Mutated human ADP-ribosyltransferase 2 (PARP2) catalytic domain bound to Olaparib (AZD2281). Determined by X-ray diffraction at 2.24 Å resolution. Released 1 May 2024.
Explore 8HLJ in 3D Show helices and sheets RCSB PDB PDBe
8HLJ contains 39 α-helices and 34 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 | 236-245 | 10 | |
| α-helix | 248-257 | 10 | |
| β-strand | 260 | 1 | 1 |
| α-helix | 267-269 | 3 | |
| α-helix | 272-290 | 19 | |
| α-helix | 296-308 | 13 | |
| β-strand | 311 | 1 | 1 |
| α-helix | 317-321 | 5 | |
| α-helix | 324-348 | 25 | |
| α-helix | 357-365 | 9 | |
| β-strand | 367-371 | 5 | 2 |
| α-helix | 372-373 | 2 | |
| α-helix | 377-388 | 12 | |
| β-strand | 398-409 | 12 | 2 |
| α-helix | 412-415 | 4 | |
| β-strand | 423-429 | 7 | 2 |
| α-helix | 432-434 | 3 | |
| α-helix | 435-441 | 7 | |
| α-helix | 445-447 | 3 | |
| α-helix | 452-454 | 3 | |
| β-strand | 461-463 | 3 | 3 |
| β-strand | 464 | 1 | 2 |
| α-helix | 467-471 | 5 | |
| α-helix | 472-474 | 3 | |
| β-strand | 482-491 | 10 | 2 |
| β-strand | 495-498 | 4 | 3 |
| β-strand | 514-517 | 4 | 3 |
| β-strand | 519-523 | 5 | 4 |
| β-strand | 529-531 | 3 | 2 |
| β-strand | 534-536 | 3 | 2 |
| α-helix | 540 | 1 | |
| β-strand | 541-543 | 3 | 4 |
| β-strand | 554-556 | 3 | 4 |
| β-strand | 558-561 | 4 | 3 |
| α-helix | 564-566 | 3 | |
| β-strand | 567-578 | 12 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 236-245 | 10 | |
| α-helix | 248-257 | 10 | |
| β-strand | 260 | 1 | 5 |
| α-helix | 267-269 | 3 | |
| α-helix | 272-290 | 19 | |
| α-helix | 296-308 | 13 | |
| β-strand | 311 | 1 | 5 |
| α-helix | 317-321 | 5 | |
| α-helix | 324-348 | 25 | |
| α-helix | 357-365 | 9 | |
| β-strand | 367-371 | 5 | 6 |
| α-helix | 377-388 | 12 | |
| β-strand | 397-409 | 13 | 6 |
| α-helix | 412-415 | 4 | |
| β-strand | 423-429 | 7 | 6 |
| α-helix | 432-434 | 3 | |
| α-helix | 435-441 | 7 | |
| α-helix | 445-447 | 3 | |
| α-helix | 452-454 | 3 | |
| β-strand | 461-463 | 3 | 7 |
| β-strand | 464 | 1 | 6 |
| α-helix | 467-471 | 5 | |
| α-helix | 472-474 | 3 | |
| β-strand | 482-491 | 10 | 6 |
| β-strand | 495-498 | 4 | 7 |
| α-helix | 505-508 | 4 | |
| β-strand | 514-517 | 4 | 7 |
| β-strand | 519-523 | 5 | 8 |
| α-helix | 525-527 | 3 | |
| β-strand | 529-531 | 3 | 6 |
| β-strand | 534-536 | 3 | 6 |
| α-helix | 540 | 1 | |
| β-strand | 541-543 | 3 | 8 |
| β-strand | 554-556 | 3 | 8 |
| β-strand | 558-561 | 4 | 7 |
| α-helix | 564-566 | 3 | |
| β-strand | 567-579 | 13 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Poly [ADP-ribose] polymerase 2 | A, B | protein | 353 | Homo sapiens | Q9UGN5 (AlphaFold model) |
>8HLJ_1 Poly [ADP-ribose] polymerase 2 (chains A, B) GPESQLDLRVQELIKLICNVQAMEEMMMEMKYNTKKAPLGKLTVAQIKAGYQSLKKIEDC IRAGQHGRALMEACNEFYTRIPHDFGLRTPPLIRTQKELSEKIQLLEALGDIEIAIKLVK SERQGLEHPLDQHYRNLHCALRPLDHESYEFKVISQYLQSTHAPTHSDYTMTLLDLFEVE KDGEKEAFREDLHNRMLLWHGSRMSNWVGILSHGLRIAPPEAPITGYMFGKGIYFADMSS KSANYCFASRLKNTGLLLLSEVALGQCNELLEANPKAEGLLQGKHSTKGLGKMAPSSAHF VTLNGSTVPLGPASDTGILNPDGYTLNYNEYIVYNPNQVRMRYLLKVQFNFLQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| 09L | 4-(3-{[4-(cyclopropylcarbonyl)piperazin-1-yl]carbonyl}-4-fluorobenzyl)phthalazi… | C24 H23 F N4 O3 | 2 |
Engaging an engineered PARP-2 catalytic domain mutant to solve the complex structures harboring approved drugs for structure analyses. Wang, X., Zhou, J., Xu, B. Bioorg Chem (2025) 160:108471-108471. DOI 10.1016/j.bioorg.2025.108471 · PubMed
Other PDB entries of the same protein (UniProt Q9UGN5 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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