9z2c

KHK Bound to GS-1291269

Method: X-RAY DIFFRACTION Dmax: 106.3 Å Quality: REASONABLE

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

Ketohexokinase

Homo sapiens

UniProt P50053

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 5–298 Chain B; UniProt 5–298 Not recorded A1C0H 3-amino-3-(4-{7,7-difluoro-2-[(2R)-2-(trifluoromethyl)azetidin-1-yl]-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl}phenyl)-1lambda~6~-thietane-1,1-dione × 2 FRU beta-D-fructofuranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;100 mM NaCitrate pH 4.5, 200 mM Ammonium Sulfate, 10-15% PEG 8000 Resolution 2.02 Å R-free 0.231

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.

29 other PDB entries and 31 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name KHK_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 20–313; UniProt 5–298 Author chain B; PDBConstruct 20–313; UniProt 5–298

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 9z2c

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9z2c
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9z2c
Deposition date deposition_date2025-11-04
Structure title titleKHK Bound to GS-1291269
Keywords keywordsInhibitor, Fructose, Metabolism, Phosphorylation, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR complex; TRANSFERASE/TRANSFERASE INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier29.26
Radius of gyration Rg (electron density) rg_electron29.10
Forward intensity I(0) i0138919000.00
Molecular weight molecular_weight61296.0 kDa
Excluded volume excluded_volume58554 ų
Envelope volume envelope_volume100040 ų
Hydration-shell volume shell_volume30100 ų
Envelope diameter envelope_diameter103.3
Shell Rg shell_rg34.94
Envelope Rg envelope_rg29.10
Shape Rg shape_rg29.14
Total Rg total_rg29.43
Total atoms total_atoms4628
Residues n_residues598
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 dmax106.3
Rg (real space) rg_real29.46
Rg uncertainty (real space) rg_real_error1.09
I(0) (real space) i0_real1.3890e+08
I(0) uncertainty (real space) i0_real_error2.4950e+06
Rg (reciprocal space) rg_reciprocal29.38
I(0) (reciprocal space) i0_reciprocal138900000.0000
Solution quality estimate total_estimate0.7197
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary27.6
Skewness Skewness skewness0.505
Kurtosis Kurtosis kurtosis-0.459
Angular range angular_range— – 0.2700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha28360000.0000
Real-space data points n_real_points55
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.544; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.719; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)