5nik

Structure of the MacAB-TolC ABC-type tripartite multidrug efflux pump

Method: ELECTRON MICROSCOPY Dmax: 260.8 Å Quality: GOOD

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

Outer membrane protein TolC

Escherichia coli (strain 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 × 11 PDB declaration: undecameric(11) Consistent with protein copy count Chain A; UniProt 23–493 Chain B; UniProt 23–493 Chain C; UniProt 23–493 Not recorded Macrolide export protein MacA × 6 (P75830) Macrolide export ATP-binding/permease protein MacB × 2 (P75831) ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.30 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

Macrolide export protein MacA

Escherichia coli (strain K12)

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 × 11 PDB declaration: undecameric(11) Consistent with protein copy count Chain D; UniProt 1–371 Chain E; UniProt 1–371 Chain F; UniProt 1–371 Chain G; UniProt 1–371 Chain H; UniProt 1–371 Chain I; UniProt 1–371 Not recorded Outer membrane protein TolC × 3 (P02930) Macrolide export ATP-binding/permease protein MacB × 2 (P75831) ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.30 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 2
Chains and sequence ranges Author chain D; PDBConstruct 1–371; UniProt 1–371 Author chain E; PDBConstruct 1–371; UniProt 1–371 Author chain F; PDBConstruct 1–371; UniProt 1–371 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

Macrolide export ATP-binding/permease protein MacB

Escherichia coli (strain K12)

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 × 11 PDB declaration: undecameric(11) Consistent with protein copy count Chain J; UniProt 1–648 Chain K; UniProt 1–648 Not recorded Outer membrane protein TolC × 3 (P02930) Macrolide export protein MacA × 6 (P75830) ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.30 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 3
Chains and sequence ranges Author chain J; PDBConstruct 1–648; UniProt 1–648 Author chain K; PDBConstruct 1–648; UniProt 1–648

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 5nik

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id5nik
Deposition date deposition_date2017-03-24
Structure title titleStructure of the MacAB-TolC ABC-type tripartite multidrug efflux pump
Keywords keywordsABC transporter, drug efflux pump, multi-drug resistance, macrolide transporter, toxin transporter, transport protein; TRANSPORT PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier95.65
Radius of gyration Rg (electron density) rg_electron98.74
Forward intensity I(0) i03593810000.00
Molecular weight molecular_weight500830.0 kDa
Excluded volume excluded_volume626260 ų
Envelope volume envelope_volume1122400 ų
Hydration-shell volume shell_volume118930 ų
Envelope diameter envelope_diameter375.7
Shell Rg shell_rg61.45
Envelope Rg envelope_rg99.55
Shape Rg shape_rg98.79
Total Rg total_rg97.95
Total atoms total_atoms35215
Residues n_residues4582
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 dmax260.8
Rg (real space) rg_real87.28
Rg uncertainty (real space) rg_real_error1.31
I(0) (real space) i0_real3.4190e+09
I(0) uncertainty (real space) i0_real_error7.2670e+07
Rg (reciprocal space) rg_reciprocal84.87
I(0) (reciprocal space) i0_reciprocal3477000000.0000
Solution quality estimate total_estimate0.8696
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary65.2
Skewness Skewness skewness0.462
Kurtosis Kurtosis kurtosis-0.736
Angular range angular_range— – 0.0800 −1
Current regularization parameter α current_alpha0.4635
Highest regularization parameter α highest_alpha123000000.0000
Real-space data points n_real_points17
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.033; Oscil: 0.820; Stabil: 0.976; Sysdev: 1.000; Positv: 1.000; Valcen: 0.945; Smooth: 0.029

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 5 domains

CATH v4.4 (5 domains)

Domain ID domain_id5nikA00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1600 — Outer membrane efflux proteins (OEP)
Homologous superfamily homologous superfamily10 — Outer membrane efflux proteins (OEP)
Domain ID domain_id5nikB00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1600 — Outer membrane efflux proteins (OEP)
Homologous superfamily homologous superfamily10 — Outer membrane efflux proteins (OEP)
Domain ID domain_id5nikC00
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1600 — Outer membrane efflux proteins (OEP)
Homologous superfamily homologous superfamily10 — Outer membrane efflux proteins (OEP)
Domain ID domain_id5nikJ01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases
Domain ID domain_id5nikK01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases

8. Citations (1)

9. Files and Curves (10)