Human LSD1 Histone Demethylase-CoREST in complex with an FAD- tranylcypromine adduct. Determined by X-ray diffraction at 2.74 Å resolution. Released 21 Aug 2007.
Explore 2UXX in 3D Show helices and sheets RCSB PDB PDBe
2UXX contains 41 α-helices and 40 β-strands across 2 chains. 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 | 173-180 | 8 | |
| α-helix | 190-195 | 6 | |
| α-helix | 197-201 | 5 | |
| α-helix | 204-223 | 20 | |
| β-strand | 227 | 1 | 1 |
| α-helix | 231-236 | 6 | |
| α-helix | 238-239 | 2 | |
| 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 | 342-348 | 7 | |
| 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 | 408-466 | 59 | |
| α-helix | 469 | 1 | |
| α-helix | 474-513 | 40 | |
| α-helix | 523-539 | 17 | |
| 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 | 573-578 | 6 | |
| β-strand | 583-585 | 3 | 2 |
| β-strand | 588-595 | 8 | 11 |
| β-strand | 600-606 | 7 | 11 |
| β-strand | 613-618 | 6 | 11 |
| β-strand | 620-623 | 4 | 2 |
| α-helix | 627-631 | 5 | |
| 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 |
| β-strand | 766 | 1 | 13 |
| β-strand | 768 | 1 | 13 |
| α-helix | 771-777 | 7 | |
| β-strand | 780 | 1 | 2 |
| α-helix | 782-784 | 3 | |
| α-helix | 792-794 | 3 | |
| β-strand | 796-798 | 3 | 2 |
| α-helix | 801-803 | 3 | |
| α-helix | 811-830 | 20 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 312 | 1 | 14 |
| β-strand | 314 | 1 | 14 |
| α-helix | 318-324 | 7 | |
| α-helix | 330-361 | 32 | |
| α-helix | 368-370 | 3 | |
| α-helix | 383-384 | 2 | |
| α-helix | 385-398 | 14 | |
| α-helix | 402-409 | 8 | |
| α-helix | 414-423 | 10 | |
| α-helix | 430-438 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Lysine-specific histone demethylase 1 | A | protein | 666 | HOMO SAPIENS | O60341 (AlphaFold model) |
| Rest corepressor 1 | B | protein | 235 | HOMO SAPIENS | Q9UKL0 (AlphaFold model) |
>2UXX_1 LYSINE-SPECIFIC HISTONE DEMETHYLASE 1 (chains A) PSGVEGAAFQSRLPHDRMTSQEAACFPDIISGPQQTQKVFLFIRNRTLQLWLDNPKIQLT FEATLQQLEAPYNSDTVLVHRVHSYLERHGLINFGIYKRIKPLPTKKTGKVIIIGSGVSG LAAARQLQSFGMDVTLLEARDRVGGRVATFRKGNYVADLGAMVVTGLGGNPMAVVSKQVN MELAKIKQKCPLYEANGQAVPKEKDEMVEQEFNRLLEATSYLSHQLDFNVLNNKPVSLGQ ALEVVIQLQEKHVKDEQIEHWKKIVKTQEELKELLNKMVNLKEKIKELHQQYKEASEVKP PRDITAEFLVKSKHRDLTALCKEYDELAETQGKLEEKLQELEANPPSDVYLSSRDRQILD WHFANLEFANATPLSTLSLKHWDQDDDFEFTGSHLTVRNGYSCVPVALAEGLDIKLNTAV RQVRYTASGCEVIAVNTRSTSQTFIYKCDAVLCTLPLGVLKQQPPAVQFVPPLPEWKTSA VQRMGFGNLNKVVLCFDRVFWDPSVNLFGHVGSTTASRGELFLFWNLYKAPILLALVAGE AAGIMENISDDVIVGRCLAILKGIFGSSAVPQPKETVVSRWRADPWARGSYSYVAAGSSG NDYDLMAQPITPGPSIPGAPQPIPRLFFAGEHTIRNYPATVHGALLSGLREAGRIADQFL GAMYTL
>2UXX_2 REST COREPRESSOR 1 (chains B) MGSSHHHHHHSSGLVPRGSHMASMTGGQQMGRGSEFGRPTETVPQVKKEKHSTQAKNRAK RKPPKGMFLSQEDVEAVSANATAATTVLRQLDMELVSVKRQIQNIKQTNSALKEKLDGGI EPYRLPEVIQKCNARWTTEEQLLAVQAIRKYGRDFQAISDVIGNKSVVQVKNFFVNYRRR FNIDEVLQEWEAEHGKEETNGPSNQKPVKSPDNSIKMPEEEDEAPVLDVRYASAS
| ID | Name | Formula | Copies |
|---|---|---|---|
| FAJ | FAD-trans-2-Phenylcyclopropylamine Adduct | C36 H43 N9 O16 P2 | 1 |
Water and common crystallization additives (GOL, CL) are not listed.
Structural Basis for the Inhibition of the Lsd1 Histone Demethylase by the Antidepressant Trans-2-Phenylcyclopropylamine. Yang, M., Culhane, J.C., Szewczuk, L.M. et al. Biochemistry (2007) 46:8058. DOI 10.1021/BI700664Y · 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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