Crystal Structure of SETDB1 Tudor domain in complex with UNC100016. Determined by X-ray diffraction at 1.27 Å resolution. Released 2 Oct 2024.
Explore 9CUX in 3D Show helices and sheets RCSB PDB PDBe
9CUX contains 6 α-helices and 19 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 | 191-192 | 2 | 1 |
| β-strand | 194-195 | 2 | 2 |
| β-strand | 198-199 | 2 | 2 |
| β-strand | 203-207 | 5 | 1 |
| β-strand | 213-224 | 12 | 1 |
| β-strand | 227-234 | 8 | 1 |
| β-strand | 239-243 | 5 | 1 |
| α-helix | 244-246 | 3 | |
| β-strand | 247-249 | 3 | 1 |
| α-helix | 252-254 | 3 | |
| β-strand | 263-270 | 8 | 3 |
| β-strand | 273-283 | 11 | 3 |
| β-strand | 293-297 | 5 | 3 |
| β-strand | 302-305 | 4 | 3 |
| α-helix | 307-309 | 3 | |
| β-strand | 310-312 | 3 | 3 |
| β-strand | 313 | 1 | 1 |
| α-helix | 320-323 | 4 | |
| α-helix | 327-339 | 13 | |
| β-strand | 353-358 | 6 | 4 |
| β-strand | 361-371 | 11 | 4 |
| β-strand | 374-379 | 6 | 4 |
| β-strand | 385-389 | 5 | 4 |
| β-strand | 395 | 1 | 4 |
| α-helix | 396-401 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase SETDB1 | A | protein | 225 | Homo sapiens | Q15047 (AlphaFold model) |
>9CUX_1 Histone-lysine N-methyltransferase SETDB1 (chains A) MHHHHHHSSGRENLYFQGDLIVSMRILGKKRTKTWHKGTLIAIQTVGPGKKYKVKFDNKG KSLLSGNHIAYDYHPPADKLYVGSRVVAKYKDGNQVWLYAGIVAETPNVKNKLRFLIFFD DGYASYVTQSELYPICRPLKKTWEDIEDISCRDFIEEYVTAYPNRPMVLLKSGQLIKTEW EGTWWKSRVEEVDGSLVRILFLDDKRCEWIYRGSTRLEPMFSMKT
| ID | Name | Formula | Copies |
|---|---|---|---|
| A1AZ5 | (2E)-N-(4-{[6-(dimethylamino)hexyl]amino}-2-{[5-(dimethylamino)pentyl]amino}qui… | C27 H45 N7 O | 1 |
Water and common crystallization additives (SO4, EDO, UNX) are not listed.
Potent and selective SETDB1 covalent negative allosteric modulator reduces methyltransferase activity in cells. Uguen, M., Shell, D.J., Silva, M. et al. Nat Commun (2025) 16:1905-1905. DOI 10.1038/s41467-025-57005-3 · PubMed
Other PDB entries of the same protein (UniProt Q15047 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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