Crystal structure of MYST acetyltransferase domain in complex with inhibitor 92. Determined by X-ray diffraction at 2.0 Å resolution. Released 1 Apr 2020.
Explore 6OWH in 3D Show helices and sheets RCSB PDB PDBe
6OWH contains 13 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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 511-514 | 4 | 1 |
| β-strand | 517-520 | 4 | 1 |
| α-helix | 529-532 | 4 | |
| β-strand | 537-539 | 3 | 1 |
| β-strand | 546-547 | 2 | 1 |
| α-helix | 550-559 | 10 | |
| β-strand | 568-573 | 6 | 2 |
| β-strand | 576-582 | 7 | 2 |
| α-helix | 587-598 | 12 | |
| β-strand | 613-622 | 10 | 2 |
| β-strand | 625-635 | 11 | 2 |
| β-strand | 642-644 | 3 | 3 |
| β-strand | 647-649 | 3 | 2 |
| α-helix | 651-653 | 3 | |
| α-helix | 658-672 | 15 | |
| β-strand | 677 | 1 | 4 |
| β-strand | 678-679 | 2 | 3 |
| α-helix | 680 | 1 | |
| α-helix | 682-684 | 3 | |
| α-helix | 685-705 | 21 | |
| α-helix | 712-719 | 8 | |
| β-strand | 721 | 1 | 4 |
| α-helix | 723-733 | 11 | |
| β-strand | 736-739 | 4 | 5 |
| β-strand | 742-745 | 4 | 5 |
| α-helix | 749-756 | 8 | |
| α-helix | 759-761 | 3 | |
| α-helix | 764-765 | 2 | |
| β-strand | 773 | 1 | 2 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone acetyltransferase KAT8 | A | protein | 273 | Homo sapiens | Q9H7Z6 (AlphaFold model) |
>6OWH_1 Histone acetyltransferase KAT8 (chains A) VKYVDKIHIGNYEIDAWYFSPFPEDYGKQPKLWLCEYCLKYMKYEKSYRFHLGQCQWRQP PGKEIYRKSNISVHEVDGKDHKIYCQNLCLLAKLFLDHKTLYFDVEPFVFYILTEVDRQG AHIVGYFSKEKESPDGNNVSCIMILPPYQRRGYGRFLIAFSYELSKLESTVGSPEKPLSD LGKLSYRSYWSWVLLENLRDFRGTLSIKDLSQMTSITQNDIISTLQSLNMVKYWKGQHVI CVTPKLVEEHLKSAQYKKPPITVDSVCLKWAPP
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 1 |
| NBJ | N'-[(2-fluorophenyl)sulfonyl]-3-iodobenzohydrazide | C13 H10 F I N2 O3 S | 1 |
Water and common crystallization additives (GOL, DMS) are not listed.
Discovery of Acylsulfonohydrazide-Derived Inhibitors of the Lysine Acetyltransferase, KAT6A, as Potent Senescence-Inducing Anti-Cancer Agents. Priebbenow, D.L., Leaver, D.J., Nguyen, N. et al. J Med Chem (2020) 63:4655-4684. DOI 10.1021/acs.jmedchem.9b02071 · 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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