Crystal structure of human RIPK1 with Compound 22. Determined by X-ray diffraction at 2.32 Å resolution. Released 28 May 2025.
Explore 9MZY in 3D Show helices and sheets RCSB PDB PDBe
9MZY contains 37 α-helices and 20 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 | 9-10 | 2 | |
| β-strand | 11 | 1 | 1 |
| β-strand | 17-18 | 2 | 1 |
| β-strand | 31-36 | 6 | 1 |
| β-strand | 40-49 | 10 | 1 |
| α-helix | 57-68 | 12 | |
| β-strand | 75 | 1 | 2 |
| α-helix | 76-77 | 2 | |
| β-strand | 78-84 | 7 | 1 |
| β-strand | 87-92 | 6 | 1 |
| β-strand | 98-99 | 2 | 2 |
| α-helix | 100-104 | 5 | |
| α-helix | 109-111 | 3 | |
| α-helix | 112-131 | 20 | |
| α-helix | 141-143 | 3 | |
| β-strand | 144-146 | 3 | 2 |
| β-strand | 152-154 | 3 | 2 |
| α-helix | 163-169 | 7 | |
| α-helix | 190-192 | 3 | |
| α-helix | 204-205 | 2 | |
| α-helix | 207-223 | 17 | |
| α-helix | 234-242 | 9 | |
| α-helix | 249-251 | 3 | |
| α-helix | 258-267 | 10 | |
| α-helix | 272-274 | 3 | |
| α-helix | 276-277 | 2 | |
| α-helix | 278-288 | 11 | |
| α-helix | 289-293 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 9-10 | 2 | |
| β-strand | 11-12 | 2 | 3 |
| α-helix | 14-16 | 3 | |
| β-strand | 17-22 | 6 | 3 |
| β-strand | 31-36 | 6 | 3 |
| β-strand | 40-49 | 10 | 3 |
| α-helix | 57-68 | 12 | |
| β-strand | 75 | 1 | 4 |
| α-helix | 76-77 | 2 | |
| β-strand | 78-84 | 7 | 3 |
| β-strand | 87-92 | 6 | 3 |
| β-strand | 98-99 | 2 | 4 |
| α-helix | 100-104 | 5 | |
| α-helix | 109-111 | 3 | |
| α-helix | 112-131 | 20 | |
| α-helix | 141-143 | 3 | |
| β-strand | 144-146 | 3 | 4 |
| β-strand | 152-154 | 3 | 4 |
| α-helix | 163-169 | 7 | |
| α-helix | 195-197 | 3 | |
| α-helix | 204-205 | 2 | |
| α-helix | 207-223 | 17 | |
| α-helix | 234-242 | 9 | |
| α-helix | 249-251 | 3 | |
| α-helix | 258-267 | 10 | |
| α-helix | 272-274 | 3 | |
| α-helix | 276-277 | 2 | |
| α-helix | 278-288 | 11 | |
| α-helix | 289-293 | 5 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Receptor-interacting serine/threonine-protein kinase 1 | A, B | protein | 287 | Homo sapiens | Q13546 (AlphaFold model) |
>9MZY_1 Receptor-interacting serine/threonine-protein kinase 1 (chains A, B) NVIKMKSSDFLESAELDSGGFGKVSLAFHRTQGLMIMKTVYKGPNCIEHNEALLEEAKMM NRLRHSRVVKLLGVIIEEGKYSLVMEYMEKGNLMHVLKAEMSTPLSVKGRIILEIIEGMA YLHGKGVIHKDLKPENILVDNDFHIKIADLGLASFKMWSKLNNEEHNELREVDGTAKKNG GTLYYMAPEHLNDVNAKPTEKSDVYSFAVVLWAIFANKEPYENAIAEQQLIMAIKSGNRP DVDDITEYCPREIISLMKLCWEANPEARPTFPGIEEKFRPFYLSQLE
| ID | Name | Formula | Copies |
|---|---|---|---|
| A1BU6 | 1-[(2S,5S)-2,3-dihydro-2,5-methano-1,4-benzoxazepin-4(5H)-yl]-3,3-difluoro-2,2-… | C15 H17 F2 N O2 | 2 |
| GLY | Glycine | C2 H5 N O2 | 1 |
Water and common crystallization additives (IOD, CL) are not listed.
The Discovery of Bridged Benzoazepine Amides as Selective Allosteric Modulators of RIPK1. Chen, J.L., Methot, J.L., Mitcheltree, M.J. et al. ACS Med Chem Lett (2025) 16:811-818. DOI 10.1021/acsmedchemlett.5c00063 · PubMed
Other PDB entries of the same protein (UniProt Q13546 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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