RU486 bound to the progesterone receptor in a destabilized agonistic conformation. Determined by X-ray diffraction at 1.8 Å resolution. Released 28 Apr 2009.
Explore 2W8Y in 3D Show helices and sheets RCSB PDB PDBe
2W8Y contains 26 α-helices and 8 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 | 686-693 | 8 | |
| α-helix | 695-698 | 4 | |
| α-helix | 711-735 | 25 | |
| α-helix | 739-741 | 3 | |
| α-helix | 744-771 | 28 | |
| β-strand | 776-779 | 4 | 1 |
| β-strand | 782-784 | 3 | 1 |
| α-helix | 786-791 | 6 | |
| α-helix | 795-811 | 17 | |
| α-helix | 815-826 | 12 | |
| β-strand | 829-830 | 2 | 2 |
| α-helix | 838-857 | 20 | |
| α-helix | 863-896 | 34 | |
| α-helix | 898-901 | 4 | |
| α-helix | 907-921 | 15 | |
| β-strand | 926-927 | 2 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 686-693 | 8 | |
| α-helix | 696-698 | 3 | |
| α-helix | 708-709 | 2 | |
| α-helix | 711-735 | 25 | |
| α-helix | 739-741 | 3 | |
| α-helix | 744-771 | 28 | |
| β-strand | 776-779 | 4 | 3 |
| β-strand | 782-784 | 3 | 3 |
| α-helix | 786-788 | 3 | |
| α-helix | 792-801 | 10 | |
| α-helix | 803-811 | 9 | |
| α-helix | 815-826 | 12 | |
| β-strand | 829-831 | 3 | 4 |
| α-helix | 838-857 | 20 | |
| α-helix | 863-896 | 34 | |
| α-helix | 898-901 | 4 | |
| α-helix | 907-921 | 15 | |
| β-strand | 925-927 | 3 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Progesterone receptor | A, B | protein | 260 | HOMO SAPIENS | P06401 (AlphaFold model) |
>2W8Y_1 PROGESTERONE RECEPTOR (chains A, B) GSHMGQDIQLIPPLINLLMSIEPDVIYAGHDNTKPDTSSSLLTSLNQLGERQLLSVVKWS KSLPGFRNLHIDDQITLIQYSWMSLMVFGLGWRSYKHVSGQMLYFAPDLILNEQRMKESS FYSLCLTMWQIPQEFVKLQVSQEEFLCMKVLLLLNTIPLEGLRSQTQFEEMRSSYIRELI KAIGLRQKGVVSSSQRFYQLTKLLDNLHDLVKQLHLYCLNTFIQSRALSVEFPEMMSEVI AAQLPKILAGMVKPLLFHKK
| ID | Name | Formula | Copies |
|---|---|---|---|
| 486 | 11-(4-dimethylamino-phenyl)-17-hydroxy-13-methyl-17-prop-1-ynyl-1,2,6,7,8,11,12… | C29 H35 N O2 | 1 |
| NDR | Norethindrone | C20 H26 O2 | 1 |
Water and common crystallization additives (SO4, EDO) are not listed.
The X-Ray Structure of Ru486 Bound to the Progesterone Receptor in a Destabilized Agonistic Conformation. Raaijmakers, H.C.A., Versteegh, J., Uitdehaag, J.C.M. J Biol Chem (2009) 284:19572. DOI 10.1074/JBC.M109.007872 · PubMed
Other PDB entries of the same protein (UniProt P06401 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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