Structure of SETD3 bound to SAH and unmodified actin. Determined by X-ray diffraction at 2.15 Å resolution. Released 27 Feb 2019.
Explore 6ICV in 3D Show helices and sheets RCSB PDB PDBe
6ICV contains 54 α-helices and 34 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 | 22-37 | 16 | |
| α-helix | 39-40 | 2 | |
| α-helix | 46-62 | 17 | |
| α-helix | 75-78 | 4 | |
| α-helix | 79-88 | 10 | |
| β-strand | 96-101 | 6 | 1 |
| β-strand | 105-110 | 6 | 1 |
| β-strand | 114 | 1 | 2 |
| β-strand | 119-124 | 6 | 3 |
| α-helix | 125-127 | 3 | |
| β-strand | 129-130 | 2 | 4 |
| α-helix | 131-135 | 5 | |
| α-helix | 140-145 | 6 | |
| α-helix | 147-151 | 5 | |
| α-helix | 153-165 | 13 | |
| α-helix | 173-176 | 4 | |
| α-helix | 186-188 | 3 | |
| α-helix | 191-195 | 5 | |
| α-helix | 202-226 | 25 | |
| α-helix | 228-230 | 3 | |
| α-helix | 234-236 | 3 | |
| α-helix | 241-254 | 14 | |
| β-strand | 256-259 | 4 | 4 |
| β-strand | 266-270 | 5 | 4 |
| α-helix | 274-276 | 3 | |
| β-strand | 278-279 | 2 | 5 |
| β-strand | 286-289 | 4 | 3 |
| β-strand | 294-298 | 5 | 3 |
| β-strand | 303 | 1 | 2 |
| β-strand | 308-309 | 2 | 1 |
| β-strand | 310-311 | 2 | 5 |
| α-helix | 318-325 | 8 | |
| β-strand | 336-342 | 7 | 6 |
| α-helix | 350-360 | 11 | |
| β-strand | 365-371 | 7 | 6 |
| α-helix | 379-388 | 10 | |
| α-helix | 392-399 | 8 | |
| α-helix | 404-409 | 6 | |
| α-helix | 420-438 | 19 | |
| α-helix | 445-454 | 10 | |
| β-strand | 458 | 1 | 7 |
| α-helix | 459-494 | 36 | |
| α-helix | 497-500 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 22-37 | 16 | |
| α-helix | 46-62 | 17 | |
| α-helix | 75-78 | 4 | |
| α-helix | 79-88 | 10 | |
| β-strand | 96-101 | 6 | 7 |
| β-strand | 105-110 | 6 | 7 |
| β-strand | 114 | 1 | 8 |
| β-strand | 119-124 | 6 | 9 |
| α-helix | 125-127 | 3 | |
| β-strand | 129-130 | 2 | 10 |
| α-helix | 131-135 | 5 | |
| α-helix | 140-145 | 6 | |
| α-helix | 147-151 | 5 | |
| α-helix | 153-165 | 13 | |
| α-helix | 173-176 | 4 | |
| α-helix | 186-188 | 3 | |
| α-helix | 191-195 | 5 | |
| α-helix | 202-226 | 25 | |
| α-helix | 228-230 | 3 | |
| α-helix | 234-236 | 3 | |
| α-helix | 241-254 | 14 | |
| β-strand | 256-259 | 4 | 10 |
| β-strand | 266-270 | 5 | 10 |
| α-helix | 274-276 | 3 | |
| α-helix | 277 | 1 | |
| β-strand | 278-279 | 2 | 11 |
| β-strand | 286-289 | 4 | 9 |
| β-strand | 294-298 | 5 | 9 |
| β-strand | 303 | 1 | 8 |
| β-strand | 308-309 | 2 | 7 |
| β-strand | 310-311 | 2 | 11 |
| α-helix | 318-325 | 8 | |
| β-strand | 336-342 | 7 | 12 |
| α-helix | 350-359 | 10 | |
| β-strand | 365-371 | 7 | 12 |
| α-helix | 379-388 | 10 | |
| α-helix | 392-399 | 8 | |
| α-helix | 404-409 | 6 | |
| α-helix | 420-438 | 19 | |
| α-helix | 445-454 | 10 | |
| β-strand | 458 | 1 | 1 |
| α-helix | 459-494 | 36 | |
| α-helix | 497-500 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 70 | 1 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase setd3 | A, B | protein | 504 | Homo sapiens | Q86TU7 (AlphaFold model) |
| Actin, cytoplasmic 1 | C, D | protein | 23 | Homo sapiens | P60709 (AlphaFold model) |
>6ICV_1 Histone-lysine N-methyltransferase setd3 (chains A, B) GMGKKSRVKTQKSGTGATATVSPKEILNLTSELLQKCSSPAPGPGKEWEEYVQIRTLVEK IRKKQKGLSVTFDGKREDYFPDLMKWASENGASVEGFEMVNFKEEGFGLRATRDIKAEEL FLWVPRKLLMTVESAKNSVLGPLYSQDRILQAMGNIALAFHLLCERASPNSFWQPYIQTL PSEYDTPLYFEEDEVRYLQSTQAIHDVFSQYKNTARQYAYFYKVIQTHPHANKLPLKDSF TYEDYRWAVSSVMTRQNQIPTEDGSRVTLALIPLWDMCNHTNGLITTGYNLEDDRCECVA LQDFRAGEQIYIFYGTRSNAEFVIHSGFFFDNNSHDRVKIKLGVSKSDRLYAMKAEVLAR AGIPTSSVFALHFTEPPISAQLLAFLRVFCMTEEELKEHLLGDSAIDRIFTLGNSEFPVS WDNEVKLWTFLEDRASLLLKTYKTTIEEDKSVLKNHDLSVRAKMAIKLRLGEKEILEKAV KSAAVNREYYRQQMEEKAPLPKYE
>6ICV_2 Actin, cytoplasmic 1 (chains C, D) TLKYPIEHGIVTNWDDMEKIWHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| SAH | S-adenosyl-L-homocysteine | C14 H20 N6 O5 S | 2 |
Structural insights into SETD3-mediated histidine methylation on beta-actin. Guo, Q., Liao, S., Kwiatkowski, S. et al. Elife (2019) 8. DOI 10.7554/eLife.43676 · PubMed
Other PDB entries of the same protein (UniProt Q86TU7 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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