4dbl

Crystal structure of E159Q mutant of BtuCDF

Method: X-RAY DIFFRACTION Dmax: 174.9 Å Quality: GOOD

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

Vitamin B12 import system permease protein BtuC

Escherichia coli

UniProt P06609

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain A; UniProt 1–326 Chain B; UniProt 1–326 Mutation:C18S, C32S, C120S, C156S, C205S, C206S, C267S Vitamin B12 import ATP-binding protein BtuD × 2 (P06611) Vitamin B12-binding protein × 1 (P37028) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.4;293 K;0.1M sodium citrate, pH 5.4, 0.3-0.4M ammonium sulphate, 30-35% PEG-400, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 3.49 Å R-free 0.251
2 Protein heterocomplex Heteromer Protein × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain F; UniProt 1–326 Chain G; UniProt 1–326 Mutation:C18S, C32S, C120S, C156S, C205S, C206S, C267S Vitamin B12 import ATP-binding protein BtuD × 2 (P06611) Vitamin B12-binding protein × 1 (P37028) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.4;293 K;0.1M sodium citrate, pH 5.4, 0.3-0.4M ammonium sulphate, 30-35% PEG-400, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 3.49 Å R-free 0.251

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 BTUC_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 24–349; UniProt 1–326 Author chain B; PDBConstruct 24–349; UniProt 1–326 Author chain F; PDBConstruct 24–349; UniProt 1–326 Author chain G; PDBConstruct 24–349; UniProt 1–326

Vitamin B12 import ATP-binding protein BtuD

Escherichia coli

UniProt P06611

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain C; UniProt 1–249 Chain D; UniProt 1–249 Mutation:C180S Vitamin B12 import system permease protein BtuC × 2 (P06609) Vitamin B12-binding protein × 1 (P37028) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.4;293 K;0.1M sodium citrate, pH 5.4, 0.3-0.4M ammonium sulphate, 30-35% PEG-400, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 3.49 Å R-free 0.251
2 Protein heterocomplex Heteromer Protein × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain H; UniProt 1–249 Chain I; UniProt 1–249 Mutation:C180S Vitamin B12 import system permease protein BtuC × 2 (P06609) Vitamin B12-binding protein × 1 (P37028) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.4;293 K;0.1M sodium citrate, pH 5.4, 0.3-0.4M ammonium sulphate, 30-35% PEG-400, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 3.49 Å R-free 0.251

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 BTUD_ECOLI
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 1–249; UniProt 1–249 Author chain D; PDBConstruct 1–249; UniProt 1–249 Author chain H; PDBConstruct 1–249; UniProt 1–249 Author chain I; PDBConstruct 1–249; UniProt 1–249

Vitamin B12-binding protein

Escherichia coli

UniProt P37028

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain E; UniProt 22–266 Not recorded Vitamin B12 import system permease protein BtuC × 2 (P06609) Vitamin B12 import ATP-binding protein BtuD × 2 (P06611) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.4;293 K;0.1M sodium citrate, pH 5.4, 0.3-0.4M ammonium sulphate, 30-35% PEG-400, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 3.49 Å R-free 0.251
2 Protein heterocomplex Heteromer Protein × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain J; UniProt 22–266 Not recorded Vitamin B12 import system permease protein BtuC × 2 (P06609) Vitamin B12 import ATP-binding protein BtuD × 2 (P06611) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.4;293 K;0.1M sodium citrate, pH 5.4, 0.3-0.4M ammonium sulphate, 30-35% PEG-400, VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 3.49 Å R-free 0.251

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.

10 other PDB entries and 24 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BTUF_ECOLI
Isoform
PDB entities 3
Chains and sequence ranges Author chain E; PDBConstruct 2–246; UniProt 22–266 Author chain J; PDBConstruct 2–246; UniProt 22–266

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 4dbl

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id4dbl
Deposition date deposition_date2012-01-16
Structure title titleCrystal structure of E159Q mutant of BtuCDF
Keywords keywordsABC transporter for vitamin B12, ATP binding, inner membrane, 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_guinier52.74
Radius of gyration Rg (electron density) rg_electron51.91
Forward intensity I(0) i01205620000.00
Molecular weight molecular_weight301750.0 kDa
Excluded volume excluded_volume383210 ų
Envelope volume envelope_volume524180 ų
Hydration-shell volume shell_volume83741 ų
Envelope diameter envelope_diameter170.2
Shell Rg shell_rg55.35
Envelope Rg envelope_rg50.93
Shape Rg shape_rg51.87
Total Rg total_rg52.14
Total atoms total_atoms21230
Residues n_residues2778
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 dmax174.9
Rg (real space) rg_real52.78
Rg uncertainty (real space) rg_real_error1.71
I(0) (real space) i0_real1.2060e+09
I(0) uncertainty (real space) i0_real_error2.2750e+07
Rg (reciprocal space) rg_reciprocal52.69
I(0) (reciprocal space) i0_reciprocal1205000000.0000
Solution quality estimate total_estimate0.8672
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks0
Primary peak position r_peak_primary
Skewness Skewness skewness0.277
Kurtosis Kurtosis kurtosis-0.564
Angular range angular_range— – 0.1500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha143000000.0000
Real-space data points n_real_points31
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.917; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.519

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 12 domains

CATH v4.4 (12 domains)

Domain ID domain_id4dblA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3470 — ABC transporter involved in vitamin B12 uptake, BtuC
Homologous superfamily homologous superfamily10 — ABC transporter involved in vitamin B12 uptake, BtuC
Domain ID domain_id4dblB00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3470 — ABC transporter involved in vitamin B12 uptake, BtuC
Homologous superfamily homologous superfamily10 — ABC transporter involved in vitamin B12 uptake, BtuC
Domain ID domain_id4dblC00
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_id4dblD00
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_id4dblE01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1980 — Nitrogenase molybdenum iron protein domain
Domain ID domain_id4dblE02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1980 — Nitrogenase molybdenum iron protein domain
Domain ID domain_id4dblF00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3470 — ABC transporter involved in vitamin B12 uptake, BtuC
Homologous superfamily homologous superfamily10 — ABC transporter involved in vitamin B12 uptake, BtuC
Domain ID domain_id4dblG00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology3470 — ABC transporter involved in vitamin B12 uptake, BtuC
Homologous superfamily homologous superfamily10 — ABC transporter involved in vitamin B12 uptake, BtuC
Domain ID domain_id4dblH00
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_id4dblI00
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_id4dblJ01
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1980 — Nitrogenase molybdenum iron protein domain
Domain ID domain_id4dblJ02
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily1980 — Nitrogenase molybdenum iron protein domain

8. Citations (1)

9. Files and Curves (10)