9OOA: MYST acetyltransferase domain

Crystal structure of MYST acetyltransferase domain in complex with inhibitor 7. Determined by X-ray diffraction at 1.39 Å resolution. Released 11 Feb 2026.

Method
X-ray diffraction
Resolution
1.39 Å
Organism
Homo sapiens
Chains
1
Atoms
2,549
Mol. weight
35.71 kDa
Ligands
ZN, A1CD4, A1CD3
Released
11 Feb 2026

Explore 9OOA in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

9OOA contains 12 α-helices and 16 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 12 helices, 16 β-strands

ElementResiduesLengthSheet
β-strand511-51441
β-strand517-52041
α-helix529-5324
β-strand537-53931
β-strand546-54721
α-helix550-55910
β-strand568-57362
β-strand576-58272
α-helix587-59812
β-strand613-62192
β-strand626-635102
β-strand642-64433
β-strand647-64932
α-helix651-6533
α-helix658-67215
β-strand67714
β-strand678-67923
α-helix6801
α-helix683-6842
α-helix685-70420
α-helix712-7198
β-strand72114
α-helix723-73210
β-strand736-73945
β-strand742-74545
α-helix749-7579
α-helix770-7723
β-strand77312

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone acetyltransferase KAT8Aprotein295Homo sapiensQ9H7Z6 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>9OOA_1 Histone acetyltransferase KAT8 (chains A)
MGSSHHHHHHSSGLVPRGSTKVKYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCL
KYMKYEKSYRFHLGQCQWRQPPGKEIYRKSNISVHEVDGKDHKIYCQNLCLLAKLFLDHK
TLYFDVEPFVFYILTEVDRQGAHIVGYFSKEKESPDGNNVSCIMILPPYQRRGYGRFLIA
FSYELSKLESTVGSPEKPLSDLGKLSYRSYWSSVLLENLRDFRGTLSIKDLSQMTSITQN
DIISTLQSLNMVKYWKGQHVICVTPKLVEEHLKSAQYKKPPITVDSVCLKWAPPK

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn1
A1CD4N-(cyclohexylsulfamoyl)-2-hydroxy-6-methoxy-4-[(1H-pyrazol-1-yl)methyl]benzene-…C18 H25 N5 O4 S1
A1CD3N-cyclohexyl-N'-{4-methoxy-6-[(1H-pyrazol-1-yl)methyl]-1,2-benzoxazol-3-yl}sulf…C18 H23 N5 O4 S1

Water and common crystallization additives (SO4, NA, CL, GOL) are not listed.

Primary citation

Biological Activity and Structural Biology of Current KAT6A Inhibitor Chemotypes. Suwandi, A., Jin, J., Zhao, Y. et al. J Med Chem (2026) 69:2082-2114. DOI 10.1021/acs.jmedchem.5c01426 · PubMed

Other PDB entries of the same protein (UniProt Q9H7Z6 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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