4lse

Ion selectivity of OmpF porin soaked in 0.2M NaBr

Method: X-RAY DIFFRACTION Dmax: 89.5 Å Quality: EXCELLENT

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

Outer membrane protein F

Escherichia coli

UniProt P02931

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 homooligomer Homooligomer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 23–362 Chain B; UniProt 23–362 Chain C; UniProt 23–362 Fragment:UNP residues 23-362 BR BROMIDE ION × 8 MG MAGNESIUM ION × 6 PEG DI(HYDROXYETHYL)ETHER × 4 C8E (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;293 K;50% PEG200, 0.1 M sodium cacodylate, 0.2 M magnesium chloride, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293.0K Resolution 2.10 Å R-free 0.290

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.

41 other PDB entries and 64 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name OMPF_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–341; UniProt 23–362 Author chain B; PDBConstruct 2–341; UniProt 23–362 Author chain C; PDBConstruct 2–341; UniProt 23–362

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 4lse

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4lse
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4lse
Deposition date deposition_date2013-07-22
Structure title titleIon selectivity of OmpF porin soaked in 0.2M NaBr
Keywords keywordsporin, outer membrane protein, beta-barrel, ion transport, TRANSPORT PROTEIN; TRANSPORT PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.64
Radius of gyration Rg (electron density) rg_electron30.21
Forward intensity I(0) i0215002000.00
Molecular weight molecular_weight112770.0 kDa
Excluded volume excluded_volume139000 ų
Envelope volume envelope_volume179400 ų
Hydration-shell volume shell_volume47465 ų
Envelope diameter envelope_diameter91.7
Shell Rg shell_rg39.17
Envelope Rg envelope_rg29.88
Shape Rg shape_rg30.25
Total Rg total_rg30.85
Total atoms total_atoms7947
Residues n_residues1020
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 dmax89.5
Rg (real space) rg_real30.41
Rg uncertainty (real space) rg_real_error0.39
I(0) (real space) i0_real2.1500e+08
I(0) uncertainty (real space) i0_real_error2.8740e+06
Rg (reciprocal space) rg_reciprocal30.51
I(0) (reciprocal space) i0_reciprocal215000000.0000
Solution quality estimate total_estimate0.9082
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary36.2
Skewness Skewness skewness0.055
Kurtosis Kurtosis kurtosis-0.631
Angular range angular_range— – 0.2600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha19240000.0000
Real-space data points n_real_points53
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.968; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.978; Smooth: 0.921

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd4lsea_
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.4 — Transmembrane beta-barrels
Superfamily Superfamily superfamilyf.4.3 — Porins
Family Family familyf.4.3.1 — Porin
Domain ID domain_idd4lseb_
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.4 — Transmembrane beta-barrels
Superfamily Superfamily superfamilyf.4.3 — Porins
Family Family familyf.4.3.1 — Porin
Domain ID domain_idd4lsec_
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.4 — Transmembrane beta-barrels
Superfamily Superfamily superfamilyf.4.3 — Porins
Family Family familyf.4.3.1 — Porin

CATH v4.4 (3 domains)

Domain ID domain_id4lseA00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology160 — Porin
Homologous superfamily homologous superfamily10 — Porin
Domain ID domain_id4lseB00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology160 — Porin
Homologous superfamily homologous superfamily10 — Porin
Domain ID domain_id4lseC00
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology160 — Porin
Homologous superfamily homologous superfamily10 — Porin

8. Citations (1)

9. Files and Curves (10)