Structure of PDB 7lzb Chain A Binding Site BS02
Receptor Information
>7lzb Chain A (length=235) Species:
9606
(Homo sapiens) [
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GPSCVMDDFRDPQRWKECAKQGKMPCYFDLIEENVYLTERMQCECTPLSK
DERAQGEIACGEDCLNRLLMIECSSRCPNGDYCSNRRFQRKQHADVEVIL
TEKKGWGLRAAKDLPSNTFVLEYCGEVLDHKEFKARVKEYARNKNIHYYF
MALKNDEIIDATQKGNCSRFMNHSCEPNCETQKWTVNGQLRVGFFTTKLV
PSGSELTFDYQFQRYGKEAQKCFCGSANCRGYLGG
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
7lzb Chain A Residue 1802 [
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Receptor-Ligand Complex Structure
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PDB
7lzb
Discovery of a First-in-Class Inhibitor of the Histone Methyltransferase SETD2 Suitable for Preclinical Studies.
Resolution
2.28 Å
Binding residue
(original residue number in PDB)
C1516 C1529 C1533 C1539
Binding residue
(residue number reindexed from 1)
C60 C73 C77 C83
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.1.1.-
2.1.1.359
: [histone H3]-lysine(36) N-trimethyltransferase.
Gene Ontology
Molecular Function
GO:0016279
protein-lysine N-methyltransferase activity
GO:0042054
histone methyltransferase activity
GO:0046975
histone H3K36 methyltransferase activity
Cellular Component
GO:0005634
nucleus
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:7lzb
,
PDBe:7lzb
,
PDBj:7lzb
PDBsum
7lzb
PubMed
34671445
UniProt
Q9BYW2
|SETD2_HUMAN Histone-lysine N-methyltransferase SETD2 (Gene Name=SETD2)
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