Crystal structure of DNMT1 RFTS domain in complex with K18/K23 mono-ubiquitylated histone H3. Determined by X-ray diffraction at 2.0 Å resolution. Released 15 Nov 2017.
Explore 5WVO in 3D Show helices and sheets RCSB PDB PDBe
5WVO contains 18 α-helices and 32 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 |
|---|---|---|---|
| β-strand | 2-7 | 6 | 1 |
| β-strand | 12-16 | 5 | 1 |
| β-strand | 22 | 1 | 2 |
| α-helix | 23-34 | 12 | |
| α-helix | 38-40 | 3 | |
| β-strand | 41-45 | 5 | 1 |
| β-strand | 48-49 | 2 | 1 |
| α-helix | 50-51 | 2 | |
| β-strand | 55 | 1 | 2 |
| α-helix | 56-59 | 4 | |
| β-strand | 66-71 | 6 | 1 |
| β-strand | 74 | 1 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-7 | 6 | 4 |
| β-strand | 11 | 1 | 5 |
| β-strand | 12-16 | 5 | 4 |
| β-strand | 22 | 1 | 6 |
| α-helix | 23-34 | 12 | |
| α-helix | 38-40 | 3 | |
| β-strand | 41-45 | 5 | 4 |
| β-strand | 48-49 | 2 | 4 |
| α-helix | 50-51 | 2 | |
| β-strand | 55 | 1 | 6 |
| β-strand | 66-71 | 6 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 367 | 1 | 7 |
| β-strand | 375 | 1 | 8 |
| α-helix | 377-381 | 5 | |
| α-helix | 384-386 | 3 | |
| β-strand | 392 | 1 | 5 |
| α-helix | 402-403 | 2 | |
| β-strand | 404-409 | 6 | 8 |
| β-strand | 410 | 1 | 9 |
| β-strand | 411-414 | 4 | 8 |
| β-strand | 418 | 1 | 7 |
| β-strand | 419 | 1 | 8 |
| β-strand | 433-440 | 8 | 8 |
| β-strand | 453-458 | 6 | 8 |
| β-strand | 463-467 | 5 | 8 |
| β-strand | 476-480 | 5 | 8 |
| β-strand | 485-488 | 4 | 8 |
| α-helix | 490 | 1 | |
| β-strand | 491 | 1 | 9 |
| α-helix | 492 | 1 | |
| α-helix | 496-518 | 23 | |
| α-helix | 524-533 | 10 | |
| α-helix | 535-537 | 3 | |
| α-helix | 547-551 | 5 | |
| α-helix | 554-566 | 13 | |
| α-helix | 579-588 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 8 | 1 | 3 |
| β-strand | 9-14 | 6 | 8 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Ubiquitin | A, B | protein | 76 | Homo sapiens | P62979 (AlphaFold model) |
| DNA (cytosine-5)-methyltransferase 1 | C | protein | 250 | Homo sapiens | P26358 (AlphaFold model) |
| Histone H3.1 | D | protein | 37 | Homo sapiens | P68431 (AlphaFold model) |
>5WVO_1 Ubiquitin (chains A, B) MQIFVKTLTGKTITLEVEPSDTIENVKAKIQDKEGIPPDQQRLIFAGKQLEDGRTLSDYN IQKESTLHLVLRLRGC
>5WVO_2 DNA (cytosine-5)-methyltransferase 1 (chains C) PKCIQCGQYLDDPDLKYGQHPPDAVDEPQMLTNEKLSIFDANESGFESYEALPQHKLTCF SVYCKHGHLCPIDTGLIEKNIELFFSGSAKPIYDDDPSLEGGVNGKNLGPINEWWITGFD GGEKALIGFSTSFAEYILMDPSPEYAPIFGLMQEKIYISKIVVEFLQSNSDSTYEDLINK IETTVPPSGLNLNRFTEDSLLRHAQFVVEQVESYDEAGDSDEQPIFLTPCMRDLIKLAGV TLGQRRAQAR
>5WVO_3 Histone H3.1 (chains D) ARTKQTARKSTGGKAPRCQLATCAARKSAPATGGVKW
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 1 |
Structure of the Dnmt1 Reader Module Complexed with a Unique Two-Mono-Ubiquitin Mark on Histone H3 Reveals the Basis for DNA Methylation Maintenance. Ishiyama, S., Nishiyama, A., Saeki, Y. et al. Mol Cell (2017) 68:350-360.e7. DOI 10.1016/j.molcel.2017.09.037 · PubMed
Other PDB entries of the same protein (UniProt P62979 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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