CARM1 in complex with EML981. Determined by X-ray diffraction at 2.19 Å resolution. Released 6 Apr 2022.
Explore 7PUC in 3D Show helices and sheets RCSB PDB PDBe
7PUC contains 66 α-helices and 86 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 | 137-140 | 4 | |
| α-helix | 144-154 | 11 | |
| α-helix | 157-164 | 8 | |
| α-helix | 167-178 | 12 | |
| α-helix | 181-183 | 3 | |
| β-strand | 188-192 | 5 | 1 |
| α-helix | 198-205 | 8 | |
| β-strand | 210-215 | 6 | 1 |
| α-helix | 219-229 | 11 | |
| β-strand | 236-240 | 5 | 1 |
| β-strand | 252-257 | 6 | 1 |
| β-strand | 261 | 1 | 2 |
| β-strand | 264 | 1 | 2 |
| α-helix | 269-275 | 7 | |
| α-helix | 276-279 | 4 | |
| β-strand | 280-287 | 8 | 1 |
| β-strand | 290-298 | 9 | 3 |
| α-helix | 301-311 | 11 | |
| α-helix | 312-314 | 3 | |
| β-strand | 319 | 1 | 4 |
| β-strand | 322 | 1 | 4 |
| α-helix | 325-327 | 3 | |
| α-helix | 328-337 | 10 | |
| α-helix | 339 | 1 | |
| β-strand | 340-342 | 3 | 3 |
| α-helix | 346-348 | 3 | |
| β-strand | 349 | 1 | 3 |
| β-strand | 354-359 | 6 | 3 |
| α-helix | 365-368 | 4 | |
| β-strand | 370-378 | 9 | 5 |
| β-strand | 383-397 | 15 | 3 |
| β-strand | 402-406 | 5 | 3 |
| β-strand | 418-429 | 12 | 3 |
| β-strand | 434-443 | 10 | 5 |
| β-strand | 449-457 | 9 | 5 |
| β-strand | 463-469 | 7 | 5 |
| β-strand | 474-475 | 2 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 137-140 | 4 | |
| α-helix | 144-154 | 11 | |
| α-helix | 157-164 | 8 | |
| α-helix | 167-178 | 12 | |
| α-helix | 181-183 | 3 | |
| β-strand | 188-192 | 5 | 6 |
| α-helix | 198-205 | 8 | |
| β-strand | 210-215 | 6 | 6 |
| α-helix | 219-229 | 11 | |
| β-strand | 236-240 | 5 | 6 |
| β-strand | 252-257 | 6 | 6 |
| β-strand | 261 | 1 | 7 |
| β-strand | 264 | 1 | 7 |
| α-helix | 269-275 | 7 | |
| α-helix | 276-279 | 4 | |
| β-strand | 280-287 | 8 | 6 |
| β-strand | 290-298 | 9 | 8 |
| α-helix | 301-311 | 11 | |
| α-helix | 312-315 | 4 | |
| β-strand | 319 | 1 | 9 |
| β-strand | 322 | 1 | 9 |
| α-helix | 325-327 | 3 | |
| α-helix | 328-337 | 10 | |
| α-helix | 339 | 1 | |
| β-strand | 340-342 | 3 | 8 |
| α-helix | 346-348 | 3 | |
| β-strand | 349 | 1 | 8 |
| α-helix | 352-353 | 2 | |
| β-strand | 354-359 | 6 | 8 |
| α-helix | 365-368 | 4 | |
| β-strand | 370-378 | 9 | 10 |
| β-strand | 383-397 | 15 | 8 |
| β-strand | 402-406 | 5 | 8 |
| β-strand | 418-429 | 12 | 8 |
| β-strand | 434-443 | 10 | 10 |
| β-strand | 449-457 | 9 | 10 |
| β-strand | 462-469 | 8 | 10 |
| β-strand | 474-475 | 2 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 137-140 | 4 | |
| α-helix | 144-154 | 11 | |
| α-helix | 157-164 | 8 | |
| α-helix | 167-178 | 12 | |
| α-helix | 181-183 | 3 | |
| β-strand | 188-192 | 5 | 11 |
| α-helix | 198-205 | 8 | |
| β-strand | 210-215 | 6 | 11 |
| α-helix | 219-229 | 11 | |
| β-strand | 236-240 | 5 | 11 |
| β-strand | 252-257 | 6 | 11 |
| β-strand | 261 | 1 | 12 |
| β-strand | 264 | 1 | 12 |
| α-helix | 269-275 | 7 | |
| α-helix | 276-279 | 4 | |
| β-strand | 280-287 | 8 | 11 |
| β-strand | 290-298 | 9 | 13 |
| α-helix | 301-311 | 11 | |
| α-helix | 312-314 | 3 | |
| β-strand | 319 | 1 | 14 |
| β-strand | 322 | 1 | 14 |
| α-helix | 325-327 | 3 | |
| α-helix | 328-337 | 10 | |
| α-helix | 339 | 1 | |
| β-strand | 340-342 | 3 | 13 |
| α-helix | 346-348 | 3 | |
| β-strand | 349 | 1 | 13 |
| β-strand | 351 | 1 | 15 |
| β-strand | 354-359 | 6 | 13 |
| α-helix | 365-368 | 4 | |
| β-strand | 370-378 | 9 | 16 |
| β-strand | 379 | 1 | 15 |
| β-strand | 383-397 | 15 | 13 |
| β-strand | 402-406 | 5 | 13 |
| β-strand | 418-429 | 12 | 13 |
| β-strand | 434-443 | 10 | 16 |
| β-strand | 449-457 | 9 | 16 |
| β-strand | 463-469 | 7 | 16 |
| β-strand | 474-475 | 2 | 13 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone-arginine methyltransferase CARM1 | A, B, C, D | protein | 361 | Mus musculus | Q9WVG6 (AlphaFold model) |
>7PUC_1 Histone-arginine methyltransferase CARM1 (chains A, B, C, D) GHMGHTLERSVFSERTEESSAVQYFQFYGYLSQQQNMMQDYVRTGTYQRAILQNHTDFKD KIVLDVGCGSGILSFFAAQAGARKIYAVEASTMAQHAEVLVKSNNLTDRIVVIPGKVEEV SLPEQVDIIISEPMGYMLFNERMLESYLHAKKYLKPSGNMFPTIGDVHLAPFTDEQLYME QFTKANFWYQPSFHGVDLSALRGAAVDEYFRQPVVDTFDIRILMAKSVKYTVNFLEAKEG DLHRIEIPFKFHMLHSGLVHGLAFWFDVAFIGSIMTVWLSTAPTEPLTHWYQVRCLFQSP LFAKAGDTLSGTCLLIANKRQSYDISIVAQVDQTGSKSSNLLDLKNPFFRYTGTTPSPPP G
| ID | Name | Formula | Copies |
|---|---|---|---|
| 85U | methyl 6-[4-[[~{N}-[(~{E})-3-[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3… | C30 H36 N10 O7 | 4 |
Water and common crystallization additives (EDO) are not listed.
Turning Nonselective Inhibitors of Type I Protein Arginine Methyltransferases into Potent and Selective Inhibitors of Protein Arginine Methyltransferase 4 through a Deconstruction-Reconstruction and Fragment-Growing Approach. Iannelli, G., Milite, C., Marechal, N. et al. J Med Chem (2022) 65:11574-11606. DOI 10.1021/acs.jmedchem.2c00252 · PubMed
Other PDB entries of the same protein (UniProt Q9WVG6 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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