Structure of PDB 7xuc Chain A Binding Site BS03
Receptor Information
>7xuc Chain A (length=272) Species:
9606
(Homo sapiens) [
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IRTEKIICRDVARGYENVPIPCVNGVDGEPCPEDYKYISENCETSTMNID
RNITHLQHCTCVDDCSSSNCLCGQLSIRCWYDKDGRLLQEFNKPPLIFEC
NQACSCWRNCKNRVVQSGIKVRLQLYRTAKMGWGVRALQTIPQGTFICEY
VGELISDAEADVREDDSYLFDLDNKDGEVYCIDARYYGNISRFINHLCDP
NIIPVRVFMLHQDLRFPRIAFFSSRDIRTGEELGFDYGDRFWDIKSKYFT
CQCGSEKCKHSAEAIALEQSRL
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
7xuc Chain A Residue 1203 [
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Receptor-Ligand Complex Structure
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PDB
7xuc
Discovery of Novel Substrate-Competitive Lysine Methyltransferase G9a Inhibitors as Anticancer Agents.
Resolution
1.67 Å
Binding residue
(original residue number in PDB)
C974 C976 C980 C985
Binding residue
(residue number reindexed from 1)
C59 C61 C65 C70
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.1.1.-
2.1.1.367
: [histone H3]-lysine(9) N-methyltransferase.
Gene Ontology
Molecular Function
GO:0002039
p53 binding
GO:0008270
zinc ion binding
GO:0016279
protein-lysine N-methyltransferase activity
GO:0042054
histone methyltransferase activity
Cellular Component
GO:0005634
nucleus
View graph for
Molecular Function
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Cellular Component
External links
PDB
RCSB:7xuc
,
PDBe:7xuc
,
PDBj:7xuc
PDBsum
7xuc
PubMed
36882960
UniProt
Q96KQ7
|EHMT2_HUMAN Histone-lysine N-methyltransferase EHMT2 (Gene Name=EHMT2)
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