1i5d

STRUCTURE OF CHEA DOMAIN P4 IN COMPLEX WITH TNP-ATP

Method: X-RAY DIFFRACTION Dmax: 62.0 Å Quality: GOOD

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 350–540 Fragment:DOMAIN P4 SO4 SULFATE ION × 2 128 SPIRO(2,4,6-TRINITROBENZENE[1,2A]-2O',3O'-METHYLENE-ADENINE-TRIPHOSPHATE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.7;298 K;sodium acetate 0.1 M Ammonium sulfate 1.9 M, pH 4.7. VAPOR DIFFUSION, HANGING DROP at 298 K Resolution 2.90 Å R-free 0.312

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 31 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 1–191; UniProt 350–540

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 1i5d

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1i5d
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1i5d
Deposition date deposition_date2001-02-26
Structure title titleSTRUCTURE OF CHEA DOMAIN P4 IN COMPLEX WITH TNP-ATP
Keywords keywordsbeta-alpha sandwich, SIGNALING PROTEIN, TRANSFERASE; SIGNALING PROTEIN, TRANSFERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.36
Radius of gyration Rg (electron density) rg_electron17.37
Forward intensity I(0) i09275740.00
Molecular weight molecular_weight21607.0 kDa
Excluded volume excluded_volume26764 ų
Envelope volume envelope_volume32490 ų
Hydration-shell volume shell_volume16050 ų
Envelope diameter envelope_diameter63.5
Shell Rg shell_rg23.07
Envelope Rg envelope_rg17.78
Shape Rg shape_rg17.38
Total Rg total_rg18.29
Total atoms total_atoms1511
Residues n_residues190
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 dmax62.0
Rg (real space) rg_real18.29
Rg uncertainty (real space) rg_real_error0.34
I(0) (real space) i0_real9.2760e+06
I(0) uncertainty (real space) i0_real_error1.0860e+05
Rg (reciprocal space) rg_reciprocal18.30
I(0) (reciprocal space) i0_reciprocal9276000.0000
Solution quality estimate total_estimate0.8744
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary61.1
Skewness Skewness skewness0.236
Kurtosis Kurtosis kurtosis-0.318
Angular range angular_range— – 0.4350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1830000.0000
Real-space data points n_real_points75
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.793; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.983

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1i5da_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.122 — ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
Superfamily Superfamily superfamilyd.122.1 — ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
Family Family familyd.122.1.3 — Histidine kinase

CATH v4.4 (1 domains)

Domain ID domain_id1i5dA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology565 — Heat Shock Protein 90
Homologous superfamily homologous superfamily10 — Histidine kinase-like ATPase, C-terminal domain

8. Citations (1)

9. Files and Curves (10)