6owi

Crystal structure of MYST acetyltransferase domain in complex with inhibitor 85

Method: X-RAY DIFFRACTION Dmax: 79.9 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 176–448 Mutation:A142S, L145M, T146I, K157R Non-standard monomer:Yes (specific site not provided by mmCIF) ZN ZINC ION × 1 NB7 N'-[(2-fluorophenyl)sulfonyl]benzohydrazide × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;292 K;20% PEG3350, 2% Tacsimate pH 7.0, 0.1 M HEPES pH 7.0 Resolution 1.75 Å R-free 0.235

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 1–273; UniProt 176–448

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 6owi

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6owi
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6owi
Deposition date deposition_date2019-05-09
Structure title titleCrystal structure of MYST acetyltransferase domain in complex with inhibitor 85
Keywords keywordsInhibitor, Complex, MYST, TRANSFERASE, TRANSFERASE-TRANSERASE INHIBITOR complex; TRANSFERASE/TRANSERASE INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier21.22
Radius of gyration Rg (electron density) rg_electron20.40
Forward intensity I(0) i016630100.00
Molecular weight molecular_weight31995.0 kDa
Excluded volume excluded_volume40519 ų
Envelope volume envelope_volume46721 ų
Hydration-shell volume shell_volume19904 ų
Envelope diameter envelope_diameter80.7
Shell Rg shell_rg26.49
Envelope Rg envelope_rg20.83
Shape Rg shape_rg20.37
Total Rg total_rg21.39
Total atoms total_atoms2255
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 dmax79.9
Rg (real space) rg_real21.28
Rg uncertainty (real space) rg_real_error0.79
I(0) (real space) i0_real1.6630e+07
I(0) uncertainty (real space) i0_real_error2.4360e+05
Rg (reciprocal space) rg_reciprocal21.27
I(0) (reciprocal space) i0_reciprocal16630000.0000
Solution quality estimate total_estimate0.8038
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.7
Skewness Skewness skewness0.485
Kurtosis Kurtosis kurtosis-0.039
Angular range angular_range— – 0.3750 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha4197000.0000
Real-space data points n_real_points69
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.543; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.817; Smooth: 0.999

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 1 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd6owia_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.108 — Acyl-CoA N-acyltransferases (Nat)
Superfamily Superfamily superfamilyd.108.1 — Acyl-CoA N-acyltransferases (Nat)
Family Family familyd.108.1.0 — automated matches

8. Citations (1)

9. Files and Curves (10)