Crystal structure of Lysine Specific Demethylase 1 (LSD1) with TAK-418 distomer, FAD-adduct. Determined by X-ray diffraction at 2.28 Å resolution. Released 12 Oct 2022.
Explore 7XW8 in 3D Show helices and sheets RCSB PDB PDBe
7XW8 contains 36 α-helices and 36 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 |
|---|---|---|---|
| α-helix | 172-180 | 9 | |
| α-helix | 190-195 | 6 | |
| α-helix | 197-200 | 4 | |
| α-helix | 204-223 | 20 | |
| β-strand | 227 | 1 | 1 |
| α-helix | 231-237 | 7 | |
| α-helix | 239 | 1 | |
| α-helix | 242-244 | 3 | |
| α-helix | 246-258 | 13 | |
| β-strand | 268 | 1 | 1 |
| α-helix | 272-274 | 3 | |
| β-strand | 280-284 | 5 | 2 |
| β-strand | 287 | 1 | 3 |
| α-helix | 288-299 | 12 | |
| β-strand | 303-307 | 5 | 2 |
| β-strand | 314 | 1 | 3 |
| β-strand | 319-322 | 4 | 4 |
| β-strand | 325-328 | 4 | 4 |
| β-strand | 333-334 | 2 | 5 |
| β-strand | 338 | 1 | 6 |
| α-helix | 342-349 | 8 | |
| β-strand | 353-355 | 3 | 5 |
| α-helix | 356-357 | 2 | |
| β-strand | 362-363 | 2 | 7 |
| α-helix | 368 | 1 | |
| β-strand | 369 | 1 | 7 |
| α-helix | 370-371 | 2 | |
| α-helix | 372-394 | 23 | |
| β-strand | 400-401 | 2 | 8 |
| β-strand | 404-405 | 2 | 8 |
| α-helix | 406 | 1 | |
| β-strand | 407 | 1 | 9 |
| α-helix | 408-457 | 50 | |
| α-helix | 476-485 | 10 | |
| α-helix | 487-511 | 25 | |
| α-helix | 515-517 | 3 | |
| α-helix | 523-540 | 18 | |
| α-helix | 544-546 | 3 | |
| β-strand | 547 | 1 | 10 |
| β-strand | 548 | 1 | 9 |
| α-helix | 556-558 | 3 | |
| α-helix | 559-560 | 2 | |
| β-strand | 561 | 1 | 6 |
| β-strand | 565-567 | 3 | 5 |
| α-helix | 573-579 | 7 | |
| β-strand | 583-585 | 3 | 2 |
| β-strand | 588-596 | 9 | 11 |
| β-strand | 599-606 | 8 | 11 |
| β-strand | 613-618 | 6 | 11 |
| β-strand | 620-623 | 4 | 2 |
| α-helix | 627-630 | 4 | |
| β-strand | 638-640 | 3 | 11 |
| α-helix | 642-644 | 3 | |
| α-helix | 645-653 | 9 | |
| β-strand | 655-656 | 2 | 12 |
| β-strand | 660-665 | 6 | 7 |
| β-strand | 677-680 | 4 | 7 |
| β-strand | 693-695 | 3 | 7 |
| β-strand | 702-707 | 6 | 7 |
| α-helix | 710-715 | 6 | |
| α-helix | 720-735 | 16 | |
| α-helix | 741-743 | 3 | |
| β-strand | 745-748 | 4 | 7 |
| β-strand | 762-763 | 2 | 12 |
| β-strand | 765 | 1 | 10 |
| α-helix | 771-777 | 7 | |
| α-helix | 778-779 | 2 | |
| β-strand | 780 | 1 | 2 |
| α-helix | 792-794 | 3 | |
| β-strand | 796-798 | 3 | 2 |
| α-helix | 801-803 | 3 | |
| α-helix | 811-830 | 20 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Lysine-specific histone demethylase 1A | A | protein | 665 | Homo sapiens | O60341 (AlphaFold model) |
>7XW8_1 Lysine-specific histone demethylase 1A (chains A) GGSSGVEGAAFQSRLPHDRMTSQEAACFPDIISGPQQTQKVFLFIRNRTLQLWLDNPKIQ LTFEATLQQLEAPYNSDTVLVHRVHSYLERHGLINFGIYKRIKPLPTKKTGKVIIIGSGV SGLAAARQLQSFGMDVTLLEARDRVGGRVATFRKGNYVADLGAMVVTGLGGNPMAVVSKQ VNMELAKIKQKCPLYEANGQAVPKEKDEMVEQEFNRLLEATSYLSHQLDFNVLNNKPVSL GQALEVVIQLQEKHVKDEQIEHWKKIVKTQEELKELLNKMVNLKEKIKELHQQYKEASEV KPPRDITAEFLVKSKHRDLTALCKEYDELAETQGKLEEKLQELEANPPSDVYLSSRDRQI LDWHFANLEFANATPLSTLSLKHWDQDDDFEFTGSHLTVRNGYSCVPVALAEGLDIKLNT AVRQVRYTASGCEVIAVNTRSTSQTFIYKCDAVLCTLPLGVLKQQPPAVQFVPPLPEWKT SAVQRMGFGNLNKVVLCFDRVFWDPSVNLFGHVGSTTASRGELFLFWNLYKAPILLALVA GEAAGIMENISDDVIVGRCLAILKGIFGSSAVPQPKETVVSRWRADPWARGSYSYVAAGS SGNDYDLMAQPITPGPSIPGAPQPIPRLFFAGEHTIRNYPATVHGALLSGLREAGRIADQ FLGAM
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 2 |
| I00 | ~{N}-(oxan-4-yl)-5-(3-oxidanylidenepropyl)thiophene-3-carboxamide | C13 H17 N O3 S | 1 |
| FA8 | [[(2R,3S,4S)-5-[(4AS)-7,8-dimethyl-2,4-dioxo-4A,5-dihydrobenzo[g]pteridin-10-yl… | C27 H35 N9 O15 P2 | 1 |
Water and common crystallization additives (GOL) are not listed.
Design, synthesis, and structure-activity relationship of TAK-418 and its derivatives as a novel series of LSD1 inhibitors with lowered risk of hematological side effects. Hattori, Y., Matsumoto, S., Morimoto, S. et al. Eur J Med Chem (2022) 239:114522-114522. DOI 10.1016/j.ejmech.2022.114522 · PubMed
Other PDB entries of the same protein (UniProt O60341 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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