Structure of PDB 6mbp Chain A Binding Site BS02
Receptor Information
>6mbp Chain A (length=261) Species:
9606
(Homo sapiens) [
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VERIVSRDIARGYERIPIPCVNAVDSEPCPSNYKYVSQNCVTSPMNIDRN
ITHLQYCVCIDDCSSSNCMCGQLSMRCWYDKDGRLLPEFNMAEPPLIFEC
NHACSCWRNCRNRVVQNGLRARLQLYRTRDMGWGVRSLQDIPPGTFVCEY
VGELISDSEADVREEDSYLFDLDNKDGEVYCIDARFYGNVSRFINHHCEP
NLVPVRVFMAHQDLRFPRIAFFSTRLIEAGEQLGFDYGERFWDIKGKLFS
CRCGSPKCRHS
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
6mbp Chain A Residue 2002 [
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Receptor-Ligand Complex Structure
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PDB
6mbp
Discovery of a Novel Chemotype of Histone Lysine Methyltransferase EHMT1/2 (GLP/G9a) Inhibitors: Rational Design, Synthesis, Biological Evaluation, and Co-crystal Structure.
Resolution
1.947 Å
Binding residue
(original residue number in PDB)
C1037 C1074 C1080 C1084
Binding residue
(residue number reindexed from 1)
C63 C100 C106 C110
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y1124 Y1211
Catalytic site (residue number reindexed from 1)
Y150 Y237
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
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Molecular Function
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Cellular Component
External links
PDB
RCSB:6mbp
,
PDBe:6mbp
,
PDBj:6mbp
PDBsum
6mbp
PubMed
30753076
UniProt
Q9H9B1
|EHMT1_HUMAN Histone-lysine N-methyltransferase EHMT1 (Gene Name=EHMT1)
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