5LT6: Histone-lysine N-methyltransferase SETD2

Structure of the Epigenetic Oncogene MMSET and inhibition by N-Alkyl Sinefungin Derivatives. Determined by X-ray diffraction at 2.05 Å resolution. Released 5 Oct 2016.

Method
X-ray diffraction
Resolution
2.05 Å
Organism
Homo sapiens
Chains
2
Atoms
4,032
Mol. weight
69.61 kDa
Ligands
76J, SCN, ZN
Released
5 Oct 2016

Explore 5LT6 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5LT6 contains 23 α-helices and 41 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.

Chain A: 12 helices, 21 β-strands

ElementResiduesLengthSheet
β-strand1448-144921
α-helix1453-14553
α-helix1457-14659
β-strand1474-147522
β-strand1480-148123
α-helix1501-15055
α-helix1506-15105
α-helix1513-15142
α-helix1521-15244
β-strand152714
α-helix1536-15383
β-strand1552-155651
β-strand1562-156651
β-strand157015
β-strand1575-157844
β-strand1582-158433
α-helix1586-159914
β-strand1605-161063
β-strand1613-161643
β-strand1620-162122
α-helix1623-16264
β-strand1628-162926
β-strand1635-164284
β-strand1645-165284
β-strand165615
α-helix16601
β-strand1661-166221
β-strand1663-166426
α-helix1666-16683
β-strand1670-167123
β-strand1676-167727
α-helix16781
β-strand1688-168927
Chain B: 11 helices, 20 β-strands
ElementResiduesLengthSheet
β-strand1448-144928
α-helix1453-14553
α-helix1457-14659
β-strand1474-147529
β-strand1480-1481210
α-helix1501-15055
α-helix1506-15105
α-helix1513-15142
α-helix1521-15244
β-strand1527111
α-helix1536-15383
β-strand1552-155658
β-strand1562-156658
β-strand1570112
β-strand1575-1578411
β-strand1582-1584310
α-helix1586-159611
β-strand1606-1610510
β-strand1613-1616410
β-strand1620-162129
α-helix1623-16264
β-strand1628-1629213
β-strand1635-1642811
β-strand1645-1652811
β-strand1656112
α-helix16601
β-strand1661-166228
β-strand1663-1664213
α-helix1666-16683
β-strand1677114
β-strand1688114

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone-lysine N-methyltransferase SETD2A, Bprotein295Homo sapiensQ9BYW2 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5LT6_1 Histone-lysine N-methyltransferase SETD2 (chains A, B)
MHHHHHHSSGRENLYFQGETSVPPGSALVGPSCVMDDFRDPQRWKECAKQGKMPCYFDLI
EENVYLTERKKNKSHRDIKRMQCECTPLSKDERAQGEIACGEDCLNRLLMIECSSRCPNG
DYCSNRRFQRKQHADVEVILTEKKGWGLRAAKDLPSNTFVLEYCGEVLDHKEFKARVKEY
ARNKNIHYYFMALKNDEIIDATQKGNCSRFMNHSCEPNCETQKWTVNGQLRVGFFTTKLV
PSGSELTFDYQFQRYGKEAQKCFCGSANCRGYLGGENRVSIRAAGGKMKKERSRK

Ligands and cofactors

IDNameFormulaCopies
76J[(2~{S},5~{S})-1-[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxida…C20 H35 N7 O52
SCNThiocyanate ionC N S2
ZNZinc ionZn6

Primary citation

Structure of the Epigenetic Oncogene MMSET and Inhibition by N-Alkyl Sinefungin Derivatives. Tisi, D., Chiarparin, E., Tamanini, E. et al. ACS Chem Biol (2016) 11:3093-3105. DOI 10.1021/acschembio.6b00308 · 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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