5WVO: DNMT1 RFTS domain

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.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Homo sapiens
Chains
4
Atoms
3,362
Mol. weight
49.12 kDa
Ligands
ZN
Released
15 Nov 2017

Explore 5WVO in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 4 helices, 8 β-strands

ElementResiduesLengthSheet
β-strand2-761
β-strand12-1651
β-strand2212
α-helix23-3412
α-helix38-403
β-strand41-4551
β-strand48-4921
α-helix50-512
β-strand5512
α-helix56-594
β-strand66-7161
β-strand7413
Chain B: 3 helices, 8 β-strands
ElementResiduesLengthSheet
β-strand2-764
β-strand1115
β-strand12-1654
β-strand2216
α-helix23-3412
α-helix38-403
β-strand41-4554
β-strand48-4924
α-helix50-512
β-strand5516
β-strand66-7164
Chain C: 11 helices, 14 β-strands
ElementResiduesLengthSheet
β-strand36717
β-strand37518
α-helix377-3815
α-helix384-3863
β-strand39215
α-helix402-4032
β-strand404-40968
β-strand41019
β-strand411-41448
β-strand41817
β-strand41918
β-strand433-44088
β-strand453-45868
β-strand463-46758
β-strand476-48058
β-strand485-48848
α-helix4901
β-strand49119
α-helix4921
α-helix496-51823
α-helix524-53310
α-helix535-5373
α-helix547-5515
α-helix554-56613
α-helix579-58810
Chain D: 0 helices, 2 β-strands
ElementResiduesLengthSheet
β-strand813
β-strand9-1468

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
UbiquitinA, Bprotein76Homo sapiensP62979 (AlphaFold model)
DNA (cytosine-5)-methyltransferase 1Cprotein250Homo sapiensP26358 (AlphaFold model)
Histone H3.1Dprotein37Homo sapiensP68431 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5WVO_1 Ubiquitin (chains A, B)
MQIFVKTLTGKTITLEVEPSDTIENVKAKIQDKEGIPPDQQRLIFAGKQLEDGRTLSDYN
IQKESTLHLVLRLRGC
Sequence of entity 2 (C), FASTA
>5WVO_2 DNA (cytosine-5)-methyltransferase 1 (chains C)
PKCIQCGQYLDDPDLKYGQHPPDAVDEPQMLTNEKLSIFDANESGFESYEALPQHKLTCF
SVYCKHGHLCPIDTGLIEKNIELFFSGSAKPIYDDDPSLEGGVNGKNLGPINEWWITGFD
GGEKALIGFSTSFAEYILMDPSPEYAPIFGLMQEKIYISKIVVEFLQSNSDSTYEDLINK
IETTVPPSGLNLNRFTEDSLLRHAQFVVEQVESYDEAGDSDEQPIFLTPCMRDLIKLAGV
TLGQRRAQAR
Sequence of entity 3 (D), FASTA
>5WVO_3 Histone H3.1 (chains D)
ARTKQTARKSTGGKAPRCQLATCAARKSAPATGGVKW

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn1

Primary citation

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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