2qi9

ABC-transporter BtuCD in complex with its periplasmic binding protein BtuF

Method: X-RAY DIFFRACTION Dmax: 130.1 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 Non-standard monomer:Yes (specific site not provided by mmCIF) Vitamin B12 import ATP-binding protein btuD × 2 (P06611) Vitamin B12-binding protein btuF × 1 (P37028) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 1PE PENTAETHYLENE GLYCOL × 2 PEG DI(HYDROXYETHYL)ETHER × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.4;293 K;30-38% (w/v) polyethylene glycol 400, 50mM either of Tris‑HCl pH 8.4 or Glycine-NaOH pH 9.4 and 400mM (NH4)2SO4., VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 2.60 Å R-free 0.280

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 5 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 1–326; UniProt 1–326 Author chain B; PDBConstruct 1–326; 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 Non-standard monomer:Yes (specific site not provided by mmCIF) Vitamin B12 import system permease protein btuC × 2 (P06609) Vitamin B12-binding protein btuF × 1 (P37028) PO4 PHOSPHATE ION × 2 SO4 SULFATE ION × 6 1PE PENTAETHYLENE GLYCOL × 2 PEG DI(HYDROXYETHYL)ETHER × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.4;293 K;30-38% (w/v) polyethylene glycol 400, 50mM either of Tris‑HCl pH 8.4 or Glycine-NaOH pH 9.4 and 400mM (NH4)2SO4., VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 2.60 Å R-free 0.280

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 5 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

Vitamin B12-binding protein btuF

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 F; UniProt 22–266 Non-standard monomer:Yes (specific site not provided by mmCIF) 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 1PE PENTAETHYLENE GLYCOL × 2 PEG DI(HYDROXYETHYL)ETHER × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.4;293 K;30-38% (w/v) polyethylene glycol 400, 50mM either of Tris‑HCl pH 8.4 or Glycine-NaOH pH 9.4 and 400mM (NH4)2SO4., VAPOR DIFFUSION, SITTING DROP, temperature 293K Resolution 2.60 Å R-free 0.280

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 25 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 F; PDBConstruct 1–245; 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 2qi9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2qi9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2qi9
Deposition date deposition_date2007-07-03
Structure title titleABC-transporter BtuCD in complex with its periplasmic binding protein BtuF
Keywords keywordsInner membrane, Membrane, Transmembrane, Transport, ATP-binding, Hydrolase, Nucleotide-binding, Periplasm, 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_guinier38.28
Radius of gyration Rg (electron density) rg_electron37.63
Forward intensity I(0) i0343347000.00
Molecular weight molecular_weight153710.0 kDa
Excluded volume excluded_volume193400 ų
Envelope volume envelope_volume242710 ų
Hydration-shell volume shell_volume54384 ų
Envelope diameter envelope_diameter131.2
Shell Rg shell_rg43.34
Envelope Rg envelope_rg37.29
Shape Rg shape_rg37.65
Total Rg total_rg37.89
Total atoms total_atoms10676
Residues n_residues1349
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 dmax130.1
Rg (real space) rg_real38.41
Rg uncertainty (real space) rg_real_error1.25
I(0) (real space) i0_real3.4330e+08
I(0) uncertainty (real space) i0_real_error6.3430e+06
Rg (reciprocal space) rg_reciprocal38.34
I(0) (reciprocal space) i0_reciprocal343300000.0000
Solution quality estimate total_estimate0.8715
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary41.2
Skewness Skewness skewness0.412
Kurtosis Kurtosis kurtosis-0.399
Angular range angular_range— – 0.2050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha75510000.0000
Real-space data points n_real_points42
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.835; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.968; Smooth: 0.854

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

7. Fold Classification (SCOP + CATH) 11 domains

SCOP 2.08 (5 domains)

Domain ID domain_idd2qi9a_
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.22 — ABC transporter involved in vitamin B12 uptake, BtuC
Superfamily Superfamily superfamilyf.22.1 — ABC transporter involved in vitamin B12 uptake, BtuC
Family Family familyf.22.1.1 — ABC transporter involved in vitamin B12 uptake, BtuC
Domain ID domain_idd2qi9b_
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.22 — ABC transporter involved in vitamin B12 uptake, BtuC
Superfamily Superfamily superfamilyf.22.1 — ABC transporter involved in vitamin B12 uptake, BtuC
Family Family familyf.22.1.1 — ABC transporter involved in vitamin B12 uptake, BtuC
Domain ID domain_idd2qi9c_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.37 — P-loop containing nucleoside triphosphate hydrolases
Superfamily Superfamily superfamilyc.37.1 — P-loop containing nucleoside triphosphate hydrolases
Family Family familyc.37.1.12 — ABC transporter ATPase domain-like
Domain ID domain_idd2qi9d_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.37 — P-loop containing nucleoside triphosphate hydrolases
Superfamily Superfamily superfamilyc.37.1 — P-loop containing nucleoside triphosphate hydrolases
Family Family familyc.37.1.12 — ABC transporter ATPase domain-like
Domain ID domain_idd2qi9f_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.92 — Chelatase-like
Superfamily Superfamily superfamilyc.92.2 — 'Helical backbone' metal receptor
Family Family familyc.92.2.2 — TroA-like

CATH v4.4 (6 domains)

Domain ID domain_id2qi9A00
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_id2qi9B00
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_id2qi9C00
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_id2qi9D00
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_id2qi9F01
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_id2qi9F02
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)