6qgw

Crystal structure of E.coli BamA beta-barrel in complex with nanobody E6

Method: X-RAY DIFFRACTION Dmax: 93.7 Å Quality: GOOD

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

Outer membrane protein assembly factor BamA

Escherichia coli O157:H7

UniProt P0A942

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 421–810 Not recorded NanoE6 × 1 C8E (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE × 15 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;25% PEG 4000, 0.2 M MgCl2, 0.1 M Tris pH 8.5 Resolution 1.94 Å R-free 0.230

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.

7 other PDB entries and 9 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BAMA_ECO57
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 22–411; UniProt 421–810

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 6qgw

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6qgw
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6qgw
Deposition date deposition_date2019-01-14
Structure title titleCrystal structure of E.coli BamA beta-barrel in complex with nanobody E6
Keywords keywordsBeta-Barrel, outer membrane, protein insertion, protein folding, protein maturation, MEMBRANE PROTEIN; MEMBRANE PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.18
Radius of gyration Rg (electron density) rg_electron27.02
Forward intensity I(0) i049691800.00
Molecular weight molecular_weight55883.0 kDa
Excluded volume excluded_volume70232 ų
Envelope volume envelope_volume90755 ų
Hydration-shell volume shell_volume29145 ų
Envelope diameter envelope_diameter96.0
Shell Rg shell_rg33.35
Envelope Rg envelope_rg27.05
Shape Rg shape_rg27.00
Total Rg total_rg27.79
Total atoms total_atoms7756
Residues n_residues486
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 dmax93.7
Rg (real space) rg_real27.27
Rg uncertainty (real space) rg_real_error1.04
I(0) (real space) i0_real4.9690e+07
I(0) uncertainty (real space) i0_real_error7.2980e+05
Rg (reciprocal space) rg_reciprocal27.24
I(0) (reciprocal space) i0_reciprocal49690000.0000
Solution quality estimate total_estimate0.8639
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.7
Skewness Skewness skewness0.449
Kurtosis Kurtosis kurtosis-0.179
Angular range angular_range— – 0.2900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4150000.0000
Real-space data points n_real_points59
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.817; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.958; Smooth: 0.817

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd6qgwb_
Class classb — All beta proteins
Fold Fold foldb.1 — Immunoglobulin-like beta-sandwich
Superfamily Superfamily superfamilyb.1.1 — Immunoglobulin
Family Family familyb.1.1.1 — V set domains (antibody variable domain-like)

CATH v4.4 (1 domains)

Domain ID domain_id6qgwA00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology160 — Porin
Homologous superfamily homologous superfamily50 — membrane protein fhac: a member of the omp85/tpsb transporter family

8. Citations (1)

9. Files and Curves (10)