3gd7

Crystal structure of human NBD2 complexed with N6-Phenylethyl-ATP (P-ATP)

Method: X-RAY DIFFRACTION Dmax: 123.3 Å Quality: GOOD

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

;Fusion complex of Cystic fibrosis transmembrane conductance regulator, residues 1193-1427 and Maltose/maltodextrin import ATP-binding protein malK, residues 219-371 ;

Escherichia coli K-12

UniProt P13569

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 1193–1427 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
2 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1193–1427 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
3 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 1193–1427 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
4 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 1193–1427 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
5 Insufficient information Homooligomer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 1193–1427 Chain B; UniProt 1193–1427 Chain C; UniProt 1193–1427 Chain D; UniProt 1193–1427 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308

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.

52 other PDB entries and 66 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CFTR_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–237; UniProt 1193–1427 Author chain B; PDBConstruct 3–237; UniProt 1193–1427 Author chain C; PDBConstruct 3–237; UniProt 1193–1427 Author chain D; PDBConstruct 3–237; UniProt 1193–1427

;Fusion complex of Cystic fibrosis transmembrane conductance regulator, residues 1193-1427 and Maltose/maltodextrin import ATP-binding protein malK, residues 219-371 ;

Escherichia coli K-12

UniProt P68187

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 219–371 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
2 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 219–371 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
3 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 219–371 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
4 Insufficient information Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 219–371 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308
5 Insufficient information Homooligomer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 219–371 Chain B; UniProt 219–371 Chain C; UniProt 219–371 Chain D; UniProt 219–371 Mutation:Q1280E, Y1307N, E1308A, Q1309A, W1310H, H1402A, Q1411D B44 N-(2-phenylethyl)adenosine 5'-(tetrahydrogen triphosphate) × 4 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;277 K;1.1-1.25 M tri-sodium citrate, pH 5.5-8, sitting drop, temperature 277K, VAPOR DIFFUSION Resolution 2.70 Å R-free 0.308

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.

13 other PDB entries and 19 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MALK_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 238–390; UniProt 219–371 Author chain B; PDBConstruct 238–390; UniProt 219–371 Author chain C; PDBConstruct 238–390; UniProt 219–371 Author chain D; PDBConstruct 238–390; UniProt 219–371

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 3gd7

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3gd7
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3gd7
Deposition date deposition_date2009-02-23
Structure title titleCrystal structure of human NBD2 complexed with N6-Phenylethyl-ATP (P-ATP)
Keywords keywords;CFTR, ABC transporter, nucleotide binding domain, NBD, ATP, P-ATP, N6-Phenylethyl-ATP, ATP-binding, Chloride channel, Ion transport, Ionic channel, Transport, Cell inner membrane, Cell membrane, Hydrolase, Sugar transport ;; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier38.22
Radius of gyration Rg (electron density) rg_electron37.61
Forward intensity I(0) i0412184000.00
Molecular weight molecular_weight164540.0 kDa
Excluded volume excluded_volume206080 ų
Envelope volume envelope_volume286290 ų
Hydration-shell volume shell_volume63481 ų
Envelope diameter envelope_diameter123.9
Shell Rg shell_rg43.90
Envelope Rg envelope_rg36.64
Shape Rg shape_rg37.63
Total Rg total_rg37.93
Total atoms total_atoms11580
Residues n_residues1506
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 dmax123.3
Rg (real space) rg_real38.11
Rg uncertainty (real space) rg_real_error0.94
I(0) (real space) i0_real4.1220e+08
I(0) uncertainty (real space) i0_real_error6.9930e+06
Rg (reciprocal space) rg_reciprocal38.18
I(0) (reciprocal space) i0_reciprocal412200000.0000
Solution quality estimate total_estimate0.8740
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary48.1
Skewness Skewness skewness0.297
Kurtosis Kurtosis kurtosis-0.286
Angular range angular_range— – 0.2050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha46790000.0000
Real-space data points n_real_points42
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.851; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.989; Smooth: 0.814

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 12 domains

CATH v4.4 (12 domains)

Domain ID domain_id3gd7A01
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_id3gd7A02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily100 — RNA polymerase II/Efflux pump adaptor protein, barrel-sandwich hybrid domain
Domain ID domain_id3gd7A03
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily140 — Nucleic acid-binding proteins
Domain ID domain_id3gd7B01
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_id3gd7B02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily100 — RNA polymerase II/Efflux pump adaptor protein, barrel-sandwich hybrid domain
Domain ID domain_id3gd7B03
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily140 — Nucleic acid-binding proteins
Domain ID domain_id3gd7C01
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_id3gd7C02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily100 — RNA polymerase II/Efflux pump adaptor protein, barrel-sandwich hybrid domain
Domain ID domain_id3gd7C03
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily140 — Nucleic acid-binding proteins
Domain ID domain_id3gd7D01
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_id3gd7D02
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily100 — RNA polymerase II/Efflux pump adaptor protein, barrel-sandwich hybrid domain
Domain ID domain_id3gd7D03
Class class2 — Mainly Beta
Architecture architecture40 — Beta Barrel
Topology topology50 — OB fold (Dihydrolipoamide Acetyltransferase, E2P)
Homologous superfamily homologous superfamily140 — Nucleic acid-binding proteins

8. Citations (1)

9. Files and Curves (10)