Brand  (β version)

PDB ID: 5VSD

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Ligands
Code Name Style Show Link
9HJ 6,7-dimethoxy-N~2~-methyl-N~4~-(1-methylpiperidin-4-yl)-N~2~-propylquinazoline-2,4-diamine PoSSuM
DIO 1,4-diethylene dioxide PoSSuM
GOL Glycerol PoSSuM
SAM S-adenosylmethionine PoSSuM
ZN Zinc ion PoSSuM
Non-standard Residues
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Structure summary

Code : 5VSD   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/TRANSFERASE INHIBITOR
Title : Structure of human GLP SET-domain (EHMT1) in complex with inhibitor 13
Release Data : 2017-07-12
Compound :
mol_id molecule chains synonym
1 Histone-lysine N-methyltransferase EHMT1 A,B Euchromatic histone-lysine N-methyltransferase 1,Eu-HMTase1,G9a-like protein 1,GLP1,Histone H3-K9 methyltransferase 5,H3-K9-HMTase 5,Lysine N-methyltransferase 1D
ec: 2.1.1.-,2.1.1.43
fragment: GLP catalytic SET-domain residues 1006-1266
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:469008)
gene: EHMT1, EUHMTASE1, GLP, KIAA1876, KMT1D
expression_system_strain: BL21 (DE3) codon plus RIL
expression_system_vector_type: plasmid
expression_system_plasmid: pET28a-LIC
Authors : Babault, N., Xiong, Y., Liu, J., Jin, J.
Keywords : protein-small molecule inhibitor complex, TRANSFERASE-TRANSFERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.8500 Å )
Citation :

Structure-activity relationship studies of G9a-like protein (GLP) inhibitors.

Xiong, Y.,Li, F.,Babault, N.  et al.
(2017)  Bioorg. Med. Chem.  25 : 4414 - 4423

PubMed: 28662962
DOI: 10.1016/j.bmc.2017.06.021

Reaction

Chain : A, B
UniProt : Q9H9B1 (EHMT1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
N(6)-methyl-L-lysyl(9)-[histone H3] + S-adenosyl-L-methionine = H(+) + N(6),N(6)-dimethyl-L-lysyl(9)-[histone H3] + S-adenosyl-L- homocysteine - PubMed:12004135
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L-lysyl(9)-[histone H3] + S-adenosyl-L-methionine = H(+) + N(6)-methyl-L-lysyl(9)-[histone H3] + S-adenosyl-L-homocysteine 2.1.1.367 PubMed:12004135
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