5T0K: G9a SET-domain with H3K9M mutant peptide and SAM

Structure of G9a SET-domain with H3K9M mutant peptide and SAM. Determined by X-ray diffraction at 1.7 Å resolution. Released 5 Oct 2016.

Method
X-ray diffraction
Resolution
1.7 Å
Organism
Homo sapiens
Chains
4
Atoms
5,182
Mol. weight
69.38 kDa
Ligands
SAM, ZN
Released
5 Oct 2016

Explore 5T0K in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5T0K contains 27 α-helices and 43 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: 14 helices, 21 β-strands

ElementResiduesLengthSheet
β-strand92311
β-strand937-93821
α-helix944-9474
β-strand951-95222
β-strand957-95822
β-strand96713
α-helix968-9703
α-helix986-9905
β-strand99614
α-helix10011
β-strand100214
α-helix10031
α-helix1011-10133
β-strand1014-101525
α-helix1032-10343
β-strand1040-104451
β-strand1050-105451
β-strand105816
β-strand1063-106755
β-strand1069-107352
α-helix1074-10774
β-strand1086-108832
β-strand1097-110592
α-helix1107-11104
α-helix11111
β-strand1112-111327
β-strand1119-112575
β-strand1135-114065
β-strand114416
α-helix11481
β-strand114911
α-helix11501
β-strand1151-115227
α-helix1156-11627
α-helix1179-11868
Chain B: 13 helices, 20 β-strands
ElementResiduesLengthSheet
α-helix922-9243
β-strand937-93828
α-helix944-9474
β-strand951-95223
β-strand957-95823
β-strand96712
α-helix968-9703
α-helix986-9905
β-strand99619
β-strand100219
α-helix1012-10132
β-strand1014-1015210
α-helix1032-10343
β-strand1040-104458
β-strand1050-105458
β-strand1058111
β-strand1063-1067510
β-strand1069-107353
α-helix1074-10774
β-strand1086-108833
β-strand1097-110593
α-helix1107-11104
α-helix11111
β-strand1112-1113212
β-strand1119-1125710
β-strand1135-1140610
β-strand1144111
α-helix11481
β-strand114918
α-helix11501
β-strand1151-1152212
α-helix1156-11627
α-helix1179-119012
Chains P and Q: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand912

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone-lysine N-methyltransferase EHMT2A, Bprotein281Homo sapiensQ96KQ7 (AlphaFold model)
H3K9 mutant peptideP, Qprotein15Homo sapiensP68431 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5T0K_1 Histone-lysine N-methyltransferase EHMT2 (chains A, B)
NRAIRTEKIICRDVARGYENVPIPCVNGVDGEPCPEDYKYISENCETSTMNIDRNITHLQ
HCTCVDDCSSSNCLCGQLSIRCWYDKDGRLLQEFNKIEPPLIFECNQACSCWRNCKNRVV
QSGIKVRLQLYRTAKMGWGVRALQTIPQGTFICEYVGELISDAEADVREDDSYLFDLDNK
DGEVYCIDARYYGNISRFINHLCDPNIIPVRVFMLHQDLRFPRIAFFSSRDIRTGEELGF
DYGDRFWDIKSKYFTCQCGSEKCKHSAEAIALEQSRLARLD
Sequence of entity 2 (P, Q), FASTA
>5T0K_2 H3K9 mutant peptide (chains P, Q)
ARTKQTARMSTGGKA

Ligands and cofactors

IDNameFormulaCopies
SAMS-adenosylmethionineC15 H22 N6 O5 S2
ZNZinc ionZn8

Primary citation

A histone H3K9M mutation traps histone methyltransferase Clr4 to prevent heterochromatin spreading. Shan, C.M., Wang, J., Xu, K. et al. Elife (2016) 5. DOI 10.7554/eLife.17903 · PubMed

Other PDB entries of the same protein (UniProt Q96KQ7 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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