Crystal structure of RIP1 kinase in complex with necrostatin-4. Determined by X-ray diffraction at 1.8 Å resolution. Released 13 Mar 2013.
Explore 4ITJ in 3D Show helices and sheets RCSB PDB PDBe
4ITJ contains 38 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 | 11-12 | 2 | 1 |
| α-helix | 14-16 | 3 | |
| β-strand | 17 | 1 | 1 |
| β-strand | 30-36 | 7 | 1 |
| β-strand | 40-49 | 10 | 1 |
| α-helix | 54-56 | 3 | |
| α-helix | 57-68 | 12 | |
| β-strand | 75 | 1 | 2 |
| β-strand | 78-84 | 7 | 1 |
| β-strand | 87-93 | 7 | 1 |
| β-strand | 99 | 1 | 2 |
| α-helix | 100-104 | 5 | |
| α-helix | 112-131 | 20 | |
| α-helix | 141-143 | 3 | |
| β-strand | 144-146 | 3 | 2 |
| β-strand | 152-154 | 3 | 2 |
| α-helix | 163-168 | 6 | |
| 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 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 11-12 | 2 | 3 |
| α-helix | 14-16 | 3 | |
| β-strand | 17-22 | 6 | 3 |
| α-helix | 23 | 1 | |
| β-strand | 30-36 | 7 | 3 |
| β-strand | 40-49 | 10 | 3 |
| α-helix | 54-56 | 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 | 99 | 1 | 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 | 163-170 | 8 | |
| α-helix | 190-192 | 3 | |
| α-helix | 195-197 | 3 | |
| α-helix | 207-223 | 17 | |
| α-helix | 234-243 | 10 | |
| 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 | 294 | Homo sapiens | Q13546 (AlphaFold model) |
>4ITJ_1 Receptor-interacting serine/threonine-protein kinase 1 (chains A, B) MQPDMSLNVIKMKSSDFLESAELDSGGFGKVSLAFHRTQGLMIMKTVYKGPNCIEHNEAL LEEAKMMNRLRHSRVVKLLGVIIEEGKYSLVMEYMEKGNLMHVLKAEMSTPLSVKGRIIL EIIEGMAYLHGKGVIHKDLKPENILVDNDFHIKIADLGLASFKMWSKLNNEEHNELREVD GTAKKNGGTLYYMAPEHLNDVNAKPTEKSDVYSFAVVLWAIFANKEPYENAIAEQQLIMA IKSGNRPDVDDITEYCPREIISLMKLCWEANPEARPTFPGIEEKFRPFYLSQLE
| ID | Name | Formula | Copies |
|---|---|---|---|
| 1HX | N-[(1S)-1-(2-chloro-6-fluorophenyl)ethyl]-5-cyano-1-methyl-1H-pyrrole-2-carboxa… | C15 H13 Cl F N3 O | 2 |
Water and common crystallization additives (IOD) are not listed.
Structural Basis of RIP1 Inhibition by Necrostatins. Xie, T., Peng, W., Liu, Y. et al. Structure (2013) 21:493-499. DOI 10.1016/j.str.2013.01.016 · 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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