroxypropane-1,2-diyl dihexadecanoate × 3 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.48 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.

4 other PDB entries and 4 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name YBJP_ECOLI
Isoform
PDB entities 2
Chains and sequence ranges Author chain D; PDBConstruct 1–153; UniProt 19–171 Author chain E; PDBConstruct 1–153; UniProt 19–171 Author chain F; PDBConstruct 1–153; UniProt 19–171

Macrolide export protein MacA

Escherichia coli

UniProt P75830

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 × 14 PDB declaration: 14-meric(14) Consistent with protein copy count Chain G; UniProt 1–371 Chain H; UniProt 1–371 Chain I; UniProt 1–371 Chain J; UniProt 1–371 Chain K; UniProt 1–371 Chain L; UniProt 1–371 Not recorded Outer membrane protein TolC × 3 (P02930) Uncharacterized lipoprotein YbjP × 3 (P75818) Macrolide export ATP-binding/permease protein MacB × 2 (P75831) CL CHLORIDE ION × 3 Z41 (2S)-3-hydroxypropane-1,2-diyl dihexadecanoate × 3 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.48 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 MACA_ECOLI
Isoform
PDB entities 3
Chains and sequence ranges Author chain G; PDBConstruct 1–371; UniProt 1–371 Author chain H; PDBConstruct 1–371; UniProt 1–371 Author chain I; PDBConstruct 1–371; UniProt 1–371 Author chain J; PDBConstruct 1–371; UniProt 1–371 Author chain K; PDBConstruct 1–371; UniProt 1–371 Author chain L; PDBConstruct 1–371; UniProt 1–371

Macrolide export ATP-binding/permease protein MacB

Escherichia coli

UniProt P75831

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 × 14 PDB declaration: 14-meric(14) Consistent with protein copy count Chain M; UniProt 299–507 Chain N; UniProt 299–507 Not recorded Outer membrane protein TolC × 3 (P02930) Uncharacterized lipoprotein YbjP × 3 (P75818) Macrolide export protein MacA × 6 (P75830) CL CHLORIDE ION × 3 Z41 (2S)-3-hydroxypropane-1,2-diyl dihexadecanoate × 3 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.48 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.

5 other PDB entries and 8 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MACB_ECOLI
Isoform
PDB entities 4
Chains and sequence ranges Author chain M; PDBConstruct 1–209; UniProt 299–507 Author chain N; PDBConstruct 1–209; UniProt 299–507

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 9qgy

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9qgy
Deposition date deposition_date2025-03-14
Structure title titleStructure of the YbjP lipoprotein bound to the MacAB-TolC tripartite efflux pump
Keywords keywordsmulti-drug efflux pump, MacAB-TolC, AcrABZ-TolC, type I secretion, lipoprotein, membrane protein assembly, MEMBRANE PROTEIN; MEMBRANE PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier83.56
Radius of gyration Rg (electron density) rg_electron85.04
Forward intensity I(0) i03097850000.00
Molecular weight molecular_weight461900.0 kDa
Excluded volume excluded_volume575720 ų
Envelope volume envelope_volume945870 ų
Hydration-shell volume shell_volume103740 ų
Envelope diameter envelope_diameter291.9
Shell Rg shell_rg63.00
Envelope Rg envelope_rg83.44
Shape Rg shape_rg85.09
Total Rg total_rg84.53
Total atoms total_atoms64967
Residues n_residues4198
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 dmax227.8
Rg (real space) rg_real78.91
Rg uncertainty (real space) rg_real_error1.02
I(0) (real space) i0_real2.9730e+09
I(0) uncertainty (real space) i0_real_error5.5690e+07
Rg (reciprocal space) rg_reciprocal78.58
I(0) (reciprocal space) i0_reciprocal3054000000.0000
Solution quality estimate total_estimate0.8252
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary60.0
Skewness Skewness skewness0.432
Kurtosis Kurtosis kurtosis-0.920
Angular range angular_range— – 0.0950 −1
Current regularization parameter α current_alpha0.8833
Highest regularization parameter α highest_alpha523100000.0000
Real-space data points n_real_points20
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.669; Stabil: 0.960; Sysdev: 1.000; Positv: 1.000; Valcen: 0.840; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)