Crystal structure of constitutively active PARP-2. Determined by X-ray diffraction at 2.7 Å resolution. Released 27 Jul 2016.
Explore 5DSY in 3D Show helices and sheets RCSB PDB PDBe
5DSY contains 49 α-helices and 59 β-strands across 4 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 | 223-232 | 10 | |
| α-helix | 344-350 | 7 | |
| β-strand | 354-358 | 5 | 1 |
| α-helix | 364-375 | 12 | |
| β-strand | 384-396 | 13 | 1 |
| α-helix | 399-402 | 4 | |
| β-strand | 410-416 | 7 | 1 |
| α-helix | 419-421 | 3 | |
| α-helix | 422-428 | 7 | |
| α-helix | 430-434 | 5 | |
| β-strand | 448-450 | 3 | 2 |
| β-strand | 451 | 1 | 1 |
| α-helix | 454-458 | 5 | |
| β-strand | 469-478 | 10 | 1 |
| β-strand | 482-485 | 4 | 2 |
| α-helix | 494-496 | 3 | |
| β-strand | 501-504 | 4 | 2 |
| β-strand | 506-510 | 5 | 3 |
| α-helix | 512-514 | 3 | |
| β-strand | 516-518 | 3 | 1 |
| β-strand | 521-523 | 3 | 1 |
| β-strand | 528-530 | 3 | 3 |
| α-helix | 539-540 | 2 | |
| β-strand | 541-543 | 3 | 3 |
| β-strand | 545-548 | 4 | 2 |
| α-helix | 551-553 | 3 | |
| β-strand | 554-566 | 13 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 223-232 | 10 | |
| α-helix | 344-350 | 7 | |
| β-strand | 354-358 | 5 | 4 |
| α-helix | 364-375 | 12 | |
| β-strand | 384-396 | 13 | 4 |
| α-helix | 399-402 | 4 | |
| β-strand | 410-416 | 7 | 4 |
| α-helix | 419-421 | 3 | |
| α-helix | 422-428 | 7 | |
| α-helix | 432-434 | 3 | |
| β-strand | 448-450 | 3 | 5 |
| β-strand | 451 | 1 | 4 |
| α-helix | 454-458 | 5 | |
| α-helix | 459-461 | 3 | |
| β-strand | 469-478 | 10 | 4 |
| β-strand | 482-485 | 4 | 5 |
| α-helix | 494-496 | 3 | |
| β-strand | 501-504 | 4 | 5 |
| β-strand | 508-510 | 3 | 6 |
| α-helix | 512-514 | 3 | |
| β-strand | 516-518 | 3 | 4 |
| β-strand | 521-523 | 3 | 4 |
| β-strand | 528-530 | 3 | 6 |
| β-strand | 543 | 1 | 6 |
| β-strand | 545-548 | 4 | 5 |
| α-helix | 551-553 | 3 | |
| β-strand | 554-566 | 13 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 223-233 | 11 | |
| α-helix | 344-350 | 7 | |
| β-strand | 354-358 | 5 | 7 |
| α-helix | 364-375 | 12 | |
| β-strand | 384-396 | 13 | 7 |
| α-helix | 399-402 | 4 | |
| β-strand | 410-416 | 7 | 7 |
| α-helix | 419-421 | 3 | |
| α-helix | 422-428 | 7 | |
| α-helix | 430-432 | 3 | |
| α-helix | 434 | 1 | |
| β-strand | 448-450 | 3 | 8 |
| β-strand | 451 | 1 | 7 |
| α-helix | 454-458 | 5 | |
| α-helix | 459-461 | 3 | |
| β-strand | 469-478 | 10 | 7 |
| β-strand | 482-485 | 4 | 8 |
| α-helix | 490-496 | 7 | |
| β-strand | 501-504 | 4 | 8 |
| β-strand | 506-510 | 5 | 6 |
| α-helix | 512-514 | 3 | |
| β-strand | 516-518 | 3 | 7 |
| β-strand | 521-523 | 3 | 7 |
| β-strand | 528-530 | 3 | 6 |
| β-strand | 541-543 | 3 | 6 |
| β-strand | 545-548 | 4 | 8 |
| α-helix | 551-553 | 3 | |
| β-strand | 554-566 | 13 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 223-232 | 10 | |
| α-helix | 344-350 | 7 | |
| β-strand | 354-359 | 6 | 9 |
| α-helix | 364-375 | 12 | |
| β-strand | 384-396 | 13 | 9 |
| α-helix | 399-402 | 4 | |
| β-strand | 410-416 | 7 | 9 |
| α-helix | 419-421 | 3 | |
| α-helix | 422-428 | 7 | |
| α-helix | 430-434 | 5 | |
| β-strand | 448-451 | 4 | 9 |
| α-helix | 454-458 | 5 | |
| α-helix | 459-461 | 3 | |
| β-strand | 469-478 | 10 | 9 |
| β-strand | 482-485 | 4 | 9 |
| α-helix | 494-496 | 3 | |
| β-strand | 501-504 | 4 | 9 |
| β-strand | 506-510 | 5 | 3 |
| α-helix | 512-514 | 3 | |
| β-strand | 516-518 | 3 | 9 |
| β-strand | 521-523 | 3 | 9 |
| β-strand | 528-530 | 3 | 3 |
| β-strand | 541-543 | 3 | 3 |
| β-strand | 545-548 | 4 | 9 |
| α-helix | 551-553 | 3 | |
| β-strand | 554-566 | 13 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Poly [ADP-ribose] polymerase 2 | A, B, C, D | protein | 280 | Homo sapiens | Q9UGN5 (AlphaFold model) |
>5DSY_1 Poly [ADP-ribose] polymerase 2 (chains A, B, C, D) MGSSHHHHHHSSGLVPRGSHPESQLDLRVQELIKLICNVQAMEEKTELQSPEHPLDQHYR NLHCALRPLDHESYEFKVISQYLQSTHAPTHSDYTMTLLDLFEVEKDGEKEAFREDLHNR MLLWHGSRMSNWVGILSHGLRIAPPEAPITGYMFGKGIYFADMSSKSANYCFASRLKNTG LLLLSEVALGQCNELLEANPKAEGLLQGKHSTKGLGKMAPSSAHFVTLNGSTVPLGPASD TGILNPDGYTLNYNEYIVYNPNQVRMRYLLKVQFNFLQLW
| ID | Name | Formula | Copies |
|---|---|---|---|
| UHB | 2-[4-[(2S,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]carbonyl… | C24 H27 N9 O6 | 4 |
PARP-1 Activation Requires Local Unfolding of an Autoinhibitory Domain. Dawicki-McKenna, J.M., Langelier, M.F., DeNizio, J.E. et al. Mol Cell (2015) 60:755-768. DOI 10.1016/j.molcel.2015.10.013 · 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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