7apu

Structure of Adenylate kinase from Escherichia coli in complex with two ADP molecules refined at 1.36 A resolution.

Method: X-RAY DIFFRACTION Dmax: 83.9 Å Quality: GOOD

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

Adenylate kinase

Escherichia coli K-12

UniProt P69441

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–214 Not recorded ADP ADENOSINE-5'-DIPHOSPHATE × 2 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.6;291.15 K;AdK at 18.3 mg/ml was mixed with 5 mM each of AMP and GTP in 30 mM MOPS buffer pH 7, containing 50 mM NaCl. Hanging drop: 2 ul of AdK, preincubated with AMP and GTP, and 2 ul of precipitant buffer containing 30% PEG 4000, 0.2 M NH4CH3CO2 (Ammonium Acetate), buffered with 100 mM CH3COONa (Sodium Acetate) adjusted to pH 4.6. Resolution 1.36 Å R-free 0.206
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 1–214 Not recorded ADP ADENOSINE-5'-DIPHOSPHATE × 2 NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.6;291.15 K;AdK at 18.3 mg/ml was mixed with 5 mM each of AMP and GTP in 30 mM MOPS buffer pH 7, containing 50 mM NaCl. Hanging drop: 2 ul of AdK, preincubated with AMP and GTP, and 2 ul of precipitant buffer containing 30% PEG 4000, 0.2 M NH4CH3CO2 (Ammonium Acetate), buffered with 100 mM CH3COONa (Sodium Acetate) adjusted to pH 4.6. Resolution 1.36 Å R-free 0.206

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.

19 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name KAD_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–214; UniProt 1–214 Author chain B; PDBConstruct 1–214; UniProt 1–214

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 7apu

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7apu
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7apu
Deposition date deposition_date2020-10-19
Structure title titleStructure of Adenylate kinase from Escherichia coli in complex with two ADP molecules refined at 1.36 A resolution.
Keywords keywordsPHOSPHOTRANSFERASE, ADENYLATE KINASE, COMPLEX WITH TWO ADP, PROTEIN DYNAMICS, TRANSFERASE; TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.01
Radius of gyration Rg (electron density) rg_electron25.47
Forward intensity I(0) i042490500.00
Molecular weight molecular_weight48919.0 kDa
Excluded volume excluded_volume60669 ų
Envelope volume envelope_volume74844 ų
Hydration-shell volume shell_volume24906 ų
Envelope diameter envelope_diameter84.0
Shell Rg shell_rg32.20
Envelope Rg envelope_rg25.32
Shape Rg shape_rg25.47
Total Rg total_rg26.22
Total atoms total_atoms3422
Residues n_residues428
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 dmax83.9
Rg (real space) rg_real26.08
Rg uncertainty (real space) rg_real_error0.57
I(0) (real space) i0_real4.2490e+07
I(0) uncertainty (real space) i0_real_error6.1910e+05
Rg (reciprocal space) rg_reciprocal26.06
I(0) (reciprocal space) i0_reciprocal42490000.0000
Solution quality estimate total_estimate0.8855
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary24.8
Skewness Skewness skewness0.347
Kurtosis Kurtosis kurtosis-0.620
Angular range angular_range— – 0.3050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha9204000.0000
Real-space data points n_real_points62
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.871; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.925; Smooth: 0.968

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)