Rsk2 N-terminal Kinase in Complex with BI-D1870. Determined by X-ray diffraction at 2.55 Å resolution. Released 2 Sept 2015.
Explore 5D9K in 3D Show helices and sheets RCSB PDB PDBe
5D9K contains 30 α-helices and 24 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 | 65-67 | 3 | |
| β-strand | 68-76 | 9 | 1 |
| β-strand | 81-87 | 7 | 1 |
| β-strand | 89 | 1 | 2 |
| β-strand | 96-103 | 8 | 1 |
| α-helix | 109-124 | 16 | |
| β-strand | 130 | 1 | 3 |
| α-helix | 131-132 | 2 | |
| β-strand | 133-138 | 6 | 1 |
| β-strand | 142-147 | 6 | 1 |
| β-strand | 153-154 | 2 | 3 |
| α-helix | 155-162 | 8 | |
| α-helix | 167-186 | 20 | |
| β-strand | 190-191 | 2 | 4 |
| α-helix | 196-198 | 3 | |
| β-strand | 199-201 | 3 | 3 |
| β-strand | 207-209 | 3 | 3 |
| β-strand | 214-215 | 2 | 4 |
| α-helix | 232-234 | 3 | |
| α-helix | 237-240 | 4 | |
| α-helix | 247-263 | 17 | |
| α-helix | 273-282 | 10 | |
| α-helix | 283-285 | 3 | |
| α-helix | 293-302 | 10 | |
| α-helix | 318-322 | 5 | |
| α-helix | 325-327 | 3 | |
| α-helix | 332-336 | 5 | |
| α-helix | 341-342 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 65-67 | 3 | |
| β-strand | 68-76 | 9 | 5 |
| β-strand | 81-87 | 7 | 5 |
| β-strand | 90 | 1 | 2 |
| β-strand | 96-103 | 8 | 5 |
| α-helix | 111-124 | 14 | |
| β-strand | 130 | 1 | 6 |
| β-strand | 133-138 | 6 | 5 |
| β-strand | 142-147 | 6 | 5 |
| β-strand | 153-154 | 2 | 6 |
| α-helix | 155-162 | 8 | |
| α-helix | 167-186 | 20 | |
| β-strand | 189-191 | 3 | 7 |
| α-helix | 196-198 | 3 | |
| β-strand | 199-201 | 3 | 6 |
| β-strand | 207-209 | 3 | 6 |
| β-strand | 214-216 | 3 | 7 |
| α-helix | 232-234 | 3 | |
| α-helix | 237-240 | 4 | |
| α-helix | 247-263 | 17 | |
| α-helix | 273-282 | 10 | |
| α-helix | 293-302 | 10 | |
| α-helix | 318-322 | 5 | |
| α-helix | 325-327 | 3 | |
| α-helix | 332-336 | 5 | |
| α-helix | 341-342 | 2 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Ribosomal protein S6 kinase alpha-3 | A, B | protein | 330 | Homo sapiens | P51812 (AlphaFold model) |
>5D9K_1 Ribosomal protein S6 kinase alpha-3 (chains A, B) GPNPQTEEVSIKEIAITHHVKEGHEKADPSQFELLKVLGQGSFGKVFLVKKISGSDARQL YAMKVLKKATLKVRDRVRTKMERDILVEVNHPFIVKLHYAFQTEGKLYLILDFLRGGDLF TRLSKEVMFTEEDVKFYLAELALALDHLHSLGIIYRDLKPENILLDEEGHIKLTDFGLSK ESIDHEKKAYSFCGTVEYMAPEVVNRRGHTQSADWWSFGVLMFEMLTGTLPFQGKDRKET MTMILKAKLGMPQFLSPEAQSLLRMLFKRNPANRLGAGPDGVEEIKRHSFFSTIDWNKLY RREIHPPFKPATGRPEDTFYFDPEFTAKTP
| ID | Name | Formula | Copies |
|---|---|---|---|
| 584 | (7R)-2-[(3,5-difluoro-4-hydroxyphenyl)amino]-5,7-dimethyl-8-(3-methylbutyl)-7,8… | C19 H23 F2 N5 O2 | 2 |
Water and common crystallization additives (GOL) are not listed.
Discovery of Potent and Selective RSK Inhibitors as Biological Probes. Jain, R., Mathur, M., Lan, J. et al. J Med Chem (2015) 58:6766-6783. DOI 10.1021/acs.jmedchem.5b00450 · PubMed
Other PDB entries of the same protein (UniProt P51812 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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