5o66

Asymmetric AcrABZ-TolC

Method: ELECTRON MICROSCOPY Dmax: 240.6 Å Quality: GOOD

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

Outer membrane protein TolC

Escherichia coli K12

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 × 15 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain A; UniProt 1–493 Chain B; UniProt 1–493 Chain C; UniProt 1–493 Not recorded Multidrug efflux pump subunit AcrA × 6 (P0AE07) Multidrug efflux pump subunit AcrB × 3 (P31224) Multidrug efflux pump accessory protein AcrZ × 3 (P0AAX1) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.6 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 5.90 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 1–493; UniProt 1–493 Author chain B; PDBConstruct 1–493; UniProt 1–493 Author chain C; PDBConstruct 1–493; UniProt 1–493

Multidrug efflux pump subunit AcrA

Escherichia coli O157:H7

UniProt P0AE07

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 × 15 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain D; UniProt 25–397 Chain E; UniProt 25–397 Chain F; UniProt 25–397 Chain G; UniProt 25–397 Chain H; UniProt 25–397 Chain I; UniProt 25–397 Not recorded Outer membrane protein TolC × 3 (P02930) Multidrug efflux pump subunit AcrB × 3 (P31224) Multidrug efflux pump accessory protein AcrZ × 3 (P0AAX1) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.6 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 5.90 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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ACRA_ECO57
Isoform
PDB entities 2
Chains and sequence ranges Author chain D; PDBConstruct 1–373; UniProt 25–397 Author chain E; PDBConstruct 1–373; UniProt 25–397 Author chain F; PDBConstruct 1–373; UniProt 25–397 Author chain G; PDBConstruct 1–373; UniProt 25–397 Author chain H; PDBConstruct 1–373; UniProt 25–397 Author chain I; PDBConstruct 1–373; UniProt 25–397

Multidrug efflux pump subunit AcrB

Escherichia coli K12

UniProt P31224

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 × 15 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain J; UniProt 1–1049 Chain K; UniProt 1–1049 Chain L; UniProt 1–1049 Not recorded Outer membrane protein TolC × 3 (P02930) Multidrug efflux pump subunit AcrA × 6 (P0AE07) Multidrug efflux pump accessory protein AcrZ × 3 (P0AAX1) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.6 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 5.90 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.

117 other PDB entries and 124 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ACRB_ECOLI
Isoform
PDB entities 3
Chains and sequence ranges Author chain J; PDBConstruct 1–1049; UniProt 1–1049 Author chain K; PDBConstruct 1–1049; UniProt 1–1049 Author chain L; PDBConstruct 1–1049; UniProt 1–1049

Multidrug efflux pump accessory protein AcrZ

Escherichia coli O157:H7

UniProt P0AAX1

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 × 15 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain M; UniProt 1–49 Chain N; UniProt 1–49 Chain O; UniProt 1–49 Not recorded Outer membrane protein TolC × 3 (P02930) Multidrug efflux pump subunit AcrA × 6 (P0AE07) Multidrug efflux pump subunit AcrB × 3 (P31224) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.6 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 5.90 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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ACRZ_ECO57
Isoform
PDB entities 4
Chains and sequence ranges Author chain M; PDBConstruct 1–49; UniProt 1–49 Author chain N; PDBConstruct 1–49; UniProt 1–49 Author chain O; PDBConstruct 1–49; UniProt 1–49

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 5o66

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 5o66
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2. Structure Basics 2. Structure Basics

Entry ID entry_id5o66
Deposition date deposition_date2017-06-05
Structure title titleAsymmetric AcrABZ-TolC
Keywords keywordsmultidrug efflux pump, membrane transporter, membrane protein; MEMBRANE PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier85.84
Radius of gyration Rg (electron density) rg_electron88.27
Forward intensity I(0) i06768680000.00
Molecular weight molecular_weight706250.0 kDa
Excluded volume excluded_volume889310 ų
Envelope volume envelope_volume1314900 ų
Hydration-shell volume shell_volume146990 ų
Envelope diameter envelope_diameter344.5
Shell Rg shell_rg63.50
Envelope Rg envelope_rg91.34
Shape Rg shape_rg88.31
Total Rg total_rg87.75
Total atoms total_atoms49671
Residues n_residues6544
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 dmax240.6
Rg (real space) rg_real78.31
Rg uncertainty (real space) rg_real_error1.49
I(0) (real space) i0_real6.4630e+09
I(0) uncertainty (real space) i0_real_error1.4370e+08
Rg (reciprocal space) rg_reciprocal78.16
I(0) (reciprocal space) i0_reciprocal6624000000.0000
Solution quality estimate total_estimate0.8606
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary66.8
Skewness Skewness skewness0.644
Kurtosis Kurtosis kurtosis-0.400
Angular range angular_range— – 0.0900 −1
Current regularization parameter α current_alpha0.3086
Highest regularization parameter α highest_alpha892300000.0000
Real-space data points n_real_points19
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.002; Oscil: 0.694; Stabil: 0.985; Sysdev: 1.000; Positv: 1.000; Valcen: 0.997; Smooth: 0.159

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)