7qc9

HisF-C9A-D11E-V33A_L50H_I52H mutant in complex with Ni(II) from T. maritima

Method: X-RAY DIFFRACTION Dmax: 57.0 Å Quality: GOOD

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

Imidazole glycerol phosphate synthase subunit HisF

Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8)

UniProt Q9X0C6

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 2–253 Mutation:C9A, D11E, L50H, I52H NI NICKEL (II) ION × 1 SO4 SULFATE ION × 1 EDO 1,2-ETHANEDIOL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.3;292 K;100 mM TRIS, 23% PEG 3350 Resolution 1.80 Å R-free 0.189

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.

24 other PDB entries and 40 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name HIS6_THEMA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–253; UniProt 2–253

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 7qc9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7qc9
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id7qc9
Deposition date deposition_date2021-11-22
Structure title titleHisF-C9A-D11E-V33A_L50H_I52H mutant in complex with Ni(II) from T. maritima
Keywords keywordsBETA BARREL, ARTIFICIAL METALLOENZYME, PROTEIN DESIGN, OXIDOREDUCTASE, METAL BINDING PROTEIN; METAL BINDING PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.60
Radius of gyration Rg (electron density) rg_electron17.38
Forward intensity I(0) i012527700.00
Molecular weight molecular_weight26860.0 kDa
Excluded volume excluded_volume33872 ų
Envelope volume envelope_volume39175 ų
Hydration-shell volume shell_volume18515 ų
Envelope diameter envelope_diameter57.9
Shell Rg shell_rg23.96
Envelope Rg envelope_rg17.57
Shape Rg shape_rg17.37
Total Rg total_rg18.45
Total atoms total_atoms1888
Residues n_residues242
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 dmax57.0
Rg (real space) rg_real18.46
Rg uncertainty (real space) rg_real_error0.27
I(0) (real space) i0_real1.2530e+07
I(0) uncertainty (real space) i0_real_error1.4130e+05
Rg (reciprocal space) rg_reciprocal18.48
I(0) (reciprocal space) i0_reciprocal12530000.0000
Solution quality estimate total_estimate0.8185
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary23.4
Skewness Skewness skewness0.089
Kurtosis Kurtosis kurtosis-0.487
Angular range angular_range— – 0.4300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3475000.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.887; Stabil: 0.997; Sysdev: 1.000; Positv: 1.000; Valcen: 0.984; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)