Crystal structure of SETD2 bound to histone H3.3 K36M peptide. Determined by X-ray diffraction at 2.05 Å resolution. Released 2 Nov 2016.
Explore 5JJY in 3D Show helices and sheets RCSB PDB PDBe
5JJY contains 15 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 |
|---|---|---|---|
| β-strand | 1448-1450 | 3 | 1 |
| α-helix | 1451-1455 | 5 | |
| α-helix | 1457-1465 | 9 | |
| α-helix | 1470-1472 | 3 | |
| β-strand | 1474-1475 | 2 | 2 |
| β-strand | 1480-1481 | 2 | 3 |
| α-helix | 1501-1505 | 5 | |
| α-helix | 1506-1510 | 5 | |
| α-helix | 1513-1514 | 2 | |
| β-strand | 1515 | 1 | 4 |
| α-helix | 1521-1524 | 4 | |
| β-strand | 1527 | 1 | 5 |
| α-helix | 1536-1538 | 3 | |
| β-strand | 1539 | 1 | 4 |
| β-strand | 1552-1556 | 5 | 1 |
| β-strand | 1562-1566 | 5 | 1 |
| β-strand | 1570 | 1 | 6 |
| β-strand | 1575-1578 | 4 | 5 |
| β-strand | 1582-1584 | 3 | 3 |
| α-helix | 1586-1598 | 13 | |
| β-strand | 1606-1610 | 5 | 3 |
| β-strand | 1613-1616 | 4 | 3 |
| β-strand | 1620-1621 | 2 | 2 |
| α-helix | 1623-1626 | 4 | |
| α-helix | 1627 | 1 | |
| β-strand | 1628-1629 | 2 | 5 |
| β-strand | 1635-1642 | 8 | 5 |
| β-strand | 1645-1652 | 8 | 5 |
| β-strand | 1656 | 1 | 6 |
| α-helix | 1660 | 1 | |
| β-strand | 1661-1662 | 2 | 1 |
| β-strand | 1663-1664 | 2 | 5 |
| β-strand | 1669-1670 | 2 | 3 |
| α-helix | 1675-1676 | 2 | |
| β-strand | 1677 | 1 | 7 |
| α-helix | 1678 | 1 | |
| β-strand | 1688 | 1 | 7 |
| α-helix | 1697-1700 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 34-36 | 3 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase SETD2 | A | protein | 279 | Homo sapiens | Q9BYW2 (AlphaFold model) |
| Histone H3.3 | B | protein | 14 | Homo sapiens | P84243 (AlphaFold model) |
>5JJY_1 Histone-lysine N-methyltransferase SETD2 (chains A) SGETSVPPGSALVGPSCVMDDFRDPQRWKECAKQGKMPCYFDLIEENVYLTERKKNKSHR DIKRMQCECTPLSKDERAQGEIACGEDCLNRLLMIECSSRCPNGDYCSNRRFQRKQHADV EVILTEKKGWGLRAAKDLPSNTFVLEYCGEVLDHKEFKARVKEYARNKNIHYYFMALKND EIIDATQKGNCSRFMNHSCEPNCETQKWTVNGQLRVGFFTTKLVPSGSELTFDYQFQRYG KEAQKCFCGSANCRGYLGGENRVSIRAAGGKMKKERSRK
>5JJY_2 Histone H3.3 (chains B) APSTGGVMKPHRYR
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 3 |
| SAH | S-adenosyl-L-homocysteine | C14 H20 N6 O5 S | 1 |
| SCN | Thiocyanate ion | C N S | 5 |
Molecular basis for oncohistone H3 recognition by SETD2 methyltransferase. Yang, S., Zheng, X., Lu, C. et al. Genes Dev (2016) 30:1611-1616. DOI 10.1101/gad.284323.116 · PubMed
Other PDB entries of the same protein (UniProt Q9BYW2 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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