Structure of PDB 1mvh Chain A Binding Site BS03
Receptor Information
>1mvh Chain A (length=269) Species:
4896
(Schizosaccharomyces pombe) [
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KLDSYTHLSFYEKRELFRKKLREIEGPEVTLVNEVDDEPCPSLDFQFISQ
YRLTQGVIPPDPNFQSGCNCSSLGGCDLNNPSRCECLDDLDEPTHFAYDA
QGRVRADTGAVIYECNSFCSCSMECPNRVVQRGRTLPLEIFKTKEKGWGV
RSLRFAPAGTFITCYLGEVITSAEAAKRDKNYDDDGITYLFDLDMFDDAS
EYTVDAQNYGDVSRFFNHSCSPNIAIYSAVRNHGFRTIYDLAFFAIKDIQ
PLEELTFDYAGAKDFSPVQ
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
1mvh Chain A Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
1mvh
Structure of the SET domain histone lysine methyltransferase Clr4.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
C260 C268 C276
Binding residue
(residue number reindexed from 1)
C68 C76 C84
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y357 Y451
Catalytic site (residue number reindexed from 1)
Y165 Y259
Enzyme Commision number
2.1.1.355
: [histone H3]-lysine(9) N-trimethyltransferase.
2.1.1.366
: [histone H3]-N(6),N(6)-dimethyl-lysine(9) N-methyltransferase.
2.1.1.367
: [histone H3]-lysine(9) N-methyltransferase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0042054
histone methyltransferase activity
GO:0046974
histone H3K9 methyltransferase activity
Cellular Component
GO:0005634
nucleus
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1mvh
,
PDBe:1mvh
,
PDBj:1mvh
PDBsum
1mvh
PubMed
12389037
UniProt
O60016
|CLR4_SCHPO Histone-lysine N-methyltransferase, H3 lysine-9 specific (Gene Name=clr4)
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