9oob

Crystal structure of MYST acetyltransferase domain in complex with inhibitor 8

Method: X-RAY DIFFRACTION Dmax: 75.8 Å Quality: GOOD

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

Histone acetyltransferase KAT8

Homo sapiens

UniProt Q9H7Z6

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 174–449 Mutation:A142S, L145M, T146I, K157R, S204W Non-standard monomer:Yes (specific site not provided by mmCIF) A1CDK 6-(azetidin-1-yl)-N-(2-ethoxy-6-methoxybenzene-1-sulfonyl)-4-fluoro-1-benzofuran-2-carboxamide × 1 ZN ZINC ION × 1 CL CHLORIDE ION × 3 NA SODIUM ION × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;294 K;0.1 M Tris pH 7.0, 0.25 M MgCl2, 8% PEG8K Resolution 1.83 Å R-free 0.208

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.

41 other PDB entries and 44 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name KAT8_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 20–295; UniProt 174–449

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 9oob

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9oob
Deposition date deposition_date2025-05-15
Structure title titleCrystal structure of MYST acetyltransferase domain in complex with inhibitor 8
Keywords keywordsAcetyltransferase, Inhibitor, Complex, TRANSFERASE, TRANSFERASE-INHIBITOR complex; TRANSFERASE/INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.21
Radius of gyration Rg (electron density) rg_electron20.54
Forward intensity I(0) i032394800.00
Molecular weight molecular_weight30003.0 kDa
Excluded volume excluded_volume29423 ų
Envelope volume envelope_volume47561 ų
Hydration-shell volume shell_volume20070 ų
Envelope diameter envelope_diameter81.5
Shell Rg shell_rg26.58
Envelope Rg envelope_rg21.09
Shape Rg shape_rg20.53
Total Rg total_rg21.20
Total atoms total_atoms2267
Residues n_residues268
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 dmax75.8
Rg (real space) rg_real21.29
Rg uncertainty (real space) rg_real_error0.66
I(0) (real space) i0_real3.2390e+07
I(0) uncertainty (real space) i0_real_error4.4180e+05
Rg (reciprocal space) rg_reciprocal21.28
I(0) (reciprocal space) i0_reciprocal32390000.0000
Solution quality estimate total_estimate0.7510
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary23.4
Skewness Skewness skewness0.537
Kurtosis Kurtosis kurtosis0.002
Angular range angular_range— – 0.3750 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6666000.0000
Real-space data points n_real_points69
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.626; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.884; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)