6qv0

Structure of ATP-bound outward-facing TM287/288 in complex with sybody Sb_TM35

Method: X-RAY DIFFRACTION Dmax: 195.3 Å Quality: GOOD

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

ABC transporter, ATP-binding protein

Thermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099)

UniProt Q9WYC3

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 2–577 Fragment:ABC transporter Mutation:D41A Uncharacterized ABC transporter ATP-binding protein TM_0288 × 1 (Q9WYC4) Sb_TM35 × 1 ATP ADENOSINE-5'-TRIPHOSPHATE × 2 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;0.1M Sodium acetate, 0.025M NaCl, 12% (w/v) PEG 6000 Resolution 3.12 Å R-free 0.264
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 2–577 Fragment:ABC transporter Mutation:D41A Uncharacterized ABC transporter ATP-binding protein TM_0288 × 1 (Q9WYC4) Sb_TM35 × 1 ATP ADENOSINE-5'-TRIPHOSPHATE × 2 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;0.1M Sodium acetate, 0.025M NaCl, 12% (w/v) PEG 6000 Resolution 3.12 Å R-free 0.264

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.

8 other PDB entries and 11 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q9WYC3_THEMA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 12–587; UniProt 2–577 Author chain C; PDBConstruct 12–587; UniProt 2–577

Uncharacterized ABC transporter ATP-binding protein TM_0288

Thermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099)

UniProt Q9WYC4

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 1–598 Fragment:ABC transporter Mutation:D65A, E517A ABC transporter, ATP-binding protein × 1 (Q9WYC3) Sb_TM35 × 1 ATP ADENOSINE-5'-TRIPHOSPHATE × 2 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;0.1M Sodium acetate, 0.025M NaCl, 12% (w/v) PEG 6000 Resolution 3.12 Å R-free 0.264
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain D; UniProt 1–598 Fragment:ABC transporter Mutation:D65A, E517A ABC transporter, ATP-binding protein × 1 (Q9WYC3) Sb_TM35 × 1 ATP ADENOSINE-5'-TRIPHOSPHATE × 2 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4.6;293 K;0.1M Sodium acetate, 0.025M NaCl, 12% (w/v) PEG 6000 Resolution 3.12 Å R-free 0.264

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.

9 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Y288_THEMA
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–598; UniProt 1–598 Author chain D; PDBConstruct 1–598; UniProt 1–598

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 6qv0

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6qv0
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id6qv0
Deposition date deposition_date2019-03-01
Structure title titleStructure of ATP-bound outward-facing TM287/288 in complex with sybody Sb_TM35
Keywords keywordsABC exporter, ABC transporter, Membrane Transporter, MEMBRANE PROTEIN, sybody, nanobody; MEMBRANE PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier59.92
Radius of gyration Rg (electron density) rg_electron59.48
Forward intensity I(0) i01047140000.00
Molecular weight molecular_weight285320.0 kDa
Excluded volume excluded_volume362650 ų
Envelope volume envelope_volume564580 ų
Hydration-shell volume shell_volume76593 ų
Envelope diameter envelope_diameter191.6
Shell Rg shell_rg67.38
Envelope Rg envelope_rg56.75
Shape Rg shape_rg59.50
Total Rg total_rg59.62
Total atoms total_atoms20086
Residues n_residues2529
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 dmax195.3
Rg (real space) rg_real59.78
Rg uncertainty (real space) rg_real_error2.39
I(0) (real space) i0_real1.0470e+09
I(0) uncertainty (real space) i0_real_error2.0460e+07
Rg (reciprocal space) rg_reciprocal59.99
I(0) (reciprocal space) i0_reciprocal1047000000.0000
Solution quality estimate total_estimate0.8037
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary97.6
Skewness Skewness skewness-0.021
Kurtosis Kurtosis kurtosis-0.868
Angular range angular_range— – 0.1300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha66010000.0000
Real-space data points n_real_points27
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.570; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.988; Smooth: 0.745

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id6qv0A02
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_id6qv0B02
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_id6qv0C02
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_id6qv0D02
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)