8p59

Structure of the Histidine Kinase CheA ATP-Binding domain in complex with compound QUI-SV-333

Method: X-RAY DIFFRACTION Dmax: 78.1 Å Quality: EXCELLENT

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

Chemotaxis protein CheA

Thermotoga maritima

UniProt Q56310

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 355–540 Not recorded WZF 7-(2-phenylethoxy)quinazolin-2-amine × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5;294.15 K;PEG 8000 30% Ammonium acetate 0.6 M Sodium acetate 0.065 M ph 4.5 Resolution 1.80 Å R-free 0.230
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 355–540 Not recorded WZF 7-(2-phenylethoxy)quinazolin-2-amine × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5;294.15 K;PEG 8000 30% Ammonium acetate 0.6 M Sodium acetate 0.065 M ph 4.5 Resolution 1.80 Å R-free 0.230

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.

21 other PDB entries and 30 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CHEA_THEMA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–189; UniProt 355–540 Author chain B; PDBConstruct 4–189; UniProt 355–540

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 8p59

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8p59
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8p59
Deposition date deposition_date2023-05-23
最后修订 last_revision2024-06-12
Structure title titleStructure of the Histidine Kinase CheA ATP-Binding domain in complex with compound QUI-SV-333
Keywords keywordsinhibitor, Transferase, Signaling Protein; SIGNALING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier24.21
Radius of gyration Rg (electron density) rg_electron23.35
Forward intensity I(0) i024412600.00
Molecular weight molecular_weight38710.0 kDa
Excluded volume excluded_volume48891 ų
Envelope volume envelope_volume59308 ų
Hydration-shell volume shell_volume21583 ų
Envelope diameter envelope_diameter81.0
Shell Rg shell_rg29.92
Envelope Rg envelope_rg23.09
Shape Rg shape_rg23.34
Total Rg total_rg24.21
Total atoms total_atoms5518
Residues n_residues344
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 dmax78.1
Rg (real space) rg_real24.18
Rg uncertainty (real space) rg_real_error0.52
I(0) (real space) i0_real2.4410e+07
I(0) uncertainty (real space) i0_real_error3.3110e+05
Rg (reciprocal space) rg_reciprocal24.19
I(0) (reciprocal space) i0_reciprocal24410000.0000
Solution quality estimate total_estimate0.9064
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.9
Skewness Skewness skewness0.256
Kurtosis Kurtosis kurtosis-0.528
Angular range angular_range— – 0.3300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4059000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.936; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.974; Smooth: 0.996

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)